WO1996021424A2 - Mild cold pearlizing concentrates - Google Patents

Mild cold pearlizing concentrates Download PDF

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Publication number
WO1996021424A2
WO1996021424A2 PCT/IB1996/000406 IB9600406W WO9621424A2 WO 1996021424 A2 WO1996021424 A2 WO 1996021424A2 IB 9600406 W IB9600406 W IB 9600406W WO 9621424 A2 WO9621424 A2 WO 9621424A2
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WO
WIPO (PCT)
Prior art keywords
betaine
mild
ultra
surfactant
concentrate
Prior art date
Application number
PCT/IB1996/000406
Other languages
French (fr)
Other versions
WO1996021424A3 (en
Inventor
Pu Chen
Joseph Niu
Siew Fang Yoong
Original Assignee
Rhone-Poulenc Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Rhone-Poulenc Inc. filed Critical Rhone-Poulenc Inc.
Priority to AU53453/96A priority Critical patent/AU706141B2/en
Priority to JP8521543A priority patent/JPH11503109A/en
Publication of WO1996021424A2 publication Critical patent/WO1996021424A2/en
Publication of WO1996021424A3 publication Critical patent/WO1996021424A3/en

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Classifications

    • 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
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/442Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof substituted by amido group(s)
    • 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
    • A61K8/39Derivatives containing from 2 to 10 oxyalkylene groups
    • 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
    • A61K8/466Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
    • 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
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • 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
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0089Pearlescent compositions; Opacifying agents
    • 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 generally to hair and skin compositions such as soaps and shampoos for washing the skin and conditioning the hair. More particularly, the present invention relates to ultra-mild cold pearlescent concentrates used in said soaps and shampoos which impart an iridescent sheen or glow to these compositions.
  • Hair conditioning shampoos and cosmetic soaps are well known in the art and have been described extensively in both the patent and non-patent journal literature.
  • Cationic surfactants such as quaternary ammonium salts and anionic surfactants such as fatty alcohol sulfates and alkyl benzene sulfonates have been employed in hair rinses, soaps and shampoos as conditioning agents together with other water insoluble conditioning compounds such as silicones, waxes, grease and oils.
  • Shampoos and soaps have always been produced in a variety of different forms such as solid bars, gels, creams and liquids.
  • Pearlescent shampoos are comprised of a number of ingredients such as stabilizing agents, pearlescent agents, conditioners, emulsifiers and hydrating agents. Pearlescent agents produce a shiny glow-like look to the compositions by the incorporation of substances which, after cooling, precipitate in the form of fine crystals resembling mother of pearl and which remain dispersed in the preparation.
  • Known pearlizing agents include the mono- and diesters of glycol and glycerol with C 16 -C 22 fatty acids.
  • most pearlescent agents of the prior art if used by themselves, have to be heated above their melting points for incorporation into a final formulation. The heating step and the conditions after the heating, e.g., the mixing, storage and/or cooling stages are difficult to control and thus the pearlescence condition is ofttimes not optimized, i.e., less than ideal.
  • Cold pearlescent concentrates i.e., those that can be subsequently formulated at room temperature, are known to offer a more consistent final pearlescent product.
  • the room temperature blending not only saves energy, but also eliminates many inconsistencies that occur with high temperature mixing.
  • Cocodiethanolamide has been used to prepare these cold pearlescent concentrates since it is liquid at room temperature and thus does not require a melting step to prepare the formulations; however, studies have raised concern that the diethanolamine, often present as a by ⁇ product of the cocodiethanolamide production, may form potentially carcinogenic nitrosamines . Thus, the use of cocodiethanolamide in pearlescent personal hair care and skin products such as cosmetics, facial soaps and shampoos has been questioned from a health standpoint.
  • alkyl sulfates and ethoxylated alkyl sulfates such as sodium laureth (3E0) sulfate, which also 5. can be used in cold pearlescent concentrates, have been found to cause skin irritation.
  • United States Patent Nos. 5,290,480 and 5,290,482 to 5 Marschner et. al. disclose surfactant compositions comprising betaine/cocoamide complexes for use in shampoo and skin cleansing products.
  • the complexes are combined with a cationic, nonionic, amphoteric or anionic surfactant to provide improved lather and conditioning 0 characteristics.
  • Cocodiethanolamide is widely used in these shampoo compositions. See U.S. Patent No. 4,535,877 to Russell et. al. Cocoamidopropyl betaine is also a common shampoo ingredient often used as a conditioner or foam enhancer to increase the richness of the lather. See 5 U.S. Patent No. 4,490,355 to Desai.
  • United States Patent No. 5,217,711 to DeOliveira et. al. disclose a hair treatment system consisting of a shampoo comprising, among other things, a pearlizing agent consisting of glycol distearate and a cocodiethanolamide.
  • U.S. Patent No. 5,019,376 to Vick teaches pearlescent 5.
  • U.S. Patent No. 4,959,206 to Noguera et. al. teaches distearate of ethylene glycol and laurylsulfosuccinate as pearlescent agents but again, cocodiethanolamide is a necessary 0 pearlescent stabilizer.
  • United States Patent No. 4,938,953 to Pena discloses conditioning shampoos comprised of a fatty acid sulfate or a fatty alcohol ether sulfate, cocoamidopropyl betaine and cocoamidodiethanolamine. This composition also utilizes 5 sodium lauryl sulfate as a stabilizing agent.
