GB353538A - Process for the manufacture of water insoluble azo dyestuffs - Google Patents
Process for the manufacture of water insoluble azo dyestuffsInfo
- Publication number
- GB353538A GB353538A GB1335930A GB1335930A GB353538A GB 353538 A GB353538 A GB 353538A GB 1335930 A GB1335930 A GB 1335930A GB 1335930 A GB1335930 A GB 1335930A GB 353538 A GB353538 A GB 353538A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxyphenanthrene
- nitro
- toluidine
- carboxylic acid
- azo dyes
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Azo dyes; azo dyes, forming on the material.-Azo dyes are made in substance or on a substratum by coupling a diazo compound of an aromatic or heterocyclic non-sulphonated amine or derivative thereof or an aromatic aminoazo compound or diamine with an arylide of a hydroxyphenanthrene-o-carboxylic acid. In an example, cotton padded with 2-hydroxyphenanthrene-3-carboxylic acid-o-toluidide is developed with diazotized 2 : 5-dichloraniline (yellowish red). Other arylides specified are 3-hydroxyphenanthrene-2-carboxylic acid-o-toluidide and p-anisidide and other diazo components: o- and p-nitraniline, 5-nitro-o-anisidine, 5-chloro-2-toluidine, m-aminoazotoluene, 2-amino-5-benzoylaminohydroquinone diethylether, dianisidine, 1-, 2- or 3-aminocarbazole, 9-ethyl-3-aminocarbazole, 2-aminodiphenyleneoxide, p-nitro-o-toluidine, p-chlor-o-nitraniline, m-nitro-p-toluidine, 4-nitro-2 : 5-dimethoxy-41-aminoazobenzene. Arylides of hydroxyphenanthrene carboxylic acids and made from the corresponding acid and amine by boiling in an inert organic solvent in presence of a condensing agent, e.g. phosphorus oxychloride.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1335930A GB353538A (en) | 1930-04-30 | 1930-04-30 | Process for the manufacture of water insoluble azo dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1335930A GB353538A (en) | 1930-04-30 | 1930-04-30 | Process for the manufacture of water insoluble azo dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB353538A true GB353538A (en) | 1931-07-30 |
Family
ID=10021520
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1335930A Expired GB353538A (en) | 1930-04-30 | 1930-04-30 | Process for the manufacture of water insoluble azo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB353538A (en) |
-
1930
- 1930-04-30 GB GB1335930A patent/GB353538A/en not_active Expired
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