WO2023275197A1 - Composition comprenant au moins un colorant d'oxydation, au moins un agent alcalin et au moins un alcool gras liquide et au moins un alcool gras solide - Google Patents

Composition comprenant au moins un colorant d'oxydation, au moins un agent alcalin et au moins un alcool gras liquide et au moins un alcool gras solide Download PDF

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Publication number
WO2023275197A1
WO2023275197A1 PCT/EP2022/067987 EP2022067987W WO2023275197A1 WO 2023275197 A1 WO2023275197 A1 WO 2023275197A1 EP 2022067987 W EP2022067987 W EP 2022067987W WO 2023275197 A1 WO2023275197 A1 WO 2023275197A1
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solvates
weight
salts
composition
chosen
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PCT/EP2022/067987
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English (en)
Inventor
Sarah BOULEMNAKHER
Hanène MOUEDDENE
Amine MEGUENI
Laurence COTTARD-MEI
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L'oreal
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Priority claimed from FR2107046A external-priority patent/FR3124708B1/fr
Priority claimed from FR2107037A external-priority patent/FR3124720B1/fr
Application filed by L'oreal filed Critical L'oreal
Priority to EP22740850.7A priority Critical patent/EP4362890A1/fr
Publication of WO2023275197A1 publication Critical patent/WO2023275197A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A61K8/345—Alcohols containing more than one hydroxy group
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A61K8/342—Alcohols having more than seven atoms in an unbroken chain
    • 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
    • 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
    • A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
    • 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
    • A61K8/415—Aminophenols
    • 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
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4926—Cosmetics 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
    • 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
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A61K8/498—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/10—Preparations for permanently dyeing the hair
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
    • A61K2800/88—Two- or multipart kits
    • A61K2800/882—Mixing prior to application

Definitions

  • TITLE Composition comprising at least one oxidation dye, at least one alkaline agent and at least one liquid fatty alcohol and at least one solid fatty alcohol
  • the invention relates to a composition
  • a composition comprising at least one oxidation dye, at least one alkaline agent chosen from alkanolamines, at least one liquid fatty alcohol and at least one solid fatty alcohol.
  • the invention also relates to a process for dyeing keratin fibres, notably the hair, using this composition.
  • the invention relates to the use of such a composition for dyeing keratin fibres, and notably the hair.
  • oxidation dye precursors such as ortho- or para-phenylenediamines, ortho- or para-aminophenols, or heterocyclic compounds such as pyrazoles, pyrazolinones or pyrazolo-pyridines.
  • oxidation bases are colourless or weakly coloured compounds which, when combined with oxidizing products, may give rise to coloured compounds via a process of oxidative condensation.
  • the dyeing power obtained may not be entirely satisfactory, or may even be weak, and lead to a restricted range of colours.
  • the colourings may also be insufficiently persistent with respect to external agents such as light, shampoo or perspiration, and may also be too selective, i.e. the difference in colouring is too great along the same keratin fibre that is differently sensitized between its end and its root.
  • the regulatory conditions regarding certain compounds are increasingly stringent. It is thus necessary to develop compositions comprising alternative compounds.
  • composition for dyeing keratin fibres in particular human keratin fibres such as the hair, which is more environmentally friendly and which does not have the abovementioned drawbacks, i.e. which is capable of giving good colour build-up, intensity and chromaticity while at the same time having low selectivity and good persistence and which is capable of giving good dyeing performance, even after a period of storage, while at the same time having good working qualities.
  • composition comprising: - one or more oxidation dyes chosen from at least one coupler chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl- 3,4-methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof; (III) and at least one oxidation base chosen from: 2- b -hydroxyethyl-para-phenylenediamine and the addition salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-( g -hydroxypropyl)-para-phenylenediamine and the salts thereof, the
  • the composition according to the invention comprises:
  • At least one coupler chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl-3,4-methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof;
  • the composition according to the invention comprises: - at least one oxidation base chosen from: 2- b -hydroxyethyl-para-phenylenediamine and the addition salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-( g -hydroxypropyl)-para-phenylenediamine and the salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-methoxymethyl-para-phenylenediamine and the addition salts thereof, the solvates thereof and/or the solvates of salts thereof, and mixtures thereof;
  • the composition according to the invention comprises:
  • - at least one oxidation base chosen from: 2- b -hydroxyethyl-para-phenylenediamine and the addition salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-( g -hydroxypropyl)-para-phenylenediamine and the salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-methoxymethyl-para-phenylenediamine and the addition salts thereof, the solvates thereof and/or the solvates of salts thereof, and mixtures thereof;
  • the oxidation coupler(s) may be chosen from all the oxidation couplers as defined hereinbelow.
  • the composition according to the invention is a composition for dyeing keratin fibres, notably the hair.
  • composition according to the invention may notably lead to chromatic, powerful, intense and sparingly selective colourings, i.e. colourings that are uniform along the length of the fibre. It also allows various shades to be achieved in a very wide range of colours. It also enables good colour build-up.
  • This composition also gives particularly good coverage of depigmented keratin fibres such as grey hair.
  • the composition according to the invention has good working qualities, notably a creamy texture allowing quick and easy mixing with an oxidizing composition, where appropriate, and easy and uniform spreading over the entire head of hair.
  • the composition according to the invention has good stability over time, notably little or no change in its viscosity during storage.
  • a subject of the invention is also a kit comprising, in a first compartment, a composition as defined previously and, in a second compartment, an oxidizing composition comprising at least one chemical oxidizing agent.
  • the term “chemical oxidizing agent” means an oxidizing agent other than atmospheric oxygen.
  • oxidation dyes means dyes chosen from oxidation couplers and oxidation bases.
  • composition according to the invention may comprise one or more oxidation couplers.
  • composition according to the invention comprises at least one particular coupler.
  • composition according to the present invention comprises one or more couplers chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl-3,4- methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof.
  • couplers chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl-3,4- methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salt
  • the addition salts of the compounds of formulae (I), (II) and (III) are notably chosen from the addition salts with an acid, such as the hydrochlorides, hydrobromides, sulfates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, phosphates and acetates, and the addition salts with a base such as sodium hydroxide, potassium hydroxide, aqueous ammonia, amines or alkanolamines.
  • an acid such as the hydrochlorides, hydrobromides, sulfates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, phosphates and acetates
  • a base such as sodium hydroxide, potassium hydroxide, aqueous ammonia, amines or alkanolamines.
  • the solvates of the compounds of formulae (I), (II) and (III) more particularly represent the hydrates of these compounds and/or the combination of these compounds with a linear or branched Cl to C4 alcohol such as methanol, ethanol, isopropanol or n-propanol.
  • a linear or branched Cl to C4 alcohol such as methanol, ethanol, isopropanol or n-propanol.
  • the solvates are hydrates.
  • the total content of the couplers chosen from the compounds of formulae (I), (II) and (III) and also the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof preferably ranges from 0.001% to 20% by weight, more preferentially from 0.005% to 15% by weight, better still from 0.01% to 10% by weight, even better still from 0.05% to 5% by weight, and even better still from 0.1% to 3% by weight, relative to the total weight of the composition.
  • the total content of the couplers chosen from 6- hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof preferably ranges from 0.001% to 20% by weight, more preferentially from 0.005% to 15% by weight, better still 0.01% to 10% by weight, even better still from 0.05% to 5% by weight, and even better still from 0.1% to 3% by weight, relative to the total weight of the composition.
  • the total content of the couplers chosen from hydroxyethyl-3,4- methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof preferably ranges from 0.001% to 20% by weight, more preferentially from 0.005% to 15% by weight, better still from 0.01% to 10% by weight, even better still from 0.05% to 5% by weight, and even better still from 0.1% to 3% by weight, relative to the total weight of the composition.
  • the total content of the couplers chosen from 2-amino-5- ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof preferably ranges from 0.001% to 20% by weight, more preferentially from 0.005% to 15% by weight, better still from 0.01% to 10% by weight, even better still from 0.05% to 5% by weight, and even better still from 0.1% to 3% by weight, relative to the total weight of the composition.
  • composition according to the invention may optionally also comprise one or more additional couplers, other than the compounds of formulae (I), (II) and (III) and the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof advantageously chosen from those conventionally used in the dyeing of keratin fibres.
  • addition salts of the couplers that may be used in the context of the invention are chosen in particular from addition salts with an acid, such as hydrochlorides, hydrobromides, sulfates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, phosphates and acetates, and the addition salts with a base such as sodium hydroxide, potassium hydroxide, aqueous ammonia, amines or alkanolamines.
  • an acid such as hydrochlorides, hydrobromides, sulfates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, phosphates and acetates
  • a base such as sodium hydroxide, potassium hydroxide, aqueous ammonia, amines or alkanolamines.
  • the solvates more particularly represent the hydrates of these couplers and/or the combination of these couplers with a linear or branched Cl to C4 alcohol such as methanol, ethanol, isopropanol or n-propanol.
  • a linear or branched Cl to C4 alcohol such as methanol, ethanol, isopropanol or n-propanol.
  • the solvates are hydrates.
  • the composition according to the invention is free of oxidation couplers chosen from resorcinol, 2-methylresorcinol, 4-chlororesorcinol, the addition salts thereof, the solvates thereof and the solvates of the salts thereof.
  • the total content of the additional coupler(s), other than the couplers of formulae (I), (II) and (III), salts thereof, solvates thereof and solvates of the salts thereof, present in the composition according to the invention ranges from 0.001% to 20% by weight, more preferentially from 0.005% to 15% by weight, better still from 0.01% to 10% by weight, even better still from 0.05% to 5% by weight, and even better still from 0.1% to 3% by weight, relative to the total weight of the composition.
  • composition according to the present invention comprises one or more alkaline agent(s), chosen from alkanolamines, the total content of alkanolamine(s) being greater than or equal to 5% by weight relative to the total weight of the composition.
  • alkanolamine means an organic amine comprising a primary, secondary or tertiary amine function, and one or more linear or branched C j -Cg alkyl groups bearing one or more hydroxyl radicals.
  • Organic amines chosen from alkanolamines such as monoalkanolamines, dialkanolamines or trialkanolamines comprising one to three identical or different C/-C 4 hydroxyalkyl radicals are in particular suitable for performing the invention.
  • the alkanolamine(s) are chosen from monoethanolamine (MEA), diethanolamine, triethanolamine, monoisopropanolamine, diisopropanolamine, N,N- dimethylethanolamine, 2-amino-2-methyl-l-propanol, triisopropanolamine, 2-amino-2- m ethyl -1,3 -propanediol, 3-ami no- 1,2-propanediol, 3-dimethylamino- 1,2 -propanediol, tris(hydroxymethyl)aminomethane and mixtures thereof.
  • MEA monoethanolamine
  • diethanolamine triethanolamine
  • monoisopropanolamine diisopropanolamine
  • N,N- dimethylethanolamine 2-amino-2-methyl-l-propanol
  • 2-amino-2-methyl-l-propanol triisopropanolamine
  • the alkanolamine is monoethanolamine.
  • the total amount of alkanolamine(s), preferably of monoethanolamine, preferably ranges from 5% to 40% by weight, preferentially from 6% to 40% by weight, more preferentially from 7% to 35% by weight, better still from 8% to 30% by weight, even better still from 9% to 25% by weight, or even from 10% to 20% by weight, relative to the total weight of the composition.
