GB191220367A - Improvements in the Manufacture of Vat Dyestuffs. - Google Patents
Improvements in the Manufacture of Vat Dyestuffs.Info
- Publication number
- GB191220367A GB191220367A GB191220367DA GB191220367A GB 191220367 A GB191220367 A GB 191220367A GB 191220367D A GB191220367D A GB 191220367DA GB 191220367 A GB191220367 A GB 191220367A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthoquinone
- benzoquinone
- products
- chloranthraquinone
- diaminoanthraquinone
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
20,367. Ransford, R. B., [Cassella & Co., L.]. Sept. 6. [Cognate Application, 6269/13.] Samples furnished. Anthracene, dyes derived from.-Condensation products are obtained from diaminoanthraquinones and benzoquinone, its halogen derivatives, or alpha-naphthoquinone. The products from benzoquinone or its halogen derivatives dye cotton from a vat in brown to brownish-red shades; the products from a-naphthoquinone have little dyeing power. Other vat dyes are obtained by condensing the above-described condensation products with halogenanthraquinones; these dye brownish-red to claret-red shades. According to examples, 1:8-diaminoanthraquinone is condensed with benzoquinone; 1:5- or 2:6-diaminoanthraquinone give similar products; 1:5-diaminoanthraquinone is condensed with alpha-naphthoquinone, and the product is further condensed with #-chloranthraquinone; #-chloranthraquinone may be replaced by alpha-chloranthraquinone, and benzoquinone may replace the naphthoquinone. Suitable diluents for use in the process are glacial acetic acid, alcohol, and nitrobenzene; catalysts may be used or a current of air passed through the reaction mixture.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB191220367T | 1912-09-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191220367A true GB191220367A (en) | 1913-11-06 |
Family
ID=34358514
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191220367D Expired GB191220367A (en) | 1912-09-06 | 1912-09-06 | Improvements in the Manufacture of Vat Dyestuffs. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191220367A (en) |
-
1912
- 1912-09-06 GB GB191220367D patent/GB191220367A/en not_active Expired
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