US3355392A - Alkaline germicidal cleaner with color indicator - Google Patents

Alkaline germicidal cleaner with color indicator Download PDF

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US3355392A
US3355392A US317161A US31716163A US3355392A US 3355392 A US3355392 A US 3355392A US 317161 A US317161 A US 317161A US 31716163 A US31716163 A US 31716163A US 3355392 A US3355392 A US 3355392A
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blue
germicidal
alkaline
chloride
dye
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Cantor Abraham
Schmidt William
Murray W Winicov
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WEST LABORATORIES Inc
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/48Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L2/00Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
    • A61L2/26Accessories or devices or components used for biocidal treatment
    • A61L2/28Devices for testing the effectiveness or completeness of sterilisation, e.g. indicators which change colour
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/40Dyes ; Pigments

Definitions

  • Typical components may include phosphates such as sodium phosphate, trisodium phosphate and Abraham Cantor Elkins Park and William Schmidt 5 tetra-sodium phosphate; carbonates such as sodium car- Jamaica, and Murray W. Winicov, Flushing, N.Y., assignors to West Laboratories, Inc., Long Island City, N.Y., a corporation of New York No Drawing. Filed Oct. 18, 1963, Ser. No. 317,161
  • This invention relates to germicidal cleaning compositions having colorimetric means for indicating duration of a minimum germicidally effective contact time. More particularly, the invention relates to dry powdered compositions in the form of mixtures of cleaning components, quaternary ammonium germicide, a per-compound as a source of releasable oxygen and an oxidizable dye, said compositions being readily soluble or dispersible in water to form colored, germicidal cleaning solutions which will maintain their color only for the limited time required for minimum effective germicidal contact with items being cleaned.
  • Another United States Patent No. 2,498,343 discloses dry denture cleaning compositions containing oxygen yielding material and oxidizable dye supposedly providing an index of the proper length of time of the desired cleaning action upon the denture. with the color disappearance taking place within to 30 minutes. Such a time interval is impractical, since a denture user will rarely want to wait around for 10 to 30 minutes for his teeth to be cleaned.
  • the present invention constitutes a distinct departure from these prior teachings in providing germicidal watersoluble powdered cleaning compositions in which colorimetric means is provided for indicating the duration of immersion in aqueous solutions thereof for proper germicidal treatment.
  • the colorimetric means includes a combination of oxygen yielding material and a dye which loses its color rapidly through oxidation.
  • quaternary ammonium compounds are the preferred germicides for this application in that these compounds are stable in the presence of the required amounts of alkali and oxidizing agents.
  • the accepted quaternary ammonium germicides can be employed, including for example, benzethonium chloride, dodecyl benzyl trimethyl ammonium chloride, dodecyl .benzyl diethyl ethanol ammonium chloride, cetyl pyridinium chloride and bromide, dodecyl benzyl triethanol ammonium chloride, N(lauroyl colamino-formylmethyl) pyridinium chloride, and dodecyl benzyl diethanol ammonium chloride.
  • the quantity of germicide will vary to some extent depending on the intended use of the composition, but should generally be within the range of about 0.25 to 3% by weight of the composition.
  • the germicide concentration is preferably about 0.25 to 1.5%
  • an alkaline cleanser intended for home cleaning of sickroom utensils glasses, dishes, silverware, etc. used by a patient
  • a somewhat higher concentration of germicide suitably 2 to 3% should be employed.
  • the cleaning components which make up the bulk of bonate, calcium carbonate and magnesium carbonate, halide salts (particularly in denture cleaners) such as sodium chloride, and calcium chloride; borates such as boric acid and sodium borate; and oxygen releasing (peroxide) compounds such as perborates, persulfates, perphosphates,
  • compositions may include 0.5 to 5.0% of an anionic surface active agent, such as sodium lauryl sulfate, or nonionic surface active agent, such as a condensate of ethylene oxide with polypropylene oxide (molecular weight l50l-l800) containing -90% by weight ethylene oxide, or a normally liquid alkyl phenol ethylene oxide condensate or polyoxyethylene ether alcohol solidified with about an equal weight of urea.
  • the compositions can also be scented or flavored (in the case of denture cleaner) with a trace of suitable aromatic oils, such as peppermint oil, cinnamon oil, menthol, or vanillin.
