WO1996024328A1 - Cosmetic cleansing compositions comprising esters of alkylglycosides - Google Patents

Cosmetic cleansing compositions comprising esters of alkylglycosides Download PDF

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Publication number
WO1996024328A1
WO1996024328A1 PCT/EP1996/000541 EP9600541W WO9624328A1 WO 1996024328 A1 WO1996024328 A1 WO 1996024328A1 EP 9600541 W EP9600541 W EP 9600541W WO 9624328 A1 WO9624328 A1 WO 9624328A1
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WO
WIPO (PCT)
Prior art keywords
cosmetic cleansing
cleansing composition
weight
composition according
fatty acid
Prior art date
Application number
PCT/EP1996/000541
Other languages
French (fr)
Inventor
Jacob Oosterman
Heleen Peters De Boer
Original Assignee
Unichema Chemie B.V.
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 Unichema Chemie B.V. filed Critical Unichema Chemie B.V.
Priority to JP8524001A priority Critical patent/JPH10513189A/en
Priority to BR9607118A priority patent/BR9607118A/en
Priority to EP96904035A priority patent/EP0808152A1/en
Priority to AU47892/96A priority patent/AU4789296A/en
Publication of WO1996024328A1 publication Critical patent/WO1996024328A1/en

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    • 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
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/604Alkylpolyglycosides; Derivatives thereof, e.g. esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/02Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/11Encapsulated compositions
    • 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
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • 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
    • A61K8/37Esters of carboxylic acids
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • 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
    • A61K8/46Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/463Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
    • 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
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4993Derivatives containing from 2 to 10 oxyalkylene groups
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/20Chemical, physico-chemical or functional or structural properties of the composition as a whole
    • A61K2800/22Gas releasing
    • A61K2800/222Effervescent
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds

