CH150308A - Process for the preparation of a substantive polyazo dye. - Google Patents
Process for the preparation of a substantive polyazo dye.Info
- Publication number
- CH150308A CH150308A CH150308DA CH150308A CH 150308 A CH150308 A CH 150308A CH 150308D A CH150308D A CH 150308DA CH 150308 A CH150308 A CH 150308A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- acid
- naphthylamine
- dianotized
- diazo compound
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines substautiveai PolyazofarbstofFes. Es wurde gefunden, dass man zu einem wertvollen Substantiven Polyazofarbstoff ge langt, wenn man die Diazoverbindung von 2-Naphtylamin-4.8-disulfosäure mit a-Naph- tylamin kuppelt, den so erhaltenen Farbstoff dianotiert, die Diazoverbindung mit 1-Naph- tylamin-7-sulfosäure kuppelt,
den erhaltenen Disazofarbstoff abermals dianotiert und schliess lich seine Diazoverbindung in alkalischer Lösung mit dem Monoazofarbstoff vereinigt, welcher durch Kupplung von dianotierter Metanilsäure mit 2.5-Aminonaphtol-7-mono- sulfosäure in saurer Lösung erhalten wird.
überschüssiger Soda versetzte Lösung des Farbstoffes eingetragen, welcher durch saurf, Kupplung von 17,3 Teilen dianotierter Meta- nilsäure mit 24 Teilen 2.5-Aminonaphtol-7- monosulfosäure in saurer Lösung erhalten wurde. Nach beendeter Kupplung wird auf geheizt und ausgesalzen.
Der erhaltene Farbstoff ist ein dunkel- bronziges Pulver, welches in Wasser mit blauer, in konzentrierter Schwefelsäure mit blauschwarzer Farbe löslich ist. Er färbt auf Baumwolle ein grünliches Blau von ausge zeichneter Lichtechtheit. <I>Beispiel:</I> 30,3 Teile 2-Aminönaphtalin-4.8-disulfo- säure werden dianotiert und in bekannter Weise mit 15 Teilen a-Naphtylamin gekup pelt. Der erhaltene Farbstoff wird weiter dianotiert und mit 24,5 Teilen 1-naphtyl- amin-7-sulfosaurem Natron kombiniert.
Man isoliert den Farbstoff und dianotiert nochmals weiter. Der "#azokörper wird in eine -mit
Process for the preparation of a substautive polyazo dye. It has been found that a valuable noun polyazo dye is obtained if the diazo compound of 2-naphthylamine-4,8-disulfonic acid is coupled with a-naphthylamine, the dye thus obtained is dianotized and the diazo compound with 1-naphthylamine-7 -sulfonic acid couples,
the disazo dye obtained is dianotized again and finally its diazo compound is combined in alkaline solution with the monoazo dye, which is obtained by coupling dianotated metanilic acid with 2,5-aminonaphthol-7-monosulfonic acid in acidic solution.
Excess soda added solution of the dye, which was obtained by acidic coupling of 17.3 parts of dianotized metanilic acid with 24 parts of 2,5-aminonaphthol-7-monosulfonic acid in acidic solution. After the coupling is complete, the system is heated up and salted out.
The dye obtained is a dark bronze powder which is soluble in water with a blue color and in concentrated sulfuric acid with a blue-black color. It dyes cotton a greenish blue with excellent lightfastness. <I> Example: </I> 30.3 parts of 2-aminonaphthalene-4,8-disulfonic acid are dianotized and coupled in a known manner with 15 parts of a-naphthylamine. The dye obtained is further dianotized and combined with 24.5 parts of 1-naphthylamine-7-sulfonic acid sodium.
The dye is isolated and dianotized again. The "# azo body is in a -with
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE150308X | 1929-11-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH150308A true CH150308A (en) | 1931-10-31 |
Family
ID=5673832
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH150308D CH150308A (en) | 1929-11-29 | 1930-11-10 | Process for the preparation of a substantive polyazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH150308A (en) |
-
1930
- 1930-11-10 CH CH150308D patent/CH150308A/en unknown
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