EP1028694A1 - Utilisation d'indanones pour colorer des fibres a base de keratine - Google Patents

Utilisation d'indanones pour colorer des fibres a base de keratine

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Publication number
EP1028694A1
EP1028694A1 EP98954332A EP98954332A EP1028694A1 EP 1028694 A1 EP1028694 A1 EP 1028694A1 EP 98954332 A EP98954332 A EP 98954332A EP 98954332 A EP98954332 A EP 98954332A EP 1028694 A1 EP1028694 A1 EP 1028694A1
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EP
European Patent Office
Prior art keywords
group
amino
acid
hydroxy
compounds
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP98954332A
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German (de)
English (en)
Inventor
Hinrich Möller
Horst Höffkes
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Henkel AG and Co KGaA
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Henkel AG and Co KGaA
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Publication of EP1028694A1 publication Critical patent/EP1028694A1/fr
Ceased legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41—Amines
    • A61K8/418—Amines containing nitro groups
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
    • A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
    • 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

Definitions

  • the invention relates to the use of indanones for dyeing keratin-containing fibers, in particular human hair, an agent for dyeing keratin-containing fibers, which contains indanones, and a method for dyeing keratin-containing fibers.
  • keratin fibers e.g. B. hair, wool or fur
  • direct dyes or oxidation dyes which are formed by oxidative coupling of one or more developer components with one another or with one or more coupler components, are used.
  • Coupler and developer components are also referred to as oxidation color dead precursors.
  • Primary aromatic amines with a further free or substituted hydroxy or amino group in the para or ortho position, diaminopyridine derivatives, heterocyclic hydrazones, 4-aminopyrazolone derivatives and 2,4,5,6-tetraaminopyrimidine and their derivatives are usually used as developer components.
  • M-Phenylenediamine derivatives, naphthols, resorcinol and resorcinol derivatives, pyrazolones and m-aminophenols are generally used as coupler components.
  • Suitable coupler substances are, in particular, ⁇ -naphthol, 1,5-, 2,7- and 1,7-dihydroxynaphthalene, 5-amino-2-methylphenol, m-aminophenol, resorcinol, resor- cinmonomethyl ether, m-phenylenediamine, 2,4-diaminophenoxyethanol, 1-phenyl-3-methyl-pyrazolon-5, 2,4-dichloro-3-aminophenol, 1,3-bis- (2,4-diaminophenoxy) propane, 2-chlororesorcinol, 4-chlororesorcinol, 2-chloro-6-methyl-3-aminophenol, 2-methylresorcinol and 5-methylresorcinol.
  • oxidation dyes can be achieved with oxidation dyes, but the development of the color generally takes place under the influence of oxidizing agents such as H 2 O 2 , which in some cases can damage the fibers. Furthermore, some oxidation dye products or certain mixtures of oxidation dye precursors can sometimes have a sensitizing effect on people with sensitive skin. Direct dyes are applied under gentler conditions, but their disadvantage is that the dyeings often have inadequate fastness properties.
  • the published patent application DE 43 17 855 A1 discloses ninhydrin-containing agents for dyeing keratin-containing fibers. Ninhydrin or its derivatives can be used in combination with compounds containing amino groups, with heterocycles or with hydroxy-substituted aromatic compounds. From the published patent application DE 43 35 627 A1, 1,3-propanediones and their derivatives for dyeing keratin fibers are known, which can also be used in combination with amines and amino acids. However, the agents described in the above publications do not always result in colorations with the desired application properties.
  • the object of the present invention is to provide colorants for keratin fibers, in particular human hair, which are qualitatively at least equivalent in terms of color depth, gray coverage and fastness properties to conventional oxidation hair colorants, but without being dependent on oxidizing agents such as H 2 O 2 .
  • Another object of the present invention is to provide colorants with which a wide variety of color shades can be obtained. Staining of the skin areas should be avoided if possible.
  • the colorants may have no or only a very low sensitization potential.
