US20090249564A1 - Hair dye compositions - Google Patents

Hair dye compositions Download PDF

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Publication number
US20090249564A1
US20090249564A1 US12/278,715 US27871507A US2009249564A1 US 20090249564 A1 US20090249564 A1 US 20090249564A1 US 27871507 A US27871507 A US 27871507A US 2009249564 A1 US2009249564 A1 US 2009249564A1
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Prior art keywords
alkyl
substituted
hydrogen
group
cycloalkyl
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US12/278,715
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Inventor
Roxana Barbieru
Werner Russ
Dominic Pratt
Hartmut Moehring
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Dystar Textilfarben GmbH and Co Deutschland KG
Kao Corp
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Dystar Textilfarben GmbH and Co Deutschland KG
Kao Corp
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Assigned to KAO CORPORATION, DYSTAR TEXTILFARBEN GMBH & CO. DEUTSCHLAND KG reassignment KAO CORPORATION ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: RUSS, WERNER, BARBIERU, ROXANA, MOEHRING, HARTMUT, PRATT, DOMINIC
Publication of US20090249564A1 publication Critical patent/US20090249564A1/en
Abandoned legal-status Critical Current

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    • 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
    • C07C225/32—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 condensed quinone ring systems formed by at least three rings
    • C07C225/34—Amino anthraquinones
    • 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
    • A61K8/35—Ketones, e.g. benzophenone
    • A61K8/355—Quinones
    • 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
    • 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
    • C07C225/32—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 condensed quinone ring systems formed by at least three rings
    • C07C225/34—Amino anthraquinones
    • C07C225/36—Amino anthraquinones the carbon skeleton being further substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • 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
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/16—Amino-anthraquinones
    • C09B1/20—Preparation from starting materials already containing the anthracene nucleus
    • C09B1/207—Dyes with amino groups and with onium groups
    • 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
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
    • C09B1/501—Amino-hydroxy-anthraquinones; Ethers and esters thereof containing onium groups
    • 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
    • C09B69/00—Dyes not provided for by a single group of this subclass
    • C09B69/001—Dyes containing an onium group attached to the dye skeleton via a bridge

Definitions

  • the present invention relates to hair dye compositions containing anthraquinone hair dyes.
  • Hair dyes can be classified by the dye to be used therefore, or by whether they have bleaching action of melanin or not.
  • Typical examples include a two-part permanent hair dye composed of a first part containing an alkali agent, an oxidation dye and optionally a direct dye such as a nitro dye and a second part containing an oxidizing agent; and a one-part semi-permanent hair dye containing an organic acid or an alkali agent, and an acid dye, basic dye or direct dye such as a nitro dye.
  • the above-described permanent hair dye is however accompanied by the drawback that the color tone imparted by an oxidation dye is not so vivid and that they damage the hair.
  • a nitro dye or cationic dye for a two-component hair dye containing an oxidizing agent has been attempted in order to produce various color tones (refer to, for example, Japanese Patent Laid-Open No. 1994-271435 and EP 1 133 976 A2).
  • a permanent hair dye formulation containing current direct dyes typically develop a vivid color just after dyeing, but the color fades away quickly over time and which leads to a dull end result.
  • the use of many direct dyes involves such problems as decomposition when mixed with a peroxide serving as an oxidizing agent and incompatibility with the formulation.
  • the above described semi-permanent hair dye formulations are accompanied by the drawback that the color imparted typically displays low durability.
  • Such dyes must be high performing and toxicologically safe.
