n-(3-Fluorophenyl)-2-(piperazin-1-yl)propanamide CAS 1018252-85-1

Purity 97%+In StockPharmaceutical Standards
CAS No.1018252-85-1
Molecular FormulaC13H18FN3O
Molecular Weight251.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

n-(3-Fluorophenyl)-2-(piperazin-1-yl)propanamide CAS 1018252-85-1 chemical structure

Description

As a certified reference material (CRM), n-(3-Fluorophenyl)-2-(piperazin-1-yl)propanamide 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.

CATO supplies n-(3-Fluorophenyl)-2-(piperazin-1-yl)propanamide (CAS 1018252-85-1), a certified reference material (molecular formula C13H18FN3O, MW 251.30 g/mol) for analytical method development and quality control.

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution, n-(3-Fluorophenyl)-2-(piperazin-1-yl)propanamide is typically off-white to pale yellow low-melting solid. Its solid-state physicochemical attributes — including a molecular weight of 251.30 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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.

Physical & Chemical Properties

Molecular FormulaC13H18FN3O
Molecular Weight251.30 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)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1988
Halogen ContentF-containing
Nitrogen Atoms3

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