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GB1568767A – Biscationic disazo dyestuffs based on bis (amino benzoylamino) alkanes and pyridones
– Google Patents

GB1568767A – Biscationic disazo dyestuffs based on bis (amino benzoylamino) alkanes and pyridones
– Google Patents
Biscationic disazo dyestuffs based on bis (amino benzoylamino) alkanes and pyridones

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Publication number
GB1568767A

GB1568767A
GB3193477A
GB3193477A
GB1568767A
GB 1568767 A
GB1568767 A
GB 1568767A
GB 3193477 A
GB3193477 A
GB 3193477A
GB 3193477 A
GB3193477 A
GB 3193477A
GB 1568767 A
GB1568767 A
GB 1568767A
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Prior art keywords
compound
parts
hydrogen
formula
methyl
Prior art date
1976-08-04
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Sandoz AG

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Sandoz AG
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1976-08-04
Filing date
1977-07-29
Publication date
1980-06-04

1977-07-29
Application filed by Sandoz AG
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Sandoz AG

1980-06-04
Publication of GB1568767A
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patent/GB1568767A/en

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Classifications

C—CHEMISTRY; METALLURGY

C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR

C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES

C09B44/00—Azo dyes containing onium groups

C09B44/02—Azo dyes containing onium groups containing ammonium groups not directly attached to an azo group

C09B44/08—Azo dyes containing onium groups containing ammonium groups not directly attached to an azo group from coupling components containing heterocyclic rings

C—CHEMISTRY; METALLURGY

C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR

C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES

C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films

C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions

C09B67/0075—Preparations with cationic dyes

D—TEXTILES; PAPER

D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR

D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM

D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed

D06P1/02—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes

D06P1/04—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes not containing metal

D06P1/08—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using azo dyes not containing metal cationic azo dyes

D—TEXTILES; PAPER

D21—PAPER-MAKING; PRODUCTION OF CELLULOSE

D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR

D21H21/00—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties

D21H21/14—Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper

D21H21/28—Colorants ; Pigments or opacifying agents

Abstract

Disazo compounds of the formula in which the symbols can have the meanings given in Claim 1 are prepared by coupling the tetrazo compounds from the corresponding diamines with pyridinio pyridone compounds. The dyestuffs are suitable for dyeing paper, polyacrylonitrile or alternatively polyamide and polyester fibres modified by acidic groups.