  • the present invention provides hair dye compositions comprising one or more dyestuffs of the general formula (I)
  • R is hydrogen, alkyl, alkyl substituted by —OR 2 —, —SR 3 or —NR 5 R 4 , hydroxyalkyl, polyhydroxyalkyl, cycloalkyl, aryl substituted by R 10 , R 11 O-alkyl, —OR 12 , —R 13 , —N 14 R 15 , —CONR 15 R 16 , —C(O)OR 17 , —SO 2 —NR 18 R 19 , —SO 2 OR 20 , —C(O)R 21 or —SO 2 R 22 , —C(O)R 6 , —SO 2 NR 7 R 8 or —SO 2 R 9 ;
  • X is hydrogen, —OR 230 , —SR 240 , —NR 250 R 260 , —SO 2 NR 270 R 280 , —CONR 290 R 300 , —SO 2 OR 310 , —C(O)OR 320 , —C(O)
  • each of R′, R′′ and R′′′ is alkyl, aryl, arylalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, heterocycloalkyl, heterocycloalkyl-alkyl, either of which can be substituted by heteroatom containing groups or R′ and R′′ form together with the nitrogen to which they are bonded a 5- or 6-membered heterocyclic ring; and
  • a ⁇ is a cosmetically acceptable anion; whereby the dyestuff of the formula (I) contains exactly one group Q; whereby at least one of the groups Y and Z are groups other than hydrogen; and whereby T and R 1 are hydrogen if X is different from hydrogen.
  • Alkyl groups may be straight-chain or branched and are preferably (C 1 -C 6 )-alkyl groups, for example methyl, ethyl, n-propyl, isopropyl, n-butyl, n-pentyl, isopentyl or n-hexyl.
  • Cycloalkyl is preferably (C 3 -C 8 )-cycloalkyl and especially preferably cyclopentyl and cyclohexyl.
  • Aryl groups are preferably phenyl or naphthyl groups.
  • Halogen is preferably chlorine, bromine and fluorine.
  • a 5- or 6-membered heterocyclic ring which is formed by R′ and R′′ is preferably a pyrrolidine, piperidine, morpholine or piperazine ring.
  • R′, R′′ and R′′′ are preferably benzyl or (C 1 -C 6 )-alkyl and especially preferably benzyl, methyl and ethyl.
  • the dyestuffs of the general formula (I) may be salts of an organic or inorganic acid. Consequently, A ⁇ may be for example chloride, bromide, iodide, hydroxide, hydrogenphosphate, phosphate, carbonate, hydrogencarbonate, hydrogensulfate, perchlorate, fluoroborate, chlorozincate, methylsulfate, ethylsulfate, acetate, propionate, lactate or citrate or mixtures thereof.
  • a ⁇ is generally given by the preparation method of the dyestuff of the general formula (I).
  • Preferred meanings of A ⁇ are chloride, sulfate, hydrogensulfate, methylsulfate, ethylsulfate, phosphate, formate, acetate and lactate.
  • Especially preferred dye compositions of the present invention comprise one or more dyestuffs of the general formula (I) in which
  • Z, T and R 1 are hydrogen;
  • R is hydrogen or (C 1 -C 6 )-alkyl;
  • Y is —NR 51 R 52 , —NHSO 2 R 58 or —OR 58 , wherein R 51 is hydrogen and R 52 is hydrogen, (C 1 -C 6 )-alkyl, hydroxy-(C 1 -C 6 )-alkyl or phenyl;
  • R 53 is hydrogen, (C 1 -C 6 )-alkyl or phenyl; and
  • R 58 is (C 1 -C 6 )-alkyl or phenyl;
  • X is —OR 230 or —SR 240 , wherein R 230 and R 240 are (C 1 -C 6 )-alkyl substituted by Q, phenyl substituted by Q, (C 1 -C 6 )-alkyl-SO 2 -phenyl wherein the alkyl group is substituted by Q or (C 1 -C 6
  • dyestuffs of this type are the dyestuffs of the formulae (Ic), (Ig), (Ih), (Ii), (Ir), (Is), (Idd), (Iee and (Iff)
  • compositions of the present invention comprise one or more dyestuffs of the general formula (I) in which
