GB834270A - Improvements in or relating to monoazo dyestuffs of the pyrazolone series and their chromium complex compounds - Google Patents
Improvements in or relating to monoazo dyestuffs of the pyrazolone series and their chromium complex compoundsInfo
- Publication number
- GB834270A GB834270A GB31036/56A GB3103656A GB834270A GB 834270 A GB834270 A GB 834270A GB 31036/56 A GB31036/56 A GB 31036/56A GB 3103656 A GB3103656 A GB 3103656A GB 834270 A GB834270 A GB 834270A
- Authority
- GB
- United Kingdom
- Prior art keywords
- complexes
- chroming
- dyes
- free
- coupling
- 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
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
The invention comprises dyes and their chromium complexes which in their metal-free form are of formula <FORM:0834270/IV(c)/1> where X is H or the residue of a sulphonamide group which may be N-substituted by alkyl, hydroxy-, alkoxy- or cyclo-alkyl, aralkyl or aryl groups free from COOH or SO3H groups, and R is the residue of 1-(51,61,71,81-tetrahydro-11) -naphthyl - 3 - methyl - 5 - pyrazolone - 41 - sulphonamide which may be N-substituted as in X and also by a morpholide group. They are made by conventional diazotizing and coupling methods from appropriate anthranilic acids and pyrazolones and, if desired, with subsequent chroming in substance or on the fibre. Coupling is preferably effected in an alkaline medium. The metal-free dyes dye wool by the single bath chroming or after-chroming process in yellow shades and the complexes dye wool, silk, leather and artificial nitrogenous fibres, e.g. polyamides, also in yellow shades. The complexes also colour spinning solutions, lacquer media, oils and synthetic resins and plastics. In examples which illustrate the preparation of the dyes and their complexes and the use of both in dyeing processes, the diazo components are 2-amino-benzene-1-carboxylic acid and its 5-sulphon-and sulphonmethyl- and sulphonphenyl-amides and the N-substituents of the coupling components are H, ethyl, isopropyl, 2-hydroxyethyl, 3-methoxypropyl, phenyl, morpholyl and dimethyl radicles. Specification 753,550 is referred to. Reference has been directed by the Comptroller to Specification 775,005.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH834270X | 1955-10-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB834270A true GB834270A (en) | 1960-05-04 |
Family
ID=4540547
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB31036/56A Expired GB834270A (en) | 1955-10-12 | 1956-10-11 | Improvements in or relating to monoazo dyestuffs of the pyrazolone series and their chromium complex compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB834270A (en) |
-
1956
- 1956-10-11 GB GB31036/56A patent/GB834270A/en not_active Expired
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