GB422287A - Manufacture of mordant dyestuffs - Google Patents
Manufacture of mordant dyestuffsInfo
- Publication number
- GB422287A GB422287A GB23564/33A GB2356433A GB422287A GB 422287 A GB422287 A GB 422287A GB 23564/33 A GB23564/33 A GB 23564/33A GB 2356433 A GB2356433 A GB 2356433A GB 422287 A GB422287 A GB 422287A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- nitraniline
- sulphonic acid
- sulphonic
- amino
- 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
- C09B35/38—Trisazo dyes ot the type
- C09B35/44—Trisazo dyes ot the type the component K being a hydroxy amine
- C09B35/46—Trisazo dyes ot the type the component K being a hydroxy amine the component K being an amino naphthol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Abstract
Mordant trisazo dyes are made by coupling H acid first in an acid medium with diazotized aniline or a derivative thereof (R1) and then in an alkaline medium with a diazotized aminoazo compound of the type R3--N = --R2--NH2 in which R2 = a sulphonated benzene nucleus and R3 = a benzene nucleus which contains a hydroxyl group and a carboxyl group in o-position and may also contain further substituents, e.g. methyl or halogen. They yield in chrome printing on cotton green to blue-green shades having good fastness properties, particularly to chlorine. In examples the following dyes are described 3-amino-4-sulphobenzeneazosalicylic acid --> (MgCO2) H acid \sM 4-nitraniline-2-sulphonic acid or 2-nitraniline-4-sulphonic acid; 4 - amino - 2 - sulphobenzene - azo - salicylic acid may also be used. Other components specified are 3-nitraniline-4-sulphonic acid, 4-nitraniline-3-sulphonic acid, p-nitraniline, 4 - chloraniline - 2 - sulphonic acid, sulphanilic or metanilic acid, 4-chloraniline-3-sulphonic acid, 2-chlor-4-nitraniline and 4-chlor-3-nitraniline; instead of salicylic acid there may be used, e.g. cresotinic acid, chloro-salicylic acids and b -resorcylic acid. Specifications 15725/91, 15056/92, [both in Class 2], and 231,885, [Class 2 (iii)], are referred to. The Specification as open to inspection under Sect. 91 also specifies 4-amino-3-sulphobenzene-azosalicylic acid as the aminoazo compound. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE422287X | 1932-08-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB422287A true GB422287A (en) | 1935-01-09 |
Family
ID=6463007
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB23564/33A Expired GB422287A (en) | 1932-08-24 | 1933-08-24 | Manufacture of mordant dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB422287A (en) |
-
1933
- 1933-08-24 GB GB23564/33A patent/GB422287A/en not_active Expired
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