  • U.S. Patent No. 5,271,930 to Walele et. al. discloses the use of novel benzoic acid esters of polyalkoxylated block co-polymers as pearlescent agents in hair and skin care compositions.
  • Pearlizing agents conventionally can contain ethylene 0 glycol monostearate, ethylene glycol distearate, guanine bismuth oxychloride on mica and mixtures thereof.
  • U.S. Patent No. 4,654,207 to Preston teaches a pearlescent shampoo wherein the pearlescing agent is a fatty acid ester, such as myristyl myristate or cetyl myristate, which 5 is added to the shampoo base from a substantially anhydrous solubilizing agent such as a surfactant.
  • a fatty acid ester such as myristyl myristate or cetyl myristate
  • a number of other prior art patents such as U.S. Patent No. 4,608,392 to Jaquet et. al. describe the use of fatty alcohols and fatty acid quaternary ammonium compounds in the pearlescent blends.
  • U.S. Patent No. 5,019,376 to Vick et. al. also 5. teaches the use of a quaternary ammonium compounds such as stearyl dimethyl benzyl ammonium chloride together with a C 12 -C 16 fatty acid and cetyl alcohol.
  • U.S. Patent No. 5,213,792 to Grundemen discloses hair conditioning compositions containing a pearlescent agent 0 comprised of glycerin, a monolauric acid ester, a C 10 -C 18 fatty alcohol, a quaternary ammonium compound, water and any one of a number of dyes, antioxidants and the like. All of these compositions also use cocodiethanolamide in one form or another for pearlescence or some other related 5 function.
  • U.S. Patent No. 4,777,038 to Scheuffgen discloses a free flowing pearlescent concentrate which allegedly remains stable without the sedimentation of the pearlescent crystals during storage.
  • the composition is comprised of 0 at least one mono- and diester of ethylene glycol or propylene glycol, a fatty acid mono-ethanolamine, ethylene glycol distearate, coconut oil and fatty alcohol.
  • the sheen is provided by the appearance of fine, pearlescent crystals.
  • a free flowing pearlescent concentrate comprising a C 12 -C 18 coconut oil fatty acid monoethanolamide, a C 16 -C 22 fatty alkyl ester, and at least one ethylene or propylene glycol ester or diester.
  • These pearlescent agents act as emulsifier ⁇ which provide free flowing 5.
  • dispersions that allegedly combine high brilliance and stability with other cationic surfactant components.
  • U.S. Patent No. 5,198,209 to Zhou et. al. discloses a conditioning shampoo comprising a mixture of anionic, cationic and nonionic surfactants and suggests the use of 0 ethylene glycol stearate among others as a pearlescent agent.
  • U.S. Patent No. 5,252,325 to Bires e . al. teaches polyvinyl-pyrrolidone stabilized silicone shampoos together with a cationic surfactant and ethylene glycol distearate as a suggested pearlescent agent.
  • the present invention is a novel ultra-mild cold pearlescent concentrate for use in shampoo, lipstick, skin 5 creams, lotions and the like.
  • the pearlizing concentrate is a unique formulation of ingredients comprised of an emulsifier, a zwitterionic surfactant, a nonionic alcohol ethoxylate, and an isethionate or N-methyl taurate which, when processed with other surfactants under conditions well 0 known in the art, impart a brilliant sheen when incorporated into shampoo and soap products.
  • a stable, ultra-mild free flowing cold pearlescent concentrate is prepared using i) a suspending agent 5 emulsifier, preferably a glycol stearate; ii) a zwitterionic surfactant co-emulsifier; iii) a nonionic alcohol ethoxylate; and iv) an isethionate or an N-methyl t aura t e to obviate the use of cocodiethanolamide and the alkyl sulfates and ethoxylated alkyl sulfates.
  • a suspending agent 5 emulsifier preferably a glycol stearate
  • ii) a zwitterionic surfactant co-emulsifier iii) a nonionic alcohol ethoxylate
  • an isethionate or an N-methyl t aura t e to obviate the use of cocodiethanolamide and the alkyl sulfates and ethoxy
  • the emulsifier comprises from about 15 to about 25
  • the emulsifier is preferably selected from the group consisting of hydroxy stearate, polyethylene glycol mono- and distearates, ethylene glycol mono- and 0 distearates, stearic monoethanolamide, stearic monoe th anolamide stearate and mixtures thereof.
  • the most preferred emulsifier is ethylene glycol monostearate
  • a second component of the pearlizing concentrate is a 5 nonionic surfactant.
  • This surfactant which functions as an emulsion stabilizer in the formulation, is preferably an alcohol ethoxylate, of the formula
  • the most preferred nonionic is a lauryl alcohol ethoxylate such as Rhodasurf ® LA-7, a C 12 alkyl ( 7 E O ) ethoxylated alcohol sold by Rhone-Poulenc Inc.
  • the nonionic surfactant is incorporated in the cold pearlizing concentrate in an amount of from approximately
  • a zwitterionic surfactant comprises the fourth component of the present 5.
  • Zwitterionic surfactants are those in which the positive and negative groups are equally ionized.
  • zwitterionic surfactants known as the betaines and their derivatives are incorporated to provide an enhanced pearlizing effect.
  • Betaines and amidobetaines are compounds of the general structures :
  • R 2 is C 8 - C 22 alkyl or alkenyl
  • R « is H or C ⁇ - C- « alkyl.
  • the more preferred betaines useful herein include the
  • 20 high alkyl betaines such as cocodimethyl carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl alpha-carboxy-ethyl betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis- (2-hydroxy-ethyl) carboxy methyl betaine, stearyl bis- (2-hydroxy-propyl) carboxymethyl
  • the sulfobetaines are also preferred and may be represented by cocodimethyl sulfopropyl betaine, stearyldimethyl sulfopropyl betaine, lauryl dimethyl sulfoethyl betaine, and lauryl bis- (2-hydroxy-ethyl) sulfopropyl betaine.
  • a particularly preferred composition utilizes cocoamidopropyl betaine.
  • the zwitterionic can be present from 5. approximately 1.0 weight percent to about 10 weight percent based on the total weight of the pearlizing concentrate.
  • the zwitterionic will comprise from about 2.0 to about 7.0 weight percent of the composition and most preferably from about 3.0 to about 5.0 weight percent of 0 the pearlizing concentrate.
