CH115468A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH115468A CH115468A CH115468DA CH115468A CH 115468 A CH115468 A CH 115468A CH 115468D A CH115468D A CH 115468DA CH 115468 A CH115468 A CH 115468A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- azo dye
- new
- oxynaphthalene
- new 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
-
- 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
- C09B29/0014—Monoazo dyes prepared by diazotising and coupling from diazotized aminonaphthalene
-
- 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
- C09B29/103—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the naphthalene series
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 101614. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man das 2-Oxy- naphthalin-6-sulfamid mit diazotierter 1-Oxy- naphthalin - 2 - a,mino-8-sulfamicl-4-sulfosäura kuppelt. Der neue Farbstoff bildet ein dunk les Pulver und färbt Wolle im essigsauren Bade in blauroten Farbtönen, welche beim Nachchromieren hellblau, beim Nachkupfern rotviolett und echt werden.
<I>Beispiel:</I> 22,3 Teile 2-Oxynaphthalin-6-sulfamid werden in eine Lösung von 56 Teilen Ätzkali in 48 Teilen Wasser bei 40-45 eingetra gen. Die so erhaltene Mischung wird hierauf mit der Diazoverbindung aus 31,8 Teilen 1- Oxynaphthalin-2-amino-8-sulfamid - 4 - sul.fo- säure in Form einer 49 %igen Paste versetzt. Nach beendeter Kupplung verdünnt man mit 200 Teilen kaltem Wasser, lässt 280 Teile 15 %ige Salzsäure unter Rühren einlaufen und salzt den gebildeten Farbstoff aus.
Additional patent to main patent no. 101614. Process for the production of a new azo dye. It has been found that a new azo dye is obtained when 2-oxynaphthalene-6-sulfamide is coupled with diazotized 1-oxynaphthalene-2-a, mino-8-sulfamicl-4-sulfosacid. The new dye forms a dark powder and dyes wool in the acetic acid bath in blue-red shades, which become light blue when chromium plating and red-violet and real when copper plating.
<I> Example: </I> 22.3 parts of 2-oxynaphthalene-6-sulfamide are introduced into a solution of 56 parts of caustic potash in 48 parts of water at 40-45. The mixture thus obtained is then mixed with the diazo compound from 31 , 8 parts of 1-oxynaphthalene-2-amino-8-sulfamide - 4 - sulpho acid added in the form of a 49% paste. After coupling has ended, the mixture is diluted with 200 parts of cold water, 280 parts of 15% strength hydrochloric acid are run in with stirring and the dyestuff formed is salted out.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH101614T | 1922-11-18 | ||
CH115468T | 1924-04-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH115468A true CH115468A (en) | 1926-06-16 |
Family
ID=25706022
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH115468D CH115468A (en) | 1922-11-18 | 1924-04-20 | Process for the production of a new azo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH115468A (en) |
-
1924
- 1924-04-20 CH CH115468D patent/CH115468A/en unknown
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