US20030074747A1 - Composition for the oxidation dyeing of keratin fibres, comprising at least one fatty alcohol chosen from mono- and polyglycerolated fatty alcohols and a particular polyol - Google Patents

Composition for the oxidation dyeing of keratin fibres, comprising at least one fatty alcohol chosen from mono- and polyglycerolated fatty alcohols and a particular polyol Download PDF

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Publication number
US20030074747A1
US20030074747A1 US10/206,569 US20656902A US2003074747A1 US 20030074747 A1 US20030074747 A1 US 20030074747A1 US 20656902 A US20656902 A US 20656902A US 2003074747 A1 US2003074747 A1 US 2003074747A1
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United States
Prior art keywords
equal
chosen
composition
composition according
radicals
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Abandoned
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US10/206,569
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English (en)
Inventor
Patricia Vuarier
Jean-Marie Millequant
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LOreal SA
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LOreal SA
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Assigned to L'OREAL S.A. reassignment L'OREAL S.A. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: VUARIER, PATRICIA, MILLEQUANT, JEAN-MARIE
Publication of US20030074747A1 publication Critical patent/US20030074747A1/en
Priority to US11/483,637 priority Critical patent/US7402180B2/en
Abandoned legal-status Critical Current

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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
    • 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
    • A61K8/18—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
    • A61K8/345—Alcohols containing more than one hydroxy group

Definitions

  • polyethylene glycols such as, for example, the product known as PEG-6 in the CTFA publication (International Cosmetic Ingredient Dictionary, Seventh Edition).
  • R 9 denotes a hydrogen atom or a methyl radical
  • R 7 and R 8 independently of each other, denote an alkyl group comprising from 1 to 6 carbon atoms, a hydroxyalkyl group in which the alkyl group comprises 1 to 5 carbon atoms, a lower C 1 -C 4 amidoalkyl group, or R 7 and R 8 can denote, together with the nitrogen atom to which they are attached, heterocyclic groups such as piperidyl or morpholinyl
  • R 7 and R 8 independently of each other, denote an alkyl group comprising from 1 to 4 carbon atoms
  • Y ⁇ is an anion such as bromide, chloride, acetate, borate, citrate, tartrate, bisulphate, bisulphite, sulphate, or phosphate.
  • R 10 , R 11 , R 12 and R 13 which may be identical or different, represent aliphatic, alicyclic, or arylaliphatic radicals comprising from 1 to 20 carbon atoms or lower hydroxyalkylaliphatic radicals, or alternatively R 10 , R 1 , R 12 and R 13 , together or separately, constitute, with the nitrogen atoms to which they are attached, heterocycles optionally comprising a second hetero atom other than nitrogen, or alternatively R 10 , R 11 , R 12 and R 13 represent a linear or branched C 1 -C 6 alkyl radical substituted with a nitrile, ester, acyl, or amide group or a group —CO—O—R 14 —D or —CO—NH—R 14 —D where R 14 is an alkylene and D is a quaternary ammonium group;
  • a 1 and B 1 represent polymethylene groups comprising from 2 to 20 carbon atoms which may be linear or branched, saturated or unsaturated, and which may comprise, linked to or intercalated in the main chain, one or more aromatic rings or one or more oxygen or sulphur atoms or sulphoxide, sulphone, disulphide, amino, alkylamino, hydroxyl, quaternary ammonium, ureido, amide, or ester groups, and
  • Such polymers may be prepared according to the processes described, for example, in U.S. Pat. Nos. 4,157,388, 4,702,906, and 4,719,282 (the disclosures of which are incorporated herein by reference). They are also described, for example, in patent application EP-A-122 324 (the disclosure of which is incorporated herein by reference).
  • copolymers whose CTFA (4th edition, 1991) name is octylacrylamide/acrylates/butylaminoethyl methacrylate copolymer such as the products sold under the name Amphomer or Lovocryl 47 by the company National Starch can be used.
  • R 20 denotes a polymerizable unsaturated group such as an acrylate, methacrylate, acrylamide, or methacrylamide group
  • y and z represent an integer from 1 to 3
  • R 2 , and R 22 represent a hydrogen atom, methyl, ethyl or propyl
  • R 23 and R 24 represent a hydrogen atom or an alkyl radical such that the sum of the carbon atoms in R 23 and R 24 does not exceed 10.
  • E or E′, E or E′ which may be identical or different, denote a divalent radical which is an alkylene radical with a straight or branched chain comprising up to 7 carbon atoms in the main chain, which is unsubstituted or substituted with hydroxyl groups and which can contain, in addition to the oxygen, nitrogen and sulphur atoms, 1 to 3 aromatic and/or heterocyclic rings; the oxygen, nitrogen and sulphur atoms being present in the form of ether, thioether, sulphoxide, sulphone, sulphonium, alkylamine or alkenylamine groups, hydroxyl, benzylamine, amine oxide, quaternary ammonium, amide, imide, alcohol, ester and/or urethane groups;
  • nonionic surfactants are, themselves also, compounds that are well known by one of ordinary skill in the art (see, for example, “Handbook of Surfactants” by M. R. Porter, published by Blackie & Son (Glasgow and London), 1991, pp. 116-178) and their nature is not a critical factor in the context of the present invention.
  • they can be chosen from (non-limiting list) polyethoxylated or polypropoxylated, alkylphenols, alpha-diols or alcohols, comprising a fatty chain that comprises, for example, 8 to 18 carbon atoms, wherein the number of ethylene oxide or propylene oxide groups can range from 2 to 50, for example.
  • fatty-chain anionic thickening polymers of this type which can be used are polymers formed from a monomer blend comprising:
  • hydroxyethylcelluloses modified with groups comprising at least one fatty chain such as alkyl, arylalkyl, or alkylaryl groups, or mixtures thereof, and in which the alkyl groups can be C 8 -C 22 , for instance the product Natrosol Plus Grade 330 CS (C 16 alkyls) sold by the company Aqualon, or the product Bermocoll EHM 100 sold by the company Berol Nobel,
  • Such polymers are prepared by reacting, in a solvent medium, ammonia gas with a hydrophobic maleic acid monoamide, polyoxyalkylenated and modified with a linear or branched C 8 -C 30 alkyl or alkenyl chain, optionally as a mixture with a maleic acid monoester.
US10/206,569 2001-07-27 2002-07-29 Composition for the oxidation dyeing of keratin fibres, comprising at least one fatty alcohol chosen from mono- and polyglycerolated fatty alcohols and a particular polyol Abandoned US20030074747A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/483,637 US7402180B2 (en) 2001-07-27 2006-07-11 Composition for the oxidation dyeing of keratin fibres, comprising at least one fatty alcohol chosen from mono- and polyglycerolated fatty alcohols and a particular polyol