  • composition according to the present invention may also comprise other mineral, organic or hybrid alkaline agents, other than alkanolamines.
  • alkaline agent and “ basifying agent” are used interchangeably.
  • the mineral basifying agent(s) are preferably chosen from aqueous ammonia, alkali metal carbonates or bicarbonates such as sodium (hydrogen) carbonate and potassium (hydrogen) carbonate, alkali metal or alkaline-earth metal phosphates such as sodium phosphates or potassium phosphates, sodium or potassium hydroxides, alkali metal or alkaline-earth metal silicates or metasilicates such as sodium metasilicate, and mixtures thereof.
  • the organic basifying agent(s) are preferably chosen from amino acids, organic amines other than alkanolamines, oxyethylenated and/or oxypropylenated ethylenediamines, 1,3-diaminopropane, spermine, spermidine and mixtures thereof.
  • the amino acids are basic amino acids comprising an additional amine function.
  • Such basic amino acids are preferably chosen from histidine, lysine, arginine, ornithine and citru Mine.
  • the organic amine may also be chosen from organic amines of heterocyclic type. Besides histidine that has already been mentioned in the amino acids, mention may in particular be made of pyridine, piperidine, imidazole, triazole, tetrazole and benzimidazole.
  • the organic amine may also be chosen from amino acid dipeptides.
  • amino acid dipeptides that may be used in the present invention, mention may notably be made of carnosine, anserine and balenine.
  • the organic amine may also be chosen from compounds including a guanidine function.
  • amines of this type other than arginine that may be used in the present invention, mention may notably be made of creatine, creatinine, 1,1-dimethylguanidine, 1,1-diethylguanidine, glycocyamine, metformin, agmatine, n-amidoalanine, 3-guanidinopropionic acid, 4-guanidinobutyric acid and 2-([amino(imino)methyl]amino)ethane-l-sulfonic acid.
  • the additional alkaline agent(s) that are useful according to the invention are preferably chosen from aqueous ammonia, carbonates or bicarbonates such as sodium (hydrogen) carbonate and potassium (hydrogen) carbonate, alkali metal or alkaline-earth metal silicates or metasilicates such as sodium metasilicate, and mixtures thereof.
  • composition according to the invention is free of aqueous ammonia.
  • the total content of the alkaline agent(s) other than the alkanolamines preferably ranges from 0.1% to 20% by weight, more preferentially from 0.5% to 10% by weight, better still from 1% to 5% by weight, and even better still from 2% to 4% by weight, relative to the total weight of the composition.
  • the pH of the composition according to the invention is between 8 and 13; preferably between 9.0 and 12.
  • the pH of the composition may be adjusted to the desired value by means of acidic or alkaline agent(s) commonly used in the dyeing of keratin fibres, such as those described previously, or alternatively using buffer systems known to those skilled in the art.
  • composition according to the invention comprises at least one liquid fatty alcohol and at least one solid fatty alcohol, the total content of liquid fatty alcohol(s) and of solid fatty alcohol(s) being greater than or equal to 5% by weight relative to the total weight of the composition.
  • the total content of solid fatty alcohol(s) is greater than or equal to 5% by weight relative to the total weight of the composition.
  • fatty alcohols means compounds containing at least one linear or branched, saturated or unsaturated hydrocarbon-based group comprising from 6 to 40 and better still from 8 to 30 carbon atoms, which are optionally substituted, in particular with one or more hydroxyl groups (in particular 1 to 4). If they are unsaturated, these compounds may comprise one to three conjugated or unconjugated carbon-carbon double bonds.
  • the fatty alcohols that may be used in the present invention are neither (poly)oxyalkylenated nor (poly)glycerolated.
  • liquid fatty alcohol means a fatty alcohol with a melting point of less than or equal to 25° C at atmospheric pressure (1.013 x 10 5 Pa) and the term “solid fatty alcohol” means a fatty alcohol with a melting point of greater than 25° C at atmospheric pressure (1.013 x 10 5 Pa).
  • the melting point corresponds to the temperature of the most endothermic peak observed on thermal analysis (differential scanning calorimetry or DSC) as described in the standard ISO 11357-3; 1999.
  • the melting point may be measured using a differential scanning calorimeter (DSC), for example the calorimeter sold under the name MDSC 2920 by the company TA Instruments.
  • DSC differential scanning calorimeter
  • all the melting points are determined at atmospheric pressure (1.013 x 10 5 Pa).
  • the liquid fatty alcohols that are suitable for use in the invention are more particularly chosen from linear or branched, saturated or unsaturated alcohols, preferably unsaturated or branched alcohols, including from 6 to 40 carbon atoms and preferably from 8 to 30 carbon atoms. These fatty alcohols are neither oxyalkylenated nor glycerolated.
  • Examples that may be mentioned include octyldodecanol, 2-butyloctanol, 2-hexyldecanol, 2-undecylpentadecanol, isostearyl alcohol, oleyl alcohol, linolenyl alcohol, ricinoleyl alcohol, undecylenyl alcohol and linoleyl alcohol, and mixtures thereof.
  • oleyl alcohol will be used.
  • the solid fatty alcohols may be saturated or unsaturated, and linear or branched, and include from 8 to 40 carbon atoms, preferably from 10 to 30 carbon atoms.
  • the solid fatty alcohols have the structure R-OH with R denoting a linear alkyl group, optionally substituted with one or more hydroxyl groups, comprising from 8 to 40, preferentially from 10 to 30 carbon atoms, better still from 12 to 24 atoms and even better still from 14 to 22 carbon atoms.
  • the solid fatty alcohols that may be used are preferably chosen from saturated or unsaturated, linear or branched, preferably linear and saturated, (mono)alcohols including from 8 to 40 carbon atoms, preferentially from 10 to 30, better still from 12 to 24 and even better still from 14 to 22 carbon atoms.
  • the solid fatty alcohols that may be used may be chosen, alone or as a mixture, from: myristyl alcohol (or 1-tetradecanol); cetyl alcohol (or 1-hexadecanol); stearyl alcohol (or 1-octadecanol); arachidyl alcohol (or 1-eicosanol); behenyl alcohol (or 1-docosanol); lignoceryl alcohol (or 1-tetracosanol); ceryl alcohol (or 1-hexacosanol); montanyl alcohol (or 1-octacosanol); myricyl alcohol (or 1-triacontanol).
  • the solid fatty alcohol is chosen from cetyl alcohol, stearyl alcohol, behenyl alcohol, myristyl alcohol, arachidyl alcohol, and mixtures thereof, such as cetylstearyl alcohol or cetearyl alcohol.
  • the solid fatty alcohol is chosen from cetyl alcohol, stearyl alcohol and mixtures thereof such as cetylstearyl alcohol or cetearyl alcohol.
  • the total content of liquid fatty alcohol(s) and of solid fatty alcohol(s) preferably ranges from 6% to 40% by weight, preferentially from 7% to 35% by weight, better still from 8% to 30% by weight, even better still from 9% to 25% by weight, or even from 10% to 20% by weight, relative to the total weight of the composition.
  • the total content of solid fatty alcohol(s) is greater than or equal to 5% by weight, preferably ranges from 6% to 40% by weight, more preferentially from 7% to 35% by weight, better still from 8% to 30% by weight, even better still from 9% to 25% by weight, or even from 10% to 20% by weight, relative to the total weight of the composition.
  • the total content of liquid fatty alcohol(s) preferably ranges from 0.5% to 15% by weight, more preferentially from 1% to 10% by weight and better still from 2% to 5% by weight relative to the total weight of the composition.
  • composition according to the invention may also comprise one or more fatty substances other than the fatty acids and other than the liquid fatty alcohols and the solid fatty alcohols as defined previously.
  • the additional fatty substances that are useful according to the invention may be liquid fatty substances (or oils) and/or solid fatty substances.
  • liquid fatty substance means a fatty substance with a melting point of less than or equal to 25° C at atmospheric pressure (1.013 x 10 5 Pa) and the term “solid fatty substance” means a fatty substance with a melting point of greater than 25° C at atmospheric pressure (1.013 x lO 5 Pa).
  • fatty substance means an organic compound that is insoluble in water at 25° C and at atmospheric pressure (1.013 x 10 5 Pa) (solubility of less than 5% by weight, preferably less than 1% by weight, even more preferentially less than 0.1% by weight).
  • the fatty substances bear in their structure at least one hydrocarbon-based chain including at least 6 carbon atoms and/or a sequence of at least two siloxane groups.
  • the fatty substances are generally soluble in organic solvents under the same temperature and pressure conditions, for instance chloroform, dichloromethane, carbon tetrachloride, ethanol, benzene, toluene, tetrahydrofuran (THF), liquid petroleum jelly or decamethylcyclopentasiloxane.
  • the additional fatty substances other than the fatty acids and other than the solid fatty alcohols and the liquid fatty alcohols, that may be used in the present invention, are neither (poly)oxyalkylenated nor (poly)glycerolated.
  • the additional fatty substances other than the fatty acids and other than the solid fatty alcohols and the liquid fatty alcohols, that are useful according to the invention are non-silicone.
  • non-silicone fatty substance refers to a fatty substance not containing any Si-0 bonds and the term “silicone fatty substance” refers to a fatty substance containing at least one Si-0 bond.
  • the additional liquid fatty substance(s) other than the liquid fatty acids and the liquid fatty alcohols may be chosen from C6 to C16 liquid hydrocarbons, liquid hydrocarbons comprising more than 16 carbon atoms, non-silicone oils of animal origin, oils of triglyceride type of plant or synthetic origin, fluoro oils, liquid esters of fatty acid and/or of fatty alcohol other than triglycerides, and mixtures thereof.
  • the fatty esters more particularly contain at least one saturated or unsaturated, linear or branched hydrocarbon-based group, comprising 6 to 40 and better still from 8 to 30 carbon atoms, which is optionally substituted, in particular, with one or more hydroxyl groups (in particular 1 to 4). If they are unsaturated, these compounds may comprise one to three conjugated or unconjugated carbon-carbon double bonds.
  • C6 to C16 liquid hydrocarbons these may be linear, branched, or optionally cyclic, and are preferably chosen from alkanes. Examples that may be mentioned include hexane, cyclohexane, undecane, dodecane, isododecane, tridecane or isoparaffins, such as isohexadecane or isodecane, and mixtures thereof.
  • the liquid hydrocarbons comprising more than 16 carbon atoms may be linear or branched, and of mineral or synthetic origin, and are preferably chosen from liquid paraffins or liquid petroleum jelly (or mineral oil), polydecenes, hydrogenated polyisobutene such as Parleam ® , and mixtures thereof.
  • a hydrocarbon-based oil of animal origin that may be mentioned is perhydrosqualene.
  • the triglyceride oils of plant or synthetic origin are preferably chosen from liquid fatty acid triglycerides including from 6 to 30 carbon atoms, for instance heptanoic or octanoic acid triglycerides, or alternatively, for example, sunflower oil, maize oil, soybean oil, marrow oil, grapeseed oil, sesame seed oil, hazelnut oil, apricot oil, macadamia oil, arara oil, castor oil, avocado oil, caprylic/capric acid triglycerides, for instance those sold by the company Stearinerie Dubois or those sold under the names Miglyol ® 810, 812 and 818 by the company Dynamit Nobel, jojoba oil and shea butter oil, and mixtures thereof.
