EP0441652A1 - Detergent composition - Google Patents

Detergent composition Download PDF

Info

Publication number
EP0441652A1
EP0441652A1 EP19910301046 EP91301046A EP0441652A1 EP 0441652 A1 EP0441652 A1 EP 0441652A1 EP 19910301046 EP19910301046 EP 19910301046 EP 91301046 A EP91301046 A EP 91301046A EP 0441652 A1 EP0441652 A1 EP 0441652A1
Authority
EP
European Patent Office
Prior art keywords
sulfosuccinate
isethionate
composition according
acyl
composition
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.)
Granted
Application number
EP19910301046
Other languages
German (de)
French (fr)
Other versions
EP0441652B1 (en
Inventor
Karla Jean Rys
Alan Paul Greene
Frederick Sylvio Osmer
Joseph James Podgorsky
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.)
Unilever PLC
Unilever NV
Original Assignee
Unilever PLC
Unilever NV
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 Unilever PLC, Unilever NV filed Critical Unilever PLC
Publication of EP0441652A1 publication Critical patent/EP0441652A1/en
Application granted granted Critical
Publication of EP0441652B1 publication Critical patent/EP0441652B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/006Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/37Mixtures of compounds all of which are anionic
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/123Sulfonic acids or sulfuric acid esters; Salts thereof derived from carboxylic acids, e.g. sulfosuccinates
    • 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
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/02Anionic compounds
    • C11D1/12Sulfonic acids or sulfuric acid esters; Salts thereof
    • C11D1/126Acylisethionates

