CH106435A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106435A CH106435A CH106435DA CH106435A CH 106435 A CH106435 A CH 106435A CH 106435D A CH106435D A CH 106435DA CH 106435 A CH106435 A CH 106435A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- production
- dye
- indigoid dye
- orange
- 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 Herstellung eines neuen indigoiden Farbstoffes. Es wurde gefunden, dass man einen neuen indgoiden Farbstoff erhält, wenn man .das 7-Chlor-2,1-thionaphthisatin (welches erhal ten werden kann durch Kondensseren von 7- Chlor-2-thionaphthol mit Ox:alylchlorid) mit Acenaphthenon kondensiert.
Der neue Farbstoff bildet ein .orangerotes Pulver, löst sich in konzentrierter Schwefel säure mit olivgrüner Farbe, gibt mit Hydro- sulfit und Natronlauge eine gelbbraune Küpe und erzeugt auf Baumwolle Färbungen, wel che nach dem Seifen orange und sehr echt werden.
<I>Beispiel:</I> 248,5 Teile 7-Chlar-2,1-thianaphthis,a in arid 168 Teile Acenaphthenon werden in 2000 Teilen Chlorbenzol suspendiert. Nach Zu gabe von 200 Teilen Chlorzink wird längere Zeit zum sch-,vachen Sieden erhitzt. Der sich abscheidende Farbstoff wird filtriert.
Process for the production of a new indigoid dye. It has been found that a new indgoid dye is obtained if the 7-chloro-2,1-thionaphthisatin (which can be obtained by condensing 7-chloro-2-thionaphthol with Ox: alyl chloride) is condensed with acenaphthenone.
The new dye forms an orange-red powder, dissolves in concentrated sulfuric acid with an olive-green color, gives a yellow-brown vat with hydrosulphite and caustic soda and creates dyes on cotton that turn orange and very fast after soaking.
<I> Example: </I> 248.5 parts of 7-chloro-2,1-thianaphthis, a in arid 168 parts of acenaphthenone are suspended in 2000 parts of chlorobenzene. After adding 200 parts of zinc chloride, the mixture is heated to low boiling 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 | ||
CH106435T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106435A true CH106435A (en) | 1924-09-01 |
Family
ID=25705850
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106435D CH106435A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106435A (en) |
-
1922
- 1922-12-07 CH CH106435D patent/CH106435A/en unknown
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