CH114283A - Process for the production of a new dye. - Google Patents

Process for the production of a new dye.

Info

Publication number
CH114283A
CH114283A CH114283DA CH114283A CH 114283 A CH114283 A CH 114283A CH 114283D A CH114283D A CH 114283DA CH 114283 A CH114283 A CH 114283A
Authority
CH
Switzerland
Prior art keywords
new dye
production
yellow
acid
sulfo
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 CH114283A publication Critical patent/CH114283A/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
    • C09B29/3665Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic ring with two nitrogen atoms
    • C09B29/3669Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic ring with two nitrogen atoms from a pyrimidine ring
    • C09B29/3673Barbituric acid and derivatives thereof

Landscapes

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

Description

  

  Verfahren zur Herstellung eines neuen     Farbstoffes.       Es wurde gefunden,. dass man einen neuen  Farbstoff erhält,     -wenn    man     Barbitursäure     mit dianotierter     4-Sulfo-2-amino-l-phenol-fi-          karbonsäure        kuppelt.    Der neue Farbstoff  bildet ein oranges Pulver, löst sich in Was  ser auf Zusatz von     Sodalösung    mit gelb  oranger Farbe und färbt Wolle aus saurem  Bade in gelben Tönen, die beim     Nachebro-          mieren    braungelb und echt werden.  



  <I>Beispiel:</I>  233 Teile     4-Sulfo-2-amino-l-phenol-6-          karbansäure    werden wie üblich dianotiert  und in ein Gemisch aus 134 Teilen     Barbitur-          säure,    133 Teilen 30     %iger    Natronlauge, 170  Teilen Soda und 1500 Teilen Wasser     ein-          hetragen.    Die     Kupplung    setzt sofort ein, zu    ihrer Vervollständigung rührt man noch  einige Zeit. Der gebildete Farbstoff     wird     dann filtriert und getrocknet.



  Process for the production of a new dye. It was found,. that a new dye is obtained if barbituric acid is coupled with dianotated 4-sulfo-2-amino-1-phenol-ficarboxylic acid. The new dye forms an orange powder, dissolves in water with the addition of soda solution with a yellow-orange color and dyes wool from acid baths in yellow tones, which become brown-yellow and real when they are rebrowned.



  <I> Example: </I> 233 parts of 4-sulfo-2-amino-1-phenol-6-carbanic acid are dianotized as usual and converted into a mixture of 134 parts of barbituric acid, 133 parts of 30% sodium hydroxide solution, 170 parts Soda and 1500 parts of water are introduced. The clutch works immediately, and stir for some time to complete. The dye formed is then filtered and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Farbstoffes, dadurch gekennzeichnet, dass man Barbitursäure mit dianotierter 4-Sulf o- 2-amino-l-phenol-6-karbonsäure kuppelt. Der neue Farbstoff bildet ein oranges Pulver, löst sich in Wasser auf Zusatz von Soda lösung mit gelboranger Farbe- und färbt Wolle aus saurem Bade in gelben Tönen, die beim Nachchromieren braungelb und echt werden. PATENT CLAIM: Process for the production of a new dye, characterized in that barbituric acid is coupled with dianotated 4-sulfo-2-amino-1-phenol-6-carboxylic acid. The new dye forms an orange powder, dissolves in water with the addition of soda solution with a yellow-orange color and dyes wool from acidic baths in yellow tones, which become brown-yellow and real when chromium-plating.
CH114283D 1924-12-24 1924-12-24 Process for the production of a new dye. CH114283A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH114283T 1924-12-24

Publications (1)

Publication Number Publication Date
CH114283A true CH114283A (en) 1926-03-16

Family

ID=4373383

Family Applications (1)

Application Number Title Priority Date Filing Date
CH114283D CH114283A (en) 1924-12-24 1924-12-24 Process for the production of a new dye.

Country Status (1)

Country Link
CH (1) CH114283A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993013458A1 (en) * 1991-12-20 1993-07-08 E.I. Du Pont De Nemours And Company Photographic elements with reduced print-through

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993013458A1 (en) * 1991-12-20 1993-07-08 E.I. Du Pont De Nemours And Company Photographic elements with reduced print-through
US5298658A (en) * 1991-12-20 1994-03-29 E. I. Du Pont De Nemours And Company Photographic elements with reduced print-through
US5298378A (en) * 1991-12-20 1994-03-29 E. I. Du Pont De Nemours And Company Photographic elements with reduced print-through

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