CH86850A - Process for the preparation of a substantive o-oxyazo dye. - Google Patents

Process for the preparation of a substantive o-oxyazo dye.

Info

Publication number
CH86850A
CH86850A CH86850DA CH86850A CH 86850 A CH86850 A CH 86850A CH 86850D A CH86850D A CH 86850DA CH 86850 A CH86850 A CH 86850A
Authority
CH
Switzerland
Prior art keywords
oxyazo
dye
substantive
preparation
sulfonic acid
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 CH86850A publication Critical patent/CH86850A/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
    • 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
    • C09B45/14Monoazo compounds
    • C09B45/18Monoazo compounds containing copper
    • 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
    • C09B33/056Disazo dyes in which the coupling component is a dihydroxy or polyhydroxy compound the coupling component being a bis-(naphthol-urea)

Landscapes

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

Description

  

      \'erfahren    zur Herstellung eines     direktziehenden        o-Oiyazofarbstoffes.       Es wurde gefunden, dass     dureli        Kuppeln     von dianotierter     2-Amitio-l-oxybenzol-4-sulfo-          säure    mit dem Harnstoffe der     2-Amino-5-oxy-          n.iphtalin-7-sulfosäure    ein direktziehender       o-Oxyazofarbstofferhalteu    wird,     welclierBaum-          wollc    in licht- und ,     alkali-empfindlichen     gelbrosa Tönen anfärbt.

   Durch     Nachkupfern     oder noch besser durch Färben in der für  direktziehende     Farbstoffe    üblichen Weise un  ter     Zusatz    von     Kupferverbindungen    zum Bade  werden hervorragend licht-     arid        alkalieclite     blaurote Töne erhalten.  



       Beispiel:     37,8 kg     2-Ainino-l-ox@#betizol-4-stilfosiitire     werden in die     Diazoverbindting    übergeführt  Lind diese in eine Lösung     voll        50,-1    kg     Harn-          stoff    der     2-Aiiiino-5-oxynaphtalin-7-sulfosäiire          und        501c-    Soda einfliessen gelassen. Nach    12     Stunden    wird der     Farbstoff    aasgesalzen,       filtriert    und getrocknet.



      \ 'experienced in the production of a substantive o-oiyazo dye. It has been found that by coupling dianotated 2-amino-1-oxybenzene-4-sulfonic acid with the urea of 2-amino-5-oxy-n.iphtalin-7-sulfonic acid, a substantive o-oxyazo dye is obtained, welclierTree- wollc dyes in light and alkali-sensitive yellow-pink tones.

   By re-coppering or, even better, by dyeing in the manner customary for substantive dyes with the addition of copper compounds to the bath, excellent light-arid alkaline blue-red tones are obtained.



       Example: 37.8 kg of 2-ainino-l-ox @ # betizol-4-stilfosiitire are converted into the diazo compound and this is converted into a solution full of 50.1 kg of urea of the 2-aiiiino-5-oxynaphthalene-7- sulfosäiire and 501c soda allowed to flow in. After 12 hours the dyestuff is salted ashes, filtered and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines direkt ziehenden o-Oxy-tizufai#bsto$es, dadurch ge- kennzE#ichnet, dafj dianotierte 2-Amino-l-o-xy- benzol-4-sulfosiiure mit dem Harnstoffe der An üno-5-oxynaphtalin-7-sulfosäure kombi niert wird. PATENT CLAIM: Process for the production of a direct o-oxy-tizufai # bsto $ es, characterized by the fact that dianotated 2-amino-lo-xy-benzene-4-sulfonic acid with the urea of an uno-5-oxynaphthalene -7-sulfonic acid is combined. Der erhaltene Oxyazofarbstoff färbt direkt Baumwolle in lieht- und alkali- empfindlielien gelbrosa Tönen. Dureli Nach kupfern oder besser durch Färben in der für direktziehende Farbstoffe üblichen Weise un ter Zusatz von Kupfervei#bindungen zum Bade werden hervorragend licht- und alkalieclite blaurote Tune erhalten. The oxyazo dye obtained directly dyes cotton in light- and alkali-sensitive yellow-pink shades. Dureli after copper or better by coloring in the usual way for direct dyes with the addition of copper compounds to the bath, excellent light and alkaline blue-red tones are obtained.
CH86850D 1919-05-01 1915-12-30 Process for the preparation of a substantive o-oxyazo dye. CH86850A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH86850T 1919-05-01

Publications (1)

Publication Number Publication Date
CH86850A true CH86850A (en) 1920-10-16

Family

ID=4343501

Family Applications (1)

Application Number Title Priority Date Filing Date
CH86850D CH86850A (en) 1919-05-01 1915-12-30 Process for the preparation of a substantive o-oxyazo dye.

Country Status (1)

Country Link
CH (1) CH86850A (en)

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