CH198320A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH198320A CH198320A CH198320DA CH198320A CH 198320 A CH198320 A CH 198320A CH 198320D A CH198320D A CH 198320DA CH 198320 A CH198320 A CH 198320A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- production
- new azo
- new
- dye
- Prior art date
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
- C09B29/32—Monoazo dyes prepared by diazotising and coupling from coupling components containing a reactive methylene group
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbatoff erhält, wenn man diazotiertes 1-Amino-2-methyl-4-nitrobenzol mit dem Arylid, das erhalten wird durch Kondensieren von 5-Aminophenyl-pseudo-azimidobenzol mit Acetessigester, vereinigt.
Der neue @ Farbstoff bildet ein gelbes, in Wasser unlösliches Pulver. Auf geeigneten Substraten, wie z. B. Baumwolle, hergestellt, färbt er diese in echten gelben Tönen. <I>Beispiel:</I> 15,2 Teile 1-Amino-2-methyl-4-nitrobenzol werden wie üblich diazotiert Lind in eine Lösung von 29,4 Teilen des Kondensations produktes aus 5-Aminophenyl-pseudo-azimido- benzol mit Acetessigester, 100 Teilen Natrium hydroxydlösung von<B>360</B> Bö,<B>16</B> Teilen Na- triumacetat und 2000 Teilen Wasser einge tragen.
Der gebildete gelbe Farbstoff fällt sofort aus. Er wird filtriert, und getrocknet.
Process for the production of a new azo dye. It has been found that a new azo carbate is obtained when diazotized 1-amino-2-methyl-4-nitrobenzene is combined with the arylide, which is obtained by condensing 5-aminophenyl-pseudo-azimidobenzene with acetoacetic ester.
The new @ dye forms a yellow, water-insoluble powder. On suitable substrates, such as. B. cotton, he dyes them in real yellow tones. <I> Example: </I> 15.2 parts of 1-amino-2-methyl-4-nitrobenzene are diazotized as usual and in a solution of 29.4 parts of the condensation product of 5-aminophenyl-pseudo-azimidobenzene with acetoacetic ester, 100 parts of sodium hydroxide solution of <B> 360 </B> Bo, <B> 16 </B> parts of sodium acetate and 2000 parts of water.
The yellow dye formed precipitates immediately. It is filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH195072T | 1936-07-14 | ||
CH198320T | 1936-07-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH198320A true CH198320A (en) | 1938-06-15 |
Family
ID=25722722
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH198320D CH198320A (en) | 1936-07-14 | 1936-07-14 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH198320A (en) |
-
1936
- 1936-07-14 CH CH198320D patent/CH198320A/en unknown
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