N-(4-(N-(2-(6-Oxo-3-phenylpyridazin-1(6H)-yl)ethyl)sulfamoyl)phenyl)propionamide CAS 921535-32-2

Purity 97%+In StockPharmaceutical Standards
CAS No.921535-32-2
Molecular FormulaC21H22N4O4S
Molecular Weight426.49 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-(N-(2-(6-Oxo-3-phenylpyridazin-1(6H)-yl)ethyl)sulfamoyl)phenyl)propionamide CAS 921535-32-2 chemical structure

Description

CATO manufactures N-(4-(N-(2-(6-Oxo-3-phenylpyridazin-1(6H)-yl)ethyl)sulfamoyl)phenyl)propionamide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

N-(4-(N-(2-(6-Oxo-3-phenylpyridazin-1(6H)-yl)ethyl)sulfamoyl)phenyl)propionamide (CAS 921535-32-2) is a high-purity analytical reference standard with the molecular formula C21H22N4O4S and a molecular weight of 426.49 g/mol.

The molecular framework of N-(4-(N-(2-(6-Oxo-3-phenylpyridazin-1(6H)-yl)ethyl)sulfamoyl)phenyl)propionamide (C21H22N4O4S) is characterized by a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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

Physical & Chemical Properties

Molecular FormulaC21H22N4O4S
Molecular Weight426.49 g/mol
Purity97%+
StorageStore in a cool place (≤25°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
Degree of Unsaturation (DBE)13.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms4
Sulfur Atoms1

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