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WO1993001792A1 - Procede pour la teinture oxydante des cheveux - Google Patents

Procede pour la teinture oxydante des cheveux Download PDF

Info

Publication number
WO1993001792A1
WO1993001792A1 PCT/EP1992/001431 EP9201431W WO9301792A1 WO 1993001792 A1 WO1993001792 A1 WO 1993001792A1 EP 9201431 W EP9201431 W EP 9201431W WO 9301792 A1 WO9301792 A1 WO 9301792A1
Authority
WO
WIPO (PCT)
Prior art keywords
hair
preparation
mixture
amino
mixed
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/EP1992/001431
Other languages
German (de)
English (en)
Inventor
Herbert Mager
Dieter Hoch
Johann Aeby
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
Application filed by Wella GmbH filed Critical Wella GmbH
Priority to BR9205371A priority Critical patent/BR9205371A/pt
Publication of WO1993001792A1 publication Critical patent/WO1993001792A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

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
    • A61Q5/10—Preparations for permanently dyeing the hair
    • 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
    • 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
    • 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
    • A61K2800/884—Sequential application

Definitions

  • the present invention relates to a process for the oxidative coloring of hair, in which an optimal color balance between the hairline on the one hand and hair lengths and hair tips on the other hand is achieved.
  • a process for the oxidative dyeing of hair based on a dye carrier mass F, which contains a developer substance-coupler substance combination and which is used after mixing with an oxidizing agent, in which a first Step the dye carrier mass F is mixed with a preparation A containing an oxidizing agent and then the mixture FA thus obtained is applied to the hairline (hair growth) and allowed to act and in a second step the dye carrier mass F is mixed with a preparation B containing an oxidizing agent and then the mixture FB thus obtained is applied to the hair lengths and hair tips and allowed to act, the preparation B having a more acidic pH than the preparation A, and finally rinsing the hair with water, optionally aftertreated and then drying, the task set being convincing is solved.
  • the dye carrier composition F contains developer substances, in particular 1,4-diaminobenzene, 2,5-diamino toluene, 2,5-diaminobenzyl alcohol, 2- (2'-hydroxyethyl) -1, 4-diaminobenzene, 4-aminophenol , 4-amino-2-aminomethylphenol, 4-amino-3-methylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-ethoxymethylphenol as well as tetraaminopyridine or their physiologically compatible, water-soluble salts.
  • developer substances in particular 1,4-diaminobenzene, 2,5-diamino toluene, 2,5-diaminobenzyl alcohol, 2- (2'-hydroxyethyl) -1, 4-diaminobenzene, 4-aminophenol , 4-amino-2-aminomethylphenol, 4-amino-3-methylphenol, 4-amino-2-methoxymethyl
  • the developer substances and the coupler substances are contained in the dye carrier mass F in an amount of 0.01 to 8.0 percent by weight, preferably 0.02 to 4.0 percent by weight.
  • the total amount of developer-coupler-substance combination contained in the dye carrier mass F described here should be about 0.01 to 12.0 percent by weight, but preferably 0.2 to 6.0 percent by weight.
  • the dye carrier mass F can also contain other color components, for example the self-coupling dyes 6-amino-2-methylphenol, 2-amino5-ethoxyphenol and 2-amino-5-methylphenol and also 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-nitro-l, 4-diamino-benzene, 2-amino-4-nitrophenol, 2-amino-4-nitro-6 -chlorophenol, 4-amino-3-nitrotoluene.
  • the self-coupling dyes 6-amino-2-methylphenol, 2-amino5-ethoxyphenol and 2-amino-5-methylphenol and also conventional direct dyes, for example triphenylmethane dyes such as
  • constituents mentioned are used in the amounts customary for such purposes, for example the wetting agents and emulsifiers in concentrations of about 0.5 to 30 percent by weight, the thickeners in an amount of about 0.1 to 25 percent by weight and the care substances in one Concentration from about 0.1 to 5.0 percent by weight.
  • the dye carrier mass F described above is mixed with the preparation A or B containing an oxidizing agent immediately before use, and an amount sufficient for the hair dye treatment, depending on the fullness of the hair, is generally about 60 to 200 g , this mixture according to the inventive method on the hair.
  • the preparation A is adjusted to a pH of 2.3 to 5, preferably 2.3 to 4.0, while the preparation B a pH of 0.8 to 3, preferably 0.8 to 2, 5 has.
  • the pH of the preparations A or B is adjusted by adding physiologically compatible organic or inorganic acids, with phosphoric acid being preferred. This can also be used in combination with primary, secondary and tertiary phosphates.
  • the dye carrier mass F is mixed with the preparations A or B containing an oxidizing agent mixed in a ratio of about 4: 1 to 1: 4, with a mixing ratio of about 1: 1 being preferred.
  • the pH value of the dye carrier mass F is reduced by mixing with the preparations A or B, the lowering of the pH value in connection with preparation B being greater.
  • the pH of the mixtures FA and FB is between 7.5 and 13, the pH of the mixture FA being 0.5 to 1.5 higher than the pH of the mixture FB.
  • the dye carrier mass F1 is mixed in a ratio of 1: 1 with the preparation A, so that the mixture FIA is formed.
  • the dye carrier mass F1 is mixed in a ratio of 1: 1 with the preparation B, so that the mixture FIB is formed.
  • the pH of the mixture FIA is 10.4, while the mixture FIB has a pH of 9.4.
  • the FIA mixture is applied to the hairline (hair regrowth) of gold-orange colored hair 4 weeks ago and left to act at room temperature for 20 minutes. 7 minutes before the end of the exposure time of the mixture FIA, the mixture FIB is applied to the lengths and tips of the hair and allowed to act. After these 7 minutes, the mixtures FIA and FIB are rinsed out with water and the hair is dried.
  • the hair has taken on a very balanced golden orange color, which has excellent stability against shampoo treatments.
  • the dye carrier mass F2 is mixed in a ratio of 1: 1 with the preparation A, so that the mixture F2A is formed.
  • the dye carrier mass F2 is mixed in a ratio of 1: 1 with the preparation B, so that the mixture F2B is formed.
  • the pH of the mixture F2A is 10.5, while the mixture F2B has a pH of 9.5.
  • the mixture F2A is applied to the Hairline (hair growth) of a hair dyed red 4 weeks ago and leaves it to act at room temperature for 30 minutes. 10 minutes before the end of the exposure time of the mixture F2A, the mixture F2B is applied to the lengths and tips of the hair and allowed to act.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)

