CH138773A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH138773A CH138773A CH138773DA CH138773A CH 138773 A CH138773 A CH 138773A CH 138773D A CH138773D A CH 138773DA CH 138773 A CH138773 A CH 138773A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- dye
- indigoid dye
- indigoid
- methyl
- 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 befunden, dass man einen in- digoiden Farbstoff herstellen kann, wenn man ein a-Ketomonoanil des Thion.aphthen- chinons mit 1-Methyl-2,3-nap.hthooxythio- phen kondensiert.
Der erhaltene Farbstoff stellt ein dunkel blaues Pulver dar, das sich in konzentrierter Schwefelsäure mit grünoliver Farbe löst. Es bildet eine orangebraune Kvipe. Daraus wird Baumwolle in grauer Nuance von sehr guter Echtheit gefärbt.
Beispiel: 21,4 Teile 1-Methyl-2,3-naphthooxythio- phen werden mit 28,2 Teilen Thionaphthen- chinon-p-dimethylamide-anil in 400 Teilen Eisessig suspendiert und einige Stunden rückfliessend gekocht. Hierauf wird filtriert, mit Alkohol gewaschen und .der Farbstoff ge trocknet.
Process for the production of an indigoid dye. It has been found that an indigo dye can be produced by condensing an α-ketomonoanil of thion.aphthene-quinone with 1-methyl-2,3-nap.hthooxythiophene.
The dye obtained is a dark blue powder which dissolves in concentrated sulfuric acid with a green-olive color. It forms an orange-brown kvipe. From this, cotton is dyed in a gray shade of very good fastness.
Example: 21.4 parts of 1-methyl-2,3-naphthooxythiophene are suspended with 28.2 parts of thionaphthene-quinone-p-dimethylamide-anil in 400 parts of glacial acetic acid and refluxed for a few hours. It is then filtered, washed with alcohol and the dye is dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH138773T | 1927-11-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH138773A true CH138773A (en) | 1930-03-15 |
Family
ID=25705878
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH138773D CH138773A (en) | 1922-11-18 | 1927-11-17 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH138773A (en) |
-
1927
- 1927-11-17 CH CH138773D patent/CH138773A/en unknown
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