GB383967A - Process for the manufacture of azo-dyestuffs - Google Patents
Process for the manufacture of azo-dyestuffsInfo
- Publication number
- GB383967A GB383967A GB1598731A GB1598731A GB383967A GB 383967 A GB383967 A GB 383967A GB 1598731 A GB1598731 A GB 1598731A GB 1598731 A GB1598731 A GB 1598731A GB 383967 A GB383967 A GB 383967A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aminoindole
- diazotized
- methoxynaphthaleneindigo
- nitroisatin
- indigo
- 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
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Azo dyes are made in substance or on the fibre by coupling a diazotized amino-indolenaphthalene or amino-indoleanthracene indigo with an acyl acetic acid arylide. Green dyestuffs insoluble in water are obtained. In examples: (1) cotton impregnated with diaceto - acetyl - o - tolidine is developed with diazotized 5 - aminoindole - 4<1> - methoxynaphthaleneindigo or (2) with diazotized 5-aminoindole - 4<1> - chloronaphthaleneindigo, (3) the dyestuff 5-aminoindole-4<1>-methoxynaphthaleneindigo----> acetoacetic acid-o-anisidide is prepared in substance, (4) cotton is padded with benzoylacetic acid anilide and developed with diazotized 5-aminoindole-4<1>-methoxynaphthaleneindigo. Specification 210,217, [Class 2 (iii). Dyes &c.], is referred to. Aminoindolenaphthalene and aminoindoleanthracene indigos are made by converting the corresponding nitroisatin (obtained by nitration) into the nitroisatin chloride by the action of phosphorus pentachloride, condensing with the corresponding naphthol or hydroxyanthracene and reducing the nitro-indigo thus obtained.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1598731A GB383967A (en) | 1931-06-01 | 1931-06-01 | Process for the manufacture of azo-dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1598731A GB383967A (en) | 1931-06-01 | 1931-06-01 | Process for the manufacture of azo-dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB383967A true GB383967A (en) | 1932-12-01 |
Family
ID=10069166
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1598731A Expired GB383967A (en) | 1931-06-01 | 1931-06-01 | Process for the manufacture of azo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB383967A (en) |
-
1931
- 1931-06-01 GB GB1598731A patent/GB383967A/en not_active Expired
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