CH135389A - Process for the production of a new azo dye. - Google Patents

Process for the production of a new azo dye.

Info

Publication number
CH135389A
CH135389A CH135389DA CH135389A CH 135389 A CH135389 A CH 135389A CH 135389D A CH135389D A CH 135389DA CH 135389 A CH135389 A CH 135389A
Authority
CH
Switzerland
Prior art keywords
new
azo dye
production
dye
good
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 CH135389A publication Critical patent/CH135389A/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
    • C09B29/34Monoazo 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

  

      Zusatzpatent    zum Hauptpatent Nr. 132916.    Verfahren zur Herstellung eines neuen     Azofarbstoffes.       Es wurde gefunden, dass man einen neuen       Farbstoff    erhält,     wenn    man dianotiertes     2,5-          Dichloranilin    mit     1(2,5-Dichlor-4-sulfo)-phenyl-          3-rnethyl-5-pyi-azolori    kuppelt.  



  Der neue     Farbstoff    bildet ein gelbes Pul  ver, er löst sich in Wasser mit gelber Farbe  und ist zum Färben von Wolle und Seide  geeignet. Er zeichnet sich durch sehr gutes       Egalisierungsvermögen,    sehr gute Lichtecht  heit und gute Wasch-, Säure- und Walk  echtheit seiner Färbungen aus. Der neue  Farbstoff kann auch in unlösliche Metallsalze  übergeführt werden und als Lack Verwen  dung finden.  



       Beispiel:     16,2 Teile     2,5-Dichloranilin    werden wie  üblich dianotiert. Bei 5-10  wird diese     Diazo-          lösung    mit einer überschüssiges     Natriumcar-          bonat    enthaltenden Lösung von 34 Teilen       1(2,5-Dichlor-4-sulfo)-phenyl-3-rnethyl-5-pyra-          zolon    vereinigt. Die Kupplung setzt sofort    ein. Man rührt bis zum Verschwinden der       Diazoverbindung;    filtriert den ausgefällten       Farbstoff    und trocknet ihn.



      Additional patent to main patent No. 132916. Process for the production of a new azo dye. It has been found that a new dye is obtained when dianotated 2,5-dichloroaniline is coupled with 1 (2,5-dichloro-4-sulfo) -phenyl-3-methyl-5-pyi-azolori.



  The new dye forms a yellow powder, it dissolves in water with a yellow color and is suitable for dyeing wool and silk. It is characterized by very good leveling properties, very good lightfastness and good wash, acid and milled fastness of its dyeings. The new dye can also be converted into insoluble metal salts and used as a varnish.



       Example: 16.2 parts of 2,5-dichloroaniline are dianotized as usual. At 5-10 this diazo solution is combined with a solution of 34 parts of 1 (2,5-dichloro-4-sulfo) -phenyl-3-methyl-5-pyrazolone containing excess sodium carbonate. The clutch works immediately. Stir until the diazo compound disappears; filter the precipitated dye and dry it.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Azofarbstoffes, dadurch gekennzeichnet, dass man dianotiertes 2,5-Dichloranilin mit 1(2,5- Dichlor - 4 - sulfo)-pheriyl-3-methyl-5-pyrazolon kuppelt. Der neue Farbstoff bildet ein gelbes Pul ver, er löst sich in Wasser mit gelber Farbe und ist zum Färben von Wolle und Seide geeignet. Er zeichnet sich durch sehr gutes Egalisierungsvermögen, sehr gute Lichtecht heit und gute Wasch-, Säure- und Walk- echtheit seiner Färbungen aus. PATENT CLAIM: Process for the preparation of a new azo dye, characterized in that dianotated 2,5-dichloroaniline is coupled with 1 (2,5-dichloro-4-sulfo) -pheriyl-3-methyl-5-pyrazolone. The new dye forms a yellow powder, it dissolves in water with a yellow color and is suitable for dyeing wool and silk. It is characterized by very good leveling properties, very good lightfastness and good wash, acid and milled fastness of its dyeings. Der neue Farbstoff kann auch in unlösliche Metallsalze übergeführt werden und als Lack Verwen dung finden. The new dye can also be converted into insoluble metal salts and used as a varnish.
CH135389D 1927-11-24 1927-11-24 Process for the production of a new azo dye. CH135389A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH132916T 1927-11-24
CH135389T 1927-11-24

Publications (1)

Publication Number Publication Date
CH135389A true CH135389A (en) 1929-09-15

Family

ID=25711951

Family Applications (1)

Application Number Title Priority Date Filing Date
CH135389D CH135389A (en) 1927-11-24 1927-11-24 Process for the production of a new azo dye.

Country Status (1)

Country Link
CH (1) CH135389A (en)

Similar Documents

Publication Publication Date Title
CH266557A (en) Process for the preparation of a copper-compatible polyazo dye.
CH135389A (en) Process for the production of a new azo dye.
CH135390A (en) Process for the production of a new azo dye.
CH135388A (en) Process for the production of a new azo dye.
CH135392A (en) Process for the production of a new azo dye.
CH135391A (en) Process for the production of a new azo dye.
CH132916A (en) Process for the production of a new azo dye.
CH144489A (en) Process for the preparation of a disazo dye.
CH144485A (en) Process for the preparation of a disazo dye.
CH221198A (en) Process for the preparation of an azo dye.
CH202751A (en) Process for the preparation of an azo dye.
CH200063A (en) Process for the preparation of an azo dye.
CH221166A (en) Process for the preparation of an azo dye.
CH117270A (en) Process for the production of a new dye.
CH164437A (en) Process for the production of a chromium-containing dye which coloring in red shades.
CH202745A (en) Process for the preparation of an azo dye.
CH202747A (en) Process for the preparation of an azo dye.
CH228818A (en) Process for the preparation of a stilbene dye.
CH106927A (en) Process for the preparation of a monoazo dye.
CH107128A (en) Process for the preparation of a monoazo dye.
CH124678A (en) Process for the preparation of a monoazo dye.
CH133805A (en) Process for the preparation of an azo dye.
CH128145A (en) Process for the preparation of a dye of the phenonaphtosafranine series.
CH164439A (en) Process for the production of a chromium-containing dye which coloring in red shades.
CH138227A (en) Process for the production of a new azo dye.