US20020004955A1 - Dye composition for keratin fibers, with a cationic direct dye and a polyol or polyol ether - Google Patents

Dye composition for keratin fibers, with a cationic direct dye and a polyol or polyol ether Download PDF

Info

Publication number
US20020004955A1
US20020004955A1 US09/321,889 US32188999A US2002004955A1 US 20020004955 A1 US20020004955 A1 US 20020004955A1 US 32188999 A US32188999 A US 32188999A US 2002004955 A1 US2002004955 A1 US 2002004955A1
Authority
US
United States
Prior art keywords
chosen
radicals
alkyl
radical
alkyl radicals
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.)
Granted
Application number
US09/321,889
Other versions
US6371994B2 (en
Inventor
Gerard Lang
Jean Cotteret
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.)
LOreal SA
Original Assignee
LOreal SA
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9526825&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=US20020004955(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by LOreal SA filed Critical LOreal SA
Assigned to L'OREAL S.A. reassignment L'OREAL S.A. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: COTTERET, JEAN, LANG, GERARD
Publication of US20020004955A1 publication Critical patent/US20020004955A1/en
Application granted granted Critical
Publication of US6371994B2 publication Critical patent/US6371994B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B44/00Azo dyes containing onium groups
    • C09B44/10Azo dyes containing onium groups containing cyclammonium groups attached to an azo group by a carbon atom of the ring system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/06Preparations for styling the hair, e.g. by temporary shaping or colouring
    • A61Q5/065Preparations for temporary colouring the hair, e.g. direct dyes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4926Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A61K8/4946Imidazoles or their condensed derivatives, e.g. benzimidazoles
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/58Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing atoms other than carbon, hydrogen, halogen, oxygen, nitrogen, sulfur or phosphorus
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/02Material containing basic nitrogen

