CH202750A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH202750A CH202750A CH202750DA CH202750A CH 202750 A CH202750 A CH 202750A CH 202750D A CH202750D A CH 202750DA CH 202750 A CH202750 A CH 202750A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye
- azo
- nitrobenzene
- 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
- C09B29/06—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)
- Coloring (AREA)
Description
Verfahren zur Rerstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen Azo- farbstoff erhält, wenn man die Diazoverbin- duug des 1-Amino-4-nitrobenzol-2-m6thylsul- fons mit (2-Ätlioxy-5-metllyl-29'-sulionsäuxe- 6'- chlor <B>-</B> 4'- chloracatylamino) <B>-</B> diplionylamin der Formel
EMI0001.0016
vereinigt.
Der neue Farbstoff bildet ein dunkles Pulver, das sich in Wasser mit roter Farbe löst und das Wolle und Seide aus sau rem Bade in -violetten Tönen färbt <I>Beispiel:</I> <B>216</B> Teile 1:- A-mino-4-nitrobenzol-2-methyl- sulfon werden diazotiert und in die mineral saure Lösung dieser Diazoverbindung die Lösung des NatriumsaIzes aus 433 Teilen (2-Ätlic>xy- 5-methyl-2'-sulfonsäure-6'- chlor- V- chloracotylamiuo,) <B>-</B> diplienylamin eingetra gen.
Nachdem die Farbstoffbildung beendet ist, wird abfiltriert, der Farbstoff in Wasser suspendiert und durch Verrühren mit einem Alkali neutral gestellt. Der Farbstoff wird eventuell durch Zusatz -eines Salzes ausge schieden, abfiltriert und getrocknet.
Process for the preparation of an azo dye. It has been found that an azo dye is obtained if the diazo compound of 1-amino-4-nitrobenzene-2-methylsulfone is used with (2-Ätlioxy-5-metllyl-29'-sulionsäuxe- 6'- chlorine <B> - </B> 4'- chloracatylamino) <B> - </B> diplionylamine of the formula
EMI0001.0016
united.
The new dye forms a dark powder that dissolves in water with a red color and colors the wool and silk from acid baths in violet tones <I> Example: </I> <B> 216 </B> Part 1: - A-mino-4-nitrobenzene-2-methyl-sulfone are diazotized and in the mineral acid solution of this diazo compound the solution of the sodium salt of 433 parts (2-Ätlic> xy- 5-methyl-2'-sulfonic acid-6'- chlor- V- chloracotylamiuo,) <B> - </B> diplienylamine entered.
After the formation of the dye has ended, it is filtered off, the dye is suspended in water and neutralized by stirring with an alkali. The dye is possibly separated out by adding a salt, filtered off and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH202750T | 1937-03-15 | ||
CH200063T | 1938-11-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH202750A true CH202750A (en) | 1939-01-31 |
Family
ID=25723423
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH202750D CH202750A (en) | 1937-03-15 | 1937-03-15 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH202750A (en) |
-
1937
- 1937-03-15 CH CH202750D patent/CH202750A/en unknown
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