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WO2010142776A1 - Colorants directs d'azométhine n-oxydés ou précurseurs de ces colorants obtenus à partir de para-phénylènediamines n-alkylaminées secondaires, et procédé de coloration capillaire utilisant ces colorants - Google Patents

Colorants directs d'azométhine n-oxydés ou précurseurs de ces colorants obtenus à partir de para-phénylènediamines n-alkylaminées secondaires, et procédé de coloration capillaire utilisant ces colorants Download PDF

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Publication number
WO2010142776A1
WO2010142776A1 PCT/EP2010/058188 EP2010058188W WO2010142776A1 WO 2010142776 A1 WO2010142776 A1 WO 2010142776A1 EP 2010058188 W EP2010058188 W EP 2010058188W WO 2010142776 A1 WO2010142776 A1 WO 2010142776A1
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radical
formula
linear
iii
alkyl radical
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English (en)
Inventor
Stéphane SABELLE
Madeleine Leduc
Eric Metais
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LOreal SA
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LOreal SA
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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
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41—Amines
    • A61K8/418—Amines containing nitro groups
    • 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
    • A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
    • C07C225/24—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings
    • C07C225/26—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings
    • C07C225/28—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones the carbon skeleton containing carbon atoms of quinone rings having amino groups bound to carbon atoms of quinone rings or of condensed ring systems containing quinone rings of non-condensed quinone rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/02—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
    • C07C251/20—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups being part of rings other than six-membered aromatic rings
    • C07C251/22—Quinone imines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/90—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having more than three double bonds between ring members or between ring members and non-ring members
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B55/00—Azomethine dyes
    • C09B55/009—Azomethine dyes, the C-atom of the group -C=N- being part of a ring (Image)