Definitions

  • the invention relates to a dye composition for keratin fibers, in particular for human keratin fibers such as the hair, comprising, in a medium which is suitable for dyeing, at least one cationic direct dye of given formula, and at least glycerol and/or one specific polyol and/or polyol ether.
  • the invention also relates to the dyeing processes and devices using the composition.
  • the first is semi-permanent or temporary dyeing, or direct dyeing, which involves dyes capable of giving the hair's natural color a more or less pronounced color change which may withstand shampooing several times.
  • These dyes are known as direct dyes; they can be used with or without an oxidizing agent.
  • the aim is to obtain a lightening coloration.
  • the lightening coloration is carried out by applying to the hair the mixture, prepared at the time of use, of a direct dye and an oxidizing agent, and in particular makes it possible to obtain, by lightening the melanin in the hair, an advantageous effect such as a unified color in the case of grey hair, or to bring out the color in the case of naturally pigmented hair.
  • the second is permanent dyeing or oxidation dyeing.
  • This is carried out with dyes known as “oxidation” dyes comprising oxidation dye precursors and couplers.
  • Oxidation dye precursors commonly known as “oxidation bases” are initially colorless or weakly colored compounds which develop their dyeing power on the hair in the presence of oxidizing agents added at the time of use, leading to the formation of colored compounds and dyes.
  • the formation of these colored compounds and dyes results either from an oxidative condensation of the “oxidation bases” with themselves or from an oxidative condensation of the “oxidation bases” with coloration modifier compounds commonly known as “couplers”, which are generally present in the dye compositions used in oxidation dyeing.
  • a first subject of the present invention is thus a composition for dyeing keratin fibers, and in particular human keratin fibers such as the hair, containing, in a medium which is suitable for dyeing, (i) at least one cationic direct dye whose structure corresponds to formula (I) below, characterized in that it also contains (ii) at least glycerol and/or one specific polyol and/or polyol ether.
  • the cationic direct dye which can be used according to the present invention is a compound of formula (I) below:
  • R is chosen from C 1 -C 4 alkyl radicals and a phenyl radical having a substituent chosen from C 1 -C 4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
  • R 2 is chosen from C 1 -C 4 alkyl radicals and a phenyl radical
  • R 3 and R 4 which may be identical or different, are chosen from C 1 -C 4 alkyl radicals and a phenyl radical or, in the case of structure A 1 , can together form a substituted benzene ring, and in the case of structure A 2 , can together form a benzene ring optionally having at least one substituent chosen from C 1 -C 4 alkyl, C 1 -C 4 alkoxy and NO 2 radicals;
  • R 3 can ailso denote a hydrogen atom
  • Z is chosen from an oxygen atom, a sulphur atom, and —NR 2 groups;
  • M is chosen from —CH, —CR, where R is chosen from C 1 -C 4 alkyl radicals, and —N + R 5 (X ⁇ ) r groups;
  • K is chosen from —CH, —CR, where R is chosen from C 1 -C 4 alkyl radicals, and —N + R 5 (X ⁇ ) r groups;
  • P is chosen from —CH, —CR, where R is chosen from C 1 -C 4 alkyl radicals, and —N + R 5 (X ⁇ ) r groups;
  • r denotes 0 or 1
  • R 5 is chosen from an atom O ⁇ , C 1 -C 4 alkoxy radicals and C 1 -C 4 alkyl radicals;
  • R 6 and R 7 which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C 1 -C 4 alkyl radicals, C 1 -C 4 alkoxy radicals and an —NO 2 radical;
  • X ⁇ is an anion, preferably chosen from chloride, iodide, methyl sulphate, ethyl sulphate, acetate and perchlorate;
  • R 4 is a C 1 -C 4 alkyl radical and Z is a sulphur atom, R 3 is not a hydrogen atom;
  • R 6 or R 7 is other than a hydrogen atom
  • K is ⁇ N + R 5 (X ⁇ ) r , then M ⁇ P and is —CH or —CR;
  • R 8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C 1 -C 4 alkyl radicals, C 1 -C 4 alkoxy radicals, a radical —OH, a radical —NO 2 , —NHR 11 radicals, —NR 12 R 13 radicals, and —NHCO(C 1 -C 4 )alkyl radicals or forms, with R 9 , a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
  • R 9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C 1 -C 4 alkyl radicals, and C 1 -C 4 alkoxy radicals, or forms, with R 10 or R 11 , a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
  • R 10 is chosen from a hydrogen atom, an —OH radical, —NHR 11 radicals and —NR 12 R 13 radicals;
  • R 11 is chosen from a hydrogen atom, C 1 -C 4 alkyl radicals, C 1 -C 4 monohydroxyalkyl radicals, C 2 -C 4 polyhydroxyalkyl radicals and a phenyl radical;
  • R 12 and R 13 which may be identical or different, are chosen from C 1 -C 4 alkyl radicals, C 1 -C 4 monohydroxyalkyl radicals and C 2 -C 4 polyhydroxyalkyl radicals; or
  • R 14 and R 15 which may be identical or different, are chosen from a hydrogen atom and C 1 -C 4 alkyl and phenyl radicals;
  • Y denotes a —CO— radical or a radical
  • n 0 or 1 where, when n denotes 1, U denotes a —CO— radical.
  • the C 1 -C 4 alkyl or alkoxy group preferably denotes methyl, ethyl, butyl, methoxy or ethoxy.
  • the cationic direct dyes of formula (I) which can be used in the dye compositions in accordance with the invention are known compounds and are described, for example, in patent applications FR-2,189,006, FR-2,285,851 and FR-2,140,205 and its Certificates of Addition, the disclosures of all of which are specifically incorporated by reference herein.
  • cationic direct dyes of formula (I) which can be used in the dye compositions in accordance with the invention, those of formula (I) in which the symbol A denotes structure A3 while the symbol B denotes structure B1 or B2 are particularly preferred.
  • the cationic direct dye(s) used according to the invention preferably represent(s) from 0.001 to 10% by weight approximately relative to the total weight of the dye composition, and even more preferably from 0.005 to 5% by weight approximately relative to this weight.
  • polyol denotes a compound of linear, branched or cyclic, saturated or unsaturated alkyl type bearing at least two —OH functions on the alkyl chain, as well as the polymers (polyethers) of these polyhydroxyalkyl compounds.
  • the specific polyols used according to the invention contain at least 4 carbon atoms and can be chosen in particular from C 4 -C 9 polyols and polyalkylene glycols such as, more particularly, polyethylene glycols and polypropylene glycols.
  • C 4 -C 9 polyols mention may be made in particular of 2-butene-1,4-diol, pentane-1,5-diol, 2,2-dimethylpropane-1,3-diol, 3-methylpentane-1,5-diol, pentane-1,2-diol, 2,2,4-trimethylpentane-1,3-diol, 2-methylpropane-1,3-diol, hexylene glycol, 1,3-butylene glycol, dipropylene glycol, diethylene glycol and triethylene glycol.
  • the specific polyol ethers according to the invention are chosen from C 1 -C 8 aliphatic ethers of C 3 -C 9 polyols and C 6 -C 8 aromatic ethers of C 2 -C 9 polyols.
  • C 1 -C 8 aliphatic ethers of C 3 -C 9 polyols mention may be made in particular of propylene glycol monomethyl ether, propylene glycol monoethyl ether, isopropylene glycol dimethyl ether, diethylene glycol monomethyl ether and monoethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether and diethylene glycol dimethyl ether;
  • the glycerol and/or the polyol(s) and/or polyol ether(s) described for the purposes of the invention are present in the dye composition in accordance with the invention in proportions generally ranging from 0.1 to 40% by weight, and even more particularly from 0.5 to 20% by weight, relative to the total weight of the composition.
  • the medium which is suitable for dyeing (or support) generally comprises a mixture of water and at least glycerol and/or a polyol and/or polyol ether as defined above. It can also contain one or more organic solvents other than glycerol and/or the polyol(s) and/or polyol ether(s) used in accordance with the invention, to dissolve the compounds which would not be sufficiently soluble in water.
  • Organic solvents which may be mentioned, for example, are C 1 -C 4 alkanols such as ethanol and isopropanol, as well as aromatic alcohols such as benzyl alcohol, similar products and mixtures thereof.
  • the said additional organic solvents can be present in proportions preferably approximately ranging from 0.5 to 40% by weight relative to the total weight of the dye composition, and even more preferably approximately from 1 to 20% by weight.
  • the pH of the dye composition in accordance with the invention generally approximately ranges from 2 to 11, and preferably approximately from 5 to 10 . It can be adjusted to the desired value using acidifying or basifying agents usually used for dyeing keratin fibers.
  • acidifying agents which may be mentioned, for example, are 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, and sulphonic acids.
  • 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, and sulphonic acids.
  • basifying agents which may be mentioned, for example, are aqueous ammonia, alkaline carbonates, alkanolamines such as mono-, di- and triethanolamine and derivatives thereof, sodium hydroxide, potassium hydroxide and the compounds of formula (II) below:
  • W is a propylene residue optionally having a substituent chosen from a hydroxyl group and C 1 -C 6 alkyl radicals
  • R 16 , R 17 , R 18 and R 19 which may be identical or different, are chosen from a hydrogen atom and C 1 -C 6 alkyl and C 1 -C 6 hydroxyalkyl radicals.
  • the dye composition in accordance with the invention can contain one or more additional direct dyes which may be chosen, for example, from nitrobenzene dyes, anthraquinone dyes, naphthoquinone dyes, triarylmethane dyes, xanthene dyes and azo dyes which are non-cationic.
  • the dye composition in accordance with the invention contains one or more oxidation bases chosen from the oxidation bases conventionally used for oxidation dyeing and among which mention may be made in particular of para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases.
  • the oxidation base(s) preferably represent(s) from 0.0005 to 12% by weight approximately relative to the total weight of the dye composition, and even more preferably from 0.005 to 6% by weight approximately relative to this weight.
  • the dye composition in accordance with the invention can also contain one or more couplers so as to modify or enrich with glints the shades obtained using the cationic direct dye(s) and the oxidation bases.
  • the couplers which can be used in the dye composition in accordance with the invention can be chosen from the couplers used conventionally in oxidation dyeing and among which mention may be made in particular of meta-phenylenediamines, meta-aminophenols, meta-diphenols and heterocyclic couplers.
  • the coupler(s) preferably represent(s) from 0.0001 to 10% by weight approximately relative to the total weight of the dye composition, and even more preferably from 0.005 to 5% by weight approximately relative to this weight.
  • the dye composition in accordance with the invention can also contain various adjuvants conventionally used in compositions for dyeing the hair, such as antioxidants, penetrating agents, sequestering agents, fragrances, buffers, dispersing agents, surfactants, film-forming agents, ceramides, preserving agents, screening agents and opacifiers.
  • adjuvants conventionally used in compositions for dyeing the hair such as antioxidants, penetrating agents, sequestering agents, fragrances, buffers, dispersing agents, surfactants, film-forming agents, ceramides, preserving agents, screening agents and opacifiers.
  • the dye composition according to the invention can be in various forms, such as in the form of liquids, shampoos, creams or gels or any other form which is suitable for dyeing keratin fibers, and in particular human hair. It can be obtained by mixing, at the time of use, a composition, which may be in pulverulent form, containing the cationic direct dye(s) with a composition containing the glycerol and/or the specific polyol and/or polyol ether.
  • the dye composition in accordance with the invention also contains at least one oxidizing agent chosen, for example, from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulphates, and enzymes such as peroxidases, laccases and two-electron oxidoreductases.
  • oxidizing agent chosen, for example, from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulphates, and enzymes such as peroxidases, laccases and two-electron oxidoreductases.
  • the use of hydrogen peroxide or enzymes is particularly preferred.
  • Another subject of the invention is a process for dyeing keratin fibers, and in particular human keratin fibers such as the hair, using the dye composition as defined above.
  • At least one dye composition as defined above is applied to the fibers, for a period which is sufficient to develop the desired coloration, after which the fibers are rinsed, optionally washed with shampoo, rinsed again and dried.
  • the time required to develop the coloration on the keratin fibers generally ranges from 3 to 60 minutes and even more preferably from 5 to 40 minutes.
  • At least one dye composition as defined above is applied to the fibers, for a period which is sufficient to develop the desired coloration, without final rinsing.
  • the dyeing process includes a preliminary step which comprises separately storing, on the one hand, a composition (A1) comprising, in a medium which is suitable for dyeing, at least one cationic direct dye and at least glycerol and/or one specific polyol and/or polyol ether as defined above and at least one oxidation base, and, on the other hand, a composition (B1) containing, in a medium which is suitable for dyeing, at least one oxidizing agent, and then in mixing them together at the time of use, after which this mixture is applied to the keratin fibers.
  • a composition (A1) comprising, in a medium which is suitable for dyeing, at least one cationic direct dye and at least glycerol and/or one specific polyol and/or polyol ether as defined above and at least one oxidation base
  • B1 containing, in a medium which is suitable for dyeing, at least one oxidizing agent, and then in mixing them together at the time of use, after which this mixture is
  • the dyeing process includes a preliminary step which comprises separately storing, on the one hand, a composition (A2) comprising, in a medium which is suitable for dyeing, at least one cationic direct dye and at least glycerol and/or one specific polyol and/or polyol ether as defined above, and, on the other hand, a composition (B1) containing, in a medium which is suitable for dyeing, at least one oxidizing agent, and then in mixing them together at the time of use, after which this mixture is applied to the keratin fibers.
  • a composition (A2) comprising, in a medium which is suitable for dyeing, at least one cationic direct dye and at least glycerol and/or one specific polyol and/or polyol ether as defined above
  • a composition (B1) containing, in a medium which is suitable for dyeing, at least one oxidizing agent, and then in mixing them together at the time of use, after which this mixture is applied to the keratin fibers.
  • Another subject of the invention is a multi-compartment dyeing device or “kit” or any other multi-compartment packaging system, a first compartment of which comprises composition (A1) or (A2) as defined above and a second compartment of which comprises composition (B1) as defined above.
  • These devices can be equipped with means for delivering the desired mixture onto the hair, such as the devices described in patent FR 2,586,913, assigned to the present assignee.
  • Cationic direct dye of formula (I) 27 0.1 g Glycerol 10.0 g 2-Amino-2-methylpropanol qs pH9 Demineralized water qs 100 g

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Cosmetics (AREA)

Abstract

The invention relates to a dye composition for keratin fibers, in particular for human keratin fibers such as the hair, comprising at least one cationic direct dye of given formula and at least glycerol and/or one specific polyol and/or polyol ether. The invention also relates to the dyeing processes and devices using this composition.

