3-[(2-methyl-3-phenylprop-2-en-1-yl)amino]propane-1,2-diol CAS 1807938-64-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1807938-64-2
Molecular FormulaC13H19NO2
Molecular Weight221.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-[(2-methyl-3-phenylprop-2-en-1-yl)amino]propane-1,2-diol CAS 1807938-64-2 chemical structure

Description

The molecular framework of 3-[(2-methyl-3-phenylprop-2-en-1-yl)amino]propane-1,2-diol (C13H19NO2) is characterized by a nitrogen-containing heterocyclic scaffold, 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. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

3-[(2-methyl-3-phenylprop-2-en-1-yl)amino]propane-1,2-diol (CAS 1807938-64-2) is a high-purity analytical reference standard with the molecular formula C13H19NO2 and a molecular weight of 221.30 g/mol.

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), 3-[(2-methyl-3-phenylprop-2-en-1-yl)amino]propane-1,2-diol 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 FormulaC13H19NO2
Molecular Weight221.30 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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Nitrogen Atoms1

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