IP Library Granted Patent US 8,460,397
Granted Patent B2
US 8,460,397 · App. 13/398,201 · Granted Jun 11, 2013

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

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,460,397
App. No.
13/398,201
Granted
Jun 11, 2013
Kind
B2
Abstract

A composition for the oxidative dyeing of keratin fibers, in particular human keratin fibers, comprising (A) a 1-hexyl/heptyl-4,5-diaminopyrazole compound of the general formula (I), its physiologically compatible water-soluble salt, or mixtures thereof; (B) a pyridine compound of the general formula (II), its physiologically compatible water-soluble salt, or mixtures thereof; and (C) an oxidizing agent. wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 8 are as defined herein and a=1 or 2.

Claims (55)

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 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;

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

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

wherein R 4 , R 5 , R 6 , R 7 and R 8 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 pyridine compound (II) is selected from the group consisting of compounds with formula (II.1) to (II.4) and combinations thereof:

4. A composition according to claim 3 wherein the pyridine compound has the formula (II.2):

5. A composition according to claim 1 further comprising an auxiliary coupler.

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

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 further comprising a chelant selected from the group consisting of: diethylenetriamine-N,N′,N″-polyacids, diethylenetriaminepentaacetic acid (DTPA), diethylenetriaminepenta(methylene phosphonic acid) (DTPMP), diamine-N,N′-dipolyacid, monoamine monoamide-N,N′-dipolyacid, and N,N′-bis(2-hydroxybenzyl)ethylenediamine-N,N′-diacetic acid chelants, carboxylic acids, phosphonic acids and polyphosphoric acids, their salts and derivatives.

13. 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.

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 pyridine 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 any of the preceding claims; 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-diamino pyrazole compound of the general formula (I) as defined in claim 1 , a physiologically compatible water-soluble salt thereof or mixtures thereof and,

(b) a pyridine 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 pyridine 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 →