Dye composition using at least one coupler of meta-phenylenediamine type substituted in position 4 in a medium comprising a fatty substance, processes and device

10383803 · 2019-08-20

Assignee

Inventors

Cpc classification

International classification

Abstract

The present invention relates to a composition for dyeing keratin fibers, in particular human keratin fibers such as the hair, comprising one or more fatty substances, one or more surfactants, one or more oxidation bases chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and the addition salts thereof and/or solvates thereof one or more particular couplers of meta-phenylenediamine type substituted in position 4, and one or more basifying agents, the fatty substance content in the dye composition representing in total at least 10% by weight relative to the total weight of the said composition. The invention also relates to a dyeing process using such a composition, and also to multi-compartment devices suitable for performing the said process.

Claims

1. Composition for dyeing keratin fibres, characterized in that it comprises: i) one or more fatty substances chosen from C.sub.6-C.sub.16 hydrocarbons, hydrocarbons containing more than 16 carbon atoms, non-silicone oils of animal origin, triglycerides of plant or synthetic origin, fluoro oils, saturated fatty alcohols comprising 6 to 30 carbon atoms, fatty acid esters other than triglycerides, fatty alcohol esters other than triglycerides, non-silicone waxes, silicones, and mixtures thereof, ii) one or more surfactants, iii) one or more oxidation bases chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and the addition salts thereof or solvates thereof, iv) one or more basifying agents, v) one or more meta-phenylenediamine-based couplers of formula (I), compound (4), compound (8), compound (8), compound (9), compound (10), compound (11), compound (13), addition salts thereof, optical isomers thereof, geometrical isomers thereof, tautomers thereof, or solvates thereof, wherein formula (I) is ##STR00078## in which: R.sub.1 and R.sub.3 represent, independently of each other: a hydrogen atom, a linear or branched C.sub.1-C.sub.6 alkyl radical, substituted with one or more of the following: CONH.sub.2 radicals, NHSO.sub.2CH.sub.3 radicals, hydroxyl radicals, COOH radicals, wherein R.sub.1 and R.sub.3 are different, R.sub.2 represents: a C.sub.1-C.sub.6 alkyl radical which may be substituted with one or more hydroxyl radicals, a branched C.sub.1-C.sub.6 alkoxy radical, a linear or branched C.sub.1-C.sub.6 alkoxy radical substituted with one or more of the following: CONH.sub.2 radicals, NHSO.sub.2CH.sub.3 radicals, hydroxyl radicals, COOH radicals, C.sub.1-C.sub.6 alkoxy radicals; and wherein compound (4), compound (8), compound (9), compound (10), compound (11), and compound (13) are: ##STR00079## (vii) one or more chemical oxidizing agents, the fatty substance content representing in total at least 10% by weight relative to the total weight of the said dye composition.

2. Dye composition according to claim 1, characterized in that the fatty substance(s) are chosen from liquid petroleum jelly, C.sub.6-C.sub.16 alkanes, polydecenes, and 2-octyldodecanol.

3. Dye composition according to claim 1, characterized in that it comprises at least 15% by weight of fatty substance relative to the weight of the composition.

4. Dye composition according to claim 1, characterized in that the surfactants are chosen from nonionic surfactants.

5. Dye composition according to claim 1, characterized in that the meta-phenylenediamine-based couplers are chosen from those of formula (I) in which R.sub.1 and R.sub.3 represent a hydrogen atom, a methyl radical or a linear C.sub.1-C.sub.6, substituted with a hydroxyl group.

6. Dye composition according to claim 1, characterized in that the meta-phenylenediamine-based couplers are chosen from those of formula (I) in which R.sub.2 represents a linear C.sub.1-C.sub.6 alkoxy radical, optionally substituted with the radical(s) defined in claim 1.

7. Dye composition according to claim 1, characterized in that the meta-phenylenediamine-based couplers are chosen from the following compounds, and also the addition salts thereof, optical isomers, geometrical isomers and tautomers thereof, solvates thereof: TABLE-US-00006 embedded image N-[2-(2,4- diaminophenoxy)- ethyl]methane- sulfonamide embedded image 2-[5-amino-2-(2- methoxyethoxy)- phenylamino]- ethanol embedded image N-{2-[4- amino-2-(2- hydroxy- ethylamino)- phenoxy]ethyl}- methane- sulfonamide embedded image 2-(2,4- diamino- phenyl)ethanol embedded image 2-(5-amino-2- methylphenyl- amino)ethanol.