  • the present invention accordingly relates to the use of indanones of the following formula I.
  • R 1 and R 2 each independently represent a hydrogen atom, a halogen atom, a (CC 4 ) alkyl group, (CC 4 ) alkoxy group, hydroxy (C r C 4 ) alkoxy group, hydroxy group, nitro group, carboxy group, sulfo group, amino group , which can be substituted by (C, -C 4 ) alkyl groups, or (C, - C 4 ) acyl group, where the radicals R 1 and R 2 together can form a fused-on benzene ring, X is a nitromethylene group, an isonitrosomethylene group or one
  • Y represents a methylene group, ethylene group or carbonyl group, with the proviso that X and Y are not simultaneously a carbonyl group, in the presence of at least one compound having a primary or secondary amino group or hydroxyl group selected from primary or secondary aliphatic or aromatic amines, nitrogen-containing heterocyclic compounds, ⁇ - to ⁇ - amino acids, oligopeptides and aromatic hydroxy compounds composed of 2 to 9 amino acids, and / or at least one CH-active compound for dyeing fibers containing keratin.
  • a primary or secondary amino group or hydroxyl group selected from primary or secondary aliphatic or aromatic amines, nitrogen-containing heterocyclic compounds, ⁇ - to ⁇ - amino acids, oligopeptides and aromatic hydroxy compounds composed of 2 to 9 amino acids, and / or at least one CH-active compound for dyeing fibers containing keratin.
  • Another object of the present invention is an agent for dyeing keratin fibers, in particular human hair, which contains
  • a primary or secondary amino group or hydroxy group selected from primary or secondary aliphatic or aromatic amines, nitrogen-containing heterocyclic compounds, ⁇ - to ⁇ -amino acids, oligopeptides and aromatic hydroxy compounds composed of 2 to 9 amino acids, and / or at least a CH active compound.
  • Keratin-containing fibers are wool, furs, feathers and in particular human hair.
  • the colorants according to the invention can also be used to dye other natural fibers, such as Cotton, jute, sisal, linen or silk, modified natural fibers, e.g. Regenerated cellulose, nitro, alkyl or hydroxyalkyl or acetyl cellulose and synthetic fibers such as e.g. Polyamide, polyacrylonitrile, polyurethane and polyester fibers can be used.
  • the present invention also includes the use of substances which represent reaction products of the individual components with one another.
  • Suitable compounds of the formula I which can be used as component A are 1,2-indanedione, 2-oximo-1-indanone, indan-1, 2,3-trione-2-oxime, 5-methoxy-indane 1, 2,3-trione-2-oxime and 2-nitro-1,3-indanedione.
  • Suitable compounds with a primary or secondary amino group as component B are, for example, primary aromatic amines such as N, N-dimethyl-, N, N-diethyl-, N- (2-hydroxyethyl) -N-ethyl-, N, N-bis- ( 2-hydroxyethyl) -, N- (2-methoxyethyl-), 2,3-, 2,4-, 2,5-dichloro-p-phenylenediamine, 2-chloro-p-phenylenediamine, 2,5-dihydroxy-4 morpholinoaniline dihydrobromide, 2-, 3-, 4-aminophenol, 2-aminomethyl-4-aminophenol, 2-hydroxymethyl-4-aminophenol, o-, p-phenylenediamine, o-toluenediamine, 2,5-diamino-toluene, -phenol, -phenethol, 4-amino-3-methylphenol, 2- (2,5-diamin
  • R 3 represents a hydroxy or an amino group which can be substituted by C 1-4 alkyl, C 1-4 hydroxyalkyl or C alkoxy-C 1-4 alkyl
  • R 4 , R 5 , R 6 , R 7 and R 8 represent hydrogen, a hydroxy or an amino group, which is replaced by a C M alkyl, C 1-4 hydroxyalkyl, C M aminoalkyl or C 1-4 Alkoxy-C M alkyl group can be substituted, represent a carbon or sulfonic acid group
  • Z represents a direct bond, a saturated or unsaturated carbon chain with 1 to 4 carbon atoms, optionally substituted by hydroxyl groups, a carbonyl, sulfonyl or Imino group, an oxygen or sulfur atom, or a group with the formula III
  • the abovementioned compounds can be used both in free form and in the form of their physiologically tolerable salts, in particular as salts of inorganic acids, such as hydrochloric or sulfuric acid.
