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WO2006061095A1 - Gels pigmentes en aerosol - Google Patents

Gels pigmentes en aerosol Download PDF

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Publication number
WO2006061095A1
WO2006061095A1 PCT/EP2005/012423 EP2005012423W WO2006061095A1 WO 2006061095 A1 WO2006061095 A1 WO 2006061095A1 EP 2005012423 W EP2005012423 W EP 2005012423W WO 2006061095 A1 WO2006061095 A1 WO 2006061095A1
Authority
WO
WIPO (PCT)
Prior art keywords
alkyl
microns
sprayable
hair
alkylamino
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2005/012423
Other languages
German (de)
English (en)
Inventor
Winfried Emmerling
Helga Van Flodrop
Dirk Hentrich
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
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 Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Priority to EP05813649A priority Critical patent/EP1819314A1/fr
Publication of WO2006061095A1 publication Critical patent/WO2006061095A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
    • A61K8/04—Dispersions; Emulsions
    • A61K8/046—Aerosols; Foams
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • A61K8/8141—Compositions 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
    • A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers

Definitions

  • the invention relates to a sprayable gel for the treatment of hair, which contains at least one thixotropic thickener and optionally pigments, the use of a thixotropic thickener to stabilize insoluble pigments in sprayable gels, the use of the gel for shaping and / or luster of the hair and a corresponding method for shaping and / or luster of the hair.
  • Keratinic fibers are now undergoing a variety of treatments. Treatments that serve permanent or temporary styling of the hair to create attractive-looking hairstyles play an important role. Due to current fashion trends hairstyles are always considered chic, which build up in many hair types only with the use of certain firming agents or can be maintained for a longer period of time, in contrast to a permanent deformation of the hair due to a chemical intervention in the hair structure with the help of a Permanent waving agents are used to achieve a temporary shaping hair treatment agent whose main components are film-forming polymers. As a temporary shapes, for example, designs such as curl, smoothing, Toup réelle or consolidation in question.
  • the temporary shaping is also referred to as hair styling or styling, shaping agents are also referred to as styling agents.
  • these products are often also glossing effects. This is achieved by the addition of certain insoluble pigments, which produce light reflections on the hair.
  • lower viscosity hair gels are known from the prior art which can be mixed with a conventional mechanical spray device, e.g. spray a spray pump, or with a propellant from a conventional aerosol pressure vessel with a conventional spray head as a finely divided gel.
  • the sprayable gels are much easier to dose and distribute in the hair than the high-viscosity gels.
  • the sprayable hair gels known from the prior art have good hair-firming properties.
  • sprayable hair gels containing solid pigments are also known from the prior art.
  • a disadvantage of the sprayable hair gels known from the prior art is that added glossy solid pigments sediment sometimes in part, and sometimes after longer periods of time in the spray bottles, so that these products are not optically satisfactory.
  • a first subject of the present invention is therefore a sprayable hair treatment gel containing at least one thixotropic thickener.
  • the dependent claims represent preferred embodiments of this subject invention.
  • Another object is the use of this gel for the temporary shaping / glossing of the hair.
  • Another object of the present invention is the use of thixotropic thickening agents to stabilize insoluble pigments in sprayable gels.
  • Another object of the invention is a method for temporary hair shaping / glossing.
  • Thixotropic behavior is understood to mean the phenomenon that gels, when exposed to mechanical forces, e.g. by stirring or shaking, liquefy, but after completion of the mechanical stress solidify again.
