CH166666A - Process for the preparation of an o-oxyazo dye. - Google Patents
Process for the preparation of an o-oxyazo dye.Info
- Publication number
- CH166666A CH166666A CH166666DA CH166666A CH 166666 A CH166666 A CH 166666A CH 166666D A CH166666D A CH 166666DA CH 166666 A CH166666 A CH 166666A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- oxyazo
- preparation
- parts
- dioxyquinoline
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines o-Oxyazofarbstoffes. Nach dem durch das Hauptpatent ge schützten Verfahren erhält man einen Wolle in Gegenwart von Chrombeizen echt an färbenden Farbstoff, wenn man 4-Chlor-2- diazo-l-oxybenzol-6-sulfosäure mit 7.8-Benzo- 2.4-dioxychinolin kuppelt.
Wie nun weiter gefunden wurde, erhält man einen Farbstoff mit ganz ähnlichen guten Eigenschaften, wenn man 4-1Titro-2-diazo-l- oxybenzol-6-sulfosäure mit 5.6-Benzo-2.4- dioxychinolin kuppelt.
Beispiel: 23,4 Teile 4-Nitro-2-amino-l-oxybenzol-6- sulfosäure werden mit etwa 300 Teilen Wasser angeschlämmt und nach Zusatz von 5 Teilen Salzsäure von 12 B6 mit 6,9 Tei len Natriumnitrit bei<B>100</B> diazotiert. Die fertige Diazoverbindung läuft in eine kalte Lösung von 23 Teilen 5.6-Benzo-2.4-dioxy- chinolin und 6 Teilen Natriumhydroxyd in etwa 500 Teilen Wasser. Nach beendeter Kombination wird der Farbstoff in bekannter Weise aufgearbeitet.
Er stellt in trockenem Zustand ein dunkles Pulver dar und färbt Wolle nach dem Einbad-Chromverfahren in granatfarbenen Tönen von sehr guter Wasch und Walkechtheit an.
Process for the preparation of an o-oxyazo dye. According to the process protected by the main patent ge one obtains a wool in the presence of chrome stains really on coloring dye, if one couples 4-chloro-2-diazo-1-oxybenzene-6-sulfonic acid with 7.8-benzo-2,4-dioxyquinoline.
As has now been further found, a dye with very similar good properties is obtained if 4-1-nitro-2-diazo-l-oxybenzene-6-sulfonic acid is coupled with 5,6-benzo-2,4-dioxyquinoline.
Example: 23.4 parts of 4-nitro-2-amino-1-oxybenzene-6-sulfonic acid are slurried with about 300 parts of water and, after the addition of 5 parts of hydrochloric acid of 12 B6, with 6.9 parts of sodium nitrite at <B> 100 </B> diazotized. The finished diazo compound runs into a cold solution of 23 parts of 5.6-benzo-2.4-dioxyquinoline and 6 parts of sodium hydroxide in about 500 parts of water. When the combination is complete, the dye is worked up in a known manner.
When dry, it is a dark powder and uses the single-bath chrome process to dye wool in garnet-colored shades of very good wash and milled fastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE166666X | 1932-04-18 | ||
CH164201T | 1932-11-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH166666A true CH166666A (en) | 1934-01-15 |
Family
ID=25717942
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH166666D CH166666A (en) | 1932-04-18 | 1932-11-11 | Process for the preparation of an o-oxyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH166666A (en) |
-
1932
- 1932-11-11 CH CH166666D patent/CH166666A/en unknown
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