GB952123A - Water-soluble organic dyestuffs - Google Patents
Water-soluble organic dyestuffsInfo
- Publication number
- GB952123A GB952123A GB3916761A GB3916761A GB952123A GB 952123 A GB952123 A GB 952123A GB 3916761 A GB3916761 A GB 3916761A GB 3916761 A GB3916761 A GB 3916761A GB 952123 A GB952123 A GB 952123A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- sulphonic acid
- fluoro
- dyes
- benzene
- 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
- C09B62/00—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves
- C09B62/44—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring
- C09B62/78—Reactive dyes, i.e. dyes which form covalent bonds with the substrates or which polymerise with themselves with the reactive group not directly attached to a heterocyclic ring with other reactive groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises water-soluble organic dyestuffs characterized by containing at least one grouping of the general formula <FORM:0952123/C3/1> wherein one Y is a fluorine atom or a nitro group, the other Y is a hydrogen atom and A is a nitrile or -SO2R group, R being an aliphatic, araliphatic, aromatic, cycloaliphatic or heterocyclic residue. The dyes are prepared by reacting amino groups of water-soluble dyestuffs with functional derivatives of aromatic carboxylic acids of the general formula <FORM:0952123/C3/2> or they are prepared in known manner from intermediates containing at least one grouping of the first general formula above. The dyes contain at least one water-solubilizing group, e.g. the sulphonic acid group. The dyes may be of the azo, anthraquinone, azine, oxazine, thiazine, nitroso, nitro, azomethine, phthalocyanine, acridine, quinoline, triarylmethane, perinone or indigoid series. The azo dyes may be mono-, dis- or polyazo dyes and may contain in complex linkage metal atoms such as copper, chromium and cobalt. The dyes may be used for dyeing wool, silk, polyamide fibres or leather and react with material containing hydroxyl groups, e.g. cotton or regenerated cellulose whilst heating in the presence of alkaline agents. In examples: 1-amino-3-(41-fluoro-31-methyl-sulphonbenzoylamino) - benzene - 6 - sulphonic acid is diazotized and coupled with the sodium salt of 1-(41-sulphophenyl)-3-methylpyrazolone to form a yellow dye; representative of many alternative coupling components specified are 1 - methylpyrazolone - 3 - carboxylic acid, 2-naphthol - 6, 8 - disulphonic acid and 2-(31-sulphophenylamino) - 8 - naphthol - 6 - sulphonic acid, and of alternative diazo components specified are 1-amino-3-(61-nitro-31-methyl-sulphon - benzoylamino) - benzene - 6 - sulphonic acid and 1-amino-3-(41-fluoro-31-cyano-benzoylamino) - benzene - 6 - sulphonic acid (1); 1 - amino - 3 - (41 - fluoro - 31 - methyl-sulpho - benzoylamino) - benzene - 6 - sulphonic acid is diazotized and coupled with 2-amino-8-naphthol-3, 6-disulphonic acid (2); 1-amino - 3 - (41 - fluoro - 31 - methyl-sulphon - 11 - benzoyl)-aminobenzene-6-sulphonic acid is diazotized and coupled with 1,3-diamino-benzene-4-sulphonic acid and the product is coupled with diazotized 1 - amino - 3 - (41 - fluoro 31 - methyl-sulphonbenzoyl) - aminobenzene - 6 - sulphonic acid (3); copper phthalocyanine is converted to a sulphochloride and reacted with 4,41-diamino-diphenyl-2, 21-disulphonic acid and the product is reacted with 4-fluoro-3-methylsulphon-1-benzoyl chloride. Additional alternative starting materials are listed.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEC22649A DE1263949B (en) | 1960-11-02 | 1960-11-02 | Process for the production of water-soluble azo and phthalocyanine dyes |
Publications (1)
Publication Number | Publication Date |
---|---|
GB952123A true GB952123A (en) | 1964-03-11 |
Family
ID=7017262
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3916761A Expired GB952123A (en) | 1960-11-02 | 1961-11-01 | Water-soluble organic dyestuffs |
Country Status (2)
Country | Link |
---|---|
DE (1) | DE1263949B (en) |
GB (1) | GB952123A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7098319B2 (en) | 2004-09-16 | 2006-08-29 | Everlight Usa, Inc. | Disazo reactive dyestuffs containing the quaternary groups and their use |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE881853C (en) * | 1937-03-18 | 1953-07-02 | Bayer Ag | Process for the preparation of aminoazo dyes |
-
1960
- 1960-11-02 DE DEC22649A patent/DE1263949B/en active Pending
-
1961
- 1961-11-01 GB GB3916761A patent/GB952123A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7098319B2 (en) | 2004-09-16 | 2006-08-29 | Everlight Usa, Inc. | Disazo reactive dyestuffs containing the quaternary groups and their use |
Also Published As
Publication number | Publication date |
---|---|
DE1263949B (en) | 1968-03-21 |
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