Definitions

  • the invention relates to solid skin cleansing, detergent compositions containing acyl isethionates.
  • soap has been utilized as a skin cleanser. Soap is, however, a very harsh chemical. Irritated and cracked skin result from use of soap, especially in colder climates. There are, however, certain benefits from the use of soap including low cost, ease of manufacture into bars, and good lathering properties.
  • U.S. 4,335,025 discusses synthetic detergent bars containing critical amounts of components.
  • alkali metal salts of C8 ⁇ 16 alkyl sulfosuccinate together with a selected water soluble anionic detergent which may include a C10 ⁇ 16 acyl isethionate, a waxy extender such as a C12 ⁇ 22 fatty acid or alcohol and the like, and other optional extenders.
  • U.S. 3,901,832 discusses a detergent bar containing a monoalkyl sulfosuccinate and a specific plasticizer in detergent cakes.
  • U.S. 3,989,642 discusses a synthetic toilet bar containing selected amounts of an alkane sulfonate, a fatty acid, and a binder modifier, which may be an alkyl sulfosuccinate.
  • U.S. 4,812,253 discusses various compositions containing polymeric skin mildness aids, moisturizers, soap and selected surfactants which include acyl isethionates and alkyl sulfosuccinate.
  • the present invention aims to provide compositions with excellent skin mildness while also possessing good lather, mush and processing properties.
  • a skin cleansing toilet bar composition comprising:
  • Preferred skin cleansing compositions have acyl isethionates as the main active in combination with monoalkyl sulfosuccinates as the co-active. Such compositions can be substantially milder to the skin than previously known compositions.
  • compositions within this invention may contain some free fatty acid. They may contain some free isethionate. They may contain some soap.
  • a preferred solid skin cleansing composition comprises:
  • Preferred weight ratios of acyl isethionate to sulfosuccinates are 6:1 to 2:1 and most preferred to maintain mildness are 2:1 to 4.5:1.
  • the irritancy of the already mild main active, acyl isethionate can be reduced significantly by the incorporation of sulfosuccinates.
  • the cleansers resulting from this mixture of actives have superior skin mildness together with good bar properties such as processability, low mush, good lather, and good tactile characteristics. In addition, they are easily processable using standard manufacturing equipment. In order for processability to be good, it is usually required for the composition to have an appropriate hardness and stickiness.
  • Isethionate salts in the range of about C6-C18 such as those derived from coconut fatty acids, for example, have been employed in a number of commercial cleansing products and are known to produce a voluminous, creamy lather.
  • This active by itself, has been shown to be very mild to the skin. These actives are solid at room temperature and serve as excellent structurants when used in bar formulations.
  • the isethionate ester salts that may be employed herein are preferably acyl ester isethionates and most preferably the cocoyl ester.
  • These preferred esters may be prepared from the usual cocoyl fatty acids having a small percentage of fatty acid chains below C8 with over 95% of the carbon chain distribution being between C8 and C18 and more than half being C12 or less.
  • the acyl chain length of the esters will have at least about 90% C6-C18 and more than about 30% C14 or lower.
  • a typical cocoyl fraction will contain:
  • the sulfosuccinates useful in the invention may be any suitable sulfosuccinate esther mono-esters (half esters) or di-esters and any alkali metal, alkaline earth metal or ammonium salt, but the sulfosuccinates are preferably monoesters and preferably prepared through an alkanolamine intermediate so as to introduce an amido group into the molecule.
  • the sulfosuccinate monoester is prepared through a monoethanolamine intermediate.
  • the most preferable sulfosuccinates are, Disodium Cocamido Monoethanolamide Sulfosuccinate of the Structure 1:
  • R in Structure 1 is derived from coconut fatty acids, but in other forms may be any convenient alkyl group.
  • the chain length distribution of coconut fatty acids is similar to that for the coco group on the isethionate.
  • the chain length distribution will contain at least 90% of C8 to C18 with more than half made up of C8 to C14.
  • a typical fatty acid distribution in the cocoyl portion is as follows:
  • the sulfosuccinate of Structure 1 may conveniently be prepared by a two step reaction:
  • the relative amounts of isethionate esters to sulfosuccinate will preferably lie in the weight ratio of 2:1 to 4.5:1, or even as high as 6:1, preferably from 3:1 to 4:1, optimally about 3.5:1.
  • soap may be somewhat harsh and when present in the compositions of this invention should be at a level no higher than about 25%, preferably less than 5%, and advantageously totally absent.
  • Free fatty acids of about 8-22 carbon atoms are desirably incorporated within the compositions of the present invention. Some of these fatty acids are present to operate as superfatting agents and others as skin feel and creaminess enhancers. Fatty alcohols, fatty amides and the like may also be employed. Superfatting agents enhance lathering properties and may be selected from fatty acids of carbon atoms numbering 8-18, preferably 10-18, in an amount up to 40% by weight of the composition. Skin feel and creaminess enhancers, the most important of which is stearic acid, are also desirably present in these compositions.
  • humectants such as glycerine
  • anti wear agents such as polymer JR and natural and synthetic gums and the like
  • germicides perfumes, colorants, dyes, pigments such as titanium dioxide, electrolytes, and water.
  • the products skin mildness properties were evaluated by comparison to Dove toilet bars (Dove is a registered trademark of Lever Brothers Co.), which are very mild commercial bars, through the following test procedure.
  • the Flex Wash test procedure consists of three daily two minute washes of the antecubital fossa (flex area of elbow). This method is an "exaggerated use” method designed to differentiate very mild products. Erythemal response varies only slightly with temperature and humidity fluctuations making the protocol suitable for year round testing.
  • Panelist flex areas must be free of any skin condition (eczema, dryness, irritation, cuts or abrasions).
  • Any skin condition eczema, dryness, irritation, cuts or abrasions.
  • An antihistamines, anti-inflammatory drugs (more than 8 per week) or topical, oral or injectable cortisone on a regular basis was excluded from the study.
  • the panel was divided into two sub-groups which were balanced for left handedness. Group I was assigned composition "A" for the left flex and "B" for the right flex. Group II reversed the order.
  • the panelist was instructed to moisten the left flex area, the sponge and test compositions formulated as toilet bars were dampened with tap water (100 ppm calcium/magnesium ions). The sponge was then stroked over the test bar 10 times by the evaluator. The "dosed" sponge was placed in the panelist's right hand. The panelist then washed the left flex area for exactly two minutes. Thereupon, the flex was rinsed and patted dry. This washing procedure was repeated on the right arm with the appropriate composition. Thus, both arms are tested simultaneously. Washing by this procedure was repeated three times daily for 5 consecutive days for a total of 15 washes. Treatment times were scheduled 1.5 hours apart. Each test site was evaluated immediately prior to washing and 4 hours after the third daily wash.
  • Mean Rank Scores is the sum total of grade scores for 15 assessments per panelist averaged over the scores from all panelists. Thus, theoretically, the average score could range from 0 to 30; the lower score indicating absolutely no skin irritation while the 30 score being the most severe.
  • Mean Endpoint Erythema scores are the mean of the evaluation scores, for each panelist, at which the first arm received a grade of "2" or greater erythema score or at the completion of fifteen washes.
  • This example illustrates the difference in mildness between Dove and a toilet bar employing the Acyl Isethionate/Alkyl Sulfosuccinate active system, where the ratio of Isethionate to Sulfosuccinate is 2.20:1.
  • PEG-150 a polymer of ethylene oxide
  • the ratio of Cocoyl Isethionate to Amido Sulfosuccinate is 3.64:1. Mildness, superior to Dove, is proven by-the Flex Wash.
  • Mush - Pre-weighed bars were immersed in water for 2 hours. The increase in weight was noted. Mush was removed and the remainder of the bar was dried. After reweighing, mush was calculated as the weight of mush per 50 cm2 of surface mushed. Lower values indicated better performance.

