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CH249785A - Process for the preparation of a substantive azo dye. - Google Patents

Process for the preparation of a substantive azo dye.

Info

Publication number
CH249785A
CH249785A CH249785DA CH249785A CH 249785 A CH249785 A CH 249785A CH 249785D A CH249785D A CH 249785DA CH 249785 A CH249785 A CH 249785A
Authority
CH
Switzerland
Prior art keywords
azo dye
weight
parts
preparation
substantive azo
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellschaft Ciba
Original Assignee
Ciba Geigy
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 Ciba Geigy filed Critical Ciba Geigy
Publication of CH249785A publication Critical patent/CH249785A/en

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
    • C09B45/00—Complex metal compounds of azo dyes
    • C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14—Monoazo compounds
    • C09B45/18—Monoazo compounds containing copper
    • 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
    • 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
    • C09B43/00—Preparation of azo dyes from other azo compounds
    • C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
    • C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
    • C09B43/16—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents linking amino-azo or cyanuric acid residues

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Paper (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Description

  

  Verfahren zur Herstellung eines Substantiven     Azofarbstoffes.       Gegenstand des vorliegenden Zusatz  patentes ist ein Verfahren zur Herstellung  eines Substantiven     Azofarbstoffes,        dadureh     gekennzeichnet,

   dass man     diazotiertes        1-Oxy--          2-Aminobenzol-4-earbonsäure-phenylamid    mit       2-Phenylamino    - 5 -     oxynaphthalin    - 7 -     sulfon-          säure    in alkalischem Medium vereinigt und  den neuen Farbstoff durch     Behandeln    mit       kupferabgebenden        Mitteln    in eine komplexe       Kupferverbindung    überführt. Diese färbt  Baumwolle in echten rotvioletten Tönen.  



       Beispiel:     22,8     Gewichtsteile        1-Oxy-2-aminobenzol-          4-carbonsäurephenylamid    werden unter Zu  satz von 6,9 Gewichtsteilen     Natriumnitrit     und 27 Gewichtsteilen konzentrierter Salz  säure bei 0      diazotiert    und die     Diazoverbin-          dung    mit<B>31,5</B> Gewichtsteilen     2-Phenylamino-          5-oxynaphthalin-7-sulfonsäure,

      die als     Na.-          trzumsalz        unter    Zusatz von 100 Gewichts  teilen 20 %     igem        Calciumhydroxyd    in 1000 Ge  wichtsteilen     Wasser    gelöst wurden, vereinigt.

    Nach 4     Stunden    wird der gebildete Farb-         stoff    durch     Zusatz        voll    Salzsäure abgeschie  den und     filtriert.    Der     Filterrückstand        wird          in    bekannter Weise durch Behandeln mit       einer        Lösung    von 25     Gewichtsteilen        kristal-          lisiertem        Kupfersulfat    in 100 Gewichtsteilen  25%igem Ammoniak in 1000 Gewichtsteilen       Wasser    bei 35-40  in seine Kupferverbin  dung 

  übergeführt. Die     gebildete    Kupferver  bindung fällt aus, wird filtriert und getrock  net. Der neue Farbstoff bildet     ein        dunkles     Pulver, das Baumwolle in echten     rotvioletten     Tönen färbt.



  Process for the production of a noun azo dye. The subject of the present additional patent is a process for the production of a noun azo dye, dadureh,

   that diazotized 1-oxy- 2-aminobenzene-4-carboxylic acid-phenylamide is combined with 2-phenylamino-5-oxynaphthalene-7-sulfonic acid in an alkaline medium and the new dye is converted into a complex copper compound by treatment with copper-releasing agents. This dyes cotton in real red-violet tones.