Definitions

  • the present invention relates to a cosmetic cleansing composition in a water-soluble capsule.
  • the cosmetic cleansing composition should have a relatively high viscosity, so as to enable its encapsulation, whereas upon use the composition after breakage of the capsule should quickly dissolve or disperse in the aqueous environment.
  • a cosmetic cleansing composition in a water- soluble capsule, preferably made of gelatin, which composition comprises an alkali metal salt of an alkyl sulphate, a fatty acid ester of an alkylglycoside having an alkyl group with from 1 to 4 carbon atoms and a sorbitan
  • the viscosity of the product was dependent on the shear exerted upon it. For example 1 it was found that at very low shear (below to 10 sec “1 ) the viscosity of the product was 8,000 mPas; then with increasing shear (to 50 sec “1 ) the viscosity increased to 8,300 mPas and at constant shear of 50 sec "1 the viscosity increased further to 9,100 mPas. If the shear was then decreased, the viscosity further increased to 15,000 mPas. After some time, the viscosity started to decrease again. It may therefore be stated that the product is both shear thickening or dilatant and exhibits rheopexy.
  • This rheological behaviour is of advantage during finishing and in using the product.
  • a relatively high viscosity is required (in the order of 8,000 to 12,000 mPas) . If the product after finishing is left to rest, its viscosity will decrease to its original value at low shear, so that upon use the product will easily dissolve or disperse in water.
  • the present invention relates to a cosmetic cleansing composition in a water-soluble capsule, which composition comprises:
  • the fatty acid ester of the alkylglycoside having an alkyl group with from 1 to 4 carbon atoms preferably is a fatty acid ester of methyl glucoside, methyl fructoside, ethyl glycoside or ethyl fructoside.
  • the fatty acid may be a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms.
  • lauric acid, palmitic acid, stearic acid and iso-stearic acid is preferred.
  • fatty acid mixtures may be used, such as coconut fatty acids, palm kernel fatty acids and tallow fatty acids.
  • coconut fatty acids of which the fatty acids up to and including octanoic acid have mainly been removed, is preferred.
  • the fatty acid esters of the alkylglycosides comprise mono-, di-, tri- and higher esters.
  • the use of esters comprising at least 50% by weight, preferably at least 75% by weight, of mono esters is preferred.
  • the esters may comprise up to 15% by weight of free fatty acids, but preferably the free fatty acid content is as low as possible, e.g.below 3% by weight.
  • from 30 to 85% by weight of alkylglycoside ester is used, preferably from 60% to 85% by weight, and most preferably from 70% to 80% by weight.
  • the alkali metal salt of the alkyl sulphate preferably is the sodium salt.
  • the alkyl sulphate contains from 10 to 20 carbon atoms, such as dodecyl, lauryl, hexadecyl, myristyl and octadecyl sulphate. The use of lauryl sulphate is preferred. In general amine salts or alkanolamine salts are not used in view of the possibility of skin irritation. Generally from 10% to 20% by weight of the alkali metal salt of C 10 - C 20 alkyl sulphate is used.
  • the alkoxylated sorbitan fatty acid esters are derived from sorbitan (or anhydrohexitol) .
  • the fatty acids may be straight or branched chain, saturated or unsaturated fatty acids having from 10 to 22 carbon atoms, such as lauric acid, stearic acid, palmitic acid, oleic acid, iso-stearic acid and the like.
  • the sorbitan fatty acid esters have been alkoxylated with C1-C4 alkylene oxides, preferably ethylene oxide, or mixtures of such alkylene oxides. On an average from 10 to 80 moles of alkylene oxide per mole of sorbitan fatty acid ester are reacted.
