CH106433A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106433A CH106433A CH106433DA CH106433A CH 106433 A CH106433 A CH 106433A CH 106433D A CH106433D A CH 106433DA CH 106433 A CH106433 A CH 106433A
- 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
- C09B7/12—Other thionaphthene indigos
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Yerfahren zur Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, dass man einen neuen indigoiden Farbstoff erhält, wenn man das 1- Chlar-2,3-thionaphthisatin (welches erhalten werden kann durch Kondensieren von 1- Chlor-2-thionaphthol mit Oxalylchlorid) mit Acenaphthenon kondensiert.
Der neue Farbstoff bildet ein blaurotes Pulver, löst sich in konzentrierter Schwefel säure mit grüner Farbe, gibt mit Hydrosulfit und Natronlauge eine braungelbe Küpe und erzeugt auf Baumwolle Färbungen, welche nach dem Seifen heliotrop und sehr echt werden.
Beispiel: <B>293</B> Teile 1- Chlor - 2,3 - thionaphthisatin und 168 Teile Acenaphthenon werden in 2000 Teilen Chlorbenzol suspendiert. Nach Zugabe von 200 Teilen Chlorzink wird längere Zeit zum schwachen Sieden erhitzt. Der sich ab scheidende Farbstoff wird filtriert.
Process for the production of a new indigoid dye. It has been found that a new indigoid dye is obtained when 1-chloro-2,3-thionaphthisatin (which can be obtained by condensing 1-chloro-2-thionaphthol with oxalyl chloride) is condensed with acenaphthenone.
The new dye forms a blue-red powder, dissolves in concentrated sulfuric acid with a green color, gives a brown-yellow vat with hydrosulfite and sodium hydroxide solution and produces dyes on cotton which become heliotropic and very real after soaking.
Example: 293 parts 1-chloro-2,3-thionaphthisatin and 168 parts acenaphthenone are suspended in 2000 parts of chlorobenzene. After adding 200 parts of zinc chloride, the mixture is heated to a gentle boil for a long time. The dye which separates out is filtered off.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106433T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106433A true CH106433A (en) | 1924-09-01 |
Family
ID=25705848
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106433D CH106433A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106433A (en) |
-
1922
- 1922-12-07 CH CH106433D patent/CH106433A/en unknown
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