GB456768A - Process for the manufacture of polyazo dyestuffs - Google Patents
Process for the manufacture of polyazo dyestuffsInfo
- Publication number
- GB456768A GB456768A GB14271/35A GB1427135A GB456768A GB 456768 A GB456768 A GB 456768A GB 14271/35 A GB14271/35 A GB 14271/35A GB 1427135 A GB1427135 A GB 1427135A GB 456768 A GB456768 A GB 456768A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- mol
- nitroaniline
- sulphonic
- acids
- 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
- C09B35/50—Tetrazo dyes
- C09B35/52—Tetrazo dyes of the type
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Polyazo dyes are made by coupling 1 mol. of a naphthol sulphonic acid capable of coupling both in an acid and in an alkaline medium, in either order, with 1 mol of a tetrazodiphenyl and 1 mol. of a diazo compound, one of the couplings being effected in an acid and the other in an alkaline medium, combining the diazo disazo compound obtained with 1 mol. of resorcinol or a derivative thereof, and causing the trisazo dyestuff to react in an alkaline medium with 1 mol. of a monodiazo compound or at the same time or successively with 2 mols. of the same or different monodiazo compounds. Instead of the tetrazodiphenyl a diazo compound of the benzene series containing a group which is convertible into an amino group may be used. They yield brown to blackish brown shades on leather fast to acids and alkalies. In the examples the following dyes are described: (1) sulphanilic acid --> (alk.) H acid \sM (acid) benzidine --> resorcinol \sx p-nitroaniline; (2) 4-nitroaniline-2-sulphonic acid is used instead of sulphanilic acid in (1); this component and the p-nitroaniline may also be substituted by aniline disulphonic acids, naphthionic acid, naphthylamine disulphonic acids, chloraniline sulphonic acids, anisidine sulphonic acids, aminoazobenzene mono- or disulphonic acids, etc.; (3) sulphanilic acid (1 mol.) and p-nitroaniline (1 mol.) are used as end components in (1); p-nitraniline disulphonic acids, substituted anilines and aniline sulphonic acids, picramic acid and 1 : 3-diamino-4-nitrobenzene may also be used; (4) sulphanilic acid --> (alk.) J acid \sM (acid) benzidine --> resorcinol \sx 4-nitroaniline-2-sulphonic acid (1 mol.) and p-nitroaniline (1 mol.); p-aminobenzoic acid, 1-hydroxy-4-aminobenzene-2-carboxylic acid &c. may also be used as components; (5) sulphanilic acid --> (acid) J acid \sM (alk.) benzidine --> resorcinol \sx 4-nitraniline-2-sulphonic acid (1 mol.) and p-nitroaniline (1 mol.); (6) sulphanilic acid --> (alk.) J acid \sM (acid) p-nitroaniline (reduced) --> resorcinol \sx 4-nitraniline-2-sulphonic acid (1 mol.) and p-nitroaniline (1 mol.); (7) H acid is used instead of J acid. Further similar combinations are specified in a table. Other double coupling components mentioned are 1-amino-8-naphthol-4 - sulphonic acid, phenyl J acid and 2 : 5-dihydroxynaphthalene - 7 - sulphonic acid and other diaminodiphenyls are m-nitrobenzidine and benzidine-m-disulphonic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB14271/35A GB456768A (en) | 1935-05-15 | 1935-05-15 | Process for the manufacture of polyazo dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB14271/35A GB456768A (en) | 1935-05-15 | 1935-05-15 | Process for the manufacture of polyazo dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB456768A true GB456768A (en) | 1936-11-16 |
Family
ID=10038137
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14271/35A Expired GB456768A (en) | 1935-05-15 | 1935-05-15 | Process for the manufacture of polyazo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB456768A (en) |
-
1935
- 1935-05-15 GB GB14271/35A patent/GB456768A/en not_active Expired
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