Definitions

  • the invention relates to the dyeing of keratin fibres using N-oxidized azomethine direct dyes or reduced precursors of azomethine direct dyes obtained from secondary, N-alkylaminated para-phenylenediamines .
  • the subject of the present application is N-oxidized direct dyes or dye precursors thereof derived from secondary, N-alkylaminated para-phenylene diamines, especially from 2- [ ⁇ 2- [ (4-aminophenyl) amino] - ethyl ⁇ (2-hydroxyethyl) amino] ethanol, a dye composition comprising the N-oxidized direct dyes, a method for dyeing keratin fibres using the N-oxidized direct dyes and the use of these dyes for dyeing keratin fibres.
  • the method conventionally used in direct dyeing comprises applying, to the keratin fibres, direct dyes, or colouring molecules, having an affinity for said fibres, leaving them on, and then rinsing the fibres.
  • the direct dyes used up until now are nitrobenzene dyes, anthraquinones, nitropyridines or dyes of azo, xanthene, acridine, azine or triarylmethane benzene derivative type.
  • dyes result from oxidation bases and oxidation couplers which, once condensed, are applied to the hair.
  • diphenylamines such as leuco derivatives of indophenols, of indamine and of indoaniline, are used, either alone or in combination with other dyes, in dye compositions.
  • Other compounds corresponding to oxidized derivatives of leuco derivatives such as those described in documents FR 2254557 and FR 2234277, are also known to dye keratin fibres.
  • the colourings which result from direct dyeings are temporary or semi-permanent colourings, since the nature of the interactions which bind direct dyes to the keratin fibre and their desorption from the surface and/or from the core of the fibre are responsible for their low dyeing power and for their poor hold with regard to washing operations or perspiration.
  • these direct dyes are generally sensitive to the action of oxidizing agents such as aqueous hydrogen peroxide, which makes them generally unusable in lightening direct dye compositions based on aqueous hydrogen peroxide and on a basifying agent, which would be similar to oxidation dyeings.
  • Direct dyes also exhibit a certain lack of stability towards light related to the low resistance of the chromophore with respect to photochemical attacks.
  • their sensitivity to light is dependent on the distribution of their molecules, uniform or aggregated, in the substrate. Consequently, there exists a real need to search for direct dyes which make it possible to dye keratin fibres, which are stable towards light, which are also resistant to bad weather, to washing operations and to perspiration, and which are sufficiently stable in the presence of oxidizing agents such as aqueous hydrogen peroxide, so as to be able to obtain simultaneous lightening of the fibre with the advantages set out above, while at the same time exhibiting an improved toxicological profile compatible with cosmetic use on keratin fibres.
  • n represents an integer equal to 0, 1 or 2 ;
  • m represents an integer equal to 1 or 2 ;
  • R is a methyl or ethyl radical
  • halogen atom such as chlorine, or - a linear or branched Ci-C 5 , preferably C1-C2, alkyl radical;
  • Ci-C 5 a linear or branched Ci-C 5 , preferably C1-C2, alkyl radical,
  • R 3 represents: - a hydrogen atom
  • R 3 represents a radical R 6 ;
  • R 4 and R 5 which may be identical or different, represent a linear or branched Ci-C 5 alkyl radical which may be functionalized with a hydroxyl radical; in particular, the alkyl radical is a linear Ci-C 5 alkyl radical optionally functionalized with a hydroxyl radical; preferably, the alkyl radical is a linear C1-C4 alkyl radical or a linear C2 hydroxyalkyl radical; or else
  • R 4 and R 5 form, together with the nitrogen atom which bears them, a heterocycloalkyl group optionally substituted with one or more hydroxyl or (Ci-C 4 ) alkyl radicals, comprising from 5 to 7 ring members, and from 1 to 3 heteroatoms such as oxygen, sulphur or a nitrogen atom; in particular, R 4 and R 5 together form a pyrrolidino, piperidino, morpholino or piperazino ring, more particularly a pyrrolidino or piperidino ring; preferably, R 4 and R 5 represent a Ci-C 5 alkyl radical which may be functionalized with a hydroxyl radical; more particularly, the alkyl radical is a linear Ci-C 5 alkyl radical optionally functionalized with a hydroxyl radical; preferably, the alkyl radical is a linear Ci-C 4 , in particular C 2 , alkyl radical or is a linear Ci-C 4 , in particular C 2 , hydroxyalkyl
  • R 6 represents the radical corresponding to formula (a), (b) or (c) :
  • X represents an oxygen atom 0 or an NH radical
  • Y represents: - a hydroxyl radical
  • R 7 represents: o a linear or branched Ci-C 5 alkyl radical which may be functionalized with a hydroxyl radical
  • Rg and Rg which may be identical or different, represent: o a hydrogen atom, o a linear or branched Ci-C 5 alkyl radical, or o a linear or branched Ci-C 5 alkyl radical functionalized with a hydroxyl radical, preferably a linear C1-C3 hydroxyalkyl radical.
  • Another subject of the invention relates to reduced precursors of N-oxidized azomethine dyes which are colourless, which, once oxidized, generate the compounds of formula (I) , (II) or (III) as defined above. These precursors correspond to the compounds of formulae (IV) , (V) and (VI) :
  • Another subject of the invention is a dye composition for dyeing keratin fibres, comprising, in a cosmetic medium, at least one compound of formula (I) , (II), (III), (IV), (V) or (VI) as defined previously.
  • Another subject of the invention is a method for dyeing keratin fibres using a composition comprising at least one compound of formula (I) , (II) , (III) , (IV) , (V) or (VI) as defined previously.
  • Another subject of the invention is the use of the compounds of formula (I) , (II) or (III) as defined previously, as a direct dye for hair dyeing, and the use of the compounds of formula (IV) , (V) or (VI) as defined previously, as direct dye precursors for hair dyeing.
  • the direct dyes of formula (I), (II) or (III) as defined previously make it possible to remedy the drawbacks of the direct dyes conventionally used previously, and result in dyeings by direct dyeing, which exhibit very good resistance to light, to bad weather, to washing operations, to perspiration and to rubbing.
  • Their good stability with regard to oxidizing agents, such as aqueous hydrogen peroxide also makes it possible to use them for lightening direct dyeing.