  • an isethionate or N-methyl taurate is utilized in the concentrates of this invention.
  • the isethionates are of the formula: 5 0
  • R,. is a fatty alkyl group and M is a counterion selected from the group consisting of sodium, calcium, magnesium, ammonium and triethanolamine, some of which are 0 commercially available as the Geropon ® AS series (Rhone- Poulenc Inc.) .
  • the preferred isethionate is sodium cocoyl isethionate.
  • N-methyl taurates are of the formula: 0 CH 3
  • the preferred N-methyl taurate is sodium cocoyl N-methyl taurate.
  • the isethionates and/or taurates of this invention may be any one of the isethionates and/or taurates of this invention.
  • the pearlizing concentrates 5. be incorporated into the pearlizing concentrates at from about 5.0 to about 25 weight percent, preferably about 8 to about 20 weight percent based on the total weight of the concentrate.
  • Water preferably deionized, is then added in an amount from about 20 weight percent to about 78 weight 5 percent, preferably from about 41 to about 67 weight percent based on the total weight of the concentrate.
  • the formulated shampoo and soap systems utilizing the cold pearlizing concentrate of the present invention can contain a variety of non-essential optional components 0 suitable for rendering such compositions more acceptable.
  • non-essential optional components are well known to those skilled in the art, e.g., preservatives such as benzyl alcohol, methyl paraben, propyl paraben and imidazolidinyl urea; cationic surfactants such as cetyl 5 trimethyl ammonium chloride, lauryl trimethyl ammonium chloride, tricetyl methyl ammonium chloride, stearyldimethyl benzyl ammonium chloride, and di (partially hydrogenated tallow) dimethylammonium chloride; thickeners and viscosity modifiers such as block polymers of ethylene oxide and propylene oxide, e.g.
  • Antarox F-88 (Rhone-Poulenc 5. Inc.) , sodium chloride, sodium sulfate, polyvinyl alcohol, and ethyl alcohol; pH adjusting agents such as citric acid, succinic acid, phosphoric acid, sodium hydroxide, sodium carbonate; perfumes; dyes; and sequestering agents such as disodium ethylenediamine tetra-acetate.
  • Such agents 0 generally are used individually at levels of from about 0.01% to about 10%, preferably from 0.5% to about 5.0% by weight of the composition.
  • the pH of the present compositions is not critical and may be in the range of from about 5 to about 9.
  • the pH can 5 be adjusted using a buffer such as citric acid.
  • the order of addition to the mixing tank of the individual components of the concentrate is not critical nor is the reasonably elevated temperature; however, preferably the water, emulsifier and isethionate or N- 0 methyl taurate surfactant are intimately blended at from about 60" to 80"C, more preferably from about 70 * to 75 * C with high agitation until the emulsifier is solubilized.
  • the nonionic surfactant and zwitterionic are then blended into the mix.
  • the concentrate is then stored at a 5 temperature of from about 35 * C to about 60 * C, preferably from about 45°C to about 55°C for at least one day and preferably two (2) days in order to fully develop its pearlescent characteristics.
  • the shampoos and soaps of the present invention can be made by merely mixing the materials together with the 5. concentrate at room temperature.
  • the ultra-mild cold pearlizing concentrate of the present invention may be specifically formulated into a number of different blended soap products.
  • the pearlizing concentrate not only imparts a high luster pearlescence and 0 sheen to the products, but also contributes emollient and moisturizing qualities to the skin. It provides superior shampoo, bath and shower soap systems and markedly improves wet comb-out of the hair.
  • compositions of the present invention are for illustrative purposes only, and it is realized that minor changes and variations may be made with respect to these compositions that are not shown below. Such changes that do not materially alter the compositions formulation 0 or function are still considered to fall within the spirit and scope of the invention as recited by the claims that follow.
  • Example I The following components and their respective amounts in a weight percent of the total basis are assembled.
  • Cocoamidopropyl betaine 5.
  • the ethylene glycol monostearate is mixed with water and the sodium cocoyl N-methyl taurate or the sodium cocoyl isethionate at 70 * to 75°C with high speed agitation.
  • the lauryl (7E0) alcohol and the cocoamidopropyl betaine are added into the mixture with stirring and kept at 50°C for one to two days in order to develop the pearlescence fully. The maintenance of the emulsion at this temperature for 5. this period of time is important for the full development of the pearlescence.
  • the pearlescence concentrate produced is an iridescent or shiny white to off-white viscous liquid with a pH of from about 6.5-7.5 and realizes excellent dispersibility in 0 water.
  • compositions of this invention require no heating for blending and are readily compatible with most anionic-based liquid hand 5 cleaner, shampoo, bubble bath and cosmetic systems to form attractive high-performance very mild products.
  • Example II The following ingredients and their respective amounts are combined to produce a pearlescent liquid hand soap.
  • the 0 amounts given are weight percent based on the total weight.
  • Example III The following ingredients and their respective amounts are combined to produce an ultra-mild pearlescent body 0 shampoo. The amounts given are in weight percent based on the total weight.
  • Example II The ingredients are easily blended as in Example II. These pearlescent specialty bath and shower formulations contribute to a luxurious, smooth feel and they help to 0 keep the skin soft and supple.
  • Example IV A body shampoo is prepared as in Example III with the use of Formulation C concentrate in lieu of Formulation B. 35 As in Example II, the pearlescent liquid products are prepared easily at room temperature and the Formulation C concentrate provides enhanced viscosity building, foam stability and lather enrichment properties; all combined in an extremely mild formulation.