  • liquid fatty acid triglycerides including from 6 to 30 carbon atoms, for instance heptanoic or octanoic acid triglycerides, or alternatively, for example, sunflower oil, mai
  • fluoro oils they may be chosen from perfluoromethylcyclopentane and perfluoro-l,3-dimethylcyclohexane, sold under the names Flutec ® PCI and Flutec ® PC3 by the company BNFL Fluorochemicals; perfluoro-l,2-dimethylcyclobutane; perfluoroalkanes such as dodecafluoropentane and tetradecafluorohexane, sold under the names PF 5050 ® and PF 5060 ® by the company 3M, or bromoperfluorooctyl sold under the name Foralkyl ® by the company Atochem; nonafluoromethoxybutane and nonafluoroethoxyisobutane; perfluoromorpholine derivatives such as 4- trifluoromethylperfluoromorpholine sold under the name PF 5052 ® by the company 3M.
  • liquid esters of fatty acids and/or of fatty alcohols other than the triglycerides mentioned previously, mention may be made notably of esters of saturated or unsaturated, linear Cl to C26 or branched C3 to C26 aliphatic mono- or polyacids and of saturated or unsaturated, linear Cl to C26 or branched C3 to C26 aliphatic mono- or polyalcohols, the total carbon number of the esters being greater than or equal to 6 and more advantageously greater than or equal to 10.
  • esters of monoalcohols Preferably, for the esters of monoalcohols, at least one from among the alcohol and the acid is branched.
  • dihydroabietyl behenate octyldodecyl behenate; isocetyl behenate; isostearyl lactate; lauryl lactate; linoleyl lactate; oleyl lactate; isostearyl octanoate; isocetyl octanoate; octyl octanoate; decyl oleate; isocetyl isostearate; isocetyl laurate; isocetyl stearate; isodecyl octanoate; isodecyl oleate; isononyl isononanoate; isostearyl palmitate; methyl acetyl ricinoleate; octyl isononanoate; 2-ethyl hexyl isononate; octyldodecyl
  • ethyl palmitate and isopropyl palmitate alkyl myristates such as isopropyl myristate or ethyl myristate, isocetyl stearate, 2-ethyl hexyl isononanoate, isodecyl neopentanoate and isostearyl neopentanoate, and mixtures thereof.
  • Esters of C4 to C22 dicarboxylic or tricarboxylic acids and of Cl to C22 alcohols and esters of monocarboxylic, dicarboxylic or tricarboxylic acids and of C2 to C26 dihydroxy, trihydroxy, tetrahydroxy or pentahydroxy alcohols may also be used.
  • composition may also comprise, as fatty ester, sugar esters and diesters of C6 to C30 and preferably C12 to C22 fatty acids.
  • sugar esters refers to oxygen-bearing hydrocarbon-based compounds bearing several alcohol functions, with or without aldehyde or ketone functions, and which include at least 4 carbon atoms.
  • sugars may be monosaccharides, oligosaccharides or polysaccharides other than the anionic polysaccharides described hereinbelow.
  • suitable sugars include sucrose, glucose, galactose, ribose, fucose, maltose, fructose, mannose, arabinose, xylose and lactose, and derivatives thereof, notably alkyl derivatives, such as methyl derivatives, for instance methylglucose.
  • the sugar esters of fatty acids may be chosen notably from the group comprising the esters or mixtures of esters of sugars described above and of linear or branched, saturated or unsaturated C6 to C30 and preferably C12 to C22 fatty acids. If they are unsaturated, these compounds may comprise one to three conjugated or unconjugated carbon-carbon double bonds.
  • the esters may also be chosen from monoesters, diesters, triesters, tetraesters and polyesters, and mixtures thereof.
  • esters may be, for example, oleates, laurates, palmitates, myristates, behenates, cocoates, stearates, linoleates, linolenates, caprates, arachidonates or mixtures thereof notably such as the mixed oleo-palmitate, oleo-stearate and palmito-stearate esters
  • monoesters and diesters and notably sucrose, glucose or methylglucose mono- or di-oleates, -stearates, -behenates, -oleopalmitates, - linoleates, -linolenates and -oleostearates, and mixtures thereof.
  • liquid ester of a monoacid and of a monoalcohol Preferably, use will be made of a liquid ester of a monoacid and of a monoalcohol.
  • the additional solid fatty substances other than the solid fatty alcohols preferably have a viscosity of greater than 2 Pa.s, measured at 25° C and at a shear rate of 1 s _1 .
  • the additional solid fatty substance(s) other than the solid fatty alcohols are preferably chosen from solid esters of fatty acids and/or of fatty alcohols, waxes, ceramides and mixtures thereof.
  • the solid esters of a fatty acid and/or of a fatty alcohol that may be used are preferably chosen from esters derived from a C9-C26 carboxylic fatty acid and/or from a C9-C26 fatty alcohol.
  • these solid fatty esters are esters of a linear or branched, saturated carboxylic acid including at least 10 carbon atoms, preferably from 10 to 30 carbon atoms and more particularly from 12 to 24 carbon atoms, and of a linear or branched, saturated monoalcohol, including at least 10 carbon atoms, preferably from 10 to 30 carbon atoms and more particularly from 12 to 24 carbon atoms.
  • the saturated carboxylic acids may optionally be hydroxylated, and are preferably monocarboxylic acids.
  • Esters of C4-C22 dicarboxylic or tricarboxylic acids and of C1-C22 alcohols and esters of monocarboxylic, dicarboxylic or tricarboxylic acids and of C2-C26 dihydroxy, trihydroxy, tetrahydroxy or pentahydroxy alcohols may also be used.
  • the solid esters of a fatty acid and/or of a fatty alcohol are chosen from C9- C26 alkyl palmitates, notably myristyl palmitate, cetyl palmitate or stearyl palmitate; C9- C26 alkyl myristates, such as cetyl myristate, stearyl myristate and myristyl myristate; and C9-C26 alkyl stearates, notably myristyl stearate, cetyl stearate and stearyl stearate; and mixtures thereof.
  • C9- C26 alkyl palmitates notably myristyl palmitate, cetyl palmitate or stearyl palmitate
  • C9- C26 alkyl myristates such as cetyl myristate, stearyl myristate and myristyl myristate
  • C9-C26 alkyl stearates notably myristyl stearate, cety
  • a wax is a lipophilic compound, which is solid at 25° C and atmospheric pressure, with a reversible solid/liquid change of state, having a melting point greater than about 40° C, which may be up to 200° C, and having in the solid state anisotropic crystal organization.
  • the size of the wax crystals is such that the crystals diffract and/or scatter light, giving the composition that comprises them a more or less opaque cloudy appearance.
  • the waxes that are suitable for use in the invention may be chosen from waxes of animal, plant or mineral origin, non-silicone synthetic waxes, and mixtures thereof.
  • hydrocarbon-based waxes for instance beeswax, notably of organic origin, lanolin wax and Chinese insect waxes; rice bran wax, carnauba wax, candelilla wax, ouricury wax, esparto grass wax, berry wax, shellac wax, Japan wax and sumac wax; montan wax, orange wax and lemon wax, microcrystalline waxes, paraffins and ozokerite; polyethylene waxes, the waxes obtained by Fischer-Tropsch synthesis and waxy copolymers, and also esters thereof.
  • beeswax notably of organic origin, lanolin wax and Chinese insect waxes
  • rice bran wax carnauba wax, candelilla wax, ouricury wax, esparto grass wax, berry wax, shellac wax, Japan wax and sumac wax
  • montan wax orange wax and lemon wax
  • microcrystalline waxes microcrystalline waxes
  • polyethylene waxes the waxes obtained
  • C20 to C60 microcrystalline waxes such as Microwax HW.
  • waxes obtained by catalytic hydrogenation of animal or plant oils containing linear or branched C8 to C32 fatty chains may also be made of.
  • isomerized jojoba oil such as the trans-isomerized partially hydrogenated jojoba oil, notably the product manufactured or sold by the company Desert Whale under the commercial reference Iso-Jojoba-50 ® , hydrogenated sunflower oil, hydrogenated castor oil, hydrogenated coconut kernel oil, hydrogenated lanolin oil and bis(l,l,l-trimethylolpropane) tetrastearate, notably the product sold under the name Hest 2T-4S ® by the company Heterene.
  • the waxes obtained by hydrogenation of castor oil esterified with cetyl alcohol such as those sold under the names Phytowax Castor 16L64 ® and 22L73 ® by the company Sophim, may also be used.
  • a wax that may also be used is a C20-C40 alkyl (hydroxystearyloxy)stearate (the alkyl group containing from 20 to 40 carbon atoms), alone or as a mixture.
  • Such a wax is notably sold under the names Kester Wax K 82 P ® , Hydroxypolyester K 82 P ® and Kester Wax K 80 P ® by the company Koster Keunen.
  • microwaxes in the compositions of the invention; mention may notably be made of carnauba microwaxes, such as the product sold under the name MicroCare 350 ® by the company Micro Powders, synthetic-wax microwaxes, such as the product sold under the name MicroEase 114S ® by the company Micro Powders, microwaxes constituted of a mixture of carnauba wax and polyethylene wax, such as the products sold under the names Micro Care 300 ® and 310 ® by the company Micro Powders, microwaxes constituted of a mixture of carnauba wax and of synthetic wax, such as the product sold under the name Micro Care 325 ® by the company Micro Powders, polyethylene microwaxes, such as the products sold under the names Micropoly 200 ® , 220 ® , 220L ® and 250S ® by the company Micro Powders, and polytetrafluoroethylene microwaxes, such as the products sold under the names Microslip 519 ® and 5
  • the waxes are preferably chosen from mineral waxes, for instance paraffin, petroleum jelly, lignite or ozokerite wax; plant waxes, for instance cocoa butter or cork fibre or sugar cane waxes, olive tree wax, rice wax, hydrogenated jojoba wax, ouricury wax, carnauba wax, ca nd el i I la wax, esparto grass wax, or absolute waxes of flowers, such as the essential wax of blackcurrant blossom sold by the company Bertin (France); waxes of animal origin, for instance beeswaxes or modified beeswaxes (cera bellina), spermaceti, lanolin wax and lanolin derivatives; microcrystalline waxes; and mixtures thereof.
  • mineral waxes for instance paraffin, petroleum jelly, lignite or ozokerite wax
  • plant waxes for instance cocoa butter or cork fibre or sugar cane waxes, olive tree wax, rice wax, hydrogenated jojoba wax, ouricury wax
  • the ceramides, or ceramide analogues such as glycoceramides, which may be used in the compositions according to the invention, are known; mention may be made in particular of ceramides of classes I, II, III and V according to the Dawning classification.
