CH176226A - Process for the preparation of an o-oxyazo dye. - Google Patents
Process for the preparation of an o-oxyazo dye.Info
- Publication number
- CH176226A CH176226A CH176226DA CH176226A CH 176226 A CH176226 A CH 176226A CH 176226D A CH176226D A CH 176226DA CH 176226 A CH176226 A CH 176226A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- oxyazo
- bath
- parts
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines o-Ogyazofarbstoffes. Nach dem im Hauptpatent beschützten Verfahren erhält man einen Wolle nach dem Einbad-Chromverfahren echt färbenden Farbstoff, wenn man 4-Nitro-6-chlor-2- amino-l-oxybenzo.1 diazotiert und mit 1-(2'- Naphthyl) - 3 -methyl - 5 -pyrazolon - 6'- sulfo- s aure kuppelt.
Wie nun weiter gefunden wurde, erhält man einen ähnlichen, Wolle nach dem Ein bad-Chromverfahren in granatfarbenen Tönen anfärbenden Farbstoff, wenn man 4-Chlor-5- nitro-2-ainino-1-oxybenzol diazotiert und mit l.-(2'-Naplithyl)-3-methyl-5-pyrazolon-8'-sul- fosäurekuppelt.
<I>Beispiel:</I> Eine aus 18,9 Teilen 4-Chlor-5-nitro-2- amino-l-oxybenzol, 6,9 Teilen Natriumnitrit und 25 Teilen Salzsäure von 12 B6 bereitete Diazoverbindunb wird zu einer kalten Lö sung von 31 Teilen 1-(2'-Naphthyl)-3-methyl- 5-pyrazolan-8'-sulfosäure und 25 Teilen Soda in etwa 1500 Teilen Wasser begeben. Der in üblicher Weise aufgearbeitete Farbstoff ist getrocknet ein dunkles Pulver, welches in Wasser mit roter Farbe löslich ist.
Wolle wird nach dem Einbad-Chromverfahren in granatfarbenen Tönen von guter Wasch- und Walkechtheit angefärbt.
Process for the preparation of an o-ogyazo dye. According to the process protected in the main patent, a dye that really dyes wool by the single-bath chromium process is obtained if 4-nitro-6-chloro-2- amino-l-oxybenzo.1 is diazotized and 1- (2'-naphthyl) - 3-methyl-5-pyrazolone-6'-sulfonic acid couples.
As has now been found, a similar dye is obtained which dyes wool in garnet-colored shades by the one-bath chrome process if 4-chloro-5-nitro-2-ainino-1-oxybenzene is diazotized and l .- (2 ' -Naplithyl) -3-methyl-5-pyrazolone-8'-sulphonic acid coupled.
<I> Example: </I> A diazo compound prepared from 18.9 parts of 4-chloro-5-nitro-2-amino-1-oxybenzene, 6.9 parts of sodium nitrite and 25 parts of hydrochloric acid of 12 B6 is converted into a cold solution solution of 31 parts of 1- (2'-naphthyl) -3-methyl-5-pyrazolane-8'-sulfonic acid and 25 parts of soda in about 1500 parts of water. The dye, worked up in the usual way, is dried, a dark powder which is soluble in water with a red color.
Wool is dyed using the single-bath chrome process in garnet-colored tones with good wash and milled fastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE176226X | 1932-12-07 | ||
CH173738T | 1933-08-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH176226A true CH176226A (en) | 1935-03-31 |
Family
ID=25719406
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH176226D CH176226A (en) | 1932-12-07 | 1933-08-05 | Process for the preparation of an o-oxyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH176226A (en) |
-
1933
- 1933-08-05 CH CH176226D patent/CH176226A/en unknown
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