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WO1991011985A1 - Colorant d'oxydation pour teinture des cheveux comprenant un mordant liquide et une composition en emulsion renfermant un agent oxydant, et procede de teinture oxydante des cheveux - Google Patents

Colorant d'oxydation pour teinture des cheveux comprenant un mordant liquide et une composition en emulsion renfermant un agent oxydant, et procede de teinture oxydante des cheveux Download PDF

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Publication number
WO1991011985A1
WO1991011985A1 PCT/EP1991/000204 EP9100204W WO9111985A1 WO 1991011985 A1 WO1991011985 A1 WO 1991011985A1 EP 9100204 W EP9100204 W EP 9100204W WO 9111985 A1 WO9111985 A1 WO 9111985A1
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WO
WIPO (PCT)
Prior art keywords
component
hair
agent
composition according
weight
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/EP1991/000204
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German (de)
English (en)
Inventor
Johann Aeby
Herbert Mager
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.)
Procter and Gamble Deutschland GmbH
Original Assignee
Wella GmbH
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
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6400392&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO1991011985(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Wella GmbH filed Critical Wella GmbH
Publication of WO1991011985A1 publication Critical patent/WO1991011985A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A61K8/342—Alcohols having more than seven atoms in an unbroken chain
    • 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
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36—Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361—Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • 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
    • A61Q5/10—Preparations for permanently dyeing the hair
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88—Two- or multipart kits