  • the preparation of many alkaline cleansers employing combinations of the components noted above is described in Bennetts Chemical Formulary, and in other standard references, and in adapting such known preparations to the present invention, two conditions must be satisfied.
  • the pH of the composition in its intended use dilution should be within the range of about pH 10 11.5, and the amount of per-compound employed should be adjusted to the amount and type of dye to be employed as hereinafter described.
  • the pH range is of importance in that we find that lower pHs tend to lengthen both the cleaning time and d olorati tim
  • the selection of-a'dyefor use in the new compositions is greatly limited by the short time interval in which it must lose its color through oxidation.
  • an effective germicidal action may be achieved in about 0.5 to 5 minutes, and the purpose of the dye is to provide a reliable indication to users of the compositions that treatment of objects, such as dentures, sickroom utensils, dishes, urinals, and the like, is continued for at least the interval required for complete germicidal effectiveness.
  • objects such as dentures, sickroom utensils, dishes, urinals, and the like
  • the purpose of the dye is to provide a reliable indication to users of the compositions that treatment of objects, such as dentures, sickroom utensils, dishes, urinals, and the like, is continued for at least the interval required for complete germicidal effectiveness.
  • objects such as dentures, sickroom utensils, dishes, urinals, and the like
  • Dyes which give a measurable decoloration time of less than 5 minutes according to this test procedure are dyes which may be used in the new alkaline germicidal cleansers. (By measurable time is meant an interval of one second or more.)
  • the actual decoloration time for a particular product can be adjusted by varying the pH within the range of 10.5 to 11.5, a lower pH generally prolonging the decoloration time.
  • the temperature of 37 C. employed in the test procedure above described is selected as an approximate midpoint between room temperature and 5 C., the temperature range within which germicidal alkaline cleaners should generally be used. Within this temperature range the speed of decoloration increases as the temperature increases. At the same time, however, the rate of germicidal activity of the quaternary ammonium germicide is also increased as the temperature increases, and it has been found that the temperature coefhcients for decoloration and germicidal activity are sufliciently close in the new compositions so that within the 35 to 50 C. temperature range at which the compositions will normally be employed, decoloration time, although changing, will indicate a substantially constant degree of germicidal activ ity.
  • the germicide in use of the new compositions, the germicide remains active long after the dye has become decolorized and articles being treated can be kept immersed in cleaning solution for extended periods if desired. In many instances, however, the user will wish to minimize the cleaning time, and the presence of the oxidizable dye in the manner herein described provides a definite indication to the user of the minimum immersion time which will provide the desired germicidal action.
  • the amount of dye to be employed in an alkaline germicidal cleaner will depend upon the color intensity desired in the recommended use dilution of a particular product. This will generally require about 2 to 20 p.p.m. of dye in a use dilution, or about 0.01 to 0.1% in a composition intended to be used at a 2% concentration in use dilution.
  • the amount of per-compound should be at least equivalent in active oxygen to the amount of hydrogen peroxide necessary to decolorize the dye within min. under the conditions described in the dye screening test. As the amount of per-compound is increased, the rate of decoloration of dye will increase, and adjustment of the amount of per-compound provides one means for setting.the decoloration time for a product.
  • compositions of the following examples perform in substantially the same manner when the benzethonium chloride is replaced by an equivalent concentration of other quaternary ammonium germicides.
  • compositions of the examples also perform in the same manner when the F.D. & C. Blue No. 1 is replaced by D. & C. Blue No. 4, or Blue No. 7, and shows substantially more rapid decoloration when the dye is replaced by F.D. & C. Violet No. 1, or F.D. & C. Blue No. 2.
  • EXAMPLE I An alkaline germicidal cleaner is prepared by dry mixing the following components:
  • This composition provides an effective denture cleaner when added to water at a concentration of about 2.5%. At this concentration the blue color disappears in about 3% min. at 37 C. and 1% min. at 45 C. The pH of the use dilution is about 11.1.
