US20090258889A1 - Pesticidal compositions - Google Patents

Pesticidal compositions Download PDF

Info

Publication number
US20090258889A1
US20090258889A1 US12/418,466 US41846609A US2009258889A1 US 20090258889 A1 US20090258889 A1 US 20090258889A1 US 41846609 A US41846609 A US 41846609A US 2009258889 A1 US2009258889 A1 US 2009258889A1
Authority
US
United States
Prior art keywords
composition
mineral oil
weight
active ingredient
alcohol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/418,466
Inventor
Steven R. Sims
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Corp
Whitmire Holdings Inc
Original Assignee
Whitmire Micro Gen Research Laboratories Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Whitmire Micro Gen Research Laboratories Inc filed Critical Whitmire Micro Gen Research Laboratories Inc
Priority to US12/418,466 priority Critical patent/US20090258889A1/en
Priority to PCT/US2009/039664 priority patent/WO2009126577A2/en
Priority to MX2010011081A priority patent/MX2010011081A/en
Priority to MYPI20104721 priority patent/MY149026A/en
Priority to KR20107025258A priority patent/KR20100134105A/en
Priority to EA201201028A priority patent/EA201201028A1/en
Priority to CN2009801215262A priority patent/CN102083311A/en
Priority to AU2009233944A priority patent/AU2009233944A1/en
Priority to CN2013101326390A priority patent/CN103190446A/en
Priority to EA201201029A priority patent/EA201201029A1/en
Priority to CN2013101327181A priority patent/CN103210959A/en
Priority to BRPI0911664-8A priority patent/BRPI0911664A2/en
Priority to EP09730159A priority patent/EP2271216A4/en
Priority to EA201001616A priority patent/EA018969B1/en
Priority to CA2720953A priority patent/CA2720953A1/en
Assigned to WHITMIRE MICRO-GEN RESEARCH LABORATORIES, INC. reassignment WHITMIRE MICRO-GEN RESEARCH LABORATORIES, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SIMS, STEVEN R.
Priority to JP2011504111A priority patent/JP2011517685A/en
Priority to PH12010502295A priority patent/PH12010502295A1/en
Priority to ARP090101274 priority patent/AR071468A1/en
Priority to TW98112120A priority patent/TW200948273A/en
Priority to UY31759A priority patent/UY31759A/en
Publication of US20090258889A1 publication Critical patent/US20090258889A1/en
Assigned to WHITMIRE HOLDINGS, INC. reassignment WHITMIRE HOLDINGS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: WHITMIRE MICRO-GEN RESEARCH LABORATORIES, INC.
Assigned to BASF CORPORATION reassignment BASF CORPORATION MERGER (SEE DOCUMENT FOR DETAILS). Assignors: WHITMIRE HOLDINGS, INC.
Priority to IL208553A priority patent/IL208553A0/en
Priority to CR11720A priority patent/CR11720A/en
Priority to MA33331A priority patent/MA32292B1/en
Priority to ZA2010/08005A priority patent/ZA201008005B/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N27/00Biocides, pest repellants or attractants, or plant growth regulators containing hydrocarbons
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/02Acyclic compounds
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/02Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/32Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms six-membered rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N61/00Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action
    • A01N61/02Mineral oils; Tar oils; Tar; Distillates, extracts or conversion products thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K35/00Medicinal preparations containing materials or reaction products thereof with undetermined constitution
    • A61K35/02Medicinal preparations containing materials or reaction products thereof with undetermined constitution from inanimate materials
    • A61K35/04Tars; Bitumens; Mineral oils; Ammonium bituminosulfonate
    • A61K35/06Mineral oils, e.g. paraffinic oils or aromatic oils based on aromatic hydrocarbons
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11BPRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00Essential oils; Perfumes

