GB191202948A - Manufacture of New Derivatives and Dyestuffs of the Anthraquinone Series. - Google Patents
Manufacture of New Derivatives and Dyestuffs of the Anthraquinone Series.Info
- Publication number
- GB191202948A GB191202948A GB191202948DA GB191202948A GB 191202948 A GB191202948 A GB 191202948A GB 191202948D A GB191202948D A GB 191202948DA GB 191202948 A GB191202948 A GB 191202948A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloranthrone
- halogenpyridazoneanthrones
- sulphonic acids
- dye
- wool
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/16—Benz-diazabenzanthrones, e.g. anthrapyrimidones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
2948. Ullmann, F. July 7, 1911, [Convention date]. Arylaminopyridazoneanthrones are obtained by condensing halogenpyridazoneanthrones with primary aromatic monamines; their sulphonic acids, obtained either by subsequent sulphonation, or by using halogenpyridazoneanthrone sulphonic acids, dye wool yellow to orange tints. According to examples, pyridazone - 4 - chloranthrone is condensed with aniline, and the product is sulphonated, giving a yellow wool dye; phenylpyridazone-4-chloranthrone is condensed with p-toluidine, and the product is sulphonated, giving an orange wool dye; o- and p-anisidine are also specified as suitable amines. Halogenpyridazoneanthrones. - Pyridazone- 4 - chloranthrone and phenylpyridazone - 4 - chloranthrone are prepared by the process of Specification 25,183/10 from 4-chloranthraquinone-1-carboxylic chloride and hydrazine, and 4-chloranthraquinone-1-carhoxylic acid and phenylhydrazine respectively; phenylhydrazine sulphonic acids &c. may be used in the production of the halogenpyridazoneanthrones.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE191202948X | 1911-07-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB191202948A true GB191202948A (en) | 1912-09-26 |
Family
ID=32522255
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB191202948D Expired GB191202948A (en) | 1911-07-07 | 1912-02-05 | Manufacture of New Derivatives and Dyestuffs of the Anthraquinone Series. |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB191202948A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2992220A (en) * | 1956-12-05 | 1961-07-11 | Ici Ltd | New anthra-1':9'(n):10'(n):5'-dipyridazones and anthra-1':9'(n):10'(n):4'-dipyridazones chemical compounds |
-
1912
- 1912-02-05 GB GB191202948D patent/GB191202948A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2992220A (en) * | 1956-12-05 | 1961-07-11 | Ici Ltd | New anthra-1':9'(n):10'(n):5'-dipyridazones and anthra-1':9'(n):10'(n):4'-dipyridazones chemical compounds |
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