8. Dye composition according to claim 7, characterized in that the coupler(s) are chosen from couplers (2), (5), and (6), and also the addition salts thereof, optical isomers, geometrical isomers and tautomers thereof, and solvates thereof.

9. Dye composition according to claim 1, characterized in that the basifying agent(s) are mineral, organic or hybrid.

10. Dye composition according to claim 1, characterized in that the basifying agents are chosen from alkanolamines, and amino acids in neutral or ionic form.

11. Dye composition according to claim 1, characterized in that it comprises at least hydrogen peroxide as chemical oxidizing agent.

12. Process for dyeing keratin fibres which consists in applying to the said fibres a dye composition as defined according to claim 1.

13. Dyeing process according to claim 12, characterized in that the composition results from the extemporaneous mixing of two compositions: a composition (A) comprising one or more oxidation bases chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and the addition salts thereof or solvates thereof; one or more meta-phenylenediamine-based couplers of formula (I); and one or more basifying agents; and a composition (B) comprising one or more chemical oxidizing agents; at least one of the compositions (A) and (B) comprising one or more fatty substances and one or more surfactants, the fatty substance content of the composition resulting from the extemporaneous mixing of compositions (A) and (B) corresponding to at least 10% by weight of fatty substance.

14. Process according to claim 12, characterized in that the composition results from the extemporaneous mixing of three compositions: two aqueous compositions (B) and (C) and an anhydrous composition (A), the anhydrous composition (A) comprising one or more fatty substances, the composition (B) comprising one or more oxidation bases chosen from para-phenylenediamines, bis(phenyl)alkylenediamines, para-aminophenols, ortho-aminophenols and the addition salts thereof or solvates thereof; and one or more meta-phenylenediamine-based couplers of formula (I); the composition (C) comprising one or more chemical oxidizing agents; one or more basifying agents being included in the compositions (A) or (B); one or more surfactants being included in at least one of the compositions (A), (B) and (C), the fatty substance content of the composition resulting from the extemporaneous mixing of the three compositions (A), (B) and (C) representing at least 10% by weight of fatty substance.

15. Multi-compartment device comprising a first compartment containing composition (A) as described in claim 13 and at least a second compartment containing composition (B) as described in claim 13, the compositions of the compartments being intended to be mixed together before application, on condition that the amount of fatty substance represents at least 10% by weight relative to the weight of the composition resulting from the mixing of (A) and (B).

16. Multi-compartment device comprising a first compartment containing composition (A) as described in claim 14; and a second compartment containing a cosmetic composition (B) as described in claim 14 and at least a third compartment comprising composition (C) as described in claim 14, the compositions of the compartments being intended to be mixed together before application, on condition that the amount of fatty substance represents at least 10% by weight relative to the weight of the composition resulting from the mixing of (A), (B) and (C).

17. Dye composition according to claim 2, characterized in that the fatty substance(s) are chosen from liquid petroleum jelly, C.sub.6-C.sub.16 alkanes, polydecenes, liquid esters of fatty acids other than triglycerides, liquid esters of fatty alcohols other than triglycerides, and liquid fatty alcohols, or mixtures thereof.

18. Dye composition according to claim 9, characterized in that the basifying agent(s) are chosen from aqueous ammonia, alkali metal carbonates or bicarbonates, sodium hydroxide, potassium hydroxide, organic amines chosen from alkanolamines, oxyethylenated ethylenediamines, oxypropylenated ethylenediamines, amino acids and the compounds of formula (II) or mixtures thereof: ##STR00085## in which formula (II) W is a divalent C.sub.1-C.sub.6 alkylene radical optionally substituted with one or more hydroxyl groups or a C.sub.1-C.sub.6 alkyl radical, optionally interrupted with one or more heteroatoms include O, or NR.sub.u, R.sub.x, R.sub.y, R.sub.z, R.sub.t and R.sub.u, which may be identical or different, represent a hydrogen atom or a C.sub.1-C.sub.6 alkyl, C.sub.1-C.sub.6 hydroxyalkyl or C.sub.1-C.sub.6 aminoalkyl radical.

