GB560451A - Manufacture of azo-dyestuffs - Google Patents
Manufacture of azo-dyestuffsInfo
- Publication number
- GB560451A GB560451A GB4468/42A GB446842A GB560451A GB 560451 A GB560451 A GB 560451A GB 4468/42 A GB4468/42 A GB 4468/42A GB 446842 A GB446842 A GB 446842A GB 560451 A GB560451 A GB 560451A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- free
- groups
- substituted
- group
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
- C09B35/38—Trisazo dyes ot the type
- C09B35/44—Trisazo dyes ot the type the component K being a hydroxy amine
- C09B35/46—Trisazo dyes ot the type the component K being a hydroxy amine the component K being an amino naphthol
- C09B35/463—D being derived from diaminodiphenyl
Abstract
Trisazo dyes, suitable for dyeing or printing animal fibres, e.g. wool, silk or leather, or cellulose fibres, e.g. cotton, linen, ramie, hemp or regenerated cellulose, the after-coppered dyeings being specially fast to light, to washing and to acid, are obtained by coupling (alkaline) a diazotised 4-chloro-2-aminophenol, free from sulphonic acid groups and carrying a nitro group in the 5- or 6-position, with an azo dyestuff of the general formula <FORM:0560451/IV/1> wherein R1 represents a residue of the benzene series, which may be substituted, e.g. by methyl, and carries the OH and COOH groups in o-position to each other and R2 represents a 4 : 41-diphenyl residue, which may be substituted, e.g. by halogen or by alkyl or alkoxy groups but is free from sulphonic acid groups. The products may be treated in substance, in the dyebath or on the fibre with an agent yielding metal, e.g. copper. In an example the preparation is described of the dyestuffs, salicylic acid\sMbenzidine-->(acid 2 : 5 : 7-acid (alkaline)\sM4-chloro -5- or 6-nitro-2-aminophenol. An example is also given of the dyeing process for cotton with after-coppering in the dyebath. Specifications 12932/15, 101,601, [both in Class 2 (iii)], 455,274, 468,362 and 516,076 are referred to. The Specification as open to inspection under Sect. 91 comprises also (a) the use as diazo component of any amine of the benzene series, free from sulphonic acid groups and containing a lake-forming group, e.g. a hydroxy, carboxy or carboxymethoxy group, in o-position to the diazotised amino group and at least one halogen atom, (b) the use of any substituted benzidine component. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH560451X | 1941-04-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB560451A true GB560451A (en) | 1944-04-05 |
Family
ID=4520245
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4468/42A Expired GB560451A (en) | 1941-04-03 | 1942-04-03 | Manufacture of azo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB560451A (en) |
-
1942
- 1942-04-03 GB GB4468/42A patent/GB560451A/en not_active Expired
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