Definitions

  • the invention relates to a means for oxidative
  • Ratio of 1: 1.5 to 1: 4 is obtained, as well as a process for the oxidative dyeing of hair.
  • Oxidation hair colors are, just as in the past, a central component of a cosmetic product range used for hair treatment. They consist of two components, which are mixed shortly before use and then applied to the hair to be colored.
  • the first component contains the dyestuff substances. You can as
  • the second component is an aqueous, creamy or powdery product in which a suitable oxidizing agent is contained.
  • a suitable oxidizing agent for example hydrogen peroxide.
  • 1,4-Diaminobenzene, 2,5-diaminotoluene, 2,5-diaminophenylethanol, 4-aminophenol and 4-amino-3-methylphenol are preferably used as developer substances.
  • Coupler substances examples include resorcinol, 4-chlororesorcinol, sesamol, 2-methylresorcinol, 3-aminophenol, 4- (2'-hydroxyethyl) amino-1,2-methylenedioxybenzene and 2-amino-4- (2'-hydroxyethylamino) - anisole.
  • Coloring compounds are preferably used in liquid form in some countries, for example in the USA.
  • Liquid colorants are also of great importance in the area of public hair colors. They have the advantage that the raw materials they contain are available inexpensively and that the liquid colorant masses are easy to produce in terms of production technology.
  • liquid dye compositions are mostly used in conjunction with aqueous hydrogen peroxide solutions, for example in a ratio of 1: 1 or 1: 2.
  • the mixing of the liquid color carrier mass with the hydrogen peroxide solution can take place, for example, in an application bottle with which the ready-to-use oxidation hair colorant is applied to the hair to be colored after mixing.
  • liquid dyes have a number of serious disadvantages.
  • the liquid colorants quickly turn dark after adding the hydrogen peroxide solution.
  • the hair brought into contact with the ready-to-use oxidation hair dye takes on the coloring much more slowly.
  • the premature darkening of the hair of the oxidation hair has the disadvantageous effect that the coloring agent is rinsed out too early, so that the intended color intensity is often not achieved by a too short exposure time on the hair.
  • liquid colorants also have the disadvantage that they very easily release the ammonia contained in the environment, which has an undesirable odor nuisance.
  • liquid hair dyes are known for their inadequate skin tolerance, especially if they serve to lighten the hair.
  • the object of the present invention was therefore to provide an agent for the oxidative dyeing of hair on the basis of a liquid dyestuff and a hair dyeing process using this agent, which has the disadvantages described of known agents based on liquid dyestuffs for oxidative dyeing of hair does not have.
  • agents for the oxidative dyeing of hair can be prepared by mixing a liquid colorant and an emulsion-like preparation containing the oxidizing agent which are well tolerated by the skin and in which the premature darkening, which adversely affects the coloring result, after the admixing of the oxidizing agent, largely is avoided and which, compared to known agents, emits a far lower odor burden due to ammonia escaping from the agent.
  • the present invention therefore relates to compositions for the oxidative dyeing of hair, obtained by mixing a component (A) which is a liquid colorant composition with a viscosity below 100 mPa.s at 30 degrees Celsius, and a component (B) which is an emulsion , 2.5 to 12 percent by weight of at least one C 10 to C 24 fatty alcohol of natural or synthetic origin and a composition containing an oxidizing agent, in the weight ratio of component (A) to component (B) 1: 1.5 to 1: 4 .
  • a component (A) which is a liquid colorant composition with a viscosity below 100 mPa.s at 30 degrees Celsius
  • a component (B) which is an emulsion , 2.5 to 12 percent by weight of at least one C 10 to C 24 fatty alcohol of natural or synthetic origin and a composition containing an oxidizing agent, in the weight ratio of component (A) to component (B) 1: 1.5 to 1: 4 .
  • the weight ratio of component (A) to component (B) is 1: 2 to 1: 3.
  • the viscosity of the liquid colorant composition was 30 at 30 using a Haake-Visco balance (rod II, 5 grams) Degrees Celsius.
  • Component (B) contained fatty alcohol of natural or synthetic origin is preferably a C 1 4 - bis
  • component (B) C 20 fatty alcohol.
  • fatty alcohols which can be contained in component (B) are cetyl and stearyl alcohol or a mixture thereof.
  • Component (B) contains 1 to 18 percent by weight, but particularly preferably 4 to 14 percent by weight of an oxidizing agent.
  • the main oxidizing agents used to develop hair color are hydrogen peroxide and its addition compounds to urea, melanin and sodium borate.
  • Component (B) particularly preferably contains 1 to 18 percent by weight of hydrogen peroxide.
  • Component (A) contains 2 to 30 percent by weight, particularly preferably 8 to 16 percent by weight, but saturated or unsaturated C 10 to C 24 fatty acids of natural or synthetic origin, but preferably C 16 to