Description

EXAMPLES

I. Protocol

(1) Compositions (A) and (B) below are prepared from the ingredients indicated in the table below. The amounts mentioned are indicated in grams of active material.

(2) Composition (A)

(3) TABLE-US-00002 Composition A 2-Octyldodecanol 11.5 g Liquid petroleum jelly 75.5 g Oxyethylenated lauryl alcohol (2 OE) 3 g Oxyethylenated sorbitan monolaurate (4 OE) 11 g

(4) Composition (B)

(5) TABLE-US-00003 Composition B Monoethanolamine 15.05 g Sodium metabisulfite 0.7 g Ascorbic acid 0.25 g Diethylenetriaminepentaacetic acid 1 g Propylene glycol 6.2 g 96% ethanol 8.8 g Hexylene glycol 3 g Dipropylene glycol 3 g Oxidation base 1.45 10.sup.2 mol Coupler 1.45 10.sup.2 mol Water qs 100 g

(6) Procedure

(7) At the time of use, 0.828 ml of composition (A), 0.33 ml of composition (B) and 1.242 ml of a composition (C) of 20-volumes aqueous hydrogen peroxide solution are mixed together.

(8) The mixture obtained is applied to 200 mg of locks of natural hair containing 90% white hairs. After a leave-on time of 30 minutes at room temperature, the locks are rinsed and then washed with a standard shampoo.

II. Calculation of the Colour Variation (Eab*)

(9) The coloration build-up (E.sub.ab*) was evaluated in the CIE L* a* b* system. In this L* a* b* system, L* represents the intensity of the colour, a* indicates the green/red colour axis and b* indicates the blue/yellow colour axis. The lower the value of L*, the darker or more intense the colour.

(10) The value of E.sub.ab* was calculated from the values of L*a*b* according to equation (i) below:
E.sub.ab*={square root over ((L*L.sub.o*).sup.2+(a*a.sub.o*).sup.2(b*b.sub.o*).sup.2)}(i)

(11) The coloration build-up (E.sub.Lab*) was calculated on the locks of untreated hair (L.sub.0*, a.sub.0* and b.sub.0*) and on locks of dyed hair (L*, a* and b*). The values of L.sub.0*, a.sub.0* and b.sub.0* for the untreated natural white hairs are, respectively, 55.56, 2.06 and 12.29.

(12) The greater the value of E.sub.ab*, the better the coverage of the treated fibres.

IV. Results

(13) TABLE-US-00004 TABLE 1 (invention) Coupler Base L* a* b* E.sub.ab 0embedded image embedded image 13.8 1.6 5 45.1 embedded image embedded image 13.5 1.3 7.8 46.6 embedded image embedded image 12.14 2.47 6.05 47.1 embedded image embedded image 13.6 2.2 8 46.6 embedded image embedded image 12.3 1.75 5 46.5 0embedded image embedded image 13.4 1.9 9 47.2 embedded image embedded image 14.3 1.6 6.1 45.1 embedded image embedded image 15.1 1.1 10.7 46.6 embedded image embedded image 12.7 2.2 5.7 46.4 embedded image embedded image 14 1.6 9.2 46.8 0embedded image embedded image 13.2 1.9 5.4 45.8 embedded image embedded image 13.4 1.6 9.6 47.6

(14) TABLE-US-00005 TABLE 2 (Reference) Coupler Base L* a* b* E.sub.ab embedded image embedded image 14.4 6.6 0.13 43.2 embedded image embedded image 20.9 14.3 7.8 37.2 embedded image embedded image 14 8.2 0.26 43.7 0embedded image embedded image 23.7 22.2 12.2 37.9 embedded image embedded image 14.2 9 1.1 43.4 embedded image embedded image 23.5 21.7 12.9 37.8 embedded image embedded image 15 11.7 1.7 43.1 embedded image embedded image 28.3 23.7 15 35.29 0embedded image embedded image 14.6 11.2 1.1 43.5 embedded image embedded image 20.3 22.5 9.9 41.1 embedded image embedded image 15.5 10.0 1.3 42.4 embedded image embedded image 19.5 21.7 10.1 41.3

(15) The coloration up-takes of the dyes are significantly higher than that obtained with a standard oxidation dye support.