CH205814A - Process for the production of a new, metal-containing stain dye. - Google Patents
Process for the production of a new, metal-containing stain dye.Info
- Publication number
- CH205814A CH205814A CH205814DA CH205814A CH 205814 A CH205814 A CH 205814A CH 205814D A CH205814D A CH 205814DA CH 205814 A CH205814 A CH 205814A
- Authority
- CH
- Switzerland
- Prior art keywords
- new
- amino
- chromium
- molecule
- 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
- 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
- C09B33/08—Disazo dyes in which the coupling component is a hydroxy-amino compound
- C09B33/10—Disazo dyes in which the coupling component is a hydroxy-amino compound in which the coupling component is an amino naphthol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen, metallhaltigen Beizenfarbstofes. Es wurde gefunden, dass man einen neuen, chromhaltigen Beizenfarbstoff erhält, wenn man ein Molekül 2-Amino-5-oxynaphthaliri-7- sulfonsäure zuerst in schwach saurem Medium mit einem Molekül dianotierter 2-Amino-l- oxybenzol-6-carbonsäure und nachher in schwach alkalischem Medium mit einem Mole kül dianotierter 1-Oxy-2-amino-6-nitrobenzol- 4-sulfonsäure kuppelt und den erhaltenen Disazofarbatoff mit einer chromabgebenden Substanz behandelt.
<I>Beispiel:</I> 15,3 Teile 2-Amino-l-oxybenzol-6-carbon- säure werden wie üblich dianotiert und in essigsaurer Lösung auf 23,9 Teile 2-Amino- 5-oxynaphthalin-7-sulfonsäuregekuppelt. Dann wird der erhaltene Monoazofarbstoff in alka lischer Lösung mit der Diazoverbindung aus 23,4 Teilen 1-Oxy-2-amino-6-nitrobenzol-4- sulfonsäure weitergekuppelt.
Nach beendeter Kupplung wird der erhaltene Disazofarbstoff ausgesalzen, abgenutscht, in 2000 Teilen kochendem Wasser gelöst und die Lösung unter Zusatz von 80 Teilen Ameisensäure und einer Ohromformiatlösung entsprechend 30,4 Teilen Crs03 während 15 Stunden unter Rückfluss gekocht. Die neue Chromverbindung wird durch Eindampfen der Lösung in fester Form gewonnen.
Der neue chromhaltige Farbstoff bildet, wenn getrocknet, ein graues Pulver, löst sich in Wasser mit graublauer, in konzentrierter Schwefelsäure mit violetter Farbe und liefert im Chromdruck auf Baumwolle, Kunstseide aus regenerierter Cellulose oder auf Natur seide graublaue Töne, die sich durch gute Echtheiten auszeichnen.
Process for the production of a new, metal-containing stain dye. It has been found that a new, chromium-containing mordant dye is obtained if one molecule of 2-amino-5-oxynaphthalene-7-sulfonic acid is first mixed with a molecule of dianotized 2-amino-l-oxybenzene-6-carboxylic acid in a weakly acidic medium and then coupling in a weakly alkaline medium with a mole of kül dianotized 1-oxy-2-amino-6-nitrobenzene-4-sulfonic acid and treated the disazo carbate obtained with a chromium-releasing substance.
<I> Example: </I> 15.3 parts of 2-amino-1-oxybenzene-6-carboxylic acid are dianotized as usual and coupled to 23.9 parts of 2-amino-5-oxynaphthalene-7-sulfonic acid in acetic acid solution . The monoazo dye obtained is then coupled further in alkali solution with the diazo compound from 23.4 parts of 1-oxy-2-amino-6-nitrobenzene-4-sulfonic acid.
When the coupling is complete, the disazo dye obtained is salted out, suction filtered, dissolved in 2000 parts of boiling water and the solution is refluxed for 15 hours with the addition of 80 parts of formic acid and an odor formate solution corresponding to 30.4 parts of Crs03. The new chromium compound is obtained in solid form by evaporating the solution.
The new chromium-containing dye forms a gray powder when dried, dissolves in water with a gray-blue color, in concentrated sulfuric acid with a violet color and, when printed with chrome on cotton, rayon made from regenerated cellulose or on natural silk, it produces gray-blue tones that are characterized by good fastness properties .
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE205814X | 1936-05-28 | ||
CH202856T | 1937-05-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH205814A true CH205814A (en) | 1939-06-30 |
Family
ID=25723861
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH205814D CH205814A (en) | 1936-05-28 | 1937-05-20 | Process for the production of a new, metal-containing stain dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH205814A (en) |
-
1937
- 1937-05-20 CH CH205814D patent/CH205814A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH205814A (en) | Process for the production of a new, metal-containing stain dye. | |
CH205812A (en) | Process for the production of a new, metal-containing stain dye. | |
CH205816A (en) | Process for the production of a new, metal-containing stain dye. | |
CH205815A (en) | Process for the production of a new, metal-containing stain dye. | |
CH205817A (en) | Process for the production of a new, metal-containing stain dye. | |
CH205813A (en) | Process for the production of a new, metal-containing stain dye. | |
CH203871A (en) | Process for the production of a new, metal-containing stain dye. | |
CH189040A (en) | Process for the preparation of a water-soluble monoazo dye. | |
CH203041A (en) | Process for the production of a new, metal-containing stain dye. | |
CH119125A (en) | Process for the production of a new dye. | |
CH214808A (en) | Process for the production of a new stain dye. | |
CH214807A (en) | Process for the production of a new stain dye. | |
CH153829A (en) | Process for the production of a new metal-containing dye. | |
CH238336A (en) | Process for the preparation of a new disazo dye. | |
CH205818A (en) | Process for the production of a new, metal-containing stain dye. | |
CH189037A (en) | Process for the preparation of a water-soluble monoazo dye. | |
CH200250A (en) | Process for the preparation of a new chromable disazo dye. | |
CH203037A (en) | Process for the preparation of an azo dye containing complexed chromium. | |
CH200999A (en) | Process for the preparation of an azo dye. | |
CH148008A (en) | Process for the production of a new metal-containing dye. | |
CH203042A (en) | Process for the production of a new, metal-containing stain dye. | |
CH150182A (en) | Process for the production of a new metal-containing dye. | |
CH119139A (en) | Process for the production of a new metal-containing dye. | |
CH119140A (en) | Process for the production of a new metal-containing dye. | |
CH117996A (en) | Process for the production of a new dye. |