Abstract

Novel ultra-mild cold pearlizing concentrates provide pearlescent personal hair and skin compositions such as shampoos and beauty soaps with added luster and sheen.

Description

96/21424 PCMB96/00406
Mild Cold Pearlizinα Concentrates
Field of Invention
The present invention relates generally to hair and skin compositions such as soaps and shampoos for washing the skin and conditioning the hair. More particularly, the present invention relates to ultra-mild cold pearlescent concentrates used in said soaps and shampoos which impart an iridescent sheen or glow to these compositions.
Background of the Invention Hair conditioning shampoos and cosmetic soaps are well known in the art and have been described extensively in both the patent and non-patent journal literature. Cationic surfactants such as quaternary ammonium salts and anionic surfactants such as fatty alcohol sulfates and alkyl benzene sulfonates have been employed in hair rinses, soaps and shampoos as conditioning agents together with other water insoluble conditioning compounds such as silicones, waxes, grease and oils. Shampoos and soaps have always been produced in a variety of different forms such as solid bars, gels, creams and liquids.
Pearlescent shampoos are comprised of a number of ingredients such as stabilizing agents, pearlescent agents, conditioners, emulsifiers and hydrating agents. Pearlescent agents produce a shiny glow-like look to the compositions by the incorporation of substances which, after cooling, precipitate in the form of fine crystals resembling mother of pearl and which remain dispersed in the preparation. Known pearlizing agents include the mono- and diesters of glycol and glycerol with C16-C22 fatty acids. However, most pearlescent agents of the prior art, if used by themselves, have to be heated above their melting points for incorporation into a final formulation. The heating step and the conditions after the heating, e.g., the mixing, storage and/or cooling stages are difficult to control and thus the pearlescence condition is ofttimes not optimized, i.e., less than ideal.
"Cold pearlescent concentrates" i.e., those that can be subsequently formulated at room temperature, are known to offer a more consistent final pearlescent product.
The room temperature blending not only saves energy, but also eliminates many inconsistencies that occur with high temperature mixing.
Cocodiethanolamide has been used to prepare these cold pearlescent concentrates since it is liquid at room temperature and thus does not require a melting step to prepare the formulations; however, studies have raised concern that the diethanolamine, often present as a by¬ product of the cocodiethanolamide production, may form potentially carcinogenic nitrosamines . Thus, the use of cocodiethanolamide in pearlescent personal hair care and skin products such as cosmetics, facial soaps and shampoos has been questioned from a health standpoint.
Furthermore, alkyl sulfates and ethoxylated alkyl sulfates such as sodium laureth (3E0) sulfate, which also 5. can be used in cold pearlescent concentrates, have been found to cause skin irritation.
It would certainly be advantageous then, to have a safe pearlescent agent for use in shampoo, lipstick and personal skin care products without the presence of 1) the 0 cocodiethanolamide as a component of the formulation if the health concerns have any basis whatsoever and 2) the irritation producing alkyl sulfates and ethoxylated alkyl sulfates.
United States Patent Nos. 5,290,480 and 5,290,482 to 5 Marschner et. al. disclose surfactant compositions comprising betaine/cocoamide complexes for use in shampoo and skin cleansing products. The complexes are combined with a cationic, nonionic, amphoteric or anionic surfactant to provide improved lather and conditioning 0 characteristics. Cocodiethanolamide is widely used in these shampoo compositions. See U.S. Patent No. 4,535,877 to Russell et. al. Cocoamidopropyl betaine is also a common shampoo ingredient often used as a conditioner or foam enhancer to increase the richness of the lather. See 5 U.S. Patent No. 4,490,355 to Desai.
United States Patent No. 5,217,711 to DeOliveira et. al. disclose a hair treatment system consisting of a shampoo comprising, among other things, a pearlizing agent consisting of glycol distearate and a cocodiethanolamide. U.S. Patent No. 5,019,376 to Vick teaches pearlescent 5. "crystals" in -a shampoo formulation formed by the reaction between a fatty acid and a fatty monoalcohol. U.S. Patent No. 4,959,206 to Noguera et. al. teaches distearate of ethylene glycol and laurylsulfosuccinate as pearlescent agents but again, cocodiethanolamide is a necessary 0 pearlescent stabilizer.
United States Patent No. 4,938,953 to Pena discloses conditioning shampoos comprised of a fatty acid sulfate or a fatty alcohol ether sulfate, cocoamidopropyl betaine and cocoamidodiethanolamine. This composition also utilizes 5 sodium lauryl sulfate as a stabilizing agent. U.S. Patent No. 5,271,930 to Walele et. al. discloses the use of novel benzoic acid esters of polyalkoxylated block co-polymers as pearlescent agents in hair and skin care compositions.
Pearlizing agents conventionally can contain ethylene 0 glycol monostearate, ethylene glycol distearate, guanine bismuth oxychloride on mica and mixtures thereof. U.S. Patent No. 4,654,207 to Preston teaches a pearlescent shampoo wherein the pearlescing agent is a fatty acid ester, such as myristyl myristate or cetyl myristate, which 5 is added to the shampoo base from a substantially anhydrous solubilizing agent such as a surfactant. A number of other prior art patents such as U.S. Patent No. 4,608,392 to Jaquet et. al. describe the use of fatty alcohols and fatty acid quaternary ammonium compounds in the pearlescent blends. U.S. Patent No. 5,019,376 to Vick et. al. also 5. teaches the use of a quaternary ammonium compounds such as stearyl dimethyl benzyl ammonium chloride together with a C12-C16 fatty acid and cetyl alcohol.
U.S. Patent No. 5,213,792 to Grundemen discloses hair conditioning compositions containing a pearlescent agent 0 comprised of glycerin, a monolauric acid ester, a C10-C18 fatty alcohol, a quaternary ammonium compound, water and any one of a number of dyes, antioxidants and the like. All of these compositions also use cocodiethanolamide in one form or another for pearlescence or some other related 5 function.
U.S. Patent No. 4,777,038 to Scheuffgen discloses a free flowing pearlescent concentrate which allegedly remains stable without the sedimentation of the pearlescent crystals during storage. The composition is comprised of 0 at least one mono- and diester of ethylene glycol or propylene glycol, a fatty acid mono-ethanolamine, ethylene glycol distearate, coconut oil and fatty alcohol. The sheen is provided by the appearance of fine, pearlescent crystals. United States Patent Nos. 4,824,594, 4,948,528 5 and 5,017,305 to Hoeffkes et. al. all disclose and claim variations of a free flowing pearlescent concentrate comprising a C12-C18 coconut oil fatty acid monoethanolamide, a C16-C22 fatty alkyl ester, and at least one ethylene or propylene glycol ester or diester. These pearlescent agents act as emulsifierε which provide free flowing 5. dispersions that allegedly combine high brilliance and stability with other cationic surfactant components.