  • C 2 2 fatty acids or mixtures thereof examples of such fatty acids which can be contained in component (A) are erucic acid, myristic acid, ricinoleic acid, lauric acid, palmitic acid and oleic acid.
  • the fatty acids are preferably dissolved in the hair dye according to the invention by the addition of ammonia in the form of their ammonium soaps. Instead of ammonia, however, aliphatic amines, for example monoethanolamine, can also be used.
  • Component (A) can further contain 2 to 30, but preferably 12 to 28, percent by weight of low molecular weight C 1 to C 4 alcohols, C 2 to C 6 glycols, such as, for example, ethanol, propanol, isopranol, ethylene glycol, 1,2 propylene glycol or butyl glycol, or mixtures thereof may be included.
  • C 1 to C 4 alcohols such as, for example, ethanol, propanol, isopranol, ethylene glycol, 1,2 propylene glycol or butyl glycol, or mixtures thereof may be included.
  • C 2 to C 6 glycols such as, for example, ethanol, propanol, isopranol, ethylene glycol, 1,2 propylene glycol or butyl glycol, or mixtures thereof may be included.
  • Component (A) can also contain 0.1 to 25 percent by weight of nonionic emulsifiers.
  • the hair dye according to the invention particularly preferably contains 10 to 20 percent by weight of nonionic emulsifiers.
  • non-ionic emulsifiers which can be used are oxyethylated C 10 -C 20 -fatty alcohols or oxyethylated alkylphenols with a C 6 -C 14 -alkyl radical or mixtures thereof.
  • the fatty alcohols and alkylphenols contained in component (A) are ethoxylated with 1 and 8, but preferably with 1 and 6, ethylene oxide units.
  • Component (A) contains at least one coupler substance and at least one developer substance and, if appropriate, additionally with self-coupling color pre-mares and dyes which are absorbed directly onto the hair.
  • the developer and coupler substances are used in the hair dye either as such or in the form of their physiologically acceptable salts with inorganic or organic acids, such as, for example, chloride, sulfate, phosphate, acetate, propionate, lactate or citrate.
  • the coupler substances are generally used in an approximately equimolar amount, based on the developer substances used. Even if the equimolar use proves to be expedient, it is not disadvantageous if the coupler substances are used in a certain excess or deficit. It is also not necessary for the developer component and the coupler component to be uniform products; rather, both the developer component can be a mixture of known developer substances and the coupler component can be a mixture of known coupler substances.
  • the liquid colorant, component (A) contains known coupler substances, alone or as a mixture with one another, in particular 1-naphthol, 4-methoxy-1-napthol, resorcinol, 4-chlororesorcinol, 4,6-dichlororesorcinol, 2-methylresorcinol, 3 Aminophenol, 4-hydroxy-1,2-methylenedioxybenzene, 4-amino-1,2-methylenedioxybenzene, 4- (ß-hydroxyethylamino) -1,2-methylenedioxybenzene, 4-hydroxyindole,
  • 1,4-diaminobenzene, 2,5-diaminotoluene, 2,5-diaminoanisole, 2,5-diaminobenzyl alcohol, 3-methyl-4-aminophenol are the main constituents of the color carrier composition according to the invention.
  • Oxidation dyes known and customary for hair coloring which may be contained in component (A), are found, inter alia, in the book by E. Sagarin, "Cosmetics, Science and Technology", Interscience Pubtishers Inc., New York (1957), pages 503 ff. and in the book by H. Janistyn, "Handbook of cosmetics and fragrances"
  • the total amount of the developer substance-coupler substance combination contained in component (A) should be 0.01 to 12.0 weight percent, in particular 0.2 to 4.0 weight percent.
  • conventional direct dyes for example triphenylmethane dyes such as Diamond Fuchsine (CI 42 510) and Leather Ruby HF (CI 42 520), aromatic nitro dyes such as 2-amino-4,6-dinitro-phenol, 2-nitro- 4- (ß-hydroxyethylamino) aniline, 2-N-ß, -dihydroxypropylamino- 5- (N-methyl, N-hydroxyethyl) amino-nitrobenzene and 2-amino-4-nitrophenol, azo dyes such as Acid Brown 4 (CI 14 805) and Acid Blue 135 (CI 13 385), Anthrachi non-dyes such as Disperse Violet 4 (CI 61 105), Disperse Blue 1 (CI 64 500), Disperse Red 15 (CI 60 710), Disperse Violet 1 (CI 61 100), also 1, 4,5,8-tetra aminoanthraquinone and 1,4-diaminoanthraquinone, can be contained in component (A).
  • Component (A) can also be used with self-coupling color precursors, such as 2-amino-5-methylphenol, 2-amino-6-methylphenol, 2-amino-5-ethoxypheno L or also 2-propylamino-5- aminopyridine.
  • the total amount of the direct dyes and of the self-coupling dye precursors in component (A) is 0.01 to 7.0 percent by weight, preferably 0.2 to 4.0 percent by weight.
  • antioxidants such as ascorbic acid, resorcinol or sodium sulfite and
  • Complexing agents for heavy metals for example ethylenediaminetetraacetate and nitriloacetic acid, can be contained in an amount of up to 0.5 percent by weight.
  • Perfume oils can be contained in the color carrier composition according to the invention in an amount of up to 1 percent by weight.
  • Component (A) can also contain wetting agents, emulsifiers,
  • Contain care agents Contain care agents, cationic resins and other common additives.