  • Suitable nitrogen-containing heterocyclic compounds are, for example, 2-, 3-, 4-amino, 2-amino-3-hydroxy, 2,6-diamino, 2,5-diamino, 2,3-diamino, 2-dimethylamino -5-amino-, 2-methylamino-3-amino-6-methoxy-, 2,3-diamino-6-methoxy-, 2,6-dimethoxy-3,5-diamino-, 2,4,5-triamino -, 2,6-dihydroxy-3,4-dimethylpyridine, 2,4-dihydroxy-5,6- diamino-, 4,5,6-triamino-, 4-hydroxy-2,5,6-triamino-, 2-hydroxy-4,5,6-triamino-, 2,4,5,6-tetraamino-, 2 -Methylamino-4,5,6-thamino-, 2,4-, 4,5-diamino-, 2-amino-4
  • Preferred amino acids are all naturally occurring and synthetic ⁇ -amino acids, e.g. obtained by hydrolysis from vegetable or animal proteins, e.g. Collagen, keratin, casein, elastin, soy protein, wheat gluten or almond protein, accessible amino acids. Both acidic and alkaline amino acids can be used. Preferred amino acids are arginine, histidine, tyrosine, phenylalanine, DOPA (dihydroxyphenylalanine), ornithine, lysine and tryptophan. But also other amino acids, e.g. 6-aminocaproic acid can be used.
  • the oligopeptides can be naturally occurring or synthetic oligopeptides, but also the oligopeptides contained in polypeptide or protein hydrolyzates, provided that they have sufficient water solubility for use in the colorants according to the invention.
  • examples are e.g. Glutathione or the oligopeptides contained in the hydrolyzates of collagen, keratin, casein, elastin, soy protein, wheat gluten or almond protein.
  • Use together with compounds having a primary or secondary amino group or with aromatic hydroxy compounds is preferred.
  • Suitable aromatic hydroxy compounds are, for example, 2-, 4-, 5-methylresorcinol, 2,5-dimethylresorcinol, resorcinol, 3-methoxyphenol, pyrocatechol, hydroquinone, pyrogallol, phloroglucinol, hydroxyhydroquinone, 2-, 3-, 4-methoxy, 3- Dimethylamino-, 2- (2-hydroxyethyl) -, 3,4-methylenedioxyphenol, 2,4-, 3,4-dihydroxybenzoic acid, phenylacetic acid, gallic acid, 2,4,6-trihydroxybenzoic acid, -acetophenone, 2-, 4- Chlororesorcinol, 1-naphthol, 1, 5-, 2,3-, 2,7-dihydroxynaphthalene, 6-dimethyiamino-4-hydroxy-2-naphthalenesulfonic acid, 3,6-dihydroxy-2,7-naphthalenesulfonic acid.
  • CH-active compounds which may be mentioned are 1, 2,3,3-tetramethyl-3H-indolium iodide, 1, 2,3,3-tetramethyl-3H-indolium-p-toluenesulfonate, 1, 2,3,3-tetrams - 3-H-indolium methanesulfonate, Fischer's base (1, 3,3-trimethyl-2-methylene indoline), 2,3-dimethyl-benzothiazolium iodide, 2,3-dimethyl-benzothiazolium p-toluenesulfonate, rhodanine, rhodanine -3-acetic acid, 1-ethyl-2-quinaldinium iodide, 1-methyl-2-quinaldinium iodide, barbituric acid, thiobarbituric acid, 1, 3-dimethylthiobarbituric acid, diethylthiobarbituric acid, oxindole, 3-
  • compositions preferably contain the compounds of components A and B in an amount of 0.03 to 65, in particular 1 to 40 mmol, based in each case on 100 g of the total colorant.
