Composition for the dyeing of human hair

Bleaching and dyeing; fluid treatment and chemical modification – Dyeing involving animal-derived natural fiber material ,... – Hair dyeing

Reexamination Certificate

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C008S406000, C008S407000, C008S421000, C008S614000

Reexamination Certificate

active

06733541

ABSTRACT:

The invention concerns a composition for the dyeing of human hair on aqueous basis, which comprises at least one direct-acting hair dyestuff. Such hair dyeing compositions have been known for some time.
They usually comprise several anionic or cationic direst-acting dyestuffs and, in difference to the permanent hair dyeing compositions on the basis of oxidation dyestuff precursor products, they require no prior development with oxidation agents.
These direct-acting compositions are either applied together with surface-active substances as so-called tinting shampoos, or they are applied onto the hair as lotions, emulsions or thickened lotions, i.e. gels.
With regard to their color stability and especially intensity as well as evenness of the coloration and color gloss, these direct-acting hair dyeing compositions can still be improved.
The invention therefore starts from the task of creating a hair dyeing composition on the basis of direct-acting dyestuffs, which can be applied onto the hair as a lotion, emulsion, solution, gel, suspension or, also, with the addition of propellants, as aerosol preparation, and which shows excellent coloration properties, providing stable colorations over an extended period of time.
This problem is solved by adding to such a composition at least one direct-acting dyestuff on the basis of a compound of formula (1)
wherein R
1
is a halogen atom; R
2
and R
4
are an optionally OH— or NH
2
-substituted C
1
-C
4
-alkyl group or phenyl group and R
3
stands for H
1
or an optionally OH— or NH
2
-substituted C
1
-C
4
-alkyl group or phenyl group.
Preferred compounds are those of the formulas (2) and (3)
The preparation of these compounds is known per se and is carried out by transfer of the respectively substituted acetamides or acetanilides with the respectively substituted haloaminobenzoles.
The colors thus obtained are mainly in the range of intensive yellow and gold but can be varied by the addition of further dyestuff shades.
The proportion of direct-acting dyestuffs in the compositions according to the invention is variable and ranges between about 0.001% to about 5%, preferably 0.01% to 2.5%, in particular 0.1% to 1% by weight, calculated to the total composition.
As stated above, in addition to the compounds of formula (1), it is possible to incorporate further direct-acting hair dyestuffs to modify the shades.
Preferred are the so-called “Arianor” dyestuffs; see K. Schrader, “Grundlagen und Rezepturen der Kosmetika”, 2nd Ed., (1989), p. 811.
Especially suited basic (cationic) dyestuffs are.
Basic Blue 6,
C.I.-No. 51,175;
Basic Blue 7,
C.I.-No. 42,595;
Basic Blue 9,
C.I.-No. 52,015;
Basic Blue 26,
C.I.-No. 44,045;
Basic Blue 41,
C.I.-No. 11,154;
Basic Blue 99,
C.I.-No. 56,059;
Basic Brown 4,
C.I.-No. 21,010;
Basic Brown 16,
C.I.-No. 12,250;
Basic Brown 17,
C.I.-No. 12,251;
Natural Brown 7,
C.I.-No. 75,500;
Basic Green 1,
C.I.-No 42,040;
Basic Red 2,
C.I.-No. 50,240;
Basic Red 12
C.I.-No. 48,070;
Basic Red 22,
C.I.-No. 11,055;
Basic Red 76,
C.I.-No. 12,245;
Basic Violet 1,
C.I.-No. 42,535;
Basic Violet 3,
C.I.-No. 42,555;
Basic Violet 10,
C.I.-No. 45,170;
Basic Violet 14,
C.I.-No. 42,510;
Basic Yellow 57,
C.I.-No. 12,719.
as well as the dyestuffs known from EP 0681 464 B1.
It is, of course, also possible to use the respective direct-acting plant dyestuffs or also anionic (acidic), direct-acting hair dyestuffs.
These are customarily also used in an amount of about 0.005% to about 5%, preferably about 0.05% to about 2.5%, in particular about 0.1% to about 1% by weight, calculated to the total composition, which is present as solution, dispersion, emulsion, gel or aerosol preparation for direct application.
Suitable as anionic dyestuffs are, for example:
Acid Black 1,
C.I.-No. 20,470;
Acid Blue 1,
C.I.-No. 42,045;
Food Blue 5,
C.I.-No. 42,051;
Acid Blue 9,
C.I.-No. 42,090;
Acid Blue 74,
