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Acrylic or methacrylic acid copolymer in resinous aerosol hair preparations

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US3577517A
US3577517A US3577517DA US3577517A US 3577517 A US3577517 A US 3577517A US 3577517D A US3577517D A US 3577517DA US 3577517 A US3577517 A US 3577517A
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acid
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hair
alcohol
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Ikuo Kubot
Masakatsu Mikami
Seikichi Kitamura
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Mitsubishi Rayon Co Ltd
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Mitsubishi Rayon Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J131/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid, or of a haloformic acid; Adhesives based on derivatives of such polymers
    • C09J131/02Homopolymers or copolymers of esters of monocarboxylic acids
    • C09J131/04Homopolymers or copolymers of vinyl acetate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K8/00Cosmetics or similar toilet preparations
    • A61K8/02Cosmetics or similar toilet preparations characterised by special physical form
    • A61K8/04Dispersions; Emulsions
    • A61K8/046Aerosols; Foams
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
    • A61K8/00Cosmetics or similar toilet preparations
    • A61K8/18Cosmetics or similar toilet preparations characterised by the composition
    • A61K8/72Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
    • A61K8/8152Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILET PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/06Preparations for styling the hair, e.g. by temporary shaping or colouring
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/62Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D131/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid, or of a haloformic acid; Coating compositions based on derivatives of such polymers
    • C09D131/02Homopolymers or copolymers of esters of monocarboxylic acids
    • C09D131/04Homopolymers or copolymers of vinyl acetate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/062Copolymers with monomers not covered by C09D133/06
    • C09D133/064Copolymers with monomers not covered by C09D133/06 containing anhydride, COOH or COOM groups, with M being metal or onium-cation
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; MISCELLANEOUS COMPOSITIONS; MISCELLANEOUS APPLICATIONS OF MATERIALS
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J133/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Adhesives based on derivatives of such polymers
    • C09J133/04Homopolymers or copolymers of esters
    • C09J133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09J133/062Copolymers with monomers not covered by C09J133/06
    • C09J133/064Copolymers with monomers not covered by C09J133/06 containing anhydride, COOH or COOM groups, with M being metal or onium-cation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S424/00Drug, bio-affecting and body treating compositions
    • Y10S424/01Aerosol hair preparation
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S526/00Synthetic resins or natural rubbers -- part of the class 520 series
    • Y10S526/936Physiological use, e.g. pharmaceutical, veterinary, dental

Abstract

A COMPOSITION SUITABLE FOR USE AS AN AEROSOL HAIR LACQUER COMPRISES 30-70% OF AN ORGANIC SOLUTION CONTAINING 1-10 WEIGHT PERCENT OF A COPOLYMER OF (1) 5-40 WEIGHT PERCENT OF AN ESTER OF AN ALIPHATIC ALCOHOL WITH ACRYLIC OR METHACRYLIC ACID; (2) 6-35 WEIGHT PERCENT ACRYLIC OR METHACRYLIC ACID; AND (2) 25-89 WEIGHT PERCENT OF SOME OTHER VINYL MONOMER NEUTRALIZED WITH A WATER SOLUBLE BASE AND 70-30% OF A SPRAYING AGENT.

Description

United States Patent 3,577,517 ACRYLIC OR METHACRYLIC ACID COPOLYMER IN RESINOUS AEROSOL HAIR PREPARATIONS Ikuo Kubot, Sakai-shi, and Masakatsu Mikami and Seikichi Kitamura, Kyoto, Japan, assignors to Mitsubishi Rayon Co., Ltd., Tokyo, and Goo Chemical Industry Co., Ltd., Kyoto, Japan No Drawing. Filed Mar. 21, 1966, Ser. No. 535,675 Claims priority, application Japan, Mar. 26, 1965,

40/17,174 Int. Cl. A61k 7/06 U.S. Cl. 424-47 6 Claims ABSTRACT OF THE DISCLOSURE A composition suitable for use as an aerosol hair lacquer comprises 30-70% of an organic solution containing 1-10 weight percent of a copolymer of (1) 5-40 weight percent of an ester of an aliphatic alcohol with acrylic or methacrylic acid; (2) 6-35 weight percent acrylic or methacrylic acid; and (3) 25-89 weight percent of some other vinyl monomer neutralized with a water soluble base and 70-30% of a spraying agent.

The present invention relates to a method for producing a resinous composition which adheres to hair, displaying an excellent effect of hair preparation.

As the conventional adherents for hair preparation, shellac, polyvinyl pyrrolidone and polyvinyl ether are used but film formed by those of the shellac family is brittle so that when one of them is sprayed and made to adhere to hair, its film is impaired by combing or brushing and peeled off hair and educe like dandrulf on its surface, presenting the so-called flaking phenomenon. Shellac is also defective in being hardly soluble in water. As to an adherent belonging to the family of polyvinyl pyrrolidone, when it is aerosolized, its solution in a water-soluble alcohol shows a good mutual solubility with a halogenated hydrocarbon, gaseous at atmospheric pressure, a liquefied petroleum gas or the like as a spraying agent but film formed by it is hard before it is humidified and becomes soft rapidly when humidified, a large change between such states being defective. lWhen it is used in an especially high concentration, it presents the flaking phenomenon when it is dry and becomes humidified and sticky when it is wet, as the result of which hair sticks together, making its combing or brushing impossible. As to polyvinyl ether, it is more adhesive, as it is only added to shellac or polyvinyl pyrrolidone for giving a plasticizing effect to it.

For correcting the above-mentioned defects of the conventional adherents, there are saponified shellac and a copolymer of vinyl pyrrolidone and vinyl acetate. However, they cannot be prevented from flaking or adhering at a high temperature and a high humidity.