  • hair treatment gels containing at least one thixotropic thickener are very readily sprayable and solid pigment particles remain stable over longer periods of more than 6 months without sedimentation.
  • the gel of the invention can be sprayed with a conventional mechanical spray device, such as a spray pump, or with a propellant from a conventional aerosol pressure vessel with a conventional spray head as a finely divided gel.
  • a conventional mechanical spray device such as a spray pump
  • a propellant from a conventional aerosol pressure vessel with a conventional spray head as a finely divided gel.
  • the gel of the invention can be dosed more accurately and distributed to the hair evenly than conventional gels that hold solid pigments stable in solution and are offered in tubes or crucibles because of their high viscosity.
  • contamination of the hands by the gel can be avoided by the gels according to the invention.
  • the gel of the invention holds stable pigment particles stable for longer periods of more than 6 months in solution and is therefore visually very appealing even after long storage times in contrast to commercially available pigmented spray gels, where already after a few weeks of storage significantly sedimentation phenomena are observed.
  • pseudo cationic polymers are thixotropic copolymers of an acrylate component, an aminoacrylate component and a compound of the formula I,
  • R 1 and R 2 are independently a Ci-C 30 alkyl group or a group - [(CH 2 CH 2 O) XR 3 ], wherein R 3 is hydrogen or a Ci-C 30 alkyl group and X is stands for an integer of 1-30.
  • Particularly preferred is the pseudo cationic copolymer of an acrylate, an amino acrylate and Cio-C 3 o-alkyl-PEG-20-itaconate according to formula I, wherein the acrylate component of acrylic acid, C 1 -C 6 -alkylacrylic acid esters and C 1 -C 6 -alkyl methacrylates and
  • the pseudo cationic polymer is preferably contained in an amount of 1-2% by weight based on the composition of the gel. In the context of the invention it is particularly preferred to use 5-10% by weight, based on the composition of the gel, of a 20% strength solution of the pseudo-cationic polymer.
  • the sprayable gels according to the invention may preferably contain inorganic pigments as insoluble pigments. Preference is given to pigments having a particle size distribution in the range from about 2 ⁇ m to 150 ⁇ m, preferably from 10 ⁇ m to 125 ⁇ m and from 10 ⁇ m to 60 ⁇ m.
  • the inorganic pigments may be, for example, titanium dioxide, zinc oxide, iron oxide, silicon dioxide or, for example, silicates, for example mica, which may be coated, for example with titanium dioxide, zinc oxide, iron oxide or silicon dioxide.
  • Suitable examples are the pigments available from Merck under the trade name Timiron® ®, especially Timiron ® Super Gold and Timiron ® Sun Gold Sparkle MP-29th
  • the pigments are preferably contained in an amount of 0.01-0.2 wt .-%, particularly preferably 0.05-0.1 wt .-%.
  • the gels of the invention may contain film-forming polymers. Preference is given to nonionogenic oil-forming polymers or cationic film-forming polymers.
  • Cationic polymers are polymers which have groups in the main and / or side chain which may be “temporary” or “permanent” cationic.
  • “permanently cationic” refers to those polymers which have a cationic group independently of the pH of the agent These are generally polymers which contain a quaternary nitrogen atom, for example in the form of an ammonium group
  • Preferred cationic groups are quaternary ammonium groups .
  • those polymers in which the quaternary ammonium group -4 hydrocarbon group bound to a synthesized from acrylic acid, methacrylic acid or derivatives thereof main polymer chain via a C have been found to be particularly suitable.
  • R 18 is a methyl group
  • R 19 , R 20 and R 21 are methyl groups
  • Suitable physiologically tolerated counterions X " are, for example, halide ions, sulfate ions, phosphate ions, methosulfate ions and organic ions such as lactate, citrate, tartrate and acetate ions, preference being given to halide ions, in particular chloride.
  • a particularly suitable homopolymer is, if desired, crosslinked, poly (methacryloyloxyethyltrimethylammonium chloride) with the INCI name Polyquaternium-37.