Definitions

  • the present disclosure relates to pesticidal compositions and a method of controlling insects and other pests. More particularly, the disclosure relates to pesticidal compositions containing mineral oil and one or more additional components which, when used in combination, act synergistically to control pests such as arthropods.
  • insects and other arthropod pests can have negative effects on the quality of human life. For instance, when found in the home, insects and other arthropods can be a source of annoyance due purely to their presence. They may also spread disease and allergens. Additionally, when found on plants and crops, insects and other pest arthropods can destroy foliage and fruit, and may adversely affect plant and crop growth, quality, and yield.
  • insects which are particularly undesirable are domestic cockroaches. These insects produce allergens in their saliva, fecal material, cast skins and body parts which may be particularly problematic for people suffering from allergies.
  • cockroaches It is domestically and commercially desirable to control cockroaches through the use of pesticide products. It is also desirable for to control other crawling arthropods, such as ants, beetles, earwigs, silverfish, crickets, spiders, centipedes and various flying insects including flies, mosquitoes, gnats, moths, wasps, hornets, bees, and the like.
  • crawling arthropods such as ants, beetles, earwigs, silverfish, crickets, spiders, centipedes and various flying insects including flies, mosquitoes, gnats, moths, wasps, hornets, bees, and the like.
  • the present disclosure relates to pesticidal compositions and a method of controlling pests such as arthropods and, in particular, insects.
  • the pesticidal compositions of embodiments of the present disclosure are particularly effective at controlling cockroaches. More particularly, the disclosure relates to a pesticidal composition containing mineral oil and one or more additional components which, when used in combination, act synergistically to control insect and other pest populations.
  • the present disclosure is directed to a pesticidal composition
  • a pesticidal composition comprising a first active ingredient and a second active ingredient.
  • the first active ingredient is a mineral oil and the second active ingredient is an ester compound.
  • the ester compound is selected from the group consisting of ethyl lactate, ⁇ -butyrolactone, triacetin and combinations thereof.
  • the pesticidal composition comprises a first active ingredient and a second active ingredient.
  • the first active ingredient is a mineral oil and the second active ingredient is an alcohol selected from the group consisting of methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • the pesticidal composition comprises a first active ingredient and a second active ingredient.
  • the first active ingredient is a mineral oil and the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, nitromethane, acetophenone, pyridine and combinations thereof.
  • the present disclosure is directed to a method of controlling arthropods.
  • An arthropod is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and a second active ingredient.
  • the first active ingredient is a mineral oil and the second active ingredient is an ester compound.
  • an arthropod is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and a second active ingredient.
  • the first active ingredient is a mineral oil and the second active ingredient is an alcohol selected from the group consisting of methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • the arthropod is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and a second active ingredient.
  • the first active ingredient is a mineral oil and the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof.
  • a further aspect of the present disclosure is directed to a method of controlling cockroaches.
  • a cockroach is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and at least 3% of a second active ingredient by weight of the composition.
  • the first active ingredient is a mineral oil and the second active ingredient is an alcohol.
  • FIG. 1 is a chart depicting the effects of compositions comprising mineral oil and/or ethyl lactate on the mortality of adult German cockroaches as discussed in Example 1.
  • FIG. 2 is a chart depicting the effects of compositions comprising mineral oil and/or butyl lactate on the mortality of adult German cockroaches as discussed in Example 2.
  • compositions comprising mineral oil in combination with ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, ⁇ -butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol or combinations thereof are more effective at killing targeted insects and pests than compositions comprising only mineral oil or compositions comprising ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol,
  • the present disclosure is directed to a pesticidal composition
  • a pesticidal composition comprising a first active ingredient and a second active ingredient, the first active ingredient being mineral oil, and the second active ingredient being selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, ⁇ -butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol and combinations thereof.
  • the composition may be sprayed or otherwise applied directly on crawling or flying insects or other arthropod pests in sufficient concentrations to kill the pests.
  • the pesticidal compositions of the present disclosure comprise a first active ingredient which is mineral oil.
  • a first active ingredient which is mineral oil.
  • the mineral oil is PD-23 (available from Chemtura Corporation, Middlebury, Conn.).
  • PD-23 is a light grade petroleum distillate having a flash point of 230° F. (110° C.), as measured by ASTM D-92, and a vapor pressure of less than 0.1 mmHg at 20° C.
  • PD-23 is a highly refined petroleum distillate that physically resembles a very light, clear oil, and is made by fractionating oil to a narrow boiling range, then catalytically hydrotreating it to remove all aromatic and other unsaturated hydrocarbons.
  • PD-23 is hydrophobic, colorless, tasteless, virtually odorless, and color fast.
  • PD-23 generally has a low viscosity, e.g., about 2.6 centistokes (cSt) at 40° C. or a Saybolt Universal Seconds (SUS) viscosity of about 34 SUS at 100° F. (38° C.).
  • cSt centistokes
  • SUS Saybolt Universal Seconds
  • Suitable mineral oils may also be used including, for example, PD-25 and PD-28 (both available from Chemtura Corporation, Middlebury, Conn.).
  • PD-25 typically has a viscosity of about 3.5 cSt at 40° C. or about 39 SUS at 100° F. (38° C.).
  • PD-28 typically has a viscosity of about 4.2 cSt at 40° C. or about 39 SUS at 100° F. (38° C.).
  • Another suitable mineral oil is Exxsol D95 (available from Exxon Mobil).
  • Exxsol D95 is a de-aromatized petroleum distillate.
  • Exxsol D95 typically has a viscosity of about 1.92 cSt at 40° C.
  • the viscosity of the mineral oil will range from about 2.0 cSt at 40° C. to about 5.0 cSt at 40° C., and more typically will be from about 2.6 cSt at 40° C. to about 4.2 cSt at 40° C. In other embodiments the viscosity of the mineral oil is from about 1.5 cSt to about 5.0 cSt at 40° C.
  • pesticidal compositions of the present disclosure that comprise a mineral oil having a relatively low viscosity are more effective at killing pests than pesticidal compositions comprising mineral oil having a higher viscosity.
  • the pesticidal composition comprises more than one mineral oil.
  • the total amount of mineral oil present in the pesticidal composition may be at least about 5% (by weight of the composition), at least about 10% (by weight of the composition), at least about 20% (by weight of the composition), at least about 30% (by weight of the composition), at least about 40% (by weight of the composition), or even at least about 50% (by weight of the composition).
  • the pesticidal compositions will comprise from about 5% (by weight of the composition) to about 90% (by weight of the composition) of mineral oil, and more typically from about 40% (by weight of the composition) to about 80% (by weight of the composition) of mineral oil.
  • the mineral oil is a petroleum distillate composition.
  • the amount of petroleum distillate composition in the pesticidal composition may generally be the same as the amounts listed for the mineral oil as described above.
  • the pesticidal compositions of the present disclosure further comprise at least one second active ingredient selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, ⁇ -butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol and combinations thereof.
  • at least one second active ingredient selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butan
  • compositions comprising a combination of mineral oil and one or more of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol and diacetone alcohol, ⁇ -butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol, are substantially more effective in killing insects than either mineral oil in the absence of one of these second active ingredients, or any of the second active ingredients in the absence of mineral oil.
  • the pesticidal composition comprises more than one second active ingredient.
  • the additional second active ingredient or ingredients may generally be selected from the list of compounds described above or below as potential second active ingredients.
  • the total amount of second active ingredient or ingredients present in the pesticidal composition may be at least about 3% (by weight of the composition), at least about 5% (by weight of the composition), at least about 10% (by weight of the composition), at least about 20% (by weight of the composition), at least about 30% (by weight of the composition), at least about 40% (by weight of the composition), or even at least about 50% (by weight of the composition).
  • the total amount of second active ingredient present in the pesticidal compositions will typically be from about 3% (by weight of the composition) to about 95% (by weight of the composition), more typically from about 5% (by weight of the composition) to about 95% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition).
  • the amount of each particular second active ingredient present in the composition may vary depending on the ingredient, the amount of mineral oil in the composition, and whether or not more than one second active ingredient is present in the composition.
  • the second active ingredient is selected from ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene and combinations thereof. In another embodiment, the second active ingredient is selected from ethyl lactate, butyl lactate, isopropyl myristate, d-limonene and combinations thereof.
  • the second active ingredient is selected from the group consisting of ethyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene and combinations thereof and, in a further embodiment, ethyl lactate, isopropyl myristate, d-limonene and combinations thereof.
  • ethyl lactate may be present in the composition in an amount of from about 5% (by weight of the composition) to about 95% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition).
  • compositions comprising about 12.5% (by weight of the composition) mineral oil and about 37.5% (by weight of the composition) ethyl lactate, or about 25% (by weight of the composition) mineral oil and about 25% (by weight of the composition) ethyl lactate, or about 37.5% (by weight of the composition) mineral oil and about 12.5% (by weight of the composition) ethyl lactate, or about 5% (by weight of the composition) mineral oil and about 45% (by weight of the composition) ethyl lactate have been found to be particularly effective at killing insects such as cockroaches.
  • Butyl lactate may be present in the composition in an amount of from about 5% (by weight of the composition) to about 90% (by weight of the composition), more preferably from about 10% (by weight of the composition) to about 80% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition).
  • compositions comprising about 12.5% (by weight of the composition) mineral oil and about 37.5% (by weight of the composition) butyl lactate, or about 25% (by weight of the composition) mineral oil and about 25% (by weight of the composition) butyl lactate, or about 37.5% (by weight of the composition) mineral oil and about 12.5% (by weight of the composition) butyl lactate have been found to be particularly effective at killing insects such as cockroaches.
  • Isopropyl myristate may be present in the composition in an amount of from about 5% (by weight of the composition) to about 95% (by weight of the composition), more preferably from about 10% (by weight of the composition) to about 80% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition).
  • compositions comprising about 60% (by weight of the composition) mineral oil and about 20% (by weight of the composition) isopropyl myristate, or about 50% (by weight of the composition) mineral oil and about 30% (by weight of the composition) isopropyl myristate, or about 40% (by weight of the composition) mineral oil and about 40% (by weight of the composition) isopropyl myristate have been found to be particularly effective at killing insects such as cockroaches.
  • Hexylene glycol may be present in the composition in an amount of from about 5% (by weight of the composition) to about 90% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition).
  • Compositions comprising about 60% (by weight of the composition) mineral oil and about 20% (by weight of the composition) hexylene glycol have been found to be particularly effective at killing insects such as cockroaches.
  • Dioxane may be present in the composition in an amount of from about 5% (by weight of the composition) to about 80% (by weight of the composition), more preferably from about 5% (by weight of the composition) to about 60% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition).
  • Compositions comprising about 40% (by weight of the composition) mineral oil and about 40% (by weight of the composition) dioxane have been found to be particularly effective at killing insects such as cockroaches.
  • D-limonene may be present in the composition in an amount of from about 3% (by weight of the composition) to about 90% (by weight of the composition), and more preferably from about 5% (by weight of the composition) to about 90% (by weight of the composition), and more preferably from about 5% (by weight of the composition) to about 60% (by weight of the composition).
  • Compositions comprising about 40% (by weight of the composition) mineral oil and about 40% (by weight of the composition) d-limonene have been found to be particularly effective at killing insects such as cockroaches.
  • the second active ingredient is an ester compound.
  • ester compounds When ester compounds are present in the pesticidal composition as a second active ingredient, additional second active ingredients that are not ester compounds may also be present in the composition.
  • the amount of ester compounds that are present in the pesticidal composition may be at least about 50% of all the second active ingredients, at least about 65% of all the second active ingredients, at least about 75% of all the second active ingredients, at least about 85% of all the second active ingredients, at least about 95% of all the second active ingredients, or even at least about 99% of all the second active ingredients.
  • the total amount (i.e., about 100%) of second active ingredients present in the pesticidal composition is ester compounds.
  • the ester compounds present in the pesticidal composition may be selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, ⁇ -butyrolactone, triacetin and combinations thereof. These listed esters may be present in the pesticidal composition in an amount of at least about 1% by weight of the composition, at least about 3%, at least about 5%, at least about 10% or even at least about 15% by weight of the composition. In one embodiment, the ester compounds are present in an amount from about 10% to about 60% by weight of the composition.
  • ester compounds are selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate and combinations thereof. In yet another embodiment, the ester compounds are selected from the group consisting of ethyl lactate, y-butyrolactone, triacetin and combinations thereof. In yet another aspect, the ester compounds are selected from the group consisting of ethyl lactate, ⁇ -butyrolactone, triacetin and combinations thereof.
  • the second active ingredient is an alcohol.
  • the pesticidal composition may include one alcohol compound or more than one alcohol compound without departing from the scope of the present disclosure.
  • additional second active ingredients that are not alcohols may also be present in the composition.
  • the amount of alcohol present in the pesticidal composition may be at least about 50% of all the second active ingredients, at least about 65% of all the second active ingredients, at least about 75% of all the second active ingredients, at least about 85% of all the second active ingredients, at least about 95% of all the second active ingredients, or even at least about 99% of all the second active ingredients.
  • the total amount (i.e., about 100%) of second active ingredients present in the pesticidal composition is an alcohol or alcohols.
  • the alcohol utilized in the second active ingredient may be selected from the group consisting of C1-C14 saturated straight-chain alcohols, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof. These alcohols may be present in the pesticidal composition in at least about 1%, at least about 3%, at least about 5%, at least about 10% or even at least about 15% by weight of the composition. In one embodiment, the alcohols are present in an amount from about 10% to about 60% by weight of the composition.
  • the alcohol is selected from the group consisting of methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • the alcohol is selected from methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol and combinations thereof.
  • the alcohol may also be selected from the group consisting of 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • the alcohol is selected from the group consisting of C1-C14 saturated straight-chain alcohols, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • the pesticidal composition may include a plurality of alcohol compounds including a plurality of C1-C14 saturated straight chain alcohols.
  • the C1-C14 saturated straight-chain alcohol is selected from the group consisting of methanol, ethanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol and combinations thereof.
  • the alcohol is a C1-C9 saturated straight-chain alcohol and, in another embodiment, is a C1-C6 straight chain alcohol. In one embodiment, the alcohol is a C3-C7 saturated straight-chain alcohol.
  • mineral oil and a second active ingredient selected from the group consisting of C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol or diacetone alcohol may be present in the composition in a ratio based on the LD 10 or LD 50 value of the alcohol, which optimizes the biological effect of the blend.
  • the LD 10 of each of the active ingredients is determined, for instance, by the methods described in Example 9. A ratio is then determined based on about half of the LD 10 for mineral oil and about the LD 10 of the second active ingredient. For example, as detailed in Example 9, the LD 10 for PD23 mineral oil was determined to be 0.754 mg/insect and the LD 10 for diacetone alcohol was determined to be 0.255 mg/insect.
  • a ratio corresponding to the above amounts is 4 parts PD23 to 3 parts diacetone alcohol, or 4:3.
  • a composition of this particular embodiment may comprise PD23 and diacetone alcohol, among other things, in a ratio of 4:3.
  • those active ingredients may be present in the composition in a ratio of about 4:4.5 or about 1:1.
  • the ratio is determined based on the LD 10 for 1-propanol and PD23, respectively, of 0.472 mg/insect and 0.754 mg/insect.
  • About half the LD 10 of PD23 is about 0.4 mg
  • the LD 10 of 1-propanol is about 0.45 mg, giving a ratio of about 4:4.5, or about 1:1.
  • the ratio may be determined as above, but based on the LD 10 :LD 10 of the mineral oil and second active ingredient. So, for example, in a composition comprising PD23 and 1-propanol, the PD23 and 1-propanol are present in a ratio of 8:4.5, or about 2:1.
  • a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol or diacetone alcohol may be present in the composition in a ratio relative to the mineral oil in the composition, where this ratio is determined based on the LD 50 for the alcohol and the LD 50 of the mineral oil. As above with respect to ratios based on LD 10 , such ratios may be determined based on LD 50 :LD 50 ; or may alternatively be determined based on 0.5 LD 50 for mineral oil and LD 50 for the second active ingredient.
  • mineral oil and a second active ingredient selected from the group consisting of C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol or combinations thereof may be present in the composition in a ratio which may be determined based on the LD 1 o or LD 50 .
  • the second active ingredient is a compound selected from the group consisting of hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof. These listed compounds may be included with other second active ingredients.
  • the amount of the listed compounds in the pesticidal composition may be at least about 50% of all the second active ingredients, at least about 65% of all the second active ingredients, at least about 75% of all the second active ingredients, at least about 85% of all the second active ingredients, at least about 95% of all the second active ingredients, or even at least about 99% of all the second active ingredients.
  • the total amount (i.e., about 100%) of second active ingredients present in the pesticidal composition is compounds selected from hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof.
  • the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof.
  • the second active ingredient is selected from hexylene glycol, dioxane, d-limonene and combinations thereof. In a further embodiment, the second active ingredient is selected from nitromethane, acetophenone, pyridine and combinations thereof.
  • These compounds may be present in the pesticidal composition in at least about 1%, at least about 3%, at least about 5%, at least about 10% or even at least about 15% by weight of the composition. In one embodiment, the listed compounds are present in an amount from about 10% to about 60% by weight of the composition.
  • the pesticidal compositions may comprise mineral oil plus two or more of the second active ingredients.
  • the pesticidal composition comprises mineral oil, ethyl lactate, and isopropyl myristate.
  • the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 30% (by weight of the composition) of ethyl lactate, and more typically from about 5% (by weight of the composition) to about 15% (by weight of the composition) of ethyl lactate; from about 5% (by weight of the composition) to about 60% (by weight of the composition) of isopropyl myristate, and more typically from about 5% (by weight of the composition) to about 30% (by weight of the composition) of isopropyl myristate; and from about 20% (by weight of the composition) to about 70% (by weight of the composition) of mineral oil.
  • the pesticidal composition comprises mineral oil, d-limonene, and ethyl lactate.
  • the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 60% (by weight of the composition) of d-limonene, from about 5% (by weight of the composition) to about 30% (by weight of the composition) of ethyl lactate, and from about 20% (by weight of the composition) to about 90% (by weight of the composition) of mineral oil.
  • the pesticidal composition comprises mineral oil, d-limonene, and butyl lactate.
  • the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 20% (by weight of the composition) of d-limonene, from about 5% (by weight of the composition) to about 20% (by weight of the composition) of butyl lactate, and from about 30% (by weight of the composition) to about 80% (by weight of the composition) of mineral oil.
  • the pesticidal composition may comprise mineral oil, d-limonene, ethyl lactate, and isopropyl myristate.
  • the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 20% (by weight of the composition) of d-limonene, from about 5% (by weight of the composition) to about 20% (by weight of the composition) of ethyl lactate, from about 20% (by weight of the composition) to about 40% (by weight of the composition) of isopropyl myristate, and from about 30% (by weight of the composition) to about 80% (by weight of the composition) of mineral oil.
  • the pesticidal compositions of the present disclosure may further comprise a plant essential oil or derivative thereof, which may also have pesticidal properties.
  • plant essential oils or derivatives may be extracted from natural sources or synthetically made, and generally contain, as at least one major constituent, an acyclic monoterpene alcohol or aldehyde, a benzenoid aromatic compound containing at least one oxygenated substituent or side chain, or a monocarbocyclic terpene generally having a six membered ring bearing one or more oxygenated substituents.
  • oils or their derivatives include, but are not limited to, members selected from the group consisting of aldehyde C16 (pure), alpha-terpineol, amyl cinnamic aldehyde, amyl salicylate, anisic aldehyde, benzyl alcohol, benzyl acetate, cinnamaldehyde, cinnamic alcohol, carvacrol, carveol, citral, citronellal, citronellol, dimethyl salicylate, eucalyptol (cineole), eugenol, iso-eugenol, galaxolide, geraniol, guaiacol, ionone, menthol, methyl anthranilate, methyl ionone, methyl salicylate, nerol, alpha-phellandrene, pennyroyal oil, perillaldehyde, 1- or 2-phenyl ethyl alcohol
  • suitable oils include, for example, castor oil, cedar oil, cinnamon and cinnamon oil, citronella and citronella oil, cloves and clove oil, corn oil, cottonseed oil, garlic and garlic oil, geranium oil, lemongrass oil, linseed oil, mint and mint oil, peppermint and peppermint oil, rosemary and rosemary oil, sesame and sesame oil, soybean oil, white pepper, and the like.
  • the plant essential oil or derivative is geraniol.
  • the pesticidal compositions will typically comprise from about 1% (by weight of the composition) to about 60% (by weight of the composition of the plant essential oil or derivative, more typically from about 2% (by weight of the composition) to about 60% (by weight of the composition), and more typically from about 2% (by weight of the composition) to about 20% (by weight of the composition) of the plant essential oil or derivative.
  • the pesticidal composition includes a first active ingredient that is a mineral oil, at least one second active ingredient that is selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, and combinations thereof and a third active ingredient that is a plant essential oil or derivative.
  • the plant essential oil or derivative is geraniol.
  • the composition also includes nerol.
  • the composition comprises from about 10% to about 70% of the first ingredient by weight of the composition, from about 5% to about 50% of the second ingredient by weight of the composition and from about 0.5% to about 15% of the third active ingredient by weight of the composition.
  • the amount of geraniol present in the composition may be at least about 2% by weight of the composition, at least about 4% or at least about 6% by weight of the composition. In one embodiment, the amount of geraniol present in the composition is from about 0.5% to about 8% by weight of the composition. Nerol may be present in the composition in an amount from about 0.5% to about 3% by weight of the composition.
  • the pesticidal composition comprises mineral oil, and at least two second active ingredients, each second active ingredient being selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, and combinations thereof and a third active ingredient that is a plant essential oil or derivative.
  • the plant essential oil or derivative is geraniol.
  • the composition also includes nerol.
  • the pesticidal composition comprises a mineral oil, ethyl lactate, isopropyl myristate and geraniol.
  • the composition may also include nerol.
  • Additional additives may include essential oils such as lemongrass oil and carbon dioxide (described below).
  • the pesticidal composition comprises, by weight of the composition, about 43% mineral oil, about 15% ethyl lactate, about 30% isopropyl myristate and about 6% geraniol.
  • the composition may also include about 3% nerol and about 1% lemongrass oil.
  • the pesticidal composition may further comprise other known insecticidal or pesticidal agents, including, for example, synergists such as piperonyl butoxide, MGK 264, and dillapiol; as well as other plant-derived insecticidal or pesticidal materials such as pyrethrum.
  • synergists such as piperonyl butoxide, MGK 264, and dillapiol
  • other plant-derived insecticidal or pesticidal materials such as pyrethrum.
  • the composition may also comprise an amount of water.
  • the composition contains water in an amount of, by weight of the composition, at least about 10%, at least about 25%, at least about 50% or even at least about 75%.
  • the amount of water in the solution is from about 10% to about 50% by weight of the composition and, in another embodiment, from about 25% to about 75% by weight of the composition.
  • compositions of the present disclosure may further comprise a suitable solvent, carrier or emulsifier.
  • suitable solvents or carriers include water, acetone, alcohols such as ethanol and isopropyl alcohol, dimethyl ether, and chlorinated hydrocarbon solvents such as methylene chloride and methyl chloroform.
  • emulsifiers would include soaps (such as fatty acid soaps), cationic, ionic and non-ionic compounds.
  • Additional carriers for use in various granular formulations include, for example, corn cob grits, diatomaceous earth, sand, clay, and the like.
  • the pesticidal compositions of the present disclosure may be dispensed in any conventional manner, e.g., from a standard pump-spray container.
  • the pesticide is in a ready-to-use form in which the composition does not need to be diluted before application.
  • the pesticidal composition may be in a concentrate form. The end-user of the concentrate composition may dilute the concentrate prior to use by, for example, addition of water.
  • the pesticidal composition is diluted in the pump spray bottle.
  • the concentrate pesticidal composition may be diluted by addition of water in an amount of, by weight of the concentrate composition, at least about 40%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200% or even at least about 300%.
  • dilution may cause formation of a water-concentrate emulsion.
  • the pesticidal concentrate may include emulsifiers such as surfactants (e.g., surfactants such as fatty acid soaps).
  • emulsifiers such as surfactants (e.g., surfactants such as fatty acid soaps).
  • Suitable compounds may be cationic, ionic, and non-ionic.
  • Suitable emulsifying compounds include alkyl arly sulionate-based emulsifiers, polyoxyethylenes and long-chain alcohols.
  • the pesticidal composition is packaged in a pressurized container such as a conventional aerosol container or the like.
  • the composition may be pressurized utilizing any suitable propellant.
  • suitable propellants include expandable gases such as carbon dioxide, nitrogen, propane, n-butane, isobutane, blends of propane and butane, HFC-152a (difluoroethane), HFC-134a (1,1,1,2-tetrafluoroethane), and combinations thereof.
  • the gasser-shaker method may be used. This method involves shaking or agitating the container and its contents as the carbon dioxide (or other gas) is forced into the container through a valve, with the rest of the composition having been introduced into the container prior to installation of the valve.
  • the rate of injection of the gas depends on the valve orifice size, and the shaking time depends on the container size, the amount of liquid, and the degree of agitation, as well as the temperature.
  • the pesticidal composition may be saturated with carbon dioxide prior to introduction into the container, and then pumped under pressure to a rotary undercap filler and filled as in a normal undercap operation, or pressured into containers already equipped with valves.
  • Other suitable methods known in the art may also be used.
  • propellants which may be used are known in the art and include, for example, dimethyl ether, methyl ethyl ether, nitrous oxide, and the like.
  • the composition will comprise propellant in an amount of from about 2% (by weight of the composition) to about 90% (by weight of the composition), and more typically in an amount of from about 2% (by weight of the composition) to about 10% (by weight of the composition).
  • the pesticidal compositions of the present disclosure may be sprayed or otherwise contacted with insects or other pests to effectively control insect or other pest populations.
  • the present disclosure is directed to a method of controlling insects and pests. The method comprises contacting the insects and pests with a pesticidally effective amount of a composition of the present disclosure.
  • an arthropod is contacted with the pesticidal composition in a pesticidally effective amount.
  • a “pesticidally effective amount” of the composition includes amounts that repel the arthropod or other pest and may include, in another embodiment, amounts of the composition that kill the arthropod or other pest.
  • the pesticidal compositions of embodiments of the present disclosure may be used to control arthropods and, in another embodiment, to control insects.
  • the pesticidal composition is used to control cockroaches.
  • Control of the pest may include contacting the pest with the pesticidal composition.
  • the pest is contacted with the pesticidal composition by spraying the composition directly on the crawling arthropod, flying insect or other pest.
  • the composition may be sprayed in a sufficient amount to cause death.
  • the pesticidal composition may also be sprayed in locations at which the pest is likely to come into contact with the composition.
  • the amount of the pesticidal composition required to kill insects or other pests and the time until pest death will vary depending on the composition components, the type of insect species and its life stage, and the like.
  • the time required to kill a pest contacted with the pesticidal composition of the present disclosure will typically range from mere seconds to several hours.
  • the pesticidal compositions of the present disclosure are particularly effective against cockroaches, including the species Periplaneta Americana (American cockroach), Blattella germanica (German cockroach), Blattella asahinai (Asian cockroach), and Blatta orientalis (Oriental cockroach).
  • the pesticidal compositions may also be used against a wide variety of other crawling insects or other arthropods, such as ants, water bugs, silverfish, crickets, spiders, ticks, mites, sowbugs, pillbugs, beetles, earwigs, centipedes, and the like.
  • water bugs refers to aquatic insects in the order Hemiptera.
  • the pesticidal compositions are effective against various flying insects including flies, mosquitoes, gnats, moths, wasps, hornets, bees, and the like.
  • the pesticidal compositions of the present disclosure generally result in at least 80% mortality, more preferably at least 95% mortality, and more preferably 100% mortality of the insects on contact, depending on the specific composition, the amount of composition applied to the insect and the insect species and life stage.
  • the mineral oil used in the following examples was PD-23 (available from Chemtura Corporation, Middlebury, Conn.), which is a light grade petroleum distillate having a flash point of 230° F. (110° C.), as measured by ASTM D-92, and a vapor pressure of less than 0.1 mmHg at 20° C.
  • PD-23 is a highly refined petroleum distillate that resembles a very clear oil, and is made by fractionating oil to a narrow boiling range, then catalytically hydrotreating it to remove all aromatic and other unsaturated hydrocarbons.
  • PD-23 is hydrophobic, colorless, tasteless, virtually odorless, and color fast.
  • compositions comprising various concentrations of mineral oil and/or ethyl lactate at killing German cockroaches was tested.
  • compositions comprising mineral oil and/or ethyl lactate in the following concentrations were prepared: 100% (wt/wt) mineral oil/0% (wt/wt) ethyl lactate; 90% (wt/wt) mineral oil/10% (wt/wt) ethyl lactate; 75% (wt/wt) mineral oil/25% (wt/wt) ethyl lactate; 50% (wt/wt) mineral oil/50% (wt/wt) ethyl lactate; 25% (wt/wt) mineral oil/75% (wt/wt) ethyl lactate; 10% (wt/wt) mineral oil/90% (wt/wt) ethyl lactate; 0% (wt/wt) mineral oil/100% (wt/wt) ethyl lactate.
  • the ethyl lactate was obtained from Vertech Biosolvents, Inc., Downers Grove, Ill.
  • each composition containing either mineral oil, ethyl lactate, or a combination of mineral oil and ethyl lactate was diluted by 50% by mixing the composition with acetone in a 1:1 ratio (wt/wt) to reduce viscosity prior to application of the compositions to the cockroaches.
  • the amount of mineral oil, ethyl lactate, and acetone present in the final composition (A-G) is set forth below in Table 1.
  • Toxicity evaluations were performed on 7-14 day old adult male and female German cockroaches (SCJ Strain, S.C. Johnson & Son, Racine, Wis.). Approximately 12 cockroaches were transferred to individual 100 ⁇ 20 mm polystyrene Petri dishes and anesthetized with a 15-25 second exposure to carbon dioxide. The inside edge of each Petri dish was lightly coated with mineral oil plus petroleum jelly in a 1:3 (wt/wt) ratio to minimize escape.
  • cockroaches were positioned with their ventral side up, and a 1 ⁇ l drop of the diluted test composition was applied to the area between the meso- and metathoracic legs using a Rainin L-10, 10 ⁇ l capacity pipette (Rainin Instrument, LLC, Oakland, Calif.). Five replications of 12 male cockroaches were done for each test composition. Separate tests were done using female cockroaches. Results were evaluated at 24 hours following treatment. Cockroaches were scored as either alive (dorsal side up, active movement when abdomen prodded with dissecting probe) or moribund/dead (dorsal side up and no movement when abdomen prodded or ventral side up and insect unable to right itself).
  • Results are shown in FIG. 1 and Table 1, which lists the number of dead cockroaches out of 60 total cockroaches for each test performed using the diluted test compositions (A-G).
  • composition C-F containing both mineral oil and ethyl lactate
  • composition G ethyl lactate
  • compositions comprising various concentrations of mineral oil and/or butyl lactate at killing cockroaches was tested.
  • compositions comprising mineral oil and/or butyl lactate in the following concentrations were prepared: 100% (wt/wt) mineral oil/0% (wt/wt) butyl lactate; 90% (wt/wt) mineral oil/10% (wt/wt) butyl lactate; 75% (wt/wt) mineral oil/25% (wt/wt) butyl lactate; 50% (wt/wt) mineral oil/50% (wt/wt) butyl lactate; 25% (wt/wt) mineral oil/75% (wt/wt) butyl lactate; 10% (wt/wt) mineral oil/90% (wt/wt) butyl lactate; 0% (wt/wt) mineral oil/ 100% (wt/wt) butyl lactate.
  • the butyl lactate was obtained from Vertech Biosolvents, Inc., Downers Grove, Ill.
  • each composition containing either mineral oil, butyl lactate, or a combination of mineral oil and butyl lactate was diluted by 50% by mixing the composition with acetone in a 1:1 ratio (wt/wt) to reduce viscosity prior to application of the composition to the cockroaches.
  • the amount of mineral oil, butyl lactate, and acetone present in the final compositions (H-N) is set forth below in Table 2.
  • composition H cockroaches treated with test composition J-L (containing both mineral oil and butyl lactate) had significantly higher mortality rates than cockroaches treated with only mineral oil (composition H) or only butyl lactate (composition N), indicating a synergistic effect when the combination of mineral oil and butyl lactate is used.
  • compositions comprising various concentrations of mineral oil and/or hexylene glycol at killing cockroaches was tested.
  • compositions comprising mineral oil, hexylene glycol, or a combination of mineral oil and hexylene glycol were prepared.
  • the amount of mineral oil and/or hexylene glycol in each composition is set forth below in Table 3, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 3, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing.
  • Table 3 lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • cockroaches treated with compositions containing both mineral oil and hexylene glycol had significantly higher mortality rates than cockroaches treated with only mineral oil or only hexylene glycol, indicating a synergistic effect when the combination of mineral oil and hexylene glycol is used.
  • compositions comprising various concentrations of mineral oil and/or isopropyl myristate at killing cockroaches was tested.
  • compositions comprising mineral oil, isopropyl myristate, or a combination of mineral oil and isopropyl myristate were prepared.
  • the amount of mineral oil and/or isopropyl myristate in each composition is set forth below in Table 4, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 4, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing.
  • Table 4 lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • cockroaches treated with compositions containing both mineral oil and isopropyl myristate at all tested concentrations had significantly higher mortality rates than cockroaches treated with only mineral oil or only isopropyl myristate, indicating a synergistic effect when the combination of mineral oil and isopropyl myristate is used.
  • compositions comprising various concentrations of mineral oil and/or dioxane at killing cockroaches was tested.
  • compositions comprising mineral oil, dioxane, or a combination of mineral oil and dioxane were prepared.
  • the amount of mineral oil and/or dioxane in each composition is set forth below in Table 6, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 6, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 6, which lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • cockroaches treated with compositions containing both mineral oil and dioxane had significantly higher mortality rates than cockroaches treated with only mineral oil or only dioxane, indicating a synergistic effect when the combination of mineral oil and dioxane is used.
  • compositions comprising various concentrations of mineral oil and/or d-limonene at killing cockroaches was tested.
  • compositions comprising mineral oil, d-limonene, or a combination of mineral oil and d-limonene were prepared.
  • the amount of mineral oil and/or d-limonene in each composition is set forth below in Table 7, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 7, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 7, which lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • cockroaches treated with compositions containing both mineral oil and d-limonene had significantly higher mortality rates than cockroaches treated with only mineral oil or only d-limonene, indicating a synergistic effect when the combination of mineral oil and d-limonene is used.
  • compositions comprising various types of mineral oil were tested.
  • compositions comprising one of three different types of mineral oil in varying concentrations were prepared.
  • the mineral oils used in this example were PD-23 (Sample No. 88446, 1997, available from Chemtura Corporation, Middlebury, Conn.), which is a low viscosity (e.g., about 2.6 cSt at 40° C. or about 34 SUS at 100° F. (38° C.)) petroleum distillate; PD-25 (Sample No. 88447, available from Chemtura Corporation, Middlebury, Conn.), which is a medium viscosity (e.g., about 3.5 cSt at 40° C. or about 39 SUS at 100° F.
  • Tests were generally performed as described in Example 1, except 2 ⁇ l of the compositions were applied to each cockroach, the number of cockroaches (all male) tested for each diluted composition is set forth below in Table 9, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 9.
  • compositions containing the higher concentration of mineral oil were more effective against adult German cockroaches than the lower concentration compositions (i.e., the 20% compositions).
  • the 20% compositions only the PD-23 had any effect against the cockroaches.
  • an aerosol pesticidal composition of the present disclosure was prepared.
  • the ingredients and amounts used to prepare the composition are set forth in Table 10 below.
  • the composition was prepared by mixing the mineral oil, ethyl lactate, isopropyl myristate and geraniol together until homogenous.
  • the resulting composition was placed in an aerosol can.
  • the lid and actuator of the aerosol can were sealed onto the top of the can.
  • the carbon dioxide was introduced into the can through the actuator to pressurize the can.
  • the resulting product can be used as an aerosol spray pesticidal composition.
  • PD23 and PD28 mineral oils were obtained from Sonneborn LLC, Mahwah, N.J. The physical properties of these oils are shown in Table 11. Each mineral oil was tested to determine the LD 50 and LD 10 (Table 12).
  • the alcohols tested comprise C1-C14 saturated straight chain alcohols, and alcohols selected from the group consisting of isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol and diacetone alcohol.
  • the tested alcohols were obtained from Sigma-Aldrich Corp., St. Louis, Mo. Each alcohol was tested to determine the LD 50 and LD 10 (Table 12).
  • the dose-response mortality data were analyzed using probit analysis (PoloPlus ⁇ , LeOra Software Co., Petaluma Calif., 2003) to estimate LD 50 and LD 10 values and their 95% confidence intervals.
  • compositions comprising various alcohols and/or mineral oil at killing cockroaches was tested.
  • compositions comprising alcohol and/or mineral oil are described in Table 13. The tests were performed as described in Example 1.
  • the composite data for certain compositions is presented below (Table 14), also including the calculated proportion of cockroaches dead at 24 hours for the group treated with alcohol alone and for the group treated with the composition comprising PD23 and alcohol.
  • Table 14 The difference between the proportion of dead cockroaches in the group treated with the composition comprising PD23 and alcohol and the group treated with alcohol alone was calculated, and is also presented in Table 14.
  • the increase in mortality indicates a synergistic effect with the combination compared to the alcohol or mineral oil alone, with a higher difference indicating a greater synergy.
  • the straight chain saturated alcohols with chain lengths of C3-C7 demonstrated the greatest increase, or difference, in mortality when combined with PD23 mineral oil, as compared to the other alcohols tested.
  • an aerosol pesticidal composition of the present disclosure was prepared.
  • the ingredients and amounts used to prepare the composition are set forth in Table 15 below.
  • the composition was prepared by mixing a geraniol/nerol composition with the mineral oil, ethyl lactate, isopropyl myristate and lemongrass oil until homogenous.
  • the resulting composition was placed in an aerosol can.
  • the lid and actuator of the aerosol can were sealed onto the top of the can.
  • the carbon dioxide was introduced into the can through the actuator to pressurize the can.
  • the resulting product can be used as an aerosol pesticidal composition.
  • compositions comprising various compounds and/or mineral oil at killing cockroaches was tested.
  • the compounds tested are shown in Table 16. The tests were performed as described in Example 1.
  • the composite data for certain compositions is presented below (Table 17), also including the calculated proportion of cockroaches dead at 24 hours for the group treated with the specific compounds alone and for the group treated with the composition comprising PD23 and the compound.
  • Table 17 The difference between the proportion of dead cockroaches in the group treated with the composition comprising PD23 and the compounds and the group treated with the compounds alone was calculated, and is also presented in Table 17.
  • the increase in mortality indicates a synergistic effect with the combination compared to the tested compound or mineral oil alone, with a higher difference indicating a greater synergy.
  • ⁇ -butyrolactone, nitromethane, acetophenone, triacetin, pyridine and 2-ethoxyethanol demonstrated the greatest increase in mortality when combined with PD23 mineral oil, as compared to the other compounds tested.

