CH170326A - Process for the preparation of a chromium-containing azo dye. - Google Patents
Process for the preparation of a chromium-containing azo dye.Info
- Publication number
- CH170326A CH170326A CH170326DA CH170326A CH 170326 A CH170326 A CH 170326A CH 170326D A CH170326D A CH 170326DA CH 170326 A CH170326 A CH 170326A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- oxynaphthalene
- chromium
- acid
- containing azo
- 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
Zusatzpatent zum Hauptpatent Nr. <B>166497.</B> Verfahren zur Herstellung eines ehromhaltigen Azofarbstoffes. Es wurde gefunden, dass man einen chrom- haltigen Azofarbstoff durch Einwirkung des ehromhaltigen Azofarbstoffes, der durch Cht-o- mieren des Azofarbstoffes aus nitrierterl-Diazo- 2-oxynaphtbaliii-4-sulfoi)
säure unid 2-Oxynaph- thalin entsteht, auf den Azofarbstoff aus di- azotierter 1-Amino-2-oxynaphthaliii-4-sulfon- säure und 1-Oxynaplithaliii erhalten kann, wenn diese Einwirkung in alkalischem Medium ei-folgt.
Der neue chromhaltige Azofarbstoff wird als schwarzes Pulver erhalten, das sich in Wasser leicht mit violettschwarzer Farbe löst und das Wolle aus organischsaurem-schwefel- saurem Bade in schwarzen Tönen von vorzüg lichen Eehtheiten färbt.
<I>Beispiel:</I> Der aus<B>92,2'</B> Teilen des Azofarbstoffes aus nitrierter 1-Diazo-2-oxynaphthalin-4-sul- fonsäure und 2-Oxynaphthalin in saurem Me dium hergestellte chromierte Farbstoff wird zusammen mit 41,6 Teilen des Azofarbstoffes aus diazotierter 1-Amino-2-oxynaphthalin-4- sulfonsäure und 1-Oxynaphthalin und einer Lösung von 1200 Teilen Wasser, 200 Teilen 30 %iger Natronlange,
sowie <B>5</B> Teilen Zucker 4 Stunden am Rückflusskühler gekocht. Dann wird filtriert, mit<B>10</B> O/oiger Salzsäure neutra- lisiert, mit etwa <B>5</B> Teilen 85 %iger Ameisen- säure schwach lackmussauer gestellt und der neue ehromhaltige Farbstoff durch Beigabe von Kochsalz ausgefällt.
Zu demselben chroinhaltigen Azofarbstoff gelangt man, wenn statt Natronlauge andere Alkalien, wie z. B. Kalilauge, Soda, Pottasche, Borax, Magnesiumoxyd, Caleiumhydroxyd, Ammoniak oder Trialkaliphosphat verwendet werden.
Additional patent to main patent no. <B> 166497. </B> Process for the production of an azo dye containing Ehrom. It has been found that a chromium-containing azo dye can be obtained by the action of the Ehrom-containing azo dye, which is obtained from nitrated-diazo-2-oxynaphtbaliii-4-sulfoi) by cht-omizing the azo dye
Acid and 2-oxynaphthalene are formed, to which azo dye can be obtained from diacotized 1-amino-2-oxynaphthalene-4-sulfonic acid and 1-oxynaplithaliii if this action takes place in an alkaline medium.
The new chromium-containing azo dye is obtained as a black powder which dissolves easily in water with a violet-black color and dyes the wool from organic-acid-sulfuric acid bath in black shades of excellent lightness.
<I> Example: </I> The chromed produced from <B> 92.2 '</B> parts of the azo dye from nitrated 1-diazo-2-oxynaphthalene-4-sulphonic acid and 2-oxynaphthalene in acidic medium Dye is made from diazotized 1-amino-2-oxynaphthalene-4-sulfonic acid and 1-oxynaphthalene and a solution of 1200 parts of water, 200 parts of 30% strength sodium long, together with 41.6 parts of the azo dye,
and <B> 5 </B> parts of sugar boiled for 4 hours on the reflux condenser. Then it is filtered, neutralized with <B> 10 </B> O / B hydrochloric acid, made weakly lacquer wall with about <B> 5 </B> parts of 85% formic acid and the new Ehrom-containing dye is added by adding table salt failed.
The same chroin-containing azo dye is obtained if, instead of sodium hydroxide, other alkalis, such as. B. potassium hydroxide, soda, potash, borax, magnesium oxide, calcium hydroxide, ammonia or trialkali phosphate can be used.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH170326T | 1932-11-07 | ||
CH166497T | 1934-01-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH170326A true CH170326A (en) | 1934-06-30 |
Family
ID=25718308
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH170326D CH170326A (en) | 1932-11-07 | 1932-11-07 | Process for the preparation of a chromium-containing azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH170326A (en) |
-
1932
- 1932-11-07 CH CH170326D patent/CH170326A/en unknown
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