  • the ceramides or analogues thereof that may be used preferably correspond to the following formula: R 3 CH(OH)CH(CH 2 OR 2 )(NHCOR 1 ), in which:
  • R 1 denotes a linear or branched, saturated or unsaturated alkyl group, derived from C 14 - C 30 fatty acids, it being possible for this group to be substituted with a hydroxyl group in the alpha position, or a hydroxyl group in the omega position esterified with a saturated or unsaturated C 16 -C 30 fatty acid;
  • R 2 denotes a hydrogen atom, a (glycosyl)n group, a (galactosyl)m group or a sulfogalactosyl group, in which n is an integer ranging from 1 to 4 and m is an integer ranging from 1 to 8;
  • R 3 denotes a C 15 -C 26 hydrocarbon-based group, saturated or unsaturated in the alpha position, this group possibly being substituted with one or more C j -C ⁇ alkyl groups; it being understood that in the case of natural ceramides or glycoceramides, R 3 may also denote a C 15 -C 26 alpha-hydroxyalkyl group, the hydroxyl group being optionally esterified with a C 16 -C 30 alpha-hydroxy acid.
  • the ceramides that are more particularly preferred are the compounds for which R 1 denotes a saturated or unsaturated alkyl derived from C 16 -C 22 fatty acids; R 2 denotes a hydrogen atom and R 3 denotes a saturated linear C 15 group.
  • R 1 denotes a saturated or unsaturated alkyl radical derived from C 12 -C 22 fatty acids
  • R 2 denotes a galactosyl or sulfogalactosyl radical
  • 2-N- linoleoylaminooctadecane-l,3-diol 2-N-oleoylaminooctadecane-l,3-diol
  • 2-N-stearoylaminooctadecane-l,3,4-triol and in particular N- stearoylphytosphingosine, 2-N-palmitoylaminohexadecane-l,3-diol, N-
  • N-Oleoyldihydrosphingosine will preferably be used.
  • the term “butter” (also referred to as a “pasty fatty substance”) means a lipophilic fatty compound with a reversible solid/liquid change of state, including at a temperature of 25° C and at atmospheric pressure (760 mmHg) a liquid fraction and a solid fraction.
  • the butter(s) according to the invention have a melting start temperature of more than 25° C and a melting end temperature of less than 60° C.
  • the particular butter(s) are of plant origin, such as those described in Ullmann's Encyclopedia of Industrial Chemistry (“Fats and Fatty Oils”, A. Thomas, published online: 15 JUN 2000, DOI: 10.1002/14356007. al0_173, point 13.2.2.2. Shea Butter, Borneo Tallow, and Related Fats (Vegetable Butters)).
  • mango butter Mangifera indica
  • murumuru butter Astrocaryum murumuru
  • kokum butter Garcinia indica
  • ucuuba butter Virola sebifera
  • tucuma butter painya butter (Kpangnan) ( Pentadesma butyracea ), coffee butter ( Coffea arabica ), apricot butter ( Prunus armeniaca), macadamia butter ( Macadamia ternifolia ), grapeseed butter (Vitis vinifera ), avocado butter ( Persea gratissima ), olive butter ( Olea europaea ), sweet almond butter ( Prunus amygdalus dulcis ), cocoa butter and sunflower butter.
  • An example of a preferred butter is shea butter.
  • shea butter is extracted from the fruit (also called “kernels” or “nuts”) of the Butyrospemum parkii tree.
  • Each fruit contains between 45% and 55% fatty substance, which is generally extracted and refined.
  • the total content of the additional fatty substance(s) other than fatty acids and other than fatty alcohols described previously preferably ranges from 1% to 20% by weight, more preferentially from 2% to 15% by weight and better still from 3% to 10% by weight relative to the total weight of the composition.
  • composition according to the present invention may comprise one or more surfactants. These surfactants may be chosen from anionic surfactants, nonionic surfactants and cationic surfactants and/or mixtures thereof.
  • composition according to the present invention comprises one or more surfactants.
  • anionic surfactant means a surfactant including, as ionic or ionizable groups, only anionic groups. These anionic groups are preferably chosen from the following groups: , POH a
  • anionic surfactants that can be used in the composition according to the invention, mention may be made of alkyl sulfates, alkyl ether sulfates, alkylamido ether sulfates, alkylaryl polyether sulfates, monoglyceride sulfates, alkyl sulfonates, alkylamide sulfonates, alkylaryl sulfonates, a -olefin sulfonates, paraffin sulfonates, alkyl sulfosuccinates, alkyl ether sulfosuccinates, alkylamide sulfosuccinates, alkyl sulfoacetates, acyl sarcosinates, acyl glutamates, alkyl sulfosuccinamates, acyl isethionates and N-CC j -Cjalkyl N-acyl taurates, salts, salt
  • These compounds may be oxyethylenated and then preferably include from 1 to 50 ethylene oxide units.
  • the salts of C 6 -C 24 alkyl monoesters of polyglycoside-polycarboxylic acids may be chosen from C 6 -C 24 alkyl polyglycoside-citrates, C 6 -C 24 alkyl polyglycoside-tartrates and C 6 -C 24 alkyl polyglycoside-sulfosuccinates.
  • anionic surfactant(s) When the anionic surfactant(s) are in salt form, they may be chosen from alkali metal salts such as the sodium or potassium salt and preferably the sodium salt, ammonium salts, amine salts and in particular amino alcohol salts or alkaline-earth metal salts such as the magnesium salt.
  • alkali metal salts such as the sodium or potassium salt and preferably the sodium salt, ammonium salts, amine salts and in particular amino alcohol salts or alkaline-earth metal salts such as the magnesium salt.
  • amino alcohol salts examples include monoethanolamine, diethanolamine and triethanolamine salts, monoisopropanolamine, diisopropanolamine or triisopropanolamine salts, 2-amino-2-methyl-l-propanol salts, 2-amino-2-methyl-l, 3-propanediol salts and tris(hydroxymethyl)aminomethane salts.
  • Alkali metal or alkaline-earth metal salts and in particular the sodium or magnesium salts are preferably used.
  • the anionic surfactants that may be present may be mild anionic surfactants, i.e. anionic surfactants not bearing a sulfate function.
  • mild anionic surfactants mention may be made in particular of the following compounds and salts thereof, and also mixtures thereof: polyoxyalkylenated alkyl ether carboxylic acids, polyoxyalkylenated alkylaryl ether carboxylic acids, polyoxyalkylenated alkylamido ether carboxylic acids, in particular those including 2 to 50 ethylene oxide groups, alkyl D-galactoside uronic acids, acyl sarcosinates, acyl glutamates and al kyl polyglycoside carboxylic esters.
  • Use may be made most particularly of polyoxyalkylenated carboxylic acid alkyl ethers, for instance carboxylic acid lauryl ether (4.5 OE) sold, for example, under the name Akypo RLM 45 CA from Kao.
  • carboxylic acid lauryl ether 4.5 OE
  • the anionic surfactants that may be present may be carboxylic acids comprising at least 8 carbon atoms, also known as fatty acids, optionally in salified form.
  • fatty acid means an acid comprising at least one linear or branched, saturated or unsaturated hydrocarbon- based chain, such as an alkyl or alkenyl chain, including at least 6 carbon atoms, preferably from 8 to 24 carbon atoms, and better still from 10 to 22 carbon atoms.
  • the carboxylic acids comprising at least 6 carbon atoms (or fatty acids) according to the invention are neither (poly)oxyalkylenated, nor (poly)glycerolated; in particular, they are neither (poly)oxyethylenated, nor (poly)oxypropylenated.
  • R-COOH in which R denotes a linear or branched C 7 - C 29 , preferably Cg-C 23 and better still C 9 -C 17 alkyl or alkenyl group.
  • the fatty acid according to the invention is chosen from linear fatty acids, better still from unsaturated linear C 10 -C 22 and notably C 10 -C 18 fatty acids (R is a linear C 9 -C 23 or even C 9 -C 17 alkenyl).
  • Mention may notably be made of oleic, linoleic, linolenic and undecylenic acids, and mixtures thereof.
  • oleic acid will be used.
  • nonionic surfactant(s) that may be used in the composition of the present invention are notably described, for example, in the “Handbook of Surfactants” by M.R. Porter, published by Blackie & Son (Glasgow and London), 1991, pages 116-178.
  • nonionic surfactants examples include the following compounds, alone or as a mixture:
  • C 8 -C 80 alkyl(poly)glucosides, (C 8 -C 80 )alkenyl(poly)glucosides, which are optionally oxyalkylenated (0 to 10 oxyalkylene units) and comprising from 1 to 15 glucose units, (C 8 -C 80 )alkyl(poly)glucoside esters;
  • They are notably chosen from alcohols distinct from the fatty alcohols described in the "fatty substances" section, a -diols and (C 1 -C 20 )alkylphenols, these compounds being ethoxylated, propoxylated or glycerolated and containing at least one fatty chain including, for example, from 8 to 18 carbon atoms, the number of ethylene oxide or propylene oxide groups possibly ranging notably from 1 to 200, and the number of glycerol groups possibly ranging notably from 1 to 30.
  • fatty alcohols ethoxylated fatty amides preferably containing from 1 to 30 ethylene oxide units, polyglyce
  • the C 8 -C 30 and preferably C 12 -C 22 fatty acid esters (notably monoesters, diesters and triesters) of sorbitan may be chosen from: sorbitan caprylate; sorbitan cocoate; sorbitan isostearate; sorbitan laurate; sorbitan oleate; sorbitan palmitate; sorbitan stearate; sorbitan diisostearate; sorbitan dioleate; sorbitan distearate; sorbitan sesquicaprylate; sorbitan sesquiisostearate; sorbitan sesquioleate; sorbitan sesquistearate; sorbitan triisostearate; sorbitan trioleate; and sorbitan tristearate.
  • the polyoxyethylenated C 8 -C 30 (preferably C 12 -C 18 ) fatty acid esters (notably monoesters, diesters and triesters) of sorbitan notably containing from 2 to 20 mol of ethylene oxide may be chosen from polyoxyethylenated esters of C 12 -C 18 fatty acids, in particular lauric, myristic, cetylic or stearic acid, and of sorbitan notably containing from 2 to 30 mol of ethylene oxide, such as: polyoxyethylenated sorbitan monolaurate (4 OE) (Polysorbate-21), polyoxyethylenated sorbitan monolaurate (20 OE) (Polysorbate-20), polyoxyethylenated sorbitan monopalmitate (20 OE) (Polysorbate-40), polyoxyethylenated sorbitan monostearate (20 OE) (Polysorbate-60), polyoxyethylenated sorbitan monoste
  • the polyoxyethylenated C 8 -C 30 (preferably C 12 -C 18 ) fatty acid esters (notably monoesters, diesters, triesters and tetraesters) of sorbitan, notably containing from 2 to 20 mol of ethylene oxide may be chosen from polyoxyethylenated esters, notably containing from 2 to 20 mol of ethylene oxide, such as of C 12 -C 18 fatty acids, in particular lauric, myristic, cetylic or stearic acid, and of sorbitan, such as: - the ester polyoxyethylenated with 20 OE of sorbitan and of cocoic acid (PEG-20 sorbitan cocoate);
  • the polyoxyethylenated esters notably containing from 2 to 20 OE
  • the polyoxyethylenated esters notably containing from 2 to 20 OE
  • sorbitan and of isostearic acid such as PEG-2 sorbitan isostearate; PEG-5 sorbitan isostearate; PEG-20 sorbitan isostearate such as the product sold under the name Nikkol Tl 10 V by the company Nikkol
  • the polyoxyethylenated esters notably containing from 2 to 20 OE
  • sorbitan and of lauric acid such as PEG-10 sorbitan laurate
  • the polyoxyethylenated esters notably containing from 2 to 20 OE
  • the polyoxyethylenated esters notably containing from 2 to 20 OE
  • sorbitan and of oleic acid containing 10 oxyethylene groups such as PEG-6 sorbitan oleate; PEG- 20 sorbitan oleate
  • the polyoxyethylenated esters notably containing from 3 to 20 OE
  • sorbitan and of stearic acid such as PEG-3 sorbitan stearate; PEG-4 sorbitan stearate; PEG-6 sorbitan stearate.