Abstract

The present disclosure relates to pesticidal compositions and to methods for controlling pests such as insects and other arthropods. More particularly, the disclosure relates to a pesticidal compositions containing mineral oil and one or more additional components which, when used in combination, act synergistically to control insect and pest populations.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application claims the benefit of U.S. Provisional Application No. 61/044,297 filed Apr. 11, 2008 and U.S. Provisional Application No. 61/115,231, filed Nov. 17, 2008.
  • BACKGROUND OF THE DISCLOSURE
  • The present disclosure relates to pesticidal compositions and a method of controlling insects and other pests. More particularly, the disclosure relates to pesticidal compositions containing mineral oil and one or more additional components which, when used in combination, act synergistically to control pests such as arthropods.
  • Insects and other arthropod pests can have negative effects on the quality of human life. For instance, when found in the home, insects and other arthropods can be a source of annoyance due purely to their presence. They may also spread disease and allergens. Additionally, when found on plants and crops, insects and other pest arthropods can destroy foliage and fruit, and may adversely affect plant and crop growth, quality, and yield.
  • Among the insects which are particularly undesirable are domestic cockroaches. These insects produce allergens in their saliva, fecal material, cast skins and body parts which may be particularly problematic for people suffering from allergies.
  • It is domestically and commercially desirable to control cockroaches through the use of pesticide products. It is also desirable for to control other crawling arthropods, such as ants, beetles, earwigs, silverfish, crickets, spiders, centipedes and various flying insects including flies, mosquitoes, gnats, moths, wasps, hornets, bees, and the like.
  • A broad range of compounds have been found to be toxic to insects and other arthropods such that formulations containing the compounds may be used for their control. However, most compounds damage the environment and adversely affect human health. There is a need for new pesticides which are generally safe to the environment and non-toxic to humans and animals and which are effective at controlling insect and other pest populations.
  • SUMMARY OF THE DISCLOSURE
  • The present disclosure relates to pesticidal compositions and a method of controlling pests such as arthropods and, in particular, insects. The pesticidal compositions of embodiments of the present disclosure are particularly effective at controlling cockroaches. More particularly, the disclosure relates to a pesticidal composition containing mineral oil and one or more additional components which, when used in combination, act synergistically to control insect and other pest populations.
  • In one aspect, the present disclosure is directed to a pesticidal composition comprising a first active ingredient and a second active ingredient. The first active ingredient is a mineral oil and the second active ingredient is an ester compound. The ester compound is selected from the group consisting of ethyl lactate, γ-butyrolactone, triacetin and combinations thereof.
  • In another aspect, the pesticidal composition comprises a first active ingredient and a second active ingredient. The first active ingredient is a mineral oil and the second active ingredient is an alcohol selected from the group consisting of methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • In yet another aspect, the pesticidal composition comprises a first active ingredient and a second active ingredient. The first active ingredient is a mineral oil and the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, nitromethane, acetophenone, pyridine and combinations thereof.
  • In another aspect, the present disclosure is directed to a method of controlling arthropods. An arthropod is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and a second active ingredient. The first active ingredient is a mineral oil and the second active ingredient is an ester compound.
  • In a further aspect of the method, an arthropod is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and a second active ingredient. The first active ingredient is a mineral oil and the second active ingredient is an alcohol selected from the group consisting of methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • In yet another aspect of the method, the arthropod is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and a second active ingredient. The first active ingredient is a mineral oil and the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof.
  • A further aspect of the present disclosure is directed to a method of controlling cockroaches. A cockroach is contacted with a pesticidally effective amount of a composition comprising a first active ingredient and at least 3% of a second active ingredient by weight of the composition. The first active ingredient is a mineral oil and the second active ingredient is an alcohol.
  • Other objects and features will be in part apparent and in part pointed out hereinafter.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • FIG. 1 is a chart depicting the effects of compositions comprising mineral oil and/or ethyl lactate on the mortality of adult German cockroaches as discussed in Example 1.
  • FIG. 2 is a chart depicting the effects of compositions comprising mineral oil and/or butyl lactate on the mortality of adult German cockroaches as discussed in Example 2.
  • DETAILED DESCRIPTION OF THE DISCLOSURE
  • In accordance with the present disclosure, it has now been found that the combination of mineral oil and one or more additional compounds selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, and combinations thereof, is effective for use in controlling insect and other pest populations. In particular, it has been discovered that compositions comprising mineral oil in combination with ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, γ-butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol or combinations thereof are more effective at killing targeted insects and pests than compositions comprising only mineral oil or compositions comprising ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, γ-butyrolactone, nitromethane, acetophenone, triacetin, pyridine, or 2-ethoxyethanol but no mineral oil. Advantageously, the compositions of the present disclosure also have a generally lower or reduced non-target (e.g., humans, other mammals, birds and reptiles) toxicity as compared to many other known pest control materials.
  • Thus, in one aspect, the present disclosure is directed to a pesticidal composition comprising a first active ingredient and a second active ingredient, the first active ingredient being mineral oil, and the second active ingredient being selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, γ-butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol and combinations thereof. The composition may be sprayed or otherwise applied directly on crawling or flying insects or other arthropod pests in sufficient concentrations to kill the pests.
  • As noted above, the pesticidal compositions of the present disclosure comprise a first active ingredient which is mineral oil. Any type of mineral oil may be used in the pesticidal compositions. In one preferred embodiment, the mineral oil is PD-23 (available from Chemtura Corporation, Middlebury, Conn.). PD-23 is a light grade petroleum distillate having a flash point of 230° F. (110° C.), as measured by ASTM D-92, and a vapor pressure of less than 0.1 mmHg at 20° C. PD-23 is a highly refined petroleum distillate that physically resembles a very light, clear oil, and is made by fractionating oil to a narrow boiling range, then catalytically hydrotreating it to remove all aromatic and other unsaturated hydrocarbons. PD-23 is hydrophobic, colorless, tasteless, virtually odorless, and color fast. PD-23 generally has a low viscosity, e.g., about 2.6 centistokes (cSt) at 40° C. or a Saybolt Universal Seconds (SUS) viscosity of about 34 SUS at 100° F. (38° C.).
  • Other types of suitable mineral oils may also be used including, for example, PD-25 and PD-28 (both available from Chemtura Corporation, Middlebury, Conn.). PD-25 typically has a viscosity of about 3.5 cSt at 40° C. or about 39 SUS at 100° F. (38° C.). PD-28 typically has a viscosity of about 4.2 cSt at 40° C. or about 39 SUS at 100° F. (38° C.). Another suitable mineral oil is Exxsol D95 (available from Exxon Mobil). Exxsol D95 is a de-aromatized petroleum distillate. Exxsol D95 typically has a viscosity of about 1.92 cSt at 40° C.
  • Typically, the viscosity of the mineral oil will range from about 2.0 cSt at 40° C. to about 5.0 cSt at 40° C., and more typically will be from about 2.6 cSt at 40° C. to about 4.2 cSt at 40° C. In other embodiments the viscosity of the mineral oil is from about 1.5 cSt to about 5.0 cSt at 40° C. In general, it has been determined that pesticidal compositions of the present disclosure that comprise a mineral oil having a relatively low viscosity are more effective at killing pests than pesticidal compositions comprising mineral oil having a higher viscosity.
  • In one embodiment, the pesticidal composition comprises more than one mineral oil. The total amount of mineral oil present in the pesticidal composition may be at least about 5% (by weight of the composition), at least about 10% (by weight of the composition), at least about 20% (by weight of the composition), at least about 30% (by weight of the composition), at least about 40% (by weight of the composition), or even at least about 50% (by weight of the composition).
  • Typically, the pesticidal compositions will comprise from about 5% (by weight of the composition) to about 90% (by weight of the composition) of mineral oil, and more typically from about 40% (by weight of the composition) to about 80% (by weight of the composition) of mineral oil.
  • In some embodiments, the mineral oil is a petroleum distillate composition. The amount of petroleum distillate composition in the pesticidal composition may generally be the same as the amounts listed for the mineral oil as described above.
  • In addition to mineral oil, the pesticidal compositions of the present disclosure further comprise at least one second active ingredient selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, γ-butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol and combinations thereof. Advantageously, these second active ingredients act synergistically with mineral oil to provide a pesticidal composition that is effective in controlling insect and other pest populations. Surprisingly, as can be seen from the examples set forth hereinafter, compositions comprising a combination of mineral oil and one or more of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol and diacetone alcohol, γ-butyrolactone, nitromethane, acetophenone, triacetin, pyridine, 2-ethoxyethanol, are substantially more effective in killing insects than either mineral oil in the absence of one of these second active ingredients, or any of the second active ingredients in the absence of mineral oil.
  • In one embodiment, the pesticidal composition comprises more than one second active ingredient. The additional second active ingredient or ingredients may generally be selected from the list of compounds described above or below as potential second active ingredients.
  • The total amount of second active ingredient or ingredients present in the pesticidal composition may be at least about 3% (by weight of the composition), at least about 5% (by weight of the composition), at least about 10% (by weight of the composition), at least about 20% (by weight of the composition), at least about 30% (by weight of the composition), at least about 40% (by weight of the composition), or even at least about 50% (by weight of the composition).
  • The total amount of second active ingredient present in the pesticidal compositions will typically be from about 3% (by weight of the composition) to about 95% (by weight of the composition), more typically from about 5% (by weight of the composition) to about 95% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition).
  • The amount of each particular second active ingredient present in the composition may vary depending on the ingredient, the amount of mineral oil in the composition, and whether or not more than one second active ingredient is present in the composition.
  • In one embodiment, the second active ingredient is selected from ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene and combinations thereof. In another embodiment, the second active ingredient is selected from ethyl lactate, butyl lactate, isopropyl myristate, d-limonene and combinations thereof. In yet another embodiment, the second active ingredient is selected from the group consisting of ethyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene and combinations thereof and, in a further embodiment, ethyl lactate, isopropyl myristate, d-limonene and combinations thereof.
  • Typically, ethyl lactate may be present in the composition in an amount of from about 5% (by weight of the composition) to about 95% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition). Compositions comprising about 12.5% (by weight of the composition) mineral oil and about 37.5% (by weight of the composition) ethyl lactate, or about 25% (by weight of the composition) mineral oil and about 25% (by weight of the composition) ethyl lactate, or about 37.5% (by weight of the composition) mineral oil and about 12.5% (by weight of the composition) ethyl lactate, or about 5% (by weight of the composition) mineral oil and about 45% (by weight of the composition) ethyl lactate have been found to be particularly effective at killing insects such as cockroaches.
  • Butyl lactate may be present in the composition in an amount of from about 5% (by weight of the composition) to about 90% (by weight of the composition), more preferably from about 10% (by weight of the composition) to about 80% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition). Compositions comprising about 12.5% (by weight of the composition) mineral oil and about 37.5% (by weight of the composition) butyl lactate, or about 25% (by weight of the composition) mineral oil and about 25% (by weight of the composition) butyl lactate, or about 37.5% (by weight of the composition) mineral oil and about 12.5% (by weight of the composition) butyl lactate have been found to be particularly effective at killing insects such as cockroaches.
  • Isopropyl myristate may be present in the composition in an amount of from about 5% (by weight of the composition) to about 95% (by weight of the composition), more preferably from about 10% (by weight of the composition) to about 80% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition). Compositions comprising about 60% (by weight of the composition) mineral oil and about 20% (by weight of the composition) isopropyl myristate, or about 50% (by weight of the composition) mineral oil and about 30% (by weight of the composition) isopropyl myristate, or about 40% (by weight of the composition) mineral oil and about 40% (by weight of the composition) isopropyl myristate have been found to be particularly effective at killing insects such as cockroaches.
  • Hexylene glycol may be present in the composition in an amount of from about 5% (by weight of the composition) to about 90% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition). Compositions comprising about 60% (by weight of the composition) mineral oil and about 20% (by weight of the composition) hexylene glycol have been found to be particularly effective at killing insects such as cockroaches.
  • Dioxane may be present in the composition in an amount of from about 5% (by weight of the composition) to about 80% (by weight of the composition), more preferably from about 5% (by weight of the composition) to about 60% (by weight of the composition), and more preferably from about 10% (by weight of the composition) to about 60% (by weight of the composition). Compositions comprising about 40% (by weight of the composition) mineral oil and about 40% (by weight of the composition) dioxane have been found to be particularly effective at killing insects such as cockroaches.
  • D-limonene may be present in the composition in an amount of from about 3% (by weight of the composition) to about 90% (by weight of the composition), and more preferably from about 5% (by weight of the composition) to about 90% (by weight of the composition), and more preferably from about 5% (by weight of the composition) to about 60% (by weight of the composition). Compositions comprising about 40% (by weight of the composition) mineral oil and about 40% (by weight of the composition) d-limonene have been found to be particularly effective at killing insects such as cockroaches.
  • In one embodiment, the second active ingredient is an ester compound. When ester compounds are present in the pesticidal composition as a second active ingredient, additional second active ingredients that are not ester compounds may also be present in the composition. The amount of ester compounds that are present in the pesticidal composition may be at least about 50% of all the second active ingredients, at least about 65% of all the second active ingredients, at least about 75% of all the second active ingredients, at least about 85% of all the second active ingredients, at least about 95% of all the second active ingredients, or even at least about 99% of all the second active ingredients. In one embodiment, the total amount (i.e., about 100%) of second active ingredients present in the pesticidal composition is ester compounds.
  • The ester compounds present in the pesticidal composition may be selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, γ-butyrolactone, triacetin and combinations thereof. These listed esters may be present in the pesticidal composition in an amount of at least about 1% by weight of the composition, at least about 3%, at least about 5%, at least about 10% or even at least about 15% by weight of the composition. In one embodiment, the ester compounds are present in an amount from about 10% to about 60% by weight of the composition.
  • In another embodiment, the ester compounds are selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate and combinations thereof. In yet another embodiment, the ester compounds are selected from the group consisting of ethyl lactate, y-butyrolactone, triacetin and combinations thereof. In yet another aspect, the ester compounds are selected from the group consisting of ethyl lactate, γ-butyrolactone, triacetin and combinations thereof.
  • In one embodiment, the second active ingredient is an alcohol. The pesticidal composition may include one alcohol compound or more than one alcohol compound without departing from the scope of the present disclosure. When alcohols are present in the pesticidal composition as a second active ingredient, additional second active ingredients that are not alcohols may also be present in the composition. The amount of alcohol present in the pesticidal composition may be at least about 50% of all the second active ingredients, at least about 65% of all the second active ingredients, at least about 75% of all the second active ingredients, at least about 85% of all the second active ingredients, at least about 95% of all the second active ingredients, or even at least about 99% of all the second active ingredients. In one embodiment, the total amount (i.e., about 100%) of second active ingredients present in the pesticidal composition is an alcohol or alcohols.
  • The alcohol utilized in the second active ingredient may be selected from the group consisting of C1-C14 saturated straight-chain alcohols, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof. These alcohols may be present in the pesticidal composition in at least about 1%, at least about 3%, at least about 5%, at least about 10% or even at least about 15% by weight of the composition. In one embodiment, the alcohols are present in an amount from about 10% to about 60% by weight of the composition.
  • In one embodiment, the alcohol is selected from the group consisting of methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof. In a further embodiment, the alcohol is selected from methanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol and combinations thereof. The alcohol may also be selected from the group consisting of 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • In another embodiment, the alcohol is selected from the group consisting of C1-C14 saturated straight-chain alcohols, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol and combinations thereof.
  • The pesticidal composition may include a plurality of alcohol compounds including a plurality of C1-C14 saturated straight chain alcohols. In one embodiment, the C1-C14 saturated straight-chain alcohol is selected from the group consisting of methanol, ethanol, 1-proponal, 1-butanol, 1-hexanol, 1-heptanol, 1-octanol, 1-nonanol, 1-decanol, 1-undecanol, 1-dodecanol, 1-tetradecanol and combinations thereof.
  • In another embodiment, the alcohol is a C1-C9 saturated straight-chain alcohol and, in another embodiment, is a C1-C6 straight chain alcohol. In one embodiment, the alcohol is a C3-C7 saturated straight-chain alcohol.
  • In a particular embodiment, mineral oil and a second active ingredient selected from the group consisting of C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol or diacetone alcohol may be present in the composition in a ratio based on the LD10 or LD50 value of the alcohol, which optimizes the biological effect of the blend.
  • For example, where the second active ingredient is isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, or a C1-C14 saturated straight chain alcohol, the LD10 of each of the active ingredients is determined, for instance, by the methods described in Example 9. A ratio is then determined based on about half of the LD10 for mineral oil and about the LD10 of the second active ingredient. For example, as detailed in Example 9, the LD10 for PD23 mineral oil was determined to be 0.754 mg/insect and the LD10 for diacetone alcohol was determined to be 0.255 mg/insect. About half of the LD10 of PD23 is about 0.4 mg, while about the LD10 of diacetone alcohol is about 0.3 mg. Accordingly, for a composition comprising PD23 and diacetone alcohol, a ratio corresponding to the above amounts is 4 parts PD23 to 3 parts diacetone alcohol, or 4:3. Thus, a composition of this particular embodiment may comprise PD23 and diacetone alcohol, among other things, in a ratio of 4:3.
  • Similarly, for example, in a composition comprising PD23 and 1-propanol, those active ingredients may be present in the composition in a ratio of about 4:4.5 or about 1:1. The ratio is determined based on the LD10 for 1-propanol and PD23, respectively, of 0.472 mg/insect and 0.754 mg/insect. About half the LD10 of PD23 is about 0.4 mg, and the LD10 of 1-propanol is about 0.45 mg, giving a ratio of about 4:4.5, or about 1:1.
  • Alternatively, the ratio may be determined as above, but based on the LD10:LD10 of the mineral oil and second active ingredient. So, for example, in a composition comprising PD23 and 1-propanol, the PD23 and 1-propanol are present in a ratio of 8:4.5, or about 2:1.
  • Similarly, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol or diacetone alcohol may be present in the composition in a ratio relative to the mineral oil in the composition, where this ratio is determined based on the LD50 for the alcohol and the LD50 of the mineral oil. As above with respect to ratios based on LD10, such ratios may be determined based on LD50:LD50; or may alternatively be determined based on 0.5 LD50 for mineral oil and LD50 for the second active ingredient.
  • In another embodiment, mineral oil and a second active ingredient selected from the group consisting of C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, 2-ethoxyethanol or combinations thereof may be present in the composition in a ratio which may be determined based on the LD1o or LD50.
  • In one embodiment, the second active ingredient is a compound selected from the group consisting of hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof. These listed compounds may be included with other second active ingredients. The amount of the listed compounds in the pesticidal composition may be at least about 50% of all the second active ingredients, at least about 65% of all the second active ingredients, at least about 75% of all the second active ingredients, at least about 85% of all the second active ingredients, at least about 95% of all the second active ingredients, or even at least about 99% of all the second active ingredients. In one embodiment, the total amount (i.e., about 100%) of second active ingredients present in the pesticidal composition is compounds selected from hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof.
  • In another embodiment, the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof.
  • In another embodiment, the second active ingredient is selected from hexylene glycol, dioxane, d-limonene and combinations thereof. In a further embodiment, the second active ingredient is selected from nitromethane, acetophenone, pyridine and combinations thereof.
  • These compounds may be present in the pesticidal composition in at least about 1%, at least about 3%, at least about 5%, at least about 10% or even at least about 15% by weight of the composition. In one embodiment, the listed compounds are present in an amount from about 10% to about 60% by weight of the composition.
  • In certain embodiments, the pesticidal compositions may comprise mineral oil plus two or more of the second active ingredients. For instance, in one particular embodiment, the pesticidal composition comprises mineral oil, ethyl lactate, and isopropyl myristate. In this embodiment, the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 30% (by weight of the composition) of ethyl lactate, and more typically from about 5% (by weight of the composition) to about 15% (by weight of the composition) of ethyl lactate; from about 5% (by weight of the composition) to about 60% (by weight of the composition) of isopropyl myristate, and more typically from about 5% (by weight of the composition) to about 30% (by weight of the composition) of isopropyl myristate; and from about 20% (by weight of the composition) to about 70% (by weight of the composition) of mineral oil.
  • In another particular embodiment, the pesticidal composition comprises mineral oil, d-limonene, and ethyl lactate. In this embodiment, the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 60% (by weight of the composition) of d-limonene, from about 5% (by weight of the composition) to about 30% (by weight of the composition) of ethyl lactate, and from about 20% (by weight of the composition) to about 90% (by weight of the composition) of mineral oil.
  • In yet another particular embodiment, the pesticidal composition comprises mineral oil, d-limonene, and butyl lactate. In this embodiment, the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 20% (by weight of the composition) of d-limonene, from about 5% (by weight of the composition) to about 20% (by weight of the composition) of butyl lactate, and from about 30% (by weight of the composition) to about 80% (by weight of the composition) of mineral oil.
  • In still another particular embodiment, the pesticidal composition may comprise mineral oil, d-limonene, ethyl lactate, and isopropyl myristate. In this embodiment, the pesticidal composition preferably comprises from about 5% (by weight of the composition) to about 20% (by weight of the composition) of d-limonene, from about 5% (by weight of the composition) to about 20% (by weight of the composition) of ethyl lactate, from about 20% (by weight of the composition) to about 40% (by weight of the composition) of isopropyl myristate, and from about 30% (by weight of the composition) to about 80% (by weight of the composition) of mineral oil.
