DYEING COMPOSITION BASED ON 2-GAMMA-HYDROXYPROPYL-PARA-PHENYLENEDIAMINE AND ON A PHOSPHORIC SURFACTANT

20240000684 ยท 2024-01-04

Assignee

Inventors

Cpc classification

International classification

Abstract

The present invention relates to a dyeing composition comprising 2-y-hydroxypropyl-p-phenylenediamine and at least one phosphoric surfactant. The phosphoric surfactant is of formula (I) in which: R.sub.1, R.sub.2 and R.sub.3, which may be identical or different, represent a group chosen from: a group OM, in which M represents a hydrogen atom or an alkali metal; a group OR.sub.4, in which R.sub.4 represents a linear or branched C.sub.12-C40 alkyl group, a linear or branched C.sub.2-C.sub.40 alkenyl group, a C.sub.3-C.sub.40 cyclic alkyl group, a C.sub.3-C.sub.40 cyclic alkenyl group, a C.sub.5-C.sub.40 aromatic group or a C.sub.6-C.sub.40 aralkyl group; and an oxyalkylene group (OCH.sub.2CH.sub.2)n(OCH.sub.2CH(CH.sub.3))mOR.sub.4 in which R.sub.4 is defined as above, n represents an integer ranging from 1 to 50 and m represents an integer ranging from 0 to 50; and given that at least one of the groups R.sub.1, R.sub.2 and R.sub.3 is a group OM and that at least one of the groups R.sub.1, R.sub.2 and R.sub.3 is a group OR.sub.4 or (OCH.sub.2CH.sub.2)n(OCH.sub.2CH(CH.sub.3))mOR.sub.4. The present invention also relates to a process for dyeing keratin fibres, comprising the application of the composition according to the invention to the fibres. The invention also relates to the use of the combination 2-y-hydroxypropyl-para-phenylenediamine/phosphoric surfactant, for dyeing keratin fibres.

##STR00001##

Claims

1. Dyeing composition comprising: (i) at least one oxidation base chosen from 2--hydroxypropyl-para-phenylenediamine, salts thereof, solvates thereof, and mixtures thereof, and (ii) at least one phosphoric surfactant chosen from phosphoric surfactants having the formula (I) below: ##STR00006## in which: R.sub.1, R.sub.2 and R.sub.3, which may be identical or different, represent a group chosen from: a group OM, in which M represents a hydrogen atom or an alkali metal; a group OR.sub.4, in which R.sub.4 represents a linear or branched C.sub.12-C.sub.40 alkyl group, a linear or branched C.sub.2-C.sub.40 alkenyl group, a C.sub.3-C.sub.40 cyclic alkyl group, a C.sub.3-C.sub.40 cyclic alkenyl group, a C.sub.5-C.sub.40 aromatic group or a C.sub.6-C.sub.40 aralkyl group; and an oxyalkylene group (OCH.sub.2CH.sub.2).sub.n(OCH.sub.2CH(CH.sub.3)).sub.mOR.sub.4 in which R.sub.4 is defined as above, n represents an integer ranging from 1 to 50 and m represents an integer ranging from 0 to 50; and given that at least one of the groups R.sub.1, R.sub.2 and R.sub.3 is a group OM and that at least one of the groups R.sub.1, R.sub.2 and R.sub.3 is a group OR.sub.4 or (OCH.sub.2CH.sub.2).sub.n(OCH.sub.2CH(CH.sub.3)).sub.mOR.sub.4.

2. Composition according to claim 1, characterized in that the total content of oxidation base(s) (i) ranges from 0.001% to 20% by weight, preferably from 0.005% to 15% by weight, more preferentially from 0.01% to 10% by weight, even more preferentially 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.

3. Composition according to claim 1, characterized in that it further comprises one or more additional oxidation bases, other than the oxidation base(s) (i), preferably chosen from para-phenylenediamine, para-toluenediamine, para-aminophenol, 2--hydroxyethyl-para-phenylenediamine, N,N-bis(-hydroxyethyl)-para-phenylenediamine, 4,5-diamino-1-(-hydroxyethyl)pyrazole, 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-one, 2--hydroxyethoxy-3-aminopyrazolo[1,5-a]pyridine, addition salts thereof, solvates thereof, and mixtures thereof.

4. Composition according to claim 1, characterized in that it further comprises one or more oxidation couplers, preferably chosen from meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalene-based coupling agents, heterocyclic coupling agents, addition salts thereof, solvates thereof, and mixtures thereof; and more preferentially from 2-amino-5-ethylphenol, hydroxyethyl-3,4-methylenedioxyaniline,1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 3-aminophenol, 6-hydroxybenzomorpholine, 5-N-(-hydroxyethyl)amino-2-methylphenol, 2,4-diamino-1-(-hydroxyethyloxy)benzene, 2-methyl-5-aminophenol, 6-hydroxyindole, 4-chloro-1,3-dihydroxybenzene, 2-amino-3-hydroxypyridine, 3-amino-2-chloro-6-methylphenol, -naphthol, 2-[3-amino-4-methoxyphenyl]amino)ethanol, addition salts thereof, solvates thereof, and mixtures thereof.

