GB470398A - Improvements in the manufacture and production of azo dyestuffs - Google Patents
Improvements in the manufacture and production of azo dyestuffsInfo
- Publication number
- GB470398A GB470398A GB108536A GB108536A GB470398A GB 470398 A GB470398 A GB 470398A GB 108536 A GB108536 A GB 108536A GB 108536 A GB108536 A GB 108536A GB 470398 A GB470398 A GB 470398A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxyethyl
- nitroaniline
- compounds
- groups
- benzylaniline
- 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
- C09B29/06—Monoazo dyes prepared by diazotising and coupling from coupling components containing amino as the only directing group
- C09B29/08—Amino benzenes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
Monoazo dyes are made by coupling diazo compounds of aromatic amines free from SO3H, COOH and CN groups with aralkylarylamines free from SO3H and COOH groups of the general formula <FORM:0470398/IV/1> in which R is an alkyl group containing at least one hydroxyl group and X and Y are radicles of the benzene series which may be substituted by halogen, alkyl, hydroxyalkyl, amino or nitro groups. They dye cellulose esters and ethers and colour paraffin wax and stearine and spirit and cellulose ester lacquers. They are also suitable for use as double-tone and intaglio printing inks. In examples, dyes from the following components are described: p-nitroaniline, o-chlor-p-nitroaniline, 2 : 6- or 2 : 5-dichlor-4-nitroaniline; N-hydroxyethyl- N-benzylaniline, N-hydroxyethyl-N-(4-nitrobenzyl)-aniline, N-hydroxyethyl N-benzyl-o-toluidine. Red and brown shades are obtained. R in the above formula may also be hydroxypropyl or dihydroxypropyl. The hydroxyethyl and hydroxypropyl compounds may be made by addition of ethylene or propylene oxide to N-benzylanilines under p pressure and the dihydroxypropyl compounds from chlorpropanediol (1 mol.) and benzylaniline (2 mols.)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB108536A GB470398A (en) | 1936-01-13 | 1936-01-13 | Improvements in the manufacture and production of azo dyestuffs |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB108536A GB470398A (en) | 1936-01-13 | 1936-01-13 | Improvements in the manufacture and production of azo dyestuffs |
Publications (1)
Publication Number | Publication Date |
---|---|
GB470398A true GB470398A (en) | 1937-08-13 |
Family
ID=9715900
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB108536A Expired GB470398A (en) | 1936-01-13 | 1936-01-13 | Improvements in the manufacture and production of azo dyestuffs |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB470398A (en) |
-
1936
- 1936-01-13 GB GB108536A patent/GB470398A/en not_active Expired
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