GB481832A - Manufacture of azo-dyestuffs - Google Patents
Manufacture of azo-dyestuffsInfo
- Publication number
- GB481832A GB481832A GB11881/37A GB1188137A GB481832A GB 481832 A GB481832 A GB 481832A GB 11881/37 A GB11881/37 A GB 11881/37A GB 1188137 A GB1188137 A GB 1188137A GB 481832 A GB481832 A GB 481832A
- Authority
- GB
- United Kingdom
- Prior art keywords
- sulphonic acid
- aminophenol
- naphthol
- nitro
- acid
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyrane Compounds (AREA)
Abstract
o-Hydroxyazo-dyestuffs capable of being chromed are manufactured by coupling an o-hydroxydiazo compound with an N-alkyl-, N-aralkyl- or N-aryl-derivative of 2-amino-6-naphthol-8-sulphonic acid. Examples describe the preparation of the following dyestuffs: (1) 4-nitro-2-aminophenol --> 2-phenylamino-6-naphthol-8-sulphonic acid (the product dyes wool in an acid bath bluish green shades, becoming grey when after-chromed); (2) picramic acid --> 2-dimethylamino-6-naphthol-8-sulphonic acid (green shades becoming olive when after-chromed); (3) 4-chloro-2-aminophenol-6-sulphonic acid --> 2-phenylamino-6-naphthol-8-sulphonic acid (green shades becoming grey when after-chromed). A table shows the properties of further dyestuffs, the following additional components being specified; diazo components: 6-nitro-4-methyl-2-aminophenol, 6-nitro-4-chloro-2-aminophenol, 4 : 6-dichloro-2-aminophenol, 5-nitro-2-aminophenol, 6 nitro-2-aminophenol-4-sulphonic acid; coupling components: the N-41-ethoxyphenyl-and N-benzyl-derivatives, the glycine and the N-methyl-w-sulphonic acid of 2-amino-6-naphthol-8-sulphonic acid. 2 - Amino - 6 - naphthol - 8 - sulphonic acid derivatives.-The compounds specified as coupling components are obtainable by reacting 2-amino-6-naphthol-8-sulphonic acid with aniline and sulphite, with a methylating agent such as methyl chloride, with p-phenetidine in the presence of sulphite, with a benzyl halide, with a halogenacetic acid and with formaldehyde and bisulphite respectively.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE481832X | 1936-05-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB481832A true GB481832A (en) | 1938-03-18 |
Family
ID=6542725
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB11881/37A Expired GB481832A (en) | 1936-05-06 | 1937-04-26 | Manufacture of azo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB481832A (en) |
-
1937
- 1937-04-26 GB GB11881/37A patent/GB481832A/en not_active Expired
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