Further alkali metal or amine compounds of the polymers or copolymers of the esters of an alcohol having 1-4 carbons and acrylic or methacrylic acid or the copolymers of those monomers and vinylic monomers, copolymerizable with them, are known as the adherents (US. Pat. 2,897,172) but on their aerosolizing, they are soluble in a halogenated hydrocarbon but not in liquefied petroleum gas. They are produced by saponifying the above-mentioned polymers or copolymers with an alkali metal hydroxide. This manufacturing method is defective in an uneven quality of product and the low efficiency of production. Further film formed by these adherents are hard and cannot solve the problem of preventing flaking from taking place (British Pat. 796,318 and British Pat. 796,319).

An object of the present invention is to provide a resinous composition for hair preparation which is free from the above-mentioned defects. Another object of the present invention is to provide a method for producing such a resinous composition for hair preparation, These objects and other advantages can be attained by the method of the present invention which comprises subjecting a mixture of monomeric compounds consisting of (1) 5-40 (wt.) percent of the ester of an aliphatic alcohol having 8-18 carbons and acrylic or methacrylic acid, (2) 6-35 (Wt.) percent of acrylic or methacrylic acid, (3) 25-89 (wt.) percent of some other vinylic monomer to solution polymerization and adding a water-soluble basic substance, several of the compounds of the groups (1)-(3) being able to be used concurrently.

According to the present invention, a resinous composition having necessary properties for obtaiinng an aerosolized agent for hair preparation, that is, a resinous composition which is soluble in Water or water-soluble organic solvents, its solutions in those solvents present excellent mutual solubility with a common spraying agent and further it can be washed off with Warm water or an ordinary shampoo on washing of the hair. Further the resinous composition of the present invention has such softness and adhesion as the conventional adherents have not, therefore causing no flaking nor becoming sticky at high temperature and humidity but keeping the effect of hair dressing for a long time.

In the practice of the present invention, when the content of a monomer belonging to the group (1) is below 5 (wt.) percent, a resinous composition thus obtained, when it is aerosolized, has an insuflicient mutual solubility with a mixture of a halogenated hydrocarbon and a liquefied petroleum gas as a spraying agent. Film formed by it has insufficient softness, causing flaking to occur. On the other hand, when a monomer of (1) is used by more than (Wt.) percent, a resinous composiiton thus obtained becomes hardly soluble in water or a watersoluble organic solvent, particularly ethyl alcohol and its film becomes sticky.

It would be better to change the mixing ratio of acrylic or methacrylic acid belonging to the group (2) in accord ance with those of an acrylic acid ester and a methacrylic acid ester belonging to the groups (1) and (3). That is, when the raw material monomers contain an acrylic acid ester but not a methacrylic acid ester, a transparent solution of the copolymer can be obtained at a high ratio of polymerization without white turbidity, using only acrylic acid, or when they contain a methacrylic acid ester but not an acrylic acid ester, the same is possible, using only methacrylic acid. When the monomers contain both of them, it is preferable to use acrylic acid and methacrylic acid at such a mixing ratio as is generally proportional to their mixing ratio. When the total of the contents of monomers belonging to the group (2) is belw 6 (wt.) percent, film formed by a resinous composition thus obtained is hardly soluble'in water, making it difficult to be washed otf on washing of the hair. On the other hand, when it is above 35 (wt.) percent, the resinous composition is soluble in water but has no mutual solubility with a liquefied gas as a spraying agent, its white film is very hygroscopic and therefore becomes very sticky.

As the monomers of the group (3), esters of an aliphatic alcohol having 1-4 carbons and acrylic or methacrylic acid, acrylonitrile, acrylamide, styrene, vinyl toluene and vinyl acetate are suitable. They give to the copolymer an excellent adhesion and film obtained thereby is adequately soft. Of the monomers of the group (3), acrylic acid esters of a C aliphatic alcohol, acryionitrile and acrylamide give comparatively soft film, which methacrylic acid esters of a C aliphatic alcohol, styrene, vinyl toluene and vinyl acetate give harder and less sticky film.

As solvents used for solution polymerization in the present invention, C aliphatic alcohols are suitable and can be used as mixture or a hydrous alcohol, for example, 98% ethyl alcohol. The polymerization is carried out at the boiling point of the solution or at a temperature near it with stirring. According to this method, the temperature can be controlled easily and a homogeneous polymer can be obtained.

As the catalysts of the polymerization, such peroxides as benzoyl peroxide, acetyl peroxide and lauroyl peroxide, and azo-bis-isobutylonitrile, for example, are preferable. The polymerization can be carried out at a ratio of polymerization over 90%, using these peroxides.

The mixture after the polymerization is partially or fully neutralized by adding a water-soluble basic substance which amount is at least 60% by mole of the carboxyl radical contained in the copolymer. As such basic substances, for example, ammonia water, lithium hydroxide, potassium hydroxide, sodium hydroxide, mono-, dior tri-ethanolamine, mono-, dior tripropanolamine, morpholine, amino ethyl ethanol amine, amino methyl propanol, amino methyl propanediol, hydroxy ethyl morpholine, ammonium salts of lysine or glycine and their mixtures are illustrated.

When only amines are used as a neutralizer, the composition thus obtained is excellent in mutual solubility with a spraying agent, particularly a liquefied petroleum gas, so the aerosol product in a high concentration can be produced as desired according to the specific purposes. In this case there is the advantage that the composition, nearly neutral, can be produced, compared with the case where an alkali metal hydroxide is used.

Tables 1 and 2 show the effect of the kinds of the monomer compositions and neutralizing agents in the present invention on the mutual solubility of a liquefied gas and the resinous composition and the pH of the solution. Table 1 presents the combination of the monomers and neutralizing agents and Table 2 the result of measuring the mutual solubility and the pH of the resultant compositions at 20 C. The degree of mutual solubility is expressed in the amounts of Freon gas and a liquefied petroleum gas which are dissolved in 50 g. alcohol solutions in various concentrations shown in the table. Freon gas used therein is a mixture of 80 (wt) percent or dichlorodifluoromethane and 20 (wt) percent of trichloromonofluoromethane. The values of pH are those measured relative to the alcohol or aqueous solutions in respective concentrations. A glass electrode combined with a mercurous chloride electrode was used as an apparatus for the measurement.

