DE1617699C3 - Hair dyes and hair coloring processes - Google Patents

Description

NO ₁

NO,

R '"

where R, R 'and R "are hydrogen, lower alkyl

or hydroxyalkyl radical and R "'is a radical in which R, R' and R" are hydrogen, lower alk) I- or Formula 25 hydroxyalkyl radicals and R "'is a radical of the formula

R,

- (CH ₂ ) ,, - N

means where R ₁ and R ₂ . which can be the same or different, represent hydrogen, lower alkyl or hydroxyalkyl radicals which, together with the nitrogen atom, can also form a heterocycle and, if it is a tertiary nitrogen atom, this can also be quaternized, η is an integer from 2 to including 6, where the amino group in the ortho position to the nitro group must not be tertiary and R 'and R "cannot be hydrogen at the same time, in the event that the nitro group is in the meta position to the amino group substituted by the radical R'" stands, contains.

2. Hair dye according to claim 1, characterized in that its pH is between 6 and 10 located.

3. Hair dye according to Claims 1 and 2, characterized in that there are other dyes contains.

4. Hair dye according to Claims 1 to 3, characterized in that it is also organic Contains solvent.

5. A method for dyeing hair, characterized in that the hair with a Agent according to one of the preceding claims, impregnated at room temperature Rinses for 5 to 30 minutes, then washes and dries.

The invention relates to a hair dye based on nitroparaphenylenediamines and conventional ones Additives and a hair coloring process.

(CH ₂ ) ,, - N

denotes in which R ₁ and R ₂ , which can be identical or different, represent hydrogen, lower alkyl or hydroxyalkyl radicals which, together with the nitrogen atom, can also form a heterocycle and, if it is a tertiary nitrogen atom, this can also be quaternized can, η is an integer from 2 to 6 inclusive, where the amino group in the ortho position to the nitro group must not be tertiary and R 'and R "cannot be hydrogen at the same time, in the event that the nitro group is in the meta position to the amino group substituted by the radical R '"contains.

The hair dyeing process according to the invention is characterized in that the hair with a hair dye according to the invention impregnated at room temperature, rinses after 5 to 30 minutes, then washes and dries.

The dyes corresponding to the formula given above are prepared in such a way that accordingly substituted nitroparaphenylenedimines containing a secondary amino group with haloalkylamines or alkylene dihalides condensed, in the latter case then with primary or secondary amines implemented and optionally

6ü are then quaternized in the usual way.

The dyes of the above formula can also be prepared in such a way that N-arylsulfonylated ones N'- optionally substituted nitro-para-phenylenediamines condensed with haloalkylamines and subsequently hydrolyzed. In the latter case, the condensation is expediently carried out in the presence a preferably aprotic solvent, in particular dimethylformamide.

For example, you can use the coloring agents of the new hair dye of the general formula

R '

R "

IO

R '"

Compounds of the general formula

X- (CHJ _n -N

in which X, R ₁ , R ₂ and η have the same meaning as before, with the exception of R ₁ and R ₂ hydrogen, condense in the presence of a preferably aprotic solvent, in particular dimethylformamide, and then optionally hydrolyze. You can also use compounds of the general formula

in which R, R 'and R "hydrogen, lower alkyl or hydroxyalkyl radicals and R '"is a radical of the formula

- (CH ₂ J _n -N

denotes in which R ₁ and R _{2 can be the} same or different and represent hydrogen, lower alkyl or hydroxyalkyl radicals which, together with the nitrogen atom, can also form a heterocycle and if it is a tertiary nitrogen atom, this can also be quaternized, η is an integer from 2 to 6 inclusive, the amino group in the ortho position to the nitro group must not be tertiary and R 'and R "cannot be hydrogen at the same time if the nitro group is in the meta position to the group represented by the radical R'"Substituted amino group is prepared by adding compounds of the general formula

40

with amines of the formula

HN

where R, R ', R ", R ₁ , R ₂ , X and η have the same meaning and also have the same exceptions as before, condense.

It is also possible that for the preparation of compounds of the general formula

45

NO,

in which R and R 'have the above meaning with compounds of the general formula

55 R ₂

Compounds of the general formula
NH

X- (CH ₂ ) .-

HX

60

R ₂

NO,

NH- (CHA-N

in which X represents halogen and R ₁ , R ₂ , η have the above meaning, condensed.

One can also use N-arylsulfonated, N'- optionally substituted nitro - para - phenylenediamines in the form of their alkali or alkaline earth compounds with

65 in which formulas R ₁ , R ₂ and η have the same meaning as before and R 'and R "represent hydroxyalkyl radicals, are reacted with halohydrins.