  • R is hydrogen or (C 1 -C 6 )-alkyl; Z, T and R 1 are hydrogen; Y is —NR 51 R 52 or OR 53 , wherein R 51 and R 53 are hydrogen, R 52 is (C 1 -C 6 )-alkyl, hydroxy-(C 1 -C 6 )-alkyl or phenyl; X is —SO 2 NR 270 R 280 , —CONR 290 R 300 , —SO 2 OR 310 , —C(O)OR 320 , wherein R 270 and R 290 are hydrogen or (C 1 -C 6 )-alkyl; R 280 , R 300 , R 310 and R 320 are (C 1 -C 6 )-alkyl substituted by Q, hydroxy(C 1 -C 6 )-alkyl substituted in the alkyl group by Q or phenyl substituted by Q; Q is a tris(C 1 -C 6 )-alkyl-ammoni
  • dyestuffs of this type are the dyestuffs of the formulae (Igg) to (Ijj):
  • Still further especially preferred dye compositions of the present invention comprise one or more dyestuffs of the general formula (I) in which
  • R is hydrogen or (C 1 -C 6 )-alkyl; T and R 1 are hydrogen; Z is —NR 51 R 52 or —NHC(O)R 56 , wherein R 51 is hydrogen and R 52 is hydrogen or (C 1 -C 6 )-alkyl and R 56 is (C 1 -C 6 )-alkyl or phenyl; Y is —NR 51 R 52 , wherein R 51 is hydrogen, R 52 is (C 1 -C 6 )-alkyl, hydroxy-(C 1 -C 6 )-alkyl or phenyl; X is —OR 230 , —SO 2 NR 270 R 280 or —SO 2 OR 310 , wherein R 230 and R 310 are (C 1 -C 6 )-alkyl substituted by Q, hydroxy(C 1 -C 6 )-alkyl substituted in the alkyl group by Q, phenyl substituted by Q; R 270 is hydrogen, R 280 is
  • dyestuffs of this type are the dyestuffs of the formulae (Ix) and (Iy):
  • Still further especially preferred dye compositions of the present invention comprise one or more dyestuffs of the general formula (I) in which
  • Y, T and R 1 are hydrogen;
  • R is hydrogen or (C 1 -C 6 )-alkyl;
  • Z is —NR 51 R 52 or —NHC(O)R 56 , wherein R 51 is hydrogen and R 52 is hydrogen or (C 1 -C 6 )-alkyl and R 56 is (C 1 -C 6 )-alkyl or phenyl;
  • X is —OR 230 , —SO 2 NR 270 R 280 , —SO 2 OR 310 or —NR 250 R 260 wherein R 230 and R 310 are (C 1 -C 6 )-alkyl substituted by Q, hydroxy-(C 1 -C 6 )-alkyl substituted in the alkyl group by Q, or phenyl substituted by Q;
  • R 27 is hydrogen,
  • R 28 is (C 1 -C 6 )-alkyl substituted by Q or hydroxy-(C 1 -C 6 )-alkyl substituted in
  • dyestuffs of this type are the dyestuffs of the formulae (Iz), (Iaa), (Ibb) and (Icc):
  • Still further especially preferred dye compositions of the present invention comprise one or more dyestuffs of the general formula (I) in which
  • R is hydrogen or (C 1 -C 6 )-alkyl
  • Z is —NR 51 R 52 wherein R 51 is hydrogen and R 52 is hydrogen or (C 1 -C 6 )-alkyl
  • Y is OR 53 , wherein R 53 is hydrogen; X is hydrogen,
  • R 1 is —NH 2 or —NH-alkyl
  • T is alkyl substituted by Q or aryl substituted by —OR 230 ; wherein R 230 is (C 1 -C 6 )-alkyl substituted by Q, hydroxy(C 1 -C 6 )-alkyl substituted in the alkyl group by Q, —C(O)R 600 or —SO 2 R 900 wherein R 600 and R 900 are (C 1 -C 6 )-alkyl substituted by Q or hydroxy(C 1 -C 6 )-alkyl substituted in the alkyl group by Q; Q is a tris(C 1 -C 6 )-alkyl-ammonium group, a bis(C 1 -C 6 )-alkyl-benzyl-ammonium group, a methyl-morpholinium group or a methyl-pyrrolidinium group; and A ⁇ is chloride, sulfate, hydrogensulfate, methylsulfate, ethylsulfate, phosphat
  • dyestuffs of this type are the dyestuffs of the formulae (Ikk) to (Inn):
  • the dyestuffs of the formula (I) are partly known from for example U.S. Pat. No. 2,737,517, U.S. Pat. No. 2,888,467, CH 463666, FR 1,363,216 or DE 16 19 365.
