IP Library › Granted Patent US 9,504,639
Granted Patent B2
US 9,504,639 · App. 14/645,619 · Granted Nov 29, 2016

Composition for treating keratinous fibres, comprising specific aminosilicones, acids and direct dyes

Inventors: Konstantin Goutsis (Juechen, DE); Gabriele Weser (Neuss, DE)
Assignee: Henkel AG & Co. KGaA
A61K8/898A61K8/362A61K8/365A61K8/368A61K8/55A61Q5/065A61Q5/10A61K2800/4324
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Quick Facts
Patent No.
US 9,504,639
App. No.
14/645,619
Granted
Nov 29, 2016
Kind
B2
Abstract

Composition for treating keratinous fibers, more particularly human hair, comprising in a cosmetically appropriate vehicle a) at least one organic and/or inorganic acid, b) at least one direct dye and c) at least one compound of the formula (I).

Claims (33)

1. An agent for treating keratinic fibers in a cosmetically suitable carrier, comprising:

a) at least one inorganic and/or organic acid

b) at least one direct dye and

c) at least one compound of formula (I)

where

A=

wherein

i. x and y independently stand for numbers from 1 to 100,

ii. w stands for a number from 0 to 100,

iii. z stands for a number from 1 to 100, where, if z≧2, the respective values x, y, and w in a structural element A may be selected in each case independently of preceding structural elements A,

anda

iv. R1 and R2 independently stand for a linear or branched, saturated, unsaturated, or multiply unsaturated C 5 -C 20 alkyl group, a hydroxy group, a C 1 -C 30 alkoxy group, a carboxy-C 1 -C 30 alkyl group, or a C 1 -C 6 alkyl-(O—CH 2 —CH 2 ) n —O— group, wherein n stands for an integer from 1 to 60

d) comprising 0.1 wt % to 15 wt % of one or more compounds of formula (II)

where

R3 stands for a hydrogen atom or a methyl group and

m stands for a number from 2 to 1000.

2. The agent according to claim 1 , wherein the at least one acid includes an acid selected from the group consisting of from citric acid, tartaric acid, malic acid, lactic acid, 1-hydroxyethane-1,1-diphosphonic acid, 2,6-dipicolinic acid, and benzoic acid.

3. The agent according to claim 1 , wherein in that the agent has a pH of 2 to 7 at a temperature of 22° C.

4. The agent according to claim 1 , wherein the agent has a pH of 3 to 6.9 at a temperature of 22° C.

5. The agent according to claim 1 , wherein the agent has a pH of 4 to 6.8 at a temperature of 22° C.

6. The agent according to claim 1 , wherein the one or more direct dye comprise 0.0001 wt % to 5 wt % of the total weight of the agent.

7. The agent according to claim 1 , wherein the one or more direct dyes comprise 0.001 wt % to 2.5 wt % of the total weight of the agent.

8. The agent according to claim 1 , wherein the one or more direct dyes comprise 0.01 wt % to 1 wt % of the total weight of the agent.

