N-(tert-Butyl)-4-chlorobenzenesulfonamide CAS 29083-03-2

Purity 97%+In StockPharmaceutical Standards
CAS No.29083-03-2
Molecular FormulaC10H14ClNO2S
Molecular Weight247.74 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(tert-Butyl)-4-chlorobenzenesulfonamide CAS 29083-03-2 chemical structure

Description

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 supplies N-(tert-Butyl)-4-chlorobenzenesulfonamide (CAS 29083-03-2), a certified reference material (molecular formula C10H14ClNO2S, MW 247.74 g/mol) for analytical method development and quality control.

The molecular framework of N-(tert-Butyl)-4-chlorobenzenesulfonamide (C10H14ClNO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO manufactures N-(tert-Butyl)-4-chlorobenzenesulfonamide 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 FormulaC10H14ClNO2S
Molecular Weight247.74 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1965
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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