GB430252A - Process for the manufacture of trisazodyestuffs - Google Patents
Process for the manufacture of trisazodyestuffsInfo
- Publication number
- GB430252A GB430252A GB35370/33A GB3537033A GB430252A GB 430252 A GB430252 A GB 430252A GB 35370/33 A GB35370/33 A GB 35370/33A GB 3537033 A GB3537033 A GB 3537033A GB 430252 A GB430252 A GB 430252A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- aminophenol
- coupling
- chloranilines
- toluidines
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Abstract
Trisazo dyes are made by tetrazotizing a p : p<1> - diaminodiphenyl, coupling with H or K acid (1 mol.) in mineral acid solution, coupling the intermediate product formed in alkaline solution with a diazo compound (1 mol.) and finally coupling with a nuclear substitution product of m-aminophenol which only couples in p-position with respect to the hydroxy group. They dye cotton and leather in greenish to blue to black shades fast to acids. Mixed fabrics of cotton, wool, silk and regenerated cellulose are dyed in even shades. In examples the following dyes are described: aniline --> H or K acid \sM benzidine --> 6-chloro-3-aminophenol, 4 - amino - 2 - cresol or 6- methoxy - 3 - aminophenol; tolidine, chloranilines and toluidines are also specified as components. The Specification as open to inspection under Sect. 91 specifies also the following components: sulphanilic acid, dianisidine, 3 : 3<1>-dichlorbenzidine, benzidine-3 : 3<1>-dicarboxylic acid, 4 : 4<1> - diamino - 2 - nitrodiphenyl, o-, m- and p-anisidines, o-, m-, and p-chloranilines, o-, m- and p-toluidines and 1-naphthylamine-4-sulphonic acid. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE430252X | 1932-12-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB430252A true GB430252A (en) | 1935-06-17 |
Family
ID=6479223
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35370/33A Expired GB430252A (en) | 1932-12-21 | 1933-12-15 | Process for the manufacture of trisazodyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB430252A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4701525A (en) * | 1984-07-24 | 1987-10-20 | Ciba-Geigy Ag | Polyazo dyestuffs having high UV absorption |
-
1933
- 1933-12-15 GB GB35370/33A patent/GB430252A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4701525A (en) * | 1984-07-24 | 1987-10-20 | Ciba-Geigy Ag | Polyazo dyestuffs having high UV absorption |
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