4-Chloro-n-(2-(diisopropylamino)ethyl)-3-nitrobenzenesulfonamide CAS 744242-80-6

Purity 97%+In StockPharmaceutical Standards
CAS No.744242-80-6
Molecular FormulaC14H22ClN3O4S
Molecular Weight363.86 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-Chloro-n-(2-(diisopropylamino)ethyl)-3-nitrobenzenesulfonamide CAS 744242-80-6 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.

4-Chloro-n-(2-(diisopropylamino)ethyl)-3-nitrobenzenesulfonamide (CAS 744242-80-6) is a high-purity analytical reference standard with the molecular formula C14H22ClN3O4S and a molecular weight of 363.86 g/mol.

The molecular framework of 4-Chloro-n-(2-(diisopropylamino)ethyl)-3-nitrobenzenesulfonamide (C14H22ClN3O4S) 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 the protonation state of its nitrogen-containing groups, 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 4-Chloro-n-(2-(diisopropylamino)ethyl)-3-nitrobenzenesulfonamide 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 FormulaC14H22ClN3O4S
Molecular Weight363.86 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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