  • the ready-to-use agent for oxidative dyeing of the hair which is formed by mixing component (A) with component (B) in a quantitative ratio according to the invention, can be acidic, neutral or alkaline.
  • the pH of the agent for oxidative coloring of the hair according to the invention is preferably between 7.5 and 12.0.
  • the liquid colorant composition (component (A)) is mixed with the hydrogen peroxide emulsion (component (B)) immediately before use in a weight ratio of 1: 1.5 to 1: 4 according to the invention, and an amount is sufficient for coloring the hair, depending on the fullness of the hair, generally 90 to 160 g, this mixture on the hair.
  • the mixture is left to act on the hair at 15 to 50 degrees Celsius for about 5 to 60 minutes, preferably 30 minutes, then the hair is rinsed with water, washed if necessary, rinsed and
  • Color carrier 12.0 g erucic acid
  • Hydrogen peroxide emulsion 10.0 g cetylstearyl alcohol
  • the hair treated in this way is colored evenly light brown from the roots to the ends of the hair.
  • the agent according to the invention for oxidatively dyeing hair darkens only slightly after mixing the two components; smells only slightly of ammonia and is well tolerated by the skin.
  • the liquid colorant composition Before use, 40 g of the liquid colorant composition are mixed with 80 g of the hydrogen peroxide emulsion, corresponding to a mixing ratio of 1: 2, 120 g of the mixture are applied to gray, human hair and the mixture is left to act for 20 minutes at room temperature. The hair dye mixture is then rinsed out with water and the hair is dried.
  • the agent according to the invention for oxidative dyeing of hair smells only slightly of ammonia, hardly darkens after the addition of the oxidizing agent and is well tolerated by the skin. The hair treated in this way has taken on an even, dark brown tone.
  • Example 3 Oxidation hair dye: liquid colorant: 12.0 g oleic acid
  • a half-side test is carried out to compare the skin tolerance of the oxidation hair dyeing agent according to the invention with known oxidation hair dyeing agents.
  • a normal oxidation hair dye which is prepared by mixing 20 g of the liquid colorant composition from Example 1 and 40 g of a conventional hydrogen peroxide preparation of the following composition, is applied to human, medium-brown hair on the left half of the head of ten test participants.
  • Common hydrogen peroxide preparation is
  • 60 g of the ready-to-use oxidation hair dye according to the invention according to Example 1 are applied to the hair on the right half of the head of the test participants. Both agents are allowed to act on the hair and scalp for 20 minutes at room temperature, then rinsed out with water, the hair is washed with shampoo, rinsed and then dried. During the action of the two agents for oxidative dyeing of hair, the test subjects felt a significantly stronger burning sensation on the scalp on the left side of the head than on the right side of the head, which was treated with the oxidation hair dye according to the invention.
  • Head half of 30% of the participants showed a clear reddening of the scalp.
  • the agent according to the invention did not cause reddening of the scalp in any of the test participants.
  • the customary oxidation hair dye was first prepared by mixing 20 g of the liquid colorant composition according to Example 2 with 40 g of a customary hydrogen peroxide preparation of the following composition: Common hydrogen peroxide preparation:
  • Polyethylene glycol stearyl ether in which one or more monomers consist of acrylic acid, methacrylic acid or their simple esters and the polyethylene glycol stearyl ether contains twenty oxyethylene units
  • this oxidation hair dye 60 g were then applied to the left half of the head of ten test subjects with gray hair.
  • the oxidative hair dye according to the invention according to Example 3 was compared with a customary oxidation hair dye with regard to the darkening of the mass after the two components had been mixed.
  • the usual oxidation hair dye was first prepared by mixing 20 g of the liquid colorant of Example 3 with 40 g of a conventional hydrogen peroxide preparation of the following composition: usual hydrogen peroxide preparation:
  • the right half of the head was treated with 60 g each of the oxidation hair dye according to the invention as in Example 3. During the exposure time of 20 minutes The darkening of the two agents was assessed by the hairdressers at room temperature.
  • the comparison experiment showed that the oxidation hair dye according to the invention darkens considerably less than the usual oxidation hair dye applied to the left half of the head. Since the agent darkens only slightly. The desired color result can be achieved safely.
  • the means according to the invention can rule out the incorrect assessments of the color intensity already achieved in the case of customary oxidation hair colors as a result of rapid darkening, which lead to unintentionally weak colorations.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)
  • Exhaust Gas After Treatment (AREA)
  • Processes For Solid Components From Exhaust (AREA)

