3-[2-Chloro-4-(4-chlorophenoxy)phenyl]-1-(4-chlorobenzenesulfonyl)-1H-pyrazole CAS 321522-28-5

Purity 97%+In StockPharmaceutical Standards
CAS No.321522-28-5
Molecular FormulaC21H13Cl3N2O3S
Molecular Weight479.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[2-Chloro-4-(4-chlorophenoxy)phenyl]-1-(4-chlorobenzenesulfonyl)-1H-pyrazole CAS 321522-28-5 chemical structure

Description

As a certified reference material (CRM), 3-[2-Chloro-4-(4-chlorophenoxy)phenyl]-1-(4-chlorobenzenesulfonyl)-1H-pyrazole 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.

3-[2-Chloro-4-(4-chlorophenoxy)phenyl]-1-(4-chlorobenzenesulfonyl)-1H-pyrazole (CAS 321522-28-5) is a high-purity analytical reference standard with the molecular formula C21H13Cl3N2O3S and a molecular weight of 479.76 g/mol.

3-[2-Chloro-4-(4-chlorophenoxy)phenyl]-1-(4-chlorobenzenesulfonyl)-1H-pyrazole (C21H13Cl3N2O3S) contains a steroid core, an amide group, a sulfone 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

Physical & Chemical Properties

Molecular FormulaC21H13Cl3N2O3S
Molecular Weight479.76 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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