U.S. Patent No. 5,198,209 to Zhou et. al. discloses a conditioning shampoo comprising a mixture of anionic, cationic and nonionic surfactants and suggests the use of 0 ethylene glycol stearate among others as a pearlescent agent. U.S. Patent No. 5,252,325 to Bires e . al. teaches polyvinyl-pyrrolidone stabilized silicone shampoos together with a cationic surfactant and ethylene glycol distearate as a suggested pearlescent agent. 5 Whereas the aforementioned cold pearlescent compositions allegedly provide effective cleaning and luster-producing functionalities, all the formulations continue to use cocodiethanolamide or a derivative and/or sodium laureth sulfate as stabilizing agents for 0 pearlescence or some other related function.
It is an object of the present invention to prepare a novel ultra-mild cold pearlescent concentrate for use in shampoos, skin creams, lipstick, hair colors and the like. More particularly, it is an object of the present invention 5 to prepare a cold pearlescent composition that does not require the presence of the cocodiethanolamide with the potential health problem associated with the nitrosamines possibly formed by its diethanolamine by-product; or the skin irritants, i.e. the sodium lauryl or laureth sulfates. These ingredients are removed altogether from the 5. compositions of the present invention which continue to provide shampoo, lipstick and other skin care products with excellent pearlescent effects and cleansing properties. These pearlescent concentrates also may be prepared without the need for the application of high temperatures often 0 required for blending during the final formulation processes of the prior art.
Summary of the Invention The present invention is a novel ultra-mild cold pearlescent concentrate for use in shampoo, lipstick, skin 5 creams, lotions and the like. The pearlizing concentrate is a unique formulation of ingredients comprised of an emulsifier, a zwitterionic surfactant, a nonionic alcohol ethoxylate, and an isethionate or N-methyl taurate which, when processed with other surfactants under conditions well 0 known in the art, impart a brilliant sheen when incorporated into shampoo and soap products.
Detailed Description of the Invention A stable, ultra-mild free flowing cold pearlescent concentrate is prepared using i) a suspending agent 5 emulsifier, preferably a glycol stearate; ii) a zwitterionic surfactant co-emulsifier; iii) a nonionic alcohol ethoxylate; and iv) an isethionate or an N-methyl taurate to obviate the use of cocodiethanolamide and the alkyl sulfates and ethoxylated alkyl sulfates.
The emulsifier comprises from about 15 to about 25
5. weight percent of the present concentrate, and preferably from about 18 to 22% based on the total weight of the concentrate. The emulsifier is preferably selected from the group consisting of hydroxy stearate, polyethylene glycol mono- and distearates, ethylene glycol mono- and 0 distearates, stearic monoethanolamide, stearic monoethanolamide stearate and mixtures thereof. The most preferred emulsifier is ethylene glycol monostearate
(C17H35COO(CH2)2OH) .
A second component of the pearlizing concentrate is a 5 nonionic surfactant. This surfactant, which functions as an emulsion stabilizer in the formulation, is preferably an alcohol ethoxylate, of the formula
R-O- (CH2CH20)n H wherein R is a C9-C22 alkyl, preferably C10-C18; and n is 1-40, 0 preferably 3-20. The most preferred nonionic is a lauryl alcohol ethoxylate such as Rhodasurf® LA-7, a C12 alkyl (7EO) ethoxylated alcohol sold by Rhone-Poulenc Inc.
The nonionic surfactant is incorporated in the cold pearlizing concentrate in an amount of from approximately
25 1.0 weight percent to about 20.0 weight percent; preferably in an amount of from about 5.0 to about 10.0 weight percent; and most preferably about 7 to 10 weight percent based on the total weight of the concentrate.
In place of the cocodiethanolamides, a zwitterionic surfactant comprises the fourth component of the present 5. invention. Zwitterionic surfactants are those in which the positive and negative groups are equally ionized. Preferably, zwitterionic surfactants known as the betaines and their derivatives are incorporated to provide an enhanced pearlizing effect. 10 Betaines and amidobetaines are compounds of the general structures :
CH3 CH3
I I
R2-N*-CR3R,-C07 and R2-CO-NH(CH2) 3 - N*-CR3R4-CO "
15. I I
CH3 CH3 respectively wherein R2 is C8 - C22 alkyl or alkenyl; R3 is
H or Cl - C, alkyl; and R« is H or Cλ - C-« alkyl.
The more preferred betaines useful herein include the
20 high alkyl betaines such as cocodimethyl carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl alpha-carboxy-ethyl betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis- (2-hydroxy-ethyl) carboxy methyl betaine, stearyl bis- (2-hydroxy-propyl) carboxymethyl
25 betaine, oleyl dimethyl gamma-carboxypropyl betaine, and lauryl bis- (2-hydroxypropyl) alpha-carboxyethyl betaine. The sulfobetaines are also preferred and may be represented by cocodimethyl sulfopropyl betaine, stearyldimethyl sulfopropyl betaine, lauryl dimethyl sulfoethyl betaine, and lauryl bis- (2-hydroxy-ethyl) sulfopropyl betaine. A particularly preferred composition utilizes cocoamidopropyl betaine. The zwitterionic can be present from 5. approximately 1.0 weight percent to about 10 weight percent based on the total weight of the pearlizing concentrate. Preferably, the zwitterionic will comprise from about 2.0 to about 7.0 weight percent of the composition and most preferably from about 3.0 to about 5.0 weight percent of 0 the pearlizing concentrate.
In place of the alkyl and/or alkyl ether sulfates, an isethionate or N-methyl taurate is utilized in the concentrates of this invention.
The isethionates are of the formula: 5 0
II
R-_-C-0- (CH2)2-S03M wherein R,. is a fatty alkyl group and M is a counterion selected from the group consisting of sodium, calcium, magnesium, ammonium and triethanolamine, some of which are 0 commercially available as the Geropon® AS series (Rhone- Poulenc Inc.) . The preferred isethionate is sodium cocoyl isethionate.
The N-methyl taurates are of the formula: 0 CH3
II I
25. Ri-C-N- (CH2)2-S03M wherein R, and M are as described above, some of which are commercially available as the Geropon® T series (Rhone- Poulenc Inc.) . The preferred N-methyl taurate is sodium cocoyl N-methyl taurate.
The isethionates and/or taurates of this invention may
5. be incorporated into the pearlizing concentrates at from about 5.0 to about 25 weight percent, preferably about 8 to about 20 weight percent based on the total weight of the concentrate.
It was surprisingly discovered that the above 0 isethionates and taurates provide excellent dispersing and stabilizing properties to the ultra-mild, cold pearlizing concentrates.