Description

  • The invention relates to a dye composition for keratin fibers, in particular for human keratin fibers such as the hair, comprising, in a medium which is suitable for dyeing, at least one cationic direct dye of given formula, and at least glycerol and/or one specific polyol and/or polyol ether. [0001]
  • The invention also relates to the dyeing processes and devices using the composition. [0002]
  • Two types of coloration can be distinguished in the field of hair treatment. [0003]
  • The first is semi-permanent or temporary dyeing, or direct dyeing, which involves dyes capable of giving the hair's natural color a more or less pronounced color change which may withstand shampooing several times. These dyes are known as direct dyes; they can be used with or without an oxidizing agent. In the presence of an oxidizing agent, the aim is to obtain a lightening coloration. The lightening coloration is carried out by applying to the hair the mixture, prepared at the time of use, of a direct dye and an oxidizing agent, and in particular makes it possible to obtain, by lightening the melanin in the hair, an advantageous effect such as a unified color in the case of grey hair, or to bring out the color in the case of naturally pigmented hair. [0004]
  • The second is permanent dyeing or oxidation dyeing. This is carried out with dyes known as “oxidation” dyes comprising oxidation dye precursors and couplers. Oxidation dye precursors, commonly known as “oxidation bases”, are initially colorless or weakly colored compounds which develop their dyeing power on the hair in the presence of oxidizing agents added at the time of use, leading to the formation of colored compounds and dyes. The formation of these colored compounds and dyes results either from an oxidative condensation of the “oxidation bases” with themselves or from an oxidative condensation of the “oxidation bases” with coloration modifier compounds commonly known as “couplers”, which are generally present in the dye compositions used in oxidation dyeing. [0005]
  • In order to vary the shades obtained with the said oxidation dyes, or to enrich them with glints, it is known to add direct dyes thereto. [0006]
  • Among the cationic direct dyes available in the field of dyeing keratin fibers, in particular human keratin fibers, compounds which are already known are those whose structure is developed in the text which follows; nevertheless, these dyes lead to colorations which have properties that are still insufficient, e.g., the homogeneity of the color distributed along the fiber (“unison”), in which case it is said that the coloration is too selective, the staying power, in terms of resistance to the various attacking factors to which the hair may be subjected (light, bad weather, shampooing) and the intensity. [0007]
  • After considerable research conducted in this matter, the inventors have now discovered that it is possible to obtain novel compositions for dyeing keratin fibers, which are capable of leading to colorations which can be more resistant to the various attacking factors to which the hair may be subjected, and can be more intense and less selective, by combining at least glycerol and/or one specific polyol andlor polyol ether with at least one cationic direct dye known in the prior art, and of formula (I) defined below. [0008]
  • This discovery forms the basis of the present invention. [0009]
  • A first subject of the present invention is thus a composition for dyeing keratin fibers, and in particular human keratin fibers such as the hair, containing, in a medium which is suitable for dyeing, (i) at least one cationic direct dye whose structure corresponds to formula (I) below, characterized in that it also contains (ii) at least glycerol and/or one specific polyol and/or polyol ether. [0010]
  • (i) The cationic direct dye which can be used according to the present invention is a compound of formula (I) below:[0011]
  • A—B═N—B  (I)
  • in which: [0012]
  • the symbol A represents a group chosen from structures A[0013] 1 to A3 below:
    Figure US20020004955A1-20020117-C00001
  • in which structures A[0014] 1 to A3,
  • R, is chosen from C[0015] 1-C4 alkyl radicals and a phenyl radical having a substituent chosen from C1-C4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
  • R[0016] 2 is chosen from C1-C4 alkyl radicals and a phenyl radical;
  • R[0017] 3 and R4, which may be identical or different, are chosen from C1-C4 alkyl radicals and a phenyl radical or, in the case of structure A1, can together form a substituted benzene ring, and in the case of structure A2, can together form a benzene ring optionally having at least one substituent chosen from C1-C4 alkyl, C1-C4 alkoxy and NO2 radicals;
  • R[0018] 3 can ailso denote a hydrogen atom;
  • Z is chosen from an oxygen atom, a sulphur atom, and —NR[0019] 2 groups;
  • M is chosen from —CH, —CR, where R is chosen from C[0020] 1-C4 alkyl radicals, and —N+R5(X)r groups;
  • K is chosen from —CH, —CR, where R is chosen from C[0021] 1-C4 alkyl radicals, and —N+R5(X)r groups;
  • P is chosen from —CH, —CR, where R is chosen from C[0022] 1-C4 alkyl radicals, and —N+R5(X)r groups;
  • r denotes 0 or 1; [0023]
  • R[0024] 5 is chosen from an atom O, C1-C4 alkoxy radicals and C1-C4 alkyl radicals;
  • R[0025] 6 and R7, which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals and an —NO2 radical;
  • X[0026] is an anion, preferably chosen from chloride, iodide, methyl sulphate, ethyl sulphate, acetate and perchlorate;
  • with the proviso that, [0027]
  • if R[0028] 4 is a C1-C4 alkyl radical and Z is a sulphur atom, R3 is not a hydrogen atom;
  • if R[0029] 5 is O, then r is zero;
  • if K or P or M is —N[0030] +—C1-C4 -alkyl X, then R6 or R7 is other than a hydrogen atom;
  • if K is −N[0031] +R5(X)r, then M═P and is —CH or —CR;
  • if M is —N[0032] +R5(X)r, then K═P and is —CH or —CR;
  • if P is —N[0033] +R5(X)r, then K═M and is —CH or —CR;
  • if Z is —NR[0034] 2 and R2 is a C1-C4 alkyl radical, then at least one of the radicals R1, R3 or R4 of structure A2 is other than a C1-C4 alkyl radical;
  • the symbol B represents: [0035]
  • (a) a group of structure B[0036] 1 below:
    Figure US20020004955A1-20020117-C00002
  • in which structure B[0037] 1,
  • R[0038] 8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals, a radical —OH, a radical —NO2, —NHR11 radicals, —NR12R13 radicals, and —NHCO(C1-C4)alkyl radicals or forms, with R9, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
  • R[0039] 9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, and C1-C4 alkoxy radicals, or forms, with R10 or R11, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
  • R[0040] 10 is chosen from a hydrogen atom, an —OH radical, —NHR11 radicals and —NR12R13 radicals;
  • R[0041] 11 is chosen from a hydrogen atom, C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals and a phenyl radical;
  • R[0042] 12 and R13, which may be identical or different, are chosen from C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals and C2-C4 polyhydroxyalkyl radicals; or
  • (b) a 5- or 6-membered nitrogenous heterocyclic group which can contain at least one other hetero atom and/or at least one carbonyl group and which can have at least one substituent chosen from C[0043] 1-C4 alkyl, amino and phenyl radicals, and in particular a group of structure B2 below:
    Figure US20020004955A1-20020117-C00003
  • in which structure B2, R[0044] 14 and R15, which may be identical or different, are chosen from a hydrogen atom and C1-C4 alkyl and phenyl radicals;
  • Y denotes a —CO— radical or a radical [0045]
    Figure US20020004955A1-20020117-C00004
  • n=0 or 1, where, when n denotes 1, U denotes a —CO— radical. [0046]
  • In the structures defined above, the C[0047] 1-C4 alkyl or alkoxy group preferably denotes methyl, ethyl, butyl, methoxy or ethoxy.
  • The cationic direct dyes of formula (I) which can be used in the dye compositions in accordance with the invention are known compounds and are described, for example, in patent applications FR-2,189,006, FR-2,285,851 and FR-2,140,205 and its Certificates of Addition, the disclosures of all of which are specifically incorporated by reference herein. [0048]
  • Among the cationic direct dyes of formula (I) which can be used in the dye compositions in accordance with the invention, those of formula (I) in which the symbol A denotes structure A3 while the symbol B denotes structure B1 or B2 are particularly preferred. [0049]
  • Among these compounds, mention may especially be made more particularly of the compounds of structures (I)[0050] 1 to (II)77 below:
    Figure US20020004955A1-20020117-C00005
  • The cationic direct dye(s) used according to the invention preferably represent(s) from 0.001 to 10% by weight approximately relative to the total weight of the dye composition, and even more preferably from 0.005 to 5% by weight approximately relative to this weight. [0051]
  • (ii) For the purposes of the invention, the term “polyol” denotes a compound of linear, branched or cyclic, saturated or unsaturated alkyl type bearing at least two —OH functions on the alkyl chain, as well as the polymers (polyethers) of these polyhydroxyalkyl compounds. [0052]
  • The specific polyols used according to the invention contain at least 4 carbon atoms and can be chosen in particular from C[0053] 4-C9 polyols and polyalkylene glycols such as, more particularly, polyethylene glycols and polypropylene glycols.
  • Among the C[0054] 4-C9 polyols, mention may be made in particular of 2-butene-1,4-diol, pentane-1,5-diol, 2,2-dimethylpropane-1,3-diol, 3-methylpentane-1,5-diol, pentane-1,2-diol, 2,2,4-trimethylpentane-1,3-diol, 2-methylpropane-1,3-diol, hexylene glycol, 1,3-butylene glycol, dipropylene glycol, diethylene glycol and triethylene glycol.
  • The specific polyol ethers according to the invention are chosen from C[0055] 1-C8 aliphatic ethers of C3-C9 polyols and C6-C8 aromatic ethers of C2-C9 polyols.
  • Among the C[0056] 1-C8 aliphatic ethers of C3-C9 polyols, mention may be made in particular of propylene glycol monomethyl ether, propylene glycol monoethyl ether, isopropylene glycol dimethyl ether, diethylene glycol monomethyl ether and monoethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether and diethylene glycol dimethyl ether;