To produce the quaternized compounds the general formula

(CHA-N

in which R, R ', R ", R ₁ , R ₂ and η have the meanings given above, R _{3 represents} an alkyl or aryl radical and Y represents a halogen or a monoalkyl or mono-aryl sulfate, compounds of the general formula

NO,

(CH ₂ J _n -N

in which the symbols have the same meaning as before, with a quaternizing agent such as Dialkyl sulfate or alkyl or aryl halide are implemented.

The new colorants have the advantage that they have a great affinity for keratin fibers in the cold and therefore result in high quality colorations. The new dyes produce very strong nuances. These two properties, namely the color strength and the affinity to the keratin fibers, make it possible that these dyes can be used in dye solutions even in very small amounts. This Peculiarity is significant as it allows the use of dyes that are only proportionate have low solubility, allows.

It should also be noted that the new colorants have particularly good lightfastness and washfastness exhibit. In addition, they can be used within a wider pH range than the previously known dyes of an analogous type. The dyes are preferably at pH values of 4 to 10 from 6 to 10, usable.

The new colorants do not require any addition of oxidizing agents such as one when they are used Peroxides, or like hydrogen peroxide, to develop the color on the hair.

You can use the additives customary in the industry, such as organic solvents, thickeners, cleaning agents, contain surface-active substances, lacquers and fragrances and the like. ..... '

The duration of action of the dye solutions on the hair to be colored can be varied within wide limits vary, but is preferably 5 to 30 minutes.

When using the staining solutions, the temperature can also be changed. In most cases but it is expedient to work at ordinary temperature.

The concentration of the dye in the solutions according to the invention can be within wide limits vary. It is preferably 0.1 to 3.5%.

The dye solutions cannot merely correspond to one of the formula given at the outset Dyes, but also several of these or other dyes commonly used for dyeing hair, such as nitro, azo or anthraquinone dyes.

example 1
The following solution is made:

N-methyl-N- [ß- (4-methylamino-3-nitrophenyl-1 methylamino) ethyl piperidinium iodide 0.4 g

Lauryl alcohol oxyäthylenated with 10.5 moles of ethylene oxide .... 5 g

Sodium carbonate until a pH value of 9 is reached

Make up to 100 cm ^{3 with water}

If this solution is left on dark blonde hair for 15 minutes, it will yield Rinse and wash a bold brown.

Example 2
The following solution is made:

Dichlorohydrate of 1-methylamino-2-nitro-4- [N-methyl-N - {/? - [N'-methyl-N'-OS-hydroxyethyl) amino] ethyl} amino] benzene 0.17 g

1 - [(γ-Diethylamino) propylamino] -2-amino-4-nitro-benzene 0.5 g

Lauryl alcohol oxyäthylenated with 10.5 moles of ethylene oxide .... 5 g

Sodium carbonate until a pH value of 9 is reached

Make up to 100 cm ^{3 with water}

If this solution is left to act on 100% white hair for 15 minutes, it results in after a reddish golden blonde after rinsing and washing.

Example 3
The following solution is made:

1 -Methylamino-2-nitro-

4- [N-methyl-N - {/ 3-piperidino-

ethyl) amino] benzene 0.01 g

With 10 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol 5 g

Ethanolamine until achieved

a pH of 9

Make up to 100 cm ^{3 with water}

This solution is left on hair for 5 to 10 minutes by bleaching on platinum blonde are discolored, the result is a rosewood shade after rinsing the hair and washing.

Example 4

The following solution is made:

Dichlorohydrate of 1-methylamino-2-nitro-4- [N-methyl- N- (ß-diethylaminoethyl) -

amino] benzene 0.03 g

l - [(y-diethylaminopropyl) -

amino] -2-amino-4-nitro-benzene 0.01 g with 10.5 mol of ethylene oxide oxy-

ethylated lauryl alcohol 5 g

Ethanolamine until achieved

a pH of 9

Make up to 100 cm ^{3 with water}

This solution is left on hair that is left on by bleaching for 10 to 15 minutes Platinum blonde has been decolorized, the result is a light mahogany copper color after rinsing and washing the hair Nuance.