TABLE 1.MONOMER COMPOSITION OF THE RESINOUS COMPOSITIONS AND NEUTRALIZING AGENTS Monomer and neutralizing agent Ethyl acrylate Acrylic acid Methacrylic acid 1 Potassium hydroxide Composition Composition N0. (weight part] Ethanolamine 2-1 Butyl acrylate Z-ethyihexyl acrylate Acrylic acid Methacrylic acid- Sodium hydroxidm Butyl acrylate Z-ethyihexyl ncrylate w P 0 came? Morpholine Dodecyl acrylate Ethyl methacrylate Dodecyl acrylate Ethyll methacrylate Diethanolaminen Ethyl acrylate Dodecyi methacrylate. Acrylic acid Methacrylic acid Potassium hydroxide Ethyl acrylate Doriecyl methacrylate Acrylic acid Methacrylic acid Trieth anolamine.

TABLE 2.MUTUAL SOLUBILITY AND pH OF THE COMPOSITIONS OF TABLE 1 Description Concentration pH of solution (solid Liquefied Compoportion), Freon gas, petroleum Alcohol Aqueous sition No. percent g. gas, g. solution solution The resinous composition for hair preparation obtained by the present invention dissolved in such a Water-soluble organic solvent as an aliphatic alcohol having l-4 carbons, dioxane, methyl ethyl ketone, acetone, methyl Cellosolve, 2-methoxyethanol or ethyl Cellosolve, 2- ethoxyethanol is sealed under a superatmospheric pressure in a vessel, together with a spraying agent for delivery as the product.

The spraying agents used in the present method include halogenated hydrocarbons mainly composed of trichloromonofluoromethane, dichlorodifluoromethane or dichlorotetrafluoroethane in general use, liquefied petroleum gases mainly composed of propane or butane or their mixtures. Various additive can also be used such as glycerine, ethylene glycol, sorbitol, sorbit, polyethylene glycol, lanolin or dimethyl phthalate for modifying the hardness of the film according to the respective purposes, perfume, glazing agent, coloring agent, hair tonic and others.

As a hair lacquer product, the resinous composition obtained by the present invention, even in a high concentration does not cause flaking.

The resinous composition is superior in adhesion to the conventional adherents for hair lacquer. It enables to attain the object even in a smaller amount. For example, this resinous composition is dissolved in water at a ratio of 1-10 (wt) percent of its solid. By mixing 30-70 (vol.) percent of the resultant solution with 70-30 (vol.) percent of a liquefied gas as a spraying agent, an excellent aerosol product is obtained.

Further the resinous composition obtained by the present invention is not only dissolved in water and a watersoluble organic solvent but also has mutual solubility with raw materials for making hair dressing agents, for example, castor oil, its derivatives or aliphatic higher alcohols. Hence it can be mixed as one of the raw materials for making hair dressing agents. Hair dressing agents containing this resinous composition are product possessing increased adhering property and excellent hair dressing eifect.

Further this resinous composition can be used as one of the ingredients of hair cream, hair lotion or shaving cream or as adhesive, binding agent or coating agent in general.

The present invention may be more fully understood from the following examples which are offered by way of illustration and not by way of limitation.

EXAMPLE 1 Into a. four-necked flask equipped with a reflux condenser, a dropping funnel, a thermometer and an agitator, 350 g. of ethyl acrylate, 30 g. of styrene, 70 g. of 2- ethylhexyl acrylate, 45 g. of acrylic acid, 5 g. of methacrylic acid and 600 g. of ethyl alcohol were introduced and with 7.5 g. of benzoyl peroxide added to them, were refluxed on heating at 80-81 C. and polymerized for 3.5 hours. Further, with a solution of 5 g. of benzoyl peroxide in 70 g. of ethyl alcohol added to it, the content was heated at a refluxing temperature of 79"80 C. for 1.5 hours. As a result, a solution of the copolymer in ethyl alcohol was obtained at a polymerization ratio of 98%. Next, a solution of 38 g. of caustic potash in a small amount of water and 430 g. of ethanol was added to the solution of copolymer through the dropping funnel and the resultant mixture was agitated, whereby a resinous composition having about 32 (wt.) percent of the solid portion was obtained. The viscosity of this composition at 20 C. was about 900 centipoises. The polymerization ratio was calculated by measuring its volatile portion and the viscosity was measured with a viscometer of a Brookfield type. The values of polymerization ratios and viscosities hereinafter were measured by the same procedures.

9.4 g. mi.) (about 3 g. in terms of the solid por i tion) of the composition was dissolved in 90 g. (112 ml.) of ethyl alcohol. Further I g. of lanolin and 0.1 g. of a perfume and 120 g. (86 ml.) a mixture of equal amounts of trichloromonofluoromethane and dichloromonofluoromethane were added to the resultant solution. The mixture was charged in a closed vessel to make a hair lacquer. When the hair lacquer was used in the spray form of hair dressing, it was scarcely sticky even on a rainy day and kept the effect of hair dressing for several days. Flaking did not occur by combining or brushing.

