IP Library Granted Patent US 7,678,156
Granted Patent B2
US 7,678,156 · App. 11/662,792 · Granted Mar 16, 2010

Compositions for treating keratinic fibers, methods of treating such fibers therewith and compounds contained therein

Assignee: Henkel AG & Co. KGaA
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Quick Facts
Patent No.
US 7,678,156
App. No.
11/662,792
Granted
Mar 16, 2010
Kind
B2
Abstract

Compositions suitable for treating keratinic fibers, in particular human hair, are disclosed, which compositions comprise: (i) at least one component selected from the group consisting of salt compounds of general formula I, enamine counterparts of salt compounds of general formula I, and mixtures thereof: Where each Me represents a methyl group, R represents a substituent selected from the group consisting of an allyl group, a hydroxy-(C 2-6 )-alkyl group, a benzyl group, and substituted benzyl groups, and X − represents a physiologically compatible anion; and (ii) at least one aldehyde selected from the group consisting of 4-hydroxy-3-methoxybenzaldehyde, 3,5-dimethoxy-4-hydroxybenzaldehyde, 4-hydroxy-1-naphthaldehyde, 4-hydroxy-2-methoxybenzaldehyde, 3,4-dihydroxy-5-methoxybenzaldehyde, 3,4,5-trihydroxybenzaldehyde, 3,4-dibromo-4-hydroxybenzaldehyde, 4-hydroxy-3-nitrobenzaldehyde, 3-bromo-4-hydroxybenzaldehyde, 4-hydroxy-3-methylbenzaldehyde, 3,5-dimethyl-4-hydroxy-benzaldehyde, 5-bromo-4-hydroxy-3-methoxybenzaldehyde, 4-diethylamino-2-hydroxybenzaldehyde, 4-dimethylamino-2-methoxybenzaldehyde and mixtures thereof.

Claims (29)

1. A composition comprising:

(i) at least one component selected from the group consisting of salt compounds of general formula I, enamine counterparts of salt compounds of general formula I, and mixtures thereof:

wherein each Me represents a methyl group, R represents a substituent selected from the group consisting of an allyl group, a hydroxy-(C 2-6 )-alkyl group, a benzyl group, and substituted benzyl groups, and X − represents a physiologically compatible anion; and

(ii) at least one aldehyde selected from the group consisting of 4-hydroxy-3-methoxybenzaldehyde, 3,5-dimethoxy-4-hydroxybenzaldehyde, 4-hydroxy-1-naphthaldehyde, 4-hydroxy-2-methoxybenzaldehyde, 3,4-dihydroxy-5-methoxybenzaldehyde, 3,4,5-trihydroxybenzaldehyde, 3,5-dibromo-4-hydroxybenzaldehyde, 4-hydroxy-3-nitrobenzaldehyde, 3-bromo-4-hydroxybenzaldehyde, 4-hydroxy-3-methylbenzaldehyde, 3,5-dimethyl-4-hydroxybenzatdehyde, 5-bromo-4-hydroxy-3-methoxybenzaldehyde, 4-diethyl-amino-2-hydroxybenzaldehyde, 4-dimethylamino-2-methoxybenzaldehyde, and mixtures thereof.

2. The composition according to claim 1 , wherein R represents a substituent selected from the group consisting of an allyl group, a 3-hydroxypropyl group, a 2-hydroxypropyl group, a 2-hydroxyethyl group, and a benzyl group.

3. The composition according to claim 1 , wherein X − represents a physiologically compatible anion selected from the group consisting of a halide, a benzenesulfonate, a p-toluenesulfonate, a C 1-4 -alkanesulfonate, a triftuoromethanesulfonate, a perehiorate, a 0.5 sulfate, a hydrogensulfate, a tetrafluoroborate, a hexafluorophosphate, and a tetrachlorozincate.

4. The composition according to claim 1 , wherein the at least one component (i) comprises a physiologically compatible salt or counterpart enamine form of a compound selected from the group consisting of: 1-allyl-1,2-dihydro-3,4,6-trimethyl-2-oxopyrimidinium; 1,2-dihydro-1-(2-hydroxyethyl)-3,4,6-trimethyl-2-oxopyrimidinium; 1,2-dihydro-1-(3-hydroxypropyl)-3,4,6-trimethyl-2-oxopyrimidinium; 1-benzyl-1,2-dihydro-3,4,6-trimethyl-2-oxopyrimidinium, and mixtures thereof.

