3-Phenyl-2-[(prop-2-en-1-yl)amino]propanoic acid CAS 14463-99-1

Purity 97%+In StockPharmaceutical Standards
CAS No.14463-99-1
Molecular FormulaC12H15NO2
Molecular Weight205.25 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Phenyl-2-[(prop-2-en-1-yl)amino]propanoic acid CAS 14463-99-1 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 205.25 g/mol gives 3-Phenyl-2-[(prop-2-en-1-yl)amino]propanoic acid distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

3-Phenyl-2-[(prop-2-en-1-yl)amino]propanoic acid (CAS 14463-99-1) is a high-purity analytical reference standard with the molecular formula C12H15NO2 and a molecular weight of 205.25 g/mol.

The molecular framework of 3-Phenyl-2-[(prop-2-en-1-yl)amino]propanoic acid (C12H15NO2) is characterized by an amino-acid-derived structure, 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 high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 3-Phenyl-2-[(prop-2-en-1-yl)amino]propanoic 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 FormulaC12H15NO2
Molecular Weight205.25 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1961
Nitrogen Atoms1

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