GB786928A - Improvements in or relating to 1,2 cobalt-complexes of monoazo-dyestuffs - Google Patents
Improvements in or relating to 1,2 cobalt-complexes of monoazo-dyestuffsInfo
- Publication number
- GB786928A GB786928A GB35292/55A GB3529255A GB786928A GB 786928 A GB786928 A GB 786928A GB 35292/55 A GB35292/55 A GB 35292/55A GB 3529255 A GB3529255 A GB 3529255A GB 786928 A GB786928 A GB 786928A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxy
- methoxy
- dyestuffs
- methyl
- propylamides
- 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/20—Monoazo compounds containing cobalt
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises dyestuffs of formula <FORM:0786928/IV (b)/1> where v is H or Me, w is H, Cl, Me or NO2 and R is 31-methoxy- or 21-hydroxy-propyl, the NV group is in the 1 or 2 position of the naphthalene nucleus and o to the azo group, the SO2NHR group is in the 4, 5 or 6 position and A is A1, a compound of the same formula as A1, the residue of the dyestuff a 2-aminophenol-sulphonamide-\sY2 - (31 - chloro) - phenylnaphthylamine or the residue of a compound of formula <FORM:0786928/IV (b)/2> where X is OH or MeO, y is H, Me or CH3CONH, z is an alkyl group of up to 4 C atoms or the residue of an aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic primary or secondary amine which may contain hydroxy, methoxy, ethoxy or methyl groups, R1 is an alkyl radicle of 6-18 C atoms and R2 is an alkyl or aryl radicle. They are made by treating appropriate dyestuffs or dyestuff mixtures with cobalt-yielding agents so that the final product contains approximately 2 mols. of dyestuff per atom of metal. Cobalting may be effected in conventional fashion, preferably with the use of cobaltous acetate, formate or sulphate in aqueous or organic media and especially in an aqueous caustic alkaline medium in the presence of compounds such as tartaric, citric or lactic acids. The dyestuffs dye wool, silk, leather and especially polyamide fibres from neutral to weakly acid baths in blue, green and olive shades. In examples illustrating the preparation of the dyestuffs and their use in dyeing processes the diazo components used are 4- and 5-nitro-, 4-chloro-, 5- and 6-nitro, 4-nitro-6-methyl-, 4,6-dinitro-2-aminophenols, 2-aminophenol-4- and -5-sulphonamides, -4-sulphonmethylamide, -(21-hydroxy, -methoxy and ethoxy) - ethylamides, -(21-hydroxy and 31-methoxy) - propylamides, - di - (21 - hydroxy-ethyl)amide, -cyclohexylamide, -benzylamide, -phenylamide, -(41-methyl)-phenylamide, -pyrrolidide and -morpholide, 2-aminophenol-6-methyl- and -acetylamino-4-sulphonamides, 2-amino - 1 - methoxybenzene - 4 - sulphonamide and 2 - amino - 1 - hydroxy - 4 - methyl - and -ethylsulphonylbenzenes, the coupling components being 2-naphthylamine-5 and 6-sulphon - (21 - hydroxy) - and - 6 - sulphon - (31-methoxy) - propylamides, 1 - naphthylamine-4- and -5-sulphon-(21-hydroxy and -methoxy)-propylamides and 2-methylaminophthalene-6-sulphon-(21-hydroxy and 31-methoxy)-propylamides, 2 - (31 - chloro) - phenylnaphthylamine, 1 - acetoacetylamino - 2 - ethylhexane, -octane, -hexane, -dodecane, -octadecane and -1,1-dimethyl -3,3 - dimethyl - butane and 1 - benzoylacetylaminooctane. Reference has been directed by the Comptroller to Specification 755,113.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH786928X | 1954-12-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB786928A true GB786928A (en) | 1957-11-27 |
Family
ID=4536652
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35292/55A Expired GB786928A (en) | 1954-12-15 | 1955-12-08 | Improvements in or relating to 1,2 cobalt-complexes of monoazo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB786928A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2631830A1 (en) * | 1975-07-25 | 1977-02-10 | Sandoz Ag | ORGANIC COMPOUNDS |
-
1955
- 1955-12-08 GB GB35292/55A patent/GB786928A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2631830A1 (en) * | 1975-07-25 | 1977-02-10 | Sandoz Ag | ORGANIC COMPOUNDS |
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