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0110116 2001-07-27
FR0110116A FR2827761B1 (fr) 2001-07-27 2001-07-27 Composition pour la teinture d'oxydation des fibres keratiniques comprenant un alcool gras mono- ou poly-glycerole et un polyol particulier

Related Child Applications (1)

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US11/483,637 Continuation US7402180B2 (en) 2001-07-27 2006-07-11 Composition for the oxidation dyeing of keratin fibres, comprising at least one fatty alcohol chosen from mono- and polyglycerolated fatty alcohols and a particular polyol

Publications (1)

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US20030074747A1 true US20030074747A1 (en) 2003-04-24

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US10/206,569 Abandoned US20030074747A1 (en) 2001-07-27 2002-07-29 Composition for the oxidation dyeing of keratin fibres, comprising at least one fatty alcohol chosen from mono- and polyglycerolated fatty alcohols and a particular polyol
US11/483,637 Expired - Lifetime US7402180B2 (en) 2001-07-27 2006-07-11 Composition for the oxidation dyeing of keratin fibres, comprising at least one fatty alcohol chosen from mono- and polyglycerolated fatty alcohols and a particular polyol

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Country Status (20)

Country Link
US (2) US20030074747A1 (ja)
EP (1) EP1279395B1 (ja)
JP (2) JP2003055177A (ja)
KR (1) KR100622333B1 (ja)
CN (1) CN1196465C (ja)
AR (1) AR034908A1 (ja)
AT (1) ATE385763T1 (ja)
AU (1) AU2002300197B2 (ja)
BR (1) BR0203005B1 (ja)
CA (1) CA2395683A1 (ja)
DE (1) DE60224959T2 (ja)
DK (1) DK1279395T3 (ja)
ES (1) ES2300424T3 (ja)
FR (1) FR2827761B1 (ja)
HU (1) HUP0202509A2 (ja)
MX (1) MXPA02007237A (ja)
PL (1) PL205723B1 (ja)
PT (1) PT1279395E (ja)
RU (1) RU2220704C1 (ja)
ZA (1) ZA200205953B (ja)

