4-Bromo-2,6-dichloro-N-(3-methylbutan-2-yl)benzenesulfonamide CAS 1095871-95-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1095871-95-6
Molecular FormulaC11H14BrCl2NO2S
Molecular Weight375.11 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Bromo-2,6-dichloro-N-(3-methylbutan-2-yl)benzenesulfonamide CAS 1095871-95-6 chemical structure

Description

The molecular framework of 4-Bromo-2,6-dichloro-N-(3-methylbutan-2-yl)benzenesulfonamide (C11H14BrCl2NO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine/bromine 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO supplies 4-Bromo-2,6-dichloro-N-(3-methylbutan-2-yl)benzenesulfonamide (CAS 1095871-95-6), a certified reference material (molecular formula C11H14BrCl2NO2S, MW 375.11 g/mol) for analytical method development and quality control.

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 4-Bromo-2,6-dichloro-N-(3-methylbutan-2-yl)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 FormulaC11H14BrCl2NO2S
Molecular Weight375.11 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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.)1989
Halogen ContentCl/Br-containing
Nitrogen Atoms1
Sulfur Atoms1

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