5. Composition according to claim 1, characterized in that the phosphoric surfactant(s) are chosen from phosphoric surfactants of formula (I), in which: R.sub.1, R.sub.2 and R.sub.3, which may be identical or different, represent a group chosen from: a group OM, in which M represents a hydrogen atom or an alkali metal, such as Na, Li or K, preferably Na or K; a group OR.sub.4, in which R.sub.4 represents a linear or branched C.sub.12-C.sub.20 alkyl group, preferably a C.sub.16 or C.sub.18 alkyl group, a linear or branched C.sub.2-C.sub.40 alkenyl group, preferably a C.sub.12-C.sub.20 alkenyl group, more preferentially a C.sub.16 or C.sub.18 alkenyl group, a C.sub.3-C.sub.40 cyclic alkyl group, a C.sub.3-C.sub.40 cyclic alkenyl group, a C.sub.5-C.sub.40 aromatic group or a C.sub.6-C.sub.40 aralkyl group; and an oxyalkylene group (OCH.sub.2CH.sub.2).sub.n(OCH.sub.2CH(CH.sub.3)).sub.mOR.sub.4 in which R.sub.4 is defined as above, n represents an integer ranging from 1 to 50 and m represents an integer ranging from 0 to 50; and given that at least one of the groups R.sub.1, R.sub.2 and R.sub.3 is a group OM and that at least one of the groups R.sub.1, R.sub.2 and R.sub.3 is a group OR.sub.4 or (OCH.sub.2CH.sub.2).sub.n(OCH.sub.2CH(CH.sub.3)).sub.mOR.sub.4.

6. Composition according to claim 1, characterized in that the phosphoric surfactant(s) are chosen from ceteth-10 phosphate, dicetyl phosphate, ceteth-20 phosphate, oleth-5 phosphate and dioleyl phosphate, salts thereof, and mixtures thereof; preferably from ceteth-10 phosphate, ceteth-20 phosphate and oleth-5 phosphate, salts thereof, and mixtures thereof; and even better still from ceteth-10 phosphate, salts thereof, and mixtures thereof.

7. Composition according to claim 1, characterized in that the total content of phosphoric surfactant(s) of formula (I) ranges from 0.01% to 15% by weight, preferably from 0.05% to 10% by weight, more preferentially from 0.075% to 5% by weight, even more preferentially from 0.1% to 2% by weight, and even better still from 0.5% to 1% by weight, relative to the total weight of the composition.

8. Composition according to claim 1, characterized in that the weight ratio of the total content of phosphoric surfactant(s) of formula (I) on the one hand, to the total content of 2--hydroxypropyl-para-phenylenediamine on the other hand, is greater than or equal to 1, preferentially greater than or equal to 1.5, more preferentially greater than or equal to 2, even more preferentially greater than or equal to 2.5.

9. Composition according to claim 1, characterized in that it further comprises one or more non-silicone fatty substances, preferably chosen from non-silicone oils of mineral origin, C.sub.8-C.sub.30 fatty alcohols, and mixtures thereof, and more preferentially from C.sub.8-C.sub.30 fatty alcohols.

10. Composition according to claim 9, characterized in that the total content of non-silicone fatty substance(s) ranges from 0.1% to 40% by weight, preferably from 1% to 35% by weight, more preferentially from 5% to 30% by weight, and even more preferentially from 10% to 25% by weight, relative to the total weight of the composition.

11. Composition according to claim 1, characterized in that it further comprises one or more additional surfactants other than the phosphoric surfactants, preferably one or more non-ionic additional surfactants other than the phosphoric surfactants.

12. Composition according to claim 11, characterized in that the total content of additional surfactant(s) other than the phosphoric surfactants ranges from 0.01% to 20% by weight, preferably from 0.5% to 15% by weight, more preferentially from 1% to 15% by weight, and even more preferentially from 3% to 10% by weight, relative to the total weight of the composition.

13. Process for dyeing keratin fibres, comprising at least one step of applying to said fibres a composition as defined in claim 1.

14. Process according to claim 13, further comprising at least one step of applying to said fibres an oxidizing composition comprising one or more chemical oxidizing agents, preferably hydrogen peroxide.

15. Use of at least one oxidation base (i) chosen from 2--hydroxypropyl-para-phenylenediamine, salts thereof, solvates thereof, and mixtures thereof, in combination with at least one phosphoric surfactant of formula (I) as defined in claim 1, for dyeing keratin fibres.