Description

(54) BISCATIONIC DISAZO DYESTUFFS BASED ON
BIS(AMINO BENZOYLAMINO) ALKANES AND PYRIDONES
(71) We, SANDOZ LTD., of 35 Lichtstrasse, 4002 Basle, Switzerland, a
Swiss Body Corporate, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement:- The invention relates to biscationic disazo compounds.
The invention provides compounds of formula I,
wherein R is a straight chain C,~,alkylene radical, preferably 1,2-ethylene, each R1, independently, is hydrogen; C14alkyl, unsubstituted or substituted by a
hydroxy group; or a radical -NR4R5, where R4 and R2, independently, are unsub
stituted straight chain C,~4alkyl, each R2 independently, is hydrogen; straight chain C14alkyl, unsubstituted or substi
tuted by a hydroxy group; or C14alkoxy, each R,, independently, is hydrogen or unsubstituted C14alkyl, and Al9 is an anion.
The compounds of formula I fall within the scope of Claim 1 of our accepted patent application no. 27014/76. (Serial No. 1547 900)
Any unsubstituted alkyl as R, is preferably methyl or ethyl, more preferably methyl, any hydroxy substituted alkyl is preferably 2-hydroxyethyl, 2-hydroxypropyl or CH,CHCH2OH and any NR4Rs group is preferably N(CH2)2.
Any unsubstituted alkyl as R2 is preferably methyl, any hydroxyalkyl is preferably 2-hydroxyethyl and any alkoxy is preferably methoxy.
Any unsubstituted alkyl as R3 is preferably methyl or ethyl.
In the compounds of formula I, Rl is preferably R1,, i.e. hydrogen, methyl, ethyl, 2-hydroxyethyl, 2-hydroxypropyl, –N(CHs), or CH2CHCH2OH, more preferably R1,1, i.e. hydrogen or methyl.
R2 is preferably R2,, i.e. hydrogen, methyl, methoxy or 2-hydroxyethyl, more preferably R2″, i.e. hydrogen or methyl.
R, is preferably R,’, i.e. hydrogen, methyl or ethyl, more preferably R3″, i.e.
hydrogen.
Thus, as a preferred class of compounds, may be given those wherein R1 is R1,, R2 is R.2, and R, is R,’ and as a more preferred class may be given those wherein R, is R,”, R2 is R2″ and R, is R3″, R in such compounds being 1,2-ethylene.
The symmertical compounds are preferred.
The anion A3 in the compounds of the invention is conveniently one conventional in basic dyestuff chemistry and is preferably non-chromophoric. It may he an organic or inorganic anion and as examples may be given the halide, e.g. chloride or bromide, sulphate, bisulphate, methyl sulphate, aminosulphonate, perchiorate, propionate, lactate, succinate, benzenesulphonate, oxalate, maleate, acetate, tartrate, malate, methanesulphonate, tetrafluoroborate and benzoate anions, complex anions such as of zinc chloride double salts and the anions of the acids boric, citric, glycolic, diglycolic and adipic.
The invention also provides a process for the production of compounds of formula
I, which process comprises coupling a tetrazo derivative of a diamine of formula II,
with a coupling component of formula III,
preferably in a mol ratio of 1:2.
The diazotisation and coupling may be carried out in conventional manner, coupling suitably taking place in aqueous (acidic, neutral or alkaline) or aqueous/ organic medium at a temperature of from – 100C to room temperature, optionally in the presence of a coupling accelerator such as pyridine or urea.
The resulting compounds of formula I may be isolated and purified in conventional manner.
By the use of a mixture of two coupling components of formula III, asymmetrical compounds of formula I may be prepared in the form of a mixture with the corresponding two symmetrical compounds. They may be used in the form of the mixtures, or separated for example by chromatographic techniques.
The anion As desired in the compound of formula I may be present already in the pyridone coupling component of formula III or, if desired, having obtained a compound of formula I having a particular anion AS this anion may be exchanged for the desired anion in conventional manner, e.g. using an ion exchanger or by reaction with suitable salts, optionally in several stages, e.g. through the hydroxide or bicarbonate.
The compounds of formulae II and III are either known or may be produced in conventional manner from available starting materials.
The compounds of formula I are useful as dyes for the dyeing of basically dyeable substrates, including paper.
