3,4-Diamino-N-(2-chlorophenyl)benzenesulfonamide CAS 326023-07-8

Purity 97%+In StockPharmaceutical Standards
CAS No.326023-07-8
Molecular FormulaC12H12ClN3O2S
Molecular Weight297.76 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Diamino-N-(2-chlorophenyl)benzenesulfonamide CAS 326023-07-8 chemical structure

Description

CATO manufactures 3,4-Diamino-N-(2-chlorophenyl)benzenesulfonamide 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.

3,4-Diamino-N-(2-chlorophenyl)benzenesulfonamide (CAS 326023-07-8) is a high-purity analytical reference standard with the molecular formula C12H12ClN3O2S and a molecular weight of 297.76 g/mol.

3,4-Diamino-N-(2-chlorophenyl)benzenesulfonamide (C12H12ClN3O2S) contains a nitrogen-containing heterocyclic scaffold, 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. 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).

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 FormulaC12H12ClN3O2S
Molecular Weight297.76 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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