  • In addition to the first and one or more second active ingredients, the pesticidal compositions of the present disclosure may further comprise a plant essential oil or derivative thereof, which may also have pesticidal properties. Such plant essential oils or derivatives may be extracted from natural sources or synthetically made, and generally contain, as at least one major constituent, an acyclic monoterpene alcohol or aldehyde, a benzenoid aromatic compound containing at least one oxygenated substituent or side chain, or a monocarbocyclic terpene generally having a six membered ring bearing one or more oxygenated substituents. Examples of such essential oils or their derivatives include, but are not limited to, members selected from the group consisting of aldehyde C16 (pure), alpha-terpineol, amyl cinnamic aldehyde, amyl salicylate, anisic aldehyde, benzyl alcohol, benzyl acetate, cinnamaldehyde, cinnamic alcohol, carvacrol, carveol, citral, citronellal, citronellol, dimethyl salicylate, eucalyptol (cineole), eugenol, iso-eugenol, galaxolide, geraniol, guaiacol, ionone, menthol, methyl anthranilate, methyl ionone, methyl salicylate, nerol, alpha-phellandrene, pennyroyal oil, perillaldehyde, 1- or 2-phenyl ethyl alcohol, 1- or 2-phenyl ethyl propionate, piperonal, piperonyl acetate, piperonyl alcohol, D-pulegone, terpinen-4-ol, terpinyl acetate, 4-tert butylcyclohexyl acetate, thyme oil (white and red), thymol, trans-anethole, vanillin, ethyl vanillin, and the like.
  • Other suitable oils include, for example, castor oil, cedar oil, cinnamon and cinnamon oil, citronella and citronella oil, cloves and clove oil, corn oil, cottonseed oil, garlic and garlic oil, geranium oil, lemongrass oil, linseed oil, mint and mint oil, peppermint and peppermint oil, rosemary and rosemary oil, sesame and sesame oil, soybean oil, white pepper, and the like. Preferably, the plant essential oil or derivative is geraniol.
  • The pesticidal compositions will typically comprise from about 1% (by weight of the composition) to about 60% (by weight of the composition of the plant essential oil or derivative, more typically from about 2% (by weight of the composition) to about 60% (by weight of the composition), and more typically from about 2% (by weight of the composition) to about 20% (by weight of the composition) of the plant essential oil or derivative.
  • In one embodiment, the pesticidal composition includes a first active ingredient that is a mineral oil, at least one second active ingredient that is selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, and combinations thereof and a third active ingredient that is a plant essential oil or derivative. In one embodiment, the plant essential oil or derivative is geraniol. In another embodiment, the composition also includes nerol.
  • In one embodiment, the composition comprises from about 10% to about 70% of the first ingredient by weight of the composition, from about 5% to about 50% of the second ingredient by weight of the composition and from about 0.5% to about 15% of the third active ingredient by weight of the composition.
  • The amount of geraniol present in the composition may be at least about 2% by weight of the composition, at least about 4% or at least about 6% by weight of the composition. In one embodiment, the amount of geraniol present in the composition is from about 0.5% to about 8% by weight of the composition. Nerol may be present in the composition in an amount from about 0.5% to about 3% by weight of the composition.
  • In another embodiment, the pesticidal composition comprises mineral oil, and at least two second active ingredients, each second active ingredient being selected from the group consisting of ethyl lactate, butyl lactate, isopropyl myristate, hexylene glycol, dioxane, d-limonene, a C1-C14 saturated straight-chain alcohol, isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol, diacetone alcohol, and combinations thereof and a third active ingredient that is a plant essential oil or derivative. In one embodiment, the plant essential oil or derivative is geraniol. In another embodiment, the composition also includes nerol.
  • In another embodiment, the pesticidal composition comprises a mineral oil, ethyl lactate, isopropyl myristate and geraniol. The composition may also include nerol. Additional additives may include essential oils such as lemongrass oil and carbon dioxide (described below).
  • In one embodiment, the pesticidal composition comprises, by weight of the composition, about 43% mineral oil, about 15% ethyl lactate, about 30% isopropyl myristate and about 6% geraniol. The composition may also include about 3% nerol and about 1% lemongrass oil.
  • Additionally, the pesticidal composition may further comprise other known insecticidal or pesticidal agents, including, for example, synergists such as piperonyl butoxide, MGK 264, and dillapiol; as well as other plant-derived insecticidal or pesticidal materials such as pyrethrum.
  • The composition may also comprise an amount of water. In various embodiments, the composition contains water in an amount of, by weight of the composition, at least about 10%, at least about 25%, at least about 50% or even at least about 75%. In one embodiment, the amount of water in the solution is from about 10% to about 50% by weight of the composition and, in another embodiment, from about 25% to about 75% by weight of the composition.
  • The compositions of the present disclosure may further comprise a suitable solvent, carrier or emulsifier. Examples of suitable solvents or carriers include water, acetone, alcohols such as ethanol and isopropyl alcohol, dimethyl ether, and chlorinated hydrocarbon solvents such as methylene chloride and methyl chloroform. Examples of emulsifiers would include soaps (such as fatty acid soaps), cationic, ionic and non-ionic compounds. Additional carriers for use in various granular formulations include, for example, corn cob grits, diatomaceous earth, sand, clay, and the like.
  • The pesticidal compositions of the present disclosure may be dispensed in any conventional manner, e.g., from a standard pump-spray container. In one embodiment, the pesticide is in a ready-to-use form in which the composition does not need to be diluted before application. Alternatively, the pesticidal composition may be in a concentrate form. The end-user of the concentrate composition may dilute the concentrate prior to use by, for example, addition of water. In one embodiment, the pesticidal composition is diluted in the pump spray bottle. In various embodiments, the concentrate pesticidal composition may be diluted by addition of water in an amount of, by weight of the concentrate composition, at least about 40%, at least about 50%, at least about 75%, at least about 100%, at least about 150%, at least about 200% or even at least about 300%.
  • When the pesticidal composition is present in a concentrate form, in some embodiments, dilution may cause formation of a water-concentrate emulsion. The pesticidal concentrate may include emulsifiers such as surfactants (e.g., surfactants such as fatty acid soaps). Suitable compounds may be cationic, ionic, and non-ionic. Suitable emulsifying compounds include alkyl arly sulionate-based emulsifiers, polyoxyethylenes and long-chain alcohols.
  • In one embodiment, the pesticidal composition is packaged in a pressurized container such as a conventional aerosol container or the like. The composition may be pressurized utilizing any suitable propellant. Examples of suitable propellants include expandable gases such as carbon dioxide, nitrogen, propane, n-butane, isobutane, blends of propane and butane, HFC-152a (difluoroethane), HFC-134a (1,1,1,2-tetrafluoroethane), and combinations thereof.
  • Any conventional technique may be used to charge the aerosol container with carbon dioxide or other expandable gas. In one embodiment, the gasser-shaker method may be used. This method involves shaking or agitating the container and its contents as the carbon dioxide (or other gas) is forced into the container through a valve, with the rest of the composition having been introduced into the container prior to installation of the valve. The rate of injection of the gas depends on the valve orifice size, and the shaking time depends on the container size, the amount of liquid, and the degree of agitation, as well as the temperature.
  • Alternatively, the pesticidal composition may be saturated with carbon dioxide prior to introduction into the container, and then pumped under pressure to a rotary undercap filler and filled as in a normal undercap operation, or pressured into containers already equipped with valves. Other suitable methods known in the art may also be used.
  • Other examples of suitable propellants which may be used are known in the art and include, for example, dimethyl ether, methyl ethyl ether, nitrous oxide, and the like.
  • Typically the composition will comprise propellant in an amount of from about 2% (by weight of the composition) to about 90% (by weight of the composition), and more typically in an amount of from about 2% (by weight of the composition) to about 10% (by weight of the composition).
  • As noted above, the pesticidal compositions of the present disclosure may be sprayed or otherwise contacted with insects or other pests to effectively control insect or other pest populations. Thus, in one embodiment, the present disclosure is directed to a method of controlling insects and pests. The method comprises contacting the insects and pests with a pesticidally effective amount of a composition of the present disclosure.
  • In one embodiment, an arthropod is contacted with the pesticidal composition in a pesticidally effective amount. For purposes of the present disclosure, a “pesticidally effective amount” of the composition includes amounts that repel the arthropod or other pest and may include, in another embodiment, amounts of the composition that kill the arthropod or other pest.
  • The pesticidal compositions of embodiments of the present disclosure may be used to control arthropods and, in another embodiment, to control insects. In one embodiment, the pesticidal composition is used to control cockroaches. Control of the pest (e.g., arthropod, insect, cockroach, etc.) may include contacting the pest with the pesticidal composition. In one embodiment, the pest is contacted with the pesticidal composition by spraying the composition directly on the crawling arthropod, flying insect or other pest. The composition may be sprayed in a sufficient amount to cause death. The pesticidal composition may also be sprayed in locations at which the pest is likely to come into contact with the composition.
  • The amount of the pesticidal composition required to kill insects or other pests and the time until pest death will vary depending on the composition components, the type of insect species and its life stage, and the like. The time required to kill a pest contacted with the pesticidal composition of the present disclosure will typically range from mere seconds to several hours.
  • The pesticidal compositions of the present disclosure are particularly effective against cockroaches, including the species Periplaneta Americana (American cockroach), Blattella germanica (German cockroach), Blattella asahinai (Asian cockroach), and Blatta orientalis (Oriental cockroach). However, the pesticidal compositions may also be used against a wide variety of other crawling insects or other arthropods, such as ants, water bugs, silverfish, crickets, spiders, ticks, mites, sowbugs, pillbugs, beetles, earwigs, centipedes, and the like. As used herein, the term “water bugs” refers to aquatic insects in the order Hemiptera. Examples of water bugs include giant water bugs, creeping water bugs, water scorpions, water boatmen, backswimmers, and the like. In one embodiment, the pesticidal compositions are effective against various flying insects including flies, mosquitoes, gnats, moths, wasps, hornets, bees, and the like.
  • The pesticidal compositions of the present disclosure generally result in at least 80% mortality, more preferably at least 95% mortality, and more preferably 100% mortality of the insects on contact, depending on the specific composition, the amount of composition applied to the insect and the insect species and life stage.
  • Having described the disclosure in detail, it will be apparent that modifications and variations are possible without departing from the scope of the disclosure defined in the appended claims.
  • EXAMPLES
  • The following non-limiting examples are provided to further illustrate the present disclosure.
  • Unless otherwise indicated, the mineral oil used in the following examples was PD-23 (available from Chemtura Corporation, Middlebury, Conn.), which is a light grade petroleum distillate having a flash point of 230° F. (110° C.), as measured by ASTM D-92, and a vapor pressure of less than 0.1 mmHg at 20° C. PD-23 is a highly refined petroleum distillate that resembles a very clear oil, and is made by fractionating oil to a narrow boiling range, then catalytically hydrotreating it to remove all aromatic and other unsaturated hydrocarbons. PD-23 is hydrophobic, colorless, tasteless, virtually odorless, and color fast.
  • Example 1
  • In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or ethyl lactate at killing German cockroaches was tested.
  • To begin, compositions comprising mineral oil and/or ethyl lactate in the following concentrations were prepared: 100% (wt/wt) mineral oil/0% (wt/wt) ethyl lactate; 90% (wt/wt) mineral oil/10% (wt/wt) ethyl lactate; 75% (wt/wt) mineral oil/25% (wt/wt) ethyl lactate; 50% (wt/wt) mineral oil/50% (wt/wt) ethyl lactate; 25% (wt/wt) mineral oil/75% (wt/wt) ethyl lactate; 10% (wt/wt) mineral oil/90% (wt/wt) ethyl lactate; 0% (wt/wt) mineral oil/100% (wt/wt) ethyl lactate. The ethyl lactate was obtained from Vertech Biosolvents, Inc., Downers Grove, Ill.
  • Prior to testing, each composition containing either mineral oil, ethyl lactate, or a combination of mineral oil and ethyl lactate was diluted by 50% by mixing the composition with acetone in a 1:1 ratio (wt/wt) to reduce viscosity prior to application of the compositions to the cockroaches. The amount of mineral oil, ethyl lactate, and acetone present in the final composition (A-G) is set forth below in Table 1.
  • Toxicity evaluations were performed on 7-14 day old adult male and female German cockroaches (SCJ Strain, S.C. Johnson & Son, Racine, Wis.). Approximately 12 cockroaches were transferred to individual 100×20 mm polystyrene Petri dishes and anesthetized with a 15-25 second exposure to carbon dioxide. The inside edge of each Petri dish was lightly coated with mineral oil plus petroleum jelly in a 1:3 (wt/wt) ratio to minimize escape. Anesthetized cockroaches were positioned with their ventral side up, and a 1 μl drop of the diluted test composition was applied to the area between the meso- and metathoracic legs using a Rainin L-10, 10 μl capacity pipette (Rainin Instrument, LLC, Oakland, Calif.). Five replications of 12 male cockroaches were done for each test composition. Separate tests were done using female cockroaches. Results were evaluated at 24 hours following treatment. Cockroaches were scored as either alive (dorsal side up, active movement when abdomen prodded with dissecting probe) or moribund/dead (dorsal side up and no movement when abdomen prodded or ventral side up and insect unable to right itself).
  • Results are shown in FIG. 1 and Table 1, which lists the number of dead cockroaches out of 60 total cockroaches for each test performed using the diluted test compositions (A-G).
  • TABLE 1
    Ethyl Males Females (#
    Mineral oil lactate Acetone (# dead dead out
    Composition (wt/wt) (wt/wt) (wt/wt) out of 60) of 60)
    A 50%  0% 50% 6 1
    B 45%  5% 50% 7 0
    C 37.5%   12.5%   50% 40 20
    D 25% 25% 50% 56 44
    E 12.5%   37.5%   50% 57 40
    F  5% 45% 50% 49 38
    G  0% 50% 50% 3 0
  • As can be seen from these results, cockroaches treated with test composition C-F (containing both mineral oil and ethyl lactate) had significantly higher mortality rates than cockroaches treated with only mineral oil (composition A) or only ethyl lactate (composition G), indicating a synergistic effect when the combination of mineral oil and ethyl lactate is used.
  • Example 2
  • In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or butyl lactate at killing cockroaches was tested.
  • To begin, compositions comprising mineral oil and/or butyl lactate in the following concentrations were prepared: 100% (wt/wt) mineral oil/0% (wt/wt) butyl lactate; 90% (wt/wt) mineral oil/10% (wt/wt) butyl lactate; 75% (wt/wt) mineral oil/25% (wt/wt) butyl lactate; 50% (wt/wt) mineral oil/50% (wt/wt) butyl lactate; 25% (wt/wt) mineral oil/75% (wt/wt) butyl lactate; 10% (wt/wt) mineral oil/90% (wt/wt) butyl lactate; 0% (wt/wt) mineral oil/ 100% (wt/wt) butyl lactate. The butyl lactate was obtained from Vertech Biosolvents, Inc., Downers Grove, Ill.
  • Prior to testing, each composition containing either mineral oil, butyl lactate, or a combination of mineral oil and butyl lactate was diluted by 50% by mixing the composition with acetone in a 1:1 ratio (wt/wt) to reduce viscosity prior to application of the composition to the cockroaches. The amount of mineral oil, butyl lactate, and acetone present in the final compositions (H-N) is set forth below in Table 2.
  • Tests were performed as described in Example 1. The results are shown in FIG. 2 and Table 2 below.
  • TABLE 2
    Butyl Males Females (#
    Mineral oil lactate Acetone (# dead dead
    Composition (wt/wt) (wt/wt) (wt/wt) out of 60) out of 60)
    H 50%  0% 50% 3 0
    I 45%  5% 50% 9 3
    J 37.5%   12.5%   50% 37 29
    K 25% 25% 50% 52 35
    L 12.5%   37.5%   50% 38 18
    M  5% 45% 50% 8 4
    N  0% 50% 50% 1 4
  • As can be seen from these results, cockroaches treated with test composition J-L (containing both mineral oil and butyl lactate) had significantly higher mortality rates than cockroaches treated with only mineral oil (composition H) or only butyl lactate (composition N), indicating a synergistic effect when the combination of mineral oil and butyl lactate is used.
  • Example 3
  • In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or hexylene glycol at killing cockroaches was tested.
  • To begin, compositions comprising mineral oil, hexylene glycol, or a combination of mineral oil and hexylene glycol were prepared. The amount of mineral oil and/or hexylene glycol in each composition is set forth below in Table 3, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 3, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 3 below, which lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • TABLE 3
    # Square root % Proportion Arcsine square
    Composition (% wt/wt) # tested dead dead dead root % dead
    Hexylene glycol (20%) 14 1 0.2672612 0.07142857 0
    Hexylene glycol (20%) 12 0 0 0 0
    Hexylene glycol (20%) 13 3 0.4803845 0.23076923 28.7105148
    Hexylene glycol (20%) 14 0 0 0 0
    Mineral oil (80%) 14 2 0.3779645 0.14285714 22.2076543
    Mineral oil (80%) 14 1 0.2672612 0.07142857 15.50135957
    Mineral oil (80%) 13 2 0.3922323 0.15384615 23.09346927
    Mineral oil (80%) 14 1 0.2672612 0.07142857 15.50135957
    Mineral oil (60%), 13 11 0.9198662 0.84615385 66.90653073
    hexylene glycol (20%)
    Mineral oil (60%), 14 11 0.8864053 0.78571429 62.42495229
    hexylene glycol (20%)
    Mineral oil (60%), 14 13 0.9636241 0.92857143 74.49864043
    hexylene glycol (20%)
  • As can be seen from these results, cockroaches treated with compositions containing both mineral oil and hexylene glycol had significantly higher mortality rates than cockroaches treated with only mineral oil or only hexylene glycol, indicating a synergistic effect when the combination of mineral oil and hexylene glycol is used.
  • Example 4
  • In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or isopropyl myristate at killing cockroaches was tested.
  • To begin, compositions comprising mineral oil, isopropyl myristate, or a combination of mineral oil and isopropyl myristate were prepared. The amount of mineral oil and/or isopropyl myristate in each composition is set forth below in Table 4, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 4, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 4 below, which lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • TABLE 4
    # Square root % Proportion Arcsine square
    Composition (% wt/wt) # tested dead dead dead root % dead
    Isopropyl myristate 15 1 0.2582 0.06667 14.9632174
    (80%)
    Isopropyl myristate 17 0 0 0 0
    (80%)
    Isopropyl myristate 15 1 0.2582 0.06667 14.9632174
    (80%)
    Isopropyl myristate 12 1 0.28868 0.08333 16.7786549
    (80%)
    Mineral oil (80%) 15 2 0.36515 0.13333 21.416714
    Mineral oil (80%) 17 1 0.24254 0.05882 14.0362435
    Mineral oil (80%) 15 2 0.36515 0.13333 21.416714
    Mineral oil (80%) 12 0 0 0 0
    Mineral oil (80%) 15 2 0.36515 0.13333 21.416714
    Mineral oil (40%), 15 6 0.63246 0.4 39.2315205
    isopropyl myristate
    (40%)
    Mineral oil (40%), 16 3 0.43301 0.1875 25.6589063
    isopropyl myristate
    (40%)
    Mineral oil (40%), 15 4 0.5164 0.26667 31.0909304
    isopropyl myristate
    (40%)
    Mineral oil (40%), 12 2 0.40825 0.16667 24.0948425
    isopropyl myristate
    (40%)
    Mineral oil (50%), 15 8 0.7303 0.53333 46.9112769
    isopropyl myristate
    (30%)
    Mineral oil (50%), 16 6 0.61237 0.375 37.7612439
    isopropyl myristate
    (30%)
    Mineral oil (50%), 15 3 0.44721 0.2 26.5650512
    isopropyl myristate
    (30%)
    Mineral oil (50%), 12 4 0.57735 0.33333 35.2643897
    isopropyl myristate
    (30%)
    Mineral oil (60%), 15 4 0.5164 0.26667 31.0909304
    isopropyl myristate
    (20%)
    Mineral oil (60%), 15 7 0.68313 0.46667 43.0887231
    isopropyl myristate
    (20%)
    Mineral oil (60%), 15 4 0.5164 0.26667 31.0909304
    isopropyl myristate
    (20%)
    Mineral oil (60%), 12 3 0.5 0.25 30
    isopropyl myristate
    (20%)
  • The combined data for each treatment group is set forth in Table 5 below.
  • TABLE 5
    Average
    arcsine
    Number of sq. root %
    Composition (% wt/wt) compositions dead Variance
    Isopropyl myristate (80%) 4 11.67627243 61.3258864
    Mineral oil (80%) 5 15.6572771 86.82285408
    Mineral oil (40%), isopropyl 4 30.01904993 46.70854263
    myristate (40%)
    Mineral oil (50%), isopropyl 4 36.62549043 70.05079065
    myristate (30%)
    Mineral oil (60%), isopropyl 4 33.81764598 38.46574917
    myristate (20%)
  • As can be seen from these results, cockroaches treated with compositions containing both mineral oil and isopropyl myristate at all tested concentrations had significantly higher mortality rates than cockroaches treated with only mineral oil or only isopropyl myristate, indicating a synergistic effect when the combination of mineral oil and isopropyl myristate is used.
  • Example 5
  • In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or dioxane at killing cockroaches was tested.
  • To begin, compositions comprising mineral oil, dioxane, or a combination of mineral oil and dioxane were prepared. The amount of mineral oil and/or dioxane in each composition is set forth below in Table 6, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 6, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 6, which lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • TABLE 6
    # Square root % Proportion Arcsine square
    Composition (% wt/wt) # tested dead dead dead root % dead
    Dioxane (50%) 10 0 0 0 0
    Dioxane (50%) 14 0 0 0 0
    Dioxane (50%) 14 0 0 0 0
    Dioxane (50%) 12 0 0 0 0
    Dioxane (50%) 13 1 0.277350098 0.07692308 16.10211375
    Mineral oil (80%) 13 1 0.277350098 0.07692308 16.10211375
    Mineral oil (80%) 14 2 0.377964473 0.14285714 22.2076543
    Mineral oil (80%) 14 2 0.377964473 0.14285714 22.2076543
    Mineral oil (80%) 14 1 0.267261242 0.07142857 15.50135957
    Mineral oil (80%) 13 2 0.39223227 0.15384615 23.09346927
    Mineral oil (40%), 14 10 0.845154255 0.71428571 57.68846676
    dioxane (40%)
    Mineral oil (40%), 14 11 0.88640526 0.78571429 62.42495229
    dioxane (40%)
    Mineral oil (40%), 14 11 0.88640526 0.78571429 62.42495229
    dioxane (40%)
    Mineral oil (40%), 15 9 0.774596669 0.6 50.76847952
    dioxane (40%)
    Mineral oil (40%), 13 12 0.960768923 0.92307692 73.89788625
    dioxane (40%)
  • As can be seen from these results, cockroaches treated with compositions containing both mineral oil and dioxane had significantly higher mortality rates than cockroaches treated with only mineral oil or only dioxane, indicating a synergistic effect when the combination of mineral oil and dioxane is used.
  • Example 6
  • In this example, the effectiveness of compositions comprising various concentrations of mineral oil and/or d-limonene at killing cockroaches was tested.
  • To begin, compositions comprising mineral oil, d-limonene, or a combination of mineral oil and d-limonene were prepared. The amount of mineral oil and/or d-limonene in each composition is set forth below in Table 7, with the remainder of each composition consisting of acetone.
  • Tests were generally performed as described in Example 1, except the number of cockroaches (all male) tested for each composition is set forth below in Table 7, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 7, which lists the number of cockroaches tested for each composition, the number of dead cockroaches out of the total number of cockroaches tested, the square root percent dead cockroaches, the proportion of dead cockroaches, and the arcsine square root percent dead cockroaches.
  • TABLE 7
    # Square root % Proportion Arcsine square
    Composition (% wt/wt) # tested dead dead dead root % dead
    d-limonene (40%) 14 1 0.267261242 0.0714286 15.50135957
    d-limonene (40%) 12 0 0 0 0
    d-limonene (40%) 15 2 0.365148372 0.1333333 21.41671403
    d-limonene (40%) 14 2 0.377964473 0.1428571 22.2076543
    Mineral oil (80%) 14 2 0.377964473 0.1428571 22.2076543
    Mineral oil (80%) 14 1 0.267261242 0.0714286 15.50135957
    Mineral oil (80%) 13 2 0.39223227 0.1538462 23.09346927
    Mineral oil (80%) 14 1 0.267261242 0.0714286 15.50135957
    Mineral oil (40%), d- 14 6 0.654653671 0.4285714 40.89339465
    limonene (40%)
    Mineral oil (40%), d- 13 5 0.620173673 0.3846154 38.3288181
    limonene (40%)
    Mineral oil (40%), d- 14 12 0.9258201 0.8571429 67.7923457
    limonene (40%)
    Mineral oil (40%), d- 14 7 0.707106781 0.5 45
    limonene (40%)
  • The combined data for each treatment group is set forth in Table 8 below.
  • TABLE 8
    Number of Average arcsine
    Composition (% wt/wt) compositions sq. root % dead Variance
    d-limonene (40%) 4 14.78145 106.0618
    Mineral oil (80%) 4 19.076 17.16779
    Mineral oil (40%), 4 48.00363 181.5903
    d-limonene (40%)
  • As can be seen from these results, cockroaches treated with compositions containing both mineral oil and d-limonene had significantly higher mortality rates than cockroaches treated with only mineral oil or only d-limonene, indicating a synergistic effect when the combination of mineral oil and d-limonene is used.
  • Example 7
  • In this example, the effectiveness of compositions comprising various types of mineral oil at killing cockroaches was tested.
  • To begin, compositions comprising one of three different types of mineral oil in varying concentrations were prepared. The mineral oils used in this example were PD-23 (Sample No. 88446, 1997, available from Chemtura Corporation, Middlebury, Conn.), which is a low viscosity (e.g., about 2.6 cSt at 40° C. or about 34 SUS at 100° F. (38° C.)) petroleum distillate; PD-25 (Sample No. 88447, available from Chemtura Corporation, Middlebury, Conn.), which is a medium viscosity (e.g., about 3.5 cSt at 40° C. or about 39 SUS at 100° F. (38° C.)) petroleum distillate; and PD-28 (Sample No. 88448, 1997, available from Chemtura Corporation, Middlebury, Conn.), which is a relatively high viscosity (e.g., about 4.2 cSt at 40° C. or about 39 SUS at 100° F. (38° C.)) petroleum distillate. The amount of each type of mineral oil in each composition is set forth below in Table 9, with the remainder of the composition comprising ethanol.
