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CH187606A - Process for the preparation of a chromable yellow azo dye. - Google Patents

Process for the preparation of a chromable yellow azo dye.

Info

Publication number
CH187606A
CH187606A CH187606DA CH187606A CH 187606 A CH187606 A CH 187606A CH 187606D A CH187606D A CH 187606DA CH 187606 A CH187606 A CH 187606A
Authority
CH
Switzerland
Prior art keywords
yellow
chromable
azo dye
preparation
yellow azo
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 CH187606A publication Critical patent/CH187606A/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
    • C09B45/00Complex metal compounds of azo dyes
    • C09B45/02Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
    • C09B45/14Monoazo compounds
    • C09B45/16Monoazo compounds containing chromium
    • 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
    • C09B29/34Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3647Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms
    • C09B29/3652Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles
    • C09B29/366Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a five-membered ring with two nitrogen atoms as heteroatoms containing a 1,2-diazoles or hydrogenated 1,2-diazoles containing hydroxy-1,2-diazoles, e.g. pyrazolone

Landscapes

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

Description

  

  <B>Zusatzpatent</B> zum Hauptpatent Nr. 181808.    Verfahren zur Herstellung eines     ehromierbaren    gelben     Azofarbstoifes.       Gegenstand des vorliegenden Zusatzpa  tentes ist ein Verfahren zur Herstellung eines       chromierbaren    gelben     Azofarbstoffes,    welches  darin besteht, dass man dianotierte     ortho-          Aminobenzoesäure    mit     1-(2"-Methyl-4'-phen-          oxy-3'.s    u     lfophenyl)-5-pyrazolon-3-carbonsäure-          äthylester    kuppelt.  



  <I>Beispiel:</I>  137 Gewichtsteile     ortho-Aminobenzoesäure     werden in üblicher Weise dianotiert und mit  einer     sodaalkalischen    Lösung von 418 Ge  wichtsteilen     1-(2"-Methyl-4'-phenoxy-3'-sulfo-          phenyl)-5        -pyrazolon        -3-carbonsäureäthylester     vereinigt. Nach beendeter Kupplung wird der       Farbstoff    abgesaugt und getrocknet.  



  Er stellt ein gelbes, in Wasser leicht lös  liches Pulver dar, das Wolle in gelben Tönen  färbt, die sich nach erfolgter Behandlung mit  chromabgebenden Mitteln, wie zum Beispiel       Kaliumbichromat    und Schwefelsäure, durch    gute Echtheitseigenschaften, insbesondere sehr  gute     Walkechtheit    auszeichnen.



  <B> Additional patent </B> to main patent no. 181808. Process for the production of an honorable yellow azo dye. The subject of the present additional patent is a process for the production of a chromable yellow azo dye, which consists in that dianotated ortho-aminobenzoic acid with 1- (2 "-methyl-4'-phenoxy-3'.sulfophenyl) -5- pyrazolone-3-carboxylic acid ethyl ester couples.



  <I> Example: </I> 137 parts by weight of ortho-aminobenzoic acid are dianotized in the usual way and mixed with a soda-alkaline solution of 418 parts by weight of 1- (2 "-methyl-4'-phenoxy-3'-sulfophenyl) -5 -pyrazolone-3-carboxylic acid ethyl ester combined After the coupling, the dye is filtered off with suction and dried.



  It is a yellow, easily soluble in water powder that dyes wool in yellow tones which, after treatment with chromium-releasing agents, such as potassium dichromate and sulfuric acid, are characterized by good fastness properties, in particular very good milled fastness.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines chromier- baren gelben Azofarbstoffes, dadurch gekenn zeichnet, dass man dianotierte ortho-Amino- benzoesäure mit 1-(2"-Methyl-4'-phenoxy-3' sulfophenyl)-5-pyrazolon-3-carbonsäureäthyl- ester kuppelt. Claim: Process for the production of a chromable yellow azo dye, characterized in that dianotated ortho-amino-benzoic acid with 1- (2 "-methyl-4'-phenoxy-3 'sulfophenyl) -5-pyrazolone-3-carboxylic acid ethyl - ester couples. Der so erhaltene Farbstoff stellt ein gelbes, in Wasser leicht lösliches Pulver dar, das Wolle in gelben Tönen färbt, die sich nach erfolgter Behandlung mit ebromabgebenden Mitteln, wie zum Beispiel Kaliumbichromat und Schwefelsäure, durch gute Echtheits eigenschaften, insbesondere sehr gute Walk- echtheit auszeichnen. The dye obtained in this way is a yellow, readily soluble in water powder that dyes wool in yellow tones which, after treatment with ebroma-releasing agents such as potassium dichromate and sulfuric acid, are characterized by good fastness properties, in particular very good milled fastness .
CH187606D 1935-01-26 1935-01-26 Process for the preparation of a chromable yellow azo dye. CH187606A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH187606T 1935-01-26
CH181808T 1935-01-26

Publications (1)

Publication Number Publication Date
CH187606A true CH187606A (en) 1936-11-15

Family

ID=25720596

Family Applications (1)

Application Number Title Priority Date Filing Date
CH187606D CH187606A (en) 1935-01-26 1935-01-26 Process for the preparation of a chromable yellow azo dye.

Country Status (1)

Country Link
CH (1) CH187606A (en)

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