CH200370A - Process for the preparation of a chromable o-oxydisazo dye. - Google Patents
Process for the preparation of a chromable o-oxydisazo dye.Info
- Publication number
- CH200370A CH200370A CH200370DA CH200370A CH 200370 A CH200370 A CH 200370A CH 200370D A CH200370D A CH 200370DA CH 200370 A CH200370 A CH 200370A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- preparation
- diazotized
- oxydisazo
- chromable
- 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
- C09B31/00—Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
- C09B31/02—Disazo dyes
- C09B31/08—Disazo dyes from a coupling component "C" containing directive hydroxyl and amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines chromierbaren o-Ogydisazofarbstoffes. Es wurde gefunden, .dass man wertvolle, lichtechte, ohromierbare o - Oxydisazofarb- stoffe erhält,
wenn man die Monoazofarb- stoffe aus aromatischen Diazosulfonsäuren oder -carbonsäuren und m-Amino-p-kresol diazotiert und mit N-Alkyl- bezw. N-Aryl- derivaten der 1-Amino-8-oxynaphthalin-4- sulfonsäure kombiniert.
Gegenstand des vorliegenden Patentes ist ein Verfahren zur Darstellung eines clhro- mierbaren o-Oxydisazofarbstoffes, dadurch gekennzeichnet, dass man .den aus diazotierter Sulfanilsäure und m-Amino-p-kresol erhält lichen Monoazofarbstoff diazotiert und die so erhaltene Diazoverbindung mit 1-Phenyl- amino-8-oxynaphthalin-4-sulfonsäure kuppelt.
Der neue Farbstoff, ein dunkles Pulver, löst sich in Wasser mit blauer und in kon zentrierter Schwefelsäure mit grüner Farbe. Er färbt Wolle sauer in blauen, nach chromiert in echten, gelbstichig grünen Tönen.
<I>Beispiel:</I> 30,7 Teile des aus diazotierter Sulfanil- säure und m-Amino-p-kresol erhaltenen Monoazofarbstoffes werden in Wasser mit 6 Teilen calc. Soda gelöst, mit 7 Teilen Nitrit versetzt und mit Salzsäure in üblicher Weise angesäuert. Die Diazotierung ist bald zu Ende.
Den braungelben Diazokörper gibt man zu einer sodaalkalis lhen Lösung von 32 Teilen 1-Phenylamino-8-oxynaplhtha- lin-4-sulfonsäure, die 15 Volumprozent Pyri- din enthält. Die Kombination ist in wenigen Stunden beendet. Der neue Farbstoff wird wie üblich abfiltriert und getrocknet; er stellt ein .dunkles Pulver dar, das sich in Wasser mit blauer und in konzentrierter Schwefelsäure mit grüner Farbe löst.
Er färbt Wolle sauer in blauen, naohohromiert in echten, gelbstichig grünen Tönen.
Process for the preparation of a chromable o-ogydisazo dye. It has been found that valuable, lightfast, aurable o-oxydisazo dyes are obtained,
if you diazotized the monoazo dyes from aromatic diazosulfonic acids or carboxylic acids and m-amino-p-cresol and with N-alkyl or. N-aryl derivatives of 1-amino-8-oxynaphthalene-4-sulfonic acid combined.
The subject of the present patent is a process for the preparation of a chromable o-oxydisazo dye, characterized in that the monoazo dye obtained from diazotized sulfanilic acid and m-amino-p-cresol is diazotized and the diazo compound thus obtained is diazotized with 1-phenylamino -8-oxynaphthalene-4-sulfonic acid couples.
The new dye, a dark powder, dissolves in water with a blue color and in concentrated sulfuric acid with a green color. It dyes wool sour in blue, after chroming in real, yellowish green tones.
<I> Example: </I> 30.7 parts of the monoazo dye obtained from diazotized sulfanilic acid and m-amino-p-cresol are calcined in water with 6 parts. Dissolved soda, mixed with 7 parts of nitrite and acidified with hydrochloric acid in the usual way. The diazotization will soon end.
The brown-yellow diazo body is added to a soda-alkaline solution of 32 parts of 1-phenylamino-8-oxynaplhthalin-4-sulfonic acid which contains 15 percent by volume of pyridine. The combination is finished in a few hours. The new dye is filtered off and dried as usual; it is a dark powder that dissolves in water with a blue color and in concentrated sulfuric acid with a green color.
He dyes wool sour in blue, naohohromiert in real, yellowish green tones.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH200370T | 1937-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH200370A true CH200370A (en) | 1938-10-15 |
Family
ID=4442278
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH200370D CH200370A (en) | 1937-09-07 | 1937-09-07 | Process for the preparation of a chromable o-oxydisazo dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH200370A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003074885A1 (en) | 2002-03-04 | 2003-09-12 | Prospective Concepts Ag | Pneumatic actuator |
-
1937
- 1937-09-07 CH CH200370D patent/CH200370A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003074885A1 (en) | 2002-03-04 | 2003-09-12 | Prospective Concepts Ag | Pneumatic actuator |
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