  • Tests were generally performed as described in Example 1, except 2 μl of the compositions were applied to each cockroach, the number of cockroaches (all male) tested for each diluted composition is set forth below in Table 9, and the compositions were not further diluted with acetone in a 1:1 (wt/wt) ratio prior to testing. The results are shown in Table 9.
  • TABLE 9
    Composition (% wt/wt) # tested # dead
    PD-23 (50%) 10 10
    PD-23 (20%) 10 2
    PD-23 (20%) 9 2
    PD-25 (50%) 9 8
    PD-25 (20%) 11 0
    PD-28 (50%) 9 5
    PD-28 (20%) 10 0
  • As can be seen from these results, compositions containing the higher concentration of mineral oil (i.e., the 50% compositions) were more effective against adult German cockroaches than the lower concentration compositions (i.e., the 20% compositions). Of the 20% compositions, only the PD-23 had any effect against the cockroaches. These results indicate that the lightest weight mineral oil used in these tests, PD-23, was the most active against adult German cockroaches.
  • Example 8
  • In this embodiment, an aerosol pesticidal composition of the present disclosure was prepared. The ingredients and amounts used to prepare the composition are set forth in Table 10 below.
  • TABLE 10
    Ingredient Amount (wt/wt %)
    Mineral oil (PD-23, available from Chemtura) 56.20%
    Ethyl lactate 14.95%
    Isopropyl myristate 24.00%
    Geraniol 2.00%
    Carbon dioxide 2.85%
  • The composition was prepared by mixing the mineral oil, ethyl lactate, isopropyl myristate and geraniol together until homogenous. The resulting composition was placed in an aerosol can. The lid and actuator of the aerosol can were sealed onto the top of the can. The carbon dioxide was introduced into the can through the actuator to pressurize the can. The resulting product can be used as an aerosol spray pesticidal composition.
  • Example 9
  • In this example, various mineral oils and alcohols were tested to determine, for cockroaches, the LD50 and LD10 for each.
  • PD23 and PD28 mineral oils were obtained from Sonneborn LLC, Mahwah, N.J. The physical properties of these oils are shown in Table 11. Each mineral oil was tested to determine the LD50 and LD10 (Table 12).
  • TABLE 11
    PROPERTY PD23 PD28 Test Method
    Specific gravity 60/60 0.800 0.823 ASTM D-287
    Viscosity SUS @ 100° F. 34 39 ASTM D-2161
    (38° C.)
    Viscosity cSt @ 40° C. 2.6 4.2 ASTM-D-445
    Pour point ° F. (° C.) 0 (−18) −40 (−40) ASTM D-97
    Distillation range, ° F.
    Ibp 452 526
     50% 486 568
     95% 514 614
    100% 533 625
    Molecular weight 220 245
  • The alcohols tested comprise C1-C14 saturated straight chain alcohols, and alcohols selected from the group consisting of isopropyl alcohol, 2-butanol, isobutyl alcohol, tertiary butyl alcohol, 2-butoxyethanol, 2-phenylethanol and diacetone alcohol. The tested alcohols were obtained from Sigma-Aldrich Corp., St. Louis, Mo. Each alcohol was tested to determine the LD50 and LD10 (Table 12). The dose-response mortality data were analyzed using probit analysis (PoloPlus©, LeOra Software Co., Petaluma Calif., 2003) to estimate LD50 and LD10 values and their 95% confidence intervals.
  • TABLE 12
    n
    Test Substance LD50 mg/insect (95% LD10 mg/insect (95% (sample
    (CAS number) CI) CI) Slope (+/−SE) size)
    PD23 - mineral oil 1.453 0.754 4.500 (0.360) 394
    (8042-47-5) (1.303-1.629) (0.632-0.863)
    PD28 - mineral oil 2.013 1.463 9.259 (1.204) 249
    (8042-47-5) (1.916-2.105) (1.285-1.588)
    Methanol >7.00  Estimated at ~3.000 n/a 151
    (67-56-1)
    Ethanol 2.361 1.760 10.037 (1.285)  215
    (64-17-5) (2.084-2.659) (1.255-2.014)
    1-propanol 0.557 0.472 17.756 (2.034)  248
    (71-23-8) (0.527-0.582) (0.414-0.504)
    1-butanol 1.018 0.877 19.808 (3.556)  143
    (71-36-3) (0.980-1.070) (0.814-0.917)
    1-hexanol 0.718 0.452 6.392 (0.869) 157
    (111-27-3) (0.651-0.793) (0.371-0.514)
    1-heptanol 0.791 0.462 5.502 (0.951) 154
    (111-70-6) (0.704-0.899) (0.324-0.549)
    1-octanol 0.524 0.267 4.375 (0.720) 149
    (111-87-5) (0.390-0.635) (0.116-0.367)
    1-nonanol 0.448 0.207 3.832 (0.757) 84
    (143-08-08) (0.296-0.633) (0.051-0.309)
    1-decanol 0.421 0.275 6.931 (1.023) 272
    (112-30-1) ((0.365-0.479) (0.151-0.331)
    1-undecanol 0.406 0.265 6.956 (1.013) 165
    (112-42-5) (0.373-0.444) (0.221-0.298)
    1-dodecanol 0.357 0.245 7.809 (1.350) 135
    (112-53-8) (0.304-0.412) (0.146-0.292)
    1-tetradecanol (112- 1.745 1.193 7.756 (1.268) 131
    72-1) (1.568-1.948) (0.902-1.369)
    Isopropyl alcohol 1.172 0.676 5.370 (0.701) 195
    (67-63-0) (1.014-1.394) (0.462-0.814)
    2-butanol 1.188 0.881 9.873 (1.479) 111
    (78-92-2) (1.058-1.369) (0.709-0.997)
    isobutyl alcohol 0.517 0.253 4.129 (0.452) 299
    (78-83-1) (0.426-0.644) (0.146-0.326)
    tertiary butyl alcohol 0.716 0.553 11.392 (2.147)  112
    (75-65-0) (0.634-1.004) (0.385-0.625)
    2-butoxyethanol 0.377 0.256 7.613 (1.200) 157
    (111-76-2) (0.349-0.413) (0.217-0.282)
    2-phenylethanol 0.169 0.075 3.628 (0.546) 142
    (60-12-8) (0.114-0.327) (0.015-0.113)
    Diacetone alcohol 0.483 0.255 4.617 (0.596) 171
    (123-42-2) (0.390-0.591) (0.151-0.329)
  • Example 10
  • In this example, the effectiveness of compositions comprising various alcohols and/or mineral oil at killing cockroaches was tested.
  • The compositions comprising alcohol and/or mineral oil are described in Table 13. The tests were performed as described in Example 1.
  • TABLE 13
    Proportion
    Composition # treated # dead at 24 h dead at 24 h
    diacetone alcohol (0.4 mg) + PD23 (0.4 mg) 11 11 1.000
    diacetone alcohol (0.4 mg) + PD23 (0.4 mg) 11 10 0.909
    diacetone alcohol (0.4 mg) + PD23 (0.4 mg) 12 11 0.917
    diacetone alcohol (0.3 mg) + PD23 (0.4 mg) 13 12 0.923
    diacetone alcohol (0.3 mg) + PD23 (0.4 mg) 13 11 0.846
    diacetone alcohol (0.3 mg) + PD23 (0.4 mg) 14 12 0.857
    diacetone alcohol (0.3 mg) 13 0 0.000
    diacetone alcohol (0.3 mg) 13 0 0.000
    diacetone alcohol (0.3 mg) 14 1 0.071
    methanol (1.0 mg) + PD23 (0.4 mg) 14 1 0.071
    methanol (1.0 mg) + PD23 (0.4 mg) 14 0 0.000
    methanol (1.0 mg) + PD23 (0.4 mg) 14 1 0.071
    methanol (3.0 mg) + PD23 (0.4 mg) 12 4 0.333
    methanol (3.0 mg) + PD23 (0.4 mg) 14 4 0.286
    methanol (3.0 mg) + PD23 (0.4 mg) 12 5 0.417
    methanol (3.0 mg) 14 0 0.000
    methanol (3.0 mg) 12 0 0.000
    methanol (3.0 mg) 13 1 0.077
    ethanol (1.0 mg) + PD23 (0.4 mg) 14 1 0.071
    ethanol (1.0 mg) + PD23 (0.4 mg) 13 2 0.154
    ethanol (1.0 mg) + PD23 (0.4 mg) 13 4 0.308
    ethanol (1.25 mg) + PD23 (0.4 mg) 12 5 0.417
    ethanol (1.25 mg) + PD23 (0.4 mg) 12 3 0.250
    ethanol (1.25 mg) + PD23 (0.4 mg) 13 3 0.231
    ethanol (1.25 mg) 13 0 0.000
    ethanol (1.25 mg) 12 1 0.083
    ethanol (1.25 mg) 12 0 0.000
    1-propanol (0.6 mg) + PD23 (0.40 mg) 12 12 1.000
    1-propanol (0.6 mg) + PD23 (0.40 mg) 11 11 1.000
    1-propanol (0.6 mg) + PD23 (0.40 mg) 10 10 1.000
    1-propanol (0.50 mg) + PD23 (0.40 mg) 12 12 1.000
    1-propanol (0.50 mg) + PD23 (0.40 mg) 13 13 1.000
    1-propanol (0.50 mg) + PD23 (0.40 mg) 13 13 1.000
    1-propanol (0.45 mg) + PD23 (0.40 mg) 12 10 0.833
    1-propanol (0.45 mg) + PD23 (0.40 mg) 13 13 1.000
    1-propanol (0.45 mg) + PD23 (0.40 mg) 12 12 1.000
    1-propanol (0.45 mg) 12 1 0.083
    1-propanol (0.45 mg) 12 0 0.000
    1-propanol (0.45 mg) 12 0 0.000
    Isopropyl alcohol (0.6 mg) + PD23 (0.4 mg) 12 3 0.250
    Isopropyl alcohol (0.6 mg) + PD23 (0.4 mg) 14 4 0.286
    Isopropyl alcohol (0.6 mg) + PD23 (0.4 mg) 12 3 0.250
    Isopropyl alcohol (0.6 mg) 12 0 0.000
    Isopropyl alcohol (0.6 mg) 14 0 0.000
    Isopropyl alcohol (0.6 mg) 12 0 0.000
    Isopropyl alcohol (0.8 mg) + PD23 (0.4 mg) 12 3 0.250
    Isopropyl alcohol (0.8 mg) + PD23 (0.4 mg) 13 7 0.538
    Isopropyl alcohol (0.8 mg) + PD23 (0.4 mg) 12 10 0.833
    1-butanol (0.8 mg) + PD23 (0.4 mg) 13 8 0.615
    1-butanol (0.8 mg) + PD23 (0.4 mg) 13 10 0.769
    1-butanol (0.8 mg) + PD23 (0.4 mg) 13 10 0.769
    1-butanol (0.8 mg) 12 0 0.000
    1-butanol (0.8 mg) 13 0 0.000
    1-butanol (0.8 mg) 10 1 0.100
    2-butanol (0.8 mg) + PD23 (0.4 mg) 12 1 0.083
    2-butanol (0.8 mg) + PD23 (0.4 mg) 14 0 0.000
    2-butanol (0.8 mg) + PD23 (0.4 mg) 12 3 0.250
    2-butanol (0.8 mg) 13 0 0.000
    2-butanol (0.8 mg) 13 0 0.000
    2-butanol (0.8 mg) 12 1 0.083
    t-butyl alcohol (0.5 mg) + PD23 (0.4 mg) 10 3 0.300
    t-butyl alcohol (0.5 mg) + PD23 (0.4 mg) 11 3 0.273
    t-butyl alcohol (0.5 mg) + PD23 (0.4 mg) 12 8 0.667
    t-butyl alcohol (0.5 mg) 12 0 0.000
    t-butyl alcohol (0.5 mg) 11 0 0.000
    t-butyl alcohol (0.5 mg) 10 0 0.000
    t-butyl alcohol (0.5 mg) 11 2 0.182
    isobutyl alcohol (0.50 mg) + PD23 (0.40 mg) 14 11 0.786
    isobutyl alcohol (0.50 mg) + PD23 (0.40 mg) 13 13 1.000
    isobutyl alcohol (0.50 mg) + PD23 (0.40 mg) 15 15 1.000
    isobutyl alcohol (0.50 mg) 14 1 0.071
    isobutyl alcohol (0.20 mg) 13 0 0.000
    isobutyl alcohol (0.20 mg) 12 0 0.000
    isobutyl alcohol (0.20 mg) 13 1 0.077
    isobutyl alcohol (0.20 mg) + PD23 (0.40 mg) 14 2 0.143
    isobutyl alcohol (0.20 mg) + PD23 (0.40 mg) 13 3 0.231
    isobutyl alcohol (0.20 mg) + PD23 (0.40 mg) 15 11 0.733
    isobutyl alcohol (0.20 mg) + PD23 (0.40 mg) 12 7 0.583
    1-hexanol (0.4 mg) + PD23 (0.40 mg) 13 13 1.000
    1-hexanol (0.4 mg) + PD23 (0.40 mg) 12 12 1.000
    1-hexanol (0.4 mg) + PD23 (0.40 mg) 12 12 1.000
    1-hexanol (0.4 mg) 12 1 0.083
    1-hexanol (0.4 mg) 12 1 0.083
    1-hexanol (0.4 mg) 12 1 0.083
    1-heptanol (0.4 mg) + PD23 (0.40 mg) 12 12 1.000
    1-heptanol (0.4 mg) + PD23 (0.40 mg) 12 11 0.917
    1-hexanol (0.4 mg) + PD23 (0.40 mg) 12 12 1.000
    1-heptanol (0.4 mg) 12 1 0.083
    1-heptanol (0.4 mg) 12 0 0.000
    1-heptanol (0.4 mg) 12 0 0.000
    1-octanol (0.2 mg) + PD23 (0.40 mg) 12 3 0.250
    1-octanol (0.2 mg) + PD23 (0.40 mg) 12 3 0.250
    1-octanol (0.2 mg) + PD23 (0.40 mg) 12 3 0.250
    1-octanol (0.2 mg) 13 2 0.154
    1-octanol (0.2 mg) 12 0 0.000
    1-octanol (0.2 mg) 12 0 0.000
    1-nonanol (0.2 mg) + PD23 (0.40 mg) 12 4 0.333
    1-nonanol (0.2 mg) + PD23 (0.40 mg) 12 3 0.250
    1-nonanol (0.2 mg) + PD23 (0.40 mg) 12 1 0.083
    1-nonanol (0.2 mg) 12 0 0.000
    1-nonanol (0.2 mg) 16 1 0.063
    1-nonanol (0.2 mg) 13 0 0.000
    1-decanol (0.2 mg) + PD23 (0.40 mg) 12 0 0.000
    1-decanol (0.2 mg) + PD23 (0.40 mg) 12 1 0.083
    1-decanol (0.2 mg) + PD23 (0.40 mg) 12 0 0.000
    1-decanol (0.2 mg) 12 0 0.000
    1-decanol (0.2 mg) 12 0 0.000
    1-decanol (0.2 mg) 13 1 0.077
    1-undecanol (0.25 mg) + PD23 (0.40 mg) 12 0 0.000
    1-undecanol (0.25 mg) + PD23 (0.40 mg) 13 1 0.077
    1-undecanol (0.25 mg) + PD23 (0.40 mg) 12 0 0.000
    1-undecanol (0.25 mg) 13 2 0.154
    1-undecanol (0.25 mg) 12 0 0.000
    1-undecanol (0.25 mg) 13 2 0.154
    1-dodecanol (0.2 mg) + PD23 (0.40 mg) 13 2 0.154
    1-dodecanol (0.2 mg) + PD23 (0.40 mg) 12 3 0.250
    1-dodecanol (0.2 mg) + PD23 (0.40 mg) 12 5 0.417
    1-dodecanol (0.2 mg) 13 2 0.154
    1-dodecanol (0.2 mg) 13 0 0.000
    1-dodecanol (0.2 mg) 13 1 0.077
    1-tetradecanol (1.00 mg) + PD23 (0.40 mg) 12 1 0.083
    1-tetradecanol (1.00 mg) + PD23 (0.40 mg) 12 0 0.000
    1-tetradecanol (1.00 mg) + PD23 (0.40 mg) 12 1 0.083
    1-tetradecanol (1.00 mg) 12 1 0.083
    1-tetradecanol (1.00 mg) 12 1 0.083
    1-tetradecanol (1.00 mg) 13 2 0.154
    2-phenylethanol (0.1 mg) + PD23 (0.4 mg) 12 7 0.583
    2-phenylethanol (0.1 mg) + PD23 (0.4 mg) 14 14 1.000
    2-phenylethanol (0.1 mg) + PD23 (0.4 mg) 13 10 0.769
    2-phenylethanol (0.1 mg) 12 1 0.083
    2-phenylethanol (0.1 mg) 12 1 0.083
    2-phenylethanol (0.1 mg) 13 0 0.000
    2-phenylethanol (0.1 mg) 10 3 0.300
    2-butyoxyethanol (0.3 mg) + PD23 (0.4 mg) 12 12 1.000
    2-butyoxyethanol (0.3 mg) + PD23 (0.4 mg) 12 12 1.000
    2-butyoxyethanol (0.3 mg) + PD23 (0.4 mg) 12 12 1.000
    2-butyoxyethanol (0.2 mg) + PD23 (0.4 mg) 13 6 0.462
    2-butyoxyethanol (0.2 mg) + PD23 (0.4 mg) 13 6 0.462
    2-butyoxyethanol (0.2 mg) + PD23 (0.4 mg) 13 2 0.154
    2-butyoxyethanol (0.2 mg) 14 0 0.000
    2-butyoxyethanol (0.2 mg) 13 0 0.000
    2-butyoxyethanol (0.2 mg) 13 0 0.000
  • The composite data for certain compositions is presented below (Table 14), also including the calculated proportion of cockroaches dead at 24 hours for the group treated with alcohol alone and for the group treated with the composition comprising PD23 and alcohol. The difference between the proportion of dead cockroaches in the group treated with the composition comprising PD23 and alcohol and the group treated with alcohol alone was calculated, and is also presented in Table 14. Here, the increase in mortality indicates a synergistic effect with the combination compared to the alcohol or mineral oil alone, with a higher difference indicating a greater synergy. The straight chain saturated alcohols with chain lengths of C3-C7 demonstrated the greatest increase, or difference, in mortality when combined with PD23 mineral oil, as compared to the other alcohols tested.
  • TABLE 14
    Significance
    (* p < 0.05;
    Total # Difference ** p < 0.01;
    Individual or cockroaches # dead Proportion (combination- ns = not
    combination treatment treated at 24 h dead at 24 h alcohol) significant)
    PD23 —mineral oil 91 0 0 n/a
    (0.40 mg)
    methanol (3.0 mg) 39 1 0.026
    methanol (3.0 mg) + 38 13 0.342 0.316 *
    PD23 (0.40 mg)
    ethanol (1.25 mg) 37 1 0.027
    ethanol (1.25 mg) + 37 11 0.297 0.270 *
    PD23 (0.40 mg)
    1-propanol (0.45 mg) 36 1 0.028
    1-propanol (0.45 mg) + 37 35 0.946 0.918 **
    PD23 (0.40 mg)
    1-butanol (0.8 mg) 35 1 0.029
    1-butanol (0.8 mg) + 39 28 0.718 0.689 **
    PD23 (0.40 mg)
    1-hexanol (0.4 mg) 36 3 0.083
    1-hexanol (0.4 mg) + 37 37 1.000 0.917 **
    PD23 (0.40 mg)
    1-heptanol (0.4 mg) 36 1 0.028
    1-heptanol (0.4 mg) + 36 35 0.972 0.944 **
    PD23 (0.40 mg)
    1-octanol (0.2 mg) 37 2 0.054
    1-octanol (0.2 mg) + 36 9 0.250 0.196 *
    PD23 (0.40 mg)
    1-nonanol (0.2 mg) 41 1 0.024
    1-nonanol (0.2 mg) + 36 8 0.222 0.198 *
    PD23 (0.40 mg)
    1-decanol (0.2 mg) 37 1 0.027
    1-decanol (0.2 mg) + 36 1 0.028 0.001 ns
    PD23 (0.40 mg)
    1-undecanol (0.25 mg) 38 4 0.105
    1-undecanol (0.25 mg) + 37 1 0.027 −0.078 ns
    PD23 (0.40 mg)
    1-dodecanol (0.2 mg) 39 3 0.077
    1-dodecanol (0.2 mg) + 37 10 0.270 0.193 ns
    PD23 (0.40 mg)
    1-tetradecanol (1.0 mg) 37 4 0.108
    1-tetradecanol (1.0 mg) + 36 2 0.056 −0.052 ns
    PD23 (0.40 mg)
    diacetone alcohol (0.30 mg) 40 1 0.025
    diacetone alcohol (0.30 mg) + 40 35 0.875 0.850 **
    PD23 (0.40 mg)
    Isopropyl alcohol (0.60 mg) 38 0 0.000
    Isopropyl alcohol (0.60 mg) + 38 10 0.263 0.263 *
    PD23 (0.40 mg)
    2-butanol (0.80 mg) 38 1 0.026
    2-butanol (0.80 mg) + 38 4 0.105 0.079 ns
    PD23 (0.40 mg)
    t-butyl alcohol (0.50 mg) 44 2 0.045
    t-butyl alcohol (0.50 mg) + 33 14 0.424 0.379 *
    PD23 (0.40 mg)
    isobutyl alcohol (0.20 mg) 38 1 0.026
    isobutyl alcohol (0.20 mg) + 38 23 0.605 0.579 **
    PD23 (0.40 mg)
    2-phenylethanol (0.10 mg) 47 5 0.106
    2-phenylethanol (0.10 mg) + 39 31 0.795 0.689 **
    PD23 (0.40 mg)
    2-butyoxyethanol (0.20 mg) 40 0 0.000
    2-butyoxyethanol (0.20 mg) + 36 14 0.389 0.389 *
    PD23 (0.40 mg)
  • Example 11
  • In this embodiment, an aerosol pesticidal composition of the present disclosure was prepared. The ingredients and amounts used to prepare the composition are set forth in Table 15 below.
  • TABLE 15
    Ingredient Amount (wt/wt %)
    Mineral oil (PD-23, available from Chemtura) 43.13%
    Ethyl lactate 14.95%
    Isopropyl myristate 30.00%
    Geraniol 6.00%
    Nerol 2.57%
    Lemongrass oil 0.50%
    Carbon dioxide 2.85%
  • The composition was prepared by mixing a geraniol/nerol composition with the mineral oil, ethyl lactate, isopropyl myristate and lemongrass oil until homogenous. The resulting composition was placed in an aerosol can. The lid and actuator of the aerosol can were sealed onto the top of the can. The carbon dioxide was introduced into the can through the actuator to pressurize the can. The resulting product can be used as an aerosol pesticidal composition.
  • Example 12
  • In this example, the effectiveness of compositions comprising various compounds and/or mineral oil at killing cockroaches was tested. The compounds tested are shown in Table 16. The tests were performed as described in Example 1.
  • TABLE 16
    # dead at Proportion
    Composition # treated 24 h dead at 24 hr
    gamma butyrolactone (96-48-0) (0.25 mg) 7 3 0.429
    gamma butyrolactone (96-48-0) (0.25 mg) 10 3 0.300
    gamma butyrolactone (96-48-0) (0.25 mg) 10 5 0.500
    gamma butyrolactone (0.25 mg) + PD23 (0.40 mg) 8 8 1.000
    gamma butyrolactone (0.25 mg) + PD23 (0.40 mg) 10 9 0.900
    gamma butyrolactone (0.25 mg) + PD23 (0.40 mg) 11 10 0.909
    nitromethane (75-52-5) (0.70 mg) 11 0 0.000
    nitromethane (75-52-5) (0.70 mg) 12 0 0.000
    nitromethane (75-52-5) (0.70 mg) 11 0 0.000
    nitromethane (75-52-5) (0.80 mg) 7 0 0.000
    nitromethane (75-52-5) (0.80 mg) 10 2 0.200
    nitromethane (75-52-5) (0.80 mg) 11 3 0.273
    Nitromethane (0.70 mg) + PD23 (0.40 mg) 11 6 0.545
    Nitromethane (0.70 mg) + PD23 (0.40 mg) 11 7 0.636
    Nitromethane (0.70 mg) + PD23 (0.40 mg) 11 7 0.636
    Nitromethane (0.80 mg) + PD23 (0.40 mg) 7 7 1.000
    Nitromethane (0.80 mg) + PD23 (0.40 mg) 10 9 0.900
    Nitromethane (0.80 mg) + PD23 (0.40 mg) 11 7 0.636
    Di(ethylene) glycol (111-46-6) (0.80 mg) 10 0 0.000
    Di(ethylene) glycol (111-46-6) (0.80 mg) 10 0 0.000
    Di(ethylene) glycol (111-46-6) (0.80 mg) 13 6 0.462
    Di(ethylene) glycol (0.80 mg) + PD23 (0.40 mg) 10 0 0.000
    Acetophenone (98-86-2) (0.10 mg) 10 0 0.000
    Acetophenone (98-86-2) (0.10 mg) 10 0 0.000
    Acetophenone (98-86-2) (0.10 mg) 10 0 0.000
    Acetophenone (98-86-2) (0.10 mg) + PD23 (0.40 mg) 10 3 0.300
    Acetophenone (98-86-2) (0.10 mg) + PD23 (0.40 mg) 10 8 0.800
    Acetophenone (98-86-2) (0.10 mg) + PD23 (0.40 mg) 10 10 1.000
    diethyl ether (60-29-7) (2.00 mg) 11 0 0.000
    diethyl ether (60-29-7) (2.00 mg) 10 0 0.000
    diethyl ether (2.00 mg) + PD23 (0.40 mg) 10 1 0.000
    Isopropyl acetate (108-21-4) (1.00 mg) 10 1 0.100
    Isopropyl acetate (108-21-4) (1.00 mg) 10 2 0.200
    Isopropyl acetate (108-21-4) (1.00 mg) + PD23 (0.40 mg) 10 0 0.000
    2-butanone (methyl ethyl ketone) (78-93-3) (2.00 mg) 13 0 0.000
    2-butanone (methyl ethyl ketone) (78-93-3) (2.00 mg) 12 2 0.167
    2-butanone (methyl ethyl ketone) (78-93-3) (2.00 mg) 11 1 0.091
    2-butanone (methyl ethyl ketone) (78-93-3) (2.00 mg) + 10 3 0.300
    PD23 (0.40 mg)
    2-butanone (methyl ethyl ketone) (78-93-3) (2.00 mg) + 12 2 0.167
    PD23 (0.40 mg)
    2-butanone (methyl ethyl ketone) (78-93-3) (2.00 mg) + 12 2 0.167
    PD23 (0.40 mg)
    Triacetin (102-76-1) (2.00 mg) 10 0 0.000
    Triacetin (102-76-1) (2.00 mg) 10 1 0.100
    Triacetin (102-76-1) (2.00 mg) 10 0 0.000
    Triacetin (102-76-1) (2.0 mg) + PD23 (0.40 mg) 11 6 0.545
    Triacetin (102-76-1) (2.0 mg) + PD23 (0.40 mg) 10 8 0.800
    Triacetin (102-76-1) (2.0 mg) + PD23 (0.40 mg) 10 8 0.800
    Pyridine (110-86-1) (0.10 mg) 11 0 0.000
    Pyridine (110-86-1) (0.10 mg) 10 0 0.000
    Pyridine (110-86-1) (0.10 mg) 10 1 0.100
    Pyridine (110-86-1) (0.10 mg) + PD23 (0.40 mg) 10 10 1.000
    Pyridine (110-86-1) (0.10 mg) + PD23 (0.40 mg) 10 10 1.000
    Pyridine (110-86-1) (0.10 mg) + PD23 (0.40 mg) 10 10 1.000
    Chloroform anhydrous (67-66-3) (1.00 mg) 10 1 0.100
    Chloroform anhydrous (67-66-3) (1.00 mg) 10 0 0.000
    Chloroform anhydrous (67-66-3) (1.00 mg) + PD23 (0.40 mg) 10 0 0.000
    Methyl isobutyl ketone (108-10-1) (1.00 mg) 10 1 0.100
    Methyl isobutyl ketone (108-10-1) (1.00 mg) 11 0 0.000
    Methyl isobutyl ketone (108-10-1) (1.00 mg) + PD23 10 1 0.100
    (0.40 mg)
    Tetrahydrofuran (109-99-9) (0.80 mg) 10 3 0.300
    Tetrahydrofuran (109-99-9) (0.80 mg) + PD 23 (0.40 mg) 10 0 0.000
    2-ethoxyethanol (ethyl cellosolve) (110-80-5) (0.60 mg) 10 1 0.100
    2-ethoxyethanol (ethyl cellosolve) (110-80-5) (0.60 mg) 10 0 0.000
    2-ethoxyethanol (ethyl cellosolve) (110-80-5) (0.60 mg) 10 0 0.000
    2-ethoxyethanol (ethyl cellosolve) (110-80-5) (0.60 mg) + 10 8 0.800
    0.40 mg PD23
    2-ethoxyethanol (ethyl cellosolve) (110-80-5) (0.60 mg) + 10 5 0.500
    0.40 mg PD23
    2-ethoxyethanol (ethyl cellosolve) (110-80-5) (0.60 mg) + 11 7 0.636
    0.40 mg PD23
    n-methyl pyrrolidone (872-50-4) (0.10 mg) 10 5 0.500
    n-methyl pyrrolidone (872-50-4) (0.05 mg) 10 1 0.100
    n-methyl pyrrolidone (872-50-4) (0.10 mg) + PD23 (0.40 mg) 10 7 0.700
    n-methyl pyrrolidone (872-50-4) (0.05 mg) + PD23 (0.40 mg) 12 1 0.083
    Polyethylene glycol 200 Sigma (25322-68-3) (0.80 mg) 10 1 0.100
    Polyethylene glycol 200 Sigma (25322-68-3) (0.80 mg) 10 0 0.000
    Polyethylene glycol 200 Sigma (25322-68-3) (0.80 mg) 12 4 0.333
    Polyethylene glycol 200 Sigma (0.80 mg) + PD23 (0.40 mg) 10 3 0.300
    Dimethoxymethane (methylal) (109-87-5) (2.00 mg) 12 0 0.000
    Dimethoxymethane (methylal) (109-87-5) (2.00 mg) 10 0 0.000
    Dimethoxymethane (methylal) (109-87-5) (2.00 mg) + 10 1 0.100
    PD23 (0.40 mg)
    Methyl chloroform (71-55-6) (2.00 mg) 11 1 0.091
    Methyl chloroform (71-55-6) (2.00 mg) 10 1 0.100
    Methyl chloroform (71-55-6) (2.00 mg) + PD23 (0.40 mg) 10 0 0.000
    Diisopropyl biphenyl Nu-solv (69009-90-1) (0.80 mg) 10 0 0.000
    Diisopropyl biphenyl Nu-solv (69009-90-1) (0.80 mg) + 10 2 0.200
    PD23 (0.40 mg)
    Hexanes (110-54-3) (0.80 mg) 10 1 0.100
    Hexanes (0.80 mg) + PD23 (0.40 mg) 10 0 0.000
    Methyl t-butyl ether (1634-04-4) (2.00 mg) 12 2 0.167
    Methyl t-butyl ether (1634-04-4) (2.00 mg) 10 3 0.300
    Methyl t-butyl ether (1634-04-4) (2.00 mg) + PD23 (0.40 mg) 10 2 0.200
    Dichloromethane (methylene chloride) (75-09-02) (1.50 mg) 10 0 0.000
    Dichloromethane (methylene chloride) (1.50 mg) + 10 0 0.000
    PD23 (0.40 mg)
    Toluene (108-88-3) (0.90 mg) 10 0 0.000
    Toluene (108-88-3) (0.90 mg) + PD23 (0.40 mg) 10 1 0.100
  • The composite data for certain compositions is presented below (Table 17), also including the calculated proportion of cockroaches dead at 24 hours for the group treated with the specific compounds alone and for the group treated with the composition comprising PD23 and the compound. The difference between the proportion of dead cockroaches in the group treated with the composition comprising PD23 and the compounds and the group treated with the compounds alone was calculated, and is also presented in Table 17. Here, the increase in mortality indicates a synergistic effect with the combination compared to the tested compound or mineral oil alone, with a higher difference indicating a greater synergy. γ-butyrolactone, nitromethane, acetophenone, triacetin, pyridine and 2-ethoxyethanol demonstrated the greatest increase in mortality when combined with PD23 mineral oil, as compared to the other compounds tested.
  • TABLE 17
    Significance
    (*p < 0.05;
    Total # of Difference ** p < 0.01;
    Individual or combination cockroaches # dead Proportion (combination- ns = not
    treatment treated at 24 h dead at 24 h solvent) significant)
    PD23 - mineral oil (0.40 mg) 91 0 0.000 n/a
    gamma butyrolactone (96- 27 11 0.407
    48-0) (0.25 mg)
    gamma butyrolactone (96- 29 27 0.931 0.524 **
    48-0) (0.25 mg) + PD23
    (0.40 mg)
    nitromethane (75-52-5) 34 0 0.000
    (0.70 mg)
    nitromethane (75-52-5) 33 20 0.606 0.606 **
    (0.70 mg) + PD23 (0.40 mg)
    nitromethane (75-52-5) 28 5 0.179
    (0.80 mg)
    nitromethane (75-52-5) 28 23 0.821 0.643 **
    (0.80 mg) + PD23 (0.40 mg)
    Di(ethylene) glycol (111-46- 33 6 0.182
    6) (0.80 mg)
    Di(ethylene) glycol (111-46- 10 0 0.000 −0.182 ns
    6) (0.80 mg) + PD23 (0.40 mg)
    Acetophenone (98-86-2) 30 0 0.000
    (0.10 mg)
    Acetophenone (98-86-2) 30 21 0.700 0.700 *
    (0.10 mg) + PD23 (0.40 mg)
    diethyl ether (60-29-7) (2.0 mg) 21 0 0.000
    diethyl ether (60-29-7) (2.0 mg) + 10 1 0.100 0.100 ns
    PD23 (0.40 mg)
    Isopropyl acetate (108-21-4) 20 3 0.150
    (1.0 mg)
    Isopropyl acetate (108-21-4) 10 0 0.000 −0.150 ns
    (1.0 mg) + PD23 (0.40 mg)
    2-butanone (methyl ethyl 36 3 0.083
    ketone) (78-93-3) (2.0 mg)
    2-butanone (methyl ethyl 34 7 0.206 0.123 ns
    ketone) (78-93-3) (2.0 mg) +
    PD23 (0.40 mg)
    Triacetin (102-76-1) (2.0 mg) 30 1 0.033
    Triacetin (102-76-1) (2.0 mg) + 31 22 0.710 0.676 **
    PD23 (0.40 mg)
    Pyridine (110-86-1) (0.10 mg) 31 1 0.032
    Pyridine (110-86-1) (0.10 mg) + 30 30 1.000 0.968 **
    PD23 (0.40 mg)
    Chloroform-anhydrous (67- 20 1 0.050
    66-3) (2.0 mg)
    Chloroform-anhydrous (67- 10 0 0.000 −0.050 ns
    66-3) (2.0 mg) + PD23 (0.40 mg)
    Methyl isobutyl ketone 21 1 0.048
    (108-10-1) (1.0 mg)
    Methyl isobutyl ketone 10 1 0.100 0.052 ns
    (108-10-1) (1.0 mg) + PD23
    (0.40 mg)
    Tetrahydrofuran (109-99-9) 10 3 0.300
    (0.80 mg)
    Tetrahydrofuran (109-99-9) 10 0 0.000 −0.300 ns
    (0.80 mg) + PD 23 (0.40 mg)
    2-ethoxyethanol (ethyl 30 1 0.033
    cellosolve) (110-80-5) (0.60 mg)
    2-ethoxyethanol (ethyl 31 20 0.645 0.612 **
    cellosolve) (110-80-5) (0.60 mg) +
    PD23 (0.40 mg)
    n-methyl pyrrolidone (872- 10 1 0.100
    50-4) (0.05 mg)
    n-methyl pyrrolidone (872- 12 1 0.083 −0.017 ns
    50-4) (0.05 mg) + PD23
    (0.40 mg)
    n-methyl pyrrolidone (872- 10 5 0.500
    50-4) (0.10 mg)
    n-methyl pyrrolidone (872- 10 7 0.700 0.200 ns
    50-4) (0.10 mg) + PD23
    (0.40 mg)
    Polyethylene glycol 200 32 5 0.156
    Sigma (25322-68-3) (0.80 mg)
    Polyethylene glycol 200 10 3 0.300 0.144 ns
    Sigma (25322-68-3) (0.80 mg) +
    PD23 (0.40 mg)
    Dimethoxymethane 22 0 0.000
    (methylal) (109-87-5) (2.0 mg)
    Dimethoxymethane 10 1 0.100 0.100 ns
    (methylal) (109-87-5) (2.0 mg) +
    PD23 (0.40 mg)
    Methyl chloroform (71-55- 21 2 0.095
    6) (2.00 mg)
    Methyl chloroform (71-55- 10 0 0.000 −0.095 ns
    6) (2.00 mg) + PD23 (0.40 mg)
    Diisopropyl biphenyl Nu- 10 0 0.000
    solv (69009-90-1) (0.80 mg)
    Diisopropyl biphenyl Nu- 10 2 0.200 0.200
    solv (69009-90-1) (0.80 mg) +
    PD23 (0.40 mg)
    Hexanes (110-54-3) (0.80 mg) 10 1 0.100
    Hexanes (110-54-3) (0.80 mg) + 10 0 0.000 −0.100 ns
    PD23 (0.40 mg)
    Methyl t-butyl ether (1634- 22 5 0.227
    04-4) (2.00 mg)
    Methyl t-butyl ether (1634- 10 2 0.200 −0.027 ns
    04-4) (2.00 mg) + PD23
    (0.40 mg)
    Dichloromethane 10 0 0.000
    (methylene chloride) (75-
    09-02) (1.50 mg)
    Dichloromethane 10 0 0.000 0.000 ns
    (methylene chloride) (75-
    09-02) (1.50 mg) + PD23
    (0.40 mg)
    Toluene (108-88-3) (0.90 mg) 10 0 0.000
    Toluene (108-88-3) (0.90 mg) + 10 1 0.100 0.100 ns
    PD23 (0.40 mg)
  • Example 17
  • 1-propanol and 1-heptanol were tested alone and in combination with Exxsol D95 mineral oil. Exxsol D95 was also tested alone. The results are shown in Table 18. Both alcohols exhibited significant synergy with Exxsol D95.
  • TABLE 18
    Individual or Total # of Difference Significance
    combination cockroaches # dead at Proportion (combination- (*p < 0.05; **
    treatment treated 24 h dead at 24 h solvent) p < 0.01)
    Exxsol D95 (64742- 30 1 0.033
    47-8) (0.40 mg)
    1-heptanol (111-70- 36 1 0.028
    6) (0.40 mg)
    1-propanol (71-23- 36 1 0.028
    8) (0.45 mg)
    Exxsol D95 (0.40 mg) + 21 21 1.000 0.972 **
    1 heptanol
    (0.40 mg)
    Exxsol D95 (0.40 mg) + 21 19 0.905 0.877 **
    1-propanol
    (0.40 mg)
  • When introducing elements of the present disclosure or the preferred embodiments(s) thereof, the articles “a”, “an”, “the” and “said” are intended to mean that there are one or more of the elements. The terms “comprising”, “including” and “having” are intended to be inclusive and mean that there may be additional elements other than the listed elements.
  • In view of the above, it will be seen that the several objects of the disclosure are achieved and other advantageous results attained.
  • As various changes could be made in the above compositions and products without departing from the scope of the disclosure, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limiting sense.