Abstract

Procédé pour la teinture oxydante des cheveux réalisée à partir d'une masse-support de colorant F renfermant une combinaison d'une substance développante et d'une substance copulante qui est utilisée après mélange avec un agent d'oxydation, procédé selon lequel, dans un premier stade, on mélange la masse-support de colorant F avec une préparation A renfermant un agent d'oxydation, puis on applique et on laisse agir sur la racine des cheveux le mélange FA ainsi obtenu et, dans un deuxième stade, on mélange la masse-support de colorant F avec une préparation B renfermant un agent d'oxydation, puis on applique et laisse agir sur les longueurs et les pointes des cheveux le mélange FB ainsi obtenu, la préparation B présentant un pH plus acide que la préparation A, après quoi les cheveux sont rincés à l'eau et éventuellement traités, puis séchés. Grâce à ce nouveau procédé de teinture, on obtient une égalisation de teinte remarquable entre les racines, les longueurs et les pointes des cheveux et une très bonne solidité de la couleur.
PCT/EP1992/001431 1991-07-19 1992-06-25 Procede pour la teinture oxydante des cheveux Ceased WO1993001792A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
BR9205371A BR9205371A (pt) 1991-07-19 1992-06-25 Processo para o tingimento oxidativo de cabelos

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19914123941 DE4123941A1 (de) 1991-07-19 1991-07-19 Verfahren zur oxidativen faerbung von haaren
DEP4123941.5 1991-07-19

Publications (1)

Publication Number Publication Date
WO1993001792A1 true WO1993001792A1 (fr) 1993-02-04

Family

ID=6436530

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP1992/001431 Ceased WO1993001792A1 (fr) 1991-07-19 1992-06-25 Procede pour la teinture oxydante des cheveux

Country Status (6)

Country Link
EP (1) EP0548307A1 (fr)
JP (1) JPH06501034A (fr)
BR (1) BR9205371A (fr)
DE (1) DE4123941A1 (fr)
ES (1) ES2040197T1 (fr)
WO (1) WO1993001792A1 (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993023006A1 (fr) * 1992-05-18 1993-11-25 Wella Aktiengesellschaft Colorant d'oxydation pour cheveux, a agent-support sous forme de creme, et procede de coloration des cheveux
EP2961486B1 (fr) 2013-02-27 2018-11-21 Henkel AG & Co. KGaA Colorisation multitonale de cheveux à une étappe
GB2570993A (en) * 2017-12-19 2019-08-14 Henkel Ag & Co Kgaa Method for homogenously dyeing keratinous fibers