  • the present invention provides dyestuffs of the general formula (Ia)
  • R is hydrogen, alkyl, alkyl substituted by —OR 2 , —SR 3 or —NR 5 R 4 , hydroxyalkyl, polyhydroxyalkyl, cycloalkyl, aryl substituted by R 10 , R 11 O-alkyl, —OR 12 , —SR 13 , —NR 14 R 15 , —CONR 15 R 16 , —C(O)OR 17 —SO 2 —NR 18 R 19 , —SO 2 OR 20 , —C(O)R 21 or —SO 2 R 22 , —C(O)R 6 , —SO 2 NR 7 R 8 or —SO 2 R 9 ;
  • X is hydrogen, —OR 235 , —SO 2 NR 270 R 280 or —SO 2 OR 310 ;
  • Y is hydrogen, —NR 51 R 52 , —OR 53 , —SR 54 , —SO 2 NHR 55 , —NHC(O)R 56 ,
  • Z is hydrogen or amino;
  • R 1 is hydrogen or hydroxy;
  • R is hydrogen;
  • Y is hydroxy or amino; and
  • X is —OR 235 , wherein R 235 is (C 1 -C 6 )-alkyl-NH—SO 2 -phenyl, wherein the alkyl group is substituted by Q; and T is hydrogen or aryl substituted by —OR 230 , wherein R 230 is (C 1 -C 6 )-alkyl substituted by Q, hydroxy(C 1 -C 6 )-alkyl substituted in the alkyl group by Q, —C(O)R 600 or —SO 2 R 900 , wherein R 600 and R 900 are (C 1 -C 6 )-alkyl substituted by Q or hydroxy-(C 1 -C 6 )-alkyl substituted in the alkyl group by Q.
  • Especially preferred dyestuffs of the formula (Ia) are the dyestuffs (Ii), (Is) and (Ikk) to (Inn).
  • the dyestuffs of the general formula (I) can be obtained by generally known methods, for instance via Ullmann type substitutions of anthraquinone derivatives which contain exchangeable atoms or groups such as halogen, sulfonic acid group or nitro group by aliphatic amines, aromatic amines, alcohols, phenols, thiols, thiophenols and sulfur containing reagents.
  • General procedures are described, for example, in “Ullmann's Encyclopedia of Industrial Chemistry”, VCH Verlagsgesellschaft, Weinheim 1985, volume A2, Anthraquinone Dyes and Intermediates, pages 357-412.
  • the preparing reactions of the dyestuffs can be carried out in an organic solvent such as dimethylformamide, dimethylacetamide, halogenobenzenes etc., in water or preferably in surplus reagent. It is of advantage to carry out the reactions at elevated temperatures, preferably between 60° C. and 150° C. Acid-binding agents must be added or an excess of amine is used. Adding usual catalysts such as copper or copper salts or mixtures thereof can be advantageously.
  • the alkoxyanthraquinones of the general formula (I) can be obtained via the conversion of anthraquinonesulfonic acids by alcoholic alkali at 50-130° C.
  • the direct replacement of halogen to alkoxy- or aryloxyanthraquinones can be advantageously carried out with e.g. alcoholate or phenolate generated in situ with alkali or advantageously with metallic sodium. It is advantageously to carry out these reactions under water free conditions with dried reagents.
  • Preferred hair dye compositions according to the present invention comprise dyestuff mixtures comprising one or more dyestuffs of the general formula (I) and one or more direct or oxidation dyestuff.
  • Examples of such direct dyes include dyes from the publicly available dyestuff list issued by The European Cosmetic, Toiletry and Perfumery Association (COLIPA) and especially Acid Yellow 1, Disperse Red 17, Basic Brown 17, Acid Black I, 4-Nitro-o-phenylenediamine, Picramic acid, HC Red 13, N,N-bis(2-hydroxyethyl)-2-nitro-p-phenylenediamine, HC Red 7, HC Blue 2, HC Yellow 4, HC Yellow 2, HC Orange 1, HC Red 1, HC Red 3,4-Amino-3-nitrophenol, 2-Hydroxyethylamino-5-nitroanisole, 3-Nitro-p-hydroxyethylaminophenol, 3-Methylamino-4-nitrophenoxytheanol, 2-nitro-5-glyceryl methylaniline, HC Violet 1, HC Orange 2, HC Yellow 9,4-Nitrophenylaminoethylurea, HC Red 10, HC Red 11, 2-Hydroxy-ethyl
  • Preferred inventive hair dye compositions containing mixtures usually contain one or more dyestuffs of the general formula (I) in an amount 90 to 10 wt. % and one or more direct or oxidation dyestuff in an amount of 10 to 90 wt. % based on the total weight of the dyestuff mixture.
