CH206732A - Process for the production of an indigoid vat dye. - Google Patents
Process for the production of an indigoid vat dye.Info
- Publication number
- CH206732A CH206732A CH206732DA CH206732A CH 206732 A CH206732 A CH 206732A CH 206732D A CH206732D A CH 206732DA CH 206732 A CH206732 A CH 206732A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- vat dye
- indigoid
- dye
- indigoid 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
- C09B7/00—Indigoid dyes
- C09B7/06—Indone-thionapthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden üüpenfarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines indigoiden Küpenfarbstoffes, dadurch gekennzeichnet, dass man 5-Methoxy-6,7-dichlorisatin mit 2,1-Naphthoxythiophen kondensiert.
Der so erhaltene Farbstoff ist ein brau nes Pulver, das sich in Schwefelsäure mit violetter Farbe löst, und färbt Baumwolle aus gelber güpe in braunen Tönen von guten Echtheitseigenschaften, insbesondere von be merkenswerter Lichtechtheit.
Beispiel: 24,6 Teile 5-Methoxy-6,7-.dichlorisatin werden mit 20 Teilen 2,1-Naphthoxythiophen in etwa 100 Teilen Eisessig etwa eine Stunde auf etwa 100 erhitzt. Nach dem Erkalten wird der so gebildete Farbstoff abfiltriert, ausgewaschen und getrocknet.
Process for the production of an indigoid liquid dye. The present patent relates to a process for the production of an indigoid vat dye, characterized in that 5-methoxy-6,7-dichloroisatin is condensed with 2,1-naphthoxythiophene.
The dye obtained in this way is a brown powder which dissolves in sulfuric acid with a violet color, and dyes cotton from yellow güpe in brown shades of good fastness properties, in particular of remarkable light fastness.
Example: 24.6 parts of 5-methoxy-6,7-dichloroisatin are heated to about 100 for about one hour with 20 parts of 2,1-naphthoxythiophene in about 100 parts of glacial acetic acid. After cooling, the dye thus formed is filtered off, washed out and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH206732T | 1938-07-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH206732A true CH206732A (en) | 1939-08-31 |
Family
ID=4445189
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH206732D CH206732A (en) | 1938-07-05 | 1938-07-05 | Process for the production of an indigoid vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH206732A (en) |
-
1938
- 1938-07-05 CH CH206732D patent/CH206732A/en unknown
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