  • the use of polyoxyethylene (20) orbitan monolaurate is preferred.
  • the alkoxylated sorbitan fatty acid ester is used in an amount of from 1% to 30% by weight, preferably from 5% to 25% by weight of the total composition.
  • the fatty acid dialkylolamide is derived from a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms, such as lauric acid or coconut acids of which the fatty acids up to and including octanoic acid have mainly been removed. In the latter case the term "coconut fatty acid dialkylolamide" is used and these dialkylolamides are preferred.
  • the hydroxyalkyl groups of the dialkylolamide have from 2 to 5 carbon atoms and these groups may the same or different and may be mono- or polyhydroxyalkyl.
  • the use of coconut fatty acid diethanolamide is preferred.
  • the fatty acid dialkylolamide is used in an amount of up to 30% by weight of the total composition, preferably from 15% to 25% by weight.
  • the amount of water in the cosmetic cleansing composition is at most 4% by weight and preferably at most 3% by weight.
  • the cosmetic cleansing compositions according to the present invention may also comprise an effective amount (in general up to 10% by weight, but greater amounts may be used) of a functional additive, selected from the group consisting of perfumes, chelating or sequestering agents (like EDTA) , preservatives, bactericides, herbs (or herb extracts) , vitamins, buffering substances, moisturizers, emollients (such as esters of fatty acids and/or fatty alcohols) , viscosity controlling agents (such as monohydric alcohols with 2 to 8 carbon atoms) , anti-oxidants, dyes, lather boosters (such as higher alkyl amine oxides) , and mixtures thereof .
  • a functional additive selected from the group consisting of perfumes, chelating or sequestering agents (like EDTA) , preservatives, bactericides, herbs (or herb extracts) , vitamins, buffering substances, moisturizers, emollients (such as esters of fatty acids
  • the viscosity of the cosmetic cleansing composition as measured with a rotation viscosimeter at 20°C using spindle No SV1 is from 6,500 to 15,000 mPas, preferably from 7,000 to 12,000 mPas.
  • the water-soluble capsule material is preferably gelatin, but other material like polyvinyl alcohol may be used.
  • the release time of the capsule may be controlled by the selection of the wall thickness of the capsule and the type of gelatin (different Bloom strength) .
  • the capsule may have a well thickness of 0.1 mm to 1 mm and a volume of for example 5 ml .
  • a cosmetic cleansing composition was prepared by mixing the following ingredients (in % by weight)
  • Citric acid 60 wt% aqueous solution
  • Citric acid 60 wt% aqueous solution
  • the lauric acid ester of ethyl glucoside contained 65.5% by weight of mono-ester, 14.8% by weight of di-ester, 19.1% by weight of tri-ester and 0.6% by weight of higher ester.
  • Polysorbate-20 (Trade Mark; ex. Atlas Chem.) is poly- oxyethylene (20) sorbitan monolaurate in which on an average 20 moles of ethylene oxide are present, having a HLB value of 16.7 and a viscosity at 25°C of 330 cSt (mm 2 S "1 ) .
  • Sheets of gelatin were made and passed through a capsule making machine in a manner known per se, producing capsules having a wall thickness of 0.2-0.7 mm and a volume of 5 ml, which were filled with the above prepared cosmetic cleansing composition.
  • Example 1 was repeated, now using the following formulations (ingredients in % by weight of the total composition) :
  • Polysorbate-20 (as in Example 1) 20 % 20 % Ethanol (96%) 1 % 4 % Perfume 0.10% 0.10%
  • gelatin capsules filled with the formulations as described in Example 1 upon use yielded a copiously foaming, mild to the skin cosmetic cleansing composition.