  • the crosslinking can be carried out with the aid of poly olefinically unsaturated compounds, for example divinylbenzene, tetraallyloxyethane, methylene bisacrylamide, diallyl ether, polyallyl polyglyceryl ethers, or allyl ethers of sugars or sugar derivatives such as erythritol, pentaerythritol, arabitol, mannitol, sorbitol, sucrose or glucose.
  • Methylenebisacrylamide is a preferred crosslinking agent.
  • the homopolymer is preferably used in the form of a non-aqueous polymer dispersion which should not have a polymer content of less than 30% by weight.
  • Such polymer dispersions are available under the names Salcare ® SC 95 (about 50% polymer content, additional components: mineral oil (INCI name: Mineral Oil) and tridecyl polyoxypropylene-polyoxyethylene-ether (INCI name: PPG-l-Trideceth- 6)), and Salcare ® SC 96 (about 50% polymer content, additional components: mixture of Diestera of propylene glycol with a mixture of caprylic and capric acid (INCI name: propylene glycol Dicaprylate / Dicaprate) and tridecyl polyoxypropylene polyoxyethylene ether (INCI name: PPG-I -Trideceth-6)) commercially available.
  • Copolymers containing monomer units according to formula (II) as the non-ionic monomer preferably acrylamide, methacrylamide, acrylic acid-Ci-4 alkyl esters and methacrylic acid alkyl esters Ci- 4.
  • the acrylamide is particularly preferred.
  • These copolymers can also be crosslinked, as described above in the case of the homopolymers.
  • a copolymer preferred according to the invention is the crosslinked acrylamide-methacryloyloxyethyltrimethylammonium chloride copolymer.
  • quaternized cellulose derivatives such as are available under the names of Celquat ® and Polymer JR ® commercially.
  • the compounds Celquat ® H 100, Celquat L 200 and Polymer JR ® ® 400 are preferred quaternized cellulose derivatives
  • honey for example the commercial product Honeyquat ® 50, - cationic guar derivatives, such as in particular the products sold under the trade names Cosme- dia ® Guar and Jaguar ®,
  • - polysiloxanes with quaternary groups such as the commercially available products Q2-7224 (manufacturer: Dow Corning; a stabilized Trimethylsilylamodi- methicone), Dow Corning ® 929 Emulsion (containing a hydroxylamino-modified silicone which is also known as amodimethicone ), SM-2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil ® quat 3270 and 3272 (manufacturer: Th Goldschmidt; diquaternary polydimethylsiloxanes Quateraium-80).
  • Q2-7224 commercially available products
  • Dow Corning a stabilized Trimethylsilylamodi- methicone
  • Dow Corning ® 929 Emulsion containing a hydroxylamino-modified silicone which is also known as amodimethicone
  • SM-2059 manufactured by General Electric
  • SLM-55067 manufactured by Wacker
  • Vinylpyrrolidone vinylimidazoliummethochloride copolymers such as those offered under the names Luviquat.RTM ® FC 370, FC 550, FC 905, HM 552 and Hold. quaternized polyvinyl alcohol, as well as those under the names Polyquaternium 2, Polyquaternium 17, Polyquaternium 18 and
  • Polyquaternium 27 known polymers with quaternary nitrogen atoms in the polymer main chain.
  • cationic polymers can be used those under the designations Polyquaternium-24 (commercial product eg Quatrisoft ® LM 200), known polymers. Also erfmdungs according to use the copolymers of vinylpyrrolidone, such as the commercial products Copolymer 845 (manufactured by ISP), Gaffix ® VC 713 (manufactured by ISP), Gafquat ® ASCP 1011, Gafquat ® HS 110, Luviquat ® 8155 and Luviquat ® MS 370 are available.
  • cationic polymers of the invention are the "temporarily cationic" polymers. These polymers usually contain an amino group present at certain pH values as a quaternary ammonium group and thus cationic are preferred, for example, chitosan and its derivatives, such as, for example, under the trade designations Hydagen ®. , Hydagen® ® HCMF, Kytamer ® PC and Chitolam ® NB / 101 are freely available commercially CMF. chitosans are deacetylated, in different degrees of deacetylation and varying degrees of degradation (molecular weights) are commercially available. Their preparation is, for example, in DE 44 40 625 Al and described in DE 1 95 03 465 Al.
  • Particularly suitable chitosans have a degree of deacetylation of at least 80% and a molecular weight of 5'10 5 to 5'10 6 (g / mol).
  • the chitosan must be converted into the salt form. This can be done by dissolving in dilute aqueous acids.
