GB216527A - Manufacture of azo-dyestuffs - Google Patents
Manufacture of azo-dyestuffsInfo
- Publication number
- GB216527A GB216527A GB12626/24A GB1262624A GB216527A GB 216527 A GB216527 A GB 216527A GB 12626/24 A GB12626/24 A GB 12626/24A GB 1262624 A GB1262624 A GB 1262624A GB 216527 A GB216527 A GB 216527A
- Authority
- GB
- United Kingdom
- Prior art keywords
- cresidine
- tetrazotized
- coupling
- tetrazo
- oxynaphthoic
- 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
- C09B35/36—Trisazo dyes of the type
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Insoluble azo dyes are produced, in substance or upon substrata, by coupling arylides of 2 : 3-oxynaphthoic acid with tetrazo compounds of certain diaminoazo dyestuffs not containing sulphonic groups; such diaminoazo compounds are obtainable by coupling a tetrazo compound with a diazotizable amine such as m-aminoacetanilide, acetyltoluylenediamine, m-toluidine, p-cresidine, p-xylidine, or a -naphthylamine or a derivative coupling in the 4-position; two different amines may be employed. The following examples are given:-(1) tetrazotized dianisidine is coupled with a -naphthylamine, again tetrazotized, and coupled with 2 : 3-oxynaphthoic anilide; the product yields black lakes: (2) fibre impregnated with 2 : 3-oxynaphthoic-a -naphthalide is dyed bluish- or greenish-black by developing with the tetrazo compound of the dyestuff from tetrazotized tolidine, a -naphthylamine, and p-cresidine or that from tetrazotized p : p1-diaminodiphenylamine and p-cresidine: (3) fibre impregnated as in (2) is developed with the tetrazo compound of the dyestuff made by coupling p-cresidine with tetrazotized 4 : 41-diamino-2 : 31-dimethoxy-21-methyl-azobenzene (made by coupling diazotized 1-amino-2-methoxy-4-nitro- or 4-acetylaminobenzene with p-cresidine and reducing or hydrolyzing): (4) goods impregnated with 2 : 3-oxynaphthoic anilide are printed with a thickened tetrazo solution of the dyestuff from tetrazotized tolidine and p-cresidine. 4-Amino-3-methoxy-acetanilide is obtained by reduction of the corresponding nitro compound.ALSO:Insoluble azo dyes are produced, upon the fibre, by coupling arylides of 2 : 3-oxynaphthoic acid with tetrazo compounds of certain diamino-azo dyestuffs not containing sulphonic groups; such diamino-azo compounds are obtainable by coupling a tetrazo compound with a diazotizable amine such as m-aminoacetanilide, acetyltoluylene-diamine, m-toluidine, p-cresidine, p-xylidine, or a -naphthylamine or a derivative coupling in the 4-position; two different amines may be employed. The following examples are given:-(1) fibre impregnated with 2 : 3-oxynaphthoic-a -naphthalide is dyed bluish-or greenish-black by developing with the tetrazo compound of the dyestuff from tetrazotized tolidine, a -naphthylamine, and p-cresidine or that from tetrazotized p : p1-diaminodiphenylamine and p-cresidine: (2) fibre impregnated as in (1) is developed with the tetrazo compound of the dyestuff made by coupling p-cresidine with tetrazotized 4 : 41-diamino-2 : 31-dimethoxy-21-methyl-azobenzene (made by coupling diazotized 1-amino-2-methoxy-4-nitro- or 4-acetylamino benzene with p-cresidine and reducing or hydrolyzing: (3) goods impregnated with 2 : 3-oxynaphthoic anilide are printed with a thickened tetrazo solution of the dyestuff from tetrazotized tolidine and p-cresidine.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE216527X | 1923-05-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB216527A true GB216527A (en) | 1925-03-19 |
Family
ID=5829562
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB12626/24A Expired GB216527A (en) | 1923-05-22 | 1924-05-22 | Manufacture of azo-dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB216527A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2563381A (en) * | 1947-12-30 | 1951-08-07 | Gen Aniline & Film Corp | Azo dyeing process |
-
1924
- 1924-05-22 GB GB12626/24A patent/GB216527A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2563381A (en) * | 1947-12-30 | 1951-08-07 | Gen Aniline & Film Corp | Azo dyeing process |
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