2-(4-Fluorophenyl)-N-(piperidin-3-yl)acetamide hydrochloride CAS 1605602-91-2

Purity 97%+In StockPharmaceutical Standards
CAS No.1605602-91-2
Molecular FormulaC13H17FN2O
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Fluorophenyl)-N-(piperidin-3-yl)acetamide hydrochloride CAS 1605602-91-2 chemical structure

Description

2-(4-Fluorophenyl)-N-(piperidin-3-yl)acetamide hydrochloride (C13H17FN2OHCl) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies 2-(4-Fluorophenyl)-N-(piperidin-3-yl)acetamide hydrochloride (CAS 1605602-91-2), a certified reference material (molecular formula C13H17FN2OHCl, MW 272.75 g/mol) for analytical method development and quality control.

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-(4-Fluorophenyl)-N-(piperidin-3-yl)acetamide 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 FormulaC13H17FN2O HCl
Molecular Weight272.75 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
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.)1993
Halogen ContentF/Cl-containing
Nitrogen Atoms2

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