6 EXAMPLE 2 Into the same four-necked flask as in Example 1, 110 g, of n-butyl acrylate, 10 g. of ethyl methacrylate, 30 g. of dodecyl methacrylate, 10 g. of dodecyl acrylate, 32 g. of acrylic acid, 8 g. of methacrylic acid, g. of ethyl alcohol and 100 g. of isopropyl alcohol were introduced and, with 4 g. of lauroyl peroxide added to it, were heated, and while being refluxed at 8485 C., polymerized for 4 hours. Further, with 2 g. of lauroyl peroxide dissolved in 50 g. of isopropyl alcohol being added to it, the content was heated and maintained at a refluxing temperature for 2 hours. As a result, the copolymer was obtained at a polymerization ratio of 99%. Next, 15 g. of caustic potash and 23 g. of morpholine dissolved in g. of ethyl alcohol were added to the copolymer through the dropping funnel. The mixture was agitated. As a result, a resinous composition having about 40 (wt.) percent of its solid portion was obtained. Its viscosity at 20 C. was about 1200 centipoises.

5 g. (5.2 mi.) (about 2 g. of its solid solution) of the composition was dissolved in 45 g. (56 ml.) of ethyl alcohol. With 1 g. of polyethylene glycol and some amount of a perfume added to it, the resultant solution and 50 g. (88 ml.) of a liquefied petroleum gas were charged in a closed vessel to obtain an aerosol product. When the product was used for hair dressing, a hair-setting with a soft touch was attained. It was scarcely sticky at high temperature and humidity, not causing flaking.

EXAMPLE 3 Into the same four-necked and round-bottom flask as in Example 1, 135 g. of methyl acrylate, 20 g. of acrylonitrile, g. of 2-ethylhexyl methacrylate, 15 g. of acrylic acid, 15 g. of methacrylic acid and 470 g. of ethyl alcohol were introduced and with 3.5 g. of acetyl peroxide added to them, were refluxed on heating at 8182 C. and polymerized for 4 hours. With 3 g. of acetyl peroxide dissolved in 50 g. of ethyl alcohol being added to it, the content was heated and kept being refluxed for 2 hours. As a result, a solution of the copolymer in ethyl alcohol was obtained at a polymerization ratio of 98%. Next, with 19 g. of diethanolamine and 30 g. of triethanolamine added to it, it was agitated. As a result, a water-soluble resinous composition having about 40 (wt.) percent of its solid portion was obtained. Its viscosity at 20 C. was about 900 centipoises.

The pH of a solution of 17.5 g. (18.5 ml.) (about 7 g. of its solid portion) of the composition in 82.5 g. (103 ml.) of ethyl alcohol was 7.3. As it was nearly neutral, it did not affect various additives. With 0.2 g. of phenyl ethyl alcohol added to it, it and g. (120 ml.) of a mixture of equal amount of Freon, an equal weight mixture of monofluorotrichloromethane and difluorodichloromethane, and a liquefied petroleum gas were charged into a closed vessel to obtain a hair lacquer. When the product was used for hair dressing, it was scarcely sticky even at high temperature and humidity, causing no flaking.

What is claimed is:

1. A pressurized hair lacquer composition consisting essentially of (A) a resinous composition composed of a film-forming copolymer of (1) 5 to 40% by weight of an ester of a saturated aliphatic monohydric alcohol having 8 to 18 carbon atoms and an acid selected from the group consisting of acrylic acid and methacrylic acid, (2) 6 to 35% by weight of an acid selected from the group consisting of acrylic acid and methacrylic acid, (3) 25 to 89% by weight of a monomeric compound selected from the group consisting of acrylonitrile, acrylamide, styrene, vinyltoluene, vinyl acetate and esters of an aliphatic alcohol having 1 to 4 carbon atoms with acrylic or methacrylic acid, said copolymer having 'been neutralized with a water-soluble base added to the copolymer in an amount of at least 60 mol percent of the carboxyl group content of the copolymer, (B) a water-soluble organic solvent selected from the group consisting of a saturated aliphatic alcohol having 1 to 4 carbon atoms, dioxane, methyl ethyl ketone, acetone, Z-methoxyethanol and Z-ethoxyethanol and (C) a spraying agent selected from the group consisting of halogenated hydrocarbons, liquefied petroleum gas and mixtures thereof, wherein said (A) component is dissolved in said (B) component in an amount of 1 to 10 weight percent of the solution, the solution of (A) and (B) is 30 to 70 volume percent of the aerosol composition and (C) is 70 to 30 volume percent of the aerosol composition.

2. An aerosol composition according to claim 1, wherein the (1) component is an ester selected from the group consisting of Z-ethylhexyl acrylate, 2-ethylhexyl methacrylate, dodecyl acrylate and dodecyl methacrylate.

3. An aerosol composition according to claim 1, wherein the (3) component is a monomeric compound selected from the group consisting of styrene, n-butyl acrylate, ethyl methacrylate, ethyl acrylate and methyl acrylate.

4. An aerosol composition according to claim 1, wherein the water-soluble base is a member selected from the group consisting of ammonia water, lithium hydroxide, potassium hydroxide, sodium hydroxide, monoethanolamine, diethanolamine, triethanolamine, monopropanolamine, dipropanolamine, tripropanolamine, morpholine,

8 aminoethylethanolamine, aminomethylpropanol, aminomethylpropanediol, hydroxyethyl morpholine, ammonium salts of lysine, ammonium salts of glycine and mixtures thereof.

5. An aerosol composition according to claim 1, wherein the water-soluble organic solvent is an alcohol selected from the group consisting of ethanol and isopropanol.

6. An aerosol composition according to claim 1, wherein the spraying agent is a member selected from the group consisting of trichloromonofluoromethane, dichlorodifluorornethane and dichlorotetrafluoroethane.