  • an "organic or inorganic acid salt” is, for example, chosen from a salt derived i) from hydrochloric acid HCl, ii) from hydrobromic acid HBr, iii) from sulphuric acid H 2 SO 4 , iv) from alkylsulphonic acids: AIk-S(O) 2 OH, such as methylsulphonic acid and ethylsulphonic acid; v) from arylsulphonic acids: Ar-S(O) 2 OH, such as benzenesulphonic acid and toluenesulphonic acid; vi) from citric acid; vii) from succinic acid; viii) from tartaric acid; ix) from lactic acid; x) from alkoxysulphinic acids: AIk-O-S(O)OH, such as methoxysulphinic acid and ethoxysulphinic acid; xi) from aryloxysulphinic acids, such as tolyloxy
  • an "alkyl” radical is a saturated, linear or branched, hydrocarbon-based radical containing from 1 to 6 carbon atoms, particularly from 1 to 3 carbon atoms, such as the methyl or ethyl radical;
  • an "alkoxy" radical is an "alkyl-oxy" alkyl-O- radical in which the alkyl part is as defined previously;
  • a subject of the invention relates to N-oxidized direct dyes of formula (I) , (II) or (III) or dye precursors of formula (IV) , (V) or (VI) .
  • One particular embodiment of the invention relates to compounds of formula (I), (II), (III), (IV), (V) or (VI) for which n is zero.
  • m is 1 in formula (I) , (II) , (III) , (IV) ,
  • the compound (s) of formula (I), (II), (HI), (IV), (V) or (VI) is (are) such that n is zero and m is 1.
  • the compound (s) of formula (I), (II), (III), (IV), (V) or (VI) is (are) such that R 1 is in the 3'- position.
  • (VI) is (are) such that R 4 and R 5 , which may be identical or different, represent a linear Ci-C 5 alkyl radical optionally functionalized with a hydroxyl radical; preferably, the alkyl radical is a linear Ci-C 4 alkyl radical or a linear C 2 hydroxyalkyl radical.
  • the compound (s) of formula (I), (II), (III), (IV), (V) or (VI) is (are) such that R 4 and R 5 form, together with the nitrogen atom which bears them, a heterocycloalkyl group optionally substituted with one or more hydroxyl or (C1-C4) alkyl radicals, comprising from 5 to 7 ring members, and from 1 to 3 heteroatoms such as oxygen, sulphur or a nitrogen atom; in particular, R 4 and R 5 together form a pyrrolidino, piperidino, morpholino or piperazino ring, more particularly a pyrrolidino or piperidino ring.
  • the compound (s) of the invention is (are) such that R 4 and R 5 represent a Ci-C 5 alkyl radical which may be functionalized with a hydroxyl radical; more particularly, the alkyl radical is a linear Ci-C 5 radical optionally functionalized with a hydroxyl radical; preferably, the alkyl radical is a linear Ci-C 4 , in particular C 2 , alkyl radical or a linear Ci-C 4 , in particular C 2 , hydroxyalkyl radical.
  • the compound (s) of the invention is (are) such that R 6 represents a radical (a) as defined previously.
  • the compound (s) of the invention is (are) such that Y represents a hydroxyl radical or an -NR 8 R 9 radical with R 8 and Rg, which may be identical or different, being as defined previously, and more particularly Y is chosen from an -OH, -NH2 and -NHR 8 radical.
  • Y represents a hydroxyl radical or an -NR 8 R 9 radical with R 8 and Rg, which may be identical or different, being as defined previously, and more particularly Y is chosen from an -OH, -NH2 and -NHR 8 radical.
  • the dye precursors of formula (IV) , (V) or (VI) can be obtained by conventional reduction of the compounds of formula (I) , (II) or (III) , such as dyes 1 to 36 above.
  • the reduction can, for example, be carried out using sodium hydrosulphite and ascorbic acid.
  • the compounds of formulae (I) , (II) and (III) are obtained, in general, by reacting the derivatives 1_, 2_ or 3_ with the substituted para-phenylenediamine A, preferably in a basic medium in the presence of an oxidizing agent.
  • the base used is preferably an aqueous solution of ammonia or of sodium hydroxide and the oxidizing agent is preferably aqueous hydrogen peroxide or hydrogen peroxide.
  • the compounds corresponding to formulae (IV) , (V) and (VI) are obtained, in general, by reacting the N-oxidized compounds of formula (I) , (II) or (III) with a reducing agent.
  • This reducing agent can be chosen preferably from sodium hydrosulphite and ascorbic acid. This reducing agent is preferably sodium hydrosulphite.
  • Another subject of the invention relates to a dye composition for dyeing keratin fibres, in particular human keratin fibres such as the hair, in a cosmetic medium, comprising one or more N-oxidized direct dyes of formula (I) , (II) or (III) , or one or more dye precursors of formula (IV) , (V) or (VI) .
  • the dye composition of use in the invention generally contains an amount of dye of formula (I) , (II) or (III) , or of precursor of formula (IV) , (V) or (VI), of between 0.001% and 30% relative to the total weight of the composition. Preferably, this amount is between 0.005% and 10% by weight, and even more preferably between 0.01% and 6% by weight, relative to the total weight of the composition.
  • the dye composition containing the dye(s) of formula (I) , (II) or (III) , or preferably the precursor (s) of formula (IV), (V) or (VI), can also contain one or more oxidizing agents such as hydrogen peroxide, urea peroxide, alkali metal bromates, persalts, peracids and oxidase enzymes.
  • oxidizing agents such as hydrogen peroxide, urea peroxide, alkali metal bromates, persalts, peracids and oxidase enzymes.
  • the dye composition may also contain additional direct dyes other than those of formula (I) , (II) , (III), (IV), (V) or (VI).
  • These direct dyes are, for example, chosen from neutral, acidic or cationic nitrobenzene direct dyes, neutral, acidic or cationic azo direct dyes, tetraazapentamethine dyes, neutral, acidic or cationic quinone and in particular anthraquinone dyes, azine direct dyes, triarylmethane direct dyes, indoamine direct dyes and natural direct dyes . Mention may be made, among nitrobenzene direct dyes, without implying limitation, of the following compounds :
  • Acid Yellow 36 Acid Yellow 7
  • Acid Red 33 Acid Red 35
  • Basic Brown 17 Acid Yellow 23
  • triarylmethane dyes of the following compounds: Basic Green 1, Acid Blue 9, Basic Violet 3, Basic Violet 14, Basic Blue 7, Acid Violet 49, Basic Blue 26 and Acid Blue 7.
  • the dye composition can comprise one or more oxidation bases and/or one or more couplers conventionally used for the dyeing of keratin fibres.
  • couplers of meta-phenylenediamines, meta-aminophenols, meta- diphenols, naphthalene couplers, heterocyclic couplers and their addition salts.