  • Suitable acids are both mineral acids such as hydrochloric acid, sulfuric acid and phosphoric acid and organic acids, for example low molecular weight carboxylic acids, polycarboxylic acids and hydroxycarboxylic acids.
  • higher molecular weight alkyl sulfonic acids or alkyl sulfuric acids or organophosphoric acids can be used, provided that they have the required physiological compatibility.
  • Suitable acids for converting the chitosan into the salt form are, for example, acetic acid, glycolic acid, tartaric acid, malic acid, citric acid, lactic acid, 2-pyrrolidinone-5-carboxylic acid, benzoic acid or salicylic acid. Preference is given to using low molecular weight hydroxycarboxylic acids, for example glycolic acid or lactic acid.
  • Suitable nonionic polymers are, for example:
  • Cellulose ethers such as hydroxypropylcellulose, hydroxyethylcellulose and methylhydroxypropylcellulose, as sold, for example, under the trademarks Culminal ® and Benecel ® (AQUALON). shellac
  • Siloxanes These siloxanes can be both water-soluble and water-insoluble. Both volatile and nonvolatile siloxanes are suitable, nonvolatile siloxanes being understood as meaning those compounds whose boiling point is above 200 ° C. under normal pressure.
  • Preferred siloxanes are polydi- alkylsiloxanes, such as, for example, polydimethylsiloxane, polyalkylarylsiloxanes, such as, for example, polyphenylmethylsiloxane, ethoxylated polydialkylsiloxanes and polydialkylsiloxanes which contain amine and / or hydroxyl groups.
  • gels according to the invention may contain the other components customary in hair care or hairstyling products, such as, for example:
  • According to the invention are especially the extracts of green tea, oak bark, stinging nettle, witch hazel, hops, chamomile, burdock root, horsetail, hawthorn, linden, almond, aloe vera, spruce needle, horse chestnut, sandalwood, juniper, coconut, mango, apricot, lime, wheat , Kiwi, melon, orange, grapefruit, sage, rosemary, birch, mallow, meadowfoam, quenelle, yarrow, thyme, lemon balm, toadstool, coltsfoot, marshmallow, meristem, ginseng and ginger root.
  • Especially suitable for the use according to the invention are the extracts of green tea, almond, aloe vera, coconut, mango, apricot, lime, wheat, kiwi and melon.
  • alcohols and mixtures thereof can be used as extraction agent for the preparation of said plant extracts water.
  • the alcohols are lower alcohols such as ethanol and isopropanol, but especially polyhydric alcohols such as ethylene glycol and propylene glycol, both as sole extractant and in admixture with water, are preferred.
  • Plant extracts based on water / propylene glycol in a ratio of 1:10 to 10: 1 have proven to be particularly suitable.
  • the plant extracts can be used according to the invention both in pure and in diluted form. If they are used in diluted form, they usually contain about 2 to 80 wt .-% of active substance and as a solvent used in their extraction agent or extractant mixture.
  • compositions according to the invention mixtures of several, especially two, different plant extracts.
  • the gel of the invention may optionally contain vitamins.
  • vitamin A includes retinol (vitamin Ai) and 3,4-didehydroretinol (vitamin A 2 ).
  • the ß-carotene is the provitamin of retinol.
  • vitamin A component according to the invention for example, vitamin A acid and its esters, vitamin A aldehyde and vitamin A alcohol and its esters such as palmitate and acetate into consideration.
  • the preparations used according to the invention preferably contain the vitamin A component in amounts of 0.05-1% by weight, based on the total preparation.
  • the vitamin B group or the vitamin B complex include u. a.
  • Vitamin B 3 • Vitamin B 3 .
  • the compounds nicotinic acid and nicotinamide (niacinamide) are often performed.
  • Preferred according to the invention is the nicotinic acid amide which is contained in the agents used according to the invention preferably in amounts of from 0.05 to 1% by weight, based on the total agent.
  • Vitamin B 5 pantothenic acid and panthenol
  • panthenol is preferred.
