GB462561A - The manufacture of black sulphur dyestuffs - Google Patents
The manufacture of black sulphur dyestuffsInfo
- Publication number
- GB462561A GB462561A GB3070235A GB3070235A GB462561A GB 462561 A GB462561 A GB 462561A GB 3070235 A GB3070235 A GB 3070235A GB 3070235 A GB3070235 A GB 3070235A GB 462561 A GB462561 A GB 462561A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxyphenylamino
- naphthalene
- indophenol
- carbazole
- aminophenol
- 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
- C09B49/00—Sulfur dyes
- C09B49/10—Sulfur dyes from diphenylamines, indamines, or indophenols, e.g. p-aminophenols or leucoindophenols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Indole Compounds (AREA)
Abstract
Black sulphur dyestuffs are obtained by acting with alkali polysulphides upon a mixture of a 4-hydroxyphenylaminonaphthalene or a corresponding quinone-imine or a derivative thereof having halogen atoms or carboxylic groups in the phenyl nucleus with an indophenol or leuco indophenol derived from an amine of the benzene, naphthalene or carbazole series and a p-amino or nitroso phenol or a halogen or carboxylic acid derivative thereof. Aromatic nitro or amino compounds containing further nitro, amino or hydroxy groups may also be present. In examples, the following mixtures are sulphurized: 2-(4<1>-hydroxyphenylamino)-naphthalene, 3 - (4<1> - hydroxyphenylamino)-carbazole and p- or o-aminophenol, 1-(4<1>-hydroxyphenylamino)naphthalene, 3<1> - (4<1>-hydroxyphenylamino)carbazole and p-aminophenol, 2 - (4<1> - hydroxy - 3<1> - carboxyphenylamino)naphthalene, 3<1> - (4<1> - hydroxyphenylamino)carbazole and m - toluylenediamine, 2<1> - (4<1> - hydroxyphenylamino)naphthalene and 3 - (4<1> - hydroxyphenylamino N - ethylcarbazole, 2 - (4<1> - hydroxyphenylamino)naphthalene and the indophenol prepared from diphenylamine and p-nitrosophenol. The sulphurization is effected by means of a solution prepared from caustic soda, sulphur and n-propylalcohol, methylcyclohexanol, butanol or ethylalcohol. An oxidizing agent, e.g. sodium nitrate facilitates the reaction. The use of the indophenol obtained from m-phenylenediamine and p-aminophenol, and also phenylene diamines dinitronaphthalenes and nitrocarbazoles as the third component is mentioned. Specification 25457/11, [Class 2 (iii)], is referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3070235A GB462561A (en) | 1935-11-06 | 1935-11-06 | The manufacture of black sulphur dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB3070235A GB462561A (en) | 1935-11-06 | 1935-11-06 | The manufacture of black sulphur dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB462561A true GB462561A (en) | 1937-03-11 |
Family
ID=10311784
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB3070235A Expired GB462561A (en) | 1935-11-06 | 1935-11-06 | The manufacture of black sulphur dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB462561A (en) |
-
1935
- 1935-11-06 GB GB3070235A patent/GB462561A/en not_active Expired
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