CH109641A - Process for the production of a new vat dye. - Google Patents
Process for the production of a new vat dye.Info
- Publication number
- CH109641A CH109641A CH109641DA CH109641A CH 109641 A CH109641 A CH 109641A CH 109641D A CH109641D A CH 109641DA CH 109641 A CH109641 A CH 109641A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- vat dye
- dye
- new vat
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B49/00—Sulfur dyes
- C09B49/12—Sulfur dyes from other compounds, e.g. other heterocyclic compounds
- C09B49/128—Sulfur dyes from other compounds, e.g. other heterocyclic compounds from hydroxy compounds of the benzene or naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Nüpenfarbstoffes. Es wunde gefunden, dass man einen neuen Küpenfarbstoff erhält, wenn man Schwefel ehlorür auf 2,5-Di.-p-oxyanilidobenzochinon bei niedrigen Temperaturen einwirken lässt. Die Reaktion wird zweckmässig in Gegenwart. von Verdünnungsmitteln, wie Nitrobenzol, gegebenenfalls in Gegenwart von säurebin denden Mitteln, durchgeführt.
Der neue Farbstoff bildet ein rötlichbraunes Pulver, das sich in konzentrierter Schwefelsäure mit blauer Farbe löst und Wolle aus :der Hydro- sulfitküpe in echten gelben Nuancen färbt. Beispiel: 8 Teile 2,5-Di-p-oxyanvlid:obenzocMnon, suspendiert in 120 Teilen Nitrobenzol, wer den bei 2 bis- 6 unter gutem Rühren mit 10,1 Teilen Sehwefelehlorür (SZCl2) versetzt.
Nach längerem. Rühren wird filtriert, ge waschen und ,getrocknet.
Process for the production of a new pebble dye. It was found that a new vat dye is obtained if sulfur chloride is allowed to act on 2,5-di.-p-oxyanilidobenzoquinone at low temperatures. The reaction is conveniently carried out in the presence. of diluents such as nitrobenzene, optionally in the presence of acid-binding agents carried out.
The new dye forms a reddish-brown powder that dissolves in concentrated sulfuric acid with a blue color and turns wool: the hydrosulfite vat dyes real yellow nuances. Example: 8 parts of 2,5-di-p-oxyanvlid: obenzocMnon, suspended in 120 parts of nitrobenzene, who added 10.1 parts of sulfuric acid (SZCl2) at 2 to 6 with thorough stirring.
After a long time. Stirring is filtered, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH108932T | 1923-10-27 | ||
CH109641T | 1923-11-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH109641A true CH109641A (en) | 1925-04-01 |
Family
ID=25707484
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH109641D CH109641A (en) | 1923-10-27 | 1923-11-17 | Process for the production of a new vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH109641A (en) |
-
1923
- 1923-11-17 CH CH109641D patent/CH109641A/en unknown
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