  • Derivatives of panthenol which can be used according to the invention are, in particular, the esters and ethers of panthenol, cationically derivatized panthenols and pantolactone. Individual representatives are, for example, the panthenol triacetate, the panthenol monoethyl ether and its monoacetate and the cationic disclosed in WO 92/13829 Panthenol.
  • the said compounds of the vitamin B 5 type are preferably contained in the agents according to the invention in amounts of 0.05-10% by weight, based on the total agent. Amounts of 0.1-5 wt .-% are particularly preferred.
  • Vitamin B 6 pyridoxine and pyridoxamine and pyridoxal
  • Vitamin C (ascorbic acid). Vitamin C is used in the compositions according to the invention preferably in amounts of 0.1 to 3 wt .-%, based on the total agent. Use in the form of palmitic acid ester, glucosides or phosphates may be preferred. The use in combination with tocopherols may also be preferred.
  • Vitamin E tocopherols, especially ⁇ -tocopherol.
  • Tocopherol and its derivatives which include in particular the esters such as the acetate, the nicotinate, the phosphate and the succinate, are preferably present in the agents used according to the invention in amounts of 0.05-1% by weight, based on the total agent ,
  • Vitamin F is usually understood as meaning essential fatty acids, in particular linoleic acid, linolenic acid and arachidonic acid.
  • Vitamin H is the compound (3aS, 4S, 6ai?) - 2-oxohexa-hydrothienol [3,4-d] -irnidazoI-4-valeric acid, for which, in the meantime, the trivial name biotin has prevailed.
  • Biotin is contained in the agents used according to the invention preferably in amounts of from 0.0001 to 1.0% by weight, in particular in amounts of from 0.001 to 0.01% by weight.
  • the agents used according to the invention preferably contain vitamins, provitamins and vitamin precursors from groups A, B, E and H.
  • the gel preparations according to the invention preferably contain soluble UV filters as further optional component.
  • Soluble for the purposes of the invention are those UV filters which are soluble in the gels according to the invention in amounts of at least 0.1% by weight, based on the total preparation.
  • Such UV filters can be selected, for example, from substituted benzophenones, p-aminobenzoic acid esters, diphenylacrylic acid esters, cinnamic acid esters, salicylic acid esters, benzimidazoles and ortho-aminobenzoic acid esters.
  • UV filters which can be used according to the invention are 4-aminobenzoic acid, N, N, N-trimethyl-4- (2-oxoborn-3-ylidenemethyl) aniline methylsulfate, 3,3,5-trimethylcyclohexyl salicylate (homosalates), hydroxy-4-methoxy-benzophenone (benzophenone-3; Uvinul ® M 40, Uvasorb MET ®, ® Neo Heliopan BB, Eusolex ® 4360, l- (4-tert-butylphenyl) - 3- (4-methoxyphenyl) propane -l, 3-diol (butylmethoxydibenzoylmethane; Parsol ® 1789 Eusolex ® 9020), ethoxylated ethyl 4-aminobenzoate (PEG-25 PABA; Uvinul ® P 25), 4-dimethylaminobenzoic acid 2-ethylhexyl (octyl
  • Methoxycinnamate (Isoamyl p-Methoxycinnamate; Neo Heliopan E 1000 ®), 4-methoxycinnamic acid 2-ethylhexyl ester (Octyl Methoxycinnamate; Parsol ® MCX, Escalol ® 557, Neo Helio ⁇ an ® AV), 3- (4'-methylbenzylidene) -D, L-camphor (4-methylbenzylidene camphor; Parsol ® 5000, Eusolex ® 6300), 3-benzylidene camphor (3-benzylidene camphor), 4-isopropylbenzyl, 2,4,6-trianilino- (p-carbo-2'-ethylhexyl 1'-oxi) -l, 3,5-triazine, 3-imidazol-4-yl-ethyl acrylate, polymers of N- ⁇ (2 and 4) - [2-oxoborn-3-ylid
  • 2-hydroxy-4-methoxy-benzophenone According to the invention preferably 5-sulfonic acid, Uvinul ® MS 40th
  • suitable silicone oils and silicone gums in particular dialkyl and alkylaryl siloxanes, such as, for example, dimethylpolysiloxane and methylphenylpolysiloxane, and also their alkoxylated and quaternized analogues, may be present in the gels according to the invention as conditioning active ingredients.
  • silicones are available from Dow Corning under the names DC 190, DC 200 and DC 1401 products sold and the commercial product Fancorsil ® LIM l.
  • conditioning agents to cationic silicone oils such as, for example, the commercially available products Dow Corning® 939 emulsion (containing a hydroxylamino-modified silicone, which is also referred to as amodimethicone), SM-2059 (Herstelle ⁇ General Electric), SLM-55067 (manufacturer Wacker) and Abil ® -Quat 3270 and 3272 (manufacturer Th Goldschmidt;. diquaternary polydimethylsiloxanes, quaternium-80).

