3-Chloro-N-(4-sulfamoylphenyl)propanamide CAS 104246-29-9

Purity 97%+In StockPharmaceutical Standards
CAS No.104246-29-9
Molecular FormulaC9H11ClN2O3S
Molecular Weight262.71 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Chloro-N-(4-sulfamoylphenyl)propanamide CAS 104246-29-9 chemical structure

Description

CATO supplies 3-Chloro-N-(4-sulfamoylphenyl)propanamide (CAS 104246-29-9), a certified reference material (molecular formula C9H11ClN2O3S, MW 262.71 g/mol) for analytical method development and quality control.

Based on its molecular formula C9H11ClN2O3S, 3-Chloro-N-(4-sulfamoylphenyl)propanamide 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 262.71 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).

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.

CATO manufactures 3-Chloro-N-(4-sulfamoylphenyl)propanamide 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 FormulaC9H11ClN2O3S
Molecular Weight262.71 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 methanol, ethanol, DMSO
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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