Example 5 example

The following solution is made:

1- [N - (/ J-piperidino) ethylamino] -2-nitro-4-methylamino-benzene .. 0.084 g

l - [(γ-Diethylamino) propylamino] -2-amino-4-nitro-benzene 0.035 g

With 10.5 mol of ethylene oxide oxyäthylenierter Lauryl alcohol 5 g

Fill up with water to ........ 100 cm ^J

If this solution is left to act on 100% white hair for 15 minutes, then after Rinse and wash to obtain a reddish-blonde color.

Example 6

The following solution is made:

Dichlorohydrate of 1-methylamino-2-nitro-4- [N- (ß-hydroxy- ethyl) -N - (/? - diethylaminoethyl) -

amino] benzene 0.152 g

4-nitro-1,3-phenylenediamine 0.030 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 g of 2N sodium carbonate solution up to

Achievement of a pH value of 9 Make up to 100 cm ^{3 with water}

If this solution is left to act on 100% white hair for 15 minutes, it results in after a beige shade after rinsing and washing.

Example 7
The following solution is made:

1- [N - (/ 3-piperidino) ethyl-amino] -.

2-nitro-4-aminobenzene 0.235 g

• With 10.5 moles of ethylene oxide

Ethylenated lauryl alcohol 5 g

Make up to 100 cm ^{3 with water}

This solution will be on light maroon for 10 minutes Leaving the hair to work in, the result is a strong mahogany purple after rinsing and washing.

The following solution is made:

Dichlorohydrate of 1-methylamino-2-nitro-4 - [(/ 9-N, N-di- ethylamino-ethyl) -amino] -

benzene 0.5 g

-Methylamino-2-nitro-4- [N - (/ 3-piperidino) -ethyl-

amino] benzene 0.2 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 g ethanolamine until reached a pH of

Make up to 100 cm ^{3 with water}

If this solution is left on light auburn hair for up to 15 minutes, it will obtained a light maroon coloration with metallic pink reflections after rinsing and washing.

Example 9 The following solution is prepared:

N-methyl-N - [/ J- (4-methylamino-3-nitrophenyl-1 methylamino] ethyl] piperidinium iodide 0.4 g

Dichlorohydrate of 1-methylamino-2-nitro-4-0 (N, N-diethylamino) -ethyl-amino] -

benzene 0.2 g

Dichlorohydrate of 1-methylamino-2-nitro-4- <N-methyl-N- {| 3- [N'-methyl-N '- (/ S'-hydroxy-ethyl) -amino] -ethyl} ^:

amino> -benzene 0.15 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 g of 2N sodium carbonate solution up to

Achievement of a pH value of 8.5 Make up to 100 cm ^{3 with water}

If this solution is left on dark auburn hair for 20 minutes, it gives turns a deep mahogany violet color after rinsing and washing.

Example 10

The following solution is made:

l- [N - (/ 5-piperidinethyl) amino] -

2-nitro-4-aminobenzene 0.5 g

Dichlorohydrate of 1-methylamino-2-nitro-4- [N - (/ i-diethyl- aminoethyl) -N '- (hydroxyethyl-

amino)] benzene 0.1 g

l- [N - (/ 3-piperidinoethyl) amino] -

2-nitro-4-methylamino-benzene .. 0.1 g with 10.5 mol of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 g of 2N sodium carbonate solution up to

Achievement of a pH value of 7.5 Fill up with water to .100 cm ³

If this solution is left to act on dark auburn hair for 20 to 25 minutes, then obtained a deep maroon brown with purple highlights after spraying and washing.

509 544/364

45

55

Example 11 The following solution is prepared:

Dichlorohydrate of 1-methylamino-2-nitro-4- [N-methyl-N- (β-aminoethyl) amino] benzene 0.03 g

4-nitro-1,3-phenylenediamine 0.05 g

Lauryl alcohol oxyäthylenated with 10.5 moles of ethylene oxide .... 7 g

Sodium carbonate until a pH value of 7 is reached

Make up to 100 cm ^{3 with water}

If this solution is left to act on 100% white hair for 15 minutes, it results in after a shade of beige after rinsing and washing.

Example 12 The following solution is prepared:

l- <N - {/? - [N'-methyl-N '- (/ r-hydroxyethyl) -amino] -ethyl} -amino > -2-nitro-4-methylaminobenzene 0.14 g

1 - [γ- (Diethylaminopropyl) - ■ amino] -2-amino-4-nitro-benzene 0.05 g

Lauryl alcohol oxyäthylenated with 10.5 moles of ethylene oxide .... 5 g

Sodium carbonate until a pH value of 9 is reached

Make up to 100 cm ^{3 with water}

If this solution is left to act on 100% white hair for 15 minutes, it results in after reddish-blonde coloration after rinsing and washing.