  • coloring substances can also be used together in all coloring agents; Likewise, several different components from the groups of compounds having a primary or secondary amino group, nitrogen-containing heterocycles, aromatic hydroxy compounds or amino acids can also be used together.
  • oxidizing agents for example H 2 O 2
  • H 2 O 2 oxidizing agents
  • Oxidizing agents are generally used in an amount of 0.01 to 6% by weight, based on the application solution.
  • a preferred oxidizing agent for human hair is H 2 O 2 .
  • the colorants according to the invention result in a wide range of color shades in the range from yellow to yellow-brown, orange, brown-orange, medium brown, dark brown, violet, dark violet to blue-black and black; the fastness properties are excellent, the sensitization potential is very low.
  • the colorants according to the invention contain, in addition to the compounds contained according to the invention, customary direct dyes, for example from the group of the nitrophenylenediamines, nitroaminophenols, anthraquinones or indophenols, such as those under the international names or trade names HC Yellow, for further modification of the shades 2, HC Yellow 4, HC Yellow 6, Basic Yellow 57, Disperse Orange 3, HC Red 3, HC Red BN, Basic Red 76, HC Blue 2, Disperse Blue 3, Basic Blue 99, HC Violet 1, Disperse Violet 1, Disperse Violet 4, Disperse Black 9, Basic Brown 16 and Basic Brown 17 known compounds as well as picramic acid, 2-amino-6-chloro-4-nitrophenol, 4-amino-2-nitrodiphenylamine-2'-carboxylic acid, 6-nitro-1 , 2,3,4-tetrahydroquinoxaline, 4-N-ethyl-1,4-bis (2'-hydroxyethylamino) -2-nitrobenz
  • oxidation dye orproducts or the optional direct dyes each represent uniform compounds. Rather, in the colorants according to the invention, due to the production processes for the individual dyes, further components may also be present in minor amounts, provided that these do not adversely affect the coloring result or for other reasons, e.g. toxicological, must be excluded.
  • the colorants according to the invention produce intensive colorations even at physiologically tolerable temperatures of below 45 ° C. They are therefore particularly suitable for dyeing human hair.
  • the colorants can usually be incorporated into a water-containing cosmetic carrier.
  • Suitable water-containing cosmetic carriers are, for example, creams, emulsions, gels or also surfactant-containing foaming solutions such as shampoos or other preparations which are suitable for use on the keratin-containing fibers. If necessary, it is also possible to incorporate the colorants into anhydrous carriers.
  • the colorants according to the invention can contain all active substances, additives and auxiliaries known in such preparations.
  • the colorants contain at least one surfactant, both anionic and zwitterionic, ampholytic, nonionic and cationic surfactants being suitable in principle. In many cases, however, it has proven advantageous to select the surfactants from anionic, zwitterionic or nonionic surfactants.
  • Suitable anionic surfactants in preparations according to the invention are all anionic surface-active substances suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 10 to 22 carbon atoms.
  • anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 10 to 22 carbon atoms.
  • the molecule can contain glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups.
  • anionic surfactants are, in the form of the sodium, potassium and ammonium as well as the mono-, di- and trialkanol ammonium salts with 2 or 3 C atoms in the alkanol group, linear fatty acids with 10 to 22 C atoms (Soap),
  • Ether carboxylic acids of the formula RO- (CH 2 -CH 2 O) x -CH 2 -COOH, in which R is a linear alkyl group with 10 to 22 C atoms and x 0 or 1 to 16, acyl sarcosides with 10 to 18 C- Atoms in the acyl group, acyl taurides with 10 to 18 C atoms in the acyl group, acyiisethionates with 10 to 18 C atoms in the acyl group, sulfosuccinic acid and dialkyl esters with 8 to 18 C atoms in the alkyl group and sulfosuccinic acid mono-alkyl polyoxyethyl esters with 8 to 18 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups, linear alkane sulfonates with 12 to 18 carbon atoms, linear alpha olefin sulfonates with 12 to 18 carbon atoms, methyl alpha
  • Esters of tartaric acid and citric acid with alcohols which are adducts of about 2-15 molecules of ethylene oxide and / or propylene oxide with fatty alcohols with 8 to 22 carbon atoms.