Water, preferably deionized, is then added in an amount from about 20 weight percent to about 78 weight 5 percent, preferably from about 41 to about 67 weight percent based on the total weight of the concentrate.
The formulated shampoo and soap systems utilizing the cold pearlizing concentrate of the present invention can contain a variety of non-essential optional components 0 suitable for rendering such compositions more acceptable. Such conventional optional ingredients are well known to those skilled in the art, e.g., preservatives such as benzyl alcohol, methyl paraben, propyl paraben and imidazolidinyl urea; cationic surfactants such as cetyl 5 trimethyl ammonium chloride, lauryl trimethyl ammonium chloride, tricetyl methyl ammonium chloride, stearyldimethyl benzyl ammonium chloride, and di (partially hydrogenated tallow) dimethylammonium chloride; thickeners and viscosity modifiers such as block polymers of ethylene oxide and propylene oxide, e.g. Antarox F-88 (Rhone-Poulenc 5. Inc.) , sodium chloride, sodium sulfate, polyvinyl alcohol, and ethyl alcohol; pH adjusting agents such as citric acid, succinic acid, phosphoric acid, sodium hydroxide, sodium carbonate; perfumes; dyes; and sequestering agents such as disodium ethylenediamine tetra-acetate. Such agents 0 generally are used individually at levels of from about 0.01% to about 10%, preferably from 0.5% to about 5.0% by weight of the composition.
The pH of the present compositions is not critical and may be in the range of from about 5 to about 9. The pH can 5 be adjusted using a buffer such as citric acid.
The order of addition to the mixing tank of the individual components of the concentrate is not critical nor is the reasonably elevated temperature; however, preferably the water, emulsifier and isethionate or N- 0 methyl taurate surfactant are intimately blended at from about 60" to 80"C, more preferably from about 70* to 75*C with high agitation until the emulsifier is solubilized. The nonionic surfactant and zwitterionic are then blended into the mix. The concentrate is then stored at a 5 temperature of from about 35*C to about 60 *C, preferably from about 45°C to about 55°C for at least one day and preferably two (2) days in order to fully develop its pearlescent characteristics.
The shampoos and soaps of the present invention can be made by merely mixing the materials together with the 5. concentrate at room temperature.
The ultra-mild cold pearlizing concentrate of the present invention may be specifically formulated into a number of different blended soap products. The pearlizing concentrate not only imparts a high luster pearlescence and 0 sheen to the products, but also contributes emollient and moisturizing qualities to the skin. It provides superior shampoo, bath and shower soap systems and markedly improves wet comb-out of the hair.
The following examples are provided to better describe 5 and define the compositions of the present invention. They are for illustrative purposes only, and it is realized that minor changes and variations may be made with respect to these compositions that are not shown below. Such changes that do not materially alter the compositions formulation 0 or function are still considered to fall within the spirit and scope of the invention as recited by the claims that follow.
Example I The following components and their respective amounts in a weight percent of the total basis are assembled.
Formulation A
Ethylene glycol monostearate (EGMS) 20.0
Laureth(7EO) alcohol 8.0
Sodium cocoyl N-methyl taurate 15.0
Cocoamidopropyl betaine 3 Q
Deiomzed water 54.0
Formulation B
Ethylene glycol monostearate 25.0
Laureth(7EO) alcohol 8.0
Sodium cocoyl N-methyl taurate 17.0
Cocoamidopropyl betaine 3 Q Deiomzed water 47.0
Formulation C
Ethylene glycol monostearate 15.0
Laureth(7EO) alcohol 8.0 Sodium cocoyl isethionate 10.0
Cocoamidopropyl betaine 5.0
Deionized water 62.0
In all three formulations, in order to prepare the ultra-mild cold pearlizing concentrates of the present invention, the ethylene glycol monostearate is mixed with water and the sodium cocoyl N-methyl taurate or the sodium cocoyl isethionate at 70* to 75°C with high speed agitation. After the EGMS is completely solubilized, the lauryl (7E0) alcohol and the cocoamidopropyl betaine are added into the mixture with stirring and kept at 50°C for one to two days in order to develop the pearlescence fully. The maintenance of the emulsion at this temperature for 5. this period of time is important for the full development of the pearlescence.
The pearlescence concentrate produced is an iridescent or shiny white to off-white viscous liquid with a pH of from about 6.5-7.5 and realizes excellent dispersibility in 0 water.
As is true with all of the compositions of this invention, these unique performance stabilizing and pearlizing concentrates require no heating for blending and are readily compatible with most anionic-based liquid hand 5 cleaner, shampoo, bubble bath and cosmetic systems to form attractive high-performance very mild products.
Example II The following ingredients and their respective amounts are combined to produce a pearlescent liquid hand soap. The 0 amounts given are weight percent based on the total weight.
RHODACAL* A-246/L* 23.4
Formulation A Concentrate 12.0 Citric Acid (to pH 6.5-7.0) Q.S. 5 Perfume, Dye, Preservative Q.S. Sodium Chloride 4.0
Water, Deionized 60.6
♦Sodium alpha olefin sulfonate (40* active - Rhone-Poulenc Inc.) 0 The water is charged into a mixing vessel and the active ingredients are slowly mixed at room temperature until the mixture becomes uniform in appearance and texture. Citric acid (50%) is then added in an amount sufficient to adjust the pH to 6.0. The shampoo is then fragranced with a suitable perfume as desired and colored with an appropriate FD & C dye. The hand soap provides 5. excellent lather and cleaning, is extremely mild, and leaves the hands soft.
Example III The following ingredients and their respective amounts are combined to produce an ultra-mild pearlescent body 0 shampoo. The amounts given are in weight percent based on the total weight.
5 RHODAPON SB-Θ20Θ/S 17.2
GEROPON SBFA 30 (i) 4.2
MIRATAINE BET C-30 (ii) 7.7
Formulation B Concentrate 8.5
Perfume, Dye, Preservative Q.S. 0 Water 62.4
(i) disodium laureth (3EO) sulfo succinate (30% active - Rhone- Poulenc Inc. ) (ii) cocoam do propyl betaine (30* active - Rhone-Poulenc Inc.) 5
The ingredients are easily blended as in Example II. These pearlescent specialty bath and shower formulations contribute to a luxurious, smooth feel and they help to 0 keep the skin soft and supple.
Example IV A body shampoo is prepared as in Example III with the use of Formulation C concentrate in lieu of Formulation B. 35 As in Example II, the pearlescent liquid products are prepared easily at room temperature and the Formulation C concentrate provides enhanced viscosity building, foam stability and lather enrichment properties; all combined in an extremely mild formulation.
5
10
I
Z_
25.