Cited By (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20040258641A1 (en) * 2003-04-01 2004-12-23 Gregory Plos Cosmetic composition for dyeing human keratin materials, comprising at least one fluorescent dye and at least one cationic polymer, and a dyeing process therefor
US20040256598A1 (en) * 2003-04-01 2004-12-23 Gregory Plos Composition for dyeing human keratin materials, comprising at least one fluorescent dye and at least one compound comprising an acid functional group and processes therefor
US20050008593A1 (en) * 2003-04-01 2005-01-13 Gregory Plos Dye composition comprising at least one fluorescent dye and a non-associative thickening polymer for human keratin materials, process therefor, and method thereof
US20050005368A1 (en) * 2003-04-01 2005-01-13 Gregory Plos Process for dyeing, with a lightening effect, human keratin fibers that have been permanently reshaped, using at least one composition comprising at least one fluorescent dye
US20050005371A1 (en) * 2003-04-01 2005-01-13 Chrystel Pourille-Grethen Method of dyeing human keratin materials with a lightening effect with compositions comprising at least one fluorescent dye and at least one amphoteric or nonionic surfactant, composition thereof, process thereof, and device therefor
US20050008594A1 (en) * 2003-04-01 2005-01-13 Gregory Plos Composiiton for dyeing human keratin materials, comprising at least one fluorescent dye and at least one polyol, process therefor and use thereof
US20050028302A1 (en) * 2003-07-01 2005-02-10 Marie-Pascale Audousset Dye composition comprising at least one oxidation base, 2-chloro-6-methyl-3-aminophenol and 3-methyl-1-phenyl-5-pyrazolone
US20050031562A1 (en) * 2003-04-01 2005-02-10 Luc Gourlaouen Composition for dyeing human keratin materials, comprising at least one fluorescent dye and at least one associative polymer, process therefor and use thereof
US20050028301A1 (en) * 2001-09-28 2005-02-10 Florent Pastore Dyeing composition with a brightening effect for human kerationous fibres
US20050076457A1 (en) * 2003-04-01 2005-04-14 Gregory Plos Composition for dyeing a human keratin material, comprising at least one fluorescent dye and at least one insoluble conditioning agent, process thereof, use thereof, and devices thereof
US20050098763A1 (en) * 2003-04-01 2005-05-12 Gregory Plos Composition for dyeing human keratin materials, comprising a fluorescent dye and a particular sequestering agent, process therefor and use thereof
US20050125912A1 (en) * 2001-12-21 2005-06-16 Patricia Desenne Dyeing composition for keratinous fibers comprising an oxyethylene rapeseed fatty acid amide
US20050144739A1 (en) * 2003-12-11 2005-07-07 L'oreal Treatment of dyed keratain fibres with a surfactant composition, and use for protecting the colour
WO2005074871A1 (de) * 2004-02-05 2005-08-18 Wella Aktiengesellschaft Färbemittel mit perlglanz für keratinfasern
US20060010617A1 (en) * 2002-12-24 2006-01-19 Luc Gourlaouen Method for dyeing or coloring human keratin materials with lightening effect using a composition comprising at least one fluorescent compound and at least one optical brightener
US20060277691A1 (en) * 2005-05-31 2006-12-14 Jean-Baptiste Saunier Composition for dyeing keratin fibers, comprising a diamino-N,N-dihydropyrazolone compound, a coupler, and a polyol
US7150765B2 (en) 2003-07-11 2006-12-19 L'oreal S.A. Fatty acid-free liquid dye composition comprising at least one oxidation base and 2-methyl-1, 3-propanediol, dyeing process, and device
US20080104775A1 (en) * 2002-12-06 2008-05-08 L,Oreal S.A. Oxidation dye composition for keratin fibers, comprising at least one oxidation dye, at least one associative polymer, at least one nonionic cellulose-based compound not comprising a C8-C30 fatty chain, and at least one cationic polymer with a charge density of greater than 1 MEQ/G and not comprising a C8-C30 fatty chain
US20090288674A1 (en) * 2003-04-01 2009-11-26 L'oreal S.A. Cosmetic dye composition with a lightening effect for human keratin materials, comprising at least one fluorescent dye and at least one aminosilicone, and process of dyeing
US9192555B2 (en) 2010-12-07 2015-11-24 L'oreal Oxidation dye composition comprising a polycondensate of ethylene oxide and of propylene oxide, and a non-oxyalkylenated glycerolated nonionic surfactant
US20160151264A1 (en) * 2013-07-19 2016-06-02 L'oreal Dye composition comprising a particular amphoteric surfactant and an oxyethylenated amide surfactant or an oxyethylatenated fatty alcohol surfactant comprising less than 10 oe units and mixture thereof dye composition comprising a particular amphoteric surfactant and an oxyethylenated amide surfactant
US9662290B2 (en) 2012-04-24 2017-05-30 L'oreal Dyeing process using a mixture comprising a thickening polymer, obtained from an aerosol device, and device therefor
US9789034B2 (en) 2012-04-24 2017-10-17 L'oreal Dyeing process using a mixture obtained from an aerosol device comprising a liquid fatty, alcohol and surfactants
US9855198B2 (en) 2012-04-24 2018-01-02 L'oreal Dyeing process using a mixture obtained from an aerosol device comprising a nonionic fatty amide, and device therefor
US9999583B2 (en) 2013-07-19 2018-06-19 L'oreal Dye composition comprising a particular amphoteric surfactant and a sulfate or sulfonate surfactant
US10016344B2 (en) 2012-04-24 2018-07-10 L'oreal Dyeing process using a mixture obtained from an aerosol device comprising a glycerolated surfactant, and device therefor
US10071036B2 (en) * 2012-04-24 2018-09-11 L'oreal Dyeing process using a mixture comprising a branched C6-C12 polyol, obtained from an aerosol device, and device therefor
US10071038B2 (en) 2013-07-19 2018-09-11 L'oreal Dye composition comprising a particular amphoteric surfactant and a particular thickening polymer
US20220265537A1 (en) * 2019-06-28 2022-08-25 L'oreal Composition for dyeing keratin fibres and use thereof

