GB351431A - - Google Patents
Info
- Publication number
- GB351431A GB351431A GB38669/29A GB3866929A GB351431A GB 351431 A GB351431 A GB 351431A GB 38669/29 A GB38669/29 A GB 38669/29A GB 3866929 A GB3866929 A GB 3866929A GB 351431 A GB351431 A GB 351431A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aminophenyl
- nitroso
- azo dyes
- black
- bisulphite
- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Azo dyes; azo dyes, forming on the material.-Azo dyes are made in substance or on a substratum, e.g. the fibre by coupling the diazo- or tetrazo-compound of an arylaminonaphthalene of the type <FORM:0351431/IV/1> wherein Y = hydrogen or an amino group, with a 2 : 3-oxynaphthoylarylamine. They yield colour lakes and give fast blue to blueish black shades on the fibre. When using the N-nitroso derivatives of the diazo components the nitroso group may be split off according to Specification 313,865, [Class 2 (iii), Dyes &c.]. In examples, (1) cotton impregnated with the 4-chloranilide is developed with tetrazotized bis-(41-aminophenyl)-2 : 6- or 2 : 7-naphthylenediamine (black), (2) cotton impregnated with the b -naphthylamide is developed with diazotized N-nitroso - 6 - phenylamino-(41-aminophenyl)-2-naphthylamine and the dyeing treated with sodium carbonate, soap and sodium sulphide (blueish black). Bis-(41aminophenyl)-2 : 6- and 2 : 7 naphthylenediamines are made from 2 : 6- or 2 : 7-dioxynaphthalene and p-phenylenediamine (2 mols) in presence of bisulphite. 6-Aminophenyl-(41-aminophenyl)-2-naphthylamine is made from 2-hydroxy-6-phenylaminonaphthalene, p-phenylenediamine and bisulphite or similarly from 6-phenylamino-2-naphthol-3-carboxylic acid whereby the carboxy group is split off.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE143583X | 1927-12-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB351431A true GB351431A (en) | 1931-06-24 |
Family
ID=5669774
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB38669/29A Expired GB351431A (en) | 1927-12-10 | 1928-12-17 |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB351431A (en) |
-
1928
- 1928-12-17 GB GB38669/29A patent/GB351431A/en not_active Expired
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