Methyl 4-(4-{[4-(dimethylsulfamoyl)phenyl]carbamoyl}piperazin-1-yl)-3-nitrobenzoate CAS 692732-99-3

Purity 97%+In StockPharmaceutical Standards
CAS No.692732-99-3
Molecular FormulaC21H25N5O7S
Molecular Weight491.52 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-(4-{[4-(dimethylsulfamoyl)phenyl]carbamoyl}piperazin-1-yl)-3-nitrobenzoate CAS 692732-99-3 chemical structure

Description

Methyl 4-(4-{[4-(dimethylsulfamoyl)phenyl]carbamoyl}piperazin-1-yl)-3-nitrobenzoate (C21H25N5O7S) contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage. It is notably hygroscopic, 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.

Methyl 4-(4-{[4-(dimethylsulfamoyl)phenyl]carbamoyl}piperazin-1-yl)-3-nitrobenzoate (CAS 692732-99-3), molecular formula C21H25N5O7S and molecular weight 491.52 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), Methyl 4-(4-{[4-(dimethylsulfamoyl)phenyl]carbamoyl}piperazin-1-yl)-3-nitrobenzoate 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 FormulaC21H25N5O7S
Molecular Weight491.52 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1985
Nitrogen Atoms5
Sulfur Atoms1

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