CH106453A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106453A CH106453A CH106453DA CH106453A CH 106453 A CH106453 A CH 106453A CH 106453D A CH106453D A CH 106453DA CH 106453 A CH106453 A CH 106453A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- indigoid dye
- dye
- new indigoid
- 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 neuen indigoiden Farbstoffes. Es wurde gefunden, da.ss ein neuer, wert- voller, indigoider Farbstoff entstellt, wenn man das 2,3-Naphththi.o@indoxyl mit Thio- n.aphthenchinon-p-dimethyl,amino-2-anil kon densiert.
Der neue Farbstoff stellt ein violettblaues Pulver dar, das sich in Schwefelsäure mit rotblauer Farbe löst. Er bildet eine braun orange IMpe und färbt Baumwolle in helio- trop Tönen von sehr guter Echtheit.
<I>Beispiel:</I> 200 Teile 2,3-Naphththioindoxyl und 282 Teile Thion.apl@thenchinon-p-climethylamzno- 2-anil werden in' 5000 Teilen Alkohol suspen diert und, nachdem 5 Teile Soda zugegeben sind, unter Rühren zum Kochen erhitzt. Das Reaktionsprodukt scheidet sich sofort in braunroten Kristallen ab. Nach dem Erkal ten wird filtriert, mit Alkohol gewaschen und der in sehr guter Ausbeute erhaltene Farbgtoff getrocknet. .
Process for the production of a new indigoid dye. It has been found that a new, valuable, indigoid dye is distorted if the 2,3-naphththi.o @ indoxyl is condensed with thion-naphthenquinone-p-dimethyl, amino-2-anil.
The new dye is a violet-blue powder that dissolves in sulfuric acid with a red-blue color. It forms a brown-orange IMpe and dyes cotton in heliotropic shades of very good fastness.
<I> Example: </I> 200 parts of 2,3-naphththioindoxyl and 282 parts of Thion.apl@thenchinon-p-climethylamzno- 2-anil are suspended in 5000 parts of alcohol and, after 5 parts of soda are added, under Stir heated to a boil. The reaction product separates out immediately in brownish red crystals. After cooling, it is filtered, washed with alcohol and the dye obtained in very good yield is dried. .
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106453T | 1923-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106453A true CH106453A (en) | 1924-09-01 |
Family
ID=25705868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106453D CH106453A (en) | 1922-11-18 | 1923-03-29 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106453A (en) |
-
1923
- 1923-03-29 CH CH106453D patent/CH106453A/en unknown
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