If desired, the compounds may be converted into dyeing preparations. The processing into stable, liquid dyeing preparations may take place in a generally known manner, advantageously by dissolving them in suitable solvents, optionally adding an aid, e.g. a stabilizer; for example in accordance with the description given in French
Patent Specification No. 1,572,030.
Suitable liquid preparations are obtained, for example, by dissolving one part by weight of 100% dyestuff in the form of the dyestuff base in 1 to 6 parts by weight o!E an organic carboxylic acid and in 1.5 to 4 parts by weight of water.
The organic carboxylic acids may be mono-, di- or tri-basic, but advantageouslJ monobasic, low-molecular weight carboxylic acids, such as formic acid, acetic acid or propionic acid.
Example a of a liquid preparation: (all parts are by weight) 160 parts of the dyestuff from Example 1, below, as the dyestuff base are dissolved at 4e60″C in 320 parts of acetic acid and 160 parts of water.
The processing into solid, granulated dye preparations may also take place in a generally known manner, advantageously by granulating in accordance with French
Patent Specification 1,581,900.
A granulate preparation contains, for example, 1 part of 100% dyestuff, 0.1 to 0.7 parts of an organic carboxylic acid and 0 to 1.5 parts of a solid, non-ionic diluting or standardising agent, preferably 1 part of dyestuff, 0.25 to 0.65 parts of an organic carboxylic acid and 0 to 1.5 parts of diluting or standardising agent.
The organic carboxylic acids for the production of the granulate may be mono-, di- or tribasic, but advantageously mono- or dibasic, low-molecular weight, saturated or unsaturated carboxylic acids, optionally containing hydroxyl groups, such as formic add, acetic acid, propionic acid, oxalic acid, succinic acid, malonic acid, fumaric acid, latic acid, malic acid or citric acid.
The solid, non-ionic diluting or standardising agent may be, for example, dextrin or sugar, such as glucose, fructose or galactose.
The granulates are advantageously prepared by comminution from solutions or suspensions, e.g. of the following composition:
1 part of dyestuff 100%,
0.1 to 0.7 parts of the organic carboxylic acid, o to 1.5 parts of the non-ionic diluting or standardising agent, and
1.5 to 6 parts of water, or preferably
1 part of dyestuff 100%,
0.5 to 0.65 parts of the organic carboxylic acid,
0.0 to 1.5 parts of the diluting or standardising agent, and
2 to 4 parts of water.
Example b of a granulate (all parts are by weight).
160 parts of the dyestuff from Example 1, below, as a dyestuff base and 80 parts of dextrin are dissolved at 40–600C in 47 parts of lactic acid and 320 parts of water, and the mixture is granulated by known methods.
The new dyestuffs are especially suitable for dyeing paper, e.g. for the production of dyed, sized and unsized paper in the stock. However, they may be used similarly for dyeing sheet paper by the steeping method. Conventional techniques may be used.
The compounds of formula I have good solubility properties, and they are particularly soluble in cold water. Furthermore, in the production of dyed paper, they colour the waste water slightly, if at all. They show low mottling on paper and to a great extent are insensitive to pH. The dyeings on paper are brilliant and have good light fastness properties. After lengthy exposure to light, the shade changes tone-in-tone. The dyed papers show good wet fastness properties, not only to water but also to milk, fruit juices and sweetened mineral water, and because of their good fastness to alcohol, they are also resistant to alcoholic drinks. The dyestuffs have a high degree of sub stantiyity, i.e. they are absorbed practically quantitatively; they may be added to the paper pulp directly, i.e. without previous dissolving, as a dry powder or as a granulate, without reducing the brilliance or the yield of colour. The dyed papers are bleachable both by oxidation and by reduction.