  • EXAMPLE II An alkaline germicidal cleaner is prepared by dry mixing the following components:
  • An alkaline germicidal cleaning composition having indicator means to signify the minimum contact time for effective germicidal action in use dilutions thereof, said composition consisting essentially of a mixture of inorganic alkaline cleaning components providing a pH of 10.5 to 11.5 in aqueous use dilution containing amounts of the order of 1.0 to 2.5% by Weight of said composition, 0.25 to 3% of a quaternary ammonium germicide selected from the group consisting of benzethonium chloride, dodecyl benzyl tzimethyl ammonium chloride, dodecyl benzyl diethyl ethanol ammonium chloride, cetyl pyridinium chloride and bromide, dodecyl benzyl triethanol ammonium chloride, N(lauroyl colaminoformylmethyl)pyridinium chloride, and dodecyl benzyl diethanol ammonium chloride, 0.01 to 0.1% of a water soluble dye selected from

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  • Animal Behavior & Ethology (AREA)
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Description

3,355,392 ALKALINE GERMICIDAL CLEANER WITH COLOR INDICATOR I United States Patent Examine 3,355,392 Patented Nov. 28, 1967 "ice the compositions can be varied considerably, and in general, any alkaline cleaner can be used as a base for the new compositions. Typical components may include phosphates such as sodium phosphate, trisodium phosphate and Abraham Cantor Elkins Park and William Schmidt 5 tetra-sodium phosphate; carbonates such as sodium car- Jamaica, and Murray W. Winicov, Flushing, N.Y., assignors to West Laboratories, Inc., Long Island City, N.Y., a corporation of New York No Drawing. Filed Oct. 18, 1963, Ser. No. 317,161
5 Claims. (Cl. 252F419) This invention relates to germicidal cleaning compositions having colorimetric means for indicating duration of a minimum germicidally effective contact time. More particularly, the invention relates to dry powdered compositions in the form of mixtures of cleaning components, quaternary ammonium germicide, a per-compound as a source of releasable oxygen and an oxidizable dye, said compositions being readily soluble or dispersible in water to form colored, germicidal cleaning solutions which will maintain their color only for the limited time required for minimum effective germicidal contact with items being cleaned.
The concept of colored cleaning agents which will turn colorless in use is known in the art. In United States Patent No. 3,058,916 for example, there are disclosed laundry detergent compositions in solid form. In this patent, however, the dye is merely intended to aid in the physical appearance of the product itself for marketing and sales purposes. The color disappears within the contemplated laundering cycle, but bears no useful relationship to the duration of such cycle.
Another United States Patent No. 2,498,343 discloses dry denture cleaning compositions containing oxygen yielding material and oxidizable dye supposedly providing an index of the proper length of time of the desired cleaning action upon the denture. with the color disappearance taking place within to 30 minutes. Such a time interval is impractical, since a denture user will rarely want to wait around for 10 to 30 minutes for his teeth to be cleaned.
The present invention constitutes a distinct departure from these prior teachings in providing germicidal watersoluble powdered cleaning compositions in which colorimetric means is provided for indicating the duration of immersion in aqueous solutions thereof for proper germicidal treatment. The colorimetric means includes a combination of oxygen yielding material and a dye which loses its color rapidly through oxidation.
We have found the class of quaternary ammonium compounds to be the preferred germicides for this application in that these compounds are stable in the presence of the required amounts of alkali and oxidizing agents. The accepted quaternary ammonium germicides can be employed, including for example, benzethonium chloride, dodecyl benzyl trimethyl ammonium chloride, dodecyl .benzyl diethyl ethanol ammonium chloride, cetyl pyridinium chloride and bromide, dodecyl benzyl triethanol ammonium chloride, N(lauroyl colamino-formylmethyl) pyridinium chloride, and dodecyl benzyl diethanol ammonium chloride. The quantity of germicide will vary to some extent depending on the intended use of the composition, but should generally be within the range of about 0.25 to 3% by weight of the composition. In an alkaline cleaner intended for use as a denture cleaner, the germicide concentration is preferably about 0.25 to 1.5%, whereas in an alkaline cleanser intended for home cleaning of sickroom utensils (glasses, dishes, silverware, etc. used by a patient) a somewhat higher concentration of germicide, suitably 2 to 3% should be employed.
The cleaning components which make up the bulk of bonate, calcium carbonate and magnesium carbonate, halide salts (particularly in denture cleaners) such as sodium chloride, and calcium chloride; borates such as boric acid and sodium borate; and oxygen releasing (peroxide) compounds such as perborates, persulfates, perphosphates,
. percarbonates and stabilized (e.g. coated granular form) sodium peroxide. In addition, the compositions may include 0.5 to 5.0% of an anionic surface active agent, such as sodium lauryl sulfate, or nonionic surface active agent, such as a condensate of ethylene oxide with polypropylene oxide (molecular weight l50l-l800) containing -90% by weight ethylene oxide, or a normally liquid alkyl phenol ethylene oxide condensate or polyoxyethylene ether alcohol solidified with about an equal weight of urea. The compositions can also be scented or flavored (in the case of denture cleaner) with a trace of suitable aromatic oils, such as peppermint oil, cinnamon oil, menthol, or vanillin.