  • among the C[0057] 6-C8 aromatic ethers of C2-C9 polyols, mention may be made in particular of ethylene glycol monophenyl ether, ethylene glycol monobenzyl ether, propylene glycol monophenyl ether, propylene glycol monobenzyl ether, diethylene glycol monophenyl ether and diethylene glycol monobenzyl ether.
  • The glycerol and/or the polyol(s) and/or polyol ether(s) described for the purposes of the invention are present in the dye composition in accordance with the invention in proportions generally ranging from 0.1 to 40% by weight, and even more particularly from 0.5 to 20% by weight, relative to the total weight of the composition. [0058]
  • The medium which is suitable for dyeing (or support) generally comprises a mixture of water and at least glycerol and/or a polyol and/or polyol ether as defined above. It can also contain one or more organic solvents other than glycerol and/or the polyol(s) and/or polyol ether(s) used in accordance with the invention, to dissolve the compounds which would not be sufficiently soluble in water. Organic solvents which may be mentioned, for example, are C[0059] 1-C4 alkanols such as ethanol and isopropanol, as well as aromatic alcohols such as benzyl alcohol, similar products and mixtures thereof.
  • The said additional organic solvents can be present in proportions preferably approximately ranging from 0.5 to 40% by weight relative to the total weight of the dye composition, and even more preferably approximately from 1 to 20% by weight. [0060]
  • The pH of the dye composition in accordance with the invention generally approximately ranges from 2 to 11, and preferably approximately from 5 to 10 . It can be adjusted to the desired value using acidifying or basifying agents usually used for dyeing keratin fibers. [0061]
  • Among the acidifying agents which may be mentioned, for example, are 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, and sulphonic acids. [0062]
  • Among the basifying agents which may be mentioned, for example, are aqueous ammonia, alkaline carbonates, alkanolamines such as mono-, di- and triethanolamine and derivatives thereof, sodium hydroxide, potassium hydroxide and the compounds of formula (II) below: [0063]
    Figure US20020004955A1-20020117-C00006
  • in which W is a propylene residue optionally having a substituent chosen from a hydroxyl group and C[0064] 1-C6 alkyl radicals; R16, R17, R18 and R19, which may be identical or different, are chosen from a hydrogen atom and C1-C6 alkyl and C1-C6 hydroxyalkyl radicals.
  • In addition to the cationic direct dye(s) defined above, the dye composition in accordance with the invention can contain one or more additional direct dyes which may be chosen, for example, from nitrobenzene dyes, anthraquinone dyes, naphthoquinone dyes, triarylmethane dyes, xanthene dyes and azo dyes which are non-cationic. [0065]
  • When it is intended for oxidation dyeing, in addition to the cationic direct dye(s) and glycerol and/or specific polyol and/or polyol ether defined above, the dye composition in accordance with the invention contains one or more oxidation bases chosen from the oxidation bases conventionally used for oxidation dyeing and among which mention may be made in particular of para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases. [0066]
  • When it is (they are) used, the oxidation base(s) preferably represent(s) from 0.0005 to 12% by weight approximately relative to the total weight of the dye composition, and even more preferably from 0.005 to 6% by weight approximately relative to this weight. [0067]
  • When it is intended for oxidation dyeing, in addition to the cationic direct dye and glycerol and/or specific polyol and/or polyol ether defined above as well as oxidation bases, the dye composition in accordance with the invention can also contain one or more couplers so as to modify or enrich with glints the shades obtained using the cationic direct dye(s) and the oxidation bases. [0068]
  • The couplers which can be used in the dye composition in accordance with the invention can be chosen from the couplers used conventionally in oxidation dyeing and among which mention may be made in particular of meta-phenylenediamines, meta-aminophenols, meta-diphenols and heterocyclic couplers. [0069]
  • When it is (they are) present, the coupler(s) preferably represent(s) from 0.0001 to 10% by weight approximately relative to the total weight of the dye composition, and even more preferably from 0.005 to 5% by weight approximately relative to this weight. [0070]
  • The dye composition in accordance with the invention can also contain various adjuvants conventionally used in compositions for dyeing the hair, such as antioxidants, penetrating agents, sequestering agents, fragrances, buffers, dispersing agents, surfactants, film-forming agents, ceramides, preserving agents, screening agents and opacifiers. [0071]
  • Needless to say, a person skilled in the art will take care to select this or these optional complementary compound(s) such that the advantageous properties intrinsically associated with the dye composition in accordance with the invention are not, or are not substantially, adversely affected by the addition(s) envisaged. [0072]
  • The dye composition according to the invention can be in various forms, such as in the form of liquids, shampoos, creams or gels or any other form which is suitable for dyeing keratin fibers, and in particular human hair. It can be obtained by mixing, at the time of use, a composition, which may be in pulverulent form, containing the cationic direct dye(s) with a composition containing the glycerol and/or the specific polyol and/or polyol ether. [0073]
  • When the combination of the cationic direct dye and glycerol and/or specific polyol and/or polyol ether defined according to the invention is used in a composition intended for oxidation dyeing (one or more oxidation bases are then used, optionally in the presence of one or more couplers), or when it is used in a composition intended for lightening direct dyeing, then the dye composition in accordance with the invention also contains at least one oxidizing agent chosen, for example, from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulphates, and enzymes such as peroxidases, laccases and two-electron oxidoreductases. The use of hydrogen peroxide or enzymes is particularly preferred. [0074]
  • Another subject of the invention is a process for dyeing keratin fibers, and in particular human keratin fibers such as the hair, using the dye composition as defined above. [0075]
  • According to a first variant of this dyeing process in accordance with the invention, at least one dye composition as defined above is applied to the fibers, for a period which is sufficient to develop the desired coloration, after which the fibers are rinsed, optionally washed with shampoo, rinsed again and dried. [0076]
  • The time required to develop the coloration on the keratin fibers generally ranges from 3 to 60 minutes and even more preferably from 5 to 40 minutes. [0077]
  • According to a second variant of this dyeing process in accordance with the invention, at least one dye composition as defined above is applied to the fibers, for a period which is sufficient to develop the desired coloration, without final rinsing. [0078]
  • According to one specific embodiment of this dyeing process, and when the dye composition in accordance with the invention contains at least one oxidation base and at least one oxidizing agent, the dyeing process includes a preliminary step which comprises separately storing, on the one hand, a composition (A1) comprising, in a medium which is suitable for dyeing, at least one cationic direct dye and at least glycerol and/or one specific polyol and/or polyol ether as defined above and at least one oxidation base, and, on the other hand, a composition (B1) containing, in a medium which is suitable for dyeing, at least one oxidizing agent, and then in mixing them together at the time of use, after which this mixture is applied to the keratin fibers. [0079]
  • According to another specific embodiment of this dyeing process, and when the dye composition in accordance with the invention contains at least one oxidizing agent, the dyeing process includes a preliminary step which comprises separately storing, on the one hand, a composition (A2) comprising, in a medium which is suitable for dyeing, at least one cationic direct dye and at least glycerol and/or one specific polyol and/or polyol ether as defined above, and, on the other hand, a composition (B1) containing, in a medium which is suitable for dyeing, at least one oxidizing agent, and then in mixing them together at the time of use, after which this mixture is applied to the keratin fibers. [0080]
  • Another subject of the invention is a multi-compartment dyeing device or “kit” or any other multi-compartment packaging system, a first compartment of which comprises composition (A1) or (A2) as defined above and a second compartment of which comprises composition (B1) as defined above. These devices can be equipped with means for delivering the desired mixture onto the hair, such as the devices described in patent FR 2,586,913, assigned to the present assignee. [0081]
  • The examples which follow are intended to illustrate the invention without, however, limiting its scope. [0082]
  • EXAMPLES Example 1
  • The dye composition below was prepared: [0083]
    Cationic direct dye of formula (I)27 0.1 g
    Glycerol 10.0 g
    2-Amino-2-methylpropanol qs pH9
    Demineralized water qs 100 g
  • The above composition was applied for 30 minutes to locks of natural grey hair containing 90% white hairs. The locks of hair were then rinsed, washed with a standard shampoo and then dried. [0084]
  • They were dyed in an intense purple shade. [0085]
  • Example 2
  • The dye composition below was prepared: [0086]
    Cationic direct dye of formula (I)10 0.12 g
    Propylene glycol monomethyl ether 10.0 g
    2-Amino-2-methylpropanol qs pH9
    Demineralized water qs 100 g
  • The above composition was applied for 30 minutes to locks of natural grey hair containing 90% white hairs. The locks of hair were then rinsed, washed with a standard shampoo and then dried. [0087]
  • They were dyed in an intense red shade. [0088]