  • they contain one or more dyestuffs of the general formula (I) in an amount 80 to 20 wt. % and one or more direct or oxidation dyestuff in an amount of 20 to 80 wt. % based on the total weight of the dyestuff mixture.
  • the they contain one or more dyestuffs of the general formula (I) in an amount 65 to 35 wt. % and one or more direct or oxidation dyestuff in an amount of 35 to 65 wt. % based on the total weight of the dyestuff mixture.
  • compositions according to the present invention contain the dyestuff of the general formulae (I) in amounts of 0.0001 to 20 wt. %, preferably 0.001 to 20 wt. %, more preferably from 0.01 to 10 wt. % and especially preferably from 0.05 to 5 wt. %, based on the weight of the hair dye composition.
  • Hair dye compositions according to the present invention comprising a dyestuff mixture as described above usually have a dyestuff content between 0.001 to 20 wt. %, preferably from 0.01 to 20 wt. %, more preferably from 0.05 to 10 wt. % and especially preferably from 0.1 to 5 wt. %, based on the weight of the hair dye composition.
  • the inventive dyestuffs of the general formula (I) exhibit a high storage stability within a wide pH range from 2 to 11, which is a pH range ordinarily employed for hair dyes, so that the hair dye composition of the present invention can be used at any pH in the above-described pH range.
  • Use in a pH range of from 2 or greater is however preferred from the viewpoint of dyeing property.
  • Hair dye compositions of a pH range of 2 to 8 and hair dye compositions of a pH range of 8 to 12 are preferred.
  • the desired pH value is usually adjusted using an alkali agent.
  • alkali agents include ammonia, alkanolamines such as monoethanolamine and isopropanolamine or salts thereof, guanidium salts such as guanidine carbonate and hydroxides such as sodium hydroxide.
  • the inventive hair dye compositions contain an alkali agent preferably in an amount of from 0.01 to 20 wt. %, more preferably from 0.1 to 10 wt. %, especially preferably from 0.5 to 5 wt. % based on the total weight of the composition.
  • the inventive hair dye composition may also be applied to hair together with an oxidizing agent.
  • it can be provided as a two-part composition composed of a first part containing the dyestuff of the general formula (I) and a second part containing an oxidizing agent.
  • hair dyeing and bleaching can be carried out simultaneously, which facilitates more vivid hair dyeing.
  • oxidizing agent examples include hydrogen peroxide, persulfates such as ammonium persulfate, potassium persulfate and sodium persulfate, perborates such as sodium perborate, percarbonates such as sodium percarbonate and bromates such as sodium bromate and potassium bromate.
  • Hydrogen peroxide is especially preferred from the viewpoints of hair bleaching property, stability and effectiveness of the inventive dyestuffs of the general formula (I). Hydrogen peroxide may be used in combination with another oxidizing agent.
  • the oxidizing agent is preferably used in an amount of from 0.5 to 10 wt. %, especially preferably from 1 to 8 wt. %, based on the hair dye composition.
  • the first part containing the inventive dyestuff of the general formula (I) and the second part containing the oxidizing agent are mixed at a volume ratio preferably ranging from 2:1 to 1:3.
  • an oxidation dye in the hair dye composition of the present invention, can be used in combination with the inventive dyestuff of the general formula (I).
  • Such combined use enables considerably vivid and intense dyeing which cannot be accomplished by the single use of the oxidation dye.
  • known developers and couplers ordinarily employed for an oxidation type hair dye can be used.