  • the nonionic surfactant(s) are preferably chosen from ethoxylated C 8 -C 24 fatty alcohols comprising from 1 to 200 ethylene oxide groups, ethoxylated C 8 -C 30 fatty acid esters of sorbitan containing from 1 to 30 ethylene oxide units, (C 6 -C 24 alkyOpolyglycosides, and mixtures thereof, better still from (C 6 -C 24 alkyOpolyglycosides, even better still from (C 6 -C 24 alkyOpolyglycosides such as: coco glucoside, caprylyl/capryl glucoside, lauryl glucoside, decyl glucoside and cetearyl glucoside.
  • the cationic surfactant(s) that may be used in the composition according to the invention are generally chosen from optionally polyoxyalkylenated primary, secondary or tertiary fatty amines, quaternary ammonium salts, and mixtures thereof.
  • the fatty amines generally comprise at least one C 8 -C 80 hydrocarbon-based chain.
  • examples that may be mentioned include stearylamidopropyldimethylamine and distearylamine.
  • quaternary ammonium salts examples include:
  • the groups R 8 to R n which may be identical or different, represent a linear or branched aliphatic group including from 1 to 30 carbon atoms, or an aromatic group such as aryl or alkylaryl, at least one of the groups R 8 to R n including from 8 to 30 carbon atoms and preferably from 12 to 24 carbon atoms.
  • the aliphatic groups may include heteroatoms notably such as oxygen, nitrogen, sulfur and halogens.
  • the aliphatic groups are chosen, for example, from C j -C ⁇ alkyl, C j -C ⁇ alkoxy, polyoxy(C 2 -C 6 )alkylene, C j -C ⁇ alkylamide, (C 12 -C22)alkylamido(C 2 -C 6 )alkyl, (C 12 - C 22 ) a I ky I acetate and C j -C ⁇ hydroxyalkyl groups;
  • X is an anion chosen from the group of halides, phosphates, acetates, lactates, (C j -Cjalkyl sulfates and (C 4 - C 4 )alkylsulfonates or (C j -Cjalkylarylsulfonates.
  • quaternary ammonium salts of formula (X) preference is given, firstly, to tetraalkylammonium chlorides, for instance dialkyldimethylammonium or alkyltrimethylammonium chlorides in which the alkyl group includes from about 12 to 22 carbon atoms, in particular behenyltrimethylammonium chloride, distearyldimethylammonium chloride, cetyltrimethylammonium chloride or benzyldimethylstearylammonium chloride, or, secondly, to distearoylethylhydroxyethylmethylammonium methosulfate, dipalmitoylethylhydroxyethylammonium methosulfate or distearoylethylhydroxyethylammonium methosulfate, or also, finally, to palmitylamidopropyltrimethylammonium chloride or stearamidopropyldimethyl(myristyl acetate)ammonium
  • R12 represents an alkenyl or alkyl group including from 8 to 30 carbon atoms, for example tallow fatty acid derivatives
  • R13 represents a hydrogen atom, a C j - alkyl group or an alkenyl or alkyl group including from 8 to 30 carbon atoms
  • R14 represents a C j - alkyl group
  • R15 represents a hydrogen atom or a C j - alkyl group
  • X is an anion chosen from the group of halides, phosphates, acetates, lactates, (C 1 -C 4 )alkyl sulfates, and (C j -Cjalkylsulfonates or (C j -Cjalkylarylsulfonates.
  • R12 and R13 denote a mixture of alkenyl or alkyl groups including from 12 to 21 carbon atoms, for example tallow fatty acid derivatives, R14 denotes a methyl group and R15 denotes a hydrogen atom.
  • R12 and R13 denote a mixture of alkenyl or alkyl groups including from 12 to 21 carbon atoms, for example tallow fatty acid derivatives
  • R14 denotes a methyl group
  • R15 denotes a hydrogen atom.
  • Such a product is sold, for example, under the name Rewoquat ® W 75 by the company Rewo,
  • R16 denotes an alkyl group including approximately from 16 to 30 carbon atoms, which is optionally hydroxylated and/or interrupted with one or more oxygen atoms
  • R17 is chosen from hydrogen, an alkyl group including from 1 to 4 carbon atoms or a group -(CH 2 ) 3 -N + (R16a)(R17a)(R18a), R16a, R17a, R18a, R18, R19, R20 and R21, which may be identical or different, are chosen from hydrogen or an alkyl group including from 1 to 4 carbon atoms
  • X- is an anion chosen from the group of halides, acetates, phosphates, nitrates, (C 1 -C 4 )al kyl sulfates, (C j -Cjalkylsulfonates or (C j -Cjalky
  • the alkyl groups R22 may be linear or branched, and more particularly linear.
  • R22 denotes a methyl, ethyl, hydroxyethyl or dihydroxypropyl group, and more particularly a methyl or ethyl group.
  • the sum x + y + z is from 1 to 10.
  • R23 is a hydrocarbon-based group R27, it may be long and may contain 12 to 22 carbon atoms, or may be short and may contain from 1 to 3 carbon atoms.
  • R25 is a hydrocarbon-based group R29, it preferably contains 1 to 3 carbon atoms.
  • R24, R26 and R28 which may be identical or different, are chosen from linear or branched, saturated or unsaturated C11-C21 hydrocarbon-based groups, and more particularly from linear or branched, saturated or unsaturated Cll- C21 alkyl and alkenyl groups.
  • x and z which may be identical or different, are equal to 0 or 1.
  • y is equal to 1.
  • r, s and t which may be identical or different, are equal to 2 or 3, and even more particularly are equal to 2.
  • the anion X is preferably a halide, preferably chloride, bromide or iodide, a (Cl- C4) a I ky I sulfate or a (Cl -C4) a I ky I - or (Cl-C4)alkylaryl-sulfonate.
  • a halide preferably chloride, bromide or iodide
  • a (Cl- C4) a I ky I sulfate or a (Cl -C4) a I ky I - or (Cl-C4)alkylaryl-sulfonate may be made of methanesulfonate, phosphate, nitrate, tosylate, an anion derived from an organic acid, such as acetate or lactate, or any other anion that is compatible with the ammonium bearing an ester function.
  • the anion X is even more particularly chloride, methyl sulfate or ethyl sulfate.
  • R22 denotes a methyl or ethyl group, x and y are equal to 1, z is equal to 0 or 1, r, s and t are equal to 2;
  • R23 is chosen from: the group -C(0)R26, methyl, ethyl or C14-C22 hydrocarbon-based groups, or a hydrogen atom,
  • R25 is chosen from: the group -C(0)R28, or a hydrogen atom,
  • R24, R26 and R28 which may be identical or different, are chosen from linear or branched, saturated or unsaturated C13-C17 hydrocarbon-based groups, and preferably from linear or branched, saturated or unsaturated C13-C17 alkyl and alkenyl groups.
  • the hydrocarbon-based groups are linear.
  • acyl groups preferably contain 14 to 18 carbon atoms and are derived more particularly from a plant oil such as palm oil or sunflower oil. When the compound contains several acyl groups, these groups may be identical or different.
  • alkylating agent such as an alkyl halide, preferably methyl or ethyl halide, a dialkyl sulfate, preferably dimethyl or diethyl sulfate, methyl methanesulfonate, methyl para-toluenesulfonate, glycol chlorohydrin or glycerol chlorohydrin.
  • alkylating agent such as an alkyl halide, preferably methyl or ethyl halide, a dialkyl sulfate, preferably dimethyl or diethyl sulfate, methyl methanesulfonate, methyl para-toluenesulfonate, glycol chlorohydrin or glycerol chlorohydrin.
  • Such compounds are sold, for example, under the names Dehyquart ® by the company Henkel, Stepanquat ® by the company Stepan, Noxamium ® by the company CECA or Rewoquat ® WE 18 by the company Rewo-Witco.
  • composition according to the invention may contain, for example, a mixture of quaternary ammonium monoester, diester and triester salts with a weight majority of diester salts.
  • ammonium salts containing at least one ester function that are described in patents US-A-4 874 554 and US-A-4 137 180.
  • Use may also be made of the behenoylhydroxypropyltrimethylammonium chloride sold, for example, by the company Kao under the name Quartamin BTC 131.
  • the ammonium salts containing at least one ester function contain two ester functions.
  • cetyltrimethylammonium behenyltrimethylammonium and dipalmitoylethylhydroxyethylmethylammonium salts, and mixtures thereof, and more particularly behenyltrimethylammonium chloride, cetyltrimethylammonium chloride, and dipalmitoylethylhydroxyethylammonium methosulfate, and mixtures thereof.
  • the surfactant(s) are chosen from anionic surfactants, nonionic surfactants and mixtures thereof, preferentially from fatty acids, ethoxylated C 8 -C 24 fatty alcohols comprising from 1 to 200 ethylene oxide groups, ethoxylated C 8 -C 30 fatty acid esters of sorbitan containing from 1 to 30 ethylene oxide units, (C 6 -C 24 alkyOpolyglycosides, and mixtures thereof.
  • the surfactant(s) are chosen from fatty acids, (C 6 -C 24 alkyOpolyglycosides and mixtures thereof.
  • the total content of surfactant(s) in the composition preferably ranges from 0.01% to 15% by weight, more preferentially from 0.1% to 10% by weight, better still from 0.5% to 8% by weight, even better still from 1% to 6% by weight, relative to the total weight of the composition.
  • the total content of fatty acids in the composition preferably ranges from 0.01% to 15% by weight, more preferentially from 0.1% to 10% by weight, better still from 0.5% to 8% by weight, even better still from 1% to 6% by weight, relative to the total weight of the composition.
  • the total content of (C 6 -C 24 alkyOpolyglycosides in the composition preferably ranges from 0.01% to 15% by weight, more preferentially from 0.1% to 10% by weight, better still from 0.4% to 8% by weight, even better still from 1% to 6% by weight, relative to the total weight of the composition.
  • composition according to the invention may also comprise one or more oxidation bases, salts thereof, solvates thereof and/or solvates of the salts thereof, and mixtures thereof.
  • the composition according to the invention comprises one or more oxidation bases.
  • the oxidation bases may be present in the form of salts, solvates and/or solvates of salts.
  • the addition salts of the oxidation bases present in the composition according to the invention are notably chosen from the addition salts with an acid, such as the hydrochlorides, hydrobromides, sulfates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, methanesulfonates, phosphates and acetates, and the addition salts with a base such as sodium hydroxide, potassium hydroxide, aqueous ammonia, amines or alkanolamines.
  • an acid such as the hydrochlorides, hydrobromides, sulfates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, methanesulfonates, phosphates and acetates
  • a base such as sodium hydroxide, potassium hydroxide, aqueous ammonia, amines or alkanolamines.