Example 13 The following solution is prepared:

N-methyl-N - [/ i- (4-methylamino-2-nitro-phenyl-amino) ethyl] -

piperidinium iodide 0.21 g

l - [(y-diethylaminopropyl) -amino) -

2-amino-4-nitro-benzene 0.05 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol 5 g

Ethanolamine until achieved

a pH of 7

Make up to 100 cm ^{3 with water}

If this solution is left to act on 100% white hair for 15 minutes, it results in after a light mahogany copper-colored shade after rinsing and washing.

Example 14 The following solution is made:

N-methyl-N - [/? - (4-amino-2-nitrophenyl-amino) ethyl] piperidinium iodide 0.28 g

Lauryl alcohol oxyäthylenated with 10.5 moles of ethylene oxide .... 2 g

Sodium carbonate until a pH value of 9 is reached

Make up to 100 cm ^{3 with water}

This solution will be on light maroon for 10 minutes Leaving the hair to act, the result is a strong one after rinsing and washing Brown.

Example 15

The following solution is made:

1-methylamino-2-nitro-4- [N-methyl-N - (// - aminoethyl) -aminoj-benzene 0.09 2

l- <N - (/ ^ - [N'-methyl-N '- (/;' - hydroxyethyl) -amino] -ethyl) -amino > -2-nitro-4-methylaminobenzene 0.08 g

N-methyl-N - [/ M4-methylamino-2-nitro-phenyl-amino) -ethyl] -piperidinium iodide 0.13 g

With 10.5 mol of ethylene oxide oxyethylene lauryl alcohol 2 g

Ethanolamine until achieved

a pH of 9

Make up to 100 cm ^{3 with water}

If this solution is left on light auburn hair for 10 minutes, it results a dark mahogany violet after rinsing and washing.

Example 16 The following solution is prepared:

l- [N - (/ i-aminoethyl) -amino] -2-nitro-4- [bis- (ß'-hydroxyethyl) -amino] -benzene dichlorohydrate ... 0.36 g Lauryl alcohol oxyäthylenated with 10.5 mol of ethylene oxide .... 5 g

Sodium carbonate until a pH value of 7 is reached

Make up to 100 cm ^{3 with water}

If this solution is 100% for 15 minutes If white hair is left to act, the result is a blue-violet after rinsing and washing.

B ei s ρ i e1 17 The following hair dye is produced:

l-methylamino-2-nitro-

4- [N - (/ i-aminoethyl) -amino] -

benzene monobromohydrate 0.73 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 g of 2N sodium carbonate solution up to

Achievement of a pH value of 8 Make up to 100 g with water

If this agent is left to act on natural auburn hair for 10 minutes, it results turns deep purple after rinsing and washing.

Example 18

The following hair dye is made:

l- [N - (/ i-hydroxyethyl) amino '] - 2-nitro-4- [N - (/ i'-diethylamino- ethyl) amino] benzene dichloro

hydrate 0.296 g

l- [N - (/ i-aminoethyl) -amino] -

2-nitro-4-methyl-5-amino-benzene 0.042 g with 10.5 mol of ethylene oxide oxy-

Ethylenated lauryl alcohol 2 g

2N sodium carbonate solution up to

Achievement of a pH value of 9 Make up with water to ........ 100 g

IO

15th

If this agent is left to act on 100% natural white hair for 10 minutes, the result is reddish-blonde color after rinsing and washing.

Example 19 ⁵

The following hair dye is made:

1- [N - (/) '- Hydroxyethyl) amino] -

2-nitro-4- [N-methyl-N - (/; - di-

ethylaminoethyl) -amino] -

benzene dichlorohydrate 0.304 g

l- [N - (/ y-aminoethyl) -amino] -

2-nitro-4-methyl-5-amino-benzene 0.042 g with 10.5 mol of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 2 g of 2N sodium carbonate solution up to

Achievement of a pH value of 7 Make up to 100 g with water

If this agent is left to act on severely bleached hair for 10 minutes, it results in after a dark mahogany copper shade after rinsing and washing.

Example 20
The following hair dye is made:

l-methylamino-2-nitro-4- (fV-aminobutyl-amino) -benzene-dichloro-

hydrate 0.233 g

1- [N - (/) '- aminoethyl) amino] ^-3 °

2-nitro-4-methyl-5-amino-benzene 0.052 g with 10.5 mol of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 2 g of 2N sodium carbonate solution up to

Achievement of a pH value of 9 Make up to 100 si with water

35

If this agent is left to act on 100% natural white hair for 10 minutes, the result is after rinsing and washing a dark blonde 40 with mother-of-pearl reflections.

