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
Application number
Other languages
German (de)
Inventor
A-G Durand Huguenin
Original Assignee
Durand & Huguenin Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Durand & Huguenin Ag filed Critical Durand & Huguenin Ag
Publication of CH205814A publication Critical patent/CH205814A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B33/00Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
    • C09B33/02Disazo dyes
    • C09B33/08Disazo dyes in which the coupling component is a hydroxy-amino compound
    • C09B33/10Disazo 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)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen, chromhaltigen Beize nfarbstoffes, dadurch ge kennzeichnet, dass man ein Molekül 2-Amino- 5-oxynaphthalin-7-sulfonsäure zuerst in schwach saurem Medium mit einem Molekül dianotierter 2-Amino-l-oxybenzol-6-carbon- säure und nachher in schwach alkalischem Medium mit einem Molekül diazotierter 1- Ogy-2-amino-ö-nitrobenzol-4-sulfocisäure kup pelt und den erhaltenen Disazofarbstoff mit einer chromabgebenden Substanz behandelt. PATENT CLAIM: Process for the production of a new, chromium-containing mordant dye, characterized in that 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 and then in a weakly alkaline medium with a molecule of diazotized 1- Ogy-2-amino-ö-nitrobenzene-4-sulfocic acid and treated the disazo dye obtained with a chromium-releasing substance. 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. 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 .
CH205814D 1936-05-28 1937-05-20 Process for the production of a new, metal-containing stain dye. CH205814A (en)

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)

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