The compounds of formula I are also suitable for dyeing, pad-dyeing and printing textile material consisting of acrylonitrile or dicyanoethylene polymers or mixed polymers, or synthetic polyesters which are modified by acid groups, but especially synthetic polyamides which are modified by acid groups, these including in particular the socalled “Differential dyeing polyamide”, or mixtures of textile material which consists of a predominant portion of the above-mentioned textile materials or contain these.
The acrylonitrile mixed polymers which are dyed or printed are advantageously co-polymers consisting of 80–95% acrylonitrile and 20–5% vinyl acetate, vinyl pyridine, vinyl chloride, vinylidene chloride, acrylic acid, acrylic acid ester, methacrylic acid, methacrylic acid ester or asymmetrical dicyanoethylene.
The polyester material which is dyed or printed is advantageously of the type described in U.S. Patent Specification 3,379,723, e.g. synthetic polyester as obtained by polycondensation of aliphatic or aromatic dicarboxylic acids or their polyesterforming derivatives a) with aliphatic or alicyclic diols b) and optionally aromatic dihydroxy compounds c) and/or their glycol ethers, with compounds bearing anionic groups.
Polyester material which is modified by anionic groups may also be equally well dyed or printed, e.g. as described in U.S. Patent Specification 3,018,272, in British
Patent Specification 1,406,387, and in Japanese Published Specification No. 10,497/59.
The polyamide material which is modified by anionic groups is advantageously of the type described in Belgian Patent Specifications 549,179 and 706,104, U.S. Patent
Specifications 2,893,816 and 3,890,257 and “Textilveredlung 2″ (1967), 11, pages 856-864, so-called Nylon-Dye-Resist types, in ” Textilpraxis ” 1967, volume 2 (February) pages 737-740 in ” Du Pont Preliminary Information” of 14.7.1966 relating to “Type 844 Du Pont BCF Nylon”, and 19.9.1966 (Cationic Dyeable Nylon
Stable).
Textile material consisting of polyacrylonitrile or polyester or polyamide which is modified by anionic groups may be dyed as described in German Published Specification 2,509,095, e.g. by the exhaust method in an aqueous medium, at temperatures of 60-1000C or at temperatures of above 100″ under pressure, whereby the pH value may vary within a wide range.
Dyeing or printing may also take place in the presence of usual dyeing aids, e.g.
in the presence of condensation products of naphthalene sulphonic acids and formaldehyde, or reaction products of castor oil and ethylene oxide, etc. Printing of the said textile materials takes place by impregnation with a printing paste which contains the dyestuff, water, an organic acid, e.g. acetic acid, formic acid, and a thickener, with subsequent fixation onto the fibres.
The printing paste Is applied by stencils or rollers, the print is optionally intermediately dried and the dyestuff is fixed, e.g. by steam-treatment at temperatures of about 100″C, and the print is completed.
Fixation of the dyestuff may also take place by the pad-steam process or thermosol process, or by the pad-roll process. Temperatures of above 200″C should, however, be avoided.
The dyestuffs are also suitable for dyeing the said textile materials in the mass, e.g. for gel dyeing by the so-called neocron process, for example in accordance with
U.K. Patent Specification No. 673,738.
Fast, even dyeings with good fastness properties, for example to light, are obtained on the above-mentioned substrates.
The following examples, in which the parts and percentages are by weight and the temperatures in degrees centigrade, illustrate the invention.
Example 1.
14.9 Parts of 1,2-bis-(4′-aminobenzoylamino)-ethylene are dissolved at 0 in 100 parts of water and 31 parts of 30% hydrochloric acid, and are then tetrazotised with 6.9 parts of sodium nitrite by known methods. Subsequently, a solution consisting of 25 parts of 3-pyridinium-4-methyl-6-hydroxy-pyridone-2-chloride and 100 parts of water is added to the ice-cold diazo solution, and at the same time 15 parts of crystalline sodium acetate are sprinkled in in portions. After coupling, the reaction mixture is made acid with hydrochloric acid, whereby the dyestuff is precipitated. The dyestuff is filtered off. When dried and ground, a water-soluble powder is obtained, which dyes paper in yellow shades. The dyestuff corresponds to formula:

