CH182400A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH182400A CH182400A CH182400DA CH182400A CH 182400 A CH182400 A CH 182400A CH 182400D A CH182400D A CH 182400DA CH 182400 A CH182400 A CH 182400A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye
- violet
- diogypropyl
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Azofarbstofes. Es wurde gefunden, dass man durch Diano tierung und Kupplung von 5-Chlor-2,4-di- nitranilin mit Äthyl-,Q,r-diogypropyl-m-tolui- din einen schwerlöslichen Azofarbstoff erhält, der sehr wertvolle Eigenschaften besitzt.
Er färbt Lacke und Acetatseide lichtecht violett; die gefärbte Faser besitzt sehr gute Echt heitseigenschaften und ist rein weiss ätzbar. <I>Beispiel:</I> 217,5 Teile 5-Chlor-2,4-dinitranilin werden mit der berechneten Menge Nitrosylschwefel- säure in konzentriert schwefelsaurer Lösung dianotiert, auf Eis gegossen und die verdünnte Diazoniumlösung mineralsauer mit 209 Teilen Äthyl-ss,r-diogypropyl-m-toluidin gekuppelt.
Nach kurzer Zeit ist die Farbstoffbildung beendet; das Kupplungsprodukt wird in üblicher Weise isoliert, neutral gewaschen, vergastet oder, nach dem Trocknen bei mässiger Temperatur, zu einem Färbepräparat umgearbeitet. Der Farbstoff, ein in Wasser unlösliches, dunkles Pulver, löst sich in Alkohol oder ähnlichen, organischen Lösungs mitteln mit violetter, in konzentrierter Schw e- felsäure mit roter Farbe.
Process for the preparation of an azo dye. It has been found that by dialing and coupling 5-chloro-2,4-di-nitroaniline with ethyl-, Q, r-diogypropyl-m-toluidine, a sparingly soluble azo dye is obtained which has very valuable properties.
It dyes lacquers and acetate silk lightfast violet; the dyed fiber has very good fastness properties and can be etched in pure white. <I> Example: </I> 217.5 parts of 5-chloro-2,4-dinitraniline are dianotized with the calculated amount of nitrosylsulfuric acid in concentrated sulfuric acid solution, poured onto ice and the diluted diazonium solution is minerally acidic with 209 parts of ethyl ss , r-diogypropyl-m-toluidine coupled.
After a short time, the dye formation is complete; the coupling product is isolated in the usual way, washed neutral, gasified or, after drying at a moderate temperature, worked into a dye preparation. The dye, a dark powder that is insoluble in water, dissolves in alcohol or similar organic solvents with a purple color, in concentrated sulfuric acid with a red color.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE182400X | 1934-04-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH182400A true CH182400A (en) | 1936-02-15 |
Family
ID=5718091
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH182400D CH182400A (en) | 1934-04-09 | 1935-04-01 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH182400A (en) |
-
1935
- 1935-04-01 CH CH182400D patent/CH182400A/en unknown
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