2-Amino-3-(2,5-bis(trifluoromethyl)phenyl)propanoic acid CAS 1260002-85-4

Purity 97%+In StockPharmaceutical Standards
CAS No.1260002-85-4
Molecular FormulaC11H9F6NO2
Molecular Weight301.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Amino-3-(2,5-bis(trifluoromethyl)phenyl)propanoic acid CAS 1260002-85-4 chemical structure

Description

The molecular framework of 2-Amino-3-(2,5-bis(trifluoromethyl)phenyl)propanoic acid (C11H9F6NO2) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. 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.

2-Amino-3-(2,5-bis(trifluoromethyl)phenyl)propanoic acid (CAS 1260002-85-4) is a high-purity analytical reference standard with the molecular formula C11H9F6NO2 and a molecular weight of 301.19 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), 2-Amino-3-(2,5-bis(trifluoromethyl)phenyl)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 FormulaC11H9F6NO2
Molecular Weight301.19 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
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; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1

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