CH101092A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH101092A CH101092A CH101092DA CH101092A CH 101092 A CH101092 A CH 101092A CH 101092D A CH101092D A CH 101092DA CH 101092 A CH101092 A CH 101092A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- light
- red
- indigoid 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
- C09B7/00—Indigoid dyes
- C09B7/10—Bis-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden Farbstoffes. Es wurde gefunden, dass man einen wert vollen indigoiden Farbstoff herstellen kann, wenn man das ss-Thionaphtisatin, beispiels weise erhalten nach dem Verfahren des Pa tentes Nr. 93486, mit 6-Chioroxythionaphten- karbonsäure kondensiert. Der Farbstoff bil det ein dunkles Pulver, löst sich in konzen trierter Schwefelsäure mit dunkelblaugrüner Farbe und gibt mit Hydrosulfit und Natron lauge eine gelbe Küpe, aus welcher Wolle in licht- und waschechten roten, Baumwolle in sehr licht-, wasch- und chlorechten braun roten Tönen gefärbt wird.
Beispiel: In 7000 Teilen Alkohol werden 214 Teile P-Thionaphtisatin und 228,5 Teile 6-Chlor- oxythionaplitenkarbonsäure eingetragen und hierauf einige Stunden am Rückflusskühler gekocht. Die Kondensation kann durch Zu satz von Ammoniak oder Dimethylanilin be schleunigt werden. Nachdem sie beendet ist, wird filtriert, gewaschen und getrocknet.
Process for the production of an indigoid dye. It has been found that a valuable indigoid dye can be produced if the β-thionaphtisatin, for example obtained by the process of Patent No. 93486, is condensed with 6-chloroxythionaphthenecarboxylic acid. The dye forms a dark powder, dissolves in concentrated sulfuric acid with a dark blue-green color and, with hydrosulfite and caustic soda, gives a yellow vat, from which wool in light- and wash-fast red, cotton in very light-, wash- and chlorine-fast brown-red Tones is colored.
Example: 214 parts of P-thionaphtisatin and 228.5 parts of 6-chlorooxythionaplitic acid are added to 7000 parts of alcohol and the mixture is then boiled for a few hours on the reflux condenser. The condensation can be accelerated by adding ammonia or dimethylaniline. After it is finished, it is filtered, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH101092T | 1922-11-18 | ||
CH100705T | 1922-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH101092A true CH101092A (en) | 1923-12-17 |
Family
ID=25705815
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH101092D CH101092A (en) | 1922-11-18 | 1922-11-18 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH101092A (en) |
-
1922
- 1922-11-18 CH CH101092D patent/CH101092A/en unknown
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