  • Preferred anionic surfactants are alkyl sulfates, alkyl polyglycol ether sulfates and ether carboxylic acids with 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule, and in particular salts of saturated and in particular unsaturated C 8 -C 22 carboxylic acids, such as oleic acid, stearic acid, isostearic acid and palmitic acid.
  • Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one -COO (" > - or -SO 3 (" 'group in the molecule.
  • Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl N, N-dimethylammonium glycinate, for example the coconut alkyl dimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate, for example the coconut acylaminopropyl dimethylammonium glycinate, and 2-alkyl-3-carboxymethyl-3-hydroxyethylimidazolines each with 8 to 18 carbon atoms in the alkyl or acyl group and cocoacylaminoethylhydroxyethyicarboxymethylglycinate
  • a preferred zwitterionic surfactant is the fatty acid amide dehvate known under the CT
  • Ampholytic surfactants are surface-active compounds which, in addition to a C 8-18 alkyl or acyl group, contain at least one free amino group and at least one -COOH or -SO 3 H group in the molecule and are capable of forming internal salts.
  • suitable ampholytic surfactants are N-alkylglycine, N-alkylpropionic acid, N-alkylaminobutyric acid, N-alkyliminodipropionic acid, N-hydroxyethyl-N-alkylamidopropylglycine, N-alkyltaurine, N-alkylsarcosine, 2-alkylaminopropionic acid and alkylaminoacetic acid each with about 8 to 18 C.
  • ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethylamino propionate and C 12 . 18 acyl sarcosine.
  • Nonionic surfactants contain z as a hydrophilic group.
  • B a polyol group, a polyalkylene glycol ether group or a combination of polyol and polyglycol ether group. Such connections are, for example
  • Examples of the cationic surfactants which can be used in the hair treatment compositions according to the invention are, in particular, quaternary ammonium compounds.
  • Ammonium halides such as alkyltrimethylammonium chlorides, dialkyldimethylmonium chloride and trialkylmethylammonium chlorides, for.
  • the quaternized protein hydrolyzates are further cationic surfactants which can be used according to the invention.
  • cationic silicone oils such as, for example, the commercially available products Q2-7224 (manufacturer: Dow Corning; a stabilized trimethylsilylamodimethicone), Dow Corning 929 emulsion (containing a hydroxylamino-modified silicone, which is also referred to as amodimethicone), SM -2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil®-Quat 3270 and 3272 (manufacturer: Th. Goldschmidt; diquaternary polydimethylsiloxanes, Quaterium-80).
  • alkylamidoamines especially fatty acid amidoamines such as the stearylamidopropyldimethylamine available under the name Tego Amid®S 18, are characterized in particular by their good biodegradability.
  • quaternary sugar derivative that can be used as a cationic surfactant is the commercial product Glucquat®100, according to the CTFA nomenclature a "lauryl methyl gluceth-10 hydroxypropyl dimonium chloride".
  • the compounds with alkyl groups used as surfactants can each be uniform substances. However, it is generally preferred to start from natural vegetable or animal raw materials in the production of these substances, so that substance mixtures with different alkyl chain lengths depending on the respective raw material are obtained.
  • both products with a "normal” homolog distribution and those with a narrowed homolog distribution can be used.
  • “Normal” homolog distribution is understood to mean mixtures of homologs which are obtained as catalysts from the reaction of fatty alcohol and alkylene oxide using alkali metals, alkali metal hydroxides or alkali metal alcoholates.