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
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Abstract

L'invention concerne un gel pulvérisable pour le traitement des cheveux, ce gel comprenant au moins un agent épaississant possédant un comportement thixotrope et éventuellement des pigments. L'invention concerne également l'utilisation d'un agent épaississant thixotrope pour stabiliser des pigments insolubles dans des gels pulvérisables, l'utilisation du gel selon l'invention pour coiffer et/ou faire briller les cheveux, ainsi qu'un procédé correspondant pour coiffer et/ou faire briller les cheveux.
PCT/EP2005/012423 2004-12-06 2005-11-21 Gels pigmentes en aerosol Ceased WO2006061095A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP05813649A EP1819314A1 (fr) 2004-12-06 2005-11-21 Gels pigmentes en aerosol

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE200410058851 DE102004058851A1 (de) 2004-12-06 2004-12-06 Pigmentierte Sprühgele
DE102004058851.1 2004-12-06

Publications (1)

Publication Number Publication Date
WO2006061095A1 true WO2006061095A1 (fr) 2006-06-15

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PCT/EP2005/012423 Ceased WO2006061095A1 (fr) 2004-12-06 2005-11-21 Gels pigmentes en aerosol

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EP (1) EP1819314A1 (fr)
DE (1) DE102004058851A1 (fr)
WO (1) WO2006061095A1 (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE102011089171A1 (de) * 2011-12-20 2013-06-20 Henkel Ag & Co. Kgaa Mittel zur temporären Verformung keratinischer Fasern auf Grundlage einer Kombination spezifischer filmbildender Polymere

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000062755A1 (fr) * 1999-04-20 2000-10-26 Unilever Plc Gels douche de faible viscosite et distributeur a vaporisation par poussoir
WO2001076543A1 (fr) * 2000-04-05 2001-10-18 The Procter & Gamble Company Composition d'apres-shampooing contenant un systeme d'epaississants
US6328950B1 (en) * 1998-11-28 2001-12-11 Wella Aktiengesellschaft Pigment-containing foamable gel and device producing a foam from said gel
WO2002098375A2 (fr) * 2001-06-04 2002-12-12 National Starch And Chemical Investment Holding Corporation Composites amidon-huile destines aux applications de soins personnels
US20030049224A1 (en) * 2001-08-31 2003-03-13 Susanne Birkel Hair treatment gels containing itaconic acid monoester/acrylate copolymer
EP1302191A2 (fr) * 2001-10-10 2003-04-16 Hans Schwarzkopf GmbH & Co. KG Composition moussante pour le soin de la chevelure
US20040234486A1 (en) * 2003-05-14 2004-11-25 Tomohiro Hashimoto Aqueous composition for cosmetics and cosmetic including the same
WO2004100908A1 (fr) * 2003-05-15 2004-11-25 Henkel Kommanditgesellschaft Auf Aktien Produits de traitement capillaire a proprietes coiffantes

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6328950B1 (en) * 1998-11-28 2001-12-11 Wella Aktiengesellschaft Pigment-containing foamable gel and device producing a foam from said gel
WO2000062755A1 (fr) * 1999-04-20 2000-10-26 Unilever Plc Gels douche de faible viscosite et distributeur a vaporisation par poussoir
WO2001076543A1 (fr) * 2000-04-05 2001-10-18 The Procter & Gamble Company Composition d'apres-shampooing contenant un systeme d'epaississants
WO2002098375A2 (fr) * 2001-06-04 2002-12-12 National Starch And Chemical Investment Holding Corporation Composites amidon-huile destines aux applications de soins personnels
US20030049224A1 (en) * 2001-08-31 2003-03-13 Susanne Birkel Hair treatment gels containing itaconic acid monoester/acrylate copolymer
EP1302191A2 (fr) * 2001-10-10 2003-04-16 Hans Schwarzkopf GmbH & Co. KG Composition moussante pour le soin de la chevelure
US20040234486A1 (en) * 2003-05-14 2004-11-25 Tomohiro Hashimoto Aqueous composition for cosmetics and cosmetic including the same
WO2004100908A1 (fr) * 2003-05-15 2004-11-25 Henkel Kommanditgesellschaft Auf Aktien Produits de traitement capillaire a proprietes coiffantes

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
ANON.: "Application of acrylates/beheneth-25 methacrylate (Tinovis GT Clear) as a rheology modifier, suspending agent and polymeric emulsifier in cosmetic formulations.", IP.COM JOURNAL, vol. 4, no. 5, 6 April 2004 (2004-04-06), pages 1 - 7, XP013018780 *
M. SCHLOSSMAN ED.: "The chemistry and manufacture of cosmetics: formulating, vol.2, ed.3", 2000, ALLURED, US, XP002373790, 277870 *

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Publication number Publication date
EP1819314A1 (fr) 2007-08-22
DE102004058851A1 (de) 2006-06-14

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