Description

EXAMPLES

[0165] The compositions A (invention), B and C (comparative compositions) are prepared from the ingredients shown in Table 1 below, the amounts of which are expressed, unless otherwise indicated, as weight percentages of active material (AM).

TABLE-US-00001 TABLE 1 Compo- Compo- Compo- sition A sition B sition C Ingredients Invention Comparative Comparative 2--Hydroxypropyl-p- 1.14 mmol 1.14 mmol phenylenediamine 2-Methoxymethyl-p- 1.14 mmol phenylenediamine 2-Methyl-5- 0.002 0.002 0.002 hydroxyethylaminophenol 4-Amino-2- 0.002 0.002 0.002 hydroxytoluene 2,4- 0.006 0.006 0.006 Diaminophenoxyethanol hydrochloride Resorcinol 0.14 0.14 0.14 m-Aminophenol 0.005 0.005 0.005 p-Aminophenol 0.02 0.02 0.02 Ceteth-10 phosphate 0.7 0.7 Sodium lauryl sulfate 0.7 Cetearyl alcohol 11.1 11.1 11.1 Liquid paraffin 9 9 9 Steareth-2 1.7 1.7 1.7 PPG-15 stearyl ether 1.7 1.7 1.7 Steareth-20 1.1 1.1 1.1 PEG-20 4 4 4 2-Oleamido-1,3- 0.01 0.01 0.01 octadecanediol Preservatives and q.s. q.s. q.s. pH agents Water qs 100 qs 100 qs 100

[0166] The oxidizing composition D was prepared from the ingredients indicated in Table 2 below, the amounts of which are expressed as weight percentages of active material (AM).

TABLE-US-00002 TABLE 2 Ingredients Composition D Hydrogen peroxide 5.85 Beheneth-10 0.5 Ceteareth-33 1.7 Cetearyl alcohol 4.4 Liquid paraffin 0.8 Polyquaternium-6 0.2 Preservatives q.s. Water qs 100

[0167] Protocol:

[0168] At the time of use, each of the compositions A to C is mixed with the oxidizing composition D according to a 1:1 weight ratio.

[0169] Each of the mixtures M.sub.(A+D), M.sub.(B+D) et M.sub.(C+D) is then applied to a lock of hair containing 90% natural white hair (NW) and a lock of permanent-waved 90% natural white hair (PWNW) in a proportion of 5 g of mixture per 1 g of hair.

[0170] After a leave-on time of 30 min on a hot plate at 27 C., each lock of hair is rinsed, washed with L'Oral Professionnel Pro Classic universal concentrated shampoo, diluted to 10%, and dried.

[0171] Evaluation:

[0172] The colorimetric measurements were performed on each of the treated locks using a Konica Minolta CM-3600A spectrocolorimeter (illuminant D65, angle 10, specular component included) in the CIELab system.

[0173] In this system, L* represents the lightness: the lower the value of L*, the deeper, more powerful and more intense the colouring obtained. The chromaticity is measured by the values a* and b*, a* representing the green/red colour axis and b* the blue/yellow colour axis.

[0174] The selectivity is represented by the colour difference E between the locks of dyed natural non-permanent-waved (NW) hair and the dyed permanent-waved locks (PWNW).


E={square root over ((L*L.sub.0*).sup.2+(a*a.sub.0*).sup.2+(b*b.sub.0*).sup.2)}

[0175] In this equation, L*, a* and b* represent the values measured on the locks of dyed non-permanent-waved natural (NW) hair, and L.sub.0*, a.sub.0* and b.sub.0* represent the values measured on the locks of dyed permanent-waved (PWNW) hair. The lower the value of E, the lower and therefore better the selectivity (uniform dyeing).

[0176] The results obtained are grouped together in Table 3 below:

TABLE-US-00003 TABLE 3 Type of hair L* a* b* E Mixture M.sub.A+D NW 48.46 3.19 12.11 1.16 (invention) PWNW 47.31 3.17 11.99 Mixture M.sub.B+D NW 49.77 3.00 11.70 7.24 (comparative) PWNW 42.62 4.10 11.94 Mixture M.sub.C+D NW 48.39 2.92 12.30 8.96 (comparative) PWNW 39.50 3.83 11.70

[0177] The colouring obtained with the mixture M.sub.A+D according to the invention has E values lower than that of the colourings obtained with the comparative mixtures M.sub.B+D and M.sub.C+D.

[0178] It is thus observed that the selectivity of the colouring obtained with the composition according to the invention is better than the selectivity of the colourings obtained with the comparative compositions.

[0179] The colourings obtained with the composition according to the invention are therefore more homogeneous than the colourings obtained with the comparative compositions.