GB347236A - Improvements in the manufacture and production of vat dyestuffs - Google Patents
Improvements in the manufacture and production of vat dyestuffsInfo
- Publication number
- GB347236A GB347236A GB3605829A GB3605829A GB347236A GB 347236 A GB347236 A GB 347236A GB 3605829 A GB3605829 A GB 3605829A GB 3605829 A GB3605829 A GB 3605829A GB 347236 A GB347236 A GB 347236A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aldehyde
- aminoanthraquinone
- group
- products
- chlorbenzanthrone
- 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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/02—Benzathrones
- C09B3/06—Preparation from starting materials already containing the benzanthrone nucleus
- C09B3/10—Amino derivatives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Benzanthrone derivatives.-Derivatives of benzanthrone as defined in the parent Specification in which an anthraquinone radicle containing an aldehyde group is attached by means of an NH group to the benzanthronyl radicle are treated with alkaline condensing agents. The most valuable products are those derived from starting materials in which the aldehyde group is in o-position to the imino group. In examples the alkali fusion of the condensation products from 8-chlorbenzanthrone and 1 - aminoanthraquinone - 2 - aldehyde, 6 - chlorbenzanthrone and 1-aminoanthraquinone-2-aldehyde, and dibrom-2.21-dibenzanthronyl (which may be produced by bromination of 2.21-dibenzanthronyl) and 1-aminoanthraquinone-2-aldehyde (2 mols.) is described; the products dye grey to black shades. The starting materials may generally be prepared by condensation of negatively substituted or aminobenzanthrones with amino- or negatively substituted anthraquinone aldehydes respectively.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3605829A GB347236A (en) | 1929-11-25 | 1929-11-25 | Improvements in the manufacture and production of vat dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3605829A GB347236A (en) | 1929-11-25 | 1929-11-25 | Improvements in the manufacture and production of vat dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB347236A true GB347236A (en) | 1931-04-27 |
Family
ID=10384466
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3605829A Expired GB347236A (en) | 1929-11-25 | 1929-11-25 | Improvements in the manufacture and production of vat dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB347236A (en) |
-
1929
- 1929-11-25 GB GB3605829A patent/GB347236A/en not_active Expired
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