Claims (36)

What is claimed is:
1. A composition for dyeing keratin fibers comprising: (i) at least one cationic direct dye of formula (I) below:
A—N═N—B  (I)
in which:
the symbol A represents a group chosen from structures A1 to A3 below:
Figure US20020004955A1-20020117-C00007
in which structures A1 to A3,
R1 is chosen from C1-C4 alkyl radicals and a phenyl radical having a substituent chosen from C1-C4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
R2 is chosen from C1-C4 alkyl radicals and a phenyl radical;
R3 and R4, which may be identical or different, are chosen from C1-C4 alkyl radicals and a phenyl radical or, in the case of structure A1, can together form a substituted benzene ring, and in the case of structure A2, can together form a benzene ring optionally having at least one substituent chosen from C1-C4 alkyl, C1-C4 alkoxy and NO2 radicals;
R3 can also denote a hydrogen atom;
Z is chosen from an oxygen atom, a sulphur atom, and —NR2 groups;
M is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
K is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
P is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X+)r groups;
r denotes 0 or 1;
R5 is chosen from an atom O, C1-C4 alkoxy radicals and C1-C4 alkyl radicals;
R6 and R7, which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals and an —NO2 radical;
X is an anion;
with the proviso that,
if R4 is a C1-C4 alkyl radical and Z is a sulphur atom, R3 is not a hydrogen atom;
if R5 is O, then r is zero;
if K or P or M is —N+—C1-C4 -alkyl X, then R6 or R7 is other than a hydrogen atom;
if K is —N+R5(X)r, then M═P and is —CH or —CR;
if M is —N+R5(X)r, then K═P and is —CH or —CR;
if P is —N+R5(X)r, then K═M and is —CH or —CR;
if Z is —NR2 and R2 is a C1-C4 alkyl radical, then at least one of the radicals R1, R3 or R4 of structure A2 is other than a C1-C4 alkyl radical;
the symbol B represents:
(a) a group of structure B1 below:
Figure US20020004955A1-20020117-C00008
in which structure B1,
R8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals, a radical —OH, a radical —NO2, —NHR11 radicals, —NR12R13 radicals, and —NHCO(C1-C4)alkyl radicals or forms, with R9, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, and C1-C4 alkoxy radicals, or forms, with R10 or R11, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R10 is chosen from a hydrogen atom, an —OH radical, —NHR11 radicals and —NR12R13 radicals;
R11 is chosen from a hydrogen atom, C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals and a phenyl radical;
R12 and R13, which may be identical or different, are chosen from C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals and C2-C4 polyhydroxyalkyl radicals; or
(b) a 5- or 6-membered nitrogenous heterocyclic group which can contain at least one other hetero atom and/or at least one carbonyl group and which can have at least one substituent chosen from C1-C4 alkyl, amino and phenyl radicals, and
(ii) at least one compound chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic ethers of C3-C9 polyols, and C6-C8 aromatic ethers of C2-C9 polyols.
2. The composition according to claim 1, wherein, in formula (I), the C1-C4 alkyl radicals are chosen from methyl, ethyl, and butyl radicals and the C1-C4 alkoxy radicals are methoxy and ethoxy radicals.
3. The composition according to claim 1, wherein the symbol B represents a a group of structure B2 below:
Figure US20020004955A1-20020117-C00009
in which structure B2,
R14 and R15, which may be identical or different, are chosen from a hydrogen atom, C1-C4 alkyl radicals and a phenyl radical;
Y is chosen from a —CO— radical and a radical
Figure US20020004955A1-20020117-C00010
n=0 or 1, where, when n is 1, U is a —CO— radical.
4. The composition according to claim 1, wherein X is chosen from chloride, iodide, methyl sulphate, ethyl sulphate, acetate and perchlorate.
5. The composition according to claim 1, wherein said keratin fibers are human keratin fibers.
6. The composition according to claim 5, wherein said human keratin fibers are hair.
7. The composition according to claim 1, wherein said polyols containing at least 4 carbon atoms are chosen from C4-C9 polyols and polyalkylene glycols.
8. The composition according to claim 7, wherein said polyalkylene glycols are chosen from polyethylene glycols and polypropylene glycols.
9. The composition according to claim 7, wherein said C4-C9 polyols are chosen from 2-butene-1,4-diol pentane-1,5-diol, 2,2-dimethylpropane-1,3-diol, 3-methylpentane-1,5-diol, pentane-1,2-diol, 2,2,4-trimethylpentane-1,3-diol, 2-methylpropane-1,3-diol, hexylene glycol, 1,3-butylene glycol, dipropylene glycol, diethylene glycol and triethylene glycol.
10. The composition according to claim 1, wherein said C1-C8 aliphatic ethers of C3-C9 polyols are chosen from propylene glycol monomethyl ether, propylene glycol monoethyl ether, isopropylene glycol dimethyl ether, diethylene glycol monomethyl ether and monoethyl ether, dipropylene glycol monomethyl ether, tripropylene glycol monomethyl ether and diethylene glycol dimethyl ether.
11. The composition according to claim 1, wherein said C6-C8 aromatic ethers of C2-C9 polyols are chosen from ethylene glycol monophenyl ether, ethylene glycol monobenzyl ether, propylene glycol monophenyl ether, propylene glycol monobenzyl ether, diethylene glycol monophenyl ether and diethylene glycol monobenzyl ether.
12. The composition according to claim 1, wherein said at least one cationic direct dye is chosen from structures (I)1 to (I)77 below:
Figure US20020004955A1-20020117-C00011
13. The composition according to claim 1, wherein said at least one cationic direct dye of formula (I) is present in an amount ranging from 0.001 to 10% by weight relative to the total weight of the composition.
14. The composition according to claim 13, wherein said at least one cationic direct dye of formula (I) is present in an amount ranging from 0.005 to 5% by weight relative to the total weight of the composition.
15. The composition according to claim 1, wherein said at least one compound chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic, ethers of C3-C9 polyols and C6-C8 aromatic ethers of C2-C9 polyols is present in an amount ranging from 0.1 to 40% by weight relative to the total weight of the composition.
16. The composition according to claim 15, wherein said at least one compound is present in an amount ranging from 0.5 to 20% by weight relative to the total weight of the composition.
17. The composition according to claim 1, wherein said composition further comprises additional direct dyes.
18. The composition according to claim 1, wherein said composition further comprises a mixture of water and at least one solvent chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic ethers of C3-C8 polyols, and C6-C8 aromatic ethers of C2-C9 polyols.
19. The composition according to claim 18, wherein said composition further comprises at least one additional organic solvent.
20. The composition according to claim 1, wherein said composition has a pH ranging from 2 to 11.
21. The composition according to claim 20, wherein said pH ranges from 5 to 10.
22. The composition according to claim 1, wherein said composition further comprises at least one oxidation base chosen from para-phenylenediamines, bis(pheniyl)alkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases.
23. The composition according to claim 22, wherein said at least on e oxidation base is present in an amount ranging from 0.0005 to 12% by weight relative to the total weight of the composition.
24. The composition according to claim 23, wherein said at least one oxidation base is present in an amount ranging from 0.005 to 6% by weight relative to the total weight of the composition.
25. The composition according to claim 22, wherein said composition further comprises at least one coupler chosen from meta-phenylenediamine, meta-aminophenols, meta-diphenols and heterocyclic couplers.
26. The composition according to claim 25, wherein said at least one coupler is present in an amount ranging from 0.0001 to 10% by weight relative to the total weight of the composition.
27. The composition according to claim 26, wherein said at least one coupler is present in an amount ranging from 0.005 to 5% by weight relative to the total weight of the composition.
28. The composition according to claim 1, wherein said composition further comprises at least one oxidizing agent.
29. A process for dyeing keratin fibers, comprising applying to said fibers, for a period which is sufficient to develop the desired coloration, at least one dye composition comprising:
