1-(4-Chlorophenyl)-4-oxo-N-(o-tolyl)-1,4-dihydropyridazine-3-carboxamide CAS 478063-35-3

Purity 97%+In StockPharmaceutical Standards
CAS No.478063-35-3
Molecular FormulaC18H14ClN3O2
Molecular Weight339.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(4-Chlorophenyl)-4-oxo-N-(o-tolyl)-1,4-dihydropyridazine-3-carboxamide CAS 478063-35-3 chemical structure

Description

1-(4-Chlorophenyl)-4-oxo-N-(o-tolyl)-1,4-dihydropyridazine-3-carboxamide (C18H14ClN3O2) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. It is notably hygroscopic, halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

1-(4-Chlorophenyl)-4-oxo-N-(o-tolyl)-1,4-dihydropyridazine-3-carboxamide (CAS 478063-35-3), molecular formula C18H14ClN3O2 and molecular weight 339.78 g/mol, is a CATO reference standard with documented purity and traceability.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC18H14ClN3O2
Molecular Weight339.78 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3

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