GB871624A - Azopyrimidine compounds and process of coloring fabricated polyacrylonitriles therewith - Google Patents

Azopyrimidine compounds and process of coloring fabricated polyacrylonitriles therewith

Info

Publication number
GB871624A
GB871624A GB33546/57A GB3354657A GB871624A GB 871624 A GB871624 A GB 871624A GB 33546/57 A GB33546/57 A GB 33546/57A GB 3354657 A GB3354657 A GB 3354657A GB 871624 A GB871624 A GB 871624A
Authority
GB
United Kingdom
Prior art keywords
amino
diamino
hydroxy
dyes
hydroxypyrimidines
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB33546/57A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB871624A publication Critical patent/GB871624A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/02Disazo dyes
    • C09B31/12Disazo dyes from other coupling components "C"
    • C09B31/14Heterocyclic components
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B27/00Preparations in which the azo group is formed in any way other than by diazotising and coupling, e.g. oxidation

Abstract

Polyacrylonitrile, containing at least 85% by weight of acrylonitrile, is coloured with a 2, 4, 6-trisubstituted-5-aryl- or heterocyclic-azo-pyrimidine in which the 2-substituent is an amino group, which may be alkylated, and at least one of the 4- or 6-substituents is an amino group, the other being when not an amino group, hydroxyl, the aryl or heterocyclic group being free from ionogenic acidic groups. Preferred polyacrylonitriles are those containing no basic comonomers e.g. methylvinylpyridine and vinylpyridine. Specified as comonomers which may be present are methyl acrylate and vinyl acetate and chloride. The dyes may be used as a paste or as a fine powder. Dyeing is effected, at the boil, from an acidic aqueous dye bath and, if necessary, in the presence of dispersing agents. Printing processes may also be adopted. The polyacrylonitrile may be in such forms as fibres, granules, powders or films. Indicated arylamines from which the dyes may be derived are: aniline, chloro-, cyano- and alkoxy-anilines and their benzamido- and p-sulphonyl-derivatives, a - and b -naphthylamines, biphenylamines, aminodiphenylamines and aminoazo compounds. Specified pyrimidines are: 2, 4-diamino-6-hydroxy-, 2, 4, 6-triamino-, 2-amino-4b -hydroxyethylamino-6-hydroxy-, 2-amino- 4-ethoxycarbonylmethylamino- 6-hydroxy-, 2, 4-diamino- 6-dimethyl- and -diethyl-amino-, 4, 6-diamino-2-diethyl- and diallyl-amino-, 2-amino-4, 6-di(monomethylamino)- and 4-amino-2-diallylamino-6-hydroxypyrimidine and its 2-dialkylamino derivatives. Red, blue, yellow and brown shades are obtained. Additional diazo components used in the examples, which illustrate the colouring of fibres, are p-toluidine and 3- and 4-aminopyridine.ALSO:The invention comprises the following dyes:-2, 4-diamino- 5-(2, 5-dimethoxy-, p-methyl-sulphonyl-, 4- p-anisidino-, 4-benzamido-2, 5-diethoxy-, 4-diphenyl-, 4-phenylamino-, 4-phenylazo-, 4-sulphonamido- and 4-cyan-2, 5-dimethoxy-phenylazo)-6-hydroxypyrimidines, 2, 4-diamino- 5-(1-naphthyl- and -anthraquinonyl- and 8-quinolyl-azo)- 6-hydroxypyrimidines, 2, 4-diamino- 5-(2, 4-diamino- 6-hydroxy-5-pyrimidylazo)- and -(4-styrylphenylazo)- 6-hydroxypyrimidines, 2-dimethylamino- 4-amino- 5-p-tolyl-, (4-p-anisylphenyl)- and p-chlorophenyl-azo- 6-hydroxypyrimidines and 2-diallylamino- 4-amino- 5-(p-tolylazo)- and 2-di-(2-butenyl)-amino- 4-amino- 5-(2, 5-dimethoxyphenylazo)-6-hydroxypyrimidines and the colouring of polyacrylonitrile, comprising at least 85% by weight acrylonitrile, with 2, 4, 6-trisubstituted- 5-aryl- or -heterocyclic-azopyrimidines in which the 2-substituent is an amino, or alkylated amino, group and at least one of the 4- or 6-substituents is an amino group, the other being, when not an amino group, hydroxyl, the aryl or heterocyclic group being free from ionogenic acidic groups. The dyes are made by conventional processes and preferably by coupling a diazotized arylamine with the pyrimidine component. Indicated arylamines are:-aniline, chloro-, cyano- and alkoxy-anilines and their benzamido- and p-sulphonyl derivatives, a - and b -naphthylamines, biphenyl-amines, aminodiphenylamines and aminnoazo compounds. Specified pyrimidines are:-2, 4-diamino- 6-hydroxy-, 2, 4, 6-triamino-, 2-amino- 4-b -hydroxyethylamino- 6-hydroxy-, 2-amino- 4-ethoxy-carbonylmethylamino- 6-hydroxy-, 2, 4-diamino- 6-dimethyl- and -diethylamino-, 4, 6-diamino- 2-diethyl- and -diallylamino-, 2-amino-4, 6-di-(monomethylamino)- and 4-amino- 2-diallylamino- 6-hydroxypyrimidine and its 2-dialkylamino derivatives. The polyacrylonitrile may be in such forms as fibres, granules, powders and films. Preferably basic comonomers, e.g. methylvinylpyridine and vinylpyridine, are absent. Specified comonomers are methyl acrylate and vinyl acetate and chloride. The dyes may be used as a paste or as a fine powder. Dyeing is effected at the boil from an acidic aqueous dye bath and, if necessary, in the presence of conventional dispersion agents. In examples, which illustrate the preparation of the dyes and their use in colouring polyacrylonitrile fibres, the components used are chosen from those indicated above, with the addition of p-toluidine and 3- and 4-aminopyridine as diazo components. Red, blue, yellow and brown shades are obtained.
GB33546/57A 1957-01-11 1957-10-28 Azopyrimidine compounds and process of coloring fabricated polyacrylonitriles therewith Expired GB871624A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US871624XA 1957-01-11 1957-01-11

