CH233096A - Process for the preparation of a chromable monoazo dye. - Google Patents
Process for the preparation of a chromable monoazo dye.Info
- Publication number
- CH233096A CH233096A CH233096DA CH233096A CH 233096 A CH233096 A CH 233096A CH 233096D A CH233096D A CH 233096DA CH 233096 A CH233096 A CH 233096A
- Authority
- CH
- Switzerland
- Prior art keywords
- chromable
- preparation
- dye
- orange
- monoazo 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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines ehromierbaren Nönoazofarbstoffes. Es wurde gefunden, dass man wertvolle ehromierbare Monoazofarbstoffe erhält, wenn man diazotierte 2-Aminophenol-6-sulfonsäu- ren, die in 4-Stellung- einen Cycloalkylrest oder einen Alkylrest von 3 bis und mit 8 Kohlenstoffatomen enthalten,
mit Pyrazolo- nen ohne freie Sulfon- und Carbonsäuregrup- pen kuppelt.
Gegenstand vorliegenden Zusatzpatentes ist ein Verfahren zur Herstellung eines chro- mierbaren Monoazofarbstoffes, dadurch ge kennzeichnet, dass man diazotierte 2-Amino- 4-tert.amylphenol-6-sulfonsäure mit 1-Phe- nyl-3-methyl-5-pyrazolon -kuppelt.
Der neue Farbstoff stellt ein rotes Pul ver dar, dessen Lösung in Wasser orange, in Schwefelsäure gelborange gefärbt ist. Er färbt Wolle beim Behandeln mit Chromsal zen in gelbstichig roten Tönen. <I>Beispiel:</I> 26,1 Teile 2-Amino-4-tert.amylphenol-6- sulfonsäure (aus 4-tert.Amylphenol durch Sulfonierung, Nitrierung und Reduktion dar gestellt) werden in üblicher Weise indirekt diazotiert. Die Diazoniumverbindung kuppelt man mit 17,
9 Teilen 1-Phenyl-3-methyl-5- pyrazolon in sodaalkalischer Lösung. Nach Beendigung der Farbstoffbildung wird der Farbstoff ausgesalzen, abfiltriert und ge trocknet. Er wird als rotes Pulver erhalten, das sich in Wasser mit oranger, in konzen trierter Schwefelsäure mit gelboranger Farbe löst.
Aus saurem Bade zieht er auf Wolle beim Nachchromieren in gelbatichig roten Tönen mit guten Nass- und Lichtechtheiten. Färbungen mit den gleichen Eigenschaften werden auch direkt nach dem Einbadchro- mierverfahren erhalten.
Process for the preparation of an honorable nozoazo dye. It has been found that valuable honorable monoazo dyes are obtained if diazotized 2-aminophenol-6-sulfonic acids which contain a cycloalkyl radical or an alkyl radical of 3 to 8 carbon atoms in the 4-position,
couples with pyrazolones without free sulfonic and carboxylic acid groups.
The subject of the present additional patent is a process for the production of a chromable monoazo dye, characterized in that diazotized 2-amino-4-tert-amylphenol-6-sulfonic acid is coupled with 1-phenyl-3-methyl-5-pyrazolone .
The new dye is a red powder, the solution of which is orange in water and yellow-orange in sulfuric acid. It dyes wool in yellowish red shades when treated with chromium salts. <I> Example: </I> 26.1 parts of 2-amino-4-tert-amylphenol-6-sulfonic acid (prepared from 4-tert-amylphenol by sulfonation, nitration and reduction) are diazotized indirectly in the customary manner. The diazonium compound is coupled with 17,
9 parts of 1-phenyl-3-methyl-5-pyrazolone in a soda-alkaline solution. After the formation of the dye has ended, the dye is salted out, filtered off and dried. It is obtained as a red powder which dissolves in water with orange, in concentrated sulfuric acid with a yellow-orange color.
From an acidic bath, he pulls on wool when re-chroming in yellowish red tones with good wet and light fastness properties. Dyes with the same properties are also obtained directly using the single-bath chromating process.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH233096T | 1942-05-16 | ||
CH230906T | 1942-05-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH233096A true CH233096A (en) | 1944-06-30 |
Family
ID=25727521
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH233096D CH233096A (en) | 1942-05-16 | 1942-05-16 | Process for the preparation of a chromable monoazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH233096A (en) |
-
1942
- 1942-05-16 CH CH233096D patent/CH233096A/en unknown
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