CH187426A - Process for the production of a new azo dye. - Google Patents

Process for the production of a new azo dye.

Info

Publication number
CH187426A
CH187426A CH187426DA CH187426A CH 187426 A CH187426 A CH 187426A CH 187426D A CH187426D A CH 187426DA CH 187426 A CH187426 A CH 187426A
Authority
CH
Switzerland
Prior art keywords
production
azo dye
new azo
new
dye
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 CH187426A publication Critical patent/CH187426A/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
    • C09B29/00Monoazo dyes prepared by diazotising and coupling
    • C09B29/10Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
    • C09B29/18Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides
    • C09B29/20Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group ortho-Hydroxy carbonamides of the naphthalene series

Landscapes

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

Description

  

  Verfahren zur     Rerstellung    eines neuen     Azofarbstoffes.       Es wurde gefunden,     #dass,    man einen neuen       Azofarbstoff    erhält, wenn man das     diazo-          tierte        Diät)lylamid    der     2-Aminobenzoesä.ure     mit dem     2,#3-Oxynaplithopsäure-2'-met'hylani-          lid    vereinigt.  



  Der neue Farbstoff bildet ein     lebhauft    ge  färbtes     oranges    Pulver. Auf geeigneten Sub  straten, wie zum Beispiel Baumwolle, her  gestellt, färbt er diese in echten orangen  Tönen.  



  <I>Beispiel:</I>  <B>19,1</B> Teile des     Diätliylamids    der     2.-Ami-          nobenzoesäure    werden wie     übliell        diazotiert     und in eine Lösung von<B>27,7</B> Teilen     2,3-Oxy-          napht'hoesä,ure   <B>-</B>     2'-        metllylanilid,    40 Teilen  30%iger     Natriumhydraxydlösung,   <B>15</B> Teilen    Soda und<B>1000</B> Teilen Wasser eingetragen.  Der gebildete Farbstoff fällt sofort aus. Der  orange Niederschlag wird filtriert     und    ge  trocknet.



  Process for the preparation of a new azo dye. It has been found that a new azo dye is obtained when the diazo-tated diet) lylamide of 2-aminobenzoic acid is combined with 2, # 3-oxynaplithopic acid-2'-methylanilide.



  The new dye forms a brightly colored orange powder. Produced on suitable substrates, such as cotton, he dyes them in real orange tones.



  <I> Example: </I> <B> 19.1 </B> parts of the diethylamide of 2.-aminobenzoic acid are diazotized as usual and converted into a solution of <B> 27.7 </B> parts of 2 , 3-Oxynapht'hoesä, ure <B> - </B> 2'- metllylanilid, 40 parts of 30% sodium hydroxide solution, <B> 15 </B> parts of soda and <B> 1000 </B> parts Water entered. The dye formed precipitates immediately. The orange precipitate is filtered and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Azofarbstoffes, dadurcli gekennzeiehnet, dass man daschazotierte Diä.thylamicl der 2#-Ami- nobenzoesä;are mit dem 2:,3-Oxynaphtlioe- sä,ure-2'-met'hylanili#d vereinigt. Der neue Farbstoff bildet ein lebhaft ge färbtes oranges Pulver. Auf geeigneten Sub straten, wie zum Beispiel Baumwolle, herge stellt, färbt er diese in echten orangen Tönen. PATENT CLAIM: Process for the production of a new azo dye, dadurcli marked that the chaosotized diethylamicl of the 2 # -amino benzoic acids is combined with the 2:, 3-oxynaphtholioic acid, ure-2'-methylanili # d. The new dye forms a vividly colored orange powder. Manufactured on suitable substrates such as cotton, he dyes them in real orange tones.
CH187426D 1935-10-23 1935-10-23 Process for the production of a new azo dye. CH187426A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH187426T 1935-10-23

Publications (1)

Publication Number Publication Date
CH187426A true CH187426A (en) 1936-11-15

Family

ID=4435012

Family Applications (1)

Application Number Title Priority Date Filing Date
CH187426D CH187426A (en) 1935-10-23 1935-10-23 Process for the production of a new azo dye.

Country Status (1)

Country Link
CH (1) CH187426A (en)

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