C.I.-No. 73,015;
Acid Red 18,
C.I.-No. 16,255;
Acid Red 27,
C.I.-No. 16,185;
Acid Red 87,
C.I.-No. 45,380;
Acid Red 92,
C.I.-No. 45,410;
Acid Orange 7,
C.I.-No. 15,510;
Acid Violet 43,
C.I.-No. 60,730;
Acid Yellow 1,
C.I.-No. 10,316;
Acid Yellow 23,
C.I.-No. 19,140;
Acid Yellow 3,
C.I.-No. 47,005;
Food Yellow No. 8,
C.I.-No 14,270;
D&C Brown No. 1,
C.I.-No. 20,170;
D&C Green No. 5,
C.I.-No. 61,570;
D&C Orange No. 4,
C.I.-No. 15,510;
D&C Orange No. 10,
C.I.-No. 45,425:1;
D&C Orange No. 11,
C.I.-No. 45,425;
D&C Red No. 21,
C.I.-No. 45,380:2;
D&C Red No. 27,
C.I.-No. 45,410:1;
D&C Red No. 33,
C.I.-No. 17,200;
D&C Yellow No. 7,
C.I.-No. 45,350:1;
D&C Yellow No. 8,
C.I.-No. 45,350;
FD&C Red No. 4,
C.I.-No. 14,700;
FD&C Yellow No. 6,
C.I.-No 15,985.
Also possible is the use of plant dyestuffs alone or in combination with synthetic direct-acting dyestuffs, for example henna (red or black), alkanna root, laccaic acid, indigo, logwood powder, madder root and rhubarb powder, etc.
The compositions according to the invention may also comprise at least one oxidation dyestuff precursor product, i.e. a developing and/or coupling substance.
Examples of developing substances are in particular 1,4-diaminobenzene, 2,5-diaminotoluene, tetraaminopyrimidines, triaminohydroxypyrimidines, 1,2,4-triaminobenzene, 2-(2,5-diaminophenyl)ethanol, 2-(2-hydroxyethylamino)-5-aminotoluene and 1-amino-4-bis-(2′-hydroxyethyl)aminobenzene or the water-soluble salts thereof; examples for coupling substances are resorcinol, 2-methylresorcinol, 4-chlororesorcinol, 2-amino-4-chlorophenol, 4-(N-methyl)aminophenol, 2-aminophenol, 3-aminophenol, 1-methyl-2-hydroxy-4-aminobenzene, 3-N,N-dimethylaminophenol, 4-amino-3-methylphenol, 5-amino-2-methylphenol, 6-amino-3-methylphenol, 3-amino-2-methylamino-6-methoxypyridine, 2-amino-3-hydroxypyridine, 4-aminodiphenylamine, 4,4′-diaminodiphenylamine, 2-dimethylamino-5-aminopyridine, 2.6-diaminopyridine, 1,3-diaminobenzene, 1-amino-3-(2′-hydroxyethylamino)benzene, 1-amino-3-[bis(2′-hydroxyethyl)amino]benzene, &agr;-naphthol, 1,4-diamino-2-chlorobenzene, 4,6-dichlororesorcinol, 1,3-diaminotoluene, 1-hydroxynaphthalene, 4-hydroxy-1,2-methylendioxybenzene, 1,5-dihydroxynaphthalene, 1,7-dihydroxynaphthalene, 2,7-dihydroxynaphthalene, 2,4-diamino-3-chlorophenol and/or 1-methoxy-2-amino-4-(2′-hydroxyethylamino)benzene, whereby this list is not complete.
Developing and coupling substances are preferably present in a molecular ratio of 1:3 to 5:1, in particular about 1:1 and about 3:1; their proportion in the dyestuff compositions used according to the invention can each be about 0.05% to about 5% by weight, depending on the desired coloration.
Used as oxidizing agents in such oxidation dyestuff precursor products are mainly diluted hydrogen peroxide solutions, emulsions or gels, possible but less common is also the use of further peroxides such as earth alkali peroxides, urea peroxide, melamine peroxide, etc., in the respective stoic amounts.
The oxidation dyestuff compositions can be used as solutions, creams, pastes, gels, aerosols, etc.
The hair dyeing composition according to the invention may also comprise surface-active substances, in the event the composition is a tinting shampoo, these are obligatory in any case.
Such surface-active substances can be anionic, nonionic, cationic or amphoteric or zwitterionic surfactants.
Preferred for non-tinting shampoos are nonionic, amphoteric or zwitterionic and cationic surfactants in an amount between about 0.5% and about 5% by weight, calculated to the total composition.
Suited nonionic surfactants are compounds from the category of alkyl polyglucosides with the general formula (4)
R
5
—O—(CH
2
CH
2
O)
p
—Z
q
  (4)
wherein R
5
is an alkyl group with 8 to 20, preferably 10 to 14 carbon atoms Z is a saccharide group with 5 to 6 carbon atoms, p is a number from 0 to 10, and q is a number between 1 and 5, preferably 1.1 to 2.5.
Further nonionic surfactants useful in the compositions according to invention are C
10
-C
22
-fatty alcohol ethoxylates.
Especially suited C
10
-C
22
-fatty alcohol ethers are the alkyl polyglycol ethers known by the generic terms “Laureth”, “Myristeth”

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