5. The composition according to claim 1 , further comprising at least one additional component selected from the group consisting of CH-acidic compounds different from the at least one component (i), reactive carbonyl compounds different from the at least one aldehyde, and mixtures thereof.

6. The composition according to claim 1 , further comprising a physiologically compatible salt of a compound selected from the group consisting of 1,4-dimethylquinolinium, 1-ethyl-4-methylquinolinium, 1-ethyl-2-methylquinolinium, 1,2,3,3-tetramethyl-3H-indolium, 2,3-dimethylbenzothiazolium, 2,3-dimethylnaphtho[1,2-d]thiazolium, 3-ethyl-2-methylnaphtho[1,2-d]thiazolium, 3-ethyl-2-methylbenzoxazolium, 1,2,3-trimethylquinoxalinium, 3-ethyl-2-methylbenzothiazolium, 1,2-dihydro-1,3,4,6-tetramethyl-2-oxopyrimidinium, 1,2-dihydro-1,3,4-trimethyl-2-oxopyrimidinium, 1,2-dihydro-4,6-dimethyl-1,3-dipropyl-2-oxopyrimidinium, 1,2-dihydro-1,3,4,6-tetramethyl-2-thioxopyrimidinium, 1,2-dihydro-1,3,4,5,6-pentamethyl-2-oxopyrimidinium, 2,5-dimethyl-3-(2-propenyl)-1,3,4-thiadiazolium, 3-ethyl-2,5-dimethyl-1,3,4-thiadiazolium, 1,2-dimethylquinolinium and 1,3,3-trimethyl-2-methyleneindoline (Fischer's base), oxindole, 3-methyl-1-phenylpyrazolin-5-one, indane-1,2-dione, indane-1,3-dione, indan-1-one, 2-amino-4-imino-1,3-thiazoline hydrochloride, benzoylacetonitrile, 3-dicyanomethyleneindan-1-one, 2-(2-furanoyl)acetonitrile, 2-(2-theonyl)acetonitrile, 2-(cyanomethyl)benzimidazole, 2-(cyanomethyl)benzothiazole, 2-(2,5-dimethyl-3-furanoyl)acetonitrile, and mixtures thereof.