  • narrow homolog distributions are obtained if, for example, hydrotalcites, alkaline earth metal salts of ether carboxylic acids, alkaline earth metal oxides, hydroxides or alcoholates are used as catalysts. The use of products with a narrow homolog distribution can be preferred.
  • non-ionic polymers such as, for example, vinyl pyrrolidone / vinyl acrylate copolymers, polyvinyl pyrrolidone and vinyl pyrrolidone / vinyl acetate copolymers and
  • Polysiloxanes such as quaternized cellulose ethers, polysiloxanes with quaternary groups, dimethyldiallylammonium chloride polymers, acrylamide-dimethyldiallylammonium chloride copolymers, diethyl sulfate-quaternized dimethylaminoethyimethacrylate-vinylpyrrolidone copolymers, vinylpolymer
  • Imidazolinium methochloride copolymers and quaternized polyvinyl alcohol, zwitterionic and amphoteric polymers such as, for example, acrylamidopropyltrimethylammonium chloride / acrylate copolymers and octylacrylamide / methyl methacrylate / tert.-butylaminoethyl methacrylate / 2-hydroxypropyl methacrylate copolymers, anionic polymers such as polyacrylic acids, such as polyacids, for example polyacrylics, such as polyacids , Vinyl acetate / crotonic acid copolymers, vinyl pyrrolidone / vinyl acrylate
  • Thickeners such as agar agar, guar gum, alginates, xanthan gum, gum arabic, karaya gum, locust bean gum, linseed gums, dextrans,
  • Cellulose derivatives e.g. B. methyl cellulose, hydroxyalkyl cellulose and carboxymethyl cellulose, starch fractions and derivatives such as amylose, amylopectin and
  • Dextrins clays such as e.g. B. bentonite or fully synthetic hydrocolloids such as e.g.
  • Structurants such as glucose and maleic acid, hair-conditioning compounds such as phospholipids, for example soy lecithin, egg lecithin and cephalins, and silicone oils,
  • Protein hydrolyzates especially elastin, collagen, keratin, milk protein,
  • Solubilizers such as ethanol, isopropanol, ethylene glycol, propylene glycol,
  • Anti-dandruff agents such as piroctone olamine and zinc omadine, other substances for adjusting the pH value, Active ingredients such as panthenol, pantothenic acid, allantoin, pyrrolidone carboxylic acids and their salts, plant extracts and vitamins, cholesterol, light stabilizers,
  • Consistency generators such as sugar esters, polyol esters or polyol alkyl ethers, fats and waxes such as walrus, beeswax, montan wax, paraffins, fatty alcohols and fatty acid esters, fatty acid alkanolamides,
  • Swelling and penetration substances such as glycerol, propylene glycol monoethyl ether, carbonates, hydrogen carbonates, guanidines, ureas and primary, secondary and tertiary phosphates, imidazoles, tannins, pyrrole, opacifiers such as latex,
  • Pearlescent agents such as ethylene glycol mono- and distearate
  • Blowing agents such as propane-butane mixtures, N 2 O, dimethyl ether, CO 2 and air as well as antioxidants.
  • constituents of the water-containing carrier are used to produce the colorants according to the invention in amounts customary for this purpose; e.g. emulsifiers are used in concentrations of 0.5 to 30% by weight and thickeners in concentrations of 0.1 to 25% by weight of the total colorant.
  • Suitable metal salts are, for example, formates, carbonates, halides, sulfates, butyrates, valerates, capronates, acetates, lactates, glycolates, tartrates, citrates, gluconates, propionates, phosphates and phosphonates of alkali metals, such as potassium, sodium or lithium, alkaline earth metals, such as magnesium, Caicium, strontium or barium, or of aluminum, manganese, iron, cobalt, copper or zinc, with sodium acetate, lithium bromide, calcium bromide, calcium gluconate, zinc chloride, zinc sulfate, magnesium chloride, magnesium sulfate, ammonium carbonate, chloride and acetate being preferred.
