N-(2-(tert-Butyl)phenyl)methanesulfonamide CAS 33429-89-9

Purity 97%+In StockPharmaceutical Standards
CAS No.33429-89-9
Molecular FormulaC11H17NO2S
Molecular Weight227.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-(tert-Butyl)phenyl)methanesulfonamide CAS 33429-89-9 chemical structure

Description

The occurrence of N-(2-(tert-Butyl)phenyl)methanesulfonamide is closely related to a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies N-(2-(tert-Butyl)phenyl)methanesulfonamide (CAS 33429-89-9), a certified reference material (molecular formula C11H17NO2S, MW 227.32 g/mol) for analytical method development and quality control.

The molecular framework of N-(2-(tert-Butyl)phenyl)methanesulfonamide (C11H17NO2S) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage. 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. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC11H17NO2S
Molecular Weight227.32 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
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1966
Nitrogen Atoms1
Sulfur Atoms1

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