The preparation of many alkaline cleansers employing combinations of the components noted above is described in Bennetts Chemical Formulary, and in other standard references, and in adapting such known preparations to the present invention, two conditions must be satisfied. The pH of the composition in its intended use dilution should be within the range of about pH 10 11.5, and the amount of per-compound employed should be adjusted to the amount and type of dye to be employed as hereinafter described. The pH range is of importance in that we find that lower pHs tend to lengthen both the cleaning time and d olorati tim The selection of-a'dyefor use in the new compositions is greatly limited by the short time interval in which it must lose its color through oxidation. With the germicides employed, an effective germicidal action may be achieved in about 0.5 to 5 minutes, and the purpose of the dye is to provide a reliable indication to users of the compositions that treatment of objects, such as dentures, sickroom utensils, dishes, urinals, and the like, is continued for at least the interval required for complete germicidal effectiveness. Thus, for example, when handling sickroom utensils, they should be immersed in a freshly prepared colored solution of the composition, and left untouched until the color disappears. The cleaning solution and utensils can then be worked with, with the assurance that the danger of contamination or infection has been eliminated.
As a means for determining whether a dye will lose its color in a use solution within the desired time interval, the following screening test has been devised:
To 93ml. of 0.1M trisodium phosphate solution at a 37 C. (pH 11.5), add 2 ml. of 3% hydrogen peroxide solution and 5 ml. of a 0.01% dye solution, and note the time necessary for complete decolorization of the dye.
Dyes which give a measurable decoloration time of less than 5 minutes according to this test procedure are dyes which may be used in the new alkaline germicidal cleansers. (By measurable time is meant an interval of one second or more.) The actual decoloration time for a particular product can be adjusted by varying the pH within the range of 10.5 to 11.5, a lower pH generally prolonging the decoloration time. p
In considering alkaline germicidal cleaners generally, the oxidizable dyes potentially useful in such compositions are relatively limited. In products to be used as deI1-;
screening a number of common dyes following the test procedure above described:
FD. & C. Red No. 1 8 hrs. F.D. & (3. Red No.2 "finalis 1 hr. F.D. &C. Violet No. 1 -3225 .2-". 10 sec. D. & 0. Blue No. 4 j 2 min. D.&C. Blue No.7 -1531). 2 min. D. & C. Orange No. 4 "1.521? 2 /2 hrs. D. & c. Green No.5 2x532--- 36 hrs. D. & C. Red No. 19 d 1 1% hrs. D. & c. Red No. 22 E 1 hr.
D. & C. Red No. 28 -'.\1 d i 36 hrs. D. & C. Red NO. 33 lP=. Q 36 hrs. Crystal Violet 1 to 2 sec. Ext. D. & C. Orange No. 3 10 min. Phenolphthalein 8 hrs.
From the foregoing tabulation it follows that only 8 of these dyes are suitable for use in the compositions of the present invention, namely: F.D. & C. Blue No. 1, D. & C. Blue No. 4, D. & C. Blue No. 7, F.D. & C. Violet No. 1, RD. & C. Blue No. 2, ED. & C. Green No. 1, F.D. & C. Green No. 2, and Crystal Violet.
The temperature of 37 C. employed in the test procedure above described is selected as an approximate midpoint between room temperature and 5 C., the temperature range within which germicidal alkaline cleaners should generally be used. Within this temperature range the speed of decoloration increases as the temperature increases. At the same time, however, the rate of germicidal activity of the quaternary ammonium germicide is also increased as the temperature increases, and it has been found that the temperature coefhcients for decoloration and germicidal activity are sufliciently close in the new compositions so that within the 35 to 50 C. temperature range at which the compositions will normally be employed, decoloration time, although changing, will indicate a substantially constant degree of germicidal activ ity.
It is to be understood that in use of the new compositions, the germicide remains active long after the dye has become decolorized and articles being treated can be kept immersed in cleaning solution for extended periods if desired. In many instances, however, the user will wish to minimize the cleaning time, and the presence of the oxidizable dye in the manner herein described provides a definite indication to the user of the minimum immersion time which will provide the desired germicidal action.
