CH194666A - Process for the preparation of a leather dye. - Google Patents
Process for the preparation of a leather dye.Info
- Publication number
- CH194666A CH194666A CH194666DA CH194666A CH 194666 A CH194666 A CH 194666A CH 194666D A CH194666D A CH 194666DA CH 194666 A CH194666 A CH 194666A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- leather
- preparation
- leather dye
- main
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Lederfarbstoffes. Nach dem im schweizerischen Haupt patent Nr.189871 beschriebenen. Verfahren erhält man einen Leder in echten Tönen an färbenden Farbstoff, wenn man 4'-Nitro- 4-aminodiph.enylamin-2'-sufosäure diazotiert und die Diazoverbin.dung mit 1.
2-Ogybenzol kuppelt, dass man weiterhin 4-Nitro-l-amino- benzol diazotiert und diese Diazoverbindung mit dem vorgängig erhaltenen Monoazofarb- stoff weiterkuppelt.
Wie nun weiter gefunden: wurde, kann man den so erhaltenen Farbstoff in seinen Eigenschaften verbessern, wenn man ihn in. wä.ssriger alkalischer Lösung mit Verbindun gen des zweiwertigen Kupfers nachbehandelt.
<I>Beispiel:</I> In die gemäss dem Beispiel des Haupt- patentes Nr. 189871 erhaltene Farbstoff lösung lässt man unter Erwärmen bei Gegen wart von überschüssiger Soda oder bei Ge genwart von Ammoniak eine Lösung von 50 Teilen krist. Kupfersulfat zulaufen.
Der Farbstoff wird dann in der üblichen Weise ausgesalzen. Er färbt Chromleder und vege tabilisch gegerbtes Leder in etwas gedeckte- ren, in den Echtheiten: verbesserten Tönen an, als der Ausgangsfarbstoff.
Process for the preparation of a leather dye. According to the one described in the main Swiss patent number 189871. In the process, leather is obtained in real shades of dyestuff if 4'-nitro-4-aminodiph.enylamine-2'-sulfonic acid is diazotized and the diazo compound with 1.
2-Ogybenzene is coupled by further diazotizing 4-nitro-1-aminobenzene and coupling this diazo compound with the previously obtained monoazo dye.
As has now also been found, the properties of the dye thus obtained can be improved if it is aftertreated in an aqueous alkaline solution with compounds of divalent copper.
<I> Example: </I> In the dye solution obtained according to the example of the main patent no. 189871, a solution of 50 parts of crystalline is allowed to form under heating in the presence of excess soda or in the presence of ammonia. Copper sulphate.
The dye is then salted out in the usual way. It dyes chrome leather and vegetable tanned leather in slightly more muted, fastness: better shades than the original dye.
Claims (1)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE194666X | 1934-12-21 | ||
DE160235X | 1935-02-16 | ||
DE200735X | 1935-07-20 | ||
CH193082T | 1935-09-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH194666A true CH194666A (en) | 1937-12-15 |
Family
ID=27429696
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH194666D CH194666A (en) | 1934-12-21 | 1935-09-12 | Process for the preparation of a leather dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH194666A (en) |
-
1935
- 1935-09-12 CH CH194666D patent/CH194666A/en unknown
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