Abstract

A skin cleansing composition is provided that includes a combination of acyl isethionate ester salts with at least one sulfosuccinate. The weight ratio of acyl isethionate to sulfosuccinate will be about 10:1 to about 2:1.

Description

  • The invention relates to solid skin cleansing, detergent compositions containing acyl isethionates.
  • Traditionally, soap has been utilized as a skin cleanser. Soap is, however, a very harsh chemical. Irritated and cracked skin result from use of soap, especially in colder climates. There are, however, certain benefits from the use of soap including low cost, ease of manufacture into bars, and good lathering properties.
  • There has been much commercial activity in attempting to replace soaps with milder surfactants. The introduction of mild synthetic detergent toilet bars, especially those based on sodium cocyl isethionates, has been particularly successful. Patents relating to this technology are dicussed in a published PCT application number WO 90/12860, which is incorporated by reference herein.
  • U.S. 4,335,025 discusses synthetic detergent bars containing critical amounts of components. For example, alkali metal salts of C₈₋₁₆ alkyl sulfosuccinate together with a selected water soluble anionic detergent which may include a C₁₀₋₁₆ acyl isethionate, a waxy extender such as a C₁₂₋₂₂ fatty acid or alcohol and the like, and other optional extenders.
  • U.S. 3,901,832 discusses a detergent bar containing a monoalkyl sulfosuccinate and a specific plasticizer in detergent cakes.
  • U.S. 3,989,642 discusses a synthetic toilet bar containing selected amounts of an alkane sulfonate, a fatty acid, and a binder modifier, which may be an alkyl sulfosuccinate.
  • U.S. 4,812,253 discusses various compositions containing polymeric skin mildness aids, moisturizers, soap and selected surfactants which include acyl isethionates and alkyl sulfosuccinate.
  • The present invention aims to provide compositions with excellent skin mildness while also possessing good lather, mush and processing properties.
  • According to the present invention there is provided a skin cleansing toilet bar composition comprising:
    • i) acyl esters of isethionic acid salts, the acyl chain length distribution of said esters being at least about 90% C₆-C₁₈ and having more than about 30% C₁₄ or lower; and
    • ii) at least one sulfosuccinate wherein the weight ratio of said acyl esters to sulfosuccinate is 10:1 to 2:1.
  • Preferred skin cleansing compositions have acyl isethionates as the main active in combination with monoalkyl sulfosuccinates as the co-active. Such compositions can be substantially milder to the skin than previously known compositions.
  • Compositions within this invention may contain some free fatty acid. They may contain some free isethionate. They may contain some soap.
  • A preferred solid skin cleansing composition comprises:
    • (i) acyl esters of isethionic acid salts in an amount of 20 to 70%;
    • (ii) at least one sulfosuccinate wherein the weight ratio of said acyl esters to sulfosuccinate is 10:1 to 2:1;
    • (iii) free fatty acid in an amount of 2-40%;
    • (iv) free isethionate in an amount of 2-20%;
    • (v) soap in an amount of 0-25%;
    • (vi) water in an amount of 2-20%;
    • (vii) miscellaneous other constituents in an amount of 0-20%.
  • Preferred weight ratios of acyl isethionate to sulfosuccinates are 6:1 to 2:1 and most preferred to maintain mildness are 2:1 to 4.5:1.
  • In this invention, the irritancy of the already mild main active, acyl isethionate, can be reduced significantly by the incorporation of sulfosuccinates.
  • The cleansers resulting from this mixture of actives have superior skin mildness together with good bar properties such as processability, low mush, good lather, and good tactile characteristics. In addition, they are easily processable using standard manufacturing equipment. In order for processability to be good, it is usually required for the composition to have an appropriate hardness and stickiness.
  • Isethionate salts in the range of about C₆-C₁₈, such as those derived from coconut fatty acids, for example, have been employed in a number of commercial cleansing products and are known to produce a voluminous, creamy lather. This active, by itself, has been shown to be very mild to the skin. These actives are solid at room temperature and serve as excellent structurants when used in bar formulations.
  • The isethionate ester salts that may be employed herein are preferably acyl ester isethionates and most preferably the cocoyl ester. These preferred esters may be prepared from the usual cocoyl fatty acids having a small percentage of fatty acid chains below C₈ with over 95% of the carbon chain distribution being between C₈ and C₁₈ and more than half being C₁₂ or less. Preferably, the acyl chain length of the esters will have at least about 90% C₆-C₁₈ and more than about 30% C₁₄ or lower. A typical cocoyl fraction will contain:
    Figure imgb0001
  • Skin testing has shown that the mixed active system of this invention significantly reduced the irritancy of the already mild acyl isethionate base. Skin testing and use property evaluation have shown that the preferred ratio of isethionate to sulfosuccinate is 2:1 to 6:1.
  • The sulfosuccinates useful in the invention may be any suitable sulfosuccinate esther mono-esters (half esters) or di-esters and any alkali metal, alkaline earth metal or ammonium salt, but the sulfosuccinates are preferably monoesters and preferably prepared through an alkanolamine intermediate so as to introduce an amido group into the molecule. Preferably to give processability, mildness and other use properties the sulfosuccinate monoester is prepared through a monoethanolamine intermediate.
