CH128905A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH128905A
CH128905A CH128905TA CH128905A CH 128905 A CH128905 A CH 128905A CH 128905T A CH128905T A CH 128905TA CH 128905 A CH128905 A CH 128905A
Authority
CH
Switzerland
Prior art keywords
dye
production
new dye
sulfonic acid
acetamino
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
Priority to CH128905T priority Critical patent/CH128905A/en
Publication of CH128905A publication Critical patent/CH128905A/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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Coloring (AREA)

Description

  

      Verfahren    zur Herstellung     eines    neuen     Farbstoffes.       Es wurde gefunden, dass man einen neuen  Farbstoff erhält, wenn man     diazotierte     Farbstoff erhält, wenn man     diazotierte        4-          Acetamino-2-amino-l-benzolsulfosäure    mit 1  pyrazolon kuppelt. Der so erhaltene Farb  stoff bildet ein gelbes Pulver. Er färbt Wolle  aus schwefelsaurem Bade in sehr. gleich  mässigen, grüngelben Tönen. Die Färbungen  sind sehr gut licht-, Wasser- und     alkaliecht     und halten der sauren Walke stand.  



  <I>Beispiel:</I>  39 Teile     1-(-2'-Chlor-4'-sulfosäure)-phe-          nyl-3-methyl-5-pyrazolon    werden in 150 Tei  len Wasser mit 20 Teilen     calcinierter    Soda  gelöst, mit Eis gekühlt und hierauf mit der       Diazoverbindung    aus 23 Teilen     4-Acetamino-          2-amino-l-benzolsulfosäure    versetzt. Der sich  bildende Farbstoff scheidet sich teilweise aus.    Durch Zusatz von Kochsalz     wird    die     Fällung     vervollständigt, dann wird möglichst neutral  gestellt, filtriert und getrocknet.



      Process for the production of a new dye. It has been found that a new dye is obtained when diazotized dye is obtained when diazotized 4-acetamino-2-amino-1-benzenesulfonic acid is coupled with 1 pyrazolone. The dye obtained in this way forms a yellow powder. He dyes wool from a sulfuric acid bath in a very great deal. even, green-yellow tones. The dyeings are very resistant to light, water and alkali and withstand acidic fulling.



  <I> Example: </I> 39 parts of 1- (- 2'-chloro-4'-sulfonic acid) -phenyl-3-methyl-5-pyrazolone are dissolved in 150 parts of water with 20 parts of calcined soda, cooled with ice and then mixed with the diazo compound from 23 parts of 4-acetamino-2-amino-1-benzenesulfonic acid. The dye that forms is partially separated out. The precipitation is completed by adding sodium chloride, then it is made as neutral as possible, filtered and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass man diazotierte 4-Acetamino-2-amino-l-ben- zolsulfosäure mit 1-(-2'-Chlor-4'-sulfosäure)- phenyl-3-methyl-5-pyrazolon kuppelt. Der so erhaltene Farbstoff bildet ein gelbes Pulver. Er färbt Wolle aus schwefelsaurem Bade in sehr gleichmässigen, grüngelben Tönen. Die Färbungen sind sehr gut licht-, Wasser- und alkaliecht und halten der sauren Walke stand. PATENT CLAIM: Process for the preparation of a new dye, characterized in that diazotized 4-acetamino-2-amino-1-benzene sulfonic acid with 1 - (- 2'-chloro-4'-sulfonic acid) - phenyl-3-methyl- 5-pyrazolone couples. The dye thus obtained forms a yellow powder. He dyes wool from sulfuric acid bath in very even, green-yellow tones. The dyeings are very resistant to light, water and alkali and withstand acidic fulling.
CH128905T 1926-12-04 1926-12-04 Process for the production of a new dye. CH128905A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CH128905T CH128905A (en) 1926-12-04 1926-12-04 Process for the production of a new dye.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH128905T CH128905A (en) 1926-12-04 1926-12-04 Process for the production of a new dye.
CH127259T 1926-12-04

Publications (1)

Publication Number Publication Date
CH128905A true CH128905A (en) 1928-11-16

Family

ID=25710805

Family Applications (1)

Application Number Title Priority Date Filing Date
CH128905T CH128905A (en) 1926-12-04 1926-12-04 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH128905A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7857948B2 (en) 2006-07-19 2010-12-28 Oerlikon Trading Ag, Trubbach Method for manufacturing poorly conductive layers
EP2355126A2 (en) 2005-03-24 2011-08-10 Oerlikon Trading AG, Trübbach Hard material layer

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2355126A2 (en) 2005-03-24 2011-08-10 Oerlikon Trading AG, Trübbach Hard material layer
US7857948B2 (en) 2006-07-19 2010-12-28 Oerlikon Trading Ag, Trubbach Method for manufacturing poorly conductive layers

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