(i) at least one cationic direct dye of formula (I) below:
A—N═N—B  (I)
in which:
the symbol A represents a group chosen from structures A1 to A3 below:
Figure US20020004955A1-20020117-C00012
in which structures A1 to A3,
R1 is chosen from C1-C4 alkyl radicals and a phenyl radical having a substituent chosen from C1-C4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
R2 is chosen from C1-C4 alkyl radicals and a phenyl radical;
R3 and R4, which may be identical or different, are chosen from C1-C4 alkyl radicals and a phenyl radical or, in the case of structure A1, can together form a substituted benzene ring, and in the case of structure A2, can together form a benzene ring optionally having at least one substituent chosen from C1-C4 alkyl, C1-C4 alkoxy and NO2 radicals;
R3 can also denote a hydrogen atom;
Z is chosen from an oxygen atom, a sulphur atom, and —NR2 groups;
M is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
K is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
P is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
r denotes 0 or 1;
R5 is chosen from an atom O, C1-C4 alkoxy radicals and C1-C4 alkyl radicals;
R6 and R7, which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals and an —NO2 radical;
X is an anion;
with the proviso that,
if R4 is a C1-C4 alkyl radical and Z is a sulphur atom, R3 is not a hydrogen atom;
if R5 is O, then r is zero;
if K or P or M is —N+C1-C4 -alkyl X, then R6 or R7 is other than a hydrogen atom;
if K is —N+R5(X)r, then M═P and is —CH or —CR;
if M is —N+R5(X)r, then K═P and is —CH or —CR;
if P is —N+R5(X)r, then K═M and is —CH or —CR;
if Z is —NR2 and R2 is a C1-C4 alkyl radical, then at least one of the radicals R1, R3 or R4 of structure A2 is other than a C1-C4 alkyl radical;
the symbol B represents:
(a) a group of structure B1 below:
Figure US20020004955A1-20020117-C00013
in which structure B1,
R8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals, a radical —OH, a radical —NO2, —NHR11 radicals, —NR12R13 radicals, and —NHCO(C1-C4)alkyl radicals or forms, with R9, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, and C1-C4 alkoxy radicals, or forms, with R10 or R11, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R10 is chosen from a hydrogen atom, an —OH radical, —NHR11 radicals and —NR12R13 radicals;
R11 is chosen from a hydrogen atom, C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals and a phenyl radical;
R12 and R13, which may be identical or different, are chosen from C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals and C2-C4 polyhydroxyalkyl radicals; or
(b) a 5- or 6-membered nitrogenous heterocyclic group which can contain at least one other hetero atom and/or at least one carbonyl group and which can have at least one substituent chosen from C1-C4 alkyl, amino and phenyl radicals, and
(ii) at least one compound chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic ethers of C3-C9 polyols, and C6-C8 aromatic ethers of C2-C9 polyols,
rinsing the fibers,
optionally washing said fibers with shampoo and rinsing again, and drying.
30. A process for dyeing keratin fibers according to claim 29, wherein said keratin fibers are human keratin fibers.
31. A process for dyeing keratin fibers according to claim 30, wherein said human keratin fibers are hair.
32. A process for dyeing keratin fibers according to claim 29, wherein said fibers are not rinsed a second time before drying.
33. A process for dyeing keratin fibers comprising:
separately storing a first composition comprising:
(i) at least one cationic direct dye of formula (I) below:
A—N═N—B  (I)
in which:
the symbol A represents a group chosen from structures A1 to A3 below:
Figure US20020004955A1-20020117-C00014
in which structures A1 to A3,
R1 is chosen from C1-C4 alkyl radicals and a phenyl radical having a substituent chosen from C1-C4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
R2 is chosen from C1-C4 alkyl radicals and a phenyl radical;
R3 and R4, which may be identical or different, are chosen from C1-C4 alkyl radicals and a phenyl radical or, in the case of structure A1, can together form a substituted benzene ring, and in the case of structure A2, can together form a benzene ring optionally having at least one substituent chosen from C1-C4 alkyl, C1-C4 alkoxy and NO2 radicals;
R3 can also denote a hydrogen atom;
Z is chosen from an oxygen atom, a sulphur atom, and —NR2 groups;
M is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
K is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
P is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
r denotes 0 or 1;
R5is chosen from an atom O, C1-C4 alkoxy radicals and C1-C4 alkyl radicals;
R6 and R7, which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals and an —NO2 radical;
X is an anion;
with the proviso that,
if R4is a C1-C4 alkyl radical and Z is a sulphur atom, R3is not a hydrogen atom;
if R5 is O, then r is zero;
if K or P or M is —N+-C1-C4 -alkyl X, then R6 or R7 is other than a hydrogen atom;
if K is —N+R5(X)r, then M═P and is —CH or —CR;
if M is —N+R5(X)r, then K═P and is —CH or —CR;
if P is —N+R5(X)r, then K═M and is —CH or —CR;
if Z is —NR2 and R2 is a C1-C4 alkyl radical, then at least one of the radicals R1, R3 or R4 of structure A2 is other than a C1-C4 alkyl radical;
the symbol B represents:
(a) a group of structure B1 below:
Figure US20020004955A1-20020117-C00015
in which structure B1,
R8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals, a radical —OH, a radical —NO2, —NHR11 radicals, —NR12R13 radicals, and —NHCO(C1-C4)alkyl radicals or forms, with R9, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, and C1-C4 alkoxy radicals, or forms, with R10 or R11, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R10 is chosen from a hydrogen atom, an —OH radical, —NHR11 radicals and —NR12R13 radicals;
R11 is chosen from a hydrogen atom, C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals and a phenyl radical;
R12 and R13, which may be identical or different, are chosen from C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals and C2-C4 polyhydroxyalkyl radicals; or
(b) a 5- or 6-membered nitrogenous heterocyclic group which can contain at least one other hetero atom and/or at least one carbonyl group and which can have at least one substituent chosen from C1-C4 alkyl, amino and phenyl radicals,
(ii) at least one compound chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic ethers of C3-C9 polyols, and C6-C8 aromatic ethers of C2-C9 polyols, and
(iii) at least one oxidation base,
separately storing a second composition comprising at least one oxidizing agent, and
thereafter mixing said first composition with said second composition and applying this mixture to said keratin fibers.
34. A process for dyeing keratin fibers comprising:
separately storing a first composition comprising (i) at least one cationic direct dye of formula (I) below:
A—N═N—B  (I)
in which:
the symbol A represents a group chosen from structures A1 to A3 below:
Figure US20020004955A1-20020117-C00016
in which structures A1 to A3,
R1 is chosen from C1-C4 alkyl radicals and a phenyl radical having a substituent chosen from C1-C4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
R2 is chosen from C1-C4 alkyl radicals and a phenyl radical;
R3 and R4, which may be identical or different, are chosen from C1-C4 alkyl radicals and a phenyl radical or, in the case of structure A1, can together form a substituted benzene ring, and in the case of structure A2, can together form a benzene ring optionally having at least one substituent chosen from C1-C4 alkyl, C1-C4 alkoxy and NO2 radicals;
R3 can also denote a hydrogen atom;
Z is chosen from an oxygen atom, a sulphur atom, and —NR2 groups;
M is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
K is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
P is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
r denotes 0 or 1;
R5 is chosen from an atom O, C1-C4 alkoxy radicals and C1-C4 alkyl radicals;
R6 and R7, which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals and an —NO2 radical;
X is an anion;
with the proviso that,
if R4 is a C1-C4 alkyl radical and Z is a sulphur atom, R3 is not a hydrogen atom;
if R5 is O, then r is zero;
if K or P or M is —N+-C1-C4 -alkyl X, then R6 or R7 is other than a hydrogen atom;
if K is —N+R5(X)r, then M═P and is —CH or —CR;
if M is —N+R5(X)r, then K═P and is —CH or —CR;
if P is —N+R5(X)r, then K═M and is —CH or —CR;
if Z is —NR2 and R2 is a C1-C4 alkyl radical, then at least one of the radicals R1, R3 or R4 of structure A2 is other than a C1-C4 alkyl radical;