  • the solvates of the additional oxidation bases more particularly represent the hydrates of said oxidation bases and/or the combination of said oxidation bases with a linear or branched C/ to C 4 alcohol such as methanol, ethanol, isopropanol or n- propanol.
  • the solvates are hydrates.
  • the oxidation bases are chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols ortho-aminophenols and heterocyclic bases, and the corresponding addition salts.
  • para-phenylenediamines that may be mentioned are, for example, para- phenylenediamine, para-toluenediamine, 2-chloro-para-phenylenediamine, 2,3- dimethyl -para- phenylenedia mine, 2,6-di methyl- para- phenylenedia mine, 2,6-diethyl- para- phenylenedia mine, 2,5-di methyl -para-phenylenediamine, N, N -dimethyl -para- phenyl enediamine, N,N-diethyl-para-phenylenediamine, N,N-di propyl -para- phenylenediamine, 4-amino-N,N-diethyl-3-methylaniline, N , N - bis ( /3 -hydroxyethyl)- para-phenylenediamine, 4-N,N-bis(/> - hydroxyethyl)amino-2-
  • y -di hydroxy propyl)- para-phenylenediamine N-(4’- aminophenyl)- para-phenylenediamine, N-phenyl- para-phenylenediamine, 2- b - hydroxyethyloxy- para-phenylenediamine, 2- /3 -acety la mi noethyl oxy- para- phenylenediamine, N - ( /3 -methoxyethyl) - para - phenylenedia mine, 4- aminophenylpyrrolidine, 2-thienyl-para-phenylenediamine, 2-/3 -hydroxyethylamino-5- aminotoluene and 3-hydroxy-l-(4’-aminophenyl)pyrrolidine, and the addition salts, solvates and/or solvates of salts thereof.
  • para-phenylenediamine para-toluenediamine, 2-isopropyl-para-phenylenediamine, 2- b -hydroxyethyl-para-phenylenediamine, 2-( g -hydroxypropyl)-para- phenylenediamine, 2-methoxymethyl-para-phenylenediamine, 2- /3 -hydroxyethyloxy- para- phenylenedia mine, 2,6-di methyl -para-phenylenediamine, 2,6-diethyl -para- phenylenediamine, 2,3-dimethyl-para-phenylenediamine, N , N - bis ( /3 -hydroxyethyl)- para-phenylenediamine, 2-chloro-para-phenylenediamine and 2- b - acetylaminoethyloxy-para-phenylenediamine,
  • bis(phenyl)alkylenediamines that may be mentioned, for example, are N,N'- bis ( /3 -hydroxyethyl)-N,N’-bis(4’-a mi nophenyl)-l,3-diami no propanol, N,N’-bis( ?
  • para-aminophenols that are mentioned are, for example, para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 4-amino-3-chlorophenol, 4-amino- 3-hydroxymethylphenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4- a mi n 0-2 -m ethoxy methyl phenol, 4-a mi no-2 -a mi nomethyl phenol, 4-amino-2-(/> - hydroxyethylaminomethy phenol and 4-amino-2-fluorophenol, and the addition salts, the solvates and/or the solvates of the salts.
  • ortho-aminophenols that may be mentioned, for example, are 2- aminophenol, 2-amino-5-methylphenol, 2-amino-6-methylphenol and 5-acetamido-2- aminophenol, and the corresponding addition salts, the solvates and the solvates of the salts.
  • heterocyclic bases that may be mentioned, for example, are pyridine, pyrimidine and pyrazole derivatives.
  • pyridine derivatives that may be mentioned are the compounds described, for example, in patents GB 1 026 978 and GB 1 153 196, for example 2,5- diaminopyridine, 2-(4-methoxyphenyl)amino-3-aminopyridine and 3,4-diaminopyridine, and the corresponding addition salts, the solvates and the solvates of the salts.
  • pyridine oxidation bases that are useful in the present invention are the 3- aminopyrazolo[l,5-a]pyridine oxidation bases or the corresponding addition salts described, for example, in patent application FR 2 801 308.
  • Examples that may be mentioned include pyrazolo[l,5-a]pyrid-3-ylamine, 2-acetylaminopyrazolo[l,5-a]pyrid- 3-ylamine, 2-(morpholin-4-yl)pyrazolo[l,5-a]pyrid-3-ylamine, 3-aminopyrazolo[l,5- a]pyridine-2-carboxylic acid, 2-methoxypyrazolo[l,5-a]pyrid-3-ylamine, (3- a mi nopyrazolo[l,5-a] pyrid-7-yl) methanol, 2-(3-aminopyrazolo[l,5-a]pyrid-5- yl) ethanol, 2-(
  • the oxidation bases that are useful in the present invention are chosen from 3-aminopyrazolo[l,5-a]pyridines and preferably substituted on carbon atom 2 with: a) a (di)(Cl-C6)(alkyl)amino group, said alkyl group possibly being substituted with at least one hydroxyl, amino or imidazolium group; b) an optionally cationic 5- to 7-membered heterocycloalkyl group containing from 1 to 3 heteroatoms, optionally substituted with one or more (Cl -C6) a I ky I groups, such as a di(Cl-C4)alkylpiperazinium group; or c) a (Cl-C6)alkoxy group optionally substituted with one or more hydroxyl groups, such as a b -hydroxyalkoxy group, and the corresponding addition salts, the solvates and the solvates of the salts.
  • pyrimidine derivatives that may be mentioned are the compounds described, for example, in patents DE 2359399; JP 88-169571; JP 05-63124; EP 0770375 or patent application WO 96/15765, such as 2,4,5,6-tetraaminopyrimidine, 4-hydroxy-2,5,6- tria mi no pyrimidine, 2 -hydroxy-4,5,6-tria mi no pyrimidine, 2,4-dihydroxy-5,6- diaminopyrimidine, 2,5,6-triaminopyrimidine and the addition salts thereof, the solvates and the solvates of the salts thereof, and the tautomeric forms thereof, when a tautomeric equilibrium exists.
  • pyrazole derivatives that may be mentioned are the compounds described in patents DE 3843892 and DE 4133957 and patent applications WO 94/08969, WO 94/08970, FR-A-2 733 749 and DE 195 43 988, for instance 4,5-diamino-l- methylpyrazole, 4,5-diamino-l-(/> -hydroxyethyl)pyrazole, 3,4-diaminopyrazole, 4,5 - diami no-1 -(4’-chlorobenzyl) pyrazole, 4,5-diamino- 1,3-dimethyl pyrazole, 4,5-diamino- 3- methyl -1- phenyl pyrazole, 4,5-dia mi no-1 -methyl -3-phenyl pyrazole, 4-amino-l,3- dimethyl-5-hydrazinopyrazole, 1 -benzyl -4,5 -diami no
  • a 4,5-diaminopyrazole will preferably be used and even more preferentially 4,5-diamino- 1-(b -hydroxyethy pyrazole and/or a corresponding salt, a solvate and/or a solvate of a salt.
  • pyrazole derivatives that may also be mentioned comprise diamino-N,N- dihydropyrazolopyrazolones and in particular those described in patent application FR- A-2 886 136, such as the following compounds and the corresponding addition salts: 2,3-diamino-6,7-dihydro-lH,5H-pyrazolo[l,2-a]pyrazol-l-one, 2-amino-3-ethylamino- 6,7-dihydro-lH,5H-pyrazolo[l,2-a]pyrazol-l-one, 2-amino-3-isopropylamino-6,7- dihydro-lH,5H-pyrazolo[l,2-a]pyrazol-l-one, 2-ami n o-3 - (py r ro lidin-l-yl)-6,7-dihydro- lH,5H-pyrazolo[l,2-a]pyrazol-l-one,
  • Use will preferably be made of 2,3-diamino-6,7-dihydro-lH,5H-pyrazolo[l,2-a]pyrazol- 1-one and/or a corresponding salt, solvate and/or solvate of a salt.
  • Use will preferably be made, as heterocyclic bases, of 4,5-diamino-l-(/> - hydroxyethyl) pyrazole and/or 2,3 -dia mi no-6,7-di hydro- 1 H,5 H -py razol o [1,2-a] py razol - 1-one and/or 2- b -hydroxyethoxy-3-aminopyrazolo[l,5-a]pyridine and/or a corresponding salt, solvate and/or solvate of a salt.
  • the oxidation base(s) are chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases, and the corresponding addition salts, the solvates thereof and the solvates of the salts thereof, and mixtures thereof; more preferentially from 2-methoxymethyl- para-phenylenediamine, 2- /3 -hydroxyethyl-para-phenylenediamine, 2- g - hydroxypropyl-para-phenylenediamine, and the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof.
  • the composition comprises at least one oxidation base
  • the oxidation base(s), the salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof are preferably present in a total content ranging from 0.001% to 20% by weight, preferably from 0.005% to 15% by weight, more preferentially from 0.01% to 10% by weight, better still from 0.05% to 5%, even better still from 0.1% to 3% by weight, relative to the weight of the composition.
  • the composition comprises at least one oxidation base chosen from 2-methoxymethyl-para-phenylenediamine, 2- b - hydroxyethyl -para- phenylenedia mine, 2- y - hydroxy propyl- pa ra-phenylenedia mine, addition salts thereof, solvates thereof and/or solvates of the salts thereof and mixtures thereof
  • said base(s) are present in a total content ranging from 0.001% to 20% by weight, preferably from 0.005% to 15% by weight, more preferentially from 0.01% to 10% by weight, better still from 0.05% to 5%, even better still from 0.1% to 3% by weight, relative to the total weight of the composition.
  • composition according to the invention is free of oxidation bases chosen from para-phenylenediamine, para-toluenediamine, addition salts thereof, solvates thereof and solvates of the salts thereof.
  • composition according to the invention comprises:
  • At least one coupler chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl-3,4-methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof;
  • At least one alkaline agent chosen from alkanolamines chosen from alkanolamines, the total content of alkanolamine(s) being greater than or equal to 5% by weight relative to the total weight of the composition
  • - at least one liquid fatty alcohol and at least one solid fatty alcohol the total content of liquid fatty alcohol(s) and of solid fatty alcohol(s) being greater than or equal to 5% by weight relative to the total weight of the composition
  • - at least one surfactant preferably chosen from fatty acids, ( -C 24 alky polyglycosides and mixtures thereof; and - at least one oxidation base, preferably chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases, and the corresponding addition salts, solvates and solvates of salts thereof, and mixtures thereof; more preferentially from 2-methoxymethyl-para-phenylenediamine, 2- /3 -hydroxyethyl-para-phenylenediamine, 2- y - hydroxy propyl -para - phenylenediamine, and the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof.
  • composition according to the invention may comprise at least one sequestrant (or chelating agent).
  • the composition according to the invention comprises one or more sequestrants.
  • a “sequestrant” (or “chelating agent”) is well known to those skilled in the art and refers to a compound or a mixture of compounds that are capable of forming a chelate with a metal ion.
  • a chelate is an inorganic complex in which a compound (the sequestrant or chelating agent) is coordinated to a metal ion, i.e. it forms one or more bonds with the metal ion (formation of a ring including the metal ion).
  • a sequestrant generally comprises at least two electron-donating atoms which enable the formation of bonds with the metal ion.