  • The most preferable sulfosuccinates are, Disodium Cocamido Monoethanolamide Sulfosuccinate of the Structure 1:
    Figure imgb0002
  • R in Structure 1 is derived from coconut fatty acids, but in other forms may be any convenient alkyl group. The chain length distribution of coconut fatty acids is similar to that for the coco group on the isethionate. The chain length distribution will contain at least 90% of C₈ to C₁₈ with more than half made up of C₈ to C₁₄. A typical fatty acid distribution in the cocoyl portion is as follows:
    Figure imgb0003
  • The sulfosuccinate of Structure 1 may conveniently be prepared by a two step reaction:
    • 1. An ester condensation reaction of Coco alkanolamide with Maleic Anhydride.
    • 2. Sulfonation of the double bond with Sodium Sulfite as described below.
    Figure imgb0004
    Figure imgb0005
  • The relative amounts of isethionate esters to sulfosuccinate will preferably lie in the weight ratio of 2:1 to 4.5:1, or even as high as 6:1, preferably from 3:1 to 4:1, optimally about 3.5:1.
  • As previously noted, soap may be somewhat harsh and when present in the compositions of this invention should be at a level no higher than about 25%, preferably less than 5%, and advantageously totally absent.
  • Free fatty acids of about 8-22 carbon atoms are desirably incorporated within the compositions of the present invention. Some of these fatty acids are present to operate as superfatting agents and others as skin feel and creaminess enhancers. Fatty alcohols, fatty amides and the like may also be employed. Superfatting agents enhance lathering properties and may be selected from fatty acids of carbon atoms numbering 8-18, preferably 10-18, in an amount up to 40% by weight of the composition. Skin feel and creaminess enhancers, the most important of which is stearic acid, are also desirably present in these compositions.
  • Other performance chemicals and adjuncts may be needed or employed with these compositions. The amount of these chemicals and adjuncts may range from about 0% to about 20% by weight of the total compositions. For instance, there may be included humectants such as glycerine; anti wear agents such as polymer JR and natural and synthetic gums and the like; germicides, perfumes, colorants, dyes, pigments such as titanium dioxide, electrolytes, and water.
  • Evaluation of an active's skin mildness properties are determined through the following test procedure.
  • The Flex Wash Test
  • The products skin mildness properties were evaluated by comparison to Dove toilet bars (Dove is a registered trademark of Lever Brothers Co.), which are very mild commercial bars, through the following test procedure. The Flex Wash test procedure consists of three daily two minute washes of the antecubital fossa (flex area of elbow). This method is an "exaggerated use" method designed to differentiate very mild products. Erythemal response varies only slightly with temperature and humidity fluctuations making the protocol suitable for year round testing.
  • Approximately 15 panelists were used as the test population. Panelist flex areas must be free of any skin condition (eczema, dryness, irritation, cuts or abrasions). Anyone taking antihistamines, anti-inflammatory drugs (more than 8 per week) or topical, oral or injectable cortisone on a regular basis was excluded from the study. The panel was divided into two sub-groups which were balanced for left handedness. Group I was assigned composition "A" for the left flex and "B" for the right flex. Group II reversed the order.
  • Following an evaluation, the panelist was instructed to moisten the left flex area, the sponge and test compositions formulated as toilet bars were dampened with tap water (100 ppm calcium/magnesium ions). The sponge was then stroked over the test bar 10 times by the evaluator. The "dosed" sponge was placed in the panelist's right hand. The panelist then washed the left flex area for exactly two minutes. Thereupon, the flex was rinsed and patted dry. This washing procedure was repeated on the right arm with the appropriate composition. Thus, both arms are tested simultaneously. Washing by this procedure was repeated three times daily for 5 consecutive days for a total of 15 washes. Treatment times were scheduled 1.5 hours apart. Each test site was evaluated immediately prior to washing and 4 hours after the third daily wash.
  • One trained assessor evaluated test sites prior to each wash and 4 hours after the third wash of the fifth day for a total of 15 evaluations. The grading scale was as follows:
  • 0 - no erythema
  • 0.5 - barely perceptible erythema
  • 1 - mild spotty erythema/no edema
  • 1.5 - mild/moderate erythema/with or without edema
  • 2 - moderate confluent erythema/with or without edema or vesiculation
  • Each test site was treated in the prescribed method until a grading of "2" or greater was attained or 15 washings had been completed. When a score of "2" or greater was attained, the treatment was discontinued on that flex. The final score was then carried through for all remaining evaluations. The remaining flex was washed until either a grading of at least "2" or 15 treatments were attained, whichever was first. In the Examples of this specification, the final grading, Mean Rank Scores, is the sum total of grade scores for 15 assessments per panelist averaged over the scores from all panelists. Thus, theoretically, the average score could range from 0 to 30; the lower score indicating absolutely no skin irritation while the 30 score being the most severe. Mean Endpoint Erythema scores are the mean of the evaluation scores, for each panelist, at which the first arm received a grade of "2" or greater erythema score or at the completion of fifteen washes.