  • the coupler or couplers are each generally present in an amount of between 0.001% and 10% by weight of the total weight of the dye composition, preferably between 0.005% and 6% by weight.
  • the oxidation base or bases present in the dye composition are generally present each in an amount of between 0.001% and 10% by weight of the total weight of the dye composition, preferably between 0.005% and 6% by weight.
  • the addition salts of the oxidation bases and couplers which can be used in the context of the invention are chosen in particular from the addition salts with an acid, such as hydrochlorides, hydrobromides, sulphates, citrates, succinates, tartrates, lactates, tosylates, benzenesulphonates, phosphates and acetates, and the addition salts with a base, such as alkali metal hydroxides, such as sodium hydroxide or potassium hydroxide, aqueous ammonia, amines or alkanolamines .
  • an acid such as hydrochlorides, hydrobromides, sulphates, citrates, succinates, tartrates, lactates, tosylates, benzenesulphonates, phosphates and acetates
  • a base such as alkali metal hydroxides, such as sodium hydroxide or potassium hydroxide, aqueous ammonia, amines or alkanolamines
  • the medium appropriate for the dyeing is a cosmetic medium generally comprising water or a mixture of water and of at least one organic solvent.
  • organic solvent for example, of lower C1-C4 alkanols, such as ethanol and isopropanol, polyols and polyol ethers, such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, diethylene glycol monoethyl ether and diethylene glycol monomethyl ether, aromatic alcohols, such as benzyl alcohol or phenoxyethanol, and their mixtures.
  • the solvents when they are present, are preferably present in proportions preferably of between 1% and 50% by weight approximately, with respect to the total weight of the dye composition, more preferably still between 5% and 40% by weight approximately.
  • the dye composition can also include various adjuvants conventionally used in compositions for dyeing hair, such as anionic, cationic, nonionic, amphoteric or zwitterionic surfactants, or mixtures thereof, anionic, cationic, nonionic, amphoteric or zwitterionic polymers, or mixtures thereof, inorganic or organic thickening agents, in particular anionic, cationic, nonionic and amphoteric polymeric associative thickeners, antioxidants, penetrating agents, sequestering agents, fragrances, buffers, dispersing agents, conditioning agents, such as, for example, volatile or non-volatile and modified or unmodified silicones, such as aminated silicones, film-forming agents, ceramides, preservatives, opacifying agents or conducting polymers.
  • the above adjuvants are generally present in an amount of, for each of them, between 0.01% and 20% by weight, with respect to the weight of the composition.
  • the pH of the dye composition is generally between 3 and 14 approximately. It can be adjusted to the desired value using acidifying or basifying agents commonly used in dyeing keratin fibres or else using conventional buffer systems.
  • the composition when the dye composition comprises at least one N-oxidized dye of formula (I) , (II) or (III) as defined previously, the composition has a pH of between 6 and 11.
  • the composition when the composition comprises at least one dye precursor of formula (IV) , (V) or (VI) as defined previously, the composition has a pH of between 6 and 11.
  • inorganic or organic acids such as hydrochloric acid, orthophosphoric acid, sulphuric acid, carboxylic acids, such as acetic acid, tartaric acid, citric acid or lactic acid, or sulphonic acids.
  • basifying agents by way of example, of aqueous ammonia, alkaline carbonates, alkanolamines, such as mono-, di- and triethanolamines and their derivatives, sodium hydroxide, potassium hydroxide and the compounds of following formula ( ⁇ ) :
  • R ai , R a 2, R a 3 and R a4 which may be identical or different, represent a hydrogen atom, a linear or branched Ci-C 4 alkyl radical or a Ci-C 4 hydroxyalkyl radical .
  • the dye composition may be in various forms, such as in the form of a liquid, a cream or a gel, or in any other form suitable for carrying out dyeing of keratin fibres, and in particular of the hair.
  • Another subject of the invention is a method for dyeing keratin fibres, in particular the hair, which consists in applying, to the keratin materials, in the presence or absence of an oxidizing agent, a dye composition comprising, in a cosmetic medium, at least one N-oxidized azomethine dye of formula (I) , (II) or (III) as defined previously, or an N-oxidized dye precursor of formula (IV) , (V) or (VI) as defined previously.
  • the leave-on time is generally between 3 and 50 minutes approximately, preferably 5 to 40 minutes approximately.
  • the application of the dye composition according to the invention is generally carried out at ambient temperature. However, it can be carried out at a temperature ranging from 20 to 80 0 C.
  • the examples which follow serve to illustrate the invention without, however, being limiting in nature.
  • the dyes of the examples hereinafter were fully characterized by conventional spectroscopic and spectrometric methods.
  • the 1 H NMR spectrum is in accordance with the expected structure.
  • the coloring of the hair is evaluated visually and read on a Minolta spectrocolorimeter (CM3600d, illuminant D65, angle 10°, SCI values) for the L * , a * , b * colorimetric measurements.
  • L * represents the intensity of the color
  • a * indicates the green/red color axis
  • b * indicates the blue/yellow color axis.
  • the lower the value of L the darker or more intense the color.
  • the higher the value of a * the redder the shade; the higher the value of b * , the yellower the shade.
  • L * , a * and b * represent the values measured after dyeing the natural hair comprising 90% of white hairs and L 0 * , ao * and bo * represent the values measured for the untreated natural hair comprising 90% of white hairs.
  • the coloring of the hair is evaluated visually and read on a Minolta spectrocolorimeter (CM2600d, illuminant D65, angle 10°, SCI values) for the L * , a * , b * colorimetric measurements.
  • CM2600d Minolta spectrocolorimeter
  • the following dye composition (A) was prepared: o 0.5 mmol of compound 1 of example 1 o 79.5 ml of water o 15 ml of ethanol o 5 ml of benzyl alcohol o 0.5 g of benzoic acid.
  • composition (A) This composition was applied to natural hair containing 90% white hairs, at ambient temperature for 30 minutes with a bath ratio of (0.5 g of hair per 10 g of composition (A) ) .

