Fmoc-(S)-3-Amino-3-(2,4-dichlorophenyl)-propionic acid CAS 501015-34-5

Purity 97%+In StockPharmaceutical Standards
CAS No.501015-34-5
Molecular FormulaC24H19Cl2NO4
Molecular Weight456.32 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Fmoc-(S)-3-Amino-3-(2,4-dichlorophenyl)-propionic acid CAS 501015-34-5 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.

CATO supplies Fmoc-(S)-3-Amino-3-(2,4-dichlorophenyl)-propionic acid (CAS 501015-34-5), a certified reference material (molecular formula C24H19Cl2NO4, MW 456.32 g/mol) for analytical method development and quality control.

The molecular framework of Fmoc-(S)-3-Amino-3-(2,4-dichlorophenyl)-propionic acid (C24H19Cl2NO4) is characterized by a flavonoid core, an amide group, a hydroxyl group, an ether linkage, chlorine substitution. 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), Fmoc-(S)-3-Amino-3-(2,4-dichlorophenyl)-propionic 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 FormulaC24H19Cl2NO4
Molecular Weight456.32 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, 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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)15.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1984
Halogen ContentCl-containing
Nitrogen Atoms1

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