  • The following examples will more fully illustrate the embodiments of this invention. All parts, percentages and proportions referred to herein and in the appended claims are by weight of the total composition unless otherwise stated.
  • EXAMPLE 1
  • This example illustrates the difference in mildness between Dove and a toilet bar employing the Acyl Isethionate/Alkyl Sulfosuccinate active system, where the ratio of Isethionate to Sulfosuccinate is 2.20:1.
  • Formulation 1
  • Sodium Cocoyl Isethionate
    33.10
    Stearic Acid
    29.80
    Sodium Isethionate
    9.10
    Disodium Cocamido
    MEA Sulfosuccinate
    15.00
    Water
    10.00
    Perfume
    1.00
    Sodium Chloride
    0.35
    Titanium Dioxide
    0.20
    Miscellaneous
    1.45
    Figure imgb0006
    EXAMPLE 2
  • The addition of small amounts of PEG-150, a polymer of ethylene oxide, does not deteriously affect the mildness of a 2.87:1, Isethionate to Sulfosuccinate, formulated toilet bar.
  • Formulation 2
  • Sodium Cocoyl Isethionate
    43.6
    Stearic Acid
    22.0
    Sodium Isethionate
    9.3
    Disodium Cocamido
    MEA Sulfosuccinate
    15.2
    Sodium Chloride
    2.6
    PEG 150*
    1.0
    Water
    4.7
    Perfume
    1.0
    Titanium Dioxide
    0.5
    EHDP
    0.02
    EDTA
    0.02
  • * Carbowax 8000 (Union Carbide)
    Figure imgb0007
  • EXAMPLE 3
  • In the following example, mildness superior to that of Dove is again demonstrated. The Isethionate to Sulfosuccinate ratio here is 2.89:1.
  • Formulation 3
  • Sodium Cocoyl Isethionate
    43.9
    Stearic Acid
    20.1
    Sodium Isethionate
    11.0
    Disodium Cocamido
    MEA Sulfosuccinate
    15.2
    Sodium Chloride
    5.1
    Water
    3.2
    Perfume
    1.0
    Titanium Dioxide
    0.5
    EHDP
    0.02
    EDTA
    0.02
    Figure imgb0008
    EXAMPLE 4
  • In this example, the ratio of Cocoyl Isethionate to Amido Sulfosuccinate is 3.64:1. Mildness, superior to Dove, is proven by-the Flex Wash.
  • Formulation 4
  • Sodium cocoyl Isethionate
    43.7
    Stearic Acid
    23.9
    Disodium Cocamido
    MEA Sulfosuccinate
    12.0
    Sodium Isethionate
    13.8
    Water
    4.7
    Perfume
    1.0
    Sodium Chloride
    0.35
    Titanium Dioxide
    0.5
    EHDP
    0.02
    EDTA
    0.02
    Figure imgb0009
    EXAMPLE 5
  • A significant improvement in mildness over Dove, at the 90% confidence level, is achieved when the isethionate to sulfosuccinate ratio is 5.12:1. The Mean Endpoint Erythema is substantially lower in the mixed active, Isethionate/ Sulfosuccinate bar, than in Dove.
  • Formulation 5
  • Sodium Cocoyl Isethionate
    46.1
    Stearic Acid
    23.7
    Disodium Cocamido MEA
    Sulfosuccinate
    9.0
    Sodium Isethionate
    13.7
    PEG 150
    1.0
    Sodium Chloride
    0.35
    Water
    4.7
    Perfume
    1.0
    Titanium Dioxide
    0.5
    EHDP
    0.02
    EDTA
    0.02
  • *Carbowax 8000 (Union Carbide)
    Figure imgb0010
  • EXAMPLE 6
  • Lather Volume measurements and bar mush evaluations were performed on the forementioned formulations. A brief description of the lather and mush tests are reported below.
  • Objective Lather Volume - This test involved rotating the toilet bar 15 half turns under running 95° F water. The bar was then set aside and the resulting lather was worked by hand for 10 seconds. A measuring funnel was then placed over the hands and both were lowered into a sink filled with water to the 0 ml mark on the measuring funnel. When the hands were fully immersed, they were removed from beneath the funnel. The funnel was then lowered to the bottom of the sink and lather volume was measured.
  • Mush - Pre-weighed bars were immersed in water for 2 hours. The increase in weight was noted. Mush was removed and the remainder of the bar was dried. After reweighing, mush was calculated as the weight of mush per 50 cm² of surface mushed. Lower values indicated better performance.
    Figure imgb0011
  • All of the formulations in Table 1 have excellent lather and low bar mush values.
  • EXAMPLE 7
  • In the following example, six mixed active bars and commercial Dove, were panel tested. The panel consisted of 15 highly discriminating female Dove users. Each panelist was asked to set a water temperature and then wet her hands. A bar was then taken from the soap dish, into both hands, lathered up, and placed back into the dish. The panelist then rinsed her hands and patted them dry with a non-woven towel. At the end of the wash the panelist was asked to complete a questionnaire. This process was repeated for each of the 6 remaining bars. The questionnaire was divided into two parts, the first part inquired about use properties and asked the panelists to judge the Ease of Lather Generation, Subjective Lather Volume, Lather Creaminess and Ease of Rinsing. The second part asked about skin after effects such as dryness, softness, irritation, smoothness, and cleanliness.
  • Results of these tests show the Isethionate/Sulfosuccinate combination has excellent consumer properties.
    Figure imgb0012
    Figure imgb0013
  • These resulsts clearly show that bars 1 to 6 are quite as consumer acceptable as the commercial bar.
  • Skin Afterfeel was evaluated based upon the following scale:
    Figure imgb0014
    Figure imgb0015
  • These results show that the combination of the invention is not only equal to the commercial bar, but in some cases, perceivably better.

