CH100382A - Process for the production of a new azo dye. - Google Patents

Process for the production of a new azo dye.

Info

Publication number
CH100382A
CH100382A CH100382DA CH100382A CH 100382 A CH100382 A CH 100382A CH 100382D A CH100382D A CH 100382DA CH 100382 A CH100382 A CH 100382A
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 CH100382A publication Critical patent/CH100382A/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
    • C09B29/0003Monoazo dyes prepared by diazotising and coupling from diazotized anilines
    • 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
    • C09B29/103Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the naphthalene series
    • 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
    • C09B29/103Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group of the naphthalene series
    • C09B29/106Hydroxy carboxylic acids of the naphthalene series

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Coloring (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Zusatzpatent zum Hauptpatent     Nr.   <B>99522.</B>    Verfahren zur Herstellung eines neuen     Azofarbstoffes.       Es wurde gefunden',     dass    man einen neuen       Azofarbstoff    herstellen kann, wenn man       rIas        4-Oxynaphi-alin-l-plienylketoii    mit     di-          azotiertem        4-Chlor-2-amino-phenylbenzyläther     kuppelt.

   Der neue Farbstoff bildet ein in       M'asser    unlösliches, dunkelrotes Pulver;     auf          ,oe(eio,neter    Unterlage hergestellt, erzeugt er       I        ez          feuriae    rote, Töne,  <I>Beispiel:</I>  <B>23,8</B> Teile     4-Oxynaphtalin-l-phenylkeion     werden in<B>500</B> Teilen Wasser unter Zusatz  von 4 Teilen     Ät7natron    gelöst.

   Hierauf fügt       iii.in    noch 20 Teile Soda hinzu und versetzt       init    einer aus 24,3 Teilen -t-Chlor-2-amiilo-         phenylbenzylät-'her    bereiteten     Diazolbsung.     Der gebildete Farbstoff scheidet sich sofort  als hochroter Niederschlag aus.



  Additional patent to main patent no. <B> 99522. </B> Process for the production of a new azo dye. It has been found that a new azo dye can be produced by coupling rIas 4-Oxynaphi-alin-1-plienylketoii with azo-azotized 4-chloro-2-aminophenylbenzyl ether.

   The new dye forms a dark red powder which is insoluble in mass; on, oe (eio, neter base produced, it produces I ez feuriae red, tones, <I> Example: </I> <B> 23.8 </B> parts of 4-oxynaphthalene-l-phenylkeion are used in <B > 500 parts of water are dissolved with the addition of 4 parts of sodium hydroxide.

   Then iii.in adds 20 parts of soda and mixed with a diazole solution prepared from 24.3 parts of -t-chloro-2-amilophenylbenzyl ether. The dye formed separates out immediately as a crimson precipitate.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Azofarbstoffes, dadurch gekennzeichnet, dass man das 4-Oxynaphtalin-l-phenylkeion mit diazotiertem 4-Chlor-2-aminophenylbenzyl- äther kuppelt. Der neue Farbstoff bildet ein in Wasser unlösliches, dankelrotes Pulver; auf geeignet-er Unterlage hergestellt, erzeugt er feurige rote Töne. PATENT CLAIM: Process for the production of a new azo dye, characterized in that the 4-oxynaphthalene-1-phenylkeion is coupled with diazotized 4-chloro-2-aminophenylbenzyl ether. The new dye forms a water-insoluble, thank-you-red powder; Produced on a suitable base, it produces fiery red tones.
CH100382D 1922-07-07 1922-07-07 Process for the production of a new azo dye. CH100382A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH100382T 1922-07-07
CH99522T 1922-07-07

Publications (1)

Publication Number Publication Date
CH100382A true CH100382A (en) 1923-08-16

Family

ID=25705594

Family Applications (1)

Application Number Title Priority Date Filing Date
CH100382D CH100382A (en) 1922-07-07 1922-07-07 Process for the production of a new azo dye.

Country Status (1)

Country Link
CH (1) CH100382A (en)

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