CH101096A - Process for the production of an indigoid dye. - Google Patents
Process for the production of an indigoid dye.Info
- Publication number
- CH101096A CH101096A CH101096DA CH101096A CH 101096 A CH101096 A CH 101096A CH 101096D A CH101096D A CH 101096DA CH 101096 A CH101096 A CH 101096A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- indigoid dye
- light
- dye
- brown
- 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
- C09B7/12—Other thionaphthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Tierstellung eines indigoiden Farbstoffes. Es wurde gefunden, dass man einen wert vollen, indigoiden Farbstoff herstellen kann, wenn man das ss-Thionaphtisatin, beispiels weise erhalten nach dem Verfahren des Pa tentes Nr. 93486, mit Acenaphtenon konden siert.
Der Farbstoff bildet ein dunkles Pul ver, löst sich in konzentrierter Schwefelsäure mit braunvioletter Farbe und gibt mit Hy- drosulfit und Natronlauge eine olivegrüne Iiüpe, aus welcher Wolle in licht- und wasch echten braunen, Baumwolle in sehr licht-, wach- und chlorechten, rotbraunen Tönen befärbt wird.
<I>Beispiel:</I> 6.1 Teile ss-Thionaphtisatin, 51 Teile Acenaphtenon, 6 Teile Zinkchlorid werden mit 700 Teilen Chlorbenzol längere Zeit am R.ückflusskühler gekocht. Nach dem Erkal ten wird filtriert, der Rückstand wird nach- einander mit Alkohol, mit Natronlauge und wieder mit Alkohol gewaschen und dann getrocknet.
Process for the production of an indigoid dye. It has been found that a valuable, indigoid dye can be produced if the ss-thionaphtisatin, for example obtained by the process of Patent No. 93486, is condensed with acenaphtenone.
The dye forms a dark powder, dissolves in concentrated sulfuric acid with a brownish-violet color and, with hydrosulphite and sodium hydroxide solution, gives an olive-green shade, from which wool in light- and washable brown, cotton with very light-, wax- and chlorine-rights, red-brown tones.
<I> Example: </I> 6.1 parts of ss-thionaphtisatin, 51 parts of acenaphtenone, 6 parts of zinc chloride are boiled with 700 parts of chlorobenzene on a reflux condenser for a long time. After cooling, it is filtered, the residue is washed successively with alcohol, with sodium hydroxide solution and again with alcohol and then dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH101096T | 1922-11-18 | ||
CH100705T | 1922-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH101096A true CH101096A (en) | 1923-12-17 |
Family
ID=25705819
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH101096D CH101096A (en) | 1922-11-18 | 1922-11-18 | Process for the production of an indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH101096A (en) |
-
1922
- 1922-11-18 CH CH101096D patent/CH101096A/en unknown
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