CH100864A - Process for the production of a new azo dye. - Google Patents
Process for the production of a new azo dye.Info
- Publication number
- CH100864A CH100864A CH100864DA CH100864A CH 100864 A CH100864 A CH 100864A CH 100864D A CH100864D A CH 100864DA CH 100864 A CH100864 A CH 100864A
- Authority
- CH
- Switzerland
- Prior art keywords
- azo dye
- new azo
- production
- new
- pyrazolone
- Prior art date
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
- C09B45/00—Complex metal compounds of azo dyes
- C09B45/02—Preparation from dyes containing in o-position a hydroxy group and in o'-position hydroxy, alkoxy, carboxyl, amino or keto groups
- C09B45/14—Monoazo compounds
- C09B45/16—Monoazo compounds containing chromium
-
- 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)
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 100479. Verfahren zur Herstellung eines neuen Azofarbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff herstellen kann, wenn man die nitrierte Diazoverbindung der 1-A-mino-2- oxynaplitalin-4-suliosäure mit 1-(3-Sulf- amido)-phenyl-S-metliyl-5-pyrazolon kuppelt. Der neue Azofarbstoff bildet ein braunes Pulver. Er färbt Wolle in braunen Farb tönen, welche beim Nach-chro-mieren rot wer den.
<I>Beispiel:</I> <B>295</B> Teile der nitrierten Diazoverbindung der 1-Amino-2-oxynaphtalin <B>-</B> 4<B>-</B> sulfosäure werden in eine abgekühlte Lösung von<B>253</B> Teilen 1-(3"-SuIfami#do)-phenyl-3-methyl-5- pyrazolon in 30'/o-iger Natranlange einge tragen. Nach einstündigem Rühren wird der Farbstoff #durch schwaches Ans#mern mit Mineralsäure aus der alkalischen Reaktions flüssigkeit ausgefällt und gegebenenfalls aus Wasser umkristallisiert.
Additional patent to main patent no. 100479. Process for the production of a new azo dye. It has been found that a new azo dye can be produced if the nitrated diazo compound of 1-A-mino-2-oxynaplitalin-4-sulioic acid with 1- (3-sulfamido) -phenyl-S-metliyl-5- pyrazolone couples. The new azo dye forms a brown powder. It dyes wool in brown shades, which turn red when it is re-chromed.
<I> Example: </I> <B> 295 </B> parts of the nitrated diazo compound of 1-amino-2-oxynaphthalene <B> - </B> 4 <B> - </B> sulfonic acid are converted into a cooled solution of <B> 253 </B> parts of 1- (3 "-Sulfami # do) -phenyl-3-methyl-5-pyrazolone in 30% sodium length. After stirring for one hour, the dye # precipitated from the alkaline reaction liquid by weak acidification with mineral acid and optionally recrystallized from water.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH100479T | 1922-11-11 | ||
| CH100864T | 1922-11-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH100864A true CH100864A (en) | 1924-01-02 |
Family
ID=25705766
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH100864D CH100864A (en) | 1922-11-11 | 1922-11-11 | Process for the production of a new azo dye. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH100864A (en) |
-
1922
- 1922-11-11 CH CH100864D patent/CH100864A/en unknown
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