(R)-2-(tert-Butyl)-2-methyl-1-tosylaziridine CAS 1207754-80-0

Purity 97%+In StockPharmaceutical Standards
CAS No.1207754-80-0
Molecular FormulaC14H21NO2S
Molecular Weight267.39 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-2-(tert-Butyl)-2-methyl-1-tosylaziridine CAS 1207754-80-0 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 267.39 g/mol gives (R)-2-(tert-Butyl)-2-methyl-1-tosylaziridine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies (R)-2-(tert-Butyl)-2-methyl-1-tosylaziridine (CAS 1207754-80-0), a certified reference material (molecular formula C14H21NO2S, MW 267.39 g/mol) for analytical method development and quality control.

Based on its molecular formula C14H21NO2S, (R)-2-(tert-Butyl)-2-methyl-1-tosylaziridine contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 267.39 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

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 FormulaC14H21NO2S
Molecular Weight267.39 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1
Sulfur Atoms1

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