Example 21
The following hair dye is made:

1- [N- (p'-aminoethyl) -amino] - ⁴⁵

2-nitro-4-amino-benzene-dichloro

hydrate 1.2 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 2 g of 2N sodium carbonate solution up to ⁵ °

Achievement of a pH value of 8 Make up to 100 g with water

If this agent is left on 100% natural white hair for 10 minutes, it results in 55 after rinsing and washing a slightly purple-red color.

Example 22

The following hair dye is made:

l-methylamino-2-nitro-4- (i '> - aminohexylamino) -benzene-dichloro-

hydrate 1.5 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 g of 2N sodium carbonate solution up to

Achievement of a pH value of 8 Make up to 100 g with water

60 If this mixture is left to act on 100% naturally white hair for 10 minutes, the result is a very strong purple after rinsing and washing.

Example 23
The following hair dye is made:

-Methylamino-2-nitro-

4- <N- (y- [N'-methyI-N '- (/ i-hydroxyethyl) -amino] -propyl) -

amino> -benzene-dichlorohydrate ... 0.50 g with 10.5 mol of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 2N sodium carbonate solution up to

Achievement of a pH value of 9 Make up to 100 g with water

If this agent is left on light auburn hair for 20 minutes, it results turns dark purple after rinsing and washing.

Example 24
The following hair dye is made:

- [N- (ß-diethylaminoethyl) -

amino] -2-nitro-4- [bis - (/ i'-hydroxyethyl) -amino] -benzene-

dichlorohydrate 0.41 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 5 g of 2N sodium carbonate solution up to

Achieving a pH value of 7 Mii water make up to 100 g

If this agent is left to act on dark golden blonde hair for 10 minutes, it results after rinsing and washing, a maroon brown with mother-of-pearl reflections.

Example 25
The following hair dye is made:

Dichlorohydrate of l- [N - (/; - diethylaminoethyl) -amino] -

2-nitro-4- [bis - (/ miydroxyethyl) -

amino] benzene 0.369 g

- [N - (/> '- Aminoethyl) amino] -

2-nitro-4-methyl-5-amino-benzene 0.021 g with 10.5 mol of ethylene oxide oxy-

Ethylenated lauryl alcohol .... 4.5 g of 2N sodium carbonate solution up to

Achievement of a pH value of 9 Make up to 100 g with water

If this solution is left to act on 90% white hair for 10 minutes, it results in after a light golden blonde after rinsing and washing.

B e i s ρ i e1 26

The following hair dye is made: l- [y- (diethylamino) propyl-

amino] -2-nitro-4- [bis - (/ 7-hy-

hydroxyethyl) amino] benzene

dichlorohydrate 0.43 g

With 10.5 moles of ethylene oxide oxy-

Ethylenated lauryl alcohol 1.5 g

2N sodium carbonate solution up to

Achievement of a pH value of 9 Make up to .... 100 g with water

If this solution is left to act on 90% white hair for 15 minutes, then after Rinse and wash to obtain a gray, strong soft oak tint.

Example 27 The following hair dye is prepared:

4-Nitro-3 - [(/ i-aminoethyl) -amino] -l- (N, N-dimethyl-amino) -benzene 0.02 g - [N - () '- diethylamino) propylamino] -2-nitro-4- [bis - (/ i-hy- hydroxyethyl) amino] benzene

dichlorohydrate 0.38 g

Lauryl alcohol oxyäthylenated with 10.5 moles of ethylene oxide .... Ig

2N sodium carbonate solution until a pH value of 8.5 is reached

Make up to 100 g with water

If this agent is left to act on hair that is 90% white for 10 minutes, then after Rinse and wash to obtain an ash blonde shade.

Of course, the examples can be changed if necessary, without the framework to leave the invention.

Claims (1)

Patent claims: 1. Hair dyes based on nitro-paraphenylenediamines and customary additives, thereby marked that it is in a aqueous solution, which has a pH of 4 to 10, 0.1 to 3.5% of at least one dye of the general formula Hair dyes based on nitroparaphenylenediamines are already known (see NL-PS 98 216), however, the hair colorants according to the invention are insensitive to light and pH superior to known hair dyes. The hair dye according to the invention is characterized in that it is in an aqueous solution that has a pH of 4 to 10. 0.1 to 3.5% of at least one dye of the general formula