CH202751A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH202751A CH202751A CH202751DA CH202751A CH 202751 A CH202751 A CH 202751A CH 202751D A CH202751D A CH 202751DA CH 202751 A CH202751 A CH 202751A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- dye
- diphenylamine
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Es wurde gefunden, dass man einen Azo- farbstoff erhält, wenn man die Diazoverbin- dung des 1-Amino-4-nitrobenzol-2-benzylsul- fons mit (2-Äthogy-5-methyl-2'-sulfonsäure- 6' - chlor - 4'- chloracetylanüno)
- diphenylamin der Formel
EMI0001.0017
vereinigt. Der neue Farbstoff bildet ein dunkles Pulver, das sich in Wasser mit rot violetter Farbe löst und das Wolle und Seide aus saurem Bade in violetten Tönen färbt.
Beispiel: 292 Teile 1-Amino-4-nitrobenzol-2=benzyl- sulfon werden diazotiert und in die mineral- saure Lösung dieser Diazoverbindung die Lösung des Natriumsalzes aus 4$ä Teilen (2-Athogy-5-methyl -2'-sulfonsäure-6'- chlor- (' - chloracetylamino) - diphenylamin 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-benzylsulfone is used with (2-ethogy-5-methyl-2'-sulfonic acid-6 '- chlorine - 4'- chloroacetylanüno)
- diphenylamine of the formula
EMI0001.0017
united. The new dye forms a dark powder that dissolves in water with a red-purple color and dyes the wool and silk from acid baths in purple tones.
Example: 292 parts of 1-amino-4-nitrobenzene-2-benzylsulfone are diazotized and the solution of the sodium salt of 4 parts (2-Athogy-5-methyl-2'-sulfonic acid) is added to the mineral acid solution of this diazo compound -6'- chloro- ('- chloracetylamino) - diphenylamine 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 |
---|---|---|---|
CH202751T | 1937-03-15 | ||
CH200063T | 1938-11-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH202751A true CH202751A (en) | 1939-01-31 |
Family
ID=25723424
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH202751D CH202751A (en) | 1937-03-15 | 1937-03-15 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH202751A (en) |
-
1937
- 1937-03-15 CH CH202751D patent/CH202751A/en unknown
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