(3R,4S)-1-(tert-butoxycarbonyl)-4-(3-ethylphenyl)pyrrolidine-3-carboxylic acid CAS 1255933-99-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1255933-99-3
Molecular FormulaC18H25NO4
Molecular Weight319.40 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(3R,4S)-1-(tert-butoxycarbonyl)-4-(3-ethylphenyl)pyrrolidine-3-carboxylic acid CAS 1255933-99-3 chemical structure

Description

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.

(3R,4S)-1-(tert-butoxycarbonyl)-4-(3-ethylphenyl)pyrrolidine-3-carboxylic acid (CAS 1255933-99-3), molecular formula C18H25NO4 and molecular weight 319.40 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of (3R,4S)-1-(tert-butoxycarbonyl)-4-(3-ethylphenyl)pyrrolidine-3-carboxylic acid (C18H25NO4) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

As a certified reference material (CRM), (3R,4S)-1-(tert-butoxycarbonyl)-4-(3-ethylphenyl)pyrrolidine-3-carboxylic acid 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 FormulaC18H25NO4
Molecular Weight319.40 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 methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Nitrogen Atoms1

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