CH111496A - Process for the preparation of a monoazo dye. - Google Patents
Process for the preparation of a monoazo dye.Info
- Publication number
- CH111496A CH111496A CH111496DA CH111496A CH 111496 A CH111496 A CH 111496A CH 111496D A CH111496D A CH 111496DA CH 111496 A CH111496 A CH 111496A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- parts
- monoazo dye
- bright red
- dye
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
- C09B29/18—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
- C09B29/20—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfuhren zur Darstellung eines 1Honoazofarbstoffes. Es wurde gefunden, dass ein wertvoller roter Farbstoff entsteht, wenn man diazo- tiertes 1- Methyl - 2 - amino -4- benzoylamino- benzol mit 2 . 3-Oxynaphthoesäureanilid kup pelt.
Der Farbstoff bildet getrocknet ein leuch tend rotes Pulver, das sich in konzentrierter Schwefelsäure mit leuchtend rotvioletter Farbe löst. Er liefert sehr lichtechte Farb- lacke und kann auch auf der Faser erzeugt werden, welche blaustichig rot angefärbt wird.
Beispiel: 22,6 Teile 1-Methyl-2-amino-4-benzoyl- aminobenzol werden mit 25 Teilen Salzsäure 90 E6 und 200 Teilen Wasser gelöst und mit einer Lösung von 7 Teilen Nitrit bei 5 diazotiert. Die Diazolösung wird mit essigsaurem Natron kongoneutral gestellt und unter gutem Rühren in eine - aus 26,3 Teilen 2 . 3 - Oxynaphthoesäureanilid, 15 Teilen Natronlauge 30 % und 20 Teilen rizinusölsulfosaurem Natron mit 400 Teilen Wasser hergestellte Lösung eingegossen.
Nach beendigter Kupplung wird , der aus geschiedene Farbstoff filtriert, gewaschen und vorteilhaft als Paste verwendet.
Procedure for the preparation of a 1Honoazo dye. It has been found that a valuable red dye is formed when diazotized 1-methyl-2-amino -4-benzoylamino-benzene is mixed with 2. 3-oxynaphthoic anilide kup pelt.
When dried, the dye forms a bright red powder that dissolves in concentrated sulfuric acid with a bright red-violet color. It provides very lightfast colored lacquers and can also be produced on the fiber, which is colored red with a bluish tinge.
Example: 22.6 parts of 1-methyl-2-amino-4-benzoylaminobenzene are dissolved with 25 parts of hydrochloric acid 90 E6 and 200 parts of water and diazotized at 5 with a solution of 7 parts of nitrite. The diazo solution is made Congo-neutral with sodium acetate and, with thorough stirring, in one of 26.3 parts 2. 3 - Oxynaphthoic anilide, 15 parts of sodium hydroxide solution 30% and 20 parts of castor oil sulfonic acid of sodium with 400 parts of water poured the solution prepared.
After the coupling is complete, the separated dye is filtered, washed and advantageously used as a paste.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH109706T | 1924-05-22 | ||
CH111496T | 1924-05-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH111496A true CH111496A (en) | 1925-08-17 |
Family
ID=25707606
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH111496D CH111496A (en) | 1924-05-22 | 1924-05-22 | Process for the preparation of a monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH111496A (en) |
-
1924
- 1924-05-22 CH CH111496D patent/CH111496A/en unknown
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