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FR2853236B1 (fr) * 2003-04-01 2007-10-12 Oreal Composition de coloration pour matieres keratiniques humaines comprenant un colorant fluorescent et un polyol, procede et utilisation
FR2857259B1 (fr) * 2003-07-11 2007-08-24 Oreal Composition tinctoriale liquide exempte d'acide gras et comprenant du 2-methyl 1,3-propanediol, procede de teinture et dispositif
FR2870737B1 (fr) * 2004-05-28 2006-07-14 Oreal Composition pour le traitement de matieres keratiniques comprenant un compose polycarboxylique particulier et un polymere epaississant et procedes la mettant en oeuvre
FR2870723B1 (fr) * 2004-05-28 2006-07-28 Oreal Composition pour le traitement de matieres keratiniques comprenant un compose polycarboxylique particulier et un polyol particulier et procedes la mettant en oeuvre
FR2870730B1 (fr) * 2004-05-28 2006-07-14 Oreal Composition pour le traitement de fibres keratiniques comprenant un compose polycarboxylique particulier et une base d'oxydation et/ou un coupleur heterocycliques, procedes la mettant en oeuvre et dispositif
FR2879922B1 (fr) * 2004-12-23 2007-03-02 Oreal Nouveau procede de lavage des fibres keratiniques colorees avec une composition comprenant un tensioactif non ionique particulier et utilisation pour proteger la couleur
FR2910281B1 (fr) * 2006-12-21 2009-10-16 Oreal Composition de teinture d'oxydation comprenant un tensio-actif cationique, un bioheterooolysacchardie, un tensio-actif amphotere ou non ionique et un precurseur de colorant
FR2910282B1 (fr) 2006-12-21 2009-06-05 Oreal Composition de teinture directe comprenant un tensio-actif cationique, un bioheteropolysaccharide, un tensio-actif amphotere ou non ionique et un colorant direct
FR2920091A1 (fr) * 2007-08-24 2009-02-27 Oreal Composition tinctoriale comprenant une base d'oxydation aminopyrazolopyridine, un coupleur et un polyol particulier.
JP5093803B2 (ja) * 2007-09-14 2012-12-12 株式会社マンダム 整髪剤
JP2009096743A (ja) * 2007-10-15 2009-05-07 Kao Corp 染毛剤組成物
EP2202219A1 (en) 2008-12-24 2010-06-30 Kao Corporation, S.A. Mixture of amides and cosmetic compositions comprising said mixture
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US20050144739A1 (en) * 2003-12-11 2005-07-07 L'oreal Treatment of dyed keratain fibres with a surfactant composition, and use for protecting the colour
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US7749283B2 (en) 2004-02-05 2010-07-06 Wella Ag Colorant with nacreous luster for keratin fibers
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KR100622333B1 (ko) 2006-09-13
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HU0202509D0 (ja) 2002-09-28
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US20060248664A1 (en) 2006-11-09
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US7402180B2 (en) 2008-07-22
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