References Cited UNITED STATES PATENTS 6/1959 Stewart et al 26080.73X 8/1965 Mirands et al. 26080.73X

ALBERT T. MEYERS, Primary Examiner V. C. CLARKE, Assistant Examiner

US3577517A 1965-03-26 1966-03-21 Acrylic or methacrylic acid copolymer in resinous aerosol hair preparations Expired - Lifetime US3577517A (en)

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GB (1) GB1146155A (en)

Cited By (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3723616A (en) * 1966-07-29 1973-03-27 Hoffmann La Roche Hair spray containing vinyl ester-ester of {60 ,{62 -unsaturated mono-or dicarboxylic acid copolymer
US3726288A (en) * 1971-08-04 1973-04-10 Nat Starch Chem Corp Process for setting hair using a preparation comprising a single fixative-thickener
US3860699A (en) * 1973-02-06 1975-01-14 Shinonaga Kasei Co Ltd Resin composition suitable for use in hair dressing preparations
US3907984A (en) * 1973-02-12 1975-09-23 Gillette Co Hair holding compositions containing a water-insoluble block copolymer
US3927199A (en) * 1972-04-14 1975-12-16 Nat Starch Chem Corp Hair fixing compositions containing N-alkyl acrylamide or methacrylamide interpolymer
US3959237A (en) * 1971-08-12 1976-05-25 Hydrophilics International, Inc. Sustained release polymers
US3966087A (en) * 1973-03-30 1976-06-29 Lever Brothers Company Aerosol dispensing device containing a hairsetting preparation having a low propellant content
US3966403A (en) * 1974-04-01 1976-06-29 L'oreal Hair lacquer or hair setting composition containing a tetrapolymer
US3966404A (en) * 1974-04-01 1976-06-29 L'oreal Hair laquer or hair setting composition containing a terpolymer
US3972336A (en) * 1974-03-14 1976-08-03 National Starch And Chemical Corporation Hair fixatives based on sulfonated styrene polymers
US4012501A (en) * 1975-05-08 1977-03-15 La Maur Inc. Hair-care composition containing a thermoplastic polymer
US4018594A (en) * 1971-08-12 1977-04-19 Hydrophilics International, Inc. Sustained release polymers
US4048192A (en) * 1974-11-12 1977-09-13 Wacker-Chemie Gmbh Water-dilutable tetrapolymers of vinyl acetate, maleic diesters, crotonic acid and hydrophilic unsaturated copolymerizable esters
FR2351135A1 (en) * 1976-05-15 1977-12-09 Basf Ag Method for preparing copolymers of acrylic and methacrylic acids and acrylic and methacrylic esters
US4062817A (en) * 1977-04-04 1977-12-13 The B.F. Goodrich Company Water absorbent polymers comprising unsaturated carboxylic acid, acrylic ester containing alkyl group 10-30 carbon atoms, and another acrylic ester containing alkyl group 2-8 carbon atoms
US4128635A (en) * 1976-03-04 1978-12-05 Henkel Kommanditgesellschaft Auf Aktien Cosmetic emulsions containing copolymers of alkyl (meth) acrylates and mono- or polyhydroxyalkyl (meth) acrylates
US4128634A (en) * 1976-03-04 1978-12-05 Henkel Kommanditgesellschaft Auf Aktien Cosmetic emulsions containing copolymers of alkyl(meth)acrylates and mono-(N-hydroxyalkyl) or bis-(N-hydroxyalkyl) (meth)acrylamides
US4128636A (en) * 1976-03-26 1978-12-05 Henkel Kommanditgesellschaft Auf Aktien Cosmetic emulsions containing copolymers of 2-hydroxy-3-hydroxyalkyl-aminopropyl(meth)acrylates and alkyl (meth)acrylates
US4129711A (en) * 1965-03-03 1978-12-12 L'oreal Polymers comprising vinyl esters-crotonic acid
US4192861A (en) * 1978-05-05 1980-03-11 National Starch And Chemical Corporation Hydrocarbon propelled aerosol hair spray compositions
US4196190A (en) * 1976-07-19 1980-04-01 Rohm And Haas Company Acrylic hair setting resins having high resistance to moisture and rapid removability from the hair with shampoo
US4258104A (en) * 1979-04-27 1981-03-24 The Dow Chemical Company Aqueous polymeric dispersions, paper coating compositions and coated paper articles made therewith
US4289752A (en) * 1976-04-06 1981-09-15 Societe Anonyme Dite: L'oreal Cosmetic compositions containing N-alkylacrylamide or N-alkylmethacrylamide based copolymers
EP0062002A2 (en) * 1981-03-25 1982-10-06 Ciba-Geigy Ag Composition for fixing the hair, its preparation and its use in aerosol sprays
US4767613A (en) * 1986-08-18 1988-08-30 Basf Aktiengesellschaft Terpolymers, their use in hair treatment agents and hair treatment agents containing these terpolymers
US4842852A (en) * 1988-03-10 1989-06-27 National Starch And Chemical Corporation Hydrocarbon tolerant hair fixing compositions
