CH128906A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH128906A
CH128906A CH128906TA CH128906A CH 128906 A CH128906 A CH 128906A CH 128906T A CH128906T A CH 128906TA CH 128906 A CH128906 A CH 128906A
Authority
CH
Switzerland
Prior art keywords
production
new dye
dye
acetamino
sulfophenyl
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 CH128906T priority Critical patent/CH128906A/en
Publication of CH128906A publication Critical patent/CH128906A/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B29/00—Monoazo dyes prepared by diazotising and coupling
    • C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
    • C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
    • C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
    • C09B29/3647—Monoazo 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
    • C09B29/3652—Monoazo 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
    • C09B29/366—Monoazo 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

  

  <B>Zusatzpatent</B>     zum    Hauptpatent Nr. 127259.    Verfahren zur Herstellung     eines    neuen     Farbstoffes.       Es wurde     gefunden,        daB    man einen neuen  Farbstoff erhält, wenn man     diazotierte        4-          Acetamino-2-amino-l-benzolsulfosäure    mit     1-          p-Sulfophenyl-3-methyl-5-pyrazolon    kuppelt.  Der so erhaltene Farbstoff bildet ein gelbes  Pulver. Er färbt Wolle aus schwefelsaurem  Bade in sehr gleichmässigen, rotgelben Tönen.

    Die Färbungen sind sehr gut     licht-,        wasser-          und        alkaliecht    und halten der sauren Walke  stand.  



  <I>Beispiel:</I>  25,5 Teile     1-p-Sulfophenyl-3-methyl-5-          pyrazolon    werden in 150 Teilen Wasser mit  20 Teilen     calcinierter    Soda gelöst, mit Eis  gekühlt und hierauf mit der     Diazoverbin-          dung    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     ver-          vollständigt,    dann wird möglichst neutral  gestellt,     filtriert    und getrocknet.



  <B> Additional patent </B> to main patent no. 127259. Process for the production of a new dye. It has been found that a new dye is obtained when diazotized 4-acetamino-2-amino-1-benzenesulfonic acid is coupled with 1-p-sulfophenyl-3-methyl-5-pyrazolone. The dye thus obtained forms a yellow powder. He dyes wool from sulfuric acid bath in very even, red-yellow tones.

    The dyeings are very resistant to light, water and alkali and withstand acidic fulling.



  <I> Example: </I> 25.5 parts of 1-p-sulfophenyl-3-methyl-5-pyrazolone are dissolved in 150 parts of water with 20 parts of calcined soda, cooled with ice and then with the diazo compound from 23 Parts of 4-acetamino-2-amino-1-benzenesulfonic acid are added. 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)

<B>PATENTANSPRUCH:</B> Verfahren zur Herstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass man diazotierte 4-Acetamino-2-amino-l-ben- zolsulfosäure mit 1-p-Sulfophenyl-3-methyl- 5-pyrazolonkuppelt. Der so erhaltene Farb stoff bildet ein gelbes Pulver. Er färbt Wolle aus schwefelsaurem Bade in sehr gleichmässigen, rotgelben Tönen. Die Fär bungen sind sehr gut licht-, Wasser- und alkaliecht und halten der sauren Walke stand. Claim: Process for the production of a new dye, characterized in that diazotized 4-acetamino-2-amino-1-benzenesulfonic acid is coupled with 1-p-sulfophenyl-3-methyl-5-pyrazolone. The dye obtained in this way forms a yellow powder. He dyes wool from sulfuric acid bath in very even, red-yellow tones. The dyeings are very light, water and alkali-proof and can withstand acidic fulling.
CH128906T 1926-12-04 1926-12-04 Process for the production of a new dye. CH128906A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CH128906T CH128906A (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
CH127259T 1926-12-04
CH128906T CH128906A (en) 1926-12-04 1926-12-04 Process for the production of a new dye.

Publications (1)

Publication Number Publication Date
CH128906A true CH128906A (en) 1928-11-16

Family

ID=25710806

Family Applications (1)

Application Number Title Priority Date Filing Date
CH128906T CH128906A (en) 1926-12-04 1926-12-04 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH128906A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594411A (en) * 1981-08-24 1986-06-10 Basf Aktiengesellschaft Sulfonated monoazo colorant lake obtained by di-azo coupling of 5-acetylamino-2-aminobenzene-1-sulfonic acid with 1-(3'-sulfophenyl)-3-methylphyrazol-5-one
WO1996022333A1 (en) * 1995-01-20 1996-07-25 Zeneca Limited Monoazo pigments

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4594411A (en) * 1981-08-24 1986-06-10 Basf Aktiengesellschaft Sulfonated monoazo colorant lake obtained by di-azo coupling of 5-acetylamino-2-aminobenzene-1-sulfonic acid with 1-(3'-sulfophenyl)-3-methylphyrazol-5-one
WO1996022333A1 (en) * 1995-01-20 1996-07-25 Zeneca Limited Monoazo pigments
US5919915A (en) * 1995-01-20 1999-07-06 Zeneca Limited Azo pyrazolone pigments

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