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Abstract

L'invention concerne la coloration de fibres de kératine au moyen de colorants directs d'azométhine N-oxydés ou de précurseurs réduits de colorants directs d'azométhine obtenus à partir de para-phénylènediamines N-alkylaminées secondaires. L'invention concerne des colorants directs N-oxydés ou des précurseurs de colorants correspondants obtenus à partir de para-phénylènediamines N-alkylaminées secondaires, notamment à partir de 2-[{2-[(4- aminophényl)amino]éthyl}(2-hydroxyéthyl)amino]éthanol, une composition de colorant comprenant les colorants directs N-oxydés, un procédé de coloration de fibres de kératine utilisant les colorants N-oxydés et l'utilisation de ces colorants pour colorer des fibres de kératine. Cette composition permet d'obtenir une coloration particulièrement stable et persistante.
PCT/EP2010/058188 2009-06-11 2010-06-10 Colorants directs d'azométhine n-oxydés ou précurseurs de ces colorants obtenus à partir de para-phénylènediamines n-alkylaminées secondaires, et procédé de coloration capillaire utilisant ces colorants Ceased WO2010142776A1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR0953906 2009-06-11
FR0953906A FR2946648A1 (fr) 2009-06-11 2009-06-11 Colorants directs azomethiniques n-oxydes ou precurseurs reduits de ces colorants obtenus a partir de para-phenylenediamines secondaires n-alkylaminees, procede de coloration capilaire a partir de ces colorants.
US18780109P 2009-06-17 2009-06-17
US61/187,801 2009-06-17

Publications (1)

Publication Number Publication Date
WO2010142776A1 true WO2010142776A1 (fr) 2010-12-16

