CH223709A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH223709A CH223709A CH223709DA CH223709A CH 223709 A CH223709 A CH 223709A CH 223709D A CH223709D A CH 223709DA CH 223709 A CH223709 A CH 223709A
- 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/12—Disazo dyes in which the coupling component is a heterocyclic compound
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 2207"51. Verfahren zur Iier stellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man 1 Mol der Diphenyl-4',4"-di-(3-methyl-5-pyrazo- lon)-2',2"-disulfonsäure mit 2 Mol der Diazo- verbindung des 1-Amino-2-chlorbenzols ver einigt.
Der neue Farbstoff stellt ein gelbes Pulver dar, das Wolle aus saurem Bade in reinen gelben Tönen von bemerkenswerter Wasch echtheit färbt.
<I>Beispiel:</I> Man löst 12,7 Teile 1-Amino-2-chlor- benzol in 90 Teilen Salzsäure von 10 % , kühlt durch Zufügen von Eis auf 0 und di- azotiert mit einer Lösung von 7 Teilen Na triumnitrit in 30 Teilen Wasser.
Diese Diazo- lösung giesst man in eine mit Eis gekühlte Lösung von 25,3 Teilen Diphenyl-4',4"-di- (8-methyl-5-pyrazolon)-2',2"-disulfonsäure in 200 Teilen Wasser und 18 Teilen Natrium- carbonat. Nach beendigter Kupplung wird der Farbstoff ausgesalzen, filtriert und ge trocknet.
<B> Additional patent </B> to the main patent No. 2207 "51. Process for Iier position of a new azo dye. It has been found that a new azo dye is obtained if 1 mol of the diphenyl-4 ', 4" -di- (3-methyl-5-pyrazolone) -2 ', 2 "-disulfonic acid combined with 2 moles of the diazo compound of 1-amino-2-chlorobenzene.
The new dye is a yellow powder that dyes wool from an acid bath in pure yellow shades that are remarkably fast to wash.
<I> Example: </I> 12.7 parts of 1-amino-2-chlorobenzene are dissolved in 90 parts of 10% hydrochloric acid, the mixture is cooled to 0 by adding ice and diacotized with a solution of 7 parts of Na trium nitrite in 30 parts of water.
This diazo solution is poured into a solution, cooled with ice, of 25.3 parts of diphenyl-4 ', 4 "-di (8-methyl-5-pyrazolone) -2', 2" -disulfonic acid in 200 parts of water and 18% Share sodium carbonate. After the coupling is complete, the dye is salted out, filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH223709T | 1941-03-29 | ||
CH220751T | 1941-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH223709A true CH223709A (en) | 1942-09-30 |
Family
ID=25726496
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH223709D CH223709A (en) | 1941-03-29 | 1941-03-29 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH223709A (en) |
-
1941
- 1941-03-29 CH CH223709D patent/CH223709A/en unknown
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