Abstract

L'invention a pour objet un agent pour la teinture oxydante des cheveux, obtenu en mélangeant un mordant liquide, d'une viscosité inférieure à 100 mPa, à 30 °C, avec une composition en émulsion renfermant 2,5 à 12 % en poids d'au moins un alcool gras en C10-C24 et un oxydant, dans un rapport pondéral de 1:1,5 à 1:4, ainsi qu'un procédé pour la teinture oxydante des cheveux utilisant un tel agent. Le nouvel agent évite une coloration ultérieure plus foncée altérant le résultat de la teinture, qu'on obtient avec les colorants d'oxydation habituels pour cheveux, à base de mordants liquides. Il permet également d'éviter l'inconvénient d'une odeur désagréable consécutive à un faible dégagement d'ammoniac. Il présente en outre une bonne compatibilité avec la peau.
PCT/EP1991/000204 1990-02-19 1991-02-04 Colorant d'oxydation pour teinture des cheveux comprenant un mordant liquide et une composition en emulsion renfermant un agent oxydant, et procede de teinture oxydante des cheveux Ceased WO1991011985A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DEP4005008.4 1990-02-19
DE19904005008 DE4005008C2 (de) 1990-02-19 1990-02-19 Oxidationshaarfärbemittel aus einer flüssigen Farbträgermasse und einer emulsionsförmigen, oxidationsmittelhaltigen Zusammensetzung und Verfahren zum oxidativen Färben von Haaren

Publications (1)

Publication Number Publication Date
WO1991011985A1 true WO1991011985A1 (fr) 1991-08-22

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PCT/EP1991/000204 Ceased WO1991011985A1 (fr) 1990-02-19 1991-02-04 Colorant d'oxydation pour teinture des cheveux comprenant un mordant liquide et une composition en emulsion renfermant un agent oxydant, et procede de teinture oxydante des cheveux

Country Status (3)

Country Link
JP (1) JPH0662395B2 (fr)
DE (1) DE4005008C2 (fr)
WO (1) WO1991011985A1 (fr)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2751533A1 (fr) * 1996-07-23 1998-01-30 Oreal Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique
KR100264926B1 (ko) * 1996-09-06 2000-09-01 조지안느 플로 양친매성음이온중합체를함유하는케라틴섬유용산화염료조성물
US6641618B1 (en) 1999-01-29 2003-11-04 L'oreal S.A. Ready-to-use aqueous composition for bleaching keratin fibers, comprising a combination of a water-soluble solvent and a nonionic and/or anionic amphiphilic polymer comprising at least one fatty chain
WO2004017932A1 (fr) * 2002-07-31 2004-03-04 Arimino Co.,Ltd Compositions emulsionnees pour blanchiment et teinture des cheveux et procedes de blanchiment ou de teinture des cheveux au moyen de ces compositions
WO2006106390A3 (fr) * 2005-04-05 2007-01-04 Paolo Giannico Procede de regulation et de reduction des emissions de vapeur d'ammoniac emanant de cremes de coloration et de decoloration capillaires
WO2010100231A1 (fr) * 2009-03-04 2010-09-10 L'oreal Dispositif de distribution d'une composition colorante pour fibres de kératine, et procédé associé
US8889110B2 (en) 2008-12-19 2014-11-18 L'oreal Oxidizing composition for the treatment of keratin fibers comprising at least one oil, at least one fatty alcohol and at least one oxyalkylenated fatty alcohol
US9005594B2 (en) 2007-12-21 2015-04-14 L'oreal Method for lightening human keratin fibers using at least one anhydrous composition, at least one organic amine, and at least one oxidizing agent, and device for use thereof
US9017424B2 (en) 2008-12-19 2015-04-28 L'oreal Process for lightening keratin materials using an emulsion comprising an alkaline agent and an oxidizing composition
US11691035B2 (en) 2008-12-19 2023-07-04 L'oreal Oxidizing composition for the treatment of keratin fibers comprising at least one cationic polymer, at least one fatty amide and at least one anti-oxygen agent