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Abstract

A cosmetic cleansing composition in a water-soluble capsule (preferably gelatin) comprises: (a) 30-85 wt.% (preferably 60-85 %) of C10-C22 fatty acid ester of C1-C4 alkylglycoside (preferably having at least 50 wt.% of mono-ester); (b) 10-20 wt.% alkali metal salt of C10-C20 alkyl sulphate; (c) 1-30 wt.% of an alkoxylated sorbitan C10-C22 fatty acid ester (preferably polyoxyethylene (20) sorbitan monolaurate); (d) 0-30 wt.% of C10-C22 fatty acid dialkylolamide (preferably coconut fatty acid diethanolamide) and at most 4 wt.% (preferably at most 3 wt.%) of water, the composition having a viscosity of 6,500-15,000, preferably 7,000-12,000 mPas (at 20 °C). Effective amounts of functional additives may also be present.

Description

COSMETIC CLEANSING COMPOSITIONS COMPRISING ESTERS OF ALKYLGLYCOSIDES
The present invention relates to a cosmetic cleansing composition in a water-soluble capsule.
Traditional cosmetic cleansing compositions, like hair and body shampoos, shower products and foam bath preparations are based on sodium alkyl sulphate, and even more on sodium alkyl ether sulphates. In order to stabilise and boost foam and also for reasons of skin mildness often coconut diethanolamide is added, but this leads to a rather uncontrolled increase in viscosity and it tends to darken the colour of the solutions. Sometimes betaines are used to further reduce skin irritation and to effect a viscosity synergism between the anionic sodium lauryl ether sulphate and the amphoteric oleyl betaine to yield very viscous (gel) products.
It has been proposed in United States Patent Specification US-A-3, 705, 102 (Armour-Dial Inc.) to provide a bath composition with a high-foaming detergent and an encapsulated combination of an emollient, a fatty polyoxyethylene material (HLB=10-12) and a methyl- polysiloxane defoaming agent. In use, the detergent provides copious foam and, after a delay in time, the encapsulated materials are released to simultaneously break the foam produced by the detergent and provide an emollient for the skin of the user. The disadvantage of this method is that the capsule may release its content too early and also that the emollient is not available throughout the entire cleansing process. The presence of such an emollient yields a sensation of mildness to the skin.
It is therefore proposed to encapsulate the entire cosmetic cleansing composition in a water-soluble capsule, which is preferably made of gelatin. The problem is here that most high-foaming detergents, like the alkali metal salts and the amine salts of the high-foaming alkyl sulphates - such as e.g. triethanolamine lauryl sulphate - always contain an appreciable amount of water. The presence of this relatively large amount of water leads to an undue softening and even rupture of the gelatin capsule, thus untimely releasing its contents.
Another problem is that during the manufacture of the capsules the cosmetic cleansing composition should have a relatively high viscosity, so as to enable its encapsulation, whereas upon use the composition after breakage of the capsule should quickly dissolve or disperse in the aqueous environment.
It has now been found that these problems can be solved by providing a cosmetic cleansing composition in a water- soluble capsule, preferably made of gelatin, which composition comprises an alkali metal salt of an alkyl sulphate, a fatty acid ester of an alkylglycoside having an alkyl group with from 1 to 4 carbon atoms and a sorbitan
(or anhydrohexitol) ester of a fatty acid alkoxylated with preferably ethylene oxide, and, optionally a fatty acid dialkylolamide.
It has been found that the viscosity of the product was dependent on the shear exerted upon it. For example 1 it was found that at very low shear (below to 10 sec"1) the viscosity of the product was 8,000 mPas; then with increasing shear (to 50 sec"1) the viscosity increased to 8,300 mPas and at constant shear of 50 sec"1 the viscosity increased further to 9,100 mPas. If the shear was then decreased, the viscosity further increased to 15,000 mPas. After some time, the viscosity started to decrease again. It may therefore be stated that the product is both shear thickening or dilatant and exhibits rheopexy. This rheological behaviour is of advantage during finishing and in using the product. During finishing of this type of products a relatively high viscosity is required (in the order of 8,000 to 12,000 mPas) . If the product after finishing is left to rest, its viscosity will decrease to its original value at low shear, so that upon use the product will easily dissolve or disperse in water.
