CH190321A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH190321A CH190321A CH190321DA CH190321A CH 190321 A CH190321 A CH 190321A CH 190321D A CH190321D A CH 190321DA CH 190321 A CH190321 A CH 190321A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new azo
- new
- parts
- 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
<B>Zusatzpatent</B> zum Hauptpatent Nr. 186550. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man diazotiertes 1-Aminobenzol-2-dimethylsulfainid mit 2. 3 Oxynaphthoesäure - 2', 5' - dimethoxy-4'-chlor- anilid vereinigt. Der neue Farbstoff bildet ein scharlachrotes, in Wasser unlösliches Pulver. Auf geeigneten Substraten, wie zum Beispiel Zellulose, hergestellt, färbt er diese in rotorangen Tönen von sehr guten Echt heitseigenschaften.
Beispiel: 20 Teile 1 Aminobenzol-2-dimethylsulf- amid werden mit 40 Teilen konz. Salzsäure und 200 Teilen Wasser verrührt und mit einer Lösung von 7 Teilen Natriumnitrit in üblicher Weise diazotiert. Die klare Diazo- lösung lässt man in eine Lösung von 35,7 Tei len 2. 3 - Oxynaphthoesäure-2',5'-dimethoxy- 4'-chloranilid in 40 Teilen 30 % iger Natrium- hydroxydlösung und 1000 Teilen Wasser einlaufen.
Der gebildete Farbstoff fällt sofort aus als scharlachrot gefärbter Niederschlag. Er wird filtriert und getrocknet.
<B> Additional patent </B> to main patent No. 186550. Process for the production of a new azo dye. It has been found that a new azo dye is obtained when diazotized 1-aminobenzene-2-dimethylsulfainide is combined with 2, 3-oxynaphthoic acid - 2 ', 5' - dimethoxy-4'-chloroanilide. The new dye forms a scarlet powder that is insoluble in water. Produced on suitable substrates, such as cellulose, for example, it colors them in red-orange tones with very good fastness properties.
Example: 20 parts of 1 aminobenzene-2-dimethylsulfamide are mixed with 40 parts of conc. Stirred hydrochloric acid and 200 parts of water and diazotized in the usual way with a solution of 7 parts of sodium nitrite. The clear diazo solution is allowed to run into a solution of 35.7 parts of 2,3-oxynaphthoic acid-2 ', 5'-dimethoxy-4'-chloroanilide in 40 parts of 30% sodium hydroxide solution and 1000 parts of water.
The dye formed falls out immediately as a scarlet colored precipitate. It is filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH190321T | 1936-01-17 | ||
CH186550T | 1936-01-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH190321A true CH190321A (en) | 1937-04-15 |
Family
ID=25721380
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH190321D CH190321A (en) | 1936-01-17 | 1936-01-17 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH190321A (en) |
-
1936
- 1936-01-17 CH CH190321D patent/CH190321A/en unknown
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