GB395027A - The manufacture of new azo dyestuffs - Google Patents
The manufacture of new azo dyestuffsInfo
- Publication number
- GB395027A GB395027A GB714/32A GB71432A GB395027A GB 395027 A GB395027 A GB 395027A GB 714/32 A GB714/32 A GB 714/32A GB 71432 A GB71432 A GB 71432A GB 395027 A GB395027 A GB 395027A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthol
- dyestuff
- disulphonic acid
- acid
- acetylamino
- 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
- C09B45/01—Complex metal compounds of azo dyes characterised by the method of metallisation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Dizazo dyes containing copper are made by treating with an agent yielding copper a disazo dyestuff obtainable by coupling in alkaline solution one mol. of a tetrazotized aromatic diamine, containing an alkoxy group in o-position to each diazo group, with two mols. of 2-amino-5-naphthol-1 : 7-disulphonic acid or an N-acyl derivative thereof, or with one mol. of the above acid or an N-acyl derivative thereof and one mol. of a naphthol sulphonic acid, the coppering being formed under such conditions that the alkoxy groups are split up. In the case of urea dyestuffs, a corresponding aminoalkoxy monoazo dye may first be prepared, converted into the urea and finally coppered. They dye silk, cotton and viscose violet to blue shades of good fastness to light. In examples: (1) the dyestuff dianisidine \sQ 2 - acetylamino - 5 - naphthol - 1 : 7-disulphonic acid is treated with ammoniacal copper sulphate; (2) the dyestuff 2-amino-5-naphthol-1 : 7-disulphonic acid \sM dianisidine --> 1-naphthol - 4 - sulphonic is treated with copper sulphate; (3) the dyestuff 4 : 4<1>-diamino-3 : 3<1>-dimethoxydiphenylurea \sQ 2 - acetylamino - 5 - naphthol - 1 : 7 - disulphonic acid is coppered as in (1); the same dyestuff is obtained by reducing the dyestuff 5-nitro-2-aminoanisole --> 2-acetylamino - 5 - naphthol-1 : 7-disulphonic acid, phosgenating and coppering. Specifications 113,141, [Class 2 (iii), Dyes &c.], and 352,956 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE395027X | 1931-01-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB395027A true GB395027A (en) | 1933-07-10 |
Family
ID=6396779
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB714/32A Expired GB395027A (en) | 1931-01-09 | 1932-01-09 | The manufacture of new azo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB395027A (en) |
-
1932
- 1932-01-09 GB GB714/32A patent/GB395027A/en not_active Expired
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