  • the sequestrant(s) may be chosen from carboxylic acids, preferably aminocarboxylic acids, phosphonic acids, preferably aminophosphonic acids, polyphosphoric acids, preferably linear polyphosphoric acids, salts thereof, and derivatives thereof.
  • the salts are in particular alkali metal, alkaline-earth metal, ammonium and substituted ammonium salts.
  • chelating agents based on carboxylic acids diethylenetriaminepentaacetic acid (DTPA), ethylenediaminedisuccinic acid (EDDS) and trisodium ethylenediamine disuccinate such as Octaquest E30 from Octel, ethylenediaminetetraacetic acid (EDTA) and salts thereof such as disodium EDTA, tetrasodium EDTA, ethylenediamine-N,N’-diglutaric acid (EDDG), glycinamide-N,N’-disuccinic acid (GADS), 2-hydroxypropylenediamine- N,N’-disuccinic acid (HPDDS), ethylenediamine-N,N’-bis(ortho-hydroxyphenylacetic acid) (EDDHA), N,N’-bis(2-hydroxybenzyl)ethylenediamine-N,N’-diacetic acid (HBED), nitrilotriacetic acid (NTA),
  • DTPA diethylenetriamine
  • chelating agents based on mono- or polyphosphonic acid diethylenetriaminepenta(methylenephosphonic acid) (DTPMP), ethane-l-hydroxy-l,l,2-triphosphonic acid (E1HTP), ethane-2- hydroxy-l,l,2-triphosphonic acid (E2HTP), ethane-l-hydroxy-l,l-triphosphonic acid (EHDP), ethane-1, 1,2-triphosphonic acid (ETP), ethylenediaminetetramethylenephosphonic acid (EDTMP), hydroxyethane-1,1- diphosphonic acid (HEDP, or etidronic acid), and salts such as disodium etidronate, tetrasodium etidronate.
  • DTPMP diethylenetriaminepenta(methylenephosphonic acid)
  • E1HTP ethane-l-hydroxy-l,l,2-triphosphonic acid
  • E2HTP ethane-2- hydroxy-l,l,
  • the sequestrant(s) that are useful according to the invention are phosphorus-based sequestrants, i.e. sequestrants which comprise one or more phosphorus atoms, preferably at least two phosphorus atoms.
  • the phosphorus-based sequestrant(s) used in the composition according to the invention are preferably chosen from:
  • alkali metal or alkaline-earth metal preferably alkali metal, phosphates and pyrophosphates, such as sodium pyrophosphate, potassium pyrophosphate, sodium pyrophosphate decahydrate; and alkali metal or alkaline-earth metal, preferably alkali metal, polyphosphates, such as sodium hexametaphosphate, sodium polyphosphate, sodium tripolyphosphate, sodium trimetaphosphate; which are optionally hydrated, and mixtures thereof;
  • organic phosphorus-based derivatives such as organic (poly)phosphates and (poly)phosphonates, such as etidronic acid and/or alkali metal or alkaline-earth metal salts thereof, for instance tetrasodium etidronate, disodium etidronate, and mixtures thereof.
  • the phosphorus-based sequestrant(s) are chosen from linear or cyclic compounds comprising at least two phosphorus atoms bonded together covalently via at least one linker L comprising at least one oxygen atom and/or at least one carbon atom.
  • the phosphorus-based sequestrant(s) may be chosen from inorganic phosphorus- based derivatives, preferably comprising at least two phosphorus atoms. More preferentially, the phosphorus-based sequestrant(s) are chosen from alkali metal or alkaline-earth metal pyrophosphates, better still from alkali metal pyrophosphates, in particular sodium pyrophosphate (also known as tetrasodium pyrophosphate).
  • the phosphorus-based sequestrant(s) may be chosen from organic phosphorus-based derivatives, preferably comprising at least two phosphorus atoms. More preferentially, the phosphorus-based sequestrant(s) are chosen from etidronic acid (also known as l-hydroxyethane-l,l-diphosphonic acid) and/or alkali metal or alkaline-earth metal, preferably alkali metal, salts thereof, for instance tetrasodium etidronate and disodium etidronate.
  • etidronic acid also known as l-hydroxyethane-l,l-diphosphonic acid
  • alkali metal or alkaline-earth metal preferably alkali metal, salts thereof, for instance tetrasodium etidronate and disodium etidronate.
  • the phosphorus-based sequestrant(s) are chosen from alkali metal pyrophosphates, etidronic acid and/or alkali metal salts thereof, and a mixture of these compounds.
  • the phosphorus-based sequestrant(s) are chosen from tetrasodium etidronate, disodium etidronate, etidronic acid, tetrasodium pyrophosphate, and a mixture of these compounds.
  • the sequestrants are preferably chosen from diethylenetriaminepentaacetic acid (DTPA) and salts thereof, diethylenediaminetetraacetic acid (EDTA) and salts thereof, ethylenediaminedisuccinic acid (EDDS) and salts thereof, etidronic acid and salts thereof, N,N-dicarboxymethylglutamic acid and salts thereof (GLDA), and mixtures thereof.
  • DTPA diethylenetriaminepentaacetic acid
  • EDTA diethylenediaminetetraacetic acid
  • EDDS ethylenediaminedisuccinic acid
  • etidronic acid and salts thereof etidronic acid and salts thereof, N,N-dicarboxymethylglutamic acid and salts thereof (GLDA), and mixtures thereof.
  • the sequestrant(s) are chosen from N,N-dicarboxymethylglutamic acid and salts thereof (GLDA), and mixtures thereof.
  • the alkali metal salts and notably the sodium or potassium salts are preferred.
  • the total content of the sequestrant(s) preferably ranges from 0.001% to 15% by weight, more preferentially from 0.005% to 10% by weight, better still from 0.01% to 8% by weight, even better still from 0.05% to 5% by weight, relative to the total weight of the composition.
  • composition according to the invention may comprise at least one thickening polymer, preferably chosen from polysaccharides, more preferentially from anionic polysaccharides.
  • the composition according to the invention comprises one or more thickening polymer(s), preferably chosen from polysaccharides, more preferentially from anionic polysaccharides.
  • polysaccharides means polymers which contain at least 11 monosaccharide units. Preferentially, the polysaccharides of the invention include between 20 and 100 000 monosaccharide units.
  • the anionic polysaccharides according to the invention comprise one or more anionic or anionizable groups, and do not comprise any cationic or cationizable groups.
  • the anionic polysaccharides that are useful according to the invention may be chosen from those derived from the following sugars: glucose; galactose; arabinose; rhamnose; mannose; xylose; fucose; anhydrogalactose; galacturonic acid; glucuronic acid; mannuronic acid; galactose sulfate; anhydrogalactose sulfate.
  • the anionic polysaccharides may be natural or synthetic.
  • the anionic polysaccharides that are useful in the composition according to the invention are chosen from native gums such as:
  • acacia gum branched polymer of galactose, arabinose, rhamnose and glucuronic acid
  • ghatti gum polymer derived from arabinose, galactose, mannose, xylose and glucuronic acid
  • karaya gum polymer derived from galacturonic acid, galactose, rhamnose and glucuronic acid
  • gum tragacanth polymer of galacturonic acid, galactose, fucose, xylose and arabinose
  • gums derived from algae such as: alginates (polymers of mannuronic acid and glucuronic acid); carrageenans and furcellerans (polymers of galactose sulfate and anhydrogalactose sulfate);
  • microbial gums such as: xanthan gums (polymer of glucose, mannose acetate, mannose/pyruvic acid and glucuronic acid); gel I a n gums (polymer of partially acylated glucose, rhamnose and glucuronic acid).
  • microbial gums means substances synthesized by fermentation of sugars by microorganisms.
  • the anionic polysaccharides that are useful in the composition according to the invention are chosen from anionic gums, better still from anionic microbial gums, more preferentially from xanthan gums.
  • the total content of thickening polymers preferably ranges from 0.01% to 10% by weight relative to the total weight of the composition, preferably from 0.05% to 8% by weight, better still from 0.1% to 5% by weight relative to the total weight of the composition.
  • the total content of anionic polysaccharides as defined previously preferably ranges from 0.01% to 10% by weight relative to the total weight of the composition, preferably from 0.05% to 8% by weight, better still from 0.1% to 5% by weight relative to the total weight of the composition.
  • the total content of the microbial gums as defined previously preferably ranges from 0.01% to 10% by weight relative to the total weight of the composition, preferably from 0.05% to 5% by weight, better still from 0.1% to 2% by weight relative to the total weight of the composition.
  • the composition according to the invention comprises: - at least one coupler chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl-3,4-methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof;
  • At least one surfactant preferably chosen from fatty acids, ( -C 24 alky polyglycosides and mixtures thereof; and at least one oxidation base chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases, and the corresponding addition salts, solvates and solvates of salts thereof, and mixtures thereof; more preferentially from 2-methoxymethyl-para-phenylenediamine, 2- /3 -hydroxyethyl-para-phenylenediamine, 2- y - hydroxy propyl -para - phenylenediamine, and the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof;
  • - at least one sequestrant preferably chosen from diethylenetriaminepentaacetic acid (DTPA) and salts thereof, diethylenediaminetetraacetic acid (EDTA) and salts thereof, ethylenediaminedisuccinic acid (EDDS) and salts thereof, etidronic acid and salts thereof, N,N-dicarboxymethylglutamic acid and salts thereof (GLDA), and mixtures thereof;
  • DTPA diethylenetriaminepentaacetic acid
  • EDTA diethylenediaminetetraacetic acid
  • EDDS ethylenediaminedisuccinic acid
  • etidronic acid and salts thereof etidronic acid and salts thereof, N,N-dicarboxymethylglutamic acid and salts thereof (GLDA), and mixtures thereof;
  • composition according to the invention may also comprise at least one organic solvent.
  • the composition comprises at least one organic solvent.
  • organic solvents examples include linear or branched C 2 -C 4 alkanols, such as ethanol, propanol and isopropanol; polyols and polyol ethers, for instance 2-butoxyethanol, propylene glycol, glycerol, 1,3-propanediol, dipropylene glycol, propylene glycol monomethyl ether, diethylene glycol monomethyl ether and monoethyl ether, and also aromatic alcohols or ethers, for instance benzyl alcohol or phenoxyethanol, and mixtures thereof.
  • linear or branched C 2 -C 4 alkanols such as ethanol, propanol and isopropanol
  • polyols and polyol ethers for instance 2-butoxyethanol, propylene glycol, glycerol, 1,3-propanediol, dipropylene glycol, propylene glycol monomethyl ether, diethylene glycol monomethyl ether and monoethyl ether,
  • the organic solvent(s) are chosen from polyols, more preferentially chosen from glycerol, propane-1, 3-diol, and mixtures thereof.
  • the organic solvent(s) may be present in a total amount ranging from 0.01% to 30% by weight, preferably ranging from 2% to 25% by weight, relative to the total weight of the composition.
  • composition according to the invention is preferably an aqueous composition.
  • the composition preferably comprises water in an amount of greater than or equal to 5% by weight, preferably greater than or equal to 10% by weight, and better still greater than or equal to 15% by weight, relative to the total weight of the composition.
  • the water content ranges from 15% to 80% by weight, preferentially from 30% to 70% by weight and better still from 40% to 60% by weight.