The amount of dye to be employed in an alkaline germicidal cleaner will depend upon the color intensity desired in the recommended use dilution of a particular product. This will generally require about 2 to 20 p.p.m. of dye in a use dilution, or about 0.01 to 0.1% in a composition intended to be used at a 2% concentration in use dilution. The amount of per-compound should be at least equivalent in active oxygen to the amount of hydrogen peroxide necessary to decolorize the dye within min. under the conditions described in the dye screening test. As the amount of per-compound is increased, the rate of decoloration of dye will increase, and adjustment of the amount of per-compound provides one means for setting.the decoloration time for a product.
Further latitude in setting the decoloration time is also provided by adjusting the pH. By way of illustration, the following tabulation shows the difference in decoloration time of a particular dye (FD. & C. Blue No.1) due to variation in pH. Except for pH adjustment (i.e. 0.1M Na HPO -NaOH soln.) the test procedure is the same as described above in the dye screening test.
Decoloration time (FD. & C. Blue H: N0. 1) (Min.)
The following examples will serve to show how typical alkaline germicidal cleaners in accordance with the present invention can be prepared, but it is to be understood that these examples are given by way of illustration and not of limitation:
The compositions of the following examples perform in substantially the same manner when the benzethonium chloride is replaced by an equivalent concentration of other quaternary ammonium germicides.
The compositions of the examples also perform in the same manner when the F.D. & C. Blue No. 1 is replaced by D. & C. Blue No. 4, or Blue No. 7, and shows substantially more rapid decoloration when the dye is replaced by F.D. & C. Violet No. 1, or F.D. & C. Blue No. 2.
EXAMPLE I An alkaline germicidal cleaner is prepared by dry mixing the following components:
Component: Parts by weight Sodium chloride 17.725 Sequestrene 0.25 Sodium percarbonate 10.0 Sodium carbonate monohydrate 12.5 Tetrasodium pyrophosphate 15.0 Trisodium phosphate (12 E 0) 37.5
Sodium N-methyl-N-oleoyl taurate (28% in NaCl) 4 Magnesium carbonate 2.5 Benzethonium chloride 0.4 F.D. & C. Blue No. 1 0.025 Flavor (peppermint oil) 0.1
This composition provides an effective denture cleaner when added to water at a concentration of about 2.5%. At this concentration the blue color disappears in about 3% min. at 37 C. and 1% min. at 45 C. The pH of the use dilution is about 11.1.
EXAMPLE II An alkaline germicidal cleaner is prepared by dry mixing the following components:
Component: Parts by weight Trisodium phosphate 12 B 0) 30.0 Sodium tripolyphosphate 30.0 Sodium metasilicate 28.9 Benzethonium chloride 1.0 Sodium percarbonate 10.0 F.D. & C. Blue No. 1 .025
by the appended claims, they constitute part of the present invention.
We claim: An alkaline germicidal cleaning composition having indicator means to signify the minimum contact time for effective germicidal action in use dilutions thereof, said composition consisting essentially of a mixture of inorganic alkaline cleaning components providing a pH of 10.5 to 11.5 in aqueous use dilution containing amounts of the order of 1.0 to 2.5% by Weight of said composition, 0.25 to 3% of a quaternary ammonium germicide selected from the group consisting of benzethonium chloride, dodecyl benzyl tzimethyl ammonium chloride, dodecyl benzyl diethyl ethanol ammonium chloride, cetyl pyridinium chloride and bromide, dodecyl benzyl triethanol ammonium chloride, N(lauroyl colaminoformylmethyl)pyridinium chloride, and dodecyl benzyl diethanol ammonium chloride, 0.01 to 0.1% of a water soluble dye selected from the group consisting of F.D. 8: C. Blue No. 1, D. & C. Blue No. 4,D. & C. Blue No. 7, PD. & C. Violet N0. 1, F.D. & C. Blue No. 2, ED. & C. Green No. l, F.D. & C. Green No. 2, and Crystal Violet, and an oxygen releasing inorganic per-compound in an amount to decolorize said dye in such use dilution in a time interval of 0.5 to 5 minutes, said inorganic per-compound being selected from the group consisting of perborates, persulfates, perphosphates, percarbonates, and stabilized (granular coated) sodium peroxide.