Families Citing this family (9)

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Publication number Priority date Publication date Assignee Title
DE4332965A1 (de) * 1993-09-28 1995-03-30 Wella Ag Oxidationshaarfärbemittel aus einer cremeförmigen Farbstoffträgermasse und einer ein Polymer und ein Oxidationsmittel enthaltenden Zubereitung sowie Verfahren zum oxidativen Färben von Haaren
FR2738741B1 (fr) * 1995-09-19 1997-12-05 Oreal Composition pour la teinture des fibres keratiniques, contenant un antagoniste de substance p
DE19604932A1 (de) * 1996-02-10 1997-08-14 Wella Ag Oxidationshaarfärbemittel
DE19827434C2 (de) * 1998-06-19 2000-08-17 Goldwell Gmbh Haarfärbemittel und Verfahren zu dessen Herstellung
DE19847224C2 (de) * 1998-10-14 2001-02-08 Goldwell Gmbh Verfahren zur Herstellung von stabilen Haarfärbeemulsionen
CA2394535C (fr) * 1999-12-17 2011-03-15 Unilever Plc Compositions de coloration et de decoloration des cheveux ayant un ph superieur a 10 et contenant du cholesterol
FR2817468B1 (fr) 2000-12-04 2005-05-06 Oreal Composition destinee a la teinture d'oxydation des fibres keratiniques comprenant de la gylcerine et un polyol different de la glycerine dans un rapport donne
FR2848841B1 (fr) * 2002-12-24 2005-03-11 Oreal Composition colorante contenant une phase mesomorphe et son procede de preparation, composition prete a l'emploi pour la teinture des matieres keratiniques
US7608116B2 (en) 2002-12-24 2009-10-27 L'oreal S.A. Oxidation dye composition comprising at least one mesomorphic phase, process for preparing it and ready-to-use composition for dyeing keratin materials

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DE3329916A1 (de) * 1982-08-30 1984-04-19 Bristol-Myers Co., 10154 New York, N.Y. Oxidations-haarfaerbemittel-zusammensetzung und eine verpackungseinheit dafuer
EP0166100A1 (fr) * 1984-06-27 1986-01-02 Wella Aktiengesellschaft Composition pour la teinture d'oxydation des cheveux à base d'un véhicule de basse viscosité
EP0258586A1 (fr) * 1986-07-31 1988-03-09 Wella Aktiengesellschaft Composition de teinture des cheveux par oxydation à base d'un véhicule gélifié et procédé de teinture des cheveux
US4776855A (en) * 1986-03-19 1988-10-11 Clairol Inc. Hair dyeing process and composition
EP0308825A1 (fr) * 1987-09-24 1989-03-29 Henkel Kommanditgesellschaft auf Aktien Composition sous forme d'émulsion contenant du peroxyde d'hydrogène, pour la décoloration et pour la teinture par oxydation des cheveux

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FR2421606A1 (fr) * 1978-04-06 1979-11-02 Oreal Procede de teinture de fibres keratiniques en deux temps
JPS61130209A (ja) * 1984-11-30 1986-06-18 Sunstar Inc 白髪染毛剤
DE3508309A1 (de) * 1985-03-08 1986-09-11 Henkel KGaA, 4000 Düsseldorf Haarfaerbemittel
JP2659740B2 (ja) * 1988-02-22 1997-09-30 ホーユー株式会社 染毛剤組成物
DE3834142A1 (de) * 1988-10-07 1990-04-12 Wella Ag Lagerstabiles cremefoermiges oxidationshaarfaerbemittel mit hohem farbstoff/elektrolyt-gehalt

