CH191738A - Process for the preparation of an azo dye. - Google Patents

Process for the preparation of an azo dye.

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Publication number
CH191738A
CH191738A CH191738DA CH191738A CH 191738 A CH191738 A CH 191738A CH 191738D A CH191738D A CH 191738DA CH 191738 A CH191738 A CH 191738A
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CH
Switzerland
Prior art keywords
dye
weight
parts
preparation
azo dye
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellsc Farbenindustrie
Original Assignee
Ig Farbenindustrie 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 Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Publication of CH191738A publication Critical patent/CH191738A/en

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Description

  

  Verfahren zur Herstellung eines     Azofarbstoffes.       Gegenstand des vorliegenden Patentes ist  ein Verfahren zur Herstellung eines     Azofarb-          stoffes,    dadurch gekennzeichnet, dass man       Aminotetrazol    dianotiert, sauer mit     2-Amino-          5-rraphthol-7-arrlfonsäure    vereinigt und 2     Mol       des so erhältlichen     Monoazofarbstoffes    mit 1       Mol        tetrazotierten    4 . 4'-     Diamino    - 3 .

   3'-     di-          methoxydiphenyl    zu dem     Farbstoff    der Kon  stitution  
EMI0001.0015     
      Der neue     Farbstoff    färbt Baumwolle in       grünstichig    dunkelblauen Tönen, die durch  Nachkupfern licht- und waschecht werden.  



  <I>Beispiel:</I>  9 Gewichtsteile 2 -     amino    - 5 -     naphthol    -     7-          sulfonsaures    Natrium werden in 120 Gewichts  teilen Wasser gelöst, und die Lösung wird  mit Salzsäure bis zur kongosauren Reaktion  versetzt.

   In die saure Suspension der     Amino-          naphtholsulfonsäui-e    lässt man eine aus 3 Ge  wichtsteilen     Aminotetrazol    (kristallwasser  haltig) und 2 Gewichtsteilen     Natriumnitrit     in 100 Gewichtsteilen Wasser und 5 Ge  wichtsteilen     konz.    Salzsäure bereitete     Diazo-          lösung    auf einmal zufliessen; die Kupplung  setzt sofort ein, und nach einiger Zeit erhält  man eine klare, orangegelbe Lösung. Bald  darauf beginnt der Farbstoff auszukristalli  sieren. Durch Zugabe von Kochsalz wird  dessen     Abscheidung    vervollständigt.  



  Der in üblicher Weise isolierte     Farbstoff     wird in 100 Gewichtsteilen Wasser durch  Zugabe von 10-15 Gewichtsteilen Soda in  Lösung gebracht. Sodann lässt man die aus  3,6 Gewichtsteilen     Dianisidin    mit 2 Gewichts  teilen     Natriumnitrit    in üblicher Weise berei  tete     Tetrazolösung    einfliessen.     Pyridinzusatz     beschleunigt die Kupplung. Der fertig gebil  dete     Farbstoff    der vorgenannten Formel wird  durch     Aussalzen    und Abpressen isoliert. Auf  Baumwolle erzeugt der Farbstoff     grünstichig     dunkelblaue Töne, die durch Nachkupfern  licht- und waschecht werden.



  Process for the preparation of an azo dye. The present patent relates to a process for the preparation of an azo dye, characterized in that aminotetrazole is dianotized, acidically combined with 2-amino-5-raphthol-7-arulfonic acid and 2 mol of the monoazo dye obtainable in this way with 1 mol of tetrazotized 4. 4'- diamino - 3.

   3'-dimethoxydiphenyl to the dye of the constitution
EMI0001.0015
      The new dye dyes cotton in greenish dark blue tones, which are made light- and wash-fast by re-coppering.



  <I> Example: </I> 9 parts by weight of 2-amino-5-naphthol-7-sulphonic acid sodium are dissolved in 120 parts by weight of water, and the solution is mixed with hydrochloric acid until the Congo acid reaction occurs.

   In the acidic suspension of the amino naphtholsulfonsäui-e one leaves from 3 parts by weight of aminotetrazole (containing water of crystallization) and 2 parts by weight of sodium nitrite in 100 parts by weight of water and 5 parts by weight of conc. Hydrochloric acid prepared diazo solution flow in at once; the coupling sets in immediately and after a while a clear, orange-yellow solution is obtained. Soon afterwards the dye begins to crystallize out. Its separation is completed by adding common salt.



  The dye, isolated in the usual way, is brought into solution in 100 parts by weight of water by adding 10-15 parts by weight of soda. The tetrazo solution prepared in the usual way from 3.6 parts by weight of dianisidine with 2 parts by weight of sodium nitrite is then allowed to flow in. Addition of pyridine accelerates the coupling. The finished gebil ended dye of the above formula is isolated by salting out and pressing. On cotton, the dye creates dark blue tones with a greenish tint, which can be made light and washable by re-coppering.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Azofarb- stoffes, dadurch gekennzeichnet, dass man Aminotetrazol diazotiert, sauer mit 2-Amino- 5-naphthol-7-sulfonsäure vereinigt und 2 Mol des so erhältlichen Monoazofarbstoffes mit 1 Mol tetrazotierten 4. 4'- Diamino - 3 . 3'- di- methoxydiphenyl zu dein Farbstoff der Kon stitution EMI0002.0037 kuppelt. PATENT CLAIM: A process for the production of an azo dye, characterized in that aminotetrazole is diazotized, acidically combined with 2-amino-5-naphthol-7-sulfonic acid and 2 mol of the monoazo dye thus obtainable with 1 mol of tetrazotized 4,4'-diamino - 3. 3'-dimethoxydiphenyl to your dye of the constitution EMI0002.0037 clutch. Der neue Farbstoff färbt Baumwolle in grünstichig dunkelblauen Tönen, die durch Nachkupfern licht- und waschecht werden. The new dye dyes cotton in greenish dark blue tones, which are made light- and wash-fast by re-coppering.
CH191738D 1934-10-17 1935-10-12 Process for the preparation of an azo dye. CH191738A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE191738X 1934-10-17
CH187121T 1935-10-12

Publications (1)

Publication Number Publication Date
CH191738A true CH191738A (en) 1937-06-30

Family

ID=25721481

Family Applications (1)

Application Number Title Priority Date Filing Date
CH191738D CH191738A (en) 1934-10-17 1935-10-12 Process for the preparation of an azo dye.

Country Status (1)

Country Link
CH (1) CH191738A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2817658A (en) * 1954-12-03 1957-12-24 Geigy Ag J R Metallisable trisazo dyestuffs

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2817658A (en) * 1954-12-03 1957-12-24 Geigy Ag J R Metallisable trisazo dyestuffs

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