Moreover it was surprising to note that the mildness to the skin of the final formulation was comparable to the mildness of the pure fatty acid ester of C1-C4 alkylglycoside, notwithstanding the still appreciable level of the alkali metal salt of alkyl sulphate, known to be a skin irritant.
Therefore, the present invention relates to a cosmetic cleansing composition in a water-soluble capsule, which composition comprises:
(a) from 30 to 85% by weight of an ester of an alkylglycoside having an alkyl group with from 1 to 4 carbon atoms and a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms;
(b) from 10 to 20% by weight of an alkali metal salt of an alkyl sulphate, having from 10 to 20 carbon atoms; (c) from 1 to 30% by weight of a sorbitan ester of a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms, alkoxylated with from 10 to 80 moles of a C1-C4 alkylene oxide; (d) from 0 to 30% by weight of a straight or branched chain, saturated or unsaturated C10-C22, fatty acid dialkylol amide, and (e) at most 4% by weight of water, said composition having a viscosity from 6500 to 15000 mPas. The fatty acid ester of the alkylglycoside having an alkyl group with from 1 to 4 carbon atoms preferably is a fatty acid ester of methyl glucoside, methyl fructoside, ethyl glycoside or ethyl fructoside. The fatty acid may be a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms. The use of lauric acid, palmitic acid, stearic acid and iso-stearic acid is preferred. Also fatty acid mixtures may be used, such as coconut fatty acids, palm kernel fatty acids and tallow fatty acids. The use of coconut fatty acids, of which the fatty acids up to and including octanoic acid have mainly been removed, is preferred.
Generally, the fatty acid esters of the alkylglycosides comprise mono-, di-, tri- and higher esters. The use of esters comprising at least 50% by weight, preferably at least 75% by weight, of mono esters is preferred. The esters may comprise up to 15% by weight of free fatty acids, but preferably the free fatty acid content is as low as possible, e.g.below 3% by weight. Generally from 30 to 85% by weight of alkylglycoside ester is used, preferably from 60% to 85% by weight, and most preferably from 70% to 80% by weight.
The alkali metal salt of the alkyl sulphate preferably is the sodium salt. The alkyl sulphate contains from 10 to 20 carbon atoms, such as dodecyl, lauryl, hexadecyl, myristyl and octadecyl sulphate. The use of lauryl sulphate is preferred. In general amine salts or alkanolamine salts are not used in view of the possibility of skin irritation. Generally from 10% to 20% by weight of the alkali metal salt of C10- C20 alkyl sulphate is used.
The alkoxylated sorbitan fatty acid esters are derived from sorbitan (or anhydrohexitol) . The fatty acids may be straight or branched chain, saturated or unsaturated fatty acids having from 10 to 22 carbon atoms, such as lauric acid, stearic acid, palmitic acid, oleic acid, iso-stearic acid and the like.
The sorbitan fatty acid esters have been alkoxylated with C1-C4 alkylene oxides, preferably ethylene oxide, or mixtures of such alkylene oxides. On an average from 10 to 80 moles of alkylene oxide per mole of sorbitan fatty acid ester are reacted. The use of polyoxyethylene (20) orbitan monolaurate is preferred.
The alkoxylated sorbitan fatty acid ester is used in an amount of from 1% to 30% by weight, preferably from 5% to 25% by weight of the total composition.
The fatty acid dialkylolamide is derived from a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms, such as lauric acid or coconut acids of which the fatty acids up to and including octanoic acid have mainly been removed. In the latter case the term "coconut fatty acid dialkylolamide" is used and these dialkylolamides are preferred. The hydroxyalkyl groups of the dialkylolamide have from 2 to 5 carbon atoms and these groups may the same or different and may be mono- or polyhydroxyalkyl. The use of coconut fatty acid diethanolamide is preferred. The fatty acid dialkylolamide is used in an amount of up to 30% by weight of the total composition, preferably from 15% to 25% by weight.
Since the presence of water up to a certain level may lead to undue rupture of the gelatin capsules, the amount of water in the cosmetic cleansing composition is at most 4% by weight and preferably at most 3% by weight.