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3329916A1 (de) * 1982-08-30 1984-04-19 Bristol-Myers Co., 10154 New York, N.Y. Oxidations-haarfaerbemittel-zusammensetzung und eine verpackungseinheit dafuer
EP0166100A1 (fr) * 1984-06-27 1986-01-02 Wella Aktiengesellschaft Composition pour la teinture d'oxydation des cheveux à base d'un véhicule de basse viscosité
US4776855A (en) * 1986-03-19 1988-10-11 Clairol Inc. Hair dyeing process and composition
EP0258586A1 (fr) * 1986-07-31 1988-03-09 Wella Aktiengesellschaft Composition de teinture des cheveux par oxydation à base d'un véhicule gélifié et procédé de teinture des cheveux
EP0308825A1 (fr) * 1987-09-24 1989-03-29 Henkel Kommanditgesellschaft auf Aktien Composition sous forme d'émulsion contenant du peroxyde d'hydrogène, pour la décoloration et pour la teinture par oxydation des cheveux

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2751533A1 (fr) * 1996-07-23 1998-01-30 Oreal Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique
WO1998003150A3 (fr) * 1996-07-23 1998-03-26 Oreal Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique
US6010541A (en) * 1996-07-23 2000-01-04 L'oreal Oxidation dye composition for keratin fibers comprising a nonionic amphiphilic polymer
US6277155B1 (en) 1996-07-23 2001-08-21 L'oreal Oxidation dye composition for keratin fibers comprising a nonionic amphiphilic polymer
US6344063B1 (en) 1996-07-23 2002-02-05 L'oreal Oxidation dye composition for keratin fibers comprising nonionic amphiphilic polymer
CN1121207C (zh) * 1996-07-23 2003-09-17 莱雅公司 含有非离子两亲型聚合物的角蛋白纤维氧化染色组合物
KR100264926B1 (ko) * 1996-09-06 2000-09-01 조지안느 플로 양친매성음이온중합체를함유하는케라틴섬유용산화염료조성물
US6527814B1 (en) 1996-09-06 2003-03-04 L'oreal S.A. Oxidation dye composition for keratin fibers, comprising an anionic amphiphilic polymer
US6641618B1 (en) 1999-01-29 2003-11-04 L'oreal S.A. Ready-to-use aqueous composition for bleaching keratin fibers, comprising a combination of a water-soluble solvent and a nonionic and/or anionic amphiphilic polymer comprising at least one fatty chain
WO2004017932A1 (fr) * 2002-07-31 2004-03-04 Arimino Co.,Ltd Compositions emulsionnees pour blanchiment et teinture des cheveux et procedes de blanchiment ou de teinture des cheveux au moyen de ces compositions
WO2006106390A3 (fr) * 2005-04-05 2007-01-04 Paolo Giannico Procede de regulation et de reduction des emissions de vapeur d'ammoniac emanant de cremes de coloration et de decoloration capillaires
US9005594B2 (en) 2007-12-21 2015-04-14 L'oreal Method for lightening human keratin fibers using at least one anhydrous composition, at least one organic amine, and at least one oxidizing agent, and device for use thereof
US8889110B2 (en) 2008-12-19 2014-11-18 L'oreal Oxidizing composition for the treatment of keratin fibers comprising at least one oil, at least one fatty alcohol and at least one oxyalkylenated fatty alcohol
US9017424B2 (en) 2008-12-19 2015-04-28 L'oreal Process for lightening keratin materials using an emulsion comprising an alkaline agent and an oxidizing composition
US11691035B2 (en) 2008-12-19 2023-07-04 L'oreal Oxidizing composition for the treatment of keratin fibers comprising at least one cationic polymer, at least one fatty amide and at least one anti-oxygen agent
WO2010100231A1 (fr) * 2009-03-04 2010-09-10 L'oreal Dispositif de distribution d'une composition colorante pour fibres de kératine, et procédé associé
FR2942704A1 (fr) * 2009-03-04 2010-09-10 Oreal Dispositif de distribution d'une composition tinctoriale pour les fibres keratiniques et procede associe.

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JPH04505459A (ja) 1992-09-24
DE4005008A1 (de) 1991-08-22
JPH0662395B2 (ja) 1994-08-17
DE4005008C2 (de) 1995-01-05

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