2. An alkaline germicidal cleaning composition as defined in claim 1, wherein the dye employed is F.D. & C. Blue No. 1.
3. An alkaline germicidal cleaning composition as defined in claim 1, wherein the dye employed is D. 8: C. Blue No. 4.
4. An alkaline germicidal cleaning composition as defined in claim 1, wherein the dye employed is D. & C. Blue No. 7.
6 5. An alkaline germicidal cleaning composition as defined in claim 1 wherein the W/ W ratio of per-compound to dye is of the order of 400: 1.
References Cited UNITED STATES PATENTS 2,151,495 3/1939 Bender 167-93 2,409,718 10/1946 Snell 252-106 X 2,449,274 9/1948 Broll 252-106 X 2,498,344 2/1950 Rider et a1 25299 X 2,576,205 11/1951 Apperson 252-99 2,599,127 6/1952 Resuggan 252-106 2,658,873 11/1953 Marcoux 252-106 2,714,083 7/1955 Ferguson 167-93 X 2,931,776 4/1960 Howard 25299 2,987,435 6/1961 Davies et al 252-187 X 3,044,962 7/1962 Brunt et al 252-106 X 3,243,377 3/ 1966 Stolar 252- FOREIGN PATENTS 927,540 5/ 1963 Great Britain.
LEON D. ROSDOL, Primary Examiner.
ALBERT T. MEYERS, SAMUEL H. BLECH,
Examiners. M. WEINBLATT, Assistant Examiner.

Claims (1)

1. AN ALKALINE GERMICIDAL CLANING COMPOSITION HAVING INDICATOR MEANS TOSIGNIFY THE MINIMUM CONTACT TIME FOR EFFECTIVE GERMICIDAL ACTION IN USE DILUTIONS THEREOF, SAID COMPOSITION CONSISTING ESSENTIALLY OF AMIXTURE OF INORGANIC ALKALINE CLEANING COMPONENTS PROVIDING A PH OF 10.3 TO 11.5 IN AQUEOUS USE DILUTION CONTAINING AMOUNTS OF THE ORDER OF 1.0 TO 2.5% BY WEIGHT OF SAID COMPOSITION, 0.25 TO 3% OF A QUATERNARY AMMONIUM GERMICIDE SELECTED FROM THE GROP CONSISTING OF BENZETHONIUM CHLORIDE, DODECYL BENZYL T.IMETHYL AMMONIUM CHLORIDE, DODECYL BENZYL DIETHYL ETHANOL AMMONIUM CHORIDE,CETYL PYRIDINIUM CHLORIDE AND BROMIDE, DODECYL BENZYL TRIETHANOL AMMONIUM CHLORIDE, N(LAUROYL COLAMINOFORMYLMETHYL)PYRIDINIUM CHLORIDE, AND DODECYL BENZYL DIETHANOL AMMONIUM CHLORIDE, 0.01 TO 0.1% OF A WATER SOLUBLE DYE SELECTED FROM THE GROUP CONSISTING OF F.D.& C. BLUE NO. 1, D. & C. BLUE NO. 4, D. & C. BLUE NO. 7, F. D. & C. VIOLET NO. 1, F.D.&C. BLUE NO. 2, F.D.&C. GREEN NO. 1, F.D.&C. GREEN NO. 5, AND CRYSTAL VIOLET, AND AN OXYGEN RELEASING INORGANIC PER-COMPOUND IN AN AMOUNT TODECOLORIZE SAID DYE IN SUCH USE DILUTION INA TIME INTERVAL OF 0.5 TO 5 MINUTES, SAID INORGANIC PER-COMPOUND BEING SELECTED FROM THE GROUP CONSISTING OF PERBORATES, PERSULFATES, PERPHOSPHATES, PERCARBONATES, AND STABILIZED (GRANULAR COATED) SODIUM PEROXIDE.
