CH232607A - Process for the preparation of a new acidic monoazo dye. - Google Patents
Process for the preparation of a new acidic monoazo dye.Info
- Publication number
- CH232607A CH232607A CH232607DA CH232607A CH 232607 A CH232607 A CH 232607A CH 232607D A CH232607D A CH 232607DA CH 232607 A CH232607 A CH 232607A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- dye
- preparation
- monoazo dye
- reddish
- Prior art date
Links
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- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen sauren Nonoazofarbstoffes. Gegenstand vorliegender Erfindung ist ein Verfahren zur Herstellung eines neuen sauren Monoazofarbstoffes. Erfindungsgemäss wird der neue Farb stoff dadurch hergestellt, dass man N -Äthyl -N,--omeg%- ehlorpropionylamino- 4- aminotoluol diazotiert und die so erhaltene Diazoverbindung mit 2-1blethogyaaetylamino- 5-naphthol-7-sulfonsäure kuppelt.
Der neue Farbstoff stellt ein scharlach rotes Pulver dar, welches sich in Wasser unter Bildung einer rötlichorangen Farbe und in konz. Schwefelsäure unter Bildung einer roten Lösung löst. Der neue Farbstoff färbt Wolle aus einem Schwefelsäure und Glaubersalz enthaltenden Bade in hellen röt- liehorangen Tönen von guter Wasch.-, Walk und Lichtechtheit. Die Erfindung wird durch das folgende Beispiel erläutert. Die Teile bedeuten Ge wichtsteile.
<I>Beispiel:</I> 24 Teile 2-N-Athyl-omega-chlorpropionyl- amino-4-aminotoluol werden in 350 Teilen Wasser, enthaltend 25 Teile 36%iger Salz säure, gelöst. Hierauf wird das Amin durch Zugabe von 6,9 Teilen Natriumnitrit diazo- tiert. Die auf diese Weise erhaltene Diazo- verbindung wird unter Rühren einem gekühl ten Gemisch von 33,3 Teilen Natrium-2-me- thogyacetylamino-5-naphthol-7-sulfonat, 28 Teilen krist. Natriumacetat und 500 Teilen Wasser zugesetzt.
Nach vollendeter Kupp lung wird der neue, ausgefällte Farbstoff ab- filtriert und getrocknet.
Process for the preparation of a new acidic nonoazo dye. The present invention relates to a process for the preparation of a new acidic monoazo dye. According to the invention, the new dye is prepared by diazotizing N -ethyl -N, - omeg% - ehlorpropionylamino- 4-aminotoluene and coupling the diazo compound thus obtained with 2-1blethogyaaetylamino-5-naphthol-7-sulfonic acid.
The new dye is a scarlet red powder, which in water forms a reddish orange color and in conc. Sulfuric acid dissolves to form a red solution. The new dye dyes wool from a bath containing sulfuric acid and Glauber's salt in light reddish-orange shades of good washing, fulling and lightfastness. The invention is illustrated by the following example. The parts mean parts by weight.
<I> Example: </I> 24 parts of 2-N-ethyl-omega-chloropropionyl-amino-4-aminotoluene are dissolved in 350 parts of water containing 25 parts of 36% strength hydrochloric acid. The amine is then diazotized by adding 6.9 parts of sodium nitrite. The diazo compound obtained in this way is, with stirring, a cooled mixture of 33.3 parts of sodium 2-methogyacetylamino-5-naphthol-7-sulfonate, 28 parts of crystalline. Sodium acetate and 500 parts of water were added.
After coupling is complete, the new, precipitated dye is filtered off and dried.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB232607X | 1941-10-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH232607A true CH232607A (en) | 1944-06-15 |
Family
ID=10192773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH232607D CH232607A (en) | 1941-10-08 | 1942-10-07 | Process for the preparation of a new acidic monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH232607A (en) |
-
1942
- 1942-10-07 CH CH232607D patent/CH232607A/en unknown
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