CH159861A - Process for the production of an indigoid dye of the anthraquinone series. - Google Patents
Process for the production of an indigoid dye of the anthraquinone series.Info
- Publication number
- CH159861A CH159861A CH159861DA CH159861A CH 159861 A CH159861 A CH 159861A CH 159861D A CH159861D A CH 159861DA CH 159861 A CH159861 A CH 159861A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- indigoid dye
- anthraquinone series
- anthraquinone
- 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
<B>Zusatzpatent</B> zum Hauptpatent Nr: 156120. Verfahren zur Herstellung eines indigoiden Farbstoffes der Anthrachinonreihe. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines indigoiden Farbstoffes der Anthrachinonreihe, dadurch gekennzeichnet, dass man ein ? . 1-Naphtoxy- thiophenanil mit Anthra.chinon-1 . 2-oxythio- phen kondensiert.
Das dunkelbraun gefärbte Pulver löst sich in konzentrierter Schwefelsäure mit blaugrüner Farbe. Aus der gelbroten güpe färbi, dieser Farbstoff Baumwolle braun.
Beispiel: 80 Teile 2. 1-Naphtoxythiophen-2'-(p-di- iiiethylamino)-anil werden in etwa 2000 Tei- Ien Eisessig mit 70 Teilen Anthraehinon- 1 . ?-oxythiohhen 6 bis 7 Stunden auf<B>100</B> bis 105 erhitzt. Der Farbstoff wird ab gesaugt und getrocknet.
<B> Additional patent </B> to main patent no: 156120. Process for the production of an indigoid dye of the anthraquinone series. The present patent relates to a process for the preparation of an indigoid dye of the anthraquinone series, characterized in that one? . 1-naphthoxy-thiophenanil with anthraquinone-1. 2-oxythiophene condensed.
The dark brown colored powder dissolves in concentrated sulfuric acid with a blue-green color. From the yellow-red güpe färbi, this dye is cotton brown.
Example: 80 parts of 2. 1-naphthoxythiophene-2 '- (p-di-iiethylamino) -anil are mixed with about 2,000 parts of glacial acetic acid with 70 parts of anthraquinone-1. ? -oxythiohhen heated to <B> 100 </B> to 105 hours for 6 to 7 hours. The dye is sucked off and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH159861T | 1931-04-02 | ||
CH156120T | 1931-04-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH159861A true CH159861A (en) | 1933-01-31 |
Family
ID=25716706
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH159861D CH159861A (en) | 1931-04-02 | 1931-04-02 | Process for the production of an indigoid dye of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH159861A (en) |
-
1931
- 1931-04-02 CH CH159861D patent/CH159861A/en unknown
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