GB887971A - Dyestuffs of the perylene tetracarboxylic acid diimide series and process for their manufacture - Google Patents
Dyestuffs of the perylene tetracarboxylic acid diimide series and process for their manufactureInfo
- Publication number
- GB887971A GB887971A GB41012/59A GB4101259A GB887971A GB 887971 A GB887971 A GB 887971A GB 41012/59 A GB41012/59 A GB 41012/59A GB 4101259 A GB4101259 A GB 4101259A GB 887971 A GB887971 A GB 887971A
- Authority
- GB
- United Kingdom
- Prior art keywords
- phenylene
- tetracarboxylic acid
- formula
- dyestuff
- dyestuffs
- 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
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/62—Cyclic imides or amidines of peri-dicarboxylic acids of the anthracene, benzanthrene, or perylene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Abstract
Viscose rayon, cellulose acetate rayon, nylon, polyesters and polyvinyl chloride are spin-dyed with a dyestuff of the formula:- <FORM:0887971/IV (a)/1> where R is a p-phenylene or a 4:41-diphenylene radical. Red dyeings are obtained. In an Example (5), polyvinyl chloride, dioctyl phthalate and a dyestuff of the above formula where R is p-phenylene are mixed and rolled.ALSO:The invention comprises dyestuffs of the formula <FORM:0887971/IV (c)/1> wherein R is a p-phenylene or a 4 : 41-diphenylene radical. The dyes are made by condensing perylene-3 : 4 : 9 : 10- tetracarboxylic acid or its anhydride with a p-amino-hydroxybenzene or a 4 : 41-amino-hydroxydiphenyl at a raised temperature or by treating the diisopropyl ether of a dyestuff of the above general formula with aqueous sulphuric acid. The diisopropyl ether when R is p-phenylene is made by condensing p-isopropoxyaniline with perylene-tetracarboxylic acid anhydride. Examples are given.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH887971X | 1958-12-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB887971A true GB887971A (en) | 1962-01-24 |
Family
ID=4545431
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB41012/59A Expired GB887971A (en) | 1958-12-05 | 1959-12-02 | Dyestuffs of the perylene tetracarboxylic acid diimide series and process for their manufacture |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB887971A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001092420A2 (en) * | 2000-05-29 | 2001-12-06 | Radiant Color N.V. | Perylene dyes with persistent fluorescence caused by steric inhibition of aggregation |
-
1959
- 1959-12-02 GB GB41012/59A patent/GB887971A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001092420A2 (en) * | 2000-05-29 | 2001-12-06 | Radiant Color N.V. | Perylene dyes with persistent fluorescence caused by steric inhibition of aggregation |
WO2001092420A3 (en) * | 2000-05-29 | 2002-06-20 | Radiant Color N V | Perylene dyes with persistent fluorescence caused by steric inhibition of aggregation |
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