5-(4-Chlorophenyl)-3-(p-tolyl)-4,5-dihydro-1H-pyrazole-1-carboxamide CAS 885269-75-0

Purity 97%+In StockPharmaceutical Standards
CAS No.885269-75-0
Molecular FormulaC17H16ClN3O
Molecular Weight313.78 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(4-Chlorophenyl)-3-(p-tolyl)-4,5-dihydro-1H-pyrazole-1-carboxamide CAS 885269-75-0 chemical structure

Description

5-(4-Chlorophenyl)-3-(p-tolyl)-4,5-dihydro-1H-pyrazole-1-carboxamide (C17H16ClN3O) contains a steroid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

5-(4-Chlorophenyl)-3-(p-tolyl)-4,5-dihydro-1H-pyrazole-1-carboxamide (CAS 885269-75-0) is a high-purity analytical reference standard with the molecular formula C17H16ClN3O and a molecular weight of 313.78 g/mol.

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

As a certified reference material (CRM), 5-(4-Chlorophenyl)-3-(p-tolyl)-4,5-dihydro-1H-pyrazole-1-carboxamide meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC17H16ClN3O
Molecular Weight313.78 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)11.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Halogen ContentCl-containing
Nitrogen Atoms3

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