GB191112010A - Manufacture of New Anthraquinone Derivatives and the application thereof in Dyeing and Printing. - Google Patents
Manufacture of New Anthraquinone Derivatives and the application thereof in Dyeing and Printing.Info
- Publication number
- GB191112010A GB191112010A GB191112010DA GB191112010A GB 191112010 A GB191112010 A GB 191112010A GB 191112010D A GB191112010D A GB 191112010DA GB 191112010 A GB191112010 A GB 191112010A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthylamine
- dyes
- derivatives
- diazoanthraquinone
- sulphonic
- 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
- C09B1/206—Dyes with amino groups substituted by heterocyclic radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
12,010. Bloxam, A. G., [Chemische Fabrik Griesheim-Elektron]. May 18. #-Aziminoanthraquinone derivatives are obtained by oxidizing the azo dyes produced by combining #-diazoanthraquinone or derivatives thereof with #-naphthylamine or derivatives thereof. The products, when not containing more than one or two sulphonic groups, are vat dyes. According to examples, the following azo dyes are oxidized : -the monoazo dyes from #-diazoanthraquinone and 2-naphthylamine, 2- naphthylamine-6-sulphonic acid, or 2-naphthylamine-3:6-disulphonic acid, the primary disazo dye from two molecular proportions of #-diazoanthraquinone and 2:6-naphthylenediamine, and the disazo dyes from tetrazotized 2:6-diaminoanthraquinone and 2-naphthylamine or 2- naphthylamine-6-sulphonic acid; chlor- or nitro- #-aminoanthraquinones or #-aminoanthraquinone sulphonic acids are also specified as parent materials. The oxidizing-agents specified are sodium bichromate and sodium hypochlorite. Amino groups may be introduced into the dyes by nitrating and reducing. The products give yellow shades on cotton. Lakes.-The #-azimino derivatives above-described may also be used in the preparation of lakes.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191112010T | 1911-05-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191112010A true GB191112010A (en) | 1911-11-30 |
Family
ID=34357268
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191112010D Expired GB191112010A (en) | 1911-05-18 | 1911-05-18 | Manufacture of New Anthraquinone Derivatives and the application thereof in Dyeing and Printing. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191112010A (en) |
-
1911
- 1911-05-18 GB GB191112010D patent/GB191112010A/en not_active Expired
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