GB864227A - Disazo-dyestuffs derived from cyanuric chloride and process for their manufacture - Google Patents
Disazo-dyestuffs derived from cyanuric chloride and process for their manufactureInfo
- Publication number
- GB864227A GB864227A GB21093/57A GB2109357A GB864227A GB 864227 A GB864227 A GB 864227A GB 21093/57 A GB21093/57 A GB 21093/57A GB 2109357 A GB2109357 A GB 2109357A GB 864227 A GB864227 A GB 864227A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyes
- toluidine
- cyanuric chloride
- benzene
- amino
- 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
Links
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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/02—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring
- C09B62/04—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group directly attached to a heterocyclic ring to a triazine ring
- C09B62/08—Azo dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises disazo dyes of formula :- <FORM:0864227/IV(c)/1> wherein R1 is an aromatic residue, advantageously of the benzene or naphthalene series, containing a sulphonic acid group, R2 is a benzene or naphthalene residue and R3 is a p-phenylene residue free from water-solubilizing groups. The dyes may be prepared by condensation of 1 mol of cyanuric chloride with 1 mol of an aminodisazo dye of formula: R1-N=N-R2-N=N-R3-NH2. Components used in the preparation of the intermediate aminoazo dyes and methods of preparation are specified. The dyes give yellow, orange, red and brown shades on cotton. In examples the following aminodisazo dyes are condensed with cyanuric chloride:-4-amino - 1 : 11-azobenzene - 4 : 41-disulphonic acid --> m-toluidineor p-xylidine; 2-aminonaphthalene-4 : 8-disulphonic acid --> m-toluidine -->, 1-amino-2 --> methoxy-5-methyl-benzene; 2-aminonaphthalene-4 : 8-disulphonic acid --> o-toluidine, --> o-toluidine; 1-aminobenzene-3-sulphonic acid, --> 1-amino-naphthalene-6-sulphonic acid, --> aniline; the monoazo dye 4-acetylamino-1-aminobenzene-2-sulphonic --> 1-naphthol-3 : 6-disulphonic acid is hydrolysed, diazotized and coupled with m-toluidine. Specification 838,337 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH864227X | 1956-07-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB864227A true GB864227A (en) | 1961-03-29 |
Family
ID=4543467
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB21093/57A Expired GB864227A (en) | 1956-07-03 | 1957-07-03 | Disazo-dyestuffs derived from cyanuric chloride and process for their manufacture |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB864227A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3527746A (en) * | 1964-07-02 | 1970-09-08 | Acna | Monoazo heterocyclic containing triazine dyestuffs |
-
1957
- 1957-07-03 GB GB21093/57A patent/GB864227A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3527746A (en) * | 1964-07-02 | 1970-09-08 | Acna | Monoazo heterocyclic containing triazine dyestuffs |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1037981A (en) | New naphthalene monoazo triazine dyestuffs | |
GB864227A (en) | Disazo-dyestuffs derived from cyanuric chloride and process for their manufacture | |
GB987740A (en) | Water-insoluble disazo dyestuffs and process for their manufacture | |
GB973114A (en) | New azo-dyestuffs containing halotriazinylamino groups and process for their manufacture | |
GB883550A (en) | New triazine disazo dyestuffs and their manufacture and use | |
GB921319A (en) | Azo dyestuffs of the benzene and naphthalene series containing triazine rings | |
GB855792A (en) | New mono azo-dyestuffs containing dihalotriazine residues, their manufacture and use | |
GB707488A (en) | Manufacture of new disazo-dyestuffs | |
ES251608A1 (en) | New disazo-dyestuffs containing halogenotriazine residues and their manufacture and use | |
GB265553A (en) | Improvements in tetrakisazo dyes, and the process of manufacture | |
GB874545A (en) | New mono-azo-dyestuffs containing halo-triazinylamino residues and their manufactureand use | |
US2117425A (en) | Azo dyes | |
GB671762A (en) | Manufacture of new cupriferous azodyestuffs of the stilbene series | |
GB949502A (en) | New azophthalocyanine dyestuffs and their manufacture and use | |
GB713217A (en) | Disazo dyestuffs | |
GB704043A (en) | Manufacture of new trisazo-dyestuffs | |
GB614652A (en) | Manufacture and use of polyazo-dyestuffs | |
GB815737A (en) | New polyazo-dyestuffs derived from 3,3-dihydroxydiphenylamine and processes for their manufacture | |
GB926327A (en) | New dyestuffs of the azostilbene series containing halopyrimidyl residues | |
GB1002648A (en) | New dyestuffs containing ring-condensed halopyridazinyl residues | |
GB923887A (en) | New monoazo triazine dyestuffs | |
GB248230A (en) | Process for the manufacture of trisazo dyestuffs | |
GB685078A (en) | New trisazo dyestuffs | |
GB882750A (en) | New azo-dyestuffs containing haloacylamino groups and their manufacture and use | |
GB608897A (en) | Manufacture of trisazo-dyestuffs |