Claims (30)

1. A pesticidal composition comprising a first active ingredient and a second active ingredient, the first active ingredient being a mineral oil and the second active ingredient selected from the group consisting of hexylene glycol, dioxane, nitromethane, acetophenone, pyridine and combinations thereof.
2. The composition of claim 1 wherein the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, d-limonene and combinations thereof.
3. The composition of claim 1 wherein the second active ingredient is hexylene glycol.
4. The composition of claim 1 wherein the second active ingredient is dioxane.
5. The composition of claim 1 wherein the second active ingredient is d-limonene.
6. The composition of claim 1 wherein the second active ingredient is nitromethane.
7. The composition of claim 1 wherein the second active ingredient is acetophenone.
8. The composition of claim 1 wherein the second active ingredient is pyridine.
9. The composition of claim 1 wherein the composition comprises at least about 3% of the second active ingredient by weight of the composition.
10. The composition of claim 1 wherein the composition comprises from about 10% to about 60% of the second active ingredient by weight of the composition.
11. The composition of claim 1 wherein the composition comprises at least about 30% mineral oil by weight of the composition.
12. The composition of claim 1 wherein the composition further comprises a plant essential oil or derivative.
13. The composition of claim 12 wherein the plant essential oil or derivative is geraniol.
14. The composition of claim 1 wherein the mineral oil is a petroleum distillate.
15. The composition of claim 1 wherein the composition comprises an emulsifier.
16. A method of controlling arthropods, the method comprising contacting an arthropod with a pesticidally effective amount of a composition comprising a first active ingredient and a second active ingredient, the first active ingredient being a mineral oil and the second active ingredient selected from the group consisting of hexylene glycol, dioxane, d-limonene, nitromethane, acetophenone, pyridine and combinations thereof.
17. The method of claim 16 wherein the insect or pest is a cockroach.
18. The method of claim 16 wherein the composition is packaged as a pump spray.
19. The method of claim 16 wherein the composition is packaged in a pressurized container.
20. The method of claim 16 comprising diluting a concentrate composition with water to produce the composition.
21. The method of claim 20 wherein the concentrate composition comprises an emulsifier.
22. The method of claim 16 wherein the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, nitromethane, acetophenone, pyridine and combinations thereof.
23. The method of claim 16 wherein the second active ingredient is selected from the group consisting of hexylene glycol, dioxane, d-limonene and combinations thereof.
24. The method of claim 16 wherein the composition comprises at least about 3% of the second active ingredient by weight of the composition.
25. The method of claim 16 wherein the composition comprises from about 10% to about 60% of the second active ingredient by weight of the composition.
26. The method of claim 16 wherein the composition comprises at least about 30% mineral oil by weight of the composition.
27. The method of claim 16 wherein the composition further comprises a plant essential oil or derivative.
28. The method of claim 27 wherein the plant essential oil or derivative is geraniol.
29. The method of claim 16 wherein the mineral oil is a petroleum distillate.
30. The method of claim 16 wherein the arthropod is contacted with the pesticidal composition in an amount that causes death of the arthropod.
US12/418,466 2008-04-11 2009-04-03 Pesticidal compositions Abandoned US20090258889A1 (en)

Priority Applications (24)

Application Number Priority Date Filing Date Title
US12/418,466 US20090258889A1 (en) 2008-04-11 2009-04-03 Pesticidal compositions
EA201001616A EA018969B1 (en) 2008-04-11 2009-04-06 Pesticidal compositions
CA2720953A CA2720953A1 (en) 2008-04-11 2009-04-06 Pesticidal compositions
MYPI20104721 MY149026A (en) 2008-04-11 2009-04-06 Pesticidal compositions
KR20107025258A KR20100134105A (en) 2008-04-11 2009-04-06 Pesticidal compositions
EA201201028A EA201201028A1 (en) 2008-04-11 2009-04-06 PESTICIDAL COMPOSITIONS
CN2009801215262A CN102083311A (en) 2008-04-11 2009-04-06 Pesticidal compositions
AU2009233944A AU2009233944A1 (en) 2008-04-11 2009-04-06 Pesticidal compositions
CN2013101326390A CN103190446A (en) 2008-04-11 2009-04-06 Pesticidal compositions
EA201201029A EA201201029A1 (en) 2008-04-11 2009-04-06 PESTICIDAL COMPOSITIONS
CN2013101327181A CN103210959A (en) 2008-04-11 2009-04-06 Pesticidal compositions
BRPI0911664-8A BRPI0911664A2 (en) 2008-04-11 2009-04-06 Pesticide composition and method for controlling arthropods and controlling cockroaches
MX2010011081A MX2010011081A (en) 2008-04-11 2009-04-06 Pesticidal compositions.
PCT/US2009/039664 WO2009126577A2 (en) 2008-04-11 2009-04-06 Pesticidal compositions
EP09730159A EP2271216A4 (en) 2008-04-11 2009-04-06 Pesticidal compositions
PH12010502295A PH12010502295A1 (en) 2008-04-11 2009-04-06 Pesticidal compositions
JP2011504111A JP2011517685A (en) 2008-04-11 2009-04-06 Pesticide composition
ARP090101274 AR071468A1 (en) 2008-04-11 2009-04-08 PESTICIDED COMPOSITIONS
TW98112120A TW200948273A (en) 2008-04-11 2009-04-10 Pesticidal compositions
UY31759A UY31759A (en) 2008-04-11 2009-04-13 PESTICIDED COMPOSITIONS
IL208553A IL208553A0 (en) 2008-04-11 2010-10-07 Pesticidal compositions
CR11720A CR11720A (en) 2008-04-11 2010-10-08 PESTICIDED COMPOSITIONS
MA33331A MA32292B1 (en) 2008-04-11 2010-11-08 Pesticide formulations
ZA2010/08005A ZA201008005B (en) 2008-04-11 2010-11-09 Pesticidal compositions

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US4429708P 2008-04-11 2008-04-11
US11523108P 2008-11-17 2008-11-17
US12/418,466 US20090258889A1 (en) 2008-04-11 2009-04-03 Pesticidal compositions

Publications (1)

Publication Number Publication Date
US20090258889A1 true US20090258889A1 (en) 2009-10-15

Family

ID=41164174

Family Applications (5)

Application Number Title Priority Date Filing Date
US12/418,443 Expired - Fee Related US8231887B2 (en) 2008-04-11 2009-04-03 Pesticidal compositions
US12/418,455 Active 2029-10-09 US9005644B2 (en) 2008-04-11 2009-04-03 Pesticidal compositions
US12/418,466 Abandoned US20090258889A1 (en) 2008-04-11 2009-04-03 Pesticidal compositions
US13/562,073 Active US8591927B2 (en) 2008-04-11 2012-07-30 Pesticidal compositions
US13/889,896 Abandoned US20130245053A1 (en) 2008-04-11 2013-05-08 Pesticidal Compositions

Family Applications Before (2)

Application Number Title Priority Date Filing Date
US12/418,443 Expired - Fee Related US8231887B2 (en) 2008-04-11 2009-04-03 Pesticidal compositions
US12/418,455 Active 2029-10-09 US9005644B2 (en) 2008-04-11 2009-04-03 Pesticidal compositions

Family Applications After (2)

Application Number Title Priority Date Filing Date
US13/562,073 Active US8591927B2 (en) 2008-04-11 2012-07-30 Pesticidal compositions
US13/889,896 Abandoned US20130245053A1 (en) 2008-04-11 2013-05-08 Pesticidal Compositions

Country Status (21)

