IP Library Granted Patent US 8,444,709
Granted Patent B2
US 8,444,709 · App. 13/397,923 · Granted May 21, 2013

Oxidative dyeing compositions comprising an 1-hexyl/heptyl-4,5-diaminopyrazole and a 2-aminophenol and derivatives thereof

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Quick Facts
Patent No.
US 8,444,709
App. No.
13/397,923
Granted
May 21, 2013
Kind
B2
Abstract

An oxidative dyeing composition comprising a 1-hexyl-4,5-diaminopyrazole compound or a 1-heptyl-4,5-diaminopyrazole compound of formula (I) in combination with a 2-aminophenol compound of formula (II): wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are as defined herein and a=1 or 2. The composition provides good hair color intensity together with good wash and bleeding fastness.

Claims (54)

1. A composition for the oxidative dyeing of keratin fibers, in particular human keratin fibers, comprising:

(A) a 1-hexyl/heptyl-4,5-diamino-pyrazole compound of the general formula (I), a physiologically compatible water-soluble salt thereof, or mixtures thereof,

wherein a is equal to one or two;

wherein R 1 is selected from the group consisting of:

(a) C-linked substituents selected from the group consisting of:

(i) substituted or unsubstituted, straight or branched or cyclic, saturated or unsaturated, aliphatic or heteroaliphatic substituents, in particular alkyl or hydroxy substituted alkyl, and

(ii) substituted or unsubstituted, mono- or poly- unsaturated aromatic or heteroaromatic substituents, in particular aryl or heteroaryl,

wherein said C-linked substituents comprise from 1 to 6 carbon atoms and from 0 to 5 heteroatoms selected from the group consisting of O, F, N, P and Si;

(b) S-linked substituents selected from the group consisting of SA 1 , SO 2 A 1 , SO 3 A 1 , SSA 1 , SOA 1 , SO 2 NA 1 A 2 , SNA 1 A 2 , and SONA 1 A 2 ;

(c) O-linked substituents selected from the group consisting of OA 1 ,ONA 1 A 2 ;

(d) N-linked substituents selected from the group consisting of NA 1 A 2 , (NA 1 A 2 A 3 ) + , NA 1 SA 2 , NO 2 , NA 1 A 2 ;

(e) halogens selected from the group consisting of F, Cl, Br, and I; and

(f) hydrogen;

wherein A 1 , A 2 , and A 3 are independently selected from each other from the group consisting of hydrogen; substituted or unsubstituted, straight or branched or cyclic, saturated or unsaturated, aliphatic or heteroaliphatic or aromatic or heteroaromatic substituents, or A 1 and A 2 together with nitrogen atoms to which they are bound form a ring; wherein said substituents or ring comprise from 1 to 6 carbon atoms and from 0 to 5 heteroatoms selected from the group consisting of O, S, N, P, and Si;

and wherein R 2 and R 3 are selected independently of each other from the group consisting of hydrogen; a C1-C6 alkyl substituent; a trifluoromethyl substituent; a C1-C6 aminoalkyl substituent; a C1-C6 hydroxyalkyl substituent; and C1-C6 an alkoxyalkyl substituent; and

(B) a 2-aminophenol compound of the general formula (II), a physiologically compatible water-soluble salt thereof, or mixtures thereof,

wherein R 4 , R 5 , R 6 and R 7 are substituents selected independently of each other from the group consisting of:

(a) C-linked substituents selected from the group consisting of:

(i) substituted or unsubstituted, straight or branched or cyclic, saturated or unsaturated, aliphatic or heteroaliphatic substituents, in particular alkyl or hydroxy substituted alkyl, and

(ii) substituted or unsubstituted, mono- or poly- unsaturated aromatic or heteroaromatic substituents, in particular aryl or heteroaryl,

wherein said C-linked substituents comprise from 1 to 6 carbon atoms and from 0 to 5 heteroatoms selected from the group consisting of O, F, N, P and Si;