US4874604A (en) * 1988-06-23 1989-10-17 S. C. Johnson & Son, Inc. Hairspray with improved adhesion/removability upon washing
US4923695A (en) * 1988-03-10 1990-05-08 National Starch And Chemical Corporation Hydrocarbon tolerant hair fixing compositions
US4933170A (en) * 1988-03-10 1990-06-12 National Starch And Chemical Investment Holding Corporation Hydrocarbon tolerant hair fixing compositions
US4963348A (en) * 1987-12-11 1990-10-16 The Procter & Gamble Company Styling agents and compositions containing the same
US5019377A (en) * 1987-12-11 1991-05-28 The Procter & Gamble Company Low glass transistion temperature adhesive copolymers for use in hair styling products
US5021238A (en) * 1989-09-18 1991-06-04 National Starch And Chemical Investment Holding Corporation Water-based two-phase aerosol hairsprays
US5104642A (en) * 1990-04-06 1992-04-14 The Procter & Gamble Company Hair styling compositions containing particular hair styling polymers and non-aqueous solvents
US5120532A (en) * 1990-04-06 1992-06-09 The Procter & Gamble Company Hair styling shampoos
US5120531A (en) * 1990-04-06 1992-06-09 The Procter & Gamble Company Hair styling conditioners
USRE34157E (en) * 1988-06-23 1993-01-05 S. C. Johnson & Son, Inc. Hairspray with improved adhesion/removability upon washing
US5196188A (en) * 1990-10-08 1993-03-23 Basf Aktiengesellschaft Terpolymers, use thereof in hair setting compositions for increased stiffness, and hair setting compositions containing same
US5413775A (en) * 1992-09-29 1995-05-09 Amerchol Corporation Hairsprays and acrylic polymer compositions for use therein
US5523080A (en) * 1993-05-18 1996-06-04 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Cosmetic treatment of substrates
US5621059A (en) * 1995-02-06 1997-04-15 Monsanto Company Polymeric flow modifiers
US5897870A (en) * 1996-09-20 1999-04-27 Basf Aktiengesellschaft Aqeous or aqueous-alcoholic hair-cosmetic formulation
US6294159B1 (en) 1998-10-09 2001-09-25 Colgate Palmolive Company Volumizing hair care compositions
US20030147836A1 (en) * 2001-06-22 2003-08-07 L'oreal S.A. Reshapable hair styling composition comprising (meth)acrylic copolymers of four or more monomers
FR2840210A1 (en) * 2002-05-31 2003-12-05 Oreal capillary pressurized composition, comprising at least one amphiphilic diblock copolymer linear
US6667378B2 (en) 2001-06-22 2003-12-23 L'oreal, S.A. Reshapable hair styling composition comprising heterogeneous (meth)acrylic copolymer particles
US20040013615A1 (en) * 2002-05-31 2004-01-22 L'oreal Pressurized hair treatment compositions comprising at least one amphiphilic linear diblock copolymer
US6689346B1 (en) 2000-10-25 2004-02-10 L'oreal Reshapable hair styling composition comprising acrylic copolymers
DE10251122A1 (en) * 2002-11-02 2004-05-19 Beiersdorf Ag Hair treating agents with improved film-forming and odor properties contain a polymer with acid and/or amphoteric groups and a polyhydroxyalkylamine or salt
EP1486514A1 (en) * 2003-06-11 2004-12-15 National Starch and Chemical Investment Holding Corporation Acrylic polymer composition for cosmetics
US20080089853A1 (en) * 2004-10-22 2008-04-17 Basf Aktiengesellschaft Amphoteric Ethyl Methacrylate Copolymers and Use Thereof
US20080187495A1 (en) * 2001-12-20 2008-08-07 L'oreal S.A. Reshapable hair styling non-rinse composition comprising (meth) acrylic copolymers
US20080274069A1 (en) * 2004-10-22 2008-11-06 Basf Aktiengesellschaft Cosmetic Preparations Containing Copolymers of Ethyl Methacrylate and at Least One Monoethylenically Unsaturated Carboxylic Acid
WO2009030697A1 (en) * 2007-09-04 2009-03-12 Basf Se Method for the production of leather, copolymers that are suitable therefor, and further uses thereof
US20090104136A1 (en) * 2007-10-22 2009-04-23 Daniel Griffith Anderson Hair care compositions and methods of treating hair using same
US20100249331A1 (en) * 2007-05-16 2010-09-30 Babcock Laura M Method for stabilizing polymers containing repeating lactic acid units, and stabilized polymers so made
US20100278769A1 (en) * 2007-10-22 2010-11-04 Living Proof, Inc. Hair care compositions and methods of treating hair
WO2012168035A1 (en) * 2011-06-10 2012-12-13 Henkel Ag & Co. Kgaa Shine-producing hair-styling product with a strong hold, providing hair with a pleasant feel

