4-chloro-3-{[(4-sulfamoylphenyl)methyl]sulfamoyl}benzoic acid CAS 794573-84-5

Purity 97%+In StockPharmaceutical Standards
CAS No.794573-84-5
Molecular FormulaC14H13ClN2O6S2
Molecular Weight404.85 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-chloro-3-{[(4-sulfamoylphenyl)methyl]sulfamoyl}benzoic acid CAS 794573-84-5 chemical structure

Description

As a certified reference material (CRM), 4-chloro-3-{[(4-sulfamoylphenyl)methyl]sulfamoyl}benzoic acid 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.

4-chloro-3-{[(4-sulfamoylphenyl)methyl]sulfamoyl}benzoic acid (CAS 794573-84-5), molecular formula C14H13ClN2O6S2 and molecular weight 404.85 g/mol, is a CATO reference standard with documented purity and traceability.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution, 4-chloro-3-{[(4-sulfamoylphenyl)methyl]sulfamoyl}benzoic acid is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 404.85 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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 FormulaC14H13ClN2O6S2
Molecular Weight404.85 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)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms2

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