CH117697A - Process for the preparation of a trisazo dye. - Google Patents
Process for the preparation of a trisazo dye.Info
- Publication number
- CH117697A CH117697A CH117697DA CH117697A CH 117697 A CH117697 A CH 117697A CH 117697D A CH117697D A CH 117697DA CH 117697 A CH117697 A CH 117697A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- cleve
- dye
- gray
- coupled
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Trisazofarbstoifes. Es wurde gefunden, dass man zu einem neuen Trisazofarbstoff gelangen kann, wenn man dia.zotiertes o-Toluidin mit 1,6-Naph- thylaminsulfosäure Cleve kuppelt, das Zwi schenprodukt weiter @diazotiert, mit 1,6 NaphthylaminsulfosäureClevekombiniert, er neut dianotiert und mit 1-Phenylamidonaph- tha.Iin-8-sulfosäure kuppelt.
<I>Beispiel</I> 10,7 Teile a-Toluidin werden mit 6,9 Teilen Nitrit dianotiert, mit 22,3 Teilen 1,6- Naphthylaminsulfosäure Cleve kombiniert, der entstandene Monoa.zofarbstoff wird mit 6,9 Teilen Nitrit weiter dianotiert und mit 22,3 Teilen 1,6-Naphthylaminsulfosäure Cleve gekuppelt. Der Disazofarbstoff wird abge schieden, mit 6,9 Teilen Nitrit wieder diano tiert und zum Schluss mit einer Lösung von 32,1 Teilen 1-Phenylamidonaphthalin-8-sulfo- saurem Natrium kombiniert.
Der neue Farbstoff bildet ein grau schwarzes Pulver und färbt Baumwolle licht- und waschecht grau bis schwarz.
Process for the preparation of a trisazo dye. It has been found that a new trisazo dye can be obtained if dia.zotierter o-toluidine is coupled with 1,6-naphthylamine sulfonic acid Cleve, the intermediate product is further @diazotized, combined with 1,6 naphthylamine sulfonic acid Cleve, dianotized again and with 1-Phenylamidonaphtha.Iin-8-sulfonic acid couples.
<I> Example </I> 10.7 parts of α-toluidine are dianotized with 6.9 parts of nitrite, combined with 22.3 parts of 1,6-naphthylamine sulphonic acid Cleve, the resulting monoazo dye is added to 6.9 parts of nitrite dianotized and coupled with 22.3 parts of 1,6-naphthylamine sulfonic acid Cleve. The disazo dye is separated off, dianoed again with 6.9 parts of nitrite and finally combined with a solution of 32.1 parts of 1-phenylamidonaphthalene-8-sulphonic acid sodium.
The new dye forms a gray-black powder and dyes cotton lightfast and washable gray to black.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR117697X | 1924-01-11 | ||
CH114915T | 1926-05-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH117697A true CH117697A (en) | 1926-11-16 |
Family
ID=25708414
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH117697D CH117697A (en) | 1924-01-11 | 1924-11-04 | Process for the preparation of a trisazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH117697A (en) |
-
1924
- 1924-11-04 CH CH117697D patent/CH117697A/en unknown
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