(3S,4R)-3-Methoxy-4-phenylpyrrolidine CAS 1237171-26-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1237171-26-4
Molecular FormulaC11H15NO
Molecular Weight177.24 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3S,4R)-3-Methoxy-4-phenylpyrrolidine CAS 1237171-26-4 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including (3S,4R)-3-Methoxy-4-phenylpyrrolidine.

CATO supplies (3S,4R)-3-Methoxy-4-phenylpyrrolidine (CAS 1237171-26-4), a certified reference material (molecular formula C11H15NO, MW 177.24 g/mol) for analytical method development and quality control.

(3S,4R)-3-Methoxy-4-phenylpyrrolidine (C11H15NO) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

As a certified reference material (CRM), (3S,4R)-3-Methoxy-4-phenylpyrrolidine meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC11H15NO
Molecular Weight177.24 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-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

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