The cosmetic cleansing compositions according to the present invention may also comprise an effective amount (in general up to 10% by weight, but greater amounts may be used) of a functional additive, selected from the group consisting of perfumes, chelating or sequestering agents (like EDTA) , preservatives, bactericides, herbs (or herb extracts) , vitamins, buffering substances, moisturizers, emollients (such as esters of fatty acids and/or fatty alcohols) , viscosity controlling agents (such as monohydric alcohols with 2 to 8 carbon atoms) , anti-oxidants, dyes, lather boosters (such as higher alkyl amine oxides) , and mixtures thereof .
The viscosity of the cosmetic cleansing composition as measured with a rotation viscosimeter at 20°C using spindle No SV1 is from 6,500 to 15,000 mPas, preferably from 7,000 to 12,000 mPas.
The water-soluble capsule material is preferably gelatin, but other material like polyvinyl alcohol may be used. The release time of the capsule may be controlled by the selection of the wall thickness of the capsule and the type of gelatin (different Bloom strength) . The capsule may have a well thickness of 0.1 mm to 1 mm and a volume of for example 5 ml .
It is known from Seifen-Oele-Fette- achse, Vol. 117, No. 4, 124-131 (1991) , particularly pages 128 and 129, that methyl glucoside laurate and methyl glucoside iso-stearate exhibit excellent thickening properties, when used in combination with an aqueous solution of 12% by weight of sodium lauryl ether sulphate. There is a marked difference, however, between sodium lauryl sulphate and sodium lauryl ether sulphate and no predictions can be made, that if a certain substance has a thickening effect on an aqueous sodium lauryl ether sulphate solution, it will have the same effect on almost water-free sodium lauryl sulphate. Moreover, it is clear from Figures 9 and 10 on page 129 that in the absence of salt there is apparently no thickening effect. The present invention therefore cannot be derived from this publication.
The invention will now be illustrated on hand of the following examples.
Example 1
A cosmetic cleansing composition was prepared by mixing the following ingredients (in % by weight)
Lauric acid ester of ethyl glucoside 67.0
%
Sodium Lauryl sulphate 12.0
% Polysorbate-20 10.0
%
Ethanol (96%) 5.0
%
Ethylene diamine tetra-acetic acid (40 wt% aqueous solution) 4.0
Water 0.6
%
Perfume 0.1 %
Emollient 0.55%
Citric acid (60 wt% aqueous solution) 0,75% 100.0
The lauric acid ester of ethyl glucoside contained 65.5% by weight of mono-ester, 14.8% by weight of di-ester, 19.1% by weight of tri-ester and 0.6% by weight of higher ester. Polysorbate-20 (Trade Mark; ex. Atlas Chem.) is poly- oxyethylene (20) sorbitan monolaurate in which on an average 20 moles of ethylene oxide are present, having a HLB value of 16.7 and a viscosity at 25°C of 330 cSt (mm2 S"1) .
After mixing a transparent liquid was obtained, which in a 1% by weight solution in water has a pH value of 5.7 and has a viscosity of 8,000 mPas (measured with rotation viscosimeter, using spindle no. SV 1 at 20°C) . It was an extremely mild to the skin, copiously foaming cosmetic cleansing composition.
Rheological behaviour: at shear below 10 sec"1 viscosity was 8000 mPas; at increasing shear (up to 50 sec"1) viscosity increased to 8,300 mPas. At constant shear (50 sec"1) for 3 minutes, viscosity increased to 9,100 mPas. At decrease of shear the viscosity increased to 15,000 mPas in 3 minutes.
Sheets of gelatin were made and passed through a capsule making machine in a manner known per se, producing capsules having a wall thickness of 0.2-0.7 mm and a volume of 5 ml, which were filled with the above prepared cosmetic cleansing composition.
Examples 2 and 3
Example 1 was repeated, now using the following formulations (ingredients in % by weight of the total composition) :
Example 2 Example 3
Lauric acid ester of ethyl glucoside (as in Example 1) 39 % 40 %
Lauric acid 4 % -
Sodium lauryl sulphate 12 % 12 Coconut fatty acid diethanolamide 20 % 20 o, o
Polysorbate-20 (as in Example 1) 20 % 20 % Ethanol (96%) 1 % 4 % Perfume 0.10% 0.10%
Emollient 0.55% 0.55%
Water 3,35%
3,35% 100.00%
100.00%
In both examples the gelatin capsules filled with the formulations as described in Example 1, upon use yielded a copiously foaming, mild to the skin cosmetic cleansing composition.

