CH159855A - Process for the preparation of a trisazo dye. - Google Patents
Process for the preparation of a trisazo dye.Info
- Publication number
- CH159855A CH159855A CH159855DA CH159855A CH 159855 A CH159855 A CH 159855A CH 159855D A CH159855D A CH 159855DA CH 159855 A CH159855 A CH 159855A
- Authority
- CH
- Switzerland
- Prior art keywords
- molecule
- preparation
- dye
- acid
- combined
- Prior art date
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- Coloring (AREA)
Description
Verfahren zur Darstellung ehies Trisazofarbstoffes. Es wurde gefunden, dass ein wertvoller dunkelblauer Trisazofarbstoff entsteht, wenn man ein Molekül Tetrazobenzidin in mineral saurer Lösung mit einem Molekül 1.8-Amino- riaphthol-3.6-disulfosäure kombiniert, das Zwischenprodukt mit einem Molekül Diazo- benzol vereinigt und als Schlussazokomponente 2.8.6-Aminonaphtholsulfosäure in saurer Lö sung verwendet.
<I>Beispiel:</I> 18,4 Teile Benzidin werden in der übli chen Weise tetrazotiert und mit 34,1 Teilen 1..8-Amirioiiaphthol.3.6-disuliosäure (Mono- uatriumsalz) mineralsaurer gekuppelt. Istdie Bildung des Zwischenproduktes beendet, so wird es mit einer Diazobenzollösung aus <B>91ä</B> Teilen Anilin sodaalkalisch vereinigt.
Nach dem Verschwinden des Diazobenzols macht man dieKupplutigmitEssigsäurevor- sichtig sauer und lässt eine kurz vor Gebrauch angesäuerte Lösung von 24 Teilen 2.8.6- Aminonaphtholsulfosäure in<B>300</B> Teilen Was- ser und 15 Teilen Natronlauge 30% zu- fliessen. Die Kupplung geht schnell zu Ende.
Der Farbstoff wird aufgewärmt, mit Soda alkalisch gemacht, ausgesalzen und in übli cher Weise aufgearbeitet.
Die Kupplung kann auch kongosauer aus geführt werden.
Der neue Farbstoff stellt ein grauschwar zes Pulver dar, welches Baumwolle und Seide in alkali- und säureechten blauen Tönen an färbt.
Process for the preparation of this trisazo dye. It has been found that a valuable dark blue trisazo dye is formed when one molecule of tetrazobenzidine in mineral acidic solution is combined with one molecule of 1.8-amino riaphthol-3.6-disulfonic acid, the intermediate product is combined with one molecule of diazobenzene and 2.8.6- is the final azo component. Aminonaphtholsulfonic acid used in acidic solution.
<I> Example: </I> 18.4 parts of benzidine are tetrazotized in the usual way and coupled with 34.1 parts of 1..8-Amirioiiaphthol.3,6-disulioäure (monosodium salt) mineral acid. When the formation of the intermediate product has ended, it is combined with a diazobenzene solution made from parts of aniline in a soda-alkaline manner.
After the diazobenzene has disappeared, the coupling is carefully acidified with acetic acid and a solution, acidified shortly before use, of 24 parts of 2.8.6-aminonaphtholsulfonic acid in 300 parts of water and 15 parts of 30% sodium hydroxide solution is allowed to flow in. The clutch quickly comes to an end.
The dye is warmed up, made alkaline with soda, salted out and worked up in the usual way.
The clutch can also be made from Congo.
The new dye is a gray-black powder which dyes cotton and silk in alkali and acid-fast blue tones.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE159855X | 1931-01-16 | ||
CH157036T | 1931-12-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH159855A true CH159855A (en) | 1933-01-31 |
Family
ID=25716881
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH159855D CH159855A (en) | 1931-01-16 | 1931-12-14 | Process for the preparation of a trisazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH159855A (en) |
-
1931
- 1931-12-14 CH CH159855D patent/CH159855A/en unknown
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