CH118722A - Process for the preparation of a vat dye. - Google Patents
Process for the preparation of a vat dye.Info
- Publication number
- CH118722A CH118722A CH118722DA CH118722A CH 118722 A CH118722 A CH 118722A CH 118722D A CH118722D A CH 118722DA CH 118722 A CH118722 A CH 118722A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- blue
- vat dye
- vat
- dye
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Nüpenfarbstoffes. Es wurde gefunden, dass man einen wert vollen Küpeirfarbstoff erhält, der sich in konzentrierter Schwefelsäure mit weinroter Farbe löst und auf Baumwolle aus rein blauer Küpe eine blaue Färbung liefert, die bei der Oxydation an der Luft in ein leuch tendes grünstichiges Blau übergeht, wenn man Bzl-Halogen-Bz2-methoxybenzanthron mit alkalischen Kondensationsmitteln behandelt. Der Farbstoff zeichnet sich durch hervor ragende Schönheit der Nuance und durch gute Echtheitseigenschaften aus.
Beispiel 7 Teile Bz1-Chlor-Bz2-methoxyberrzanthron (erhältlich zum Beispiel durch Behandeln des entsprechenden Bz2-Oxybenzatrthronmethyl- äthers mit Sulfurylchlorid in Nitrobenzollösung oder durch Methylieren des durch Chlorieren von Bz2 - Oxyberrzanthron erhältlichen Bzl- Chlor-Bz2-okybetrzartthrorrs) werden bei<B>135</B> bis 140<B>0</B> in eine Schmelze aus 28 Teilen Kaliumhydroxyd und 28 Teilen Alkohol ein getragen.
Das Gemisch rührt man etwa eine Stunde bei 145 bis<B>150</B> , verdünnt sodann die Schmelze mit Wasser, kocht auf und bläst den entstandenen Farbstoff mit. Luft aus. Sodann wird filtriert, neutral gewaschen und angepastet.
Process for the preparation of a pebble dye. It has been found that a valuable vat dye is obtained which dissolves in concentrated sulfuric acid with a wine-red color and provides a blue dye on cotton from a pure blue vat, which turns into a bright greenish blue when oxidized in the air Bzl-Halogen-Bz2-methoxybenzanthrone treated with alkaline condensation agents. The dyestuff is distinguished by the outstanding beauty of the shade and good fastness properties.
Example 7 parts of Bz1-chloro-Bz2-methoxyberrzanthrone (obtainable, for example, by treating the corresponding Bz2-oxybenzatrthrone methyl ether with sulfuryl chloride in nitrobenzene solution or by methylating the Bzl-chloro-Bz2-ors > 135 </B> to 140 <B> 0 </B> in a melt of 28 parts of potassium hydroxide and 28 parts of alcohol.
The mixture is stirred for about an hour at 145 to 150, then the melt is diluted with water, boiled and the resulting dye is blown with it. Air out. It is then filtered, washed neutral and made into a paste.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE118722X | 1924-12-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH118722A true CH118722A (en) | 1927-01-17 |
Family
ID=5655708
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH118722D CH118722A (en) | 1924-12-13 | 1925-11-23 | Process for the preparation of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH118722A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4565415A (en) * | 1983-08-25 | 1986-01-21 | Advance Transformer Co. | Socket for fluorescent lamps |
-
1925
- 1925-11-23 CH CH118722D patent/CH118722A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4565415A (en) * | 1983-08-25 | 1986-01-21 | Advance Transformer Co. | Socket for fluorescent lamps |
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