Claims (10)

  1. A skin cleansing toilet bar composition comprising:
    i) acyl esters of isethionic acid salts, the acyl chain length distribution of said esters being at least about 90% C₆-C₁₈ and having more than about 30% C₁₄ or lower; and
    ii) at least one sulfosuccinate wherein the weight ratio of said acyl esters to sulfosuccinate is 10:1 to 2:1.
  2. A composition according to claim 1 wherein the sulfosuccinate is a mono ester.
  3. A composition according to claim 1 wherein the sulfosuccinate is derived from a monoethanolamide.
  4. A composition according to claim 2 wherein the sulfosuccinate is an amido sulfosuccinate.
  5. A composition according to claim 4 wherein the sulfosuccinate is a cocoamido sulfosuccinate.
  6. A composition according to any one of the preceding claims wherein the ratio of isethionate ester to sulfosuccinate is from 6:1 to 2:1.
  7. A composition according to any one of the preceding claims wherein the ratio of isethionate ester to sulfosuccinate is from 4.5:1 to 3:1.
  8. A composition according to any one of the preceding claims wherein said acyl chain length has the following distribution:
    Figure imgb0016
  9. A composition according to any one of the preceding claims wherein the amount of said acyl esters of isethionic acid salts is 20 to 70% by weight of the composition.
  10. A composition according to claim 9 which also comprises 2 to 40% of free fatty acid, 2 to 20% of sodium isethionate and 2 to 20% by weight of water, the amount of soap in the composition not exceeding 25% by weight and the amount of any other materials in the composition not exceeding 20% by weight.
EP91301046A 1990-02-09 1991-02-08 Detergent composition Expired - Lifetime EP0441652B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US47768290A 1990-02-09 1990-02-09
US477682 1990-02-09