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FR2556960B1 (en) * 1983-12-21 1990-01-19 Tondeo France Pappert Diff Composition based on resins acrylic carboxiliques, for embellishment and maintenance of the hair
DE102015225204A1 (en) * 2015-12-15 2017-06-22 Henkel Ag & Co. Kgaa "Means and methods for the temporary shaping of keratin fibers"
DE102015225210A1 (en) * 2015-12-15 2017-06-22 Henkel Ag & Co. Kgaa "Means and methods for the temporary shaping of keratin fibers"

Cited By (86)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4129711A (en) * 1965-03-03 1978-12-12 L'oreal Polymers comprising vinyl esters-crotonic acid
US3723616A (en) * 1966-07-29 1973-03-27 Hoffmann La Roche Hair spray containing vinyl ester-ester of {60 ,{62 -unsaturated mono-or dicarboxylic acid copolymer
US3726288A (en) * 1971-08-04 1973-04-10 Nat Starch Chem Corp Process for setting hair using a preparation comprising a single fixative-thickener
US4018594A (en) * 1971-08-12 1977-04-19 Hydrophilics International, Inc. Sustained release polymers
US3959237A (en) * 1971-08-12 1976-05-25 Hydrophilics International, Inc. Sustained release polymers
US3927199A (en) * 1972-04-14 1975-12-16 Nat Starch Chem Corp Hair fixing compositions containing N-alkyl acrylamide or methacrylamide interpolymer
US3860699A (en) * 1973-02-06 1975-01-14 Shinonaga Kasei Co Ltd Resin composition suitable for use in hair dressing preparations
US3907984A (en) * 1973-02-12 1975-09-23 Gillette Co Hair holding compositions containing a water-insoluble block copolymer
US3966087A (en) * 1973-03-30 1976-06-29 Lever Brothers Company Aerosol dispensing device containing a hairsetting preparation having a low propellant content
US3972336A (en) * 1974-03-14 1976-08-03 National Starch And Chemical Corporation Hair fixatives based on sulfonated styrene polymers
US3966404A (en) * 1974-04-01 1976-06-29 L'oreal Hair laquer or hair setting composition containing a terpolymer
US3966403A (en) * 1974-04-01 1976-06-29 L'oreal Hair lacquer or hair setting composition containing a tetrapolymer
US4048192A (en) * 1974-11-12 1977-09-13 Wacker-Chemie Gmbh Water-dilutable tetrapolymers of vinyl acetate, maleic diesters, crotonic acid and hydrophilic unsaturated copolymerizable esters
US4012501A (en) * 1975-05-08 1977-03-15 La Maur Inc. Hair-care composition containing a thermoplastic polymer
US4128634A (en) * 1976-03-04 1978-12-05 Henkel Kommanditgesellschaft Auf Aktien Cosmetic emulsions containing copolymers of alkyl(meth)acrylates and mono-(N-hydroxyalkyl) or bis-(N-hydroxyalkyl) (meth)acrylamides
US4128635A (en) * 1976-03-04 1978-12-05 Henkel Kommanditgesellschaft Auf Aktien Cosmetic emulsions containing copolymers of alkyl (meth) acrylates and mono- or polyhydroxyalkyl (meth) acrylates
US4128636A (en) * 1976-03-26 1978-12-05 Henkel Kommanditgesellschaft Auf Aktien Cosmetic emulsions containing copolymers of 2-hydroxy-3-hydroxyalkyl-aminopropyl(meth)acrylates and alkyl (meth)acrylates
US4289752A (en) * 1976-04-06 1981-09-15 Societe Anonyme Dite: L'oreal Cosmetic compositions containing N-alkylacrylamide or N-alkylmethacrylamide based copolymers
US4085264A (en) * 1976-05-15 1978-04-18 Basf Aktiengesellschaft Process for preparing copolymers of acrylic acid or methacrylic acid and acrylic and methacrylic acid esters
FR2351135A1 (en) * 1976-05-15 1977-12-09 Basf Ag Method for preparing copolymers of acrylic and methacrylic acids and acrylic and methacrylic esters
US4196190A (en) * 1976-07-19 1980-04-01 Rohm And Haas Company Acrylic hair setting resins having high resistance to moisture and rapid removability from the hair with shampoo
US4062817A (en) * 1977-04-04 1977-12-13 The B.F. Goodrich Company Water absorbent polymers comprising unsaturated carboxylic acid, acrylic ester containing alkyl group 10-30 carbon atoms, and another acrylic ester containing alkyl group 2-8 carbon atoms
US4192861A (en) * 1978-05-05 1980-03-11 National Starch And Chemical Corporation Hydrocarbon propelled aerosol hair spray compositions
US4258104A (en) * 1979-04-27 1981-03-24 The Dow Chemical Company Aqueous polymeric dispersions, paper coating compositions and coated paper articles made therewith
EP0062002A2 (en) * 1981-03-25 1982-10-06 Ciba-Geigy Ag Composition for fixing the hair, its preparation and its use in aerosol sprays
EP0062002A3 (en) * 1981-03-25 1983-06-22 Ciba-Geigy Ag Composition for fixing the hair, its preparation and its use in aerosol sprays
US4767613A (en) * 1986-08-18 1988-08-30 Basf Aktiengesellschaft Terpolymers, their use in hair treatment agents and hair treatment agents containing these terpolymers
US5019377A (en) * 1987-12-11 1991-05-28 The Procter & Gamble Company Low glass transistion temperature adhesive copolymers for use in hair styling products
US4963348A (en) * 1987-12-11 1990-10-16 The Procter & Gamble Company Styling agents and compositions containing the same
US4923695A (en) * 1988-03-10 1990-05-08 National Starch And Chemical Corporation Hydrocarbon tolerant hair fixing compositions
US4933170A (en) * 1988-03-10 1990-06-12 National Starch And Chemical Investment Holding Corporation Hydrocarbon tolerant hair fixing compositions
US4859455A (en) * 1988-03-10 1989-08-22 National Starch And Chemical Corporation Hydrocarbon tolerant hair fixing compositions
US4842852A (en) * 1988-03-10 1989-06-27 National Starch And Chemical Corporation Hydrocarbon tolerant hair fixing compositions
US4874604A (en) * 1988-06-23 1989-10-17 S. C. Johnson & Son, Inc. Hairspray with improved adhesion/removability upon washing
USRE34157E (en) * 1988-06-23 1993-01-05 S. C. Johnson & Son, Inc. Hairspray with improved adhesion/removability upon washing
US5021238A (en) * 1989-09-18 1991-06-04 National Starch And Chemical Investment Holding Corporation Water-based two-phase aerosol hairsprays
US5120532A (en) * 1990-04-06 1992-06-09 The Procter & Gamble Company Hair styling shampoos
US5120531A (en) * 1990-04-06 1992-06-09 The Procter & Gamble Company Hair styling conditioners
US5104642A (en) * 1990-04-06 1992-04-14 The Procter & Gamble Company Hair styling compositions containing particular hair styling polymers and non-aqueous solvents