Country Link
US (5) US8231887B2 (en)
EP (1) EP2271216A4 (en)
JP (1) JP2011517685A (en)
KR (1) KR20100134105A (en)
CN (3) CN103190446A (en)
AR (1) AR071468A1 (en)
AU (1) AU2009233944A1 (en)
BR (1) BRPI0911664A2 (en)
CA (1) CA2720953A1 (en)
CL (1) CL2009000871A1 (en)
CR (1) CR11720A (en)
EA (3) EA201201029A1 (en)
IL (1) IL208553A0 (en)
MA (1) MA32292B1 (en)
MX (1) MX2010011081A (en)
MY (1) MY149026A (en)
PH (1) PH12010502295A1 (en)
TW (1) TW200948273A (en)
UY (1) UY31759A (en)
WO (1) WO2009126577A2 (en)
ZA (1) ZA201008005B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108633932A (en) * 2011-10-04 2018-10-12 0903608 B.C.有限公司 Injurious insect control formulation and manufacture and use its method
US10905114B2 (en) 2011-10-04 2021-02-02 0903608 B.C. Ltd. Pest control formulations and methods of making and using same

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8231887B2 (en) 2008-04-11 2012-07-31 Basf Corporation Pesticidal compositions
AU2010319082B2 (en) * 2009-11-13 2014-12-04 National University Corporation Okayama University Termite egg disinfestation technique utilizing volatile calling pheromone and queen pheromone
JP5633329B2 (en) 2009-11-20 2014-12-03 住友化学株式会社 Pest control composition
ITMI20110831A1 (en) * 2011-05-12 2012-11-13 Anna Andolfi FAGODETERRENT COMPOUNDS OF MUSHROOM ORIGIN
KR101288541B1 (en) * 2011-06-24 2013-07-22 전북대학교산학협력단 Composition of acaricidal components containing Acetophenone's derivatives and acaricide using the same
CA2902282C (en) * 2013-02-27 2023-03-14 Laurie Robert BATT Transdermal formulations
WO2014149138A2 (en) * 2013-03-15 2014-09-25 Tyratech Inc. Lice control composition and method
US9089141B2 (en) * 2013-09-20 2015-07-28 John James McIntyre Natural insect repellent formula BBX2
BR112016014288B1 (en) * 2013-12-30 2021-08-24 Dow Global Technologies Llc MICROBICIDE COMPOSITION, METHOD TO INHIBIT GROWTH OR CONTROL GROWTH OF MICROORGANISMS, COATING COMPOSITION, PRODUCT AND DRY FILM
BR112017000039A2 (en) 2014-07-02 2018-07-17 Ralco Nutrition, Inc. agricultural compositions and applications using essential oils
US20160374350A1 (en) * 2015-06-29 2016-12-29 Anthony C. Watson Method of treating bed bug infestation and preventing transmission thereof
MX2018007598A (en) * 2015-12-22 2018-09-21 Bayer Cropscience Ag Emulsion concentrates of lipophilic compounds.
CN105794858A (en) * 2016-03-01 2016-07-27 江西天人生物控股有限公司 Farm-oriented insecticidal composition and application thereof
CN106035362A (en) * 2016-05-31 2016-10-26 刘园 Composition for controlling adoxophyes orana and preparation method of composition
US10874099B2 (en) 2017-12-27 2020-12-29 Mclaughlin Gormley King Company Sabadilla alkaloid emulsifiable concentrate
CN108323525A (en) * 2018-02-08 2018-07-27 青岛农业大学 Application of the nerol in preparing termiticides
CN110122487B (en) * 2019-05-23 2021-04-06 赣南师范大学 Application of alcohol in attracting diaphorina citri and diaphorina citri attractant
TWI790635B (en) * 2021-06-08 2023-01-21 誌懋股份有限公司 Uses of Australian Cypress Extract for Cockroach Repellent

Citations (83)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1516907A (en) * 1918-06-25 1924-11-25 Us Ind Alcohol Co Fuel for motors
US1858635A (en) * 1927-04-25 1932-05-17 Pan American Petroleum & Trans Sweetening hydrocarbon oils
US2023140A (en) * 1932-10-19 1935-12-03 Shell Dev Livestock spray
US2041874A (en) * 1935-02-15 1936-05-26 Frits E Stockelbach Composition for preventing sunburn
US2763614A (en) * 1954-06-04 1956-09-18 Gulf Oil Corp Corrosion-inhibiting compositions
US2809122A (en) * 1954-06-24 1957-10-08 Sherwin Williams Co Dual purpose tinting base
US3158535A (en) * 1961-10-02 1964-11-24 Exxon Research Engineering Co Pyrethrin-elastomer insecticidal composition and method
US3163607A (en) * 1962-08-02 1964-12-29 Bethlehem Steel Corp Method for removing oil lubricant film from steel
US3291557A (en) * 1963-01-07 1966-12-13 Battelle Development Corp Alkyl dicarboxylic acid treatment of leather
US3444080A (en) * 1967-04-14 1969-05-13 Shell Oil Co Lubricant for rolling metals
US3806593A (en) * 1971-06-01 1974-04-23 Medisan Ab Hygienic-cosmetic compositions
US3923997A (en) * 1971-05-11 1975-12-02 Rhodia Process for repelling dogs and cats from a selected area or from each other using {65 -n-alkyl-{65 -butyrolactones and {67 -n-alkyl-{67 -valerolactones
US4056610A (en) * 1975-04-09 1977-11-01 Minnesota Mining And Manufacturing Company Microcapsule insecticide composition
US4252796A (en) * 1979-08-17 1981-02-24 Yu Ruey J Stable water-in-oil emulsions
US4279946A (en) * 1977-09-07 1981-07-21 Foseco International Limited Coating compositions
US4285868A (en) * 1968-03-20 1981-08-25 Mobil Oil Corporation Preparation of gamma-butyrolactones
US4534128A (en) * 1983-02-01 1985-08-13 Query Grady W Method for pest control using anesthetic and insecticide
US4562214A (en) * 1979-09-10 1985-12-31 Witco Chemical Corporation Personal care emulsion
US4612331A (en) * 1982-02-02 1986-09-16 Lever Brothers Company Skin treatment composition
US4624070A (en) * 1983-02-01 1986-11-25 Query Grady W Method and composition for pest control using anesthetic and insecticide
US4774081A (en) * 1987-01-13 1988-09-27 S. C. Johnson & Son, Inc. Contact insect repellents
US4774082A (en) * 1987-01-13 1988-09-27 S. C. Johnson & Son, Inc. Volatile insect repellents
US4822614A (en) * 1986-12-19 1989-04-18 S. C. Johnson & Son, Inc. Bioactive film-forming composition for control of crawling insects and the like
US4902510A (en) * 1987-10-05 1990-02-20 Shell Internationale Research Maatschappij B.V. Ectoparasiticidal pour-on formulation
US4923698A (en) * 1986-12-19 1990-05-08 S. C. Johnson & Son, Inc. Bioactive film-forming composition for control of crawling insects and the like
US4933371A (en) * 1984-07-26 1990-06-12 Shirlo, Inc. Controlling ticks and fleas with linalool
US4961532A (en) * 1989-07-07 1990-10-09 Dow Corning Corporation Fragrance release device containing a highly adsorptive copolymer
US4962133A (en) * 1989-09-05 1990-10-09 Dow Corning Corporation Method of making highly adsorptive copolymers
US5093326A (en) * 1989-06-19 1992-03-03 Stephen Herman Repellant compositions
US5130135A (en) * 1989-08-18 1992-07-14 Smithkline Beecham Plc Pesticidal formulations
US5143900A (en) * 1989-05-19 1992-09-01 Colgate-Palmolive Company Perfumes containing N-lower alkyl neoalkanamide (s)
US5227163A (en) * 1991-01-18 1993-07-13 Clilco, Ltd. Lice-repellant compositions
US5227406A (en) * 1990-04-09 1993-07-13 Primavera Laboratories, Inc. Insect repellent lotions and sprays
US5290556A (en) * 1990-02-02 1994-03-01 The United States Of America As Represented By The Secretary Of Agriculture Plastic bait composition for attracting and killing crop pests
US5344776A (en) * 1991-03-28 1994-09-06 The United States Of America As Represented By The Department Of Health And Human Services DNA encoding an insect octopamine receptor
US5476609A (en) * 1994-07-11 1995-12-19 Wilkins, Jr.; William S. Acidic cleaning composition for removing burnt starch from cold metal press heads
US5510117A (en) * 1989-03-09 1996-04-23 Micro-Pak, Inc. Entrapment vehicle and method
US5525597A (en) * 1993-12-14 1996-06-11 Kalamazoo Holdings, Inc. Synergistic insecticidal compositions comprising capsicum and insecticidal use thereof
US5536501A (en) * 1994-12-30 1996-07-16 Proguard, Inc. Use of flavenoid aldehydes as insecticides and for killing arachnids
US5538990A (en) * 1991-07-15 1996-07-23 Pfizer Inc. Benzimidazole anthelmintics
US5559271A (en) * 1995-07-26 1996-09-24 Phillips Petroleum Company Organic polysulfide compositions having reduced odor
US5562864A (en) * 1991-04-19 1996-10-08 The Lubrizol Corporation Lubricating compositions and concentrates
US5621013A (en) * 1992-06-24 1997-04-15 Primavera Laboratories, Inc. Insect replellent blends, lotions, and sprays
US5654362A (en) * 1996-03-20 1997-08-05 Dow Corning Corporation Silicone oils and solvents thickened by silicone elastomers
US5674518A (en) * 1991-08-06 1997-10-07 Prentiss Incorporated Method of fish management by poison fish bait method of making the bait, and formulation of bait
US5698210A (en) * 1995-03-17 1997-12-16 Lee County Mosquito Control District Controlled delivery compositions and processes for treating organisms in a column of water or on land
US5753686A (en) * 1992-09-18 1998-05-19 International Flavors & Fragrances Inc. Method for repelling fire ants and horn flies and compositions for repelling fire ants and horn flies and acting as anti-feedants for fire ants and horn flies
US5753507A (en) * 1995-09-22 1998-05-19 Novartis Finance Corporation Plant geraniol/nerol 10-hydroxylase and DNA coding therefor
US5792465A (en) * 1996-06-28 1998-08-11 S. C. Johnson & Son, Inc. Microemulsion insect control compositions containing phenol
US5814325A (en) * 1993-03-24 1998-09-29 The Rod Family Trust Process for repelling and killing insects and compositions to effect the same comprising a monoterpene
US5834413A (en) * 1997-09-26 1998-11-10 Colgate-Palmolive Co. Liquid cleaning compositions
US5834533A (en) * 1996-11-20 1998-11-10 Phillips Petroleum Company Stable liquid suspension compositions
US5872143A (en) * 1996-08-07 1999-02-16 Sumitomo Chemical Company, Limited Insecticidal aerosol composition and insecticidal composition for preparation of same
US5880210A (en) * 1997-04-01 1999-03-09 Dow Corning Corporation Silicone fluids and solvents thickened with silicone elastomers
US5977023A (en) * 1993-10-05 1999-11-02 Sumitomo Chemical Company, Limited Sustained release, solid pesticidal compositions comprising water insoluble alginates
US5977186A (en) * 1998-01-27 1999-11-02 Ximed Group Plc Terpene treatments for killing lice and lice eggs
US5998484A (en) * 1998-04-15 1999-12-07 Woodstream Corporation Insecticidal compositions and method of controlling insect pests using same
US6001874A (en) * 1992-08-18 1999-12-14 Veierov; Dan Arthropod control composition for plant protection
US6024972A (en) * 1998-07-21 2000-02-15 Isp Investments Inc. Water-free concentrate of amitraz insecticide and clear pour-on formulations thereof
US6071857A (en) * 1996-06-28 2000-06-06 Novartis Crop Protection, Inc. Pesticidal compositions
US6071973A (en) * 1992-08-07 2000-06-06 The United States Of America As Represented By The Secretary Of Agriculture Repellent for ants
US6074634A (en) * 1997-10-06 2000-06-13 The United States Of America As Represented By The Secretary Of Agriculture Feeding attractant and stimulant for adult control of noctuid and/or other lepidopteran species
US6083498A (en) * 1998-03-10 2000-07-04 The United States Of America As Represented By The Secretary Of Agriculture Chemical attractants for yellowjackets and paper wasps
US6124490A (en) * 1999-10-26 2000-09-26 Mona Industries, Inc. Zwitterionic siloxane polymers and ionically cross-linked polymers formed therefrom
US6130253A (en) * 1998-01-27 2000-10-10 Ximed Group Plc Terpene based pesticide treatments for killing terrestrial arthropods including, amongst others, lice, lice eggs, mites and ants
US6184197B1 (en) * 1996-09-19 2001-02-06 The Procter & Gamble Company Polymeric compound comprising one or more active alcohols
US6197098B1 (en) * 1999-12-16 2001-03-06 Isp Investments Inc. Fast drying biocidal preservative composition
US6251415B1 (en) * 1997-10-27 2001-06-26 Fmc Corporation Solvent system for pesticide products
US6255356B1 (en) * 2000-03-30 2001-07-03 International Flavors & Fragrances Inc. Method for inhibiting from feeding, cockroaches
US6255350B1 (en) * 1997-10-14 2001-07-03 Isp Investments Inc. Stabilized concentrates of water unstable AZA compounds and o/w miniemulsions thereof
US6277415B1 (en) * 1996-03-29 2001-08-21 Orna Levin Pediculocidal and veterinary compositions
US6441051B1 (en) * 2001-09-20 2002-08-27 William B. Wheeler Insect eradicator and method
US6555121B1 (en) * 2000-05-26 2003-04-29 Ecosmart Technologies, Inc. Pesticidal compositions containing mineral oil and/or soybean oil
US6641803B1 (en) * 1998-02-06 2003-11-04 Cognis Deutschland Gmbh & Co. Kg Hair-conditioning agents
US20040220075A1 (en) * 1999-09-03 2004-11-04 Ahrens Edward R. Treatment of skin disorders
US20040253287A1 (en) * 2002-08-03 2004-12-16 Denton Robert Michael Environmentally safe insecticides
US20050232981A1 (en) * 2004-04-15 2005-10-20 Ben-Sasson Shmuel A Compositions capable of facilitating penetration across a biological barrier
US20050261379A1 (en) * 2004-05-18 2005-11-24 Petro-Canada Spray Oil and Method of Use Therefor for Controlling Turfgrass Pests
US20060115508A1 (en) * 1999-06-28 2006-06-01 Ecosmart Technologies, Inc. Synergistic and residual pesticidal compositions containing plant essential oils with enzyme inhibitors
US20060257441A1 (en) * 2005-05-10 2006-11-16 Suzuki Yushi Industrial Co., Ltd. Natural essential oil sanitary insect pest repellent and its use
US20070093551A1 (en) * 2005-10-17 2007-04-26 Yu Ruey J Hydroxy-oligocarboxylic esters: effects on nerve and use for cutaneous and mucocutaneous organs or sites
US7226579B1 (en) * 1999-10-01 2007-06-05 Daizo Co., Ltd. Aerosol composition
US8231887B2 (en) * 2008-04-11 2012-07-31 Basf Corporation Pesticidal compositions

Family Cites Families (109)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE581706A (en) * 1959-08-14
JPS5623967B2 (en) * 1972-06-09 1981-06-03
US4052353B1 (en) 1974-01-02 1990-01-30 Dispersions of water soluble polymers in oil
JPS55167204A (en) * 1979-06-15 1980-12-26 Kao Corp Composition for controlling agricultural and horticultural blight and noxious insect
JPS6163603A (en) 1984-09-04 1986-04-01 Riken Koryo Kogyo Kk Cockroach attractant
EP0208694A1 (en) * 1985-01-07 1987-01-21 ROD, Robert L. Reodorizing animal repellent process and product
GB8906382D0 (en) 1989-03-20 1989-05-04 Univ Southampton Pheromone baits for social insects
EP0400914B1 (en) 1989-06-02 1996-06-26 Pfizer Inc. Agricultural foam compositions
US6316017B1 (en) 1990-02-02 2001-11-13 The United States Of America As Represented By The Secretary Of Agriculture Composition and apparatus useful for attracting and controlling insect pests
FR2689729B1 (en) 1992-04-09 1994-06-03 Roussel Uclaf NOVEL PESTICIDE COMPOSITIONS CONTAINING A PYRETHRINOUIDE.
JPH06116101A (en) * 1992-10-05 1994-04-26 Matsuda Michihiko Spray composition for trapping small insect
AU7112294A (en) * 1993-06-17 1995-01-17 Ecoscience Corporation Method for control of conidial dispersal and improved maintenance of entomopathogenic fungal products
US5914105A (en) * 1994-06-17 1999-06-22 Ecolab Inc. Petroleum based pest bait
US5679662A (en) 1995-06-06 1997-10-21 Thermo Trilogy Corporation Synergistic use of azadirachtin and pyrethrum
MA24577A1 (en) 1997-06-26 1998-12-31 Procter & Gamble METHODS AND COMPOSITIONS FOR REDUCING MICROORGANISM FOR FOOD PRODUCTS
AU5679598A (en) 1997-07-10 1999-02-08 Earth Chemical Co. Ltd. Pesticide applicator
DE19731156A1 (en) 1997-07-21 1999-01-28 Bayer Ag Improved gel formulations containing insecticide
WO1999021891A1 (en) 1997-10-27 1999-05-06 Baylor College Of Medicine Invertebrate octopamine receptor
US6355264B1 (en) * 1998-03-20 2002-03-12 Avon Products, Inc. Insect repellent composition
US6706760B2 (en) 1998-03-20 2004-03-16 Sumitomo Chemical Company, Limited Wasp controlling agent
US6455086B1 (en) * 1998-06-26 2002-09-24 The Procter & Gamble Company Microorganism reduction methods and compositions for food cleaning
WO2000005948A1 (en) * 1998-07-27 2000-02-10 Abraham Carl J Vapor releasable, geraniols containing, tick and insect repellent compositions and methods
US6849614B1 (en) * 1998-07-28 2005-02-01 Ecosmart Technologies, Inc. Synergistic and residual pesticidal compositions containing plant essential oils
US20030194454A1 (en) * 1998-07-28 2003-10-16 Bessette Steven M. Pesticidal compositions containing rosemary oil and wintergreen oil
US6607716B1 (en) 1998-09-29 2003-08-19 Tech Labs, Inc. Pediculicidal compositions, a kit, and methods of use
JP2003535918A (en) 1998-10-29 2003-12-02 ペンレコ Gel composition
US6881776B2 (en) 1998-10-29 2005-04-19 Penreco Gel compositions
WO2000026285A1 (en) * 1998-10-29 2000-05-11 Penreco Gel compositions
JP2002533203A (en) * 1998-12-24 2002-10-08 ユニヴァーシティー オヴ サウザンプトン Method and apparatus for dispersing volatile compositions
CA2372155A1 (en) 1999-03-05 2000-09-08 Ecosmart Technologies, Inc. Herbicidal compositions containing plant essential oils and mixtures or blends thereof
WO2001000049A1 (en) 1999-06-28 2001-01-04 Ecosmart Technologies, Inc. Pesticidal compositions containing plant essential oils against mites
US6531163B1 (en) * 1999-06-28 2003-03-11 Ecosmart Technologies, Inc. Pesticidal compositions containing peppermint oil
US6949587B1 (en) * 1999-08-06 2005-09-27 Ecosmart Technologies, Inc. Pesticidal compositions containing plant essential oils against beetles
WO2001018201A1 (en) 1999-09-09 2001-03-15 Ecosmart Technologies, Inc. Pesticidal activity of plant essential oils and their constituents
ES2163999B1 (en) 1999-11-11 2003-03-01 Inabonos Sa COMPOSITION OF NATURAL ORIGIN TO CONTROL THE POST-HARVEST PATHOLOGY OF FRUIT AND VEGETABLES AND APPLICATION METHOD.
US6448219B1 (en) 2000-02-11 2002-09-10 Iced Scents, Llc Scented potpourri gel and method of making the same
AR027527A1 (en) 2000-02-17 2003-04-02 Ecosmart Technologies Inc PESTICIDE COMPOSITIONS CONTAINING ESSENTIAL VEGETABLE OILS AGAINST THE HUMAN BODY LICE
WO2001072129A1 (en) 2000-03-28 2001-10-04 Council Of Scientific And Industrial Research Acyclic monoterpenes as anti-sprouting agents for potato tubers
US6514511B1 (en) 2000-05-08 2003-02-04 Beemaster, Inc. Composition, method, and apparatus to attract bees
US6773700B2 (en) 2000-05-08 2004-08-10 Steven C. Thoenes Composition, method, and apparatus to attract bees
US7282211B2 (en) 2001-05-21 2007-10-16 Btg International Inc. Pest treatment composition
US20030060379A1 (en) * 2000-05-26 2003-03-27 The Procter & Gamble Company Pesticides
US20030026823A1 (en) * 2000-06-05 2003-02-06 The 54 Group, Ltd. Environmentally safe insect repellent composition
US7081211B2 (en) 2000-07-13 2006-07-25 The Procter & Gamble Company Multi-layer reaction mixtures and apparatuses for delivering a volatile component via a controlled exothermic reaction
US6673756B2 (en) * 2000-09-20 2004-01-06 Symrise Gmbh & Co. Kg Multiphase soaps
FR2816517B1 (en) 2000-11-14 2002-12-27 Agro Ind Rech S Et Dev Ard PROCESS FOR THE PREPARATION OF SOLUBILIZATION ADJUVANTS FROM FUSEL OILS AND BONES
ATE295743T1 (en) 2001-02-26 2005-06-15 Procter & Gamble AROMA RELEASING AGENT WITH IMPROVED STABILITY AND REDUCED FOAMING
US6592637B2 (en) 2001-03-16 2003-07-15 Mcgee Thomas Decorative candle and process for making same
CN1379988A (en) * 2001-04-12 2002-11-20 丁一沅 Environmental protection type plant source sanitary insecticide
US20020193346A1 (en) 2001-04-26 2002-12-19 Dairy Solutions, Llc. Method and mixture for protecting animals against pests
US7820187B2 (en) 2001-04-26 2010-10-26 Dairy Solutions, Llc Method and mixture for protecting animals against pests
US20050002980A1 (en) 2001-06-29 2005-01-06 Mullen Patricia A. Fragrance-containing insect repellant compositions
US6749861B2 (en) * 2001-06-29 2004-06-15 Lenco Laboratories, Llc Fragrance-containing insect repellant compositions
WO2003020024A2 (en) 2001-08-28 2003-03-13 Eden Research Plc Treatment and prevention of infections in plants
IL145767A (en) 2001-10-04 2006-10-31 Israel State Microbicidal formulation comprising an essential oil or its derivatives
US20030165452A1 (en) 2001-12-27 2003-09-04 Avon Products, Inc. Controlled released powder entrapment compositions for hydrophobic ingredient
US20030175369A1 (en) * 2002-02-19 2003-09-18 Paragon Household Products Inc. Natural moths repellent compositions
CN1481849A (en) 2002-09-12 2004-03-17 胜 刘 Oil essence for relieving fatigue and preserving health
US20060193789A1 (en) 2002-10-25 2006-08-31 Foamix Ltd. Film forming foamable composition
US8119150B2 (en) 2002-10-25 2012-02-21 Foamix Ltd. Non-flammable insecticide composition and uses thereof
US20060263403A1 (en) 2003-04-24 2006-11-23 Essam Enan Compositions and methods for controlling insects involving the tyramine receptor
US7622269B2 (en) 2004-03-19 2009-11-24 Tyratech, Inc. Methods of screening tyramine- and octopamine-expressing cells for compounds and compositions having potential insect control activity
WO2004100971A1 (en) * 2003-04-24 2004-11-25 Vanderbilt University Compositions and methods for controlling insects
WO2004095926A2 (en) 2003-04-28 2004-11-11 Monsanto Technology, Llc Treatment of plants and plant propagation materials with an antioxidant to improve plant health and/or yield
EP1504664A1 (en) 2003-07-29 2005-02-09 Novartis AG Organic compounds
GB2405339A (en) 2003-08-29 2005-03-02 Reckitt Benckiser Insecticidal stick composition
JP4393853B2 (en) * 2003-12-11 2010-01-06 株式会社ナチュラルネットワーク Cockroach spray
CN100355340C (en) * 2003-12-16 2007-12-19 金中北 Mineral oil microemulsion
CN1555699A (en) * 2004-01-08 2004-12-22 金中北 Aqueous emulsion green pesticide and its formula design and preparation method
US20050244445A1 (en) 2004-04-15 2005-11-03 Anderson David L Insecticidal compositions and methods of using same
FR2869229B1 (en) * 2004-04-26 2006-08-25 Sederma Soc Par Actions Simpli USE OF A INDUCER OF UGT BY TOPIC
US20060121073A1 (en) * 2004-07-12 2006-06-08 Sandhya Goyal Topical gel formulation comprising insecticide and its preparation thereof
US7531187B2 (en) * 2004-07-13 2009-05-12 United Phosphorus, Ltd. Synergistic insecticidal composition containing chloronicotynyle and pyrethroids compounds
US20060034898A1 (en) 2004-08-10 2006-02-16 Amodt James A Method for using FIFRA-exempt substances, materials exhibiting antimicrobial, insecticidal, biocidal and/or odor controlling properties having one or more of these substances coated thereon and/or incorporated therein, and products that are made using these materials
GB0418047D0 (en) * 2004-08-12 2004-09-15 Syngenta Participations Ag Fungicidal compositions
GB0422401D0 (en) 2004-10-08 2004-11-10 Syngenta Participations Ag Fungicidal compositions
GB0422400D0 (en) 2004-10-08 2004-11-10 Syngenta Participations Ag Fungicidal compositions
US20060083763A1 (en) 2004-10-18 2006-04-20 Michael Neale Method and apparatus for insect repellant system
US20060116353A1 (en) 2004-11-26 2006-06-01 Arthur Vanmoor Method for removal of unwanted organism from the human body and a treatment for removal of unwanted organism from the human body
US20060211575A1 (en) 2005-03-16 2006-09-21 W. Neudorff Gmbh Kg Control for plant and plant product pathogens
US20060222675A1 (en) 2005-03-29 2006-10-05 Sabnis Ram W Personal care compositions with color changing indicator
DE102005026801A1 (en) 2005-06-10 2006-12-14 Symrise Gmbh & Co. Kg sandalwood odoriferous
US8062676B2 (en) 2005-08-02 2011-11-22 Thomas Besendorfer Pesticide composition
US20070098750A1 (en) 2005-09-01 2007-05-03 Ecosmart Technologies, Inc. Pesticidal compositions containing isopropyl myristate and analogs of same as a synergist for plant essential oils
US8007820B2 (en) 2005-09-16 2011-08-30 W. Neudorff Gmbh Kg Wide spectrum insecticide and miticide composition
GB0522287D0 (en) 2005-11-01 2005-12-07 Reckitt Benckiser Uk Ltd Method and compositions
WO2007056340A2 (en) 2005-11-08 2007-05-18 Mycosol, Inc. Disinfectant and antiseptic pyridinium and thiazolium compounds and methods of using the same
EP1960421B1 (en) 2005-12-15 2013-03-13 Sederma New polypeptides and their use
US20070178128A1 (en) 2006-01-06 2007-08-02 Ecosmart Technologies, Inc. Emulsifiable concentrate (ec) formulations for pesticides
US20070190094A1 (en) * 2006-01-10 2007-08-16 Ecosmart Technologies, Inc. Pesticidal compositions containing isopropyl-containing compounds as pesticidally active ingredients
US7846464B2 (en) 2006-01-16 2010-12-07 Darling Samuel T Insect repellent composition
ES2638242T3 (en) 2006-02-16 2017-10-19 Sederma  KXK polypeptides and their use
WO2008034648A1 (en) 2006-04-05 2008-03-27 Metanomics Gmbh Process for the production of a fine chemical
WO2007127211A2 (en) 2006-04-28 2007-11-08 Buckman Laboratories International, Inc. Fungicidal compositions and methods of using the same
WO2007146114A2 (en) 2006-06-08 2007-12-21 Tyratech, Inc Compositions and methods for production of peat-like material from manure
US7824668B2 (en) 2006-07-12 2010-11-02 Cotton Incorporated Compositions for attracting stink bugs
US8685471B2 (en) * 2006-07-17 2014-04-01 Tyratech, Inc. Compositions and methods for controlling insects
DE102006044849A1 (en) * 2006-09-22 2008-04-03 Symrise Gmbh & Co. Kg Deconjugated alkadienoic esters as fragrances and / or flavorings
US8293286B2 (en) * 2006-10-16 2012-10-23 Sergeant's Pet Care Products, Inc. Natural compositions for killing parasites on a companion animal
WO2008056365A2 (en) 2006-11-09 2008-05-15 Y.A.D. Bio-Agrotech Ventures Ltd. Pediculicidal, pesticidal or insecticidal compositions
US8758787B2 (en) * 2006-12-04 2014-06-24 Fasst Products, LLC. Long-lasting insect repellant, pesticide and antifeedant compositions
US20080159970A1 (en) 2006-12-20 2008-07-03 L'oreal Kit comprising silicone compounds and a cosmetic and/or dermatological active agent
AU2008205516A1 (en) 2007-01-16 2008-07-24 Tyratech, Inc. Pest control compositions and methods
US20080187607A1 (en) 2007-02-01 2008-08-07 Ecosmart Technologies Inc. Systems, methods and apparatuses for epa exempt pesticidal compositions
US20080193387A1 (en) * 2007-02-14 2008-08-14 Ricki De Wolff Essential oil compositions for killing or repelling ectoparasites and pests and methods for use thereof
US9049814B2 (en) * 2007-02-23 2015-06-09 Vamtech, Llc Coated seeds and methods of making coated seeds
JP5326320B2 (en) 2007-03-30 2013-10-30 住友化学株式会社 Pest control composition and pest control method
US7588646B2 (en) 2007-05-03 2009-09-15 United Laboratories, Inc. Cleaning compositions containing an alkyl ester and methods of using same
WO2009012415A1 (en) 2007-07-17 2009-01-22 Tyratech, Inc. Insect repellent composition

