CH90846A - Process for the preparation of a diazotization dye. - Google Patents

Process for the preparation of a diazotization dye.

Info

Publication number
CH90846A
CH90846A CH90846DA CH90846A CH 90846 A CH90846 A CH 90846A CH 90846D A CH90846D A CH 90846DA CH 90846 A CH90846 A CH 90846A
Authority
CH
Switzerland
Prior art keywords
dye
diazotization
preparation
oxy
mole
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 CH90846A publication Critical patent/CH90846A/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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • C09B35/02Disazo dyes
    • C09B35/039Disazo dyes characterised by the tetrazo component
    • C09B35/205Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene
    • C09B35/21Disazo dyes characterised by the tetrazo component the tetrazo component being a derivative of a diaryl- or triaryl- alkane or-alkene of diarylmethane or triarylmethane
    • 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
    • C09B35/00Disazo and polyazo dyes of the type A<-D->B prepared by diazotising and coupling
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/58Material containing hydroxyl groups
    • D06P3/60Natural or regenerated cellulose
    • D06P3/68Preparing azo dyes on the material

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Coloring (AREA)

Description

  

  Verfahren zur Herstellung eines     Diäzotierängsfarbstoffes.       Es wurde gefunden, dass     durch    Einwirkung  von     Formaldehydbisulfit    auf den     Farbstoff,     erhalten durch     Kombinieren    von 1     Mol.        tetrazo-          tiertem    3 :     3'-Diainino-4        .#        4'-ditolylmethan    mit       Mol:    1 :     2-(3'-Aminophenyl)-riapbtimidazol-*          5-oxy-7-srilfosäure,    ein leichtlöslicher     Farbstoff     erhalten wird.

   Dieser     Farbstoff    färbt     uuge-          beizte    Baumwolle     gelbstichig    Bordeaux; durch       r        .Diazotieren    der Färbung und Kuppeln mit       ss-Naphtal    wird ein sehr waschechtes, volles  Blaurot erhalten.

     <I>Beispiel:</I>  50 Teile des     Farbstoffes    aus 1     Mol.        tetra-          zotiertem        3:3'-Diainino-4:4'-ditolylmetliän     und 2     Mol.    1     :

  2-(3'-Amiriopheriyl)-riaphtirnid-.          azol-5-oxy-7-srilfosäure    werden mit 300 Teilen       Wasser    angerührt und     finit    einer vorbei zum  Kochen     erhitzten    Mischung von 28,6 'feilen       Natriumbisulfitlösung        h,    400o und 3,3 Teilen    Formaldehyd in Form einer wässerigen 30  bis     40 /oigen    Lösung versetzt.- Man erhitzt  die     112asse-während        -einer    Stunde zum Sieden,  salzt aus, filtriert     ünd    trocknet.



  Process for the production of a longitudinal dyestuff. It has been found that by the action of formaldehyde bisulfite on the dye, obtained by combining 1 mole of tetrazolated 3: 3'-diainino-4. # 4'-ditolylmethane with mole: 1: 2- (3'-aminophenyl) -riapbtimidazole- * 5-oxy-7-srilfosäure, a readily soluble dye is obtained.

   This dye gives off-stained cotton a yellowish tinge of Bordeaux; by r. diazotizing the color and domes with SS-naphthalene a very washfast, full blue-red is obtained.

     <I> Example: </I> 50 parts of the dye from 1 mol. Tetrazotized 3: 3'-diainino-4: 4'-ditolylmetliän and 2 mol. 1:

  2- (3'-Amiriopheriyl) -riaphtirnid-. azole-5-oxy-7-sulfonic acid are mixed with 300 parts of water and finitely added to a mixture, heated to boiling point, of 28.6 'file sodium bisulfite solution, 400o and 3.3 parts of formaldehyde in the form of an aqueous 30 to 40% solution - The mixture is heated to the boil for one hour, salted out, filtered and dried.

 

Claims (1)

-. PATENTANSPRUCH: Verfahren zur Herstellung eines Diazo- tierungsfarbstoffes, dadurch gekennzeichnet, - dass man' auf den Farbstoff, erhalten durch . -. PATENT CLAIM: Process for the production of a diazotization dye, characterized in that - that one 'on the dye obtained by. Kombinieren vori 1 Mol. tetrazotiertein .3 @: 3' Diauiirio-4 : 4'-ditolylinethan mit 2 Mol. 1 : ,2- (3'-Ami nopheriyl)-naphtimidazöl-5-oxy-7-sulfo- säure, Formaldehydbisulfit .einwirken lässt. Combine 1 mole of tetrazotized in .3 @: 3 'Diauiirio-4: 4'-ditolylinethane with 2 moles of 1:, 2- (3'-Ami nopheriyl) -naphtimidazöl-5-oxy-7-sulfonic acid, formaldehyde bisulfite .acts. Der -erhaltene leichtlösliche Farbstoff färbt urigebeizte Baumwolle gelbstichig Bordeaux; durch Diazotieren - der Färbung und Kuppeln mit P-Naphtol wird ein sehr waschechtes, volles B-lauiot erhalten.. - The readily soluble dye obtained dyes rustic-stained cotton with a yellowish tinge of Bordeaux; by diazotizing - the coloring and doming with P-naphthol a very washfast, full B-lauiot is obtained .. -
CH90846D 1918-12-21 1918-12-21 Process for the preparation of a diazotization dye. CH90846A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH90846T 1918-12-21
CH89557T 1918-12-21

Publications (1)

Publication Number Publication Date
CH90846A true CH90846A (en) 1921-09-16

Family

ID=25704030

Family Applications (1)

Application Number Title Priority Date Filing Date
CH90846D CH90846A (en) 1918-12-21 1918-12-21 Process for the preparation of a diazotization dye.

Country Status (1)

Country Link
CH (1) CH90846A (en)

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