Dyeing Preparation A.
70 Parts of chemically bleached sulphite cellulose (from conifer wood) and 30 parts of chemically bleached sulphite cellulose (from birchwood) are ground in 2000 parts of water in a Hollander. 0.2 Parts of the dyestuff described in Example 1 are sprinkled into this pulp. After mixing for 20 minutes, paper is produced from this pulp. The absorbent paper produced in this manner is dyed yellow. The waste water is practically colourless.
Dyeing Preparation B.
0.5 Parts of the dyestuff from Example 1 are dissolved in 100 parts of hot water and cooled to room temperature. This solution is added to 100 parts of chemically bleached sulphite cellulose which has been ground with 2000 parts of water in a Hol lander. After mixing thoroughly for 15 minutes, sizing takes place. Paper which is produced from this pulp has a yellow shade of average intensity, with good wet fastness.
Dyeing Preparation C.
An absorbent strip of unsized paper is drawn through a dyestuff solution of the following composition at 40 to 50 : 0.5 parts of the dyestuff from Example 1
0.5 parts of starch and
99.0 parts of water.
The excess dyestuff solution is squeezed out through two rollers. The dried paper strip is dyed yellow.
Equally good paper dyeings are obtained using the above dyeing formulae A, B and C, by adding equivalent amounts as in Example a (liquid preparation) or Example b (granulate preparation).
Example 2.
20 Parts of the dyestuff of Example 1 and 80 parts of dextrin are ground in a powder mill for 4 hours. The same dyestuff preparation may be formed by forming the components into a paste using 100 parts of water and finally spray drying.
One part of the obtained preparation is mixed with one part of 40% acetic acid, 200 parts of demineralised water are poured onto the paste and the whole heated. Dilution takes place with 7000 parts of demineralised water, 2 parts of glacial acetic acid are added and, at 60 , 100 parts of a polyacrylonitrile material are added to the bath.
The polyacrylonitrile material may be pretreated in a bath containing 8000 parts of water and 2 parts of acetic acid for 1015 min minutes at 60″.
The bath is raised in the course of 30 minutes to 98 100 , boiled for 1+ hours at this temperature and then the substrate rinsed. A yellow dyeing with good light and wet fastness is obtained.
Example 3.
20 Parts of the dyestuff of formula 1 are mixed with 80 parts of dextrin in a ball mill for 48 hours. One part of the obtained preparation and 1 part of 40% acetic acid are intimately mixed. 200 Parts of demineralised water are poured on and the whole heated. With this stock solution dyeing is carried out as follows.
a) The solution is diluted with 7000 parts of demineralised water, then 21 parts of calcined sodium sulphate, 14 parts formic acid and 15 parts of a carrier based on the reaction product of ethylene oxide with dichlorophenols are added and, at 60 , 100 parts of acid modified polyester material are entered into the bath. The polyester material may be pretreated in a bath containing 8000 parts of water and 2 parts of acetic acid for 1 1 5 minutes at 600.
The bath is raised in the course of 30 minutes to 98–100″, boiled at this temperature for one hour and then the substrate removed and rinsed. A level yellow dyeing with good light and wet fastness is obtained.
b) The solution is diluted with 3000 parts of demineralised water after which 18 parts of calcined sodium sulphate and 6 parts each of ammonium sulphate and formic acid are added and, at 600, 100 parts of acid modified polyester material are entered into the bath. The bath is raised to 1100 over the course of 45 minutes in a closed vessel.
This temperature is held for one hour with agitation of the bath. The bath is then cooled to 60 over the course of 25 minutes and the dyed material rinsed. A level fast yellow dyeing with good wet fastness is obtained.
Example 4.
20 Parts of the dyestuff of Example 1 and 80 parts of dextrin are mixed in a ball mill for 48 hours. One part of the obtained preparation and 1 part of 40% acetic acid are intimately mixed, whereafter 200 parts of demineralised water are poured on and the whole heated.
The solution is diluted with 7000 parts of demineralised water, 14 parts of formic acid and 15 parts of a carrier based on the reaction product of ethylene oxide and dichlorophenols are added. The liquor is adjusted to pH 6 with an acid buffer solution.
At 25″ 100 part of acid modified polyamide material are entered into the bath at a liquor ratio of 1:80. The bath is heated to 98″ over the course of 45 minutes and boiled for one hour at this temperature. The substrate is then removed and rinsed under running water at 7e800 and finally under cold water. The material may then be spin dried and finally ironed. A yellow dyeing with good fastness is obtained.
Example 5.
A printing paste is prepared as follows.
One part of the dyestuff of Example 1 and 30 parts of acetic acid are intimately mixed and 280 parts of boiling water poured on. To this solution are added 50 parts of benzyl alcohol and 500 parts of a thickener based on carboxymethyl cellulose, which swells to a ratio of 1:4 in water, and 10 parts of a swelling agent.
Using this printing paste, a polyacrylonitrile, polyester or polyamide material which has been acid modified, may be printed according to known methods.
The prints are dried and then placed in an autoclave where they are steamed for 30 minutes at 110 under 1.8 atmospheres (one can also steam continuously for 5 to 30 minutes).
After rinsing with cold water, unfixed dyestuff may be removed by washing for 5 minutes at 70″ with a 0.1% soap solution, (detergent). Finally the prints are rinsed with cold water and dried by known methods. A fast level print with good fastness is obtained.
According to the procedure of Example 4, advantageous dyeings are obtained on differential dyeing polyamide material of the types 844, 845 and 847, (Du Pont).
In the following table further dyes are given which can be produced according to the procedure of Example 1. These dyes can be used in the same way as that of
Example 1 and correspond to the formula
wherein R, R1, R3, Re and R, have the meanings given in the table.
The anion AO may be any one mentioned in the foregoing description.
Example No. R R1 R3 R5 R7 6 -CH2-CH2- H H CH3 H 7 do. H H H CH3 8 do. H CH3 H H 9 do. CH2-CH2-OH H H H 10 do. do. H CH3 H 11 do. do. H H CH3 12 do. do. CH3 H H 13 do. CH3 H H H 14 do. do. H CH3 H 15 do. do. H H CH3 16 do. do. CH3 H H 17 do. N(CH3)2 H H H 18 do. do. H CH3 H 19 do. do. CH3 H H 20 do. CH2-CHOH-CH3 H H H 21 do. CH1-CH-CH2OH H H H
Example 22.

