CH106703A - Process for the production of an azo dye particularly suitable for chrome printing on cotton. - Google Patents

Process for the production of an azo dye particularly suitable for chrome printing on cotton.

Info

Publication number
CH106703A
CH106703A CH106703DA CH106703A CH 106703 A CH106703 A CH 106703A CH 106703D A CH106703D A CH 106703DA CH 106703 A CH106703 A CH 106703A
Authority
CH
Switzerland
Prior art keywords
cotton
production
particularly suitable
azo dye
chrome printing
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
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 Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH106703A publication Critical patent/CH106703A/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
    • C09B33/04Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound
    • 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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/24Disazo or polyazo compounds
    • C09B45/26Disazo or polyazo compounds containing chromium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)

Description

  

  Verfahren zur     Herstelluug    eines für den     CVromdruek    auf Baumwolle besonders  geeigneten     Azofarbstoffes.       Es wurde gefunden,     d.a,ss    man durch Kup  peln von zwei     Mol.        dia.zotiertem        4-Nirto-2-          .        ani        .ino-l-oxybenzol        mit        einem        Mol.        Resorcyl-          s#iure    einen     Azoàrbstoff    erhält, welcher bei       dF:

  ni    Chromdruck auf Baumwolle violett  braune Töne von guten     Echtheiten    erzeugt.         Beispiel:       Die     Diazoverbindung    aus 15,4 Teilen     4-          Nitro-2-amino-l-oxybenzol    lässt man in eine  Lösung von 7,7 Teilen     Resorcylsäure    und  30 Teilen Soda einfliessen. Der     gebildete     Farbstoff wird durch Fällen mit Kochsalz       abgeschieden.     



  Der neue Farbstoff bildet ein dunkles  Pulver, welches sich in Wasser mit rot  brauner Farbe löst, welche Lösung .auf Zu  satz von Soda, etwas röter     wird.    In konzen  trierter Schwefelsäure ist er mit rotbrauner  Farbe löslich. Im     Chromdru.ek    ,auf Baum-    wolle erzeugt er     violettbraune    Töne von gu  ten     Echtheiten.  



  Process for the production of an azo dye which is particularly suitable for CVromdruek on cotton. It has been found that by coupling two moles of dia.zotierter 4-Nirto-2-. ani .ino-l-oxybenzene with one mole of resorcylic acid gives an azo dye, which at dF:

  ni chrome print on cotton produces violet-brown shades of good fastness properties. Example: The diazo compound from 15.4 parts of 4-nitro-2-amino-1-oxybenzene is allowed to flow into a solution of 7.7 parts of resorcylic acid and 30 parts of soda. The dye formed is deposited by precipitating with common salt.



  The new dye forms a dark powder which dissolves in water with a red-brown color, which solution becomes a little redder with the addition of soda. It is soluble in concentrated sulfuric acid with a red-brown color. In Chromdru.ek, on cotton, it creates violet-brown tones with good fastness properties.

 

Claims (1)

PATENTANSPRUCH Verfahren zur Herstellung eines für den Chromdruck auf Baumwolle besonders geeig neten Azofarbstoffes; dadurch gekennzeich net, da,ss zwei Mol. di.azotiertes 4-Nitro--2- amino-l-oxyberizol mit einem Mol. Resorcyl- säure gekuppelt werden. PATENT CLAIM Process for the production of an azo dye particularly suitable for chrome printing on cotton; characterized in that two moles of di.azotized 4-nitro-2-amino-1-oxyberizole are coupled with one mole of resorcylic acid. Der neue Farbstoff bildet ein dunkles Pulver, welches sich in Wasser mit rot brauner Farbe löst, welche Lösung auf Zu satz von Soda etwas röter wird. In konzen trierter Schwefelsäure ist er mit rotbrauner Farbe löslich. Im Chromdruck auf Baum wolle erzeugt er violetthraune Töne von gu ten Echtheiten. The new dye forms a dark powder, which dissolves in water with a red-brown color, which solution becomes a little redder with the addition of soda. It is soluble in concentrated sulfuric acid with a red-brown color. In chrome printing on cotton, it creates violet-lime tones with good fastness properties.
CH106703D 1921-03-15 1923-06-07 Process for the production of an azo dye particularly suitable for chrome printing on cotton. CH106703A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH94229T 1921-03-15
CH106703T 1923-06-07

Publications (1)

Publication Number Publication Date
CH106703A true CH106703A (en) 1924-09-01

Family

ID=25704796

Family Applications (1)

Application Number Title Priority Date Filing Date
CH106703D CH106703A (en) 1921-03-15 1923-06-07 Process for the production of an azo dye particularly suitable for chrome printing on cotton.

Country Status (1)

Country Link
CH (1) CH106703A (en)

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