CH266278A - Process for the preparation of an o, o'-dioxyazo dye. - Google Patents
Process for the preparation of an o, o'-dioxyazo dye.Info
- Publication number
- CH266278A CH266278A CH266278DA CH266278A CH 266278 A CH266278 A CH 266278A CH 266278D A CH266278D A CH 266278DA CH 266278 A CH266278 A CH 266278A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- dioxyazo
- preparation
- propyloxyamino
- diazotized
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 7
- 239000000975 dye Substances 0.000 claims description 6
- YCTAOQGPWNTYJE-UHFFFAOYSA-N 3-amino-5-chloro-2-hydroxybenzenesulfonic acid Chemical compound NC1=CC(Cl)=CC(S(O)(=O)=O)=C1O YCTAOQGPWNTYJE-UHFFFAOYSA-N 0.000 claims description 3
- 239000000843 powder Substances 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- AXDJCCTWPBKUKL-UHFFFAOYSA-N 4-[(4-aminophenyl)-(4-imino-3-methylcyclohexa-2,5-dien-1-ylidene)methyl]aniline;hydron;chloride Chemical compound Cl.C1=CC(=N)C(C)=CC1=C(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 AXDJCCTWPBKUKL-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- 210000002268 wool Anatomy 0.000 claims description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims 1
- 238000007747 plating Methods 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 241001366278 Leptotes marina Species 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000008049 diazo compounds Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
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
<B>Verfahren</B> zur <B>Herstellung eines</B> o,o'-Dioxyazofarbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines o,o'-Dioxy- azofarbstoffes. Das Verfahren ist dadurch ge kennzeichnet, dass man diazotierte 4-Chlor-2- amino-phenol-6-sulfonsäure in alkalischem Me dium mit 1-Carbo-propyloxyamino-7-napht-hol kuppelt.
Der so erhaltene neue Farbstoff ist ein vio- lettschwarzes Pulver, das sich in Wasser mit. marineblauer, in konzentrierter Schwefelsäure mit fuchsinroter Farbe löst. Er färbt. nach dem Einbadehromierverfahren auf Wolle blaustichig graue Töne von hervorragender Lichtechtheit.
Beispiel: 44,7 Teile 4-Chlor-2-amino-phenol-6-sulfon- säure werden wie üblich diazotiert und die Diazoverbindung in eine Lösung von 49 Tei- IPn 1-Carbo-propyloxyamino-7-naphthol in 500 Teile Wasser, 22 Teile Natronlauge 40 % ig und 30 Teile calc. Soda einlaufen gelassen. Der gebildete Farbstoff fällt als dunkles Pul ver aus und wird abfiltriert.
<B> Process </B> for <B> producing </B> an o, o'-dioxyazo dye. The subject of the present patent is a process for the production of an o, o'-dioxy azo dye. The process is characterized in that diazotized 4-chloro-2-aminophenol-6-sulfonic acid is coupled with 1-carbo-propyloxyamino-7-naphthol in an alkaline medium.
The new dye obtained in this way is a violet-black powder that dissolves in water with. marine blue, dissolves in concentrated sulfuric acid with a fuchsin red color. He colors. blue-tinged gray tones of excellent lightfastness after the incorporation process on wool.
Example: 44.7 parts of 4-chloro-2-aminophenol-6-sulfonic acid are diazotized as usual and the diazo compound is dissolved in a solution of 49 parts of 1-carbo-propyloxyamino-7-naphthol in 500 parts of water, 22 parts of 40% sodium hydroxide solution and 30 parts of calc. Soda poured in. The dye formed precipitates out as a dark powder and is filtered off.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH241414T | 1944-02-21 | ||
| CH266278T | 1944-02-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH266278A true CH266278A (en) | 1950-01-15 |
Family
ID=25728590
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH266278D CH266278A (en) | 1944-02-21 | 1944-02-21 | Process for the preparation of an o, o'-dioxyazo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH266278A (en) |
-
1944
- 1944-02-21 CH CH266278D patent/CH266278A/en unknown
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