US5196188A (en) * 1990-10-08 1993-03-23 Basf Aktiengesellschaft Terpolymers, use thereof in hair setting compositions for increased stiffness, and hair setting compositions containing same
US5413775A (en) * 1992-09-29 1995-05-09 Amerchol Corporation Hairsprays and acrylic polymer compositions for use therein
US5589157A (en) * 1992-09-29 1996-12-31 Amerchol Corporation Hairsprays and acrylic polymer compositions for use therein
US5523080A (en) * 1993-05-18 1996-06-04 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Cosmetic treatment of substrates
US5525332A (en) * 1993-05-18 1996-06-11 Chesebrough-Pond's Usa Co. Cosmetic treatment of substrates
US5621059A (en) * 1995-02-06 1997-04-15 Monsanto Company Polymeric flow modifiers
US5897870A (en) * 1996-09-20 1999-04-27 Basf Aktiengesellschaft Aqeous or aqueous-alcoholic hair-cosmetic formulation
US6294159B1 (en) 1998-10-09 2001-09-25 Colgate Palmolive Company Volumizing hair care compositions
US20050265949A1 (en) * 2000-10-25 2005-12-01 L'oreal S.A. Reshapable hair styling composition comprising acrylic copolymers
US6689346B1 (en) 2000-10-25 2004-02-10 L'oreal Reshapable hair styling composition comprising acrylic copolymers
US7122175B2 (en) 2001-06-22 2006-10-17 L'oreal S.A. Reshapable hair styling composition comprising (meth)acrylic copolymers of four or more monomers
US6667378B2 (en) 2001-06-22 2003-12-23 L'oreal, S.A. Reshapable hair styling composition comprising heterogeneous (meth)acrylic copolymer particles
US20050038213A1 (en) * 2001-06-22 2005-02-17 L'oreal, S.A. Reshapable hair styling composition comprising heterogeneous (meth)acrylic copolymer particles
US20030147836A1 (en) * 2001-06-22 2003-08-07 L'oreal S.A. Reshapable hair styling composition comprising (meth)acrylic copolymers of four or more monomers
US6645478B2 (en) 2001-06-22 2003-11-11 L'oreal S.A. Reshapable hair styling composition comprising (meth)acrylic copolymers of four or more monomers
US7048916B2 (en) 2001-06-22 2006-05-23 L'oreal S.A. Reshapable hair styling composition comprising heterogeneous (meth)acrylic copolymer particles
US20080187495A1 (en) * 2001-12-20 2008-08-07 L'oreal S.A. Reshapable hair styling non-rinse composition comprising (meth) acrylic copolymers
US20040013615A1 (en) * 2002-05-31 2004-01-22 L'oreal Pressurized hair treatment compositions comprising at least one amphiphilic linear diblock copolymer
FR2840210A1 (en) * 2002-05-31 2003-12-05 Oreal capillary pressurized composition, comprising at least one amphiphilic diblock copolymer linear
DE10251122A1 (en) * 2002-11-02 2004-05-19 Beiersdorf Ag Hair treating agents with improved film-forming and odor properties contain a polymer with acid and/or amphoteric groups and a polyhydroxyalkylamine or salt
EP1486514A1 (en) * 2003-06-11 2004-12-15 National Starch and Chemical Investment Holding Corporation Acrylic polymer composition for cosmetics
US20080089853A1 (en) * 2004-10-22 2008-04-17 Basf Aktiengesellschaft Amphoteric Ethyl Methacrylate Copolymers and Use Thereof
US20080274069A1 (en) * 2004-10-22 2008-11-06 Basf Aktiengesellschaft Cosmetic Preparations Containing Copolymers of Ethyl Methacrylate and at Least One Monoethylenically Unsaturated Carboxylic Acid
US8034888B2 (en) 2004-10-22 2011-10-11 Basf Se Amphoteric ethyl methacrylate copolymers and use thereof
CN101755010B (en) 2007-05-16 2012-08-08 自然工作有限责任公司 Method for stabilizing polymers containing repeating lactic acid units, and stabilized polymers so made
US8114939B2 (en) * 2007-05-16 2012-02-14 Natureworks Llc Method for stabilizing polymers containing repeating lactic acid units, and stabilized polymers so made
US20100249331A1 (en) * 2007-05-16 2010-09-30 Babcock Laura M Method for stabilizing polymers containing repeating lactic acid units, and stabilized polymers so made
WO2009030697A1 (en) * 2007-09-04 2009-03-12 Basf Se Method for the production of leather, copolymers that are suitable therefor, and further uses thereof
US8771374B2 (en) 2007-09-04 2014-07-08 Basf Se Method for the production of leather, copolymers that are suitable therefor, and further uses thereof
CN101796088B (en) 2007-09-04 2013-04-24 巴斯夫欧洲公司 Method for the production of leather, copolymers that are suitable therefor, and further uses thereof
US20100162490A1 (en) * 2007-09-04 2010-07-01 Basf Se Method for the production of leather, copolymers that are suitable therefor, and further uses thereof
US9770399B2 (en) 2007-10-22 2017-09-26 Living Proof, Inc. Hair care compositions and methods of treating hair
US20100284953A1 (en) * 2007-10-22 2010-11-11 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US20100284939A1 (en) * 2007-10-22 2010-11-11 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US20090226382A1 (en) * 2007-10-22 2009-09-10 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US20090104136A1 (en) * 2007-10-22 2009-04-23 Daniel Griffith Anderson Hair care compositions and methods of treating hair using same
US8226934B2 (en) 2007-10-22 2012-07-24 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US20090191141A1 (en) * 2007-10-22 2009-07-30 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US8318138B2 (en) * 2007-10-22 2012-11-27 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US20100278769A1 (en) * 2007-10-22 2010-11-04 Living Proof, Inc. Hair care compositions and methods of treating hair
US7785575B2 (en) 2007-10-22 2010-08-31 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US8545818B2 (en) 2007-10-22 2013-10-01 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US8551463B2 (en) 2007-10-22 2013-10-08 Living Proof, Inc. Hair care compositions and methods of treating hair
US8557223B2 (en) 2007-10-22 2013-10-15 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US7763240B2 (en) 2007-10-22 2010-07-27 Living Proof, Inc. Hair care compositions and methods of treating hair using same
US9192553B2 (en) 2007-10-22 2015-11-24 Living Proof, Inc. Hair care compositions and methods of treating hair using same
WO2012168035A1 (en) * 2011-06-10 2012-12-13 Henkel Ag & Co. Kgaa Shine-producing hair-styling product with a strong hold, providing hair with a pleasant feel

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