CH106432A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH106432A CH106432A CH106432DA CH106432A CH 106432 A CH106432 A CH 106432A CH 106432D A CH106432D A CH 106432DA CH 106432 A CH106432 A CH 106432A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- new
- dye
- indigoid dye
- acid
- 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, .dass man einen neuen indigoi-den Farbstoff erhält, wenn man das 8-Chlor-2,1-thionaphthisatin (welches erhal ten werden kann durch Kondensieren von 8- Chlor-2-thionaphtho,1 mit Oxalylchlo@rid) mit 6-Chloroxythian.aphthenkarbonsäure konden siert.
Der neue Farbstoff bildet ein dunkelbrau- nes Pulver, löst sich in konzentrierter Schwe felsäure mit .grüner Farbe, gibt mit Hydro- sulfit und Natronlauge eine rotgelbe güpe und erzeugt auf Baumwolle Färbungen, wel che nach .dem Seifen rötlichvioilett und sehr echt gemacht werden.
Beispiel: In 10000 Teile Alkohol werden 248,5 Teile 8-Chlor-2,1-thionaphthis,atin und 228,5 Teile 6 - Chlo-roxythionaphthenkarbonsäure eingetragen und hierauf die Mischung län- gere Zeit Farn Rückflusskühler gekocht. Der gebildete Farbstoff wird filtriert, gewaschen und getrocknet.
Process for the production of a new indigoid dye. It has been found that a new indigo-the dye is obtained if the 8-chloro-2,1-thionaphthisatin (which can be obtained by condensing 8-chloro-2-thionaphtho, 1 with oxalylchloride) condenses with 6-chloroxythianaphthenecarboxylic acid.
The new dye forms a dark brown powder, dissolves in concentrated sulfuric acid with a green color, gives it a red-yellow color with hydrosulphite and caustic soda, and produces colors on cotton that are made reddish-purple and very real after soaping.
Example: 248.5 parts of 8-chloro-2,1-thionaphthis, ateine and 228.5 parts of 6-chloro-roxythionaphthenecarboxylic acid are added to 10,000 parts of alcohol and the mixture is then boiled in a Fern reflux condenser for a long time. The dye formed is filtered, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH100705T | 1922-11-18 | ||
CH106432T | 1922-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106432A true CH106432A (en) | 1924-09-01 |
Family
ID=25705847
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106432D CH106432A (en) | 1922-11-18 | 1922-12-07 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106432A (en) |
-
1922
- 1922-12-07 CH CH106432D patent/CH106432A/en unknown
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