1-Chloro-n-(3-chlorobenzyl)-n-ethylmethanesulfonamide CAS 1342554-76-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1342554-76-0
Molecular FormulaC10H13Cl2NO2S
Molecular Weight282.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-Chloro-n-(3-chlorobenzyl)-n-ethylmethanesulfonamide CAS 1342554-76-0 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 1-Chloro-n-(3-chlorobenzyl)-n-ethylmethanesulfonamide (CAS 1342554-76-0), a certified reference material (molecular formula C10H13Cl2NO2S, MW 282.19 g/mol) for analytical method development and quality control.

1-Chloro-n-(3-chlorobenzyl)-n-ethylmethanesulfonamide (C10H13Cl2NO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO manufactures 1-Chloro-n-(3-chlorobenzyl)-n-ethylmethanesulfonamide 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 FormulaC10H13Cl2NO2S
Molecular Weight282.19 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.)1991
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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