(R)-tert-Butyl 3-(benzyl(methyl)amino)pyrrolidine-1-carboxylate CAS 199336-82-8

Purity 97%+In StockPharmaceutical Standards
CAS No.199336-82-8
Molecular FormulaC17H26N2O2
Molecular Weight290.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-tert-Butyl 3-(benzyl(methyl)amino)pyrrolidine-1-carboxylate CAS 199336-82-8 chemical structure

Description

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.

(R)-tert-Butyl 3-(benzyl(methyl)amino)pyrrolidine-1-carboxylate (CAS 199336-82-8), molecular formula C17H26N2O2 and molecular weight 290.40 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (R)-tert-Butyl 3-(benzyl(methyl)amino)pyrrolidine-1-carboxylate (C17H26N2O2) is characterized by a steroid core, an amide 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC17H26N2O2
Molecular Weight290.40 g/mol
AppearanceOff-white to pale yellow crystalline powder
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
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2013
Nitrogen Atoms2

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