Publications (2)

Publication Number Publication Date
EP0441652A1 true EP0441652A1 (en) 1991-08-14
EP0441652B1 EP0441652B1 (en) 1995-07-19

Family

ID=23896912

Family Applications (1)

Application Number Title Priority Date Filing Date
EP91301046A Expired - Lifetime EP0441652B1 (en) 1990-02-09 1991-02-08 Detergent composition

Country Status (8)

Country Link
EP (1) EP0441652B1 (en)
JP (1) JP2975450B2 (en)
AU (1) AU637668B2 (en)
BR (1) BR9100525A (en)
CA (1) CA2035681C (en)
DE (1) DE69111259T2 (en)
ES (1) ES2076462T3 (en)
ZA (1) ZA91953B (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994007988A1 (en) * 1992-10-05 1994-04-14 Mona Industries, Inc. Synthetic detergent bars and the method of making the same
WO1994017167A1 (en) * 1993-01-19 1994-08-04 Unilever Plc Low soap bar composition
WO1995030737A2 (en) * 1994-05-10 1995-11-16 The Procter & Gamble Company Personal cleansing soap-synthetic bar compositions with low levels of nonionic, polyethylene/polypropylene glycol polymers for improved mildness
US5500155A (en) * 1994-03-18 1996-03-19 Henkel Kommanditgesellschaft Auf Aktien Detergent mixtures of fatty acid isethionate salts and fatty alcohols
WO1997030142A1 (en) * 1996-02-15 1997-08-21 Unilever Plc Mild bar compositions comprising blends of polyalkylene glycols
US6001787A (en) * 1996-11-18 1999-12-14 Helene Curtis, Inc. Aqueous cleansing composition
FR3007641A1 (en) * 2013-06-27 2015-01-02 Oreal STABLE CLEANING COMPOSITION AS SOFT SOLID

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3793215A (en) * 1971-08-24 1974-02-19 Colgate Palmolive Co Soap bars
US4211675A (en) * 1978-01-19 1980-07-08 Lever Brothers Company Detergent bars with improved slip properties
US4335025A (en) * 1980-02-19 1982-06-15 Witco Chemical Corporation Process for the preparation of synthetic detergent bars, and products produced thereby
DE3335705A1 (en) * 1983-10-01 1985-04-11 Chemische Werke Hüls AG, 4370 Marl Liquid carpet cleaner
US4954282A (en) * 1989-04-19 1990-09-04 Lever Brothers Company Acyl isethionate skin cleansing compositions

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0308189B1 (en) * 1987-09-17 1994-04-06 The Procter & Gamble Company Skin cleansing toilet bar with low moisture content

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3793215A (en) * 1971-08-24 1974-02-19 Colgate Palmolive Co Soap bars
US4211675A (en) * 1978-01-19 1980-07-08 Lever Brothers Company Detergent bars with improved slip properties
US4335025A (en) * 1980-02-19 1982-06-15 Witco Chemical Corporation Process for the preparation of synthetic detergent bars, and products produced thereby
DE3335705A1 (en) * 1983-10-01 1985-04-11 Chemische Werke Hüls AG, 4370 Marl Liquid carpet cleaner
US4954282A (en) * 1989-04-19 1990-09-04 Lever Brothers Company Acyl isethionate skin cleansing compositions