Claims

1. A cosmetic cleansing composition in a water-soluble capsule, said composition comprising:
(a) from 30 to 85% by weight of an ester of an alkylglycoside having an alkyl group with from 1 to 4 carbon atoms and a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms :
(b) from 10 to 20% by weight of an alkali metal salt of an alkyl sulphate having from 10 to 20 carbon atoms;
(c) from 1 to 30% by weight of a sorbitan ester of a straight or branched chain, saturated or unsaturated fatty acid having from 10 to 22 carbon atoms, alkoxylated with from 10 to 80 moles of a C1-C4 alkylene oxide;
(d) from 0 to 30% by weight of a straight or branched chain, saturated or unsaturated C10-C22, fatty acid dialkylol amide, and
(c) at most 4% by weight water, said composition having a viscosity from 6500 to
15,000 mPas.
2. A cosmetic cleansing composition according to claim 1, in which (a) is a C10-C22 fatty acid ester of an alkylglucoside having an alkyl group with 1 or 2 carbon atoms.
3. A cosmetic cleansing composition according to claim 1, in which (a) comprises at least 50% by weight of mono- ester.
4. A cosmetic cleansing composition according to Claim 1. in which (a) comprises at least 75% to weight of mono- ester.
5. A cosmetic cleansing composition, according to Claim 1, in which (a) comprises at most 3% by weight of free fatty acids .
6. A cosmetic cleansing composition according to claim 1, in which in (a) the fatty acid is selected from the group consisting of lauric acid, palmitic acid, stearic acid, iso-stearic acid and coconut fatty acids of which the fatty acids up to and including octanoic acid have been removed.
7. A cosmetic cleansing composition according to Claim 1, in which from 60% to 85% by weight of the total composition of (a) is used.
8. A cosmetic cleansing composition according to claim 1, in which (b) is sodium lauryl sulphate.
9. A cosmetic cleansing composition according to Claim 1, in which in (b) the alkylene oxide is ethylene oxide.
10. A cosmetic cleansing composition according to Claim 1, in which (b) is polyoxyethylene (20) sorbitan monolaurate.
11. A cosmetic cleansing composition according to Claim 1, comprising from 5% to 25% by weight of the total composition of (b) .
12. A cosmetic cleansing composition according to Claim 1, in which (d) is coconut fatty acid diethanolamide.
13. A cosmetic cleansing composition according to Claim, comprising from 15% to 25% by weight of the total composition of (d) .
14. A cosmetic cleansing composition according to claim 1, which comprises at most 3% by weight of water.
15. A cosmetic cleansing composition according to claim 1, which comprises up to 10% by weight of the total composition of a functional additive selected from the group consisting of perfumes, chelating agents, preservatives, bactericides, herbs, vitamins, buffering substances, moisturizers, emollients, viscosity controlling agents, antioxidants, dyes, lather boosters, and mixtures thereof.
16. A cosmetic cleansing composition according to claim 1, having a viscosity of 6,500 to 15,000 mPas (at 20°C) .
17. A cosmetic cleansing composition according to Claim 1, having a viscosity of 7,000 to 12,000 mPas (at 20°C) .
18. A cosmetic cleansing composition according to claim 1, in which the capsule material is gelatin.
19. A foam bath preparation comprising a cosmetic cleansing composition according to Claims 1 - 18.
PCT/EP1996/000541 1995-02-07 1996-02-05 Cosmetic cleansing compositions comprising esters of alkylglycosides WO1996024328A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP8524001A JPH10513189A (en) 1995-02-07 1996-02-05 Cosmetic cleaning composition containing alkyl glycoside ester
BR9607118A BR9607118A (en) 1995-02-07 1996-02-05 Cosmetic composition for cleaning a water-soluble capsule and preparation for bubble bath
EP96904035A EP0808152A1 (en) 1995-02-07 1996-02-05 Cosmetic cleansing compositions comprising esters of alkylglycosides
AU47892/96A AU4789296A (en) 1995-02-07 1996-02-05 Cosmetic cleansing compositions comprising esters of alkylglycosides

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP95200301 1995-02-07
EP95200301.0 1995-02-07

Publications (1)

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WO1996024328A1 true WO1996024328A1 (en) 1996-08-15

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Country Status (7)

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EP (1) EP0808152A1 (en)
JP (1) JPH10513189A (en)
KR (1) KR19980701954A (en)
CN (1) CN1173814A (en)
AU (1) AU4789296A (en)
BR (1) BR9607118A (en)
WO (1) WO1996024328A1 (en)

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EP0879874A2 (en) * 1997-05-23 1998-11-25 Henkel Kommanditgesellschaft auf Aktien Encapsulated detergent
WO2001085895A1 (en) * 2000-05-12 2001-11-15 Unilever N.V. Unit dose cleaning product
DE10032118C2 (en) * 2000-07-01 2003-03-27 Wella Ag Antithixotropic cosmetic
JP2007023296A (en) * 1998-06-23 2007-02-01 Union Carbide Chem & Plast Technol Corp Liquid thickener for surfactant system
US7648951B2 (en) 2000-11-27 2010-01-19 The Procter & Gamble Company Dishwashing method
US8156713B2 (en) 2000-11-27 2012-04-17 The Procter & Gamble Company Detergent products, methods and manufacture
US8283300B2 (en) 2000-11-27 2012-10-09 The Procter & Gamble Company Detergent products, methods and manufacture
US8741321B2 (en) 2003-08-27 2014-06-03 Beiersdorf Ag Capsule whose envelope is separately imperceptible during the topical use thereof
US8940676B2 (en) 2000-11-27 2015-01-27 The Procter & Gamble Company Detergent products, methods and manufacture
US9055745B2 (en) 2011-04-13 2015-06-16 Natureza, Inc. Compositions for internal and external insecticides, ovicides, repellents and wound healing
US11717473B2 (en) 2019-11-25 2023-08-08 Kao Corporation Skin cleansing agent containing a particle comprised of an ester, moisturizing agent, and polymer