Claims

Claims What We Claim is: 1. An ultra-mild, cold pearlizing concentrate comprising; a) a suspending agent emulsifier; 5. b) a nonionic, emulsion stabilizer surfactant; c) a surfactant selected from the group consisting of isethionates and N-methyl taurates; d) a zwitterionic surfactant; and e) water. 0
2. An ultra-mild, cold pearlizing concentrate comprising: a) An emulsifier selected from the group consisting of hydroxy stearate, polyethylene glycol monostearate, polyethylene glycol distearate, ethylene glycol monostearate, ethylene glycol 5 distearate, stearic monoethanolamide, stearic monoethanolamide stearate, and mixtures thereof; b) a nonionic alcohol ethoxylate of the formula:
R-O- (CH2CH20)n-H wherein R is a C8 to C22 alkyl and n is 1 to 40; 0 c) a surfactant selected from the group consisting of isethionates and N-methyl taurates wherein i) the isethionates are of the formula:
O
II
Figure imgf000020_0001
5 wherein Rx is a fatty alkyl group and M is a counterion selected from the group consisting of scdium, calcium, magnesium, ammonium and triethanolamine; and ii) the N-methyl taurates are of the formula:
0 CH3 II I 5. Rj-C-N- (CH2)2-S03M wherein R and M are as described above; d) a zwitterionic surfactant selected from the group consisting of i) betaines 0 ii) amidobetaines, and iii) sulfobetaines; and e) water.
3. The ultra-mild, cold pearlizing concentrate of claim 2 wherein the zwitterionic surfactant is selected from 5 the group consisting of cocodimethyl carboxymethyl betaine, lauryl dimethyl carboxymethyl betaine, lauryl dimethyl alpha-carboxy-ethyl betaine, cetyl dimethyl carboxymethyl betaine, lauryl bis- (2-hydroxy- ethyl) carboxy methyl betaine, stearyl bis- (2-hydroxy- 0 propyl) carboxymethyl betaine, oleyl dimethyl gamma- carboxypropy1 betaine, lauryl bis- (2- hydroxypropyl) alpha-carboxyethylbetaine, cocodimethyl sulfopropyl betaine, stearyldimethyl sulfopropyl betaine, lauryldimethyl sulfoethyl betaine, lauryl 5 bis- (2-hydroxy-ethyl) sulfopropyl betaine, and cocoamidopropyl betaine.
4. The ultra-mild, cold pearlizing concentrate of claim 3 wherein a) the emulsifier is ethylene glycol monostearate; b) the nonionic alcohol ethoxylate is lauryl (7EO) 5. alcohol ; c) the isethionate surfactant is sodium cocoyl isethionate; and d) the zwitterionic surfactant is cocoamidopropyl betaine. 0 5. The ultra-mild, cold pearlizing concentrate of claim 3 wherein a) the emulsifier is ethylene glycol monostearate; b) the nonionic alcohol ethoxylate is lauryl (7EO) alcohol ; 5 c) the N-methyl taurate surfactant is sodium cocoyl
N-methyl taurate; and d) the zwitterionic surfactant is cocoamidopropyl betaine .
6. The ultra-mild, cold pearlizing concentrate of claim 0 3 wherein a) the emulsifier is present from about 15 to 25 percent by weight; b) the nonionic alcohol ethoxylate is present from about 1 to about 20 weight percent; 5 c) the isethionate or taurate surfactant is present from about 5 to about 25 weight percent; and d) the zwitterionic surfactant is present from about
1 to about 10 weight percent; all of the weight percents being based on the total weight of the pearlizing concentrate. 5.
7. The ultra-mild, cold pearlizing concentrate of claim 6 wherein a) the emulsifier is present from about 18 to about 22 weight percent; b) the nonionic alcohol ethoxylate is present from 0 about 5 to about 10 weight percent; c) the isethionate or taurate surfactant is present from about 8 to about 20 weight percent; and d) the zwitterionic surfactant is present from about
2 to about 7 weight percent; 5 all of the weight percents being based on the total weight of the pearlizing concentrate.
8. An ultra-mild shampoo composition comprising the cold pearlizing concentrate of claim 2.
9. An ultra-mild hand and body soap composition 0 comprising the cold pearlizing concentrate of claim 2.
10. An ultra-mild bubble bath composition comprising the cold pearlizing concentrate of claim 2.
11. A method for preparing an ultra-mild pearlizing concentrate comprising: 5 intimately blending the ingredients of claim 2 at from about 60*C to about 80*C until the emulsifier is solubilized.
PCT/IB1996/000406 1994-12-30 1996-01-02 Mild cold pearlizing concentrates WO1996021424A2 (en)

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996021711A2 (en) * 1994-12-30 1996-07-18 Rhone-Poulenc Inc. Cold pearlizing concentrates
WO1997013498A1 (en) * 1995-10-13 1997-04-17 Rhone-Poulenc Inc. Mild cold pearlizing concentrates
JP2000107583A (en) * 1998-10-01 2000-04-18 Imaginative Res Assoc Inc Postfoaming transparent gel and solution
US6521238B1 (en) 1998-07-27 2003-02-18 L'oreal S.A. Composition containing an opacifier or pearlescent agent and at least one fatty alcohol
EP3461472B1 (en) 2017-10-02 2021-02-24 Peter Greven Physioderm GmbH Sensitive skin cleanser with enhanced cleaning effect
WO2023057767A1 (en) * 2021-10-06 2023-04-13 Innospec Active Chemicals Llc Compositions and methods
GB2613446A (en) * 2021-10-06 2023-06-07 Innospec Active Chemicals Llc Compositions and methods

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0964674A2 (en) * 1996-12-19 1999-12-22 Rhodia Inc. Liquid delivery systems
JP2001514627A (en) * 1997-03-06 2001-09-11 ローディア インコーポレイティド Slow cooling pearlescent concentrate
US6063390A (en) 1998-08-07 2000-05-16 Chesebrough-Pond's Usa Co., A Division Of Conopco, Inc. Cosmetic effervescent cleansing pillow
DE19837841A1 (en) * 1998-08-20 2000-02-24 Cognis Deutschland Gmbh Improving the consistency of cold-produced cosmetic oil-in-water emulsions by adding an aqueous dispersion containing a wax and an emulsifier
US6765024B1 (en) * 1999-04-14 2004-07-20 Mcintyre Group, Ltd. Alkanolamide surfactant emulsions and process therefor
US6451331B1 (en) 2000-01-31 2002-09-17 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Pleated cosmetic effervescent cleansing pillow
DE10015992A1 (en) * 2000-03-31 2001-10-18 Rwe Dea Ag Aqueous pearly luster concentrate comprises anionic surfactant component comprising anionic gemini surfactant(s) and poorly foaming anionic detergent component, nonionic surfactant and pearl luster component
US20040105831A1 (en) * 2002-08-13 2004-06-03 Seren Frantz Compositions having a pearl blend appearance additive, personal care products made therefrom
US20050158270A1 (en) * 2004-01-15 2005-07-21 Seren Frantz Pearlizer concentrate and its use in personal care compositions
US7179772B2 (en) * 2004-06-24 2007-02-20 Unilever Home & Personal Care Usa, Division Of Conopco, Inc. Extended lathering pillow article for personal care
EP2119430A4 (en) * 2007-03-12 2013-08-14 Kao Corp Pearlescent composition
CN101631531B (en) * 2007-03-12 2012-03-28 花王株式会社 Pearlescent composition
DE102007040909A1 (en) 2007-08-30 2009-03-05 Clariant International Ltd. Aqueous concentrates of isethionate, taurate and betaine
US20100105742A1 (en) * 2008-10-24 2010-04-29 Conopco, Inc., D/B/A Unilever Pearlescent liquid cosmetic composition
MX352278B (en) 2011-06-23 2017-11-16 Procter & Gamble Process of forming crystals for use in a personal care composition.
IN2014DN09937A (en) 2012-05-30 2015-08-14 Clariant Int Ltd
BR112014029759A2 (en) 2012-05-30 2017-06-27 Clariant Finance Bvi Ltd use of n-methyl-n-acylglucamines as solubilizers
DE102012021647A1 (en) 2012-11-03 2014-05-08 Clariant International Ltd. Aqueous adjuvant compositions
BR112015032536A2 (en) * 2013-06-28 2017-07-25 Clariant Int Ltd use of special n-methyl-n-acylglucamines in skin cleansing agents and hand dishwashing agents
US9474916B2 (en) 2013-08-08 2016-10-25 Evonik Degussa Gmbh Carbamates from glycerine carbonate for pearlization
WO2015059711A1 (en) * 2013-10-25 2015-04-30 Galaxy Surfactants Ltd. Sustainable cold-dispersible pearlescent concentrate
DE102014005771A1 (en) 2014-04-23 2015-10-29 Clariant International Ltd. Use of aqueous drift-reducing compositions
US9668956B2 (en) 2014-05-21 2017-06-06 Galaxy Surfactants, Ltd. Low viscous, sulfate-free cold-dispersible pearlescent concentrate
DE102015219651A1 (en) 2015-10-09 2017-04-13 Clariant International Ltd. Compositions containing sugar amine and fatty acid
DE102015219608B4 (en) 2015-10-09 2018-05-03 Clariant International Ltd Universal pigment dispersions based on N-alkylglucamines
DE102016207877A1 (en) 2016-05-09 2017-11-09 Clariant International Ltd Stabilizers for silicate paints