the symbol B represents:
(a) a group of structure B1 below:
Figure US20020004955A1-20020117-C00017
in which structure B1,
R8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals, a radical —OH, a radical —NO2, —NHR11 radicals, —NR12R13 radicals, and —NHCO(C1-C4)alkyl radicals or forms, with R9, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, and C1-C4 alkoxy radicals, or forms, with R10 or R11, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R10 is chosen from a hydrogen atom, an —OH radical, —NHR11 radicals and —NR12R13 radicals;
R11 is chosen from a hydrogen atom, C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals and a phenyl radical;
R12 and R13, which may be identical or different, are chosen from C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals and C2-C4 polyhydroxyalkyl radicals; or
(b) a 5- or 6-membered nitrogenous heterocyclic group which can contain at least one other hetero atom and/or at least one carbonyl group and which can have at least one substituent chosen from C1-C4 alkyl, amino and phenyl radicals, and
(ii) at least one compound chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic ethers of C3-C9 polyols, and C6-C8 aromatic ethers of C2-C9 polyols,
separately storing a second composition comprising at least one oxidizing agent, and
thereafter mixing said first composition with said second composition and applying this mixture to said keratin fibers.
35. A multi-compartment dyeing device or multi-compartment dyeing kit compnsing at least two separate compartments, wherein
a first compartment contains a com position comprising:
in which:
the symbol A represents a group chosen from structures A1 to A3 below:
Figure US20020004955A1-20020117-C00018
in which structures A1 to A3,
R1 is chosen from C1-C4 alkyl radicals and a phenyl radical having a substituent chosen from C1-C4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
R2 is chosen from C1-C4 alkyl radicals and a phenyl radical;
R3 and R4, which may be identical or different, are chosen from C1-C4 alkyl radicals and a phenyl radical or, in the case of structure A1, can together form a substituted benzene ring, and in the case of structure A2, can together form a benzene ring optionally having at least one substituent chosen from C1-C4 alkyl, C1-C4 alkoxy and NO2 radicals;
R3 can also denote a hydrogen atom;
Z is chosen from an oxygen atom, a sulphur atom, and —NR2 groups;
M is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
K is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
P is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
r denotes 0 or 1;
R5 is chosen from an atom O, C1-C4 alkoxy radicals and C1-C4 alkyl radicals;
R6 and R7, which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals,
C1-C4 alkoxy radicals and an —NO2 radical;
X is an anion;
with the proviso that,
if R4 is a C1-C4 alkyl radical and Z is a sulphur atom, R3 is not a hydrogen atom;
if R5 is O, then r is zero;
if K or P or M is —N+-C1-C4 -alkyl X, then R6 or R7 is other than a hydrogen atom;
if K is —N+R5(X)r, then M═P and is —CH or —CR;
if M is —N+R5(X)r, then K═P and is —CH or —CR;
if P is —N+R5(X)r, then K═M and is —CH or —CR;
if Z is —NR2 and R2 is a C1-C4 alkyl radical, then at least one of the radicals R1, R3 or R4 of structure A2 is other than a C1-C4 alkyl radical;
the symbol B represents:
(a) a group of structure B1 below:
Figure US20020004955A1-20020117-C00019
in which structure B1,
R8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals, a radical —OH, a radical —NO2, —NHR11 radicals, —NR12R13 radicals, and —NHCO(C1-C4)alkyl radicals or forms, with R9, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, and C1-C4 alkoxy radicals, or forms, with R10 or R11, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R10 is chosen from a hydrogen atom, an —OH radical, —NHR11 radicals and —NR12R13 radicals;
R11 is chosen from a hydrogen atom, C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals and a phenyl radical;
R12 and R13, which may be identical or different, are chosen from C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals and C2-C4 polyhydroxyalkyl radicals; or
(b) a 5- or 6-membered nitrogenous heterocyclic group which can contain at least one other hetero atom and/or at least one carbonyl group and which can have at least one substituent chosen from C1-C4 alkyl, amino and phenyl radicals,
(ii) at least one compound chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic ethers of C3-C9 polyols, and C6-C8 aromatic ethers of C2-C9 polyols, and
(iii) at least one oxidation base, and
a second compartment contains a composition comprising at least one oxidizing agent.
36. A multi-compartment dyeing device or multi-compartment dyeing kit comprising at least two separate compartments wherein
a first compartment contains a composition comprising:
in which:
the symbol A represents a group chosen from structures A1 to A3 below:
Figure US20020004955A1-20020117-C00020
in which structures A1 to A3,
R1 is chosen from C1-C4 alkyl radicals and a phenyl radical having a substituent chosen from C1-C4 alkyl radicals and halogen atoms chosen from chlorine, bromine, iodine and fluorine;
R2 is chosen from C1-C4 alkyl radicals and a phenyl radical;
R3 and R4, which may be identical or different, are chosen from C1-C4 alkyl radicals and a phenyl radical or, in the case of structure A1, can together form a substituted benzene ring, and in the case of structure A2, can together form a benzene ring optionally having at least one substituent chosen from C1-C4 alkyl, C1-C4 alkoxy and NO2 radicals;
R3 can also denote a hydrogen atom;
Z is chosen from an oxygen atom, a sulphur atom, and —NR2 groups;
M is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
K is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
P is chosen from —CH, —CR, where R is chosen from C1-C4 alkyl radicals, and —N+R5(X)r groups;
r denotes 0 or 1;
R5 is chosen from an atom O, C1-C4 alkoxy radicals and C1-C4 alkyl radicals;
R6 and R7, which may be identical or different, are chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals and an —NO2 radical;
X is an anion;
with the proviso that,
if R4 is a C1-C4 alkyl radical and Z is a sulphur atom, R3 is not a hydrogen atom;
if R5 is O, then r is zero;
if K or P or M is —N+C1-C4 -alkyl X, then R6 or R7 is other than a hydrogen atom;
if K is —N+R5(X)r, then M═P and is —CH or —CR;
if M is —N+R5(X)r, then K═P and is —CH or —CR;
if P is —N+R5(X)r, then K═M and is —CH or —CR;
if Z is —NR2 and R2 is a C1-C4 alkyl radical, then at least one of the radicals R1, R3 or R4 of structure A2 is other than a C1-C4 alkyl radical;
the symbol B represents:
(a) a group of structure B1 below:
Figure US20020004955A1-20020117-C00021
in which structure B1,
R8 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, C1-C4 alkoxy radicals, a radical —OH, a radical —NO2, —NHR11 radicals, —NR12R13 radicals, and —NHCO(C1-C4)alkyl radicals or forms, with R9, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R9 is chosen from a hydrogen atom, halogen atoms chosen from chlorine, bromine, iodine and fluorine, C1-C4 alkyl radicals, and C1-C4 alkoxy radicals, or forms, with R10 or R11, a 5- or 6-membered ring which may contain at least one hetero atom chosen from nitrogen, oxygen and sulphur;
R10 is chosen from a hydrogen atom, an —OH radical, —NHR11, radicals and —NR12R13 radicals;
R11 is chosen from a hydrogen atom, C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals and a phenyl radical;
R12 and R13, which may be identical or different, are chosen from C1-C4 alkyl radicals, C1-C4 monohydroxyalkyl radicals and C2-C4 polyhydroxyalkyl radicals; or
(b) a 5- or 6-membered nitrogenous heterocyclic group which can contain at least one other hetero atom and/or at least one carbonyl group and which can have at least one substituent chosen from C1-C4 alkyl, amino and phenyl radicals, and
(ii) at least one compound chosen from glycerol, polyols containing at least 4 carbon atoms, C1-C8 aliphatic ethers of C3-C9 polyols, and C6-C8 aromatic ethers of C2-C9 polyols, and
a second compartment contains a composition comprising at least one oxidizing agent.
US09/321,889 1998-05-28 1999-05-28 Dye composition for keratin fibers, with a cationic direct dye and a polyol or polyol ether Expired - Fee Related US6371994B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR9806752A FR2779056B1 (en) 1998-05-28 1998-05-28 DYE COMPOSITION FOR KERATINIC FIBERS WITH CATIONIC DIRECT DYE AND POLYOL OR POLYOL ETHER
FR9806752 1998-05-28

