GB411915A - Process for the manufacture of new azo dyestuffs - Google Patents
Process for the manufacture of new azo dyestuffsInfo
- Publication number
- GB411915A GB411915A GB35766/32A GB3576632A GB411915A GB 411915 A GB411915 A GB 411915A GB 35766/32 A GB35766/32 A GB 35766/32A GB 3576632 A GB3576632 A GB 3576632A GB 411915 A GB411915 A GB 411915A
- Authority
- GB
- United Kingdom
- Prior art keywords
- carboxylic acid
- benzocarbazole
- hydroxy
- class
- iii
- 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
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Azo dyes, insoluble in water, are made in substance or on the fibre, by coupling diazotised aminochrysene (obtained by nitrating chrysene in glacial acetic acid) with a coupling component, e.g. arylamides of naphthalene-o-hydroxycarboxylic acids, 2-hydroxyanthracene-3-carboxylic acid (see Specification 367,907), 2-hydroxycarbazole-3-carboxylic acid (Specification 343,164), and 2-hydroxy-a -benzocarbazole - 3 - carboxylic acid (see Specification 330,643, [Class 2 (iii)], and acetoaceticarylides, e.g. bisacetoacetic arylides (cf. Specification 210,217, [Class 2 (iii)]). Blue to violet to brown shades are obtained. In examples the following components are specified: anilide, m-nitranilide and a -naphthylamide of 2 : 3-oxynaphthoic acid, 1-(5<1>-hydroxy-1 : 2 : 1<1> : 2<1>-benzocarbazole-4<1>-carboylamino) -2-methyl-4-methoxybenzene, diacetoacetyl-o-tolidine and acetoaceticanilide.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE411915X | 1931-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB411915A true GB411915A (en) | 1934-06-18 |
Family
ID=6433653
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35766/32A Expired GB411915A (en) | 1931-12-18 | 1932-12-16 | Process for the manufacture of new azo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB411915A (en) |
-
1932
- 1932-12-16 GB GB35766/32A patent/GB411915A/en not_active Expired
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