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Cited By (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3506756A (en) * 1969-07-07 1970-04-14 Miles Lab Use of adipic acid as a tableting lubricant
US3518346A (en) * 1968-01-02 1970-06-30 Miles Lab Tableting
US3518343A (en) * 1967-10-02 1970-06-30 Miles Lab Effervescent tablet and process for making same
US3518344A (en) * 1967-10-02 1970-06-30 Miles Lab Tableting lubricant
US3518345A (en) * 1967-10-05 1970-06-30 Miles Lab Tableting lubricant
US3619462A (en) * 1969-12-29 1971-11-09 Miles Lab Tableting lubricant
US3936385A (en) * 1973-08-09 1976-02-03 Colgate-Palmolive Company Denture cleanser
US4016089A (en) * 1974-11-11 1977-04-05 Regan Glen B Denture cleaning concentrate
US4200606A (en) * 1978-12-22 1980-04-29 The Procter & Gamble Company Method for sanitizing toilets
US4248827A (en) * 1978-06-12 1981-02-03 The Procter & Gamble Company Method for sanitizing toilets
US4249274A (en) * 1979-12-03 1981-02-10 The Procter & Gamble Company Apparatus for sanitizing toilets
US4308625A (en) * 1978-06-12 1982-01-05 The Procter & Gamble Company Article for sanitizing toilets
US4323551A (en) * 1981-02-19 1982-04-06 The Procter & Gamble Company Mouthwash compositions
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US4597941A (en) * 1984-03-28 1986-07-01 The Drackett Company Toilet cleaning article and method for codispensing disinfectant and dye having resistance to spectral degradation
US4965063A (en) * 1985-05-24 1990-10-23 Irene Casey Cleaner and disinfectant with dye
US5482654A (en) * 1994-11-09 1996-01-09 Warnaway Corporation Safety indicator system
WO1996020995A1 (en) * 1995-01-06 1996-07-11 Texas Research Institute Compositions containing a visible colorant and methods for cleaning and decontamination
WO1997019163A1 (en) * 1995-11-17 1997-05-29 Henkel Kommanditgesellschaft Auf Aktien Coloured particles suitable for incorporation in washing and cleaning agents
WO1998057544A1 (en) * 1997-06-18 1998-12-23 Reckitt & Colman Products Limited Improvements in or relating to disinfecting materials
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US20040065350A1 (en) * 2002-10-03 2004-04-08 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Indicator kit
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US20060264346A1 (en) * 2005-05-19 2006-11-23 Sullivan Mary K Timed-release cleansing and/or treatment formulation and method for making and using the same
US20080081020A1 (en) * 2006-10-03 2008-04-03 Huang Yeong H Color change surgical prep solution
US20080227856A1 (en) * 2004-02-27 2008-09-18 Melker Richard J Materials and Methods for Creating Customized Compositions Having a Temporary Visual Indicator
US11274270B2 (en) 2017-04-07 2022-03-15 Alpha Chemical Services, Inc. Cleaning compositions with pH indicators and methods of use

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US3518343A (en) * 1967-10-02 1970-06-30 Miles Lab Effervescent tablet and process for making same
US3518344A (en) * 1967-10-02 1970-06-30 Miles Lab Tableting lubricant
US3518345A (en) * 1967-10-05 1970-06-30 Miles Lab Tableting lubricant
US3518346A (en) * 1968-01-02 1970-06-30 Miles Lab Tableting
US3506756A (en) * 1969-07-07 1970-04-14 Miles Lab Use of adipic acid as a tableting lubricant
US3619462A (en) * 1969-12-29 1971-11-09 Miles Lab Tableting lubricant
US3936385A (en) * 1973-08-09 1976-02-03 Colgate-Palmolive Company Denture cleanser
US4016089A (en) * 1974-11-11 1977-04-05 Regan Glen B Denture cleaning concentrate
US4308625A (en) * 1978-06-12 1982-01-05 The Procter & Gamble Company Article for sanitizing toilets
US4248827A (en) * 1978-06-12 1981-02-03 The Procter & Gamble Company Method for sanitizing toilets
US4200606A (en) * 1978-12-22 1980-04-29 The Procter & Gamble Company Method for sanitizing toilets
US4249274A (en) * 1979-12-03 1981-02-10 The Procter & Gamble Company Apparatus for sanitizing toilets
US4323551A (en) * 1981-02-19 1982-04-06 The Procter & Gamble Company Mouthwash compositions
EP0059012A2 (en) * 1981-02-19 1982-09-01 THE PROCTER & GAMBLE COMPANY Mouthwash compositions