The dyestuffs of Example 6-22 dye paper, polyacrylonitrile and acid modified polyamide materials in yellow shades.

Claims (25)

WHAT WE CLAIM IS:

1. A compound of formula I,
wherein R is a straight chain C2~.,alkylene radical, each R1, independently, is hydrogen; C14alkyl, unsubstituted or substituted by a
hydroxy group; or a radical -NR4K5, where R4 and R6, independently, are unsub
stituted straight chain C,4alkyl, each K2, independently, is hydrogen; straight chain C1~4alkyl, unsubstituted or substi
tuted by a hydroxy group; or Cl 4alkoxy, each R,, independently, is hydrogen or unsubstituted C1~4alkyl, and A# is an anion.

2. A compound of Claim 1, wherein R is 1,2-ethyIene.

3. A compound of Claim 1 or 2 wherein R1 is hydrogen, methyl, ethyl, 2-hydroxyethyl, 2-hydroxypropyl, -N(CH3)2 or CH3CHCH2OH.

4. A compound of Claim 3, wherein R1 is hydrogen or methyl.

5. A compound of any one of Claims 1 to 4, wherein R2 is hydrogen, methyl, methoxy, or 2-hydroxyethyl.

6. A compound of Claim 5, wherein K2 is hydrogen or methyl.

7. A compound of any one of Claims I to 6, wherein R3 is hydrogen, methyl or ethyl.

8. A compound of Claim 7, wherein K, is hydrogen.

9. A compound of Claim 2, wherein R1 is as defined in Claim 3, R2 is as defined in Claim 5 and K2 is as defined in Claim 7.

10. A compound of Claim 9, wherein R1 is as defined in Claim 4, R2 is as defined in Claim 6 and K, is as defined in Claim 8.

11. A compound of any preceding claim which is symmetrical.

12. A compound of formula
wherein A# is as defined in Claim 1.

13. The compound of Claim 12, wherein AS is C19.

14. The compound of any one of Examples 6 to 22, hereinbefore set forth.

15. A process for the production of a compound of formula I, stated in Claim 1, comprising coupling a tetrazo derivative of a diamine of formula II,
with a coupling component of formula III,

16. The process of Claim 15, substantially as hereinbefore described with reference to and as illustrated by any one of Examples 1 and 6 to 22.

17. A compound of formula I, stated in Claim 1, whenever obtained by the process of Claim 15 or 16.

18. A solid dye composition comprising, as dye component, a compound of any one of Claims 1 to 14 or 17.

19. A liquid dye composition comprising, as dye component, a compound of any one of Claims 1 to 14 or 17.

20. A process for dyeing a basic dyeable substrate comprising applying thereto a compound of any one of Claims 1 to 14 or 17.