(b) S-linked substituents selected from the group consisting of SA 1 , SO 2 A 1 , SO 3 A 1 , SSA 1 , SOA 1 , SO 2 NA 1 A 2 , SNA 1 A 2 , and SONA 1 A 2 ;

(c) O-linked substituents selected from the group consisting of OA 1 and ONA 1 A 2 ;

(d) N-linked substituents selected from the group consisting of NA 1 A 2 , (NA 1 A 2 A 3 ) + , NA 1 SA 2 , NO 2 and NA 1 A 2 ;

(e) halogens selected from the group consisting of F, Cl, Br, and I; and

(f) hydrogen;

wherein A 1 , A 2 , and A 3 are selected independently of each other from the group consisting of hydrogen; substituted or unsubstituted, straight or branched or cyclic, saturated or unsaturated, aliphatic or heteroaliphatic or aromatic or heteroaromatic substituents, or A 1 and A 2 together with nitrogen atoms to which they are bound form a ring; wherein said substituents or ring comprise from 1 to 6 carbon atoms and from 0 to 5 heteroatoms selected from the group consisting of O, S, N, P, and Si; and

(C) an oxidizing agent.

2. A composition according to claim 1 , wherein the 1-hexyl/heptyl-4,5-diamino pyrazole compound (I) is a compound with formula (I.1):

3. A composition according to claim 1 , wherein the 2-aminophenol compound (II) is selected from the group consisting of 2-amino-5-propylphenol, 2-amino-5-pentylphenol, 2-amino-5-hexylphenol, 2-amino-5-(methoxymethyl)phenol, 2-amino-5-(ethoxymethyl)phenol, 2-amino-5-((2-methoxyethoxy)methyl)phenol, 2-amino-5-ethoxyphenol, 2-amino-5-ethylphenol, 2-amino-5-(2-hydroxyethyl)phenol, and 5-ethyl-2-aminophenol and 2-amino-5-(5-hydroxypentyl)phenol.

4. A composition according to claim 3 , wherein the 2-aminophenol compound (II) is 2-amino-5-ethylphenol of formula (II.1):

5. A composition according to claim 1 , wherein said composition further comprises an auxiliary coupler.

6. A composition according to claim 5 , wherein said auxiliary coupler is an m-aminophenol compound selected from the group consisting of

salts thereof and combinations thereof.

7. A composition according to claim 1 , further comprising a primary intermediate selected from the group consisting of toluene-2,5-diamine, p-phenylenediamine, 2-hydroxyethyl-p-phenylenediamine, 2-methoxymethyl-p-phenylenediamine, 2-(2,5-diamino-4-methoxyphenyl)propane-1,3-diol, 2-chloro-p-phenylenediamine, 2-methoxy-p-phenylenediamine, 2-((2-(4-amino-phenylamino)-ethyl)-(2- hydroxyethyl)-amino)-ethanol, salts thereof and combination thereof.

8. A composition according to claim 1 further comprising at least one additional component selected from the group consisting of alkalizing agents, auxiliary primary intermediates, auxiliary couplers, direct dyes, thickeners, chelants, pH modifiers and/or buffering agents, radical scavenger systems and mixtures thereof.

9. A composition according to claim 1 , further comprising fatty alcohols comprising from 14 to 30 carbon atoms, or oxyethylenated fatty alcohols comprising from 16 to 30 carbon atoms and 2 units or less of ethylene oxide.

10. A composition according to claim 9 , further comprising at least one ionic or nonionic surfactant selected from:

anionic surfactants selected from C8-C30 alkyl sulfates,

anionic surfactants according to the formula R n X m YM, wherein R is independently selected from alkyl, alkenyl or alkylaryl groups having from 8 to 30 carbon atoms, X is independently selected from polar groups comprising at least one carbon atom and at least one oxygen or nitrogen atom, Y is an anionic group selected from carboxylates, sulfates, sulfonates or phosphates, n and m are independently 1 or 2, and M is hydrogen or a salt forming cation and mixture thereof;

non-ionic surfactant comprising one or more polyethyleneoxide chains;

cationic surfactants selected from quaternary ammonium salts or amido-amines having at least one fatty chain; and

mixtures thereof.