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Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2983855A1 (fr) * 2011-12-13 2013-06-14 Oreal Colorants directs azomethiniques particuliers, composition tinctoriale comprenant au moins un tel colorant, procede de mise en oeuvre et utilisation
US8663341B2 (en) 2012-06-25 2014-03-04 The Procter & Gamble Company Hair colorant compositions comprising 2-Methoxymethy1-1,4-diaminobenzene, methods, and kits comprising the compositions
CN103998417A (zh) * 2011-12-13 2014-08-20 欧莱雅 特定的醌直接染料、包含至少一种此染料的染料组合物、其实施方法及其用途
JP2015505887A (ja) * 2011-12-13 2015-02-26 ロレアル ３芳香族アゾメチン直接染料、少なくとも１つのかかる染料を含む染料組成物、実施方法及び使用
US9012691B2 (en) 2012-10-26 2015-04-21 The Procter & Gamble Company Process for preparing primary intermediates for dyeing keratin fibers
US9309185B2 (en) 2012-10-26 2016-04-12 The Procter & Gamble Company Process for preparing primary intermediates for dyeing keratin fibers
US9539192B2 (en) 2014-04-02 2017-01-10 Noxell Corporation Hair colouring compositions, kits, method, and use thereof
US9587116B2 (en) 2014-11-04 2017-03-07 Noxell Corporation Azo direct dyes and method for dyeing hair using these dyes
US9688609B2 (en) 2014-11-04 2017-06-27 Noxell Corporation Telescoping synthesis of 2-methoxymethyl-P-phenylenediamine
US9695109B2 (en) 2014-11-04 2017-07-04 Noxell Corporation Telescoping synthesis of 2-methoxymethyl-p-phenylenediamine
US9758469B2 (en) 2014-11-04 2017-09-12 Noxell Corporation Process for the preparation of 2-substituted-1,4-benzenediamines and salts thereof

Citations (4)

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JP2017186573A (ja) * 2011-12-13 2017-10-12 ロレアル 特定のアゾメチン直接染料、少なくとも１つのこのような化合物を含む染料組成物、そのための実施方法及びその使用
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JP2017226843A (ja) * 2011-12-13 2017-12-28 ロレアル ３芳香族アゾメチン直接染料、少なくとも１つのかかる染料を含む染料組成物、実施方法及び使用
FR2983855A1 (fr) * 2011-12-13 2013-06-14 Oreal Colorants directs azomethiniques particuliers, composition tinctoriale comprenant au moins un tel colorant, procede de mise en oeuvre et utilisation
CN103998417B (zh) * 2011-12-13 2016-10-19 欧莱雅 特定的醌直接染料、包含至少一种此染料的染料组合物、其实施方法及其用途
US8663341B2 (en) 2012-06-25 2014-03-04 The Procter & Gamble Company Hair colorant compositions comprising 2-Methoxymethy1-1,4-diaminobenzene, methods, and kits comprising the compositions
US8702814B2 (en) 2012-06-25 2014-04-22 The Procter & Gamble Company Hair colorant compositions comprising 2-methoxymethyl-1,4-diaminobenzene and 2,6-diaminopyridine, methods, and kits comprising the compositions
US8709100B2 (en) 2012-06-25 2014-04-29 The Procter & Gamble Company Hair colorant compositions comprising 2-methoxymethyl-1,4-diaminobenzene and 5-amino-4-chloro-o-cresol, methods, and kits comprising the compositions
US9309185B2 (en) 2012-10-26 2016-04-12 The Procter & Gamble Company Process for preparing primary intermediates for dyeing keratin fibers
US9012691B2 (en) 2012-10-26 2015-04-21 The Procter & Gamble Company Process for preparing primary intermediates for dyeing keratin fibers
US9539192B2 (en) 2014-04-02 2017-01-10 Noxell Corporation Hair colouring compositions, kits, method, and use thereof
US9587116B2 (en) 2014-11-04 2017-03-07 Noxell Corporation Azo direct dyes and method for dyeing hair using these dyes
US9688609B2 (en) 2014-11-04 2017-06-27 Noxell Corporation Telescoping synthesis of 2-methoxymethyl-P-phenylenediamine
US9695109B2 (en) 2014-11-04 2017-07-04 Noxell Corporation Telescoping synthesis of 2-methoxymethyl-p-phenylenediamine
US9758469B2 (en) 2014-11-04 2017-09-12 Noxell Corporation Process for the preparation of 2-substituted-1,4-benzenediamines and salts thereof

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