CH101091A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH101091A CH101091A CH101091DA CH101091A CH 101091 A CH101091 A CH 101091A CH 101091D A CH101091D A CH 101091DA CH 101091 A CH101091 A CH 101091A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- light
- indigoid dye
- dye
- wash
- 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 P a tentes Nr. 93486, mit Oxythionaphtenkarbon- sä ure kondensiert.
Der Farbstoff bildet ein dunkles Pulver, löst sich in konzentrierter Schwefelsäure mit dunkelblaugrüner Farbe und gibt mit Hydrosulfit und Natronlauge eine gelbe Küpe, aus welcher Wolle in licht- und waschechten roten, Baumwolle in sehr licht-, wasch- und chlorechten Bordeaux Tö nen gefärbt wird.
<I>Beispiel:</I> In 7000 Teilen Alkohol werden 214 Teile B-Thionaphtisatin und 194 Teile Oxythio- naphtenkarbonsäure eingetragen und hierauf einige Stunden am Rückflusskühler gekocht. Die Kondensation kann durch Zusatz von Ammoniak oder Dimethylanilin beschleunigt werden. Nachdem sie beendet ist, wird fil triert, 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-thionaphthisatin, obtained for example by the process of Patent No. 93486, is condensed with oxythionaphthenecarboxylic acid.
The dye forms a dark powder, dissolves in concentrated sulfuric acid with a dark blue-green color and, with hydrosulphite and caustic soda, gives a yellow vat, from which wool is dyed in light- and washfast red, cotton in very light-, wash- and chlorine-fast Bordeaux tones .
<I> Example: </I> 214 parts of B-thionaphthisatin and 194 parts of oxythiononaphthenecarboxylic acid are added to 7000 parts of alcohol and 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 |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH101091T | 1922-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH101091A true CH101091A (en) | 1923-12-17 |
Family
ID=25705814
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH101091D CH101091A (en) | 1922-11-18 | 1922-11-18 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH101091A (en) |
-
1922
- 1922-11-18 CH CH101091D patent/CH101091A/en unknown
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