CH184182A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH184182A CH184182A CH184182DA CH184182A CH 184182 A CH184182 A CH 184182A CH 184182D A CH184182D A CH 184182DA CH 184182 A CH184182 A CH 184182A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- preparation
- parts
- dye
- oxybenzene
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Gegenstand des Hauptpatentes ist ein Verfahren zur Herstellung eines Azofarb- stoffes, bei dem dianotiertes 5-Nitro-2-amino- I -oxybenzol mit 1-N-Oxätliyl-N-butylamino- 3-methylbenzol gekuppelt wird.
Es wurde nun gefunden, dass man einen wertvollen ähnlichen Azofarbstoff erhält, wenn man die Diazoverbindung des 5-Nitro- 2-amino-l-oxybenzols mit 1-N-Dioxäthyl- amino-3-methylbenzol kuppelt.
Der neue Farbstoff eignet sich vorzüglich zum Färben von Zelluloseestern und -äthern aus wässrigem Bade und liefert hierbei kräf tige fuehsinrote Färbungen, die sich durch besondere Klarheit und gute Lichtechtheit auszeichnen, sowie waschecht und rein weiss ützbar sind; er eignet sich ferner zum Färben von Harz- und Nitrozelluloselacken.
<I>Beispiel:</I> 154 Teile 5-Nitro-2-amino-7.-oxybenzol werden in 6000 Teilen Wasser suspendiert, mit 250 Teilen 3,5%iger Salzsäure versetzt und unter allmählicher Zugabe von 300 Tei len einer 23%igen Natriumnitritlösung dia- zotiert. Die so erhaltene Lösung der Diazo- verbindung wird zu einer Lösung von 205 Teilen 1-N-Dioxyäthylamino-3-methylbenzol in 120 Teilen 35%iger Salzsäure und 1000 Teilen Wasser gegeben. Die Farbstoffbil- <RTI
ID="0001.0037"> dting wird durch Zugabe von 500 Teilen Natriumacetat zu Ende geführt.
Process for the preparation of an azo dye. The subject of the main patent is a process for the production of an azo dye in which dianotated 5-nitro-2-amino-1-oxybenzene is coupled with 1-N-oxethyl-N-butylamino-3-methylbenzene.
It has now been found that a valuable similar azo dye is obtained if the diazo compound of 5-nitro-2-amino-1-oxybenzene is coupled with 1-N-dioxäthylamino-3-methylbenzene.
The new dye is ideally suited for dyeing cellulose esters and ethers from aqueous baths and delivers strong fiery red dyes, which are characterized by particular clarity and good lightfastness, as well as being washable and pure white; it is also suitable for dyeing resin and nitrocellulose lacquers.
<I> Example: </I> 154 parts of 5-nitro-2-amino-7th-oxybenzene are suspended in 6000 parts of water, 250 parts of 3.5% hydrochloric acid are added and, with the gradual addition of 300 parts of a 23 % sodium nitrite solution diacotized. The solution of the diazo compound thus obtained is added to a solution of 205 parts of 1-N-dioxyethylamino-3-methylbenzene in 120 parts of 35% strength hydrochloric acid and 1000 parts of water. The dye image <RTI
ID = "0001.0037"> dting is completed by adding 500 parts of sodium acetate.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE184182X | 1934-03-09 | ||
CH180691T | 1935-02-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH184182A true CH184182A (en) | 1936-05-15 |
Family
ID=25720444
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH184182D CH184182A (en) | 1934-03-09 | 1935-02-06 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH184182A (en) |
-
1935
- 1935-02-06 CH CH184182D patent/CH184182A/en unknown
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