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0205922A2 (en) * 1985-05-28 1986-12-30 Henkel Kommanditgesellschaft auf Aktien Free-flowing nacreous concentrate
EP0416447A1 (en) * 1989-09-05 1991-03-13 Shiseido Company Limited Shampoo composition
EP0485212A1 (en) * 1990-11-07 1992-05-13 Unilever Plc Detergent composition
EP0568848A1 (en) * 1992-04-27 1993-11-10 Hoechst Aktiengesellschaft Free-flowing aqueous dispersions with pearly lustre
EP0573341A2 (en) * 1992-06-03 1993-12-08 Colgate-Palmolive Company High foaming nonionic surfactant based liquid detergent

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57165308A (en) * 1981-04-03 1982-10-12 Lion Corp Production of pearlescent dispersion
US4534877A (en) * 1982-07-30 1985-08-13 The Procter & Gamble Company Shampoo compositions comprising specific betaine surfactants and a quaternary compound
US4490355A (en) * 1983-03-14 1984-12-25 Miranol Chemical Company, Inc. Betaine based cosmetic formulations
LU84979A1 (en) * 1983-08-30 1985-04-24 Oreal COSMETIC OR PHARMACEUTICAL COMPOSITION IN AQUEOUS OR ANHYDROUS FORM WHOSE FATTY PHASE CONTAINS OLIGOMER POLYETHER AND NEW OLIGOMER POLYETHERS
US4654207A (en) * 1985-03-13 1987-03-31 Helene Curtis Industries, Inc. Pearlescent shampoo and method for preparation of same
US4728457A (en) * 1986-08-25 1988-03-01 The Proctor & Gamble Company Process for making a silicone-containing shampoo
DE3640755A1 (en) * 1986-11-28 1988-06-09 Henkel Kgaa FLOWABLE Pearlescent Concentrate
US5151209A (en) * 1987-11-19 1992-09-29 The Procter & Gamble Company Shampoo compositions
JPH0653222B2 (en) * 1987-12-28 1994-07-20 花王株式会社 Pearlescent agent dispersion
US4938953A (en) * 1988-08-09 1990-07-03 The Upjohn Company Self-preserving conditioning shampoo formulation
DE3837860A1 (en) * 1988-11-08 1990-05-10 Wella Ag STORAGE HAIR CONDITIONER WITH PEARL GLOSS
US5019376A (en) * 1989-03-13 1991-05-28 S. C. Johnson & Son, Inc. Sparkling pearlescent personal care compositions
GB8912391D0 (en) * 1989-05-30 1989-07-12 Unilever Plc Shampoo composition
FR2662175B1 (en) * 1990-05-18 1994-05-13 Oreal WASHING COMPOSITIONS BASED ON SILICONE AND FATTY ALCOHOLS WITH ETHER AND / OR THIOETHER OR SULFOXIDE GROUPS.
IN184497B (en) * 1990-10-12 2000-08-26 Procter & Gamble
US5252325A (en) * 1991-01-08 1993-10-12 Isp Investments Inc. Conditioning hair care compositions
US5246695A (en) * 1991-04-03 1993-09-21 Rewo Chemische Werke Gmbh Use of alkylglycoside sulfosuccinates for the production of cosmetic preparations and cleaning agents
EP0514588B1 (en) * 1991-05-20 1997-06-11 Kao Corporation Novel phosphobetaine and detergent and cosmetic containing the same
US5217711A (en) * 1991-10-16 1993-06-08 Mariana De Oliveira Hair care system
US5271930A (en) * 1991-11-20 1993-12-21 Finetex, Inc. Benzoate esters of polyalkoxylated block copolymers
US5198209A (en) * 1992-02-11 1993-03-30 Amway Corporation Conditioning shampoo
US5290482A (en) * 1992-06-01 1994-03-01 Colgate-Palmolive Company Surfactant compositions comprising betaine/cocoamide complexes and method of making the same
JP3119967B2 (en) * 1993-04-08 2000-12-25 鐘紡株式会社 Facial cleansing composition having pearl luster

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0205922A2 (en) * 1985-05-28 1986-12-30 Henkel Kommanditgesellschaft auf Aktien Free-flowing nacreous concentrate
EP0416447A1 (en) * 1989-09-05 1991-03-13 Shiseido Company Limited Shampoo composition
EP0485212A1 (en) * 1990-11-07 1992-05-13 Unilever Plc Detergent composition
EP0568848A1 (en) * 1992-04-27 1993-11-10 Hoechst Aktiengesellschaft Free-flowing aqueous dispersions with pearly lustre
EP0573341A2 (en) * 1992-06-03 1993-12-08 Colgate-Palmolive Company High foaming nonionic surfactant based liquid detergent

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 9502 Derwent Publications Ltd., London, GB; AN 95-009538 XP002010874 & JP,A,06 293 630 (KANEBO LTD) , 21 October 1994 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996021711A2 (en) * 1994-12-30 1996-07-18 Rhone-Poulenc Inc. Cold pearlizing concentrates
WO1996021711A3 (en) * 1994-12-30 1996-11-14 Rhone Poulenc Inc Cold pearlizing concentrates
WO1997013498A1 (en) * 1995-10-13 1997-04-17 Rhone-Poulenc Inc. Mild cold pearlizing concentrates
US6521238B1 (en) 1998-07-27 2003-02-18 L'oreal S.A. Composition containing an opacifier or pearlescent agent and at least one fatty alcohol
JP2000107583A (en) * 1998-10-01 2000-04-18 Imaginative Res Assoc Inc Postfoaming transparent gel and solution
EP3461472B1 (en) 2017-10-02 2021-02-24 Peter Greven Physioderm GmbH Sensitive skin cleanser with enhanced cleaning effect
WO2023057767A1 (en) * 2021-10-06 2023-04-13 Innospec Active Chemicals Llc Compositions and methods
GB2613446A (en) * 2021-10-06 2023-06-07 Innospec Active Chemicals Llc Compositions and methods

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US5925604A (en) 1999-07-20

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