21. The process of Claim 20, wherein the substrate is paper.

22. The process of Claim 20, wherein the substrate is a textile substrate.

23. The process of Claim 22, wherein said substrate is of a homo or mixed polymer of acrylonitrile or dicyanoethylene or an acid modified polyamide or polyester.

24. The process of any one of Claims 20 to 23, substantially as hereinbefore described.

25. A basic dyeable substrate whenever dyed by the process of any one of Claims 20 to 24.

GB3193477A
1976-08-04
1977-07-29
Biscationic disazo dyestuffs based on bis (amino benzoylamino) alkanes and pyridones

Expired

GB1568767A
(en)

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CH994276A

CH623050A5
(en)

1976-08-04
1976-08-04
Process for the preparation of disazo compounds

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1976-08-04
1977-07-29
Biscationic disazo dyestuffs based on bis (amino benzoylamino) alkanes and pyridones

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Cited By (3)

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Publication number
Priority date
Publication date
Assignee
Title

EP0044059A1
(en)

1980-07-16
1982-01-20
Hoechst Aktiengesellschaft
Process for the dyeing in a gel state of fibrous articles of wet-spun acrylonitrile polymers

EP0044062A1
(en)

1980-07-16
1982-01-20
Hoechst Aktiengesellschaft
Process for the dyeing in a gel state of fibrous articles of dry spun acrylonitrile polymers

EP0044061A1
(en)

1980-07-16
1982-01-20
Hoechst Aktiengesellschaft
Process for the dyeing in a gel state of fibrous articles spun from acrylonitrile polymer solutions in organic solvents

Families Citing this family (2)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

DE3117127A1
(en)

1980-05-08
1982-02-04
Sandoz-Patent-GmbH, 7850 Lörrach

ORGANIC COMPOUNDS, THEIR PRODUCTION AND USE

CH690650A5
(en)

1995-07-21
2000-11-30
Clariant Finance Bvi Ltd
Basic azo compounds having two Pyridonringen, their preparation and use.

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* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

GB1285339A
(en)

1968-12-09
1972-08-16
Ici Ltd
New water-insoluble disazo dyestuffs containing 2-hydroxy-3-azo-6-pyridone residues

GB1424118A
(en)

1973-07-31
1976-02-11
Ici Ltd
Colouration process

1976

1976-08-04
CH
CH994276A
patent/CH623050A5/en
not_active
IP Right Cessation

1977

1977-07-27
IT
IT5045677A
patent/IT1116670B/en
active

1977-07-29
GB
GB3193477A
patent/GB1568767A/en
not_active
Expired

1977-08-02
FR
FR7723726A
patent/FR2360632A2/en
active
Granted

Cited By (4)

* Cited by examiner, † Cited by third party

Publication number
Priority date
Publication date
Assignee
Title

EP0044059A1
(en)

1980-07-16
1982-01-20
Hoechst Aktiengesellschaft
Process for the dyeing in a gel state of fibrous articles of wet-spun acrylonitrile polymers

EP0044062A1
(en)

1980-07-16
1982-01-20
Hoechst Aktiengesellschaft
Process for the dyeing in a gel state of fibrous articles of dry spun acrylonitrile polymers

EP0044061A1
(en)

1980-07-16
1982-01-20
Hoechst Aktiengesellschaft
Process for the dyeing in a gel state of fibrous articles spun from acrylonitrile polymer solutions in organic solvents

US4563191A
(en)

1980-07-16
1986-01-07
Hoechst Aktiengesellschaft
Process for dyeing, in the gel state, fiber material composed of wet spun acrylonitrile polymers using dyes with two basic groups

Also Published As

Publication number
Publication date

FR2360632B2
(en)

1981-11-06

IT1116670B
(en)

1986-02-10

CH623050A5
(en)

1981-05-15

FR2360632A2
(en)

1978-03-03

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