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994007988A1 (en) * 1992-10-05 1994-04-14 Mona Industries, Inc. Synthetic detergent bars and the method of making the same
US5543072A (en) * 1992-10-05 1996-08-06 Mona Industries, Inc. Synthetic detergent bars and method of making the same
WO1994017167A1 (en) * 1993-01-19 1994-08-04 Unilever Plc Low soap bar composition
US5500155A (en) * 1994-03-18 1996-03-19 Henkel Kommanditgesellschaft Auf Aktien Detergent mixtures of fatty acid isethionate salts and fatty alcohols
WO1995030737A2 (en) * 1994-05-10 1995-11-16 The Procter & Gamble Company Personal cleansing soap-synthetic bar compositions with low levels of nonionic, polyethylene/polypropylene glycol polymers for improved mildness
WO1995030737A3 (en) * 1994-05-10 1995-12-21 Procter & Gamble Personal cleansing soap-synthetic bar compositions with low levels of nonionic, polyethylene/polypropylene glycol polymers for improved mildness
WO1997030142A1 (en) * 1996-02-15 1997-08-21 Unilever Plc Mild bar compositions comprising blends of polyalkylene glycols
EA001464B1 (en) * 1996-02-15 2001-04-23 Унилевер Н.В. Mild bar compositions comprising blends of polyalkylene glycols
US6001787A (en) * 1996-11-18 1999-12-14 Helene Curtis, Inc. Aqueous cleansing composition
FR3007641A1 (en) * 2013-06-27 2015-01-02 Oreal STABLE CLEANING COMPOSITION AS SOFT SOLID
WO2014207697A3 (en) * 2013-06-27 2015-05-21 L'oreal Aqueous cosmetic composition in flexible solid form

Also Published As

Publication number Publication date
CA2035681A1 (en) 1991-08-10
JP2975450B2 (en) 1999-11-10
ZA91953B (en) 1992-10-28
AU637668B2 (en) 1993-06-03
JPH04234810A (en) 1992-08-24
BR9100525A (en) 1991-10-29
CA2035681C (en) 1998-12-08
DE69111259T2 (en) 1995-12-21
ES2076462T3 (en) 1995-11-01
DE69111259D1 (en) 1995-08-24
AU7020691A (en) 1991-08-15
EP0441652B1 (en) 1995-07-19

Similar Documents

Publication Publication Date Title
US5372751A (en) Acyl isethionate skin cleaning compositions containing betaines, amido sulfosuccinates or combinations of the two
EP0469029B1 (en) Acyl isethionate skin cleansing compositions
EP0203750B2 (en) Ultra mild skin cleansing composition
US4812253A (en) Ultra mild skin cleansing composition
US4695395A (en) Cleaning compositions with skin protection agents
US5096608A (en) Ultra mild skin cleansing composition
AU625494B2 (en) Skin cleansing toilet bar with low moisture content
US5076953A (en) Skin cleansing synbars with low moisture and/or selected polymeric skin mildness aids
US5310508A (en) Mild personal cleansing compositions containing sodium alcohol ethoxy glyceryl sulfonate
US5296159A (en) Mild soap-synbar
NZ226220A (en) Toilet bar soap comprising synthetic surfactant, moisturiser, soap and two or more polymeric skin-feel and mildness aids
EP0748367B1 (en) Skin cleansing composition
EP0441652B1 (en) Detergent composition
EP0472320B1 (en) Acyl isethionate skin cleansing compositions containing selected betaines
EP0542526B1 (en) Skin cleansing compositions
US5108640A (en) Personal cleansing synbar with improved rinsing
WO1996036313A1 (en) Aqueous liquid cleansing composition containing fatty acid soaps

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): CH DE ES FR GB IT LI NL SE

17P Request for examination filed

Effective date: 19911111

RAP3 Party data changed (applicant data changed or rights of an application transferred)

Owner name: UNILEVER N.V.

Owner name: UNILEVER PLC

17Q First examination report despatched

Effective date: 19941011

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): CH DE ES FR GB IT LI NL SE

REF Corresponds to:

Ref document number: 69111259

Country of ref document: DE

Date of ref document: 19950824

ET Fr: translation filed
ITF It: translation for a ep patent filed

Owner name: JACOBACCI & PERANI S.P.A.

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2076462

Country of ref document: ES

Kind code of ref document: T3

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: CH

Payment date: 19970129

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 19980116

Year of fee payment: 8

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 19980218

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980228

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19980228

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990209

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19990901

EUG Se: european patent has lapsed

Ref document number: 91301046.8

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20100225

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: IT

Payment date: 20100224

Year of fee payment: 20

Ref country code: FR

Payment date: 20100303

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20100224

Year of fee payment: 20

Ref country code: DE

Payment date: 20100226

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 69111259

Country of ref document: DE

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20110207

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20110207

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20110208

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20130805

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20110209