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KR102059398B1 (en) * 2012-06-15 2019-12-26 루브리졸 어드밴스드 머티어리얼스, 인코포레이티드 Alkyl glycoside-based micellar thickeners for surfactant systems

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Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0879874A2 (en) * 1997-05-23 1998-11-25 Henkel Kommanditgesellschaft auf Aktien Encapsulated detergent
EP0879874A3 (en) * 1997-05-23 1999-06-16 Henkel Kommanditgesellschaft auf Aktien Encapsulated detergent
JP2007023296A (en) * 1998-06-23 2007-02-01 Union Carbide Chem & Plast Technol Corp Liquid thickener for surfactant system
JP2007023055A (en) * 1998-06-23 2007-02-01 Union Carbide Chem & Plast Technol Corp Liquid thickener for surfactant system
WO2001085895A1 (en) * 2000-05-12 2001-11-15 Unilever N.V. Unit dose cleaning product
DE10032118C2 (en) * 2000-07-01 2003-03-27 Wella Ag Antithixotropic cosmetic
DE10032118B9 (en) * 2000-07-01 2006-12-07 Wella Ag Antithixotropic cosmetic agent
US8435935B2 (en) 2000-11-27 2013-05-07 The Procter & Gamble Company Detergent products, methods and manufacture
US8940676B2 (en) 2000-11-27 2015-01-27 The Procter & Gamble Company Detergent products, methods and manufacture
US8250837B2 (en) 2000-11-27 2012-08-28 The Procter & Gamble Company Detergent products, methods and manufacture
US8283300B2 (en) 2000-11-27 2012-10-09 The Procter & Gamble Company Detergent products, methods and manufacture
US8357647B2 (en) 2000-11-27 2013-01-22 The Procter & Gamble Company Dishwashing method
US7648951B2 (en) 2000-11-27 2010-01-19 The Procter & Gamble Company Dishwashing method
US8518866B2 (en) 2000-11-27 2013-08-27 The Procter & Gamble Company Detergent products, methods and manufacture
US8658585B2 (en) 2000-11-27 2014-02-25 Tanguy Marie Louise Alexandre Catlin Detergent products, methods and manufacture
US10889786B2 (en) 2000-11-27 2021-01-12 The Procter & Gamble Company Detergent products, methods and manufacture
US8156713B2 (en) 2000-11-27 2012-04-17 The Procter & Gamble Company Detergent products, methods and manufacture
US10081786B2 (en) 2000-11-27 2018-09-25 The Procter & Gamble Company Detergent products, methods and manufacture
US9382506B2 (en) 2000-11-27 2016-07-05 The Procter & Gamble Company Detergent products, methods and manufacture
US9434916B2 (en) 2000-11-27 2016-09-06 The Procter & Gamble Company Detergent products, methods and manufacture
US8741321B2 (en) 2003-08-27 2014-06-03 Beiersdorf Ag Capsule whose envelope is separately imperceptible during the topical use thereof
US9538748B2 (en) 2011-04-13 2017-01-10 Natureza, Inc. Compositions for internal and external use as an insecticide, ovicide, repellent and for wound healing
US9055745B2 (en) 2011-04-13 2015-06-16 Natureza, Inc. Compositions for internal and external insecticides, ovicides, repellents and wound healing
US11717473B2 (en) 2019-11-25 2023-08-08 Kao Corporation Skin cleansing agent containing a particle comprised of an ester, moisturizing agent, and polymer

Also Published As

Publication number Publication date
EP0808152A1 (en) 1997-11-26
BR9607118A (en) 1997-11-04
AU4789296A (en) 1996-08-27
KR19980701954A (en) 1998-06-25
CN1173814A (en) 1998-02-18
JPH10513189A (en) 1998-12-15

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