7. The composition according to claim 1 , further comprising a reactive carbonyl compound selected from the group consisting of coniferylaldehyde, 2-methoxybenzaldehyde, 3-methoxybenzaldehyde, 4-methoxybenzaldehyde, 2-ethoxybenzaldehyde, 3-ethoxybenzaldehyde, 4-ethoxybenzaldehyde, 4-hydroxy-2,3-dimethoxybenzaldehyde, 4-hydroxy-2,5-dimethoxybenzaldehyde, 4-hydroxy-2,6-dimethoxybenzaldehyde, 4-hydroxy-2-methylbenzaldehyde, 4-hydroxy-2,3-dimethylbenzaldehyde, 4-hydroxy-2,5-dimethylbenzaldehyde, 4-hydroxy-2,6-dimethylbenzaldehyde, 3,5-diethoxy-4-hydroxybenzaldehyde, 2,6-diethoxy-4-hydroxybenzaldehyde, 3-hydroxy-4-methoxybenzaldehyde, 2-hydroxy-4-methoxybenzaldehyde, 2-ethoxy-4-hydroxybenzaldehyde, 3-ethoxy-4-hydroxy-benzaldehyde, 4-ethoxy-2-hydroxybenzaldehyde, 4-ethoxy-3-hydroxybenzaldehyde, 2,3-dimethoxybenzaldehyde, 2,4-dimethoxybenzaldehyde, 2-5-dimethoxybenzaldehyde, 2,6-dimethoxybenzaldehyde, 3,4-dimethoxybenzaldehyde, 3,5-dimethoxybenzaldehyde, 2,3,4-trimethoxybenzaldehyde, 2,3,5-trimethoxybenzaldehyde, 2,3,6-trimethoxybenzaldehyde, 2,4,6-trimethoxybenzaldehyde, 2,4,5-trimethoxybenzaldehyde, 2,5,6-trimethoxybenzaldehyde, 2-hydroxybenzaldehyde, 3-hydroxybenzaldehyde, 4-hydroxybenzatdehyde, 2,3-dihydroxybenz-aldehyde, 2,4-dihydroxybenzaldehyde, 2,4-dihydroxy-3-methylbenzaldehyde, 2,4-dihydroxy-5-methylbenzaldehyde, 2,4-dihydroxy-6-methylbenzaldehyde, 2,4-dihydroxy-3-methoxybenzaldehyde, 2,4-dihydroxy-5-methoxybenzaldehyde, 2,4-di-hydroxy-6-methoxybenzaldehyde, 2,5-dihydroxybenzaldehyde, 2,6-dihydroxybenzaldehyde, 3,4-dihydroxybenzaldehyde, 3,4-dihydroxy-2-methylbenzaldehyde, 3,4-di-hydroxy-5-methylbenzaldehyde, 3,4-dihydroxy-6-methylbenzaldehyde, 3,4-dihydroxy-2-methoxybenzaldehyde, 3,5-dihydroxybenzaldehyde, 2,3,4-trihydroxy-benzaldehyde, 2,3,5-trihydroxybenzaldehyde, 2,3,6-trihydroxybenzaldehyde, 2,4,6-trihydroxybenzaldehyde, 2,4,5-trihydroxybenzaldehyde, 2,5,6-trihydroxybenzaldehyde, 4-dimethylaminobenzaldehyde, 4-diethylaminobenzaldehyde, 4-dimethylamino-2-hydroxy-benzaldehyde, 4-pyrrolidinobenzaldehyde, 4-morpholinobenzaldehyde, 2-morpholinobenzaldehyde, 4-piperidinobenzaldehyde, 3,5-dichloro-4-hydroxybenzaldehyde, 4-hydroxy-3,5-diiodobenzaldehyde, 3-chloro-4-hydroxybenzatdehyde, 5-chloro-3,4-dihyroxy-benzaldehyde, 5-bromo-3,4-dihydroxybenzaldehydro, 3-chloro-4-hydroxy-5-methoxy-beuzaldehyde, 4-hydroxy-3-iodo-5-methoxybenzaldehyde, 2-methoxy-1-naphthaldehyde, 4-methoxy-1-naphthaldehyde, 2-hydroxy-1-naphthaldehyde, 2,4-dihydroxy-1-naphthaldehyde, 4-hydroxy-3-methoxy-1-naphthaldehyde, 2-hydroxy-4-methoxy-1-naphthaldehyde, 3-hydroxy-4-methoxy-1-naphthaldehyde, 2,4-dimethoxy-1-naphthaldehyde, 3,4-dimethoxy-1-naphthaldehyde, 4-dimethylamino-1-naphthaldehyde, 2-nitrobenzaldehyde, 3-nitrobenzaldehyde, 4-nitrobenzaldehyde, 4-methyl-3-nitrobenzaldehyde, 3-hydroxy-4-nitro-benzaldehyde, 5-hydroxy-2-nitrobenzaldehyde, 2-hydroxy-5-nitrobenzaldehyde, 2-hydroxy-3-nitrobenzaldehyde, 2-fluoro-3-nitrobenzaldehyde, 3-methoxy-2-nitrobenzaldehyde, 4-chloro-3-nitrobenzaldehyde, 2-chloro-6-nitrobenzaldehyde, 5-chloro-2-nitrobenzaldehyde, 4-chloro-2-nitrobenzaldehyde, 2,4-dinitrobenzaldehyde, 2,6-dinitrobenzaldehyde, 2-hydroxy-3-methoxy-5-nitrobenzaldehyde, 4,5-dimethoxy-2-nitrobenzaldehyde, 6-nitro-piperonal, 2-nitropiperonal, 5-nitrovanillin, 2,5-dinitrosalicylaldehyde, 5-bromo-3-nitrosalicylaldehyde, 4-nitro-1-naphthaldehyde, 2-nitrocinnamaldehyde, 3-nitrocinnamaldehyde, 4-nitrocinnamaldehyde, 4-dimethylaminocinnamaldehyde, 2-dimethylaminobenzaldehyde, 2-chloro-4-dimethylaminobenzaldehyde, 4-dimethylamino-2-methylbenzaldehyde, 4-diethylaminocinnamaldehyde, 4-dibutyl-aminobenzaldehyde, 4-diphenylaminobenzaldehyde, 4-(1-imidazolyl)benzaldehyde, piperonal, and mixtures thereof.

8. The composition according to claim 1 , wherein the at least one component (i) and the at least one aldehyde are each present in an amount of 0.03 to 65 mmol per 100 g of the composition.