11. A composition according to claim 10 comprising a mixture of cetearyl alcohol and dicetyl phosphate and ceteth-10 phosphate.

12. A composition according to claim 1 wherein said oxidizing agent is selected from the group consisting of hydrogen peroxide, sodium periodate, urea peroxide, melamine peroxide, perborates, percarbonates, perphosphates, persilicates, persulfates, oxidizing enzymes such as uricases, oxidases, and peroxidases, a source of peroxymonocarbonate ions and mixtures thereof.

13. A composition according to claim 12 wherein the source of peroxymonocarbonate ions selected from the group consisting of: sodium, potassium, guanidine, arginine, lithium, calcium, magnesium, barium or ammonium salts of carbonate, carbamate and hydrocarbonate ions and mixtures thereof.

14. A composition according to claim 1 , wherein said composition is dispensed as a foam.

15. A method of dyeing hair comprising the steps of:

(i) providing a tint component comprising (a) a 1-hexyl/heptyl-4,5-diaminopyrazole compound of the general formula (I) as defined in claim 1 , a physiologically compatible water-soluble salt thereof, or mixtures thereof; and (b) a 2-aminophenol compound of the general formula (II) as defined in claim 1 , a physiologically compatible water-soluble salt thereof or mixtures thereof;

(ii) providing a developer component comprising (c) an oxidizing agent;

(iii) mixing the tint component and the developer component to obtain a composition for the oxidative dyeing of keratin fibers according to claim 1 ; and

(iv) applying said composition for the oxidative dyeing of keratin fibers onto the hair.

16. An oxidative hair dyeing kit comprising: (i) a tint component comprising (a) a 1-hexyl/heptyl-4,5-diaminopyrazole compound of the general formula (I) as defined in claim 1 , a physiologically compatible water-soluble salt thereof or mixtures thereof and, (b) a 2-aminophenol compound of the general formula (II) as defined in claim 1 , a physiologically compatible water-soluble salt thereof or mixtures thereof; and ii) a developer component comprising an oxidizing agent.

17. A tint component comprising (a) a 1-hexyl/heptyl-4,5-diaminopyrazole compound of the general formula (I) as defined in claim 1 , a physiologically compatible, water-soluble salt thereof or mixtures thereof; and (b) a 2-aminophenol compound of the general formula (II) as defined in claim 1 , a physiologically compatible water-soluble salt thereof or mixtures thereof.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2021
From: NOXELL CORPORATION
To: WELLA OPERATIONS US, LLC
Reel/Frame 056339/0928 →
RELEASE OF SECURITY INTEREST Recorded Apr 16, 2018
From: JPMORGAN CHASE BANK, N.A.
To: NOXELL CORPORATION
Reel/Frame 045950/0161 →
SECURITY INTEREST Recorded Jun 29, 2017
From: NOXELL CORPORATION
To: JPMORGAN CHASE BANK N.A.
Reel/Frame 043340/0685 →
CORRECTIVE ASSIGNMENT TO CORRECT THE THE NAME OF ASSIGNOR PREVIOUSLY RECORDED ON REEL 040437 FRAME 0133. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 15, 2016
From: THE PROCTER AND GAMBLE COMPANY
To: GALLERIA CO.
Reel/Frame 040941/0637 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2016
From: GALLERIA CO.
To: NOXELL CORPORATION
Reel/Frame 040436/0438 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2016
From: PROCTER AND GAMBLE COMPANY
To: GALLERIA CO.
Reel/Frame 040437/0133 →
IP SECURITY AGREEMENT Recorded Oct 4, 2016
From: NOXELL CORPORATION
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 040224/0630 →