       Example: 22.8 parts by weight of 1-oxy-2-aminobenzene-4-carboxylic acid phenylamide are diazotized at 0 with the addition of 6.9 parts by weight of sodium nitrite and 27 parts by weight of concentrated hydrochloric acid and the diazo compound with <B> 31.5 </ B> parts by weight of 2-phenylamino-5-oxynaphthalene-7-sulfonic acid,

      which were dissolved as sodium trzumsalz with the addition of 100 parts by weight of 20% calcium hydroxide in 1000 parts by weight of water, combined.

    After 4 hours, the dyestuff formed is separated off by adding hydrochloric acid and filtered. The filter residue is converted into its copper compound in a known manner by treatment with a solution of 25 parts by weight of crystallized copper sulfate in 100 parts by weight of 25% strength ammonia in 1000 parts by weight of water at 35-40

  convicted. The formed copper compound precipitates, is filtered and net getrock. The new dye forms a dark powder that dyes cotton in true red-purple tones.

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Substan tiven Azofarbstoffes, dadurch gekennzeich net, dass man diazotiertes 1-Oxy-2-amino- benzo@l-4-carbonsäure-phenylamid mit 2-Phe- nylamino-5-oxynaphthalin - 7 - sulfonsäure in alkalischem Medium vereinigt und den neuen Farbstoff durch Behandeln mit kupferabge benden Mitteln in eine komplexe Kupferver bindung überführt. Diese färbt Baumwolle in echten rotvioletten Tönen. PATENT CLAIM: Process for the production of a substantive azo dye, characterized in that diazotized 1-oxy-2-aminobenzo @ l-4-carboxylic acid-phenylamide with 2-phenylamino-5-oxynaphthalene-7-sulfonic acid in alkaline Medium combined and the new dye converted into a complex copper compound by treating it with copper-releasing agents. This dyes cotton in real red-violet tones.
CH249785D 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye. CH249785A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH245067T 1946-01-18

Publications (1)

Publication Number Publication Date
CH249785A true CH249785A (en) 1947-07-15

Family

ID=4464679

Family Applications (14)

Application Number Title Priority Date Filing Date
CH249787D CH249787A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249792D CH249792A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249795D CH249795A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249790D CH249790A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249785D CH249785A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249786D CH249786A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249794D CH249794A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249793D CH249793A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249788D CH249788A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249789D CH249789A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH245067D CH245067A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249791D CH249791A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH252072D CH252072A (en) 1946-01-18 1946-01-18 Process for the preparation of a substantive azo dye.
CH269047D CH269047A (en) 1946-01-18 1946-01-18 Process for the preparation of a substantive azo dye.

Family Applications Before (4)

Application Number Title Priority Date Filing Date
CH249787D CH249787A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249792D CH249792A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249795D CH249795A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249790D CH249790A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.

Family Applications After (9)

Application Number Title Priority Date Filing Date
CH249786D CH249786A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249794D CH249794A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249793D CH249793A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249788D CH249788A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249789D CH249789A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH245067D CH245067A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH249791D CH249791A (en) 1946-01-18 1945-02-20 Process for the preparation of a substantive azo dye.
CH252072D CH252072A (en) 1946-01-18 1946-01-18 Process for the preparation of a substantive azo dye.
CH269047D CH269047A (en) 1946-01-18 1946-01-18 Process for the preparation of a substantive azo dye.

Country Status (1)

Country Link
CH (14) CH249787A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3320972A1 (en) * 1982-06-19 1983-12-22 Sandoz-Patent-GmbH, 7850 Lörrach Metal-containing disazo compounds, process for preparation and process for dyeing or printing

Also Published As

Publication number Publication date
CH249788A (en) 1947-07-15
CH249792A (en) 1947-07-15
CH249791A (en) 1947-07-15
CH249793A (en) 1947-07-15
CH249789A (en) 1947-07-15
CH249790A (en) 1947-07-15
CH249795A (en) 1947-07-15
CH249786A (en) 1947-07-15
CH249794A (en) 1947-07-15
CH269047A (en) 1950-06-15
CH245067A (en) 1946-10-31
CH249787A (en) 1947-07-15
CH252072A (en) 1947-11-30

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