  • These salts are preferably present in an amount of 0.03 to 65, in particular 1 to 40 mmol, based on 100 g of the total colorant.
  • the colorants are generally applied to the hair in the form of the water-containing, cosmetic carrier in an amount of 100 g, left there for about 30 minutes and then rinsed out or with a commercially available one Washed out hair shampoo.
  • the compounds of components A and B can either be applied to the hair simultaneously or in succession, it being irrelevant which of the components is applied first.
  • the optionally contained ammonium or metal salts can be added to the first or the second component. There may be an interval of up to 30 minutes between the application of the first and the second component. Pretreatment of the fibers with the saline solution is also possible.
  • Components A and B of the agents according to the invention can either be stored separately or together, either in a liquid to pasty preparation (aqueous or anhydrous) or as a dry powder. If the components are stored together in a liquid preparation, this should be largely anhydrous to reduce a reaction of the components. When stored separately, the reactive components are only intimately mixed with one another immediately before use. In dry storage, a defined amount of warm (50 to 80 ° C) water is usually added before use and a homogeneous mixture is produced.
  • a slurry of 10 mmoles of component A, 10 mmoles of an amine, 10 mmoles of sodium acetate and a drop of a 20% fatty alkyl ether sulfate solution in 100 ml of water was prepared.
  • the slurry was briefly heated to about 80 ° C and filtered after cooling, the pH was then adjusted to 6.
  • a strand of 90% gray, untreated human hair was placed in this coloring solution at 30 ° C. for 30 minutes.
  • the colored streak was then rinsed for 30 seconds with lukewarm water, dried in a warm (30-40 ° C.) air stream and then combed out. The colorations were then assessed visually in daylight.
  • the color depth was rated on the following scale:
  • Component B Color shade Color depth
  • Component B Color shade Color depth
  • Component B Color shade Color depth
  • Component B shade nuance color depth

Abstract

L'invention concerne l'utilisation pour colorer des fibres à base de kératine, d'indanones de la formule (I) dans laquelle R1 et R2 désignent dans chaque cas indépendamment l'un de l'autre, un atome d'hydrogène, un atome d'halogène, un groupe alkyle (C¿1?-C4), un groupe alcoxy (C1-C4), un groupe hydroxy-alcoxy (C1-C4), un groupe hydroxy, un groupe nitro, un groupe carboxy, un groupe sulfo, un groupe amino, qui peut être substitué par des groupes alkyle (C1-C4), ou un groupe acyle (C1-C4), les restes R?1 et R2¿ pouvant former conjointement un composé cyclique benzène condensé, X désigne un groupe nitrométhylène, un groupe isonitrosométhylène ou un groupe carbonyle et Y désigne un groupe méthylène, un groupe éthylène ou un groupe carbonyle, sous réserve que X et Y ne désignent pas simultanément un groupe carbonyle, en présence d'au moins un composé ayant un groupe amino primaire ou secondaire ou un groupe hydroxy, sélectionné parmi des amines aliphatiques ou aromatiques primaires ou secondaires, des composés hétérocycliques contenant de l'azote, des aminoacides α à φ, des oligopeptides composés de 2 à 9 aminoacides et des composés hydroxy aromatiques, et/ou au moins un composé CH-actif.
EP98954332A 1997-10-14 1998-10-05 Utilisation d'indanones pour colorer des fibres a base de keratine Ceased EP1028694A1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE19745355 1997-10-14
DE1997145355 DE19745355A1 (de) 1997-10-14 1997-10-14 Verwendung von Indanonen zum Färben von keratinhaltigen Fasern
PCT/EP1998/006306 WO1999018914A2 (fr) 1997-10-14 1998-10-05 Utilisation d'indanones pour colorer des fibres a base de keratine

Publications (1)

Publication Number Publication Date
EP1028694A1 true EP1028694A1 (fr) 2000-08-23

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EP98954332A Ceased EP1028694A1 (fr) 1997-10-14 1998-10-05 Utilisation d'indanones pour colorer des fibres a base de keratine

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Country Link
EP (1) EP1028694A1 (fr)
JP (1) JP2001519369A (fr)
AU (1) AU732041B2 (fr)
DE (1) DE19745355A1 (fr)
WO (1) WO1999018914A2 (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19857847A1 (de) * 1998-12-15 2000-06-21 Wella Ag Mittel zum Färben von Fasern mit 1,3-Indandionen und aromatischen Aminen
MXPA00003542A (es) * 1999-04-30 2002-03-08 Squibb Bristol Myers Co Composiciones de colorante o tinte oxidante con acondicionamiento y deposicion mejorada del tinte.
