CH147041A - Process for the preparation of an azo dye. - Google Patents
Process for the preparation of an azo dye.Info
- Publication number
- CH147041A CH147041A CH147041DA CH147041A CH 147041 A CH147041 A CH 147041A CH 147041D A CH147041D A CH 147041DA CH 147041 A CH147041 A CH 147041A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- azo dye
- dye
- diazo compound
- oxynaphthalene
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Azofarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Azofarb- atoffes, dadurch gekennzeichnet, dass man die Diazoverbindung von 4=Amino-3-methylbexa- hydrodiphenyl mit 1-Toluolsulfamino-8-oxy- naphtalin-3.6-disulfosäure kuppelt. Der so erhaltene Farbstoff färbt Wolle in klaren, roten Tönen an.
Beispiel: Eine salzsaure Lösung von 18,9 kg 4- Amino-3-methylhexahydrodiphenyl in etwa 80 Liter heissem Wasser wird in eine Mischung von 20 Liter Salzsäure (spez. Gewicht<B>=</B> 1,155) und Eis zugegeben. Die so entstandene Suspension wird mit einer Lösung von 6,9 kg Natriumnitrit in etwa 50Liter Wasser bei etwa 5-10<B>0</B> diazotiert, wobei die Diazoverbindung in Lösung geht.
Die so erhaltene Diazover- bindung kuppelt man bei etwa<B>10'</B> mit einer Lösung von 50 kg 1-toluolsulfami o-8-oxy- naphtalin-3.6-disulfosaurem Natrium und 30 kg Soda.
Process for the preparation of an azo dye. The present patent relates to a process for the production of an azo carbate, characterized in that the diazo compound of 4 = amino-3-methylbexa-hydrodiphenyl is coupled with 1-toluenesulfamino-8-oxynaphthalene-3,6-disulfonic acid. The dye thus obtained stains wool in clear, red shades.
Example: A hydrochloric acid solution of 18.9 kg of 4-amino-3-methylhexahydrodiphenyl in about 80 liters of hot water is added to a mixture of 20 liters of hydrochloric acid (specific weight <B> = </B> 1.155) and ice. The resulting suspension is diazotized with a solution of 6.9 kg of sodium nitrite in about 50 liters of water at about 5-10 <B> 0 </B>, the diazo compound going into solution.
The diazo compound obtained in this way is coupled at about 10 'with a solution of 50 kg of 1-toluenesulfami, 8-oxynaphthalene-3.6-disulfonic acid and 30 kg of sodium carbonate.
Claims (1)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE147041X | 1928-06-16 | ||
CH144302T | 1929-06-10 | ||
DE280628X | 1948-10-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH147041A true CH147041A (en) | 1931-05-15 |
Family
ID=27177167
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH147041D CH147041A (en) | 1928-06-16 | 1929-06-10 | Process for the preparation of an azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH147041A (en) |
-
1929
- 1929-06-10 CH CH147041D patent/CH147041A/en unknown
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