CH109642A - Process for the production of a new vat dye. - Google Patents
Process for the production of a new vat dye.Info
- Publication number
- CH109642A CH109642A CH109642DA CH109642A CH 109642 A CH109642 A CH 109642A CH 109642D A CH109642D A CH 109642DA CH 109642 A CH109642 A CH 109642A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- vat dye
- new vat
- dye
- 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)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Küpenfarbstoffes. Es wurde gefunden, dass man einen neuen Küpenfarbstoff erhält, wenn 'man Schwefel- chlorür auf 2,55-Dianilido-6-chlorbenzochinon bei niedrigen Temperaturen einwirken lässt. Die Reaktion wird zweckmässig irr Gegen wart von Verdünnungsmitteln, wie Nitroben-, zol, gegebenenfalls in Gegenwart von säure bindenden Mitteln, durchgeführt.
Der neue Farbstoff bildet ein bräunlich gelbes, kristal- linisches Pulver, das sich in konzentrierter Schwefelsäure mit violetter Farbe löst und Wolle aus der Hydrosulfitküpe in echten gelb braunen Nuancen färbt.
<I>Beispiel:</I> 8 Teile 2,5-Diarrilido-6-chlorberrzochinon, suspendiert in 160 Teilen Nitrobenzol. wer den bei 2-6 unter gutem Rühren mit 10,1 Teilen Schwefelchlorür (S2C1s) versetzt. Nach längerem Rühren wird filtriert, gewaschen und getrocknet.
Process for the production of a new vat dye. It has been found that a new vat dye is obtained if chlorine sulfur is allowed to act on 2,55-dianilido-6-chlorobenzoquinone at low temperatures. The reaction is expediently carried out in the presence of diluents such as nitrobenzene, zene, if appropriate in the presence of acid-binding agents.
The new dye forms a brownish-yellow, crystalline powder that dissolves in concentrated sulfuric acid with a violet color and dyes wool from the hydrosulfite vat in real yellow-brown shades.
<I> Example: </I> 8 parts of 2,5-diarrilido-6-chloroberzoquinone, suspended in 160 parts of nitrobenzene. who added 10.1 parts of sulfur chloride (S2C1s) at 2-6 with thorough stirring. After prolonged stirring, it is filtered, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH108932T | 1923-10-27 | ||
CH109642T | 1923-11-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH109642A true CH109642A (en) | 1925-04-01 |
Family
ID=25707485
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH109642D CH109642A (en) | 1923-10-27 | 1923-11-17 | Process for the production of a new vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH109642A (en) |
-
1923
- 1923-11-17 CH CH109642D patent/CH109642A/en unknown
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