GB324084A - Improvements in and relating to the production of anthraquinone vat dyestuffs - Google Patents
Improvements in and relating to the production of anthraquinone vat dyestuffsInfo
- Publication number
- GB324084A GB324084A GB2379928A GB2379928A GB324084A GB 324084 A GB324084 A GB 324084A GB 2379928 A GB2379928 A GB 2379928A GB 2379928 A GB2379928 A GB 2379928A GB 324084 A GB324084 A GB 324084A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- relating
- production
- nitroanthraquinone
- arylamine
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
- C09B1/34—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups sulfonated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
324,084. British Alizarine Co., Ltd., and Beghin, P. P. Aug. 18, 1928. Samples furnished. Anthraquinoneacridone vat-dyes are prepared by condensing 1-nitroanthraquinone-2-carboxylic acid or a derivative thereof with an arylamine having a free o-position to the amino group in presence of a weakly acid catalyst or condensing agent. The catalyst preferably used is boric acid and arsenious acid, oxalic acid or phthalic acid are also suitable. An inert solvent, such as nitrobenzene, or an excess of the arylamine may be present. In examples 1-nitroanthraquinone-2- carboxylic acid is heated with boric acid and (1) an excess of #-naphthylamine, (2) nitrobenzene and #-naphthylamine, #-toluidine or aniline. Specifications 894/11 and 260,588 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2379928A GB324084A (en) | 1928-08-18 | 1928-08-18 | Improvements in and relating to the production of anthraquinone vat dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2379928A GB324084A (en) | 1928-08-18 | 1928-08-18 | Improvements in and relating to the production of anthraquinone vat dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB324084A true GB324084A (en) | 1930-01-20 |
Family
ID=10201499
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2379928A Expired GB324084A (en) | 1928-08-18 | 1928-08-18 | Improvements in and relating to the production of anthraquinone vat dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB324084A (en) |
-
1928
- 1928-08-18 GB GB2379928A patent/GB324084A/en not_active Expired
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