  • Examples of the developer include paraphenylenediamine, toluene-2,5-diamine, 2-chloro-paraphenylenediamine, N-methoxyethyl-paraphenylenediamine, N,N-bis(2-hydroxyethyl)-paraphenylenediamine, 2-(2-hydroxyethyl)-paraphenylenediamine, 2,6-dimethyl-para-phenylenediamine, 4,4′-diaminodiphenylamine, 1,3-bis(N-(2-hydroxyethyl)-N-(4-aminophenyl)amino)-2-propanol, PEG-3,2,2′-paraphenylenediamine, paraaminophenol, paramethylaminophenol, 3-methyl-4-aminophenol, 2-aminomethyl-4-aminophenol, 2-(2-hydroxyethylaminomethyl)-4-aminophenol, orthoaminophenol, 2-amino-5-methylphenol, 2-amin
  • coupler examples include metaphenylenediamine, 2,4-diaminophenoxyethanol, 2-amino-4-(2-hydroxyethylamino)anisole, 2,4-diamino-5-methylphenetole, 2,4-diamino-5-(2-hydroxyethoxy)toluene, 2,4-dimethoxy-1,3-diaminobenzene, 2,6-bis(2-hydroxyethylamino)toluene, 2,4-diamino-5-fluorotoluene, 1,3-bis(2,4-diaminophenoxy)propane, metaminophenol, 2-methyl-5-aminophenol, 2-methyl-5-(2-hydroxyethylamino)phenol, 2,4-dichloro-3-aminophenol, 2-chloro-3-amino-6-methylphenol, 2-methyl-4-chloro-5-aminophenol, N-cyclopentyl-metaaminophenol, 2-methyl-4-me
  • each of the developer and coupler at least two of the above-described developers or couplers are usable.
  • the content of each of them is preferably from 0.01 to 20 wt. %, especially preferably from 0.05 to 10 wt. % based on the hair dye composition.
  • an autoxidation dye typified by an indole or an indoline, or a known direct dye such as a nitro dye or a disperse dye can also be added.
  • Addition of a polyol, polyol alkyl ether, cationic or amphoteric polymer and/or silicone to the hair dye composition of the present invention is preferred, because the resulting composition can dye the hair uniformly and provides improved cosmetic effects of the hair.
  • those ordinarily employed as a raw material for cosmetics can be added to the hair dye composition of the present invention.
  • an optional component include hydrocarbons, animal or vegetable fats and oils, higher fatty acids, organic solvents, penetration promoters, cationic surfactants, natural or synthetic polymers, higher alcohols, ethers, amphoteric surfactants, nonionic surfactants, anionic surfactants, protein derivatives, amino acids, antiseptics, chelating agents, stabilizers, antioxidants, plant extracts, crude drug extracts, vitamins, colorants, perfumes and ultraviolet absorbers.
  • the hair dye composition of the present invention can be prepared in a conventional manner to form a one-part composition or a two-part composition having a first part containing an alkali agent and a second part containing an oxidizing agent.
  • the inventive dyestuff of the general formula (I) may be incorporated in at least one of these parts of the two-part or three-part composition.
  • the first part is typically prepared by mixing the Inventive dyestuff of the general formula (I) and optionally an oxidation dye and adjusting the pH of the mixture to 8 to 12 with an alkali agent such as ammonia.
  • the second part is prepared by incorporating about 2 to 6 wt. % of hydrogen peroxide, adjusting the mixture to weakly acidic with phosphoric.
  • the hair dye composition of the present invention can be provided in the form of powder, transparent liquid, emulsion, cream, gel, paste, aerosol, aerosol foam or the like. It preferably has a viscosity of 2000 to 100000 mPa ⁇ s upon its application to the hair (after mixing of all the parts when the composition is a two-part or three-part type). The above-described viscosity is measured at 20° C. by using a Brookfield rotary viscometer (No. 5 spindle, 5 rpm).
  • the present invention also refers to a process for colouring hair characterized in that a hair dye composition as described above is applied onto hair, left for 1 to 45 minutes and than rinsed off from hair.
  • the hair dye composition is mixed with a composition comprising at least one oxidizing agent.
  • the precipitate was filtered off and washed with acetone. Upon drying 5.8 parts of the dye of the formula Idd were obtained.