Publications (1)

Publication Number Publication Date
GB871624A true GB871624A (en) 1961-06-28

Family

ID=22203471

Family Applications (1)

Application Number Title Priority Date Filing Date
GB33546/57A Expired GB871624A (en) 1957-01-11 1957-10-28 Azopyrimidine compounds and process of coloring fabricated polyacrylonitriles therewith

Country Status (1)

Country Link
GB (1) GB871624A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2206357A1 (en) * 1972-11-13 1974-06-07 Basf Ag
FR2228092A1 (en) * 1973-05-03 1974-11-29 Ciba Geigy Ag
EP0024261A1 (en) * 1979-08-17 1981-02-25 Ciba-Geigy Ag Azo pigments and process for their preparation, and their use

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2206357A1 (en) * 1972-11-13 1974-06-07 Basf Ag
FR2228092A1 (en) * 1973-05-03 1974-11-29 Ciba Geigy Ag
EP0024261A1 (en) * 1979-08-17 1981-02-25 Ciba-Geigy Ag Azo pigments and process for their preparation, and their use
US4340430A (en) 1979-08-17 1982-07-20 Ciba-Geigy Corporation Azo pigments, process for their production and their use

Similar Documents

Publication Publication Date Title
GB871624A (en) Azopyrimidine compounds and process of coloring fabricated polyacrylonitriles therewith
JPH04173874A (en) Disperse dye composition and method for dyeing hydrophobic fiber
GB1471999A (en) Azo compounds free from sulpho groups
GB1512151A (en) Fibre-reactive disazo dyestuffs their production and their use
CA1176774A (en) Process for colouring fibre forming polyamides in the melt with azo pigments
US2211339A (en) Azo compounds and material colored therewith
JPH04173872A (en) Disperse dye composition and method for dyeing hydrophobic fiber
GB899376A (en) New naphthalene monoazo triazine dyestuffs
GB911287A (en) New copper-containing triazine monoazo dyestuffs
US2768183A (en) Anthraquinone dyestuffs
GB1109628A (en) Improvements relating to difficultly soluble azo dyestuffs which can be dispersed in water, and their use
GB1068758A (en) Water-insoluble monoazo dyestuffs and process for their manufacture
US2649353A (en) Dyeing of nylon and acetate silk in
GB1412229A (en) Monoazo pigments processes for their manufacture and use
GB901692A (en) New monoazo dyestuffs containing sulphonoxy groups, their preparation and their application to dyeing
GB1469453A (en) Monoazo dyes containing a sulphato-ethyl group
GB1308705A (en) Azo dyes process for their manufacture and use
GB1406996A (en) Dyes containing an azidosulphonyl group and their preparation
GB896472A (en) New azo colouring matters containing 2-hydroxyquinoline residues
GB1351385A (en) Fibre-reactive azo dyestuffs containing halotriazine substituents
US3934974A (en) Solution of ethylauramine hydrochloride in thiodiglycol
US3364195A (en) Hydroxyindane azo benzanilide dyes
GB890175A (en) Dyestuffs of the anthraquinone series containing sulphone groups and their production
US1692492A (en) Process of dyeing cellulose derivatives
GB1261863A (en) Water-insoluble monoazo dyestuffs containing 4(3h) quinazolone residues