EP0059012A3 (en) * 1981-02-19 1983-06-01 The Procter & Gamble Company Mouthwash compositions
US4499001A (en) * 1981-04-03 1985-02-12 Warner-Lambert Company Controlled fade effervescing cleanser
US4477361A (en) * 1983-02-22 1984-10-16 Sperti Drug Products, Inc. Antifungal-antibacterial detergents containing cinnamic compounds
US4597941A (en) * 1984-03-28 1986-07-01 The Drackett Company Toilet cleaning article and method for codispensing disinfectant and dye having resistance to spectral degradation
US4965063A (en) * 1985-05-24 1990-10-23 Irene Casey Cleaner and disinfectant with dye
US5482654A (en) * 1994-11-09 1996-01-09 Warnaway Corporation Safety indicator system
US5670469A (en) * 1995-01-06 1997-09-23 Texas Research Institute Methods and compositions for cleaning and decontamination
WO1996020995A1 (en) * 1995-01-06 1996-07-11 Texas Research Institute Compositions containing a visible colorant and methods for cleaning and decontamination
WO1997019163A1 (en) * 1995-11-17 1997-05-29 Henkel Kommanditgesellschaft Auf Aktien Coloured particles suitable for incorporation in washing and cleaning agents
WO1998057544A1 (en) * 1997-06-18 1998-12-23 Reckitt & Colman Products Limited Improvements in or relating to disinfecting materials
US6121213A (en) * 1998-07-28 2000-09-19 Block Drug Company, Inc. Stable peroxide denture paste
WO2003014282A1 (en) * 2001-08-06 2003-02-20 Colgate-Palmolive Company Color changing liquid cleaning composition
US20030220213A1 (en) * 2002-05-24 2003-11-27 Bober Andrew M. Color changing floor finish stripper
EP1382354A1 (en) * 2002-07-19 2004-01-21 Philippe Guichard Cleaning, detergent, disinfecting and decontaminating composition with broad-spectrum use
FR2842426A1 (en) * 2002-07-19 2004-01-23 Philippe Guichard CLEANING, DETERGENT, DISINFECTANT AND DECONTAMINANT COMPOSITION WITH BROAD RANGE OF USE
WO2004009140A1 (en) * 2002-07-19 2004-01-29 Braun, Jean-Paul Cleaning, detergent, disinfectant and decontaminating composition with wide spectrum of application
US20040065350A1 (en) * 2002-10-03 2004-04-08 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Indicator kit
US6814816B2 (en) 2002-10-03 2004-11-09 Unilever Home & Personal Care Usa Division Of Conopco, Inc. Indicator kit
WO2004078896A1 (en) * 2003-03-05 2004-09-16 Unilever Plc Method of treating a textile using a colour changing foam
US20060191076A1 (en) * 2003-03-05 2006-08-31 Bonfa Marcio Henrique P Method of treating a textile using a colour changing form
WO2005037974A2 (en) * 2003-10-07 2005-04-28 Henkel Kommanditgesellschaft Auf Aktien Antimicrobial treatment for bath and toilet articles
WO2005037974A3 (en) * 2003-10-07 2009-03-05 Henkel Kgaa Antimicrobial treatment for bath and toilet articles
WO2005084434A2 (en) * 2004-02-27 2005-09-15 Tvia, Llc System and methods for customized products having a temporary visual indicator
WO2005084434A3 (en) * 2004-02-27 2005-12-01 Tvia Llc System and methods for customized products having a temporary visual indicator
US20050191326A1 (en) * 2004-02-27 2005-09-01 Melker Richard J. Materials and methods for creating customized compositions having a temporary visual indicator
US20080227856A1 (en) * 2004-02-27 2008-09-18 Melker Richard J Materials and Methods for Creating Customized Compositions Having a Temporary Visual Indicator
US20060264346A1 (en) * 2005-05-19 2006-11-23 Sullivan Mary K Timed-release cleansing and/or treatment formulation and method for making and using the same
US20080081020A1 (en) * 2006-10-03 2008-04-03 Huang Yeong H Color change surgical prep solution
WO2008060355A2 (en) * 2006-10-03 2008-05-22 Allegiance Corporation Color change surgical prep solution
WO2008060355A3 (en) * 2006-10-03 2009-07-09 Allegiance Corp Color change surgical prep solution
US20100221193A1 (en) * 2006-10-03 2010-09-02 Carefusion 2200, Inc. Color change surgical prep solution
US9101134B2 (en) 2006-10-03 2015-08-11 Carefusion 2200, Inc. Color change surgical prep solution
US11274270B2 (en) 2017-04-07 2022-03-15 Alpha Chemical Services, Inc. Cleaning compositions with pH indicators and methods of use

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