GB475996A - Manufacture of polyazo-dyestuffs - Google Patents
Manufacture of polyazo-dyestuffsInfo
- Publication number
- GB475996A GB475996A GB793/37A GB79337A GB475996A GB 475996 A GB475996 A GB 475996A GB 793/37 A GB793/37 A GB 793/37A GB 79337 A GB79337 A GB 79337A GB 475996 A GB475996 A GB 475996A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- sulphonic
- mol
- methyl
- used instead
- 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
- C09B35/00—Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Polyazo dyes are made by causing to act on resorcinol in any order, 1 mol. of a diazotized sulphonic acid of the thiazole series and 1 mol. of a diazotized p-aminoazo dyestuff of the general formula R1-N=N-R2-NH2, in which R2 is the residue of a middle component and R1 is the residue of an intermediate product from 1 mol. of a tetrazo compound of the diphenyl series and 1 mol. of a yellow component, that is, a mononuclear aromatic oxy-compound, such as phenol, the cresols or xylenols and their carboxylic and sulphonic acids, or compounds which contain a methylene group capable of coupling, such as 1-phenyl-3-methyl-5-pyrazolone, acetoacetic anilide, dioxyquinoline or their sulphonic acids. They have a better affinity for vegetable fibre than the dyestuffs made according to Specification 267,162, [Class 2 (iii)], and yield brown shades on cotton and leather. The following dyestuffs are described in examples: (1) salicylic acid --> benzidine \sM 1-naphthylamine-6- or 7-sulphonic acid --> resorcinol \sM primuline; salicylic acid may be replaced by a cresotinic acid, p-cresol or xylenol, primuline by dehydrothiotoluidine monosulphonic acid and benzidine by tolidine; (2) 1-amino-2-methoxy-5-methyl-benzene is used instead of 1-naphthylamine-6-or 7-sulphonic acid in (1) and salicylic acid may be replaced by 1-(4<1>-sulphophenyl)-3-methyl-5-pyrazolone; (3) 1-(4<1>-sulphophenyl)-3-methyl-5-pyrazolone is used instead of salicylic acid in (1); dehydrothiotoluidine monosulphonic acid, tolidine, 4 : 4<1>-diamino-3 : 3<1>-dichlorodiphenyl and a sulphonic acid of acetoacetic anilide may also be used; (4) the thiazole obtained by condensing J acid with m-nitrobenzaldehyde and sodium polysulphide is used instead of primuline in (1); tolidine, dianisidine and 3 : 3<1>-dichlorobenzidine may be used instead of benzidine. p - Aminophenylnaphthothiazole sulphonic acid (cf. German Specification 165,126) is also specified. British Specification 469,646 also is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH475996X | 1936-01-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB475996A true GB475996A (en) | 1937-11-30 |
Family
ID=4516156
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB793/37A Expired GB475996A (en) | 1936-01-09 | 1937-01-11 | Manufacture of polyazo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB475996A (en) |
-
1937
- 1937-01-11 GB GB793/37A patent/GB475996A/en not_active Expired
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