Publications (2)

Publication Number Publication Date
US20020004955A1 true US20020004955A1 (en) 2002-01-17
US6371994B2 US6371994B2 (en) 2002-04-16

Family

ID=9526825

Family Applications (1)

Application Number Title Priority Date Filing Date
US09/321,889 Expired - Fee Related US6371994B2 (en) 1998-05-28 1999-05-28 Dye composition for keratin fibers, with a cationic direct dye and a polyol or polyol ether

Country Status (16)

Country Link
US (1) US6371994B2 (en)
EP (1) EP0962220B1 (en)
JP (1) JPH11349457A (en)
KR (1) KR100329412B1 (en)
CN (1) CN1237410A (en)
AR (1) AR016497A1 (en)
AT (1) ATE319412T1 (en)
AU (1) AU720852B2 (en)
BR (1) BR9901830A (en)
CA (1) CA2273411A1 (en)
DE (1) DE69930228T2 (en)
ES (1) ES2260891T3 (en)
FR (1) FR2779056B1 (en)
HU (1) HUP9901747A3 (en)
PL (1) PL333403A1 (en)
ZA (1) ZA993198B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030074747A1 (en) * 2001-07-27 2003-04-24 Patricia Vuarier 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
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

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2788432B1 (en) 1999-01-19 2003-04-04 Oreal USE FOR THE DIRECT DYEING OF KERATINIC FIBERS FROM A COMBINATION OF TWO CATIONIC DYES
JP2004099476A (en) * 2002-09-06 2004-04-02 Kanebo Ltd Hair dye
US7097668B2 (en) * 2002-09-16 2006-08-29 Combe Incorporated Temporary hair dye composition
US20040244126A1 (en) * 2003-06-04 2004-12-09 Vena Lou Ann Christine Method, compositions, and kit for coloring hair
FR2857259B1 (en) * 2003-07-11 2007-08-24 Oreal FATTY ACID-FREE LIQUID TINCTORIAL COMPOSITION COMPRISING 2-METHYL 1,3-PROPANEDIOL, DYEING METHOD AND DEVICE
US20050125913A1 (en) 2003-12-11 2005-06-16 Saroja Narasimhan Method and compositions for coloring hair
JP5669485B2 (en) 2009-11-30 2015-02-12 花王株式会社 Two-component hair dye

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2983651A (en) * 1955-12-10 1961-05-09 Oreal Dyeing of animal fibres
DE1492196A1 (en) * 1964-09-02 1969-12-04 Therachemie Chem Therapeut Process and means for facilitating the coloring of hair with cationic substantive dyes
LU53050A1 (en) * 1967-02-22 1968-08-27
US3632290A (en) * 1968-01-26 1972-01-04 Lowenstein Dyes & Cosmetics In Dyeing of human hair using ethylene glycol ethers
LU70835A1 (en) 1974-08-30 1976-08-19
CH560539A5 (en) * 1971-06-04 1975-04-15 Oreal
US4151162A (en) 1971-06-04 1979-04-24 L'oreal Diazomerocyanines and mesomeric forms thereof
US3985499A (en) * 1971-06-04 1976-10-12 L'oreal Diazamerocyanines for dyeing keratinous fibers
LU65539A1 (en) * 1972-06-19 1973-12-21
LU71015A1 (en) 1974-09-27 1976-08-19
FR2586913B1 (en) 1985-09-10 1990-08-03 Oreal PROCESS FOR FORMING IN SITU A COMPOSITION CONSISTING OF TWO SEPARATELY PACKED PARTS AND DISPENSING ASSEMBLY FOR THE IMPLEMENTATION OF THIS PROCESS
DE3829870A1 (en) 1988-09-02 1989-04-13 Henkel Kgaa Dye solutions for dyeing hair
TW311089B (en) 1993-07-05 1997-07-21 Ciba Sc Holding Ag
TW325998B (en) 1993-11-30 1998-02-01 Ciba Sc Holding Ag Dyeing keratin-containing fibers
US5474578A (en) * 1994-10-03 1995-12-12 Clairol, Inc. Erasable hair dyeing process
ES2181761T3 (en) * 1994-11-03 2003-03-01 Ciba Geigy Ag CATIONIC AZOIC COLORS OF IMIDAZOL.
FR2757388B1 (en) * 1996-12-23 1999-11-12 Oreal KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME
FR2757384B1 (en) * 1996-12-23 1999-01-15 Oreal KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME
FR2757385B1 (en) 1996-12-23 1999-01-29 Oreal KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME
FR2757387B1 (en) * 1996-12-23 1999-01-29 Oreal KERATINIC FIBER OXIDATION DYE COMPOSITION AND DYEING METHOD USING THE SAME

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030074747A1 (en) * 2001-07-27 2003-04-24 Patricia Vuarier 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
US20060248664A1 (en) * 2001-07-27 2006-11-09 Patricia Vuarier 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
US7402180B2 (en) 2001-07-27 2008-07-22 L'ORéAL S.A. 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
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

Also Published As

Publication number Publication date
EP0962220A3 (en) 2000-03-08
AR016497A1 (en) 2001-07-04
KR100329412B1 (en) 2002-03-20
HUP9901747A2 (en) 2000-07-28
HUP9901747A3 (en) 2000-11-28
ATE319412T1 (en) 2006-03-15
KR19990088441A (en) 1999-12-27
JPH11349457A (en) 1999-12-21
DE69930228T2 (en) 2006-11-23
DE69930228D1 (en) 2006-05-04
AU720852B2 (en) 2000-06-15
ZA993198B (en) 1999-11-10
FR2779056A1 (en) 1999-12-03
FR2779056B1 (en) 2001-09-07
ES2260891T3 (en) 2006-11-01
BR9901830A (en) 2000-05-30
US6371994B2 (en) 2002-04-16
EP0962220A2 (en) 1999-12-08
PL333403A1 (en) 1999-12-06
HU9901747D0 (en) 1999-07-28
CN1237410A (en) 1999-12-08
CA2273411A1 (en) 1999-11-28
AU2808199A (en) 1999-12-09
EP0962220B1 (en) 2006-03-08

Similar Documents

Publication Publication Date Title
US6436153B2 (en) Composition for the direct dyeing of keratin fibres with a cationic direct dye and a polyol and/or a polyol ether
US7198652B2 (en) Composition for dyeing keratinous fibers with a cationic direct dye and a quaternary ammonium salt
US6530959B1 (en) Dyeing composition for keratinous fibres with a direct cationic coloring agent and a surfactant
MXPA99004753A (en) Direct dyeing composition for keratinic fibers with a cationic direct coloring and a polyol and / or ether of pol
JPH04368318A (en) Method and agent for dyeing keratin fiber
US6371994B2 (en) Dye composition for keratin fibers, with a cationic direct dye and a polyol or polyol ether
JPH06199642A (en) 4-hydroxy- or 4-amino-benzimidazole and hair dyeing composition
US20030167579A1 (en) Oxidation dyeing composition for keratinous fibres and dyeing method using same
US20040205905A1 (en) Dye composition for keratin fibers, comprising at least one compound chosen from ortho- and alpha-dialdehyde compounds and at least one sulphur compound
US7270684B2 (en) Composition for dyeing keratinous fibers comprising at least one azodiazine direct dye containing an aniline group and dyeing method using it
US20030200614A1 (en) Dye composition containing 1,8-bis h(2,5-diaminophenoxy)-3,5-dioxaoctane, an additional oxidation base and a coupler, and dyeing processes
US7326257B2 (en) Composition for dyeing keratinous fibers comprising at least one azodiazine direct dye which is non-aminated at the 7-position and dyeing method using said at least one azodiazine direct dye
US20020013969A1 (en) Oxidation dyeing composition for keratinous fibers containing a paraphenylenediamine derivative and dyeing method using same
MXPA99004785A (en) Composition of dyeing for keratinic fibers with a direct cationic coloring and a polyol or ether of pol
CZ186799A3 (en) Dyeing agent for keratin fibers with cationic direct dye and polyol or polyol ether
US20020062529A1 (en) Dye composition containing 1,8-bis(2,5-diaminophenoxy)-3,6-dioxaoctane, an additional oxidation base and a coupler, and dyeing processes
US20050108833A1 (en) Composition for dyeing keratinous fibers comprising at least one azodiazine direct dye aminated at the 7-position and process for dyeing
CZ186699A3 (en) Dyeing agent for direct dyeing of keratin fibers with cationic direct dye and polyol or polyol ether
MXPA00001642A (en) DYEING COMPOSITION CONTAINING A PYRAZOLO-[1,5-a]-PYRIMIDINE AS OXIDATION BASE AND A PYRIDINE COUPLING AGENT, AND DYEING METHOD

Legal Events

Date Code Title Description
AS Assignment

Owner name: L'OREAL S.A., FRANCE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LANG, GERARD;COTTERET, JEAN;REEL/FRAME:010222/0277

Effective date: 19990614

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

CC Certificate of correction
FPAY Fee payment

Year of fee payment: 4

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Lapsed due to failure to pay maintenance fee

Effective date: 20100416