CH151335A - Process for the production of a new vat dye. - Google Patents
Process for the production of a new vat dye.Info
- Publication number
- CH151335A CH151335A CH151335DA CH151335A CH 151335 A CH151335 A CH 151335A CH 151335D A CH151335D A CH 151335DA CH 151335 A CH151335 A CH 151335A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- vat dye
- dye
- new vat
- 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 Ifferstellung eines neuen Küpenfarbstoffes. Es -wurde gefunden, dass man einen neuen Küpenfarbstoff erhält, wenn man das p-Di- methylaminoanil des 5-Methyl-6-chlorthio- indoxyls mit 1-Chlor-2,3-naphththioindoxyl kondensiert.
Der neue Farbstoff der Formel
EMI0001.0010
stellt ein violettblaues Pulver dar, das sich in konzentrierter Schwefelsäure mit grüner Farbe löst. Er gibt mit Hydrosulfit und Natronlauge eine gelbgefärbte Küpe, aus der Baumwolle in sehr echten violetten Tönen gefärbt wird.
<I>Beispiel:</I> <B>330</B> Teile p-Dimethylaininoanil des 5- Methyl-6-chloi,thioindoxyls und<B>235</B> Teile 1-Ohlor-2,3-naphththioindoxyl werden in 12,000 Teilen Benzol suspendiert und wäh rend einiger Stunden unter Rühren und Rück- flusskühlung zum Sieden erhitzt. Hierauf wird von ausgeschiedenem Farbstoff filtriert, mit Benzol gewaschen und getrocknet.
Process for producing a new vat dye. It has been found that a new vat dye is obtained when the p-dimethylaminoanil of 5-methyl-6-chlorothioindoxyl is condensed with 1-chloro-2,3-naphthioindoxyl.
The new dye in the formula
EMI0001.0010
is a purple-blue powder that dissolves in concentrated sulfuric acid with a green color. With hydrosulfite and caustic soda, he gives a yellow-dyed vat from which cotton is dyed in very real purple tones.
<I> Example: </I> <B> 330 </B> parts of p-dimethylaininoanil des 5-methyl-6-chloi, thioindoxyl and <B> 235 </B> parts of 1-chloro-2,3-naphthioindoxyl are suspended in 12,000 parts of benzene and heated to boiling for a few hours with stirring and reflux cooling. The dye which has separated out is then filtered off, washed with benzene and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH151335T | 1931-07-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH151335A true CH151335A (en) | 1931-12-15 |
Family
ID=4406636
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH151335D CH151335A (en) | 1931-07-25 | 1930-08-08 | Process for the production of a new vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH151335A (en) |
-
1930
- 1930-08-08 CH CH151335D patent/CH151335A/en unknown
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