N-tert-Butyl-4-chloro-N-[(4-methoxyphenyl)methyl]benzene-1-sulfonamide CAS 1881320-51-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1881320-51-9
Molecular FormulaC18H22ClNO3S
Molecular Weight367.89 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-tert-Butyl-4-chloro-N-[(4-methoxyphenyl)methyl]benzene-1-sulfonamide CAS 1881320-51-9 chemical structure

Description

Based on its molecular formula C18H22ClNO3S, N-tert-Butyl-4-chloro-N-[(4-methoxyphenyl)methyl]benzene-1-sulfonamide contains a steroid core, 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 367.89 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).

N-tert-Butyl-4-chloro-N-[(4-methoxyphenyl)methyl]benzene-1-sulfonamide (CAS 1881320-51-9) is a high-purity analytical reference standard with the molecular formula C18H22ClNO3S and a molecular weight of 367.89 g/mol.

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 N-tert-Butyl-4-chloro-N-[(4-methoxyphenyl)methyl]benzene-1-sulfonamide 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 FormulaC18H22ClNO3S
Molecular Weight367.89 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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