N-(4-chloro-3-nitrophenyl)benzenesulfonamide CAS 55851-37-1

Purity 97%+In StockPharmaceutical Standards
CAS No.55851-37-1
Molecular FormulaC12H9ClN2O4S
Molecular Weight312.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(4-chloro-3-nitrophenyl)benzenesulfonamide CAS 55851-37-1 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 312.73 g/mol gives N-(4-chloro-3-nitrophenyl)benzenesulfonamide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies N-(4-chloro-3-nitrophenyl)benzenesulfonamide (CAS 55851-37-1), a certified reference material (molecular formula C12H9ClN2O4S, MW 312.73 g/mol) for analytical method development and quality control.

Based on its molecular formula C12H9ClN2O4S, N-(4-chloro-3-nitrophenyl)benzenesulfonamide contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 312.73 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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

CATO manufactures N-(4-chloro-3-nitrophenyl)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.

Physical & Chemical Properties

Molecular FormulaC12H9ClN2O4S
Molecular Weight312.73 g/mol
Purity97%+
StorageStore at 2-8°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.)1972
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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