CH106702A - Process for the production of an azo dye particularly suitable for chrome printing on cotton. - Google Patents
Process for the production of an azo dye particularly suitable for chrome printing on cotton.Info
- Publication number
- CH106702A CH106702A CH106702DA CH106702A CH 106702 A CH106702 A CH 106702A CH 106702D A CH106702D A CH 106702DA CH 106702 A CH106702 A CH 106702A
- Authority
- CH
- Switzerland
- Prior art keywords
- cotton
- brown
- production
- particularly suitable
- azo 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
- C09B45/24—Disazo or polyazo compounds
- C09B45/26—Disazo or polyazo compounds containing chromium
-
- 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
- C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
- C09B33/02—Disazo dyes
- C09B33/04—Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound
-
- 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
- C09B45/38—Preparation from compounds with —OH and —COOH adjacent in the same ring or in peri position
- C09B45/40—Chromium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 94229. Verfahren zur Herstellung eines für den ühromdruck auf Baumwolle besonders geeigneten Azofarbstoffes. Es wurde gefunden, dass man durch Kup peln von zwei Mol. diazotierter 1-Oxy-2- amino-4-nitrobenzol-6-karbonsäure mit einem Mol. Resorcylsäure einen Azofarbstoff er hält, welcher bei dem Chromdruck auf Baum wolle braunstickig gelbe Töne von guten Echtheitseigenschaften erzeugt.
<I>Beispiel:</I> Die Diazoverbindung aus 19,8 Teilen 1 Oxy-2-amino-4-nitrobenzol-6-karbonsäure, 15 Teilen Salzsäure und 6,9 Teilen Natrium nitrit lässt man in eine konzentrierte Lösung von 7,7 Teilen Resorcylsäure einfliessen. Nach mehrstündigem Rühren ist keine Diazover- bindung mehr nachweisbar. Der gebildete Farbstoff wird aus der Lösung durch Sätti gen derselben mit Kochsalz ausgefällt.
Der neue Farbstoff löst sich in Wasser mit gelbbrauner Farbe, welche Lösung auf Zusatz von Natronlauge rotbraun wird. In konzentrierter Schwefelsäure ist er mit braun- roter Farbe löslich. Mit Chromacetat auf Baumwolle gedruckt, erzeugt er ein braun stickiges Gelb von guten Echtheitseigen schaften.
Additional patent to main patent no. 94229. Process for the production of an azo dye particularly suitable for chromium printing on cotton. It has been found that by coupling two moles of diazotized 1-oxy-2-amino-4-nitrobenzene-6-carboxylic acid with one mole of resorcylic acid, an azo dye is obtained which, when printed on chrome, is brownish-yellow in color good fastness properties.
<I> Example: </I> The diazo compound from 19.8 parts of 1-oxy-2-amino-4-nitrobenzene-6-carboxylic acid, 15 parts of hydrochloric acid and 6.9 parts of sodium nitrite is left in a concentrated solution of 7 7 parts of resorcylic acid are poured in. After several hours of stirring, no more diazo compound can be detected. The dye formed is precipitated from the solution by saturating the same with common salt.
The new dye dissolves in water with a yellow-brown color, which solution turns red-brown when sodium hydroxide is added. It is soluble in concentrated sulfuric acid with a brownish-red color. Printed on cotton with chrome acetate, it produces a brown, stuffy yellow with good fastness properties.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH94229T | 1921-03-15 | ||
CH106702T | 1923-06-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106702A true CH106702A (en) | 1924-09-01 |
Family
ID=25704795
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106702D CH106702A (en) | 1921-03-15 | 1923-06-07 | Process for the production of an azo dye particularly suitable for chrome printing on cotton. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106702A (en) |
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1923
- 1923-06-07 CH CH106702D patent/CH106702A/en unknown
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