CH127529A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH127529A CH127529A CH127529DA CH127529A CH 127529 A CH127529 A CH 127529A CH 127529D A CH127529D A CH 127529DA CH 127529 A CH127529 A CH 127529A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- red
- monoazo dye
- dye
- color
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Paper (AREA)
Description
Verfahren zur Darstellung eines Monoazofarbstoffes. Es wurde gefunden, dass ein wertvoller roter Monoazofarbstoff entsteht, wenn man die Diazoverbindung der 1-Amino-2-sulfo-4- chlorbenzol-5-carbonsäure mit ,B-Naphtol kombiniert.
Beispiel: 50,8 kg 1-Amino-2-sulfo-4-chlorbenzol-5- carbonsäure werden in 1000 Liter Wasser verteilt und nach Zusatz von 25 kg Salz säure 30 %ig mit 13,8 kg Natriumnitrit di- azotiert bei<B>10'.</B> In die mit Natronlauge gegen Kongopapier fast neutral gemachte Diazoverbindung läuft eine Lösung von 29, kg ss-Naphtol mit 8 kg Natriumhydroxyd in<B>MM</B> Liter Wasser. Nach beendeter Kupplung wird der Farbstoff mit 25 kg Soda in Lösung gebracht und mit Chlorkalium ausgefällt, filtriert und getrocknet.
Der Farbstoff stellt ein leuchtend rotes Pulver dar, löslich in Wasser mit orange Farbe, in konzentrierter Schwefelsäure mit fuchsinroter Farbe. Seine Calcium- und Ba riumverbindungen sind leuchtend rote Lacke von grosser Schönheit und ausgezeichneter Lichtechtheit.
Process for the preparation of a monoazo dye. It has been found that a valuable red monoazo dye is formed when the diazo compound of 1-amino-2-sulfo-4-chlorobenzene-5-carboxylic acid is combined with B-naphthol.
Example: 50.8 kg of 1-amino-2-sulfo-4-chlorobenzene-5-carboxylic acid are distributed in 1000 liters of water and, after addition of 25 kg of hydrochloric acid, 30% diacotized with 13.8 kg of sodium nitrite at <B > 10 '. </B> A solution of 29 kg ss-naphthol with 8 kg sodium hydroxide in <B> MM </B> liters of water runs into the diazo compound, which has been made almost neutral to Congo paper with sodium hydroxide. After coupling has ended, the dye is dissolved in 25 kg of soda and precipitated with potassium chloride, filtered and dried.
The dye is a bright red powder, soluble in water with an orange color, in concentrated sulfuric acid with a fuchsin red color. Its calcium and barium compounds are bright red lacquers of great beauty and excellent lightfastness.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE127529X | 1926-07-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH127529A true CH127529A (en) | 1928-09-01 |
Family
ID=5662109
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH127529D CH127529A (en) | 1926-07-29 | 1927-07-08 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH127529A (en) |
-
1927
- 1927-07-08 CH CH127529D patent/CH127529A/en unknown
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