  • the red dye Idd is very good water-soluble.
  • the analytic data are consistent with the assigned structure for dye Idd.
  • Dyestuff of general formula (I) 0.5 g iso-Propanol 5.0 g Ammonium Hydroxide (25%) 5.0 g Water up to 100 g pH 10.2
  • Dyestuff of general formula (I) 0.5 g iso-Propanol 5.0 g Ammonium Hydroxide (25%) 5.0 g Hydrogen Peroxide (50%) 6.0 g Water up to 100 g pH 10.2

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US12/278,715 2006-02-09 2007-02-02 Hair dye compositions Abandoned US20090249564A1 (en)

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EP06101466.8 2006-02-09
EP06101466A EP1820826A1 (en) 2006-02-09 2006-02-09 Dyestuffs and Hair Dye Compositions
PCT/EP2007/051043 WO2007090800A2 (en) 2006-02-09 2007-02-02 Hair dye compositions

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US12/279,003 Expired - Fee Related US7776106B2 (en) 2006-02-09 2007-02-02 Dyestuffs and hair dye compositions

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US (2) US20090249564A1 (enrdf_load_stackoverflow)
EP (3) EP1820826A1 (enrdf_load_stackoverflow)
JP (2) JP5176026B2 (enrdf_load_stackoverflow)
KR (2) KR20080093115A (enrdf_load_stackoverflow)
CN (2) CN101379144B (enrdf_load_stackoverflow)
AU (2) AU2007213796A1 (enrdf_load_stackoverflow)
CA (2) CA2641863A1 (enrdf_load_stackoverflow)
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TW (2) TW200731994A (enrdf_load_stackoverflow)
WO (2) WO2007090800A2 (enrdf_load_stackoverflow)

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DE102011089218A1 (de) * 2011-12-20 2013-06-20 Henkel Ag & Co. Kgaa Färbemittel mit kationischen direktziehenden Farbstoffen und Lecithine
DE102011089223A1 (de) 2011-12-20 2013-06-20 Henkel Ag & Co. Kgaa Färbemittel mit direktziehenden Farbstoffen und zwitterionischen Tensiden
DE102011089221A1 (de) 2011-12-20 2013-06-20 Henkel Ag & Co. Kgaa Färbemittel mit direktziehenden Farbstoffen und Phospat-Tensiden
DE102011089216A1 (de) 2011-12-20 2013-06-20 Henkel Ag & Co. Kgaa Färbemittel mit direktziehenden Farbstoffen und amphotere Tensiden
DE102011089217A1 (de) * 2011-12-20 2013-06-20 Henkel Ag & Co. Kgaa Mittel zum Färben von keratinischen Fasern enthaltend hationische Anthrachinonfarbstoffe und anionische Polymere
DE102011089220A1 (de) * 2011-12-20 2013-06-20 Henkel Ag & Co. Kgaa Mittel zum Färben von keratinischen Fasern enthaltend kationische Anthrachinonfarbstoffe und Fettsäuretriglyceride
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WO2007090799A3 (en) 2008-01-10
WO2007090799A2 (en) 2007-08-16
JP5176026B2 (ja) 2013-04-03
RU2008136053A (ru) 2010-03-20
JP2009531285A (ja) 2009-09-03
CN101379144A (zh) 2009-03-04
WO2007090800A2 (en) 2007-08-16
JP2009529582A (ja) 2009-08-20
WO2007090800A3 (en) 2007-12-21
TW200732427A (en) 2007-09-01
US20090217466A1 (en) 2009-09-03
RU2008136055A (ru) 2010-03-20
EP1984459A2 (en) 2008-10-29
CN101379144B (zh) 2012-08-22
CN101379145A (zh) 2009-03-04
CA2641838A1 (en) 2007-08-16
US7776106B2 (en) 2010-08-17
TWI412565B (zh) 2013-10-21
EP1984458A2 (en) 2008-10-29
AU2007213797A1 (en) 2007-08-16
JP5286567B2 (ja) 2013-09-11
AU2007213796A1 (en) 2007-08-16
EP1820826A1 (en) 2007-08-22
TW200731994A (en) 2007-09-01

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