US7179306B2 (en) 2003-07-25 2007-02-20 L'oreal S.A. Process for dying keratin fibers comprising at least one aryl or aryloxy substitutent-based ninhydrin derivative
FR2857866B1 (fr) 2003-07-25 2005-12-16 Oreal Utilisation en coloration capillaire de derives de ninhydrine portant un systeme insature
FR2857865B1 (fr) 2003-07-25 2005-12-16 Oreal Utilisation en coloration capillaire de derives de ninhydrine
US7179304B2 (en) 2003-07-25 2007-02-20 L'oreal S.A. Process for dyeing keratin fibers with at least one polycyclic aromatic vicinal trione
FR2857870B1 (fr) * 2003-07-25 2005-10-14 Oreal Utilisation en coloration de derives de ninhydrine a substituants aryle ou aryloxy
US7192455B2 (en) 2003-07-25 2007-03-20 L'oreal S.A. Process for dyeing keratin fibers with at least one ninhydrin derivative
FR2857867B1 (fr) 2003-07-25 2005-10-14 Oreal Utilisation en coloration capillaire de derives de ninhydrine portant un groupe heteroalkyle
FR2857857A1 (fr) * 2003-07-25 2005-01-28 Oreal Utilisation en coloration capillaire de derives de ninhydrine a substituants aryle ou aryloxy
US7374580B2 (en) 2004-06-14 2008-05-20 L'oreal S.A. Dyeing compositions comprising A 1,2-indandione derivative
FR2871374B1 (fr) 2004-06-14 2007-08-24 Oreal Compositions tinctoriales comprenant un derive de 1,3-indanedione
FR2871375B1 (fr) 2004-06-14 2007-07-13 Oreal Compositions tinctoriales comprenant un derive de 1,2-indanedione
US7367993B2 (en) 2004-06-14 2008-05-06 L'oreal S.A. Dyeing compositions comprising at least one 1,3-indandione derivative
ES2290806T3 (es) * 2005-04-02 2008-02-16 Wella Aktiengesellschaft Sistema colorante reductor para fibras de queratina.
ES2290805T3 (es) * 2005-04-02 2008-02-16 Wella Aktiengesellschaft Colorante reductor para fibras de queratina.

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3009833A1 (de) * 1980-03-14 1981-10-01 Henkel Kgaa Verbessertes haarfaerbeverfahren mittels azo-entwicklungsfarbstoffen
DE4317855A1 (de) * 1993-05-28 1994-12-01 Henkel Kgaa Ninhydrinhaltige Mittel zum Färben keratinhaltiger Fasern
DE4335627A1 (de) * 1993-10-19 1995-04-20 Henkel Kgaa 1,3-Propandione zum Färben keratinhaltiger Fasern
DE4335628A1 (de) * 1993-10-19 1995-04-20 Henkel Kgaa Mittel zum Färben keratinhaltiger Fasern
DE19527121A1 (de) * 1995-07-25 1997-01-30 Henkel Kgaa Oxidationsfärbemittel

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9918914A3 *

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WO1999018914A3 (fr) 1999-06-24
AU1149899A (en) 1999-05-03
WO1999018914A2 (fr) 1999-04-22
JP2001519369A (ja) 2001-10-23
DE19745355A1 (de) 1999-04-15
AU732041B2 (en) 2001-04-12

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