2-Fluoro-3-phenylbicyclo[1.1.1]pentan-1-amine hydrochloride CAS 2731007-31-9

Purity 97%+In StockPharmaceutical Standards
CAS No.2731007-31-9
Molecular FormulaC11H12FN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Fluoro-3-phenylbicyclo[1.1.1]pentan-1-amine hydrochloride CAS 2731007-31-9 chemical structure

Description

2-Fluoro-3-phenylbicyclo[1.1.1]pentan-1-amine hydrochloride (CAS 2731007-31-9), molecular formula C11H12FNHCl and molecular weight 213.68 g/mol, is a CATO reference standard with documented purity and traceability.

Based on its molecular formula C11H12FNHCl, 2-Fluoro-3-phenylbicyclo[1.1.1]pentan-1-amine hydrochloride contains a nitrogen-containing heterocyclic scaffold, a nitrile group, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 213.68 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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 manufactures 2-Fluoro-3-phenylbicyclo[1.1.1]pentan-1-amine 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 FormulaC11H12FN HCl
Molecular Weight213.68 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
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.)2002
Halogen ContentF/Cl-containing
Nitrogen Atoms1

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