Patent Citations (89)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1516907A (en) * 1918-06-25 1924-11-25 Us Ind Alcohol Co Fuel for motors
US1858635A (en) * 1927-04-25 1932-05-17 Pan American Petroleum & Trans Sweetening hydrocarbon oils
US2023140A (en) * 1932-10-19 1935-12-03 Shell Dev Livestock spray
US2041874A (en) * 1935-02-15 1936-05-26 Frits E Stockelbach Composition for preventing sunburn
US2763614A (en) * 1954-06-04 1956-09-18 Gulf Oil Corp Corrosion-inhibiting compositions
US2809122A (en) * 1954-06-24 1957-10-08 Sherwin Williams Co Dual purpose tinting base
US3158535A (en) * 1961-10-02 1964-11-24 Exxon Research Engineering Co Pyrethrin-elastomer insecticidal composition and method
US3163607A (en) * 1962-08-02 1964-12-29 Bethlehem Steel Corp Method for removing oil lubricant film from steel
US3291557A (en) * 1963-01-07 1966-12-13 Battelle Development Corp Alkyl dicarboxylic acid treatment of leather
US3444080A (en) * 1967-04-14 1969-05-13 Shell Oil Co Lubricant for rolling metals
US4285868A (en) * 1968-03-20 1981-08-25 Mobil Oil Corporation Preparation of gamma-butyrolactones
US3923997A (en) * 1971-05-11 1975-12-02 Rhodia Process for repelling dogs and cats from a selected area or from each other using {65 -n-alkyl-{65 -butyrolactones and {67 -n-alkyl-{67 -valerolactones
US3806593A (en) * 1971-06-01 1974-04-23 Medisan Ab Hygienic-cosmetic compositions
US4056610A (en) * 1975-04-09 1977-11-01 Minnesota Mining And Manufacturing Company Microcapsule insecticide composition
US4279946A (en) * 1977-09-07 1981-07-21 Foseco International Limited Coating compositions
US4252796A (en) * 1979-08-17 1981-02-24 Yu Ruey J Stable water-in-oil emulsions
US4562214A (en) * 1979-09-10 1985-12-31 Witco Chemical Corporation Personal care emulsion
US4612331A (en) * 1982-02-02 1986-09-16 Lever Brothers Company Skin treatment composition
US4534128A (en) * 1983-02-01 1985-08-13 Query Grady W Method for pest control using anesthetic and insecticide
US4624070A (en) * 1983-02-01 1986-11-25 Query Grady W Method and composition for pest control using anesthetic and insecticide
US4933371A (en) * 1984-07-26 1990-06-12 Shirlo, Inc. Controlling ticks and fleas with linalool
US4923698A (en) * 1986-12-19 1990-05-08 S. C. Johnson & Son, Inc. Bioactive film-forming composition for control of crawling insects and the like
US4822614A (en) * 1986-12-19 1989-04-18 S. C. Johnson & Son, Inc. Bioactive film-forming composition for control of crawling insects and the like
US4774081A (en) * 1987-01-13 1988-09-27 S. C. Johnson & Son, Inc. Contact insect repellents
US4774082A (en) * 1987-01-13 1988-09-27 S. C. Johnson & Son, Inc. Volatile insect repellents
US4902510A (en) * 1987-10-05 1990-02-20 Shell Internationale Research Maatschappij B.V. Ectoparasiticidal pour-on formulation
US5510117A (en) * 1989-03-09 1996-04-23 Micro-Pak, Inc. Entrapment vehicle and method
US5143900A (en) * 1989-05-19 1992-09-01 Colgate-Palmolive Company Perfumes containing N-lower alkyl neoalkanamide (s)
US5093326A (en) * 1989-06-19 1992-03-03 Stephen Herman Repellant compositions
US4961532A (en) * 1989-07-07 1990-10-09 Dow Corning Corporation Fragrance release device containing a highly adsorptive copolymer
US5130135A (en) * 1989-08-18 1992-07-14 Smithkline Beecham Plc Pesticidal formulations
US4962133A (en) * 1989-09-05 1990-10-09 Dow Corning Corporation Method of making highly adsorptive copolymers
US5290556A (en) * 1990-02-02 1994-03-01 The United States Of America As Represented By The Secretary Of Agriculture Plastic bait composition for attracting and killing crop pests
US5227406A (en) * 1990-04-09 1993-07-13 Primavera Laboratories, Inc. Insect repellent lotions and sprays
US5346922A (en) * 1990-04-09 1994-09-13 Primavera Laboratories, Inc. Insect repellent lotions and sprays
US5648398A (en) * 1990-04-09 1997-07-15 Primavera Laboratories, Inc. Insect repellent lotions and sprays
US5411992A (en) * 1991-01-18 1995-05-02 Clilco Ltd. Lice repellant composition
US5227163A (en) * 1991-01-18 1993-07-13 Clilco, Ltd. Lice-repellant compositions
US5344776A (en) * 1991-03-28 1994-09-06 The United States Of America As Represented By The Department Of Health And Human Services DNA encoding an insect octopamine receptor
US5562864A (en) * 1991-04-19 1996-10-08 The Lubrizol Corporation Lubricating compositions and concentrates
US5538990A (en) * 1991-07-15 1996-07-23 Pfizer Inc. Benzimidazole anthelmintics
US5674518A (en) * 1991-08-06 1997-10-07 Prentiss Incorporated Method of fish management by poison fish bait method of making the bait, and formulation of bait
US5621013A (en) * 1992-06-24 1997-04-15 Primavera Laboratories, Inc. Insect replellent blends, lotions, and sprays
US6071973A (en) * 1992-08-07 2000-06-06 The United States Of America As Represented By The Secretary Of Agriculture Repellent for ants
US6001874A (en) * 1992-08-18 1999-12-14 Veierov; Dan Arthropod control composition for plant protection
US5753686A (en) * 1992-09-18 1998-05-19 International Flavors & Fragrances Inc. Method for repelling fire ants and horn flies and compositions for repelling fire ants and horn flies and acting as anti-feedants for fire ants and horn flies
US5814325A (en) * 1993-03-24 1998-09-29 The Rod Family Trust Process for repelling and killing insects and compositions to effect the same comprising a monoterpene
US5977023A (en) * 1993-10-05 1999-11-02 Sumitomo Chemical Company, Limited Sustained release, solid pesticidal compositions comprising water insoluble alginates
US5599803A (en) * 1993-12-14 1997-02-04 Kalamazoo Holdings, Inc. Synergistic insecticidal compositions comprising capsicum and insecticidal use thereof
US5525597A (en) * 1993-12-14 1996-06-11 Kalamazoo Holdings, Inc. Synergistic insecticidal compositions comprising capsicum and insecticidal use thereof
US5476609A (en) * 1994-07-11 1995-12-19 Wilkins, Jr.; William S. Acidic cleaning composition for removing burnt starch from cold metal press heads
US5536501A (en) * 1994-12-30 1996-07-16 Proguard, Inc. Use of flavenoid aldehydes as insecticides and for killing arachnids
US5698210A (en) * 1995-03-17 1997-12-16 Lee County Mosquito Control District Controlled delivery compositions and processes for treating organisms in a column of water or on land
US5902596A (en) * 1995-03-17 1999-05-11 Lee County Mosquito Control District Controlled delivery compositions and processes for treating organisms in a column of water or on land
US5559271A (en) * 1995-07-26 1996-09-24 Phillips Petroleum Company Organic polysulfide compositions having reduced odor
US5753507A (en) * 1995-09-22 1998-05-19 Novartis Finance Corporation Plant geraniol/nerol 10-hydroxylase and DNA coding therefor
US5654362A (en) * 1996-03-20 1997-08-05 Dow Corning Corporation Silicone oils and solvents thickened by silicone elastomers
US6277415B1 (en) * 1996-03-29 2001-08-21 Orna Levin Pediculocidal and veterinary compositions
US6071857A (en) * 1996-06-28 2000-06-06 Novartis Crop Protection, Inc. Pesticidal compositions
US5792465A (en) * 1996-06-28 1998-08-11 S. C. Johnson & Son, Inc. Microemulsion insect control compositions containing phenol
US5872143A (en) * 1996-08-07 1999-02-16 Sumitomo Chemical Company, Limited Insecticidal aerosol composition and insecticidal composition for preparation of same
US6184197B1 (en) * 1996-09-19 2001-02-06 The Procter & Gamble Company Polymeric compound comprising one or more active alcohols
US5925182A (en) * 1996-11-20 1999-07-20 Phillips Petroleum Company Stable liquid suspension compositions
US5834533A (en) * 1996-11-20 1998-11-10 Phillips Petroleum Company Stable liquid suspension compositions
US5880210A (en) * 1997-04-01 1999-03-09 Dow Corning Corporation Silicone fluids and solvents thickened with silicone elastomers
US5834413A (en) * 1997-09-26 1998-11-10 Colgate-Palmolive Co. Liquid cleaning compositions
US6074634A (en) * 1997-10-06 2000-06-13 The United States Of America As Represented By The Secretary Of Agriculture Feeding attractant and stimulant for adult control of noctuid and/or other lepidopteran species
US6255350B1 (en) * 1997-10-14 2001-07-03 Isp Investments Inc. Stabilized concentrates of water unstable AZA compounds and o/w miniemulsions thereof
US6251415B1 (en) * 1997-10-27 2001-06-26 Fmc Corporation Solvent system for pesticide products
US6130253A (en) * 1998-01-27 2000-10-10 Ximed Group Plc Terpene based pesticide treatments for killing terrestrial arthropods including, amongst others, lice, lice eggs, mites and ants
US5977186A (en) * 1998-01-27 1999-11-02 Ximed Group Plc Terpene treatments for killing lice and lice eggs
US6641803B1 (en) * 1998-02-06 2003-11-04 Cognis Deutschland Gmbh & Co. Kg Hair-conditioning agents
US6083498A (en) * 1998-03-10 2000-07-04 The United States Of America As Represented By The Secretary Of Agriculture Chemical attractants for yellowjackets and paper wasps
US5998484A (en) * 1998-04-15 1999-12-07 Woodstream Corporation Insecticidal compositions and method of controlling insect pests using same
US6024972A (en) * 1998-07-21 2000-02-15 Isp Investments Inc. Water-free concentrate of amitraz insecticide and clear pour-on formulations thereof
US20060115508A1 (en) * 1999-06-28 2006-06-01 Ecosmart Technologies, Inc. Synergistic and residual pesticidal compositions containing plant essential oils with enzyme inhibitors
US20040220075A1 (en) * 1999-09-03 2004-11-04 Ahrens Edward R. Treatment of skin disorders
US7226579B1 (en) * 1999-10-01 2007-06-05 Daizo Co., Ltd. Aerosol composition
US6124490A (en) * 1999-10-26 2000-09-26 Mona Industries, Inc. Zwitterionic siloxane polymers and ionically cross-linked polymers formed therefrom
US6197098B1 (en) * 1999-12-16 2001-03-06 Isp Investments Inc. Fast drying biocidal preservative composition
US6255356B1 (en) * 2000-03-30 2001-07-03 International Flavors & Fragrances Inc. Method for inhibiting from feeding, cockroaches
US6555121B1 (en) * 2000-05-26 2003-04-29 Ecosmart Technologies, Inc. Pesticidal compositions containing mineral oil and/or soybean oil
US6441051B1 (en) * 2001-09-20 2002-08-27 William B. Wheeler Insect eradicator and method
US20040253287A1 (en) * 2002-08-03 2004-12-16 Denton Robert Michael Environmentally safe insecticides
US20050232981A1 (en) * 2004-04-15 2005-10-20 Ben-Sasson Shmuel A Compositions capable of facilitating penetration across a biological barrier
US20050261379A1 (en) * 2004-05-18 2005-11-24 Petro-Canada Spray Oil and Method of Use Therefor for Controlling Turfgrass Pests
US20060257441A1 (en) * 2005-05-10 2006-11-16 Suzuki Yushi Industrial Co., Ltd. Natural essential oil sanitary insect pest repellent and its use
US20070093551A1 (en) * 2005-10-17 2007-04-26 Yu Ruey J Hydroxy-oligocarboxylic esters: effects on nerve and use for cutaneous and mucocutaneous organs or sites
US8231887B2 (en) * 2008-04-11 2012-07-31 Basf Corporation Pesticidal compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108633932A (en) * 2011-10-04 2018-10-12 0903608 B.C.有限公司 Injurious insect control formulation and manufacture and use its method
US10791744B2 (en) 2011-10-04 2020-10-06 0903608 B.C. Ltd. Pest control formulations and methods of making and using same
US10905114B2 (en) 2011-10-04 2021-02-02 0903608 B.C. Ltd. Pest control formulations and methods of making and using same

Also Published As

Publication number Publication date
CL2009000871A1 (en) 2011-02-25
MY149026A (en) 2013-06-28
US9005644B2 (en) 2015-04-14
AR071468A1 (en) 2010-06-23
US20090257959A1 (en) 2009-10-15
WO2009126577A2 (en) 2009-10-15
CN103210959A (en) 2013-07-24
AU2009233944A1 (en) 2009-10-15
CA2720953A1 (en) 2009-10-15
CN103190446A (en) 2013-07-10
US20130245053A1 (en) 2013-09-19
US20090257958A1 (en) 2009-10-15
EA201201029A1 (en) 2013-01-30
CN102083311A (en) 2011-06-01
US20120294958A1 (en) 2012-11-22
EA201201028A1 (en) 2013-01-30
PH12010502295A1 (en) 2009-10-15
BRPI0911664A2 (en) 2015-07-28
CR11720A (en) 2011-02-04
WO2009126577A3 (en) 2010-04-22
US8591927B2 (en) 2013-11-26
KR20100134105A (en) 2010-12-22
EP2271216A2 (en) 2011-01-12
EA201001616A1 (en) 2011-06-30
IL208553A0 (en) 2010-12-30
TW200948273A (en) 2009-12-01
UY31759A (en) 2009-11-10
ZA201008005B (en) 2012-01-25
US8231887B2 (en) 2012-07-31
EP2271216A4 (en) 2012-04-04
EA018969B1 (en) 2013-12-30
JP2011517685A (en) 2011-06-16
MX2010011081A (en) 2010-12-15
MA32292B1 (en) 2011-05-02

Similar Documents

Publication Publication Date Title
US8591927B2 (en) Pesticidal compositions
JP5385534B2 (en) Limonene-containing herbicide composition, herbicide stock formulation, and methods for making and using them
US20160262404A1 (en) Pesticide Compositions Containing Thyme Oil and Cinnamon Oil
US5700473A (en) Triglyceride enhanced pyrethrin-based arthropodicidal composition
EP2572579B1 (en) Compositions for attracting Tortricidae (fruit moths)
US9609864B2 (en) Disinfectant formulation
JP3818747B2 (en) Insecticidal fungicide composition for agriculture and horticulture
KR20010052453A (en) Use Of At Least One Acid From The Citric Acid Cycle Combined With Glycerine As A Pesticide
US20210176985A1 (en) Disinfectant formulation
JP2024009844A (en) Liquid antipathogenic agricultural composition
US20230189812A1 (en) Ready-to-use barrier and knockdown pesticides
US20230354824A1 (en) Minimum Risk Pesticide Formulations Containing Mineral Oil
SHERMA Pyrethrum

Legal Events

Date Code Title Description
AS Assignment

Owner name: WHITMIRE MICRO-GEN RESEARCH LABORATORIES, INC., MI

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SIMS, STEVEN R.;REEL/FRAME:022506/0816

Effective date: 20090403

AS Assignment

Owner name: WHITMIRE HOLDINGS, INC., MISSOURI

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WHITMIRE MICRO-GEN RESEARCH LABORATORIES, INC.;REEL/FRAME:023667/0204

Effective date: 20090901

AS Assignment

Owner name: BASF CORPORATION, NEW JERSEY

Free format text: MERGER;ASSIGNOR:WHITMIRE HOLDINGS, INC.;REEL/FRAME:023771/0562

Effective date: 20090831

Owner name: BASF CORPORATION,NEW JERSEY

Free format text: MERGER;ASSIGNOR:WHITMIRE HOLDINGS, INC.;REEL/FRAME:023771/0562

Effective date: 20090831

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION