(3S,4R)-1-(tert-butyl)-4-(4-methoxyphenyl)pyrrolidine-3-carbonitrile CAS 852305-11-4

Purity 97%+In StockPharmaceutical Standards
CAS No.852305-11-4
Molecular FormulaC16H22N2O
Molecular Weight258.36 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3S,4R)-1-(tert-butyl)-4-(4-methoxyphenyl)pyrrolidine-3-carbonitrile CAS 852305-11-4 chemical structure

Description

As a certified reference material (CRM), (3S,4R)-1-(tert-butyl)-4-(4-methoxyphenyl)pyrrolidine-3-carbonitrile 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.

CATO supplies (3S,4R)-1-(tert-butyl)-4-(4-methoxyphenyl)pyrrolidine-3-carbonitrile (CAS 852305-11-4), a certified reference material (molecular formula C16H22N2O, MW 258.36 g/mol) for analytical method development and quality control.

Structurally, (3S,4R)-1-(tert-butyl)-4-(4-methoxyphenyl)pyrrolidine-3-carbonitrile (C16H22N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 7.0, corresponding to approximately 7 ring(s) or double-bond equivalent(s). With a molecular weight of 258.36 g/mol, it falls into the medium-molecular-weight range. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 FormulaC16H22N2O
Molecular Weight258.36 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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