CH138234A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH138234A CH138234A CH138234DA CH138234A CH 138234 A CH138234 A CH 138234A CH 138234D A CH138234D A CH 138234DA CH 138234 A CH138234 A CH 138234A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- dye
- new
- production
- mol
- 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
- 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
- C09B33/12—Disazo dyes in which the coupling component is a heterocyclic 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
- C09B45/02—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
- 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
- C09B45/28—Disazo or polyazo compounds containing copper
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>136650.</B> Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Farbstoff erhält, wenn man<B>1</B> Mol. des 5,5'-Dioxy-7,7'-disulfo-1,2,2',1'-dinaphth- azins mit 2 Mol. diazotierter 4-Nitro-2-amino- 1-phenol-6-suliosäure kombiniert und den erhaltenen Farbstoff mit kupfer- und ehrom- abgebenden Mitteln behandelt.
Der neue kupfer- und chromhaltige Farb stoff ist trocken ein dunkles Pulver, welches sich in Wasser mit blauvioletter, in ver dünnten Alkalien mit blauer und in konzen trierter Schwefelsäure mit schwärzlicher Farbe löst. Baumwolle wird aus soda- alkalischem Glaubersalzbade in grüngrauen Tönen angefärbt.
<I>Beispiel:</I> <B>90</B> Teile des Disazofarbstoffes aus dem 5,5'-Dic,xy-7,7'-disulfo-1,2,2',1'-dinaphthazin und 4-Nitro-2-amino-l-phenol-6-sulfosäure werden in<B>3500</B> Teilen Wasser gelöst und mit Lösungen von<B>25</B> Teilen kristallisier tem Kupfersulfat und Fluorchrom, entspre chend<B>25</B> Teilen Crf!0, versetzt und das Gemisch<B>16</B> Stunden am Rückflusskühler gekocht. Durch Zugabe von Kochsalzlösung wird die Mischkomplexverbindung abge schieden.
Additional patent to main patent no. <B> 136650. </B> Process for the production of a new azo dye. It has been found that a new dye is obtained if <B> 1 </B> mol. Of the 5,5'-dioxy-7,7'-disulfo-1,2,2 ', 1'-dinaphth- azine combined with 2 moles of diazotized 4-nitro-2-amino-1-phenol-6-sulioic acid and treated the resulting dye with copper and chromium-releasing agents.
The new dye, which contains copper and chromium, is a dry, dark powder that dissolves in water with a blue-violet color, in diluted alkalis with a blue color and in concentrated sulfuric acid with a blackish color. Cotton is dyed from a soda-alkaline Glauber's salt bath in green-gray tones.
<I> Example: </I> <B> 90 </B> parts of the disazo dye from the 5,5'-dic, xy-7,7'-disulfo-1,2,2 ', 1'-dinaphthazine and 4-Nitro-2-amino-1-phenol-6-sulfonic acid are dissolved in <B> 3500 </B> parts of water and mixed with solutions of <B> 25 </B> parts of crystallized copper sulfate and fluorochrome, accordingly B> 25 parts Crf! 0, added and the mixture boiled for 16 hours on the reflux condenser. The mixed complex compound is separated out by adding saline solution.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH138234T | 1928-09-08 | ||
CH136650T | 1929-11-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH138234A true CH138234A (en) | 1930-02-15 |
Family
ID=25712788
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH138234D CH138234A (en) | 1928-09-08 | 1928-09-08 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH138234A (en) |
-
1928
- 1928-09-08 CH CH138234D patent/CH138234A/en unknown
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