  • composition according to the invention may optionally comprise one or more additives, other than the compounds of the invention and among which mention may be made of cationic, anionic, nonionic or amphoteric polymers or mixtures thereof, other than those mentioned previously, antidandruff agents, anti-seborrhoeic agents, agents for preventing hair loss and/or for promoting hair regrowth, vitamins and provitamins including panthenol, sunscreens, mineral or organic pigments, direct dyes, plasticizers, solubilizers, opacifiers or nacreous agents, antioxidants, hydroxy acids, fragrances, and preserving agents.
  • additives other than the compounds of the invention and among which mention may be made of cationic, anionic, nonionic or amphoteric polymers or mixtures thereof, other than those mentioned previously, antidandruff agents, anti-seborrhoeic agents, agents for preventing hair loss and/or for promoting hair regrowth, vitamins and provitamins including panthenol, sunscreen
  • the above additives may generally be present in an amount, for each of them, of between 0 and 20% by weight relative to the total weight of the ready-to-use composition.
  • composition according to the invention does not comprise any chemical oxidizing agents.
  • the present invention also relates to a process for dyeing keratin fibres, preferably the hair, which comprises the application to said keratin fibres of an effective amount of a composition as defined previously.
  • the composition may be applied to wet or dry keratin fibres.
  • the keratin fibres are optionally rinsed with water, optionally washed with a shampoo and then rinsed with water, before being dried or left to dry.
  • the composition according to the invention comprises at least one oxidizing agent, preferably hydrogen peroxide.
  • the composition according to the invention is mixed at the time of use with a composition comprising at least one chemical oxidizing agent, preferably hydrogen peroxide.
  • the composition according to the invention results from the mixing of at least two compositions: a dye composition comprising:
  • - one or more oxidation dyes chosen from at least one coupler chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl- 3,4-methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof; at least one oxidation base chosen from: 2- b -hydroxyethyl-para-phenylenediamine and the addition salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-( Y -hydroxypropyl)-para-phenylenediamine and the salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-methoxymethyl-para-phenyl
  • an oxidizing composition comprising one or more chemical oxidizing agents, preferably hydrogen peroxide.
  • the process according to the invention comprises a step of mixing the composition according to the invention with an oxidizing composition comprising at least one chemical oxidizing agent.
  • This mixing step is preferably performed at the time of use, just before applying to the hair the composition resulting from the mixing.
  • the process for dyeing keratin fibres, preferably the hair comprises the step of applying to the keratin fibres a composition resulting from the mixing, at the time of use, of at least two compositions: a) a dye composition comprising:
  • - one or more oxidation dyes chosen from at least one coupler chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl- 3,4-methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof; at least one oxidation base chosen from: 2- b -hydroxyethyl-para-phenylenediamine and the addition salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-( g -hydroxypropyl)-para-phenylenediamine and the salts thereof, the solvates thereof and/or the solvates of salts thereof, 2-methoxymethyl-para-phenyl
  • At least one alkaline agent chosen from alkanolamines chosen from alkanolamines, the total content of alkanolamine(s) being greater than or equal to 5% by weight relative to the total weight of the composition
  • - at least one liquid fatty alcohol and at least one solid fatty alcohol the total content of liquid fatty alcohol(s) and of solid fatty alcohol(s) being greater than or equal to 5% by weight relative to the total weight of the composition
  • an oxidizing composition comprising one or more chemical oxidizing agents, preferably hydrogen peroxide.
  • the process for dyeing keratin fibres, preferably the hair, according to the invention comprises the step of applying to the keratin fibres a composition resulting from the mixing, at the time of use, of at least two compositions: a) a dye composition comprising:
  • At least one coupler chosen from: 6-hydroxybenzomorpholine of formula (I), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, hydroxyethyl-3,4-methylenedioxyaniline of formula (II), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, 2-amino-5-ethylphenol of formula (III), the addition salts thereof, the solvates thereof and/or the solvates of the salts thereof, and mixtures thereof; (III);
  • an oxidizing composition comprising one or more chemical oxidizing agents, preferably hydrogen peroxide.
  • the chemical oxidizing agent(s) are chosen from hydrogen peroxide, urea peroxide, alkali metal bromates or ferricyanides, peroxygenated salts, for instance persulfates, perborates, peracids and precursors thereof and percarbonates of alkali metals or alkaline-earth metals, and mixtures thereof.
  • the oxidizing agent is preferably chosen from hydrogen peroxide.
  • the oxidizing composition is preferably an aqueous composition.
  • it comprises more than 5% by weight of water, preferably more than 10% by weight of water and even more advantageously more than 20% by weight of water.
  • It may also comprise one or more organic solvents chosen from those listed previously; these solvents more particularly representing, when they are present, from 1% to 40% by weight and preferably from 5% to 30% by weight, relative to the weight of the oxidizing composition.
  • the oxidizing composition also preferably comprises one or more acidifying agents.
  • acidifying agents examples that may be mentioned include mineral or organic acids, for instance hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids, for instance acetic acid, tartaric acid, citric acid or lactic acid, and sulfonic acids.
  • the oxidizing composition may also comprise fatty substances such as those described previously, preferably chosen from fatty alcohols, liquid hydrocarbons comprising more than 16 carbon atoms and mixtures thereof, surfactants and polymers.
  • the pH of the oxidizing composition when it is aqueous, is less than 7.
  • the oxidizing composition comprises hydrogen peroxide as oxidizing agent, in aqueous solution, the concentration of which ranges, more particularly, from 0.1% to 50%, more particularly between 0.5% and 20% and even more preferentially between 1% and 15% by weight, relative to the weight of the oxidizing composition.
  • At least one of the compositions is aqueous.
  • Kits Another subject of the invention is a multi-compartment device, preferably comprising two compartments, for dyeing keratin fibres, preferably the hair, comprising at least a first compartment containing the dye composition according to the invention and at least a second compartment containing an oxidizing composition as described above.
  • the compositions of the device according to the invention are packaged in separate compartments, optionally accompanied by suitable application means, which may be identical or different, such as fine brushes, coarse brushes or sponges.
  • the device mentioned above may also be equipped with a means for dispensing the desired mixture on the hair, for instance the devices described in patent FR 2 586 913.
  • the present invention relates to the use of a composition as described above, for dyeing keratin fibres, and in particular the hair.
  • the dye compositions A1 and A2 and the oxidizing composition 0 were prepared from the ingredients of which the contents are indicated in the table below (% AM):
  • each of the dye compositions A1 and A2 is mixed with 1.5 times its weight of oxidizing agent 0.
  • Each of the mixtures is then applied to locks of natural and permanent-waved hair containing 90% grey hairs, in a proportion of 5 g of mixture/g of hair.
  • the colorimetric measurements were performed using a Konica Minolta 3600 spectrocolorimeter (illuminant D65, angle 10° , specular component included) in the CIELab system.
  • the selectivity is represented by the colour difference D E between the natural and permanent-waved dyed locks.
  • composition according to the invention leads to a lower D E value, and thus to better selectivity, in comparison with the comparative composition.
  • Example 2
  • the dye compositions A3 and A4 were prepared from the ingredients of which the contents are indicated in the table below (% AM):
  • each of the dye compositions A3 and A4 is mixed with 1.5 times its weight of oxidizing agent O disclosed in example 1.
  • Each of the mixtures is then applied to locks of 90% permanent-waved grey hair, in a proportion of 5 g of mixture/g of hair. After a leave-on time of 30 minutes on a plate thermostatically regulated at 27° C, the hair is rinsed, washed with a standard shampoo and dried.
  • the colorimetric measurements were performed using a Konica Minolta CM-3600A spectrocolorimeter (illuminant D65, angle 10° , specular component included) in the CIELab system.
  • the chromaticity is calculated by the following formula: a* indicates the green/red color axis b* indicates the blue/yellow color axis The higher the value of the chromaticity C*, the more chromatic the color of the fibers.
  • composition according to the invention leads to a higher C* value, and thus to a better chromaticity, in comparison with the comparative composition.

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Abstract

L'invention concerne une composition comprenant au moins un colorant d'oxydation, au moins un agent alcalin choisi parmi les alcanolamines, au moins un alcool gras liquide et au moins un alcool gras solide.
PCT/EP2022/067987 2021-06-30 2022-06-29 Composition comprenant au moins un colorant d'oxydation, au moins un agent alcalin et au moins un alcool gras liquide et au moins un alcool gras solide WO2023275197A1 (fr)

Priority Applications (1)

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EP22740850.7A EP4362890A1 (fr) 2021-06-30 2022-06-29 Composition comprenant au moins un colorant d'oxydation, au moins un agent alcalin et au moins un alcool gras liquide et au moins un alcool gras solide

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FRFR2107046 2021-06-30
FR2107046A FR3124708B1 (fr) 2021-06-30 2021-06-30 Composition comprenant au moins une base particulière, au moins un agent alcalin et au moins un alcool gras liquide et au moins un alcool gras solide.
FR2107037A FR3124720B1 (fr) 2021-06-30 2021-06-30 Composition comprenant au moins un coupleur particulier, au moins un agent alcalin et au moins un alcool gras liquide et au moins un alcool gras solide.
FRFR2107037 2021-06-30

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US20120276029A1 (en) * 2009-12-22 2012-11-01 L'oreal Inverse emulsion for treating the hair comprising a particular fatty substance and an alkaline agent
FR2984148A1 (fr) * 2011-12-20 2013-06-21 Oreal Procede de coloration d'oxydation mettant en oeuvre une composition riche en corps gras et des catalyseurs metalliques, et dispositif approprie
JP2013169571A (ja) 2012-02-21 2013-09-02 Nippon Steel & Sumitomo Metal Corp 鍛鋼ロールの製造方法
EP2926802A1 (fr) * 2014-04-02 2015-10-07 The Procter and Gamble Company Compositions de coloration capillaire, kits, procédé et leur utilisation
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GB1026978A (en) 1962-03-30 1966-04-20 Schwarzkopf Verwaltung G M B H Method of dyeing hair
GB1153196A (en) 1965-07-07 1969-05-29 Schwarzkopf Verwaltung G M B H Method of Dyeing Hair
DE2359399A1 (de) 1973-11-29 1975-06-12 Henkel & Cie Gmbh Haarfaerbemittel
US4137180A (en) 1976-07-02 1979-01-30 Lever Brothers Company Fabric treatment materials
FR2586913A1 (fr) 1985-09-10 1987-03-13 Oreal Procede pour former in situ une composition constituee de deux parties conditionnees separement et ensemble distributeur pour la mise en oeuvre de ce procede
US4874554A (en) 1986-07-10 1989-10-17 Henkel Kommanditgesellschaft Auf Aktien Quaternary ammonium compounds
EP0317542A2 (fr) 1987-11-13 1989-05-24 The Procter & Gamble Company Composition de nettoyage pour surfaces dures contenant des dérivés de l'acide iminodiacétique
DE3843892A1 (de) 1988-12-24 1990-06-28 Wella Ag Oxidationshaarfaerbemittel mit einem gehalt an diaminopyrazolderivaten und neue diaminopyrazolderivate
EP0399133A1 (fr) 1989-05-23 1990-11-28 The Procter & Gamble Company Compositions détergentes et de nettoyage contenant agents de chelation
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