9. The composition according to claim 1 , further comprising a color enhancer selected from the group consisting of piperidine, piperidine-2-carboxylic acid, piperidine-3-carboxylic acid, piperidine-4-carboxylic acid, pyridine, 2-hydroxypyridine, 3-hydroxypyridine, 4-hydroxypyridine, imidazole, 1-methylimidazole, arginine, histidine, pyrrolidine, proline, pyrrolidone, pyrrolidone-5-carboxylic acid, pyrazole, 1,2,4-triazole, piperazidine, and mixtures thereof.

10. The composition according to claim 1 , further comprising an oxidizing agent.

11. The composition according to claim 1 , further comprising at least one developer component.

12. The composition according to claim 1 , further comprising at least one direct dye present in an amount of 0.01 to 20% by weight, based on the composition.

13. The composition according to claim 1 , further comprising a surfactant selected from the group consisting of anionic surfactants, zwitterionic surfactants, nonionic surfactants and mixtures thereof.

14. A method comprising:

(a) providing at least one component selected from the group consisting of salt compounds of general formula I, enamine counterparts of salt compounds of general formula I, and mixtures thereof:

wherein each Me represents a methyl group, R represents a substituent selected from the group consisting of an allyl group, a hydroxy-(C 2-6 )-alkyl group, a benzyl group, and substituted benzyl groups, and X − represents a physiologically compatible anion;

(b) providing at least one aldehyde selected from the group consisting of 4 hydroxy-3-methoxybenzaldehyde, 3,5-dimethoxy-4-hydroxybenzaldehyde, 4-hydroxy-1-naphthaldehyde, 4-hydroxy-2-methoxybenzaldehyde, 3,4-dihydroxy-5-methoxybenzaldehyde, 3,4,5-trihydroxybenzaldehyde, 3,5-dibromo-4-hydroxybenzaldehyde, 4-hydroxy-3-nitrobenzaldehyde, 3-bromo-4-hydroxybenzaldehyde, 4-hydroxy-3-methylbenzaldehyde, 3,5-dimethyl-4-hydroxybenzaldehyde, 5-bromo-4-hydroxy-3-methoxybenzaldehyde, 4-diethyl-amino-2-hydroxybenzaldehyde, 4-dimethylamino-2-methoxybenzaldehyde, and mixtures thereof;

(c) contacting a keratinic fiber with the at least one component and the at least one aldehyde; and

(d) removing the at least one component and the at least one aldehyde from the keratinic fiber.

15. The method according to claim 14 , wherein the at least one component and the at least one aldehyde are applied to the keratinic fiber simultaneously.

16. The method according to claim 14 , wherein the at least one component and the at least one aldehyde are applied to the keratinic fiber sequentially.

17. The method according to claim 14 , wherein R represents a substituent selected from the group consisting of an allyl group, a 3-hydroxypropyl group, a 2-hydroxypropyl group, a 2-hydroxyethyl group, and a benzyl group.

18. The method according to claim 14 , wherein the at least one component comprises a physiologically compatible salt or counterpart enamine form of a compound selected from the group consisting of: 1-allyl-1,2-dihydro-3,4,6-trimethyl-2-oxopyrimidinium; 1,2-dihydro-1-(2-hydroxyethyl)-3,4,6-trimethyl-2-oxopyrimidinium; 1,2-dihydro-1-(3-hydroxypropyl)-3,4,6-trimethyl-2-oxopyrimidinium; 1-benzyl-1,2-dihydro-3,4,6-trimethyl-2-oxopyrimidinium, and mixtures thereof.

19. The method according to claim 14 , further comprising pretreating the keratinic fiber prior to contact with the at least one component and the at least one aldehyde, wherein pretreating the keratinic fiber comprises contacting the keratinic fiber with an agent selected from the group consisting of bleaching agents, oxidation colorants and combinations thereof.

20. A compound according to general formula I:

wherein each Me represents a methyl group, R represents a substituent selected from the group consisting of an allyl group, a hydroxy-(C 2-6 )-alkyl group, a benzyl group, and substituted benzyl groups, and X − represents a physiologically compatible anion.

Assignments (2)
CHANGE OF NAME Recorded Nov 2, 2010
From: HENKEL KGAA
To: HENKEL AG & CO. KGAA
Reel/Frame 025232/0453 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2007
From: GROSS, WIBKE; MAUSBERG, SANDRA; OBERKOBUSCH, DORIS; HOFFKES, HORST
To: HENKEL KGAA
Reel/Frame 019219/0474 →
Priority Claims (1)
DE 10 2004 044 231 · Sep 14, 2004 · national
Continuity (1)
Related Publication 20070287686A1 · Dec 13, 2007