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4314253C1 (de) * 1993-04-30 1994-11-24 Goldwell Ag Verfahren zum oxidativen Färben und/oder Nachfärben von menschlichen Haaren
JPH0940534A (ja) * 1995-07-27 1997-02-10 Shiseido Co Ltd 用時混合型の染毛剤組成物
DE19825133C1 (de) * 1998-06-05 2000-02-17 Goldwell Gmbh Verfahren zum oxidativen Färben von menschlichen Haaren
DE19825134C1 (de) * 1998-06-05 2000-02-17 Goldwell Gmbh Verfahren zum oxidativen Färben von menschlichen Haaren
DE10229420A1 (de) * 2002-06-29 2004-01-29 Henkel Kgaa Verfahren zur schonenden oxidativen Färbung von Haaren
TWI341733B (en) 2007-04-27 2011-05-11 Kao Corp Hair dyeing or bleaching method
EP3597171A1 (fr) * 2018-07-20 2020-01-22 HFC Prestige International Holding Switzerland S.a.r.l. Produits de blanchiment ou de teinture de cheveux et leurs compositions, ayant un effet d'annulation alcalin

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1151188A (en) * 1965-09-27 1969-05-07 Clairol Inc Composition and processes for Treating Hair
GB2018302A (en) * 1978-04-06 1979-10-17 Oreal Two stage process for dyeing keratin fibres
GB2018836A (en) * 1978-04-06 1979-10-24 Oreal Two-stage process for dyeing keratin fibres and composition for use therein
DE2819036A1 (de) * 1978-04-29 1979-11-08 Wella Ag Verfahren zur faerbung von haaren
WO1987001033A2 (fr) * 1985-08-24 1987-02-26 Goldwell Gmbh Procede pour teindre les cheveux ou poils par l'oxydation
GB2185498A (en) * 1986-01-20 1987-07-22 Oreal Process for dyeing keratinous fibres with 5, 6-dihydroxy indole in conjunction with an iodide
GB2205111A (en) * 1987-05-25 1988-11-30 Oreal Dyeing keratinous fibres with couplers and/or "rapid" oxidation dyes together with iodide ions
WO1989006531A1 (fr) * 1988-01-21 1989-07-27 Goldwell Gmbh Chemische Fabrik H.E. Dotter Procede et agent de decoloration par oxydation, notamment pour renouveler la teinture de cheveux vivants

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1151188A (en) * 1965-09-27 1969-05-07 Clairol Inc Composition and processes for Treating Hair
GB2018302A (en) * 1978-04-06 1979-10-17 Oreal Two stage process for dyeing keratin fibres
GB2018836A (en) * 1978-04-06 1979-10-24 Oreal Two-stage process for dyeing keratin fibres and composition for use therein
DE2819036A1 (de) * 1978-04-29 1979-11-08 Wella Ag Verfahren zur faerbung von haaren
WO1987001033A2 (fr) * 1985-08-24 1987-02-26 Goldwell Gmbh Procede pour teindre les cheveux ou poils par l'oxydation
GB2185498A (en) * 1986-01-20 1987-07-22 Oreal Process for dyeing keratinous fibres with 5, 6-dihydroxy indole in conjunction with an iodide
GB2205111A (en) * 1987-05-25 1988-11-30 Oreal Dyeing keratinous fibres with couplers and/or "rapid" oxidation dyes together with iodide ions
WO1989006531A1 (fr) * 1988-01-21 1989-07-27 Goldwell Gmbh Chemische Fabrik H.E. Dotter Procede et agent de decoloration par oxydation, notamment pour renouveler la teinture de cheveux vivants

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
J. Soc. Cosmet. Chem., Band 35, September/Oktober 1984, J.F. CORBETT: "Chemistry of hair colorant processes-science as an aid to formulation and development", Seiten 297-310, siehe das ganze Dokument *

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993023006A1 (fr) * 1992-05-18 1993-11-25 Wella Aktiengesellschaft Colorant d'oxydation pour cheveux, a agent-support sous forme de creme, et procede de coloration des cheveux
US5480459A (en) * 1992-05-18 1996-01-02 Wella Aktiengesellschaft Oxidative hair dye based on a creamlike carrier composition as well as process for the dyeing of hair
EP2961486B1 (fr) 2013-02-27 2018-11-21 Henkel AG & Co. KGaA Colorisation multitonale de cheveux à une étappe
GB2570993A (en) * 2017-12-19 2019-08-14 Henkel Ag & Co Kgaa Method for homogenously dyeing keratinous fibers
US10624825B2 (en) 2017-12-19 2020-04-21 Henkel Ag & Co. Kgaa Method for homogenously dyeing keratinous fibers
GB2570993B (en) * 2017-12-19 2020-06-10 Henkel Ag & Co Kgaa Method for the homogenous dyeing of keratinous fibers
DE102017223245B4 (de) 2017-12-19 2025-10-02 Henkel Ag & Co. Kgaa Verfahren zum homogenen Färben von keratinischen Fasern

Also Published As

Publication number Publication date
BR9205371A (pt) 1994-06-21
JPH06501034A (ja) 1994-01-27
DE4123941A1 (de) 1993-01-21
ES2040197T1 (es) 1993-10-16
EP0548307A1 (fr) 1993-06-30

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