(R)-3-amino-4-(2-fluorophenyl)butanoic acid hydrochloride CAS 331763-62-3

Purity 97%+In StockPharmaceutical Standards
CAS No.331763-62-3
Molecular FormulaC10H12FNO2
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

(R)-3-amino-4-(2-fluorophenyl)butanoic acid hydrochloride CAS 331763-62-3 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.

(R)-3-amino-4-(2-fluorophenyl)butanoic acid hydrochloride (CAS 331763-62-3), molecular formula C10H12FNO2HCl and molecular weight 233.67 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C10H12FNO2HCl, (R)-3-amino-4-(2-fluorophenyl)butanoic acid hydrochloride contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 233.67 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures (R)-3-amino-4-(2-fluorophenyl)butanoic acid hydrochloride under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC10H12FNO2 HCl
Molecular Weight233.67 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, faint amine-like odor, low volatility)
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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