CH167173A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
 - CH167173A CH167173A CH167173DA CH167173A CH 167173 A CH167173 A CH 167173A CH 167173D A CH167173D A CH 167173DA CH 167173 A CH167173 A CH 167173A
 - Authority
 - CH
 - Switzerland
 - Prior art keywords
 - production
 - azo dye
 - new azo
 - dye
 - ethyl ester
 - Prior art date
 
Links
- 239000000987 azo dye Substances 0.000 title claims description 4
 - 239000000975 dye Substances 0.000 claims description 4
 - 125000004494 ethyl ester group Chemical group 0.000 claims description 3
 - MFCDHQNPTNBIGC-UHFFFAOYSA-N 6-diazocyclohexa-2,4-diene-1-carboxylic acid Chemical compound OC(=O)C1C=CC=CC1=[N+]=[N-] MFCDHQNPTNBIGC-UHFFFAOYSA-N 0.000 claims description 2
 - 229920000742 Cotton Polymers 0.000 claims description 2
 - 229920000297 Rayon Polymers 0.000 claims description 2
 - 239000000843 powder Substances 0.000 claims description 2
 - 239000002964 rayon Substances 0.000 claims description 2
 - 239000000758 substrate Substances 0.000 claims description 2
 - -1 wool Polymers 0.000 claims description 2
 - 210000002268 wool Anatomy 0.000 claims description 2
 - 239000003086 colorant Substances 0.000 claims 1
 - HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
 - CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
 - RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 1
 - 239000002244 precipitate Substances 0.000 description 1
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
 
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
 - C09B33/00—Disazo and polyazo dyes of the types A->K<-B, A->B->K<-C, or the like, prepared by diazotising and coupling
 - C09B33/02—Disazo dyes
 - C09B33/153—Disazo dyes in which the coupling component is a bis-(aceto-acetyl amide) or a bis-(benzoyl-acetylamide)
 
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Organic Chemistry (AREA)
 - Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
 
Description
  
  Verfahren zur Herstellung eines neuen     Azofarbstoffes.       Es wurde gefunden, dass man einen neuen     Azofarbstoff    der Formel  
EMI0001.0003     
    erhält, wenn man den     Äthylester    der     1-Diazo-          2-benzolcarbonsäure    mit dem     Di-(acetacetyl)-          o.        o'-tolidid    kuppelt.  
  Der so erhaltene     Farbstoff    stellt ein gelbes  Pulver dar. Auf geeigneten Substraten, wie  zum Beispiel Baumwolle, Wolle, Kunstseide,  hergestellt, färbt er diese in leuchtenden sehr  echten gelben Tönen.  
  <I>Beispiel:</I>  33 Teile     Äthylester    der     1-Amino-2-benzol-          aarbonsäure    werden wie üblich dianotiert und    in eine Lösung von 37,8 Teilen     Di-(acet-          acetyl)-o.        o'-tolidid,    100 Teilen Natrium  hydroxydlösung, 15 Teilen Soda und 2000  Teilen Wasser eingetragen. Der gebildete       Farbstoff    fällt sofort aus. Er wird filtriert,  gewaschen und getrocknet.
  Process for the production of a new azo dye. It has been found that a new azo dye of the formula
EMI0001.0003
    obtained when the ethyl ester of 1-diazo-2-benzenecarboxylic acid is coupled with the di- (acetacetyl) - o. o'-tolidide.
  The dye thus obtained is a yellow powder. Produced on suitable substrates such as cotton, wool, rayon, it dyes them in bright, very real yellow tones.
  <I> Example: </I> 33 parts of ethyl ester of 1-amino-2-benzene-carboxylic acid are dianotized as usual and poured into a solution of 37.8 parts of di- (acet-acetyl) -o. o'-tolidide, 100 parts of sodium hydroxide solution, 15 parts of soda and 2000 parts of water entered. The dye formed precipitates immediately. It is filtered, washed and dried.
 
  
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| CH167173T | 1933-01-16 | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| CH167173A true CH167173A (en) | 1934-02-15 | 
Family
ID=4419627
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| CH167173D CH167173A (en) | 1933-01-16 | 1933-01-16 | Process for the production of a new azo dye. | 
Country Status (1)
| Country | Link | 
|---|---|
| CH (1) | CH167173A (en) | 
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| FR2558843A1 (en) * | 1984-01-26 | 1985-08-02 | Sandoz Sa | MIXTURES OF AZO PIGMENTS, THEIR PREPARATION AND USE | 
- 
        1933
        
- 1933-01-16 CH CH167173D patent/CH167173A/en unknown
 
 
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| FR2558843A1 (en) * | 1984-01-26 | 1985-08-02 | Sandoz Sa | MIXTURES OF AZO PIGMENTS, THEIR PREPARATION AND USE | 
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