9. The agent according to claim 1 , wherein the at least direct dye includes at least one nonionic nitro dye.

10. The agent according to claim 1 , wherein the at least one direct dyes includes a combination of direct dyes selected from the group consisting of: HC Blue 12/HC Yellow 2, HC Blue 12/HC Yellow 4, HC Blue 12/HC Yellow 5, HC Blue 12/HC Yellow 6, HC Blue 12/HC Yellow 12, HC Blue 12/HC Orange 1, HC Blue 12/HC Red 1, HC Blue 12/HC Red 3, HC Blue 12/HC Red 7, HC Blue 12/HC Red 10, HC Blue 12/HC Red 11, HC Blue 12/HC Red 13, HC Blue 12/HC Red BN, HC Blue 12/HC Violet 1, HC Blue 12/1,4-diamino-2-nitrobenzene, HC Blue 12/2-amino-4-nitrophenol, HC Blue 12/1,4-bis-(2-hydroxyethyl)amino-2-nitrobenzene, HC Blue 12/3-nitro-4-(2-hydroxyethyl)aminophenol, HC Blue 12/4-[(2-hydroxyethyl)amino]-3-nitro-1-methylbenzene, HC Blue 12/1-amino-4-(2-hydroxyethyl)amino-5-chloro-2-nitrobenzene, HC Blue 12/1-amino-4-(2-hydroxyethyl)amino-5-chloro-2-nitrobenzene, HC Blue 12/4-amino-3-nitrophenol, HC Blue 12/4-[(3-hydroxypropyl)amino]-3-nitrophenol, HC Blue 12/2-amino-6-chloro-4-nitrophenol, HC Blue 12/4-ethylamino-3-nitrobenzoic acid, HC Blue 12/2-chloro-6-ethylamino-4-nitrophenol, HC Yellow 2/HC Yellow 4, HC Yellow 2/HC Yellow 5, HC Yellow 2/HC Yellow 6, HC Yellow 2/HC Yellow 12, HC Yellow 2/HC Orange 1, HC Yellow 2/HC Red 1, HC Yellow 2/HC Red 3, HC Yellow 2/HC Red 7, HC Yellow 2/HC Red 10, HC Yellow 2/HC Red 11, HC Yellow 2/HC Red 13, HC Yellow 2/HC Red BN, HC Yellow 2/HC Violet 1, HC Yellow 2/HC Blue 2, HC Yellow 2/HC Blue 11, HC Yellow 2/HC Blue 12, HC Yellow 2/1,4-diamino-2-nitrobenzene, HC Yellow 2/2-amino-4-nitrophenol, HC Yellow 2/1,4-bis-(2-hydroxyethyl)amino-2-nitrobenzene, HC Yellow 2/3-nitro-4-(2-hydroxyethyl)aminophenol, HC Yellow 2/4-[(2-hydroxyethyl)amino]-3-nitro-1-methylbenzene, HC Yellow 2/1-amino-4-(2-hydroxyethyl)amino-5-chloro-2-nitrobenzene, HC Yellow 2/4-amino-3-nitrophenol, HC Yellow 2/4-[(3-hydroxypropyl)amino]-3-nitrophenol/HC Yellow 2/2-amino-6-chloro-4-nitrophenol, HC Yellow 2/4-ethylamino-3-nitrobenzoic acid, or HC Yellow 2/2-chloro-6-ethylamino-4-nitrophenol, 2-amino-6-chloro-4-nitrophenol/HC Yellow 2, 2-amino-6-chloro-4-nitrophenol/HC Yellow 4, 2-amino-6-chloro-4-nitrophenol/HC Yellow 5, 2-amino-6-chloro-4-nitrophenol/HC Yellow 6, 2-amino-6-chloro-4-nitrophenol/HC Yellow 12, 2-amino-6-chloro-4-nitrophenol/HC Orange 1, 2-amino-6-chloro-4-nitrophenol/HC Red 1, 2-amino-6-chloro-4-nitrophenol/HC Red 3, 2-amino-6-chloro-4-nitrophenol/HC Red 7, 2-amino-6-chloro-4-nitrophenol/HC Red 10, 2-amino-6-chloro-4-nitrophenol/HC Red 11, 2-amino-6-chloro-4-nitrophenol/HC Red 13, 2-amino-6-chloro-4-nitrophenol/HC Red BN, 2-amino-6-chloro-4-nitrophenol/HC Blue 2, 2-amino-6-chloro-4-nitrophenol/HC Blue 11, 2-amino-6-chloro-4-nitrophenol/HC Blue 12, 2-amino-6-chloro-4-nitrophenol/HC Violet 1, 2-amino-6-chloro-4-nitrophenol/1,4-diamino-2-nitrobenzene, 2-amino-6-chloro-4-nitrophenol/2-amino-4-nitrophenol, 2-amino-6-chloro-4-nitrophenol/1,4-bis-(2-hydroxyethyl)amino-2-nitrobenzene, 2-amino-6-chloro-4-nitrophenol/3-nitro-4-(2-hydroxyethyl)aminophenol, 2-amino-6-chloro-4-nitrophenol/4-[(2-hydroxyethyl)amino]-3-nitro-1-methylbenzene, 2-amino-6-chloro-4-nitrophenol/1-amino-4-(2-hydroxyethyl)amino-5-chloro-2-nitrobenzene, 2-amino-6-chloro-4-nitrophenol/4-amino-3-nitrophenol, 2-amino-6-chloro-4-nitrophenol/4-[(3-hydroxypropyl)amino]-3-nitrophenol, 2-amino-6-chloro-4-nitrophenol/4-ethylamino-3-nitrobenzoic acid, and 2-amino-6-chloro-4-nitrophenol/2-chloro-6-ethylamino-4-nitrophenol.

11. The agent according to claim 1 , wherein the substituents R1 and R2 independently stand for a linear or branched, saturated, unsaturated, or multiply unsaturated C 5 -C 20 alkyl chain.

12. The agent according to claim 1 , wherein the substituents R1 and R2 independently stand for a linear or branched, saturated, unsaturated, or multiply unsaturated C 14 -C 20 alkyl chain.

13. The agent according to claim 1 , wherein the substituents R1 and R2 independently are selected from the group consisting of: H 3 C—(CH 2 ) 13 —, H 3 C—(CH 2 ) 15 —, H 3 C—(CH 2 ) 17 —, and H 3 C—(CH 2 ) 19 —.

14. The agent according to claim 1 , wherein the compound or compounds of formula (I) comprise 0.005 wt % to 5 wt % of the total weight of the agent.

15. The agent according to claim 1 , wherein the compound or compounds of formula (I) comprise 0.1 wt % to 4.5 wt % of the total weight of the agent.

16. The agent according to claim 1 , wherein the compound or compounds of formula (I) comprise 1.5 wt % to 2.5 wt % of the total weight of the agent.

17. The agent according to claim 1 , wherein the agent characterized further comprises 0.1 wt % to 15 wt % of one or more solvents selected from the group consisting of: 2-butoxyethanol, propylene glycol monomethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, ethylene glycol monobutyl ether, ethylene glycol monoethyl ether, ethanol, isopropanol, n-propanol, n-butanol, 1,3-propanediol, glycerin, 1-methoxy-2-propanol, 1-ethoxy-2-propanediol, 1,4-butanediol, 1,3-butanediol, 1,2-hexanediol, benzyl alcohol, phenoxyethanol, 2-phenylethyl alcohol, methoxybutanol, n-butylene glycol, ethylene carbonate, and propylene carbonate.

18. Method for producing a long-lasting luster on keratinic fibers, in particular human hair, in which an agent according to claim 1 is applied to the keratinic fibers, left there for 30 seconds to 45 minutes, and subsequently rinsed out with water or a surfactant-containing agent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 12, 2015
From: GOUTSIS, KONSTANTIN; WESER, GABRIELE
To: HENKEL AG & CO. KGAA
Reel/Frame 035150/0074 →
Priority Claims (1)
DE 10 2012 216 606 · Sep 18, 2012 · national
Continuity (2)
Continuation PCTEP2013068973 · Sep 13, 2013
Related Publication 20150182441A1 · Jul 2, 2015