CH106456A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106456A CH106456A CH106456DA CH106456A CH 106456 A CH106456 A CH 106456A CH 106456D A CH106456D A CH 106456DA CH 106456 A CH106456 A CH 106456A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- production
- indigoid dye
- dissolves
- new
- 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 indi- goiden Farbstoff herstellen kann, wenn man das 5-Brom-2,1-thionaphthisatin mit dem 6- Thiophenoläthyläther der Oxythionaphthen- karbonsäure kondensiert. Der Farbstoff stellt ein dunkelbraunes Pulver dar, das sich in Schwefelsäure mit blauer Farbe löst.
Der Farbstoff bildet eine bräunlichgelbe Tiüpe und färbt Baumwolle in echten rotbraunen Tönen.
Beispiel: 293 Teile 5-Brom - 2,1 - thionaphthisatin und 254 Teile 6-Thiophenoläthyläther der Oxythionaphthenkarbonsäure werden mit 4000 Teilen Alkohol versetzt und zum Sie den erhitzt. Nach kurzer Zeit ist die Kon- densatio:n beendigt. Der abgeschiedene Farb- stoff wird abfiltriert, ge-vias,chen und ge trocknet.
Process for the production of an indigoid dye. It has been found that an indigoid dye can be produced if the 5-bromo-2,1-thionaphthisatin is condensed with the 6-thiophenol ethyl ether of oxythionaphthene carboxylic acid. The dye is a dark brown powder that dissolves in sulfuric acid with a blue color.
The dye forms a brownish-yellow veil and dyes cotton in real red-brown tones.
Example: 293 parts of 5-bromine-2,1-thionaphthisatin and 254 parts of 6-thiophenol ethyl ether of oxythionaphthenecarboxylic acid are mixed with 4000 parts of alcohol and heated to you. After a short time, the condensation: n is over. The deposited dye is filtered off, vias, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106456T | 1923-05-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106456A true CH106456A (en) | 1924-09-01 |
Family
ID=25705871
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106456D CH106456A (en) | 1922-11-18 | 1923-05-17 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106456A (en) |
-
1923
- 1923-05-17 CH CH106456D patent/CH106456A/en unknown
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