3-Methyl-1-(2-phenylethyl)-4-piperidone CAS 129164-39-2

Purity 97%+In StockPharmaceutical Standards
CAS No.129164-39-2
Molecular FormulaC14H19NO
Molecular Weight217.31 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Methyl-1-(2-phenylethyl)-4-piperidone CAS 129164-39-2 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 217.31 g/mol gives 3-Methyl-1-(2-phenylethyl)-4-piperidone distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 3-Methyl-1-(2-phenylethyl)-4-piperidone (CAS 129164-39-2), a certified reference material (molecular formula C14H19NO, MW 217.31 g/mol) for analytical method development and quality control.

The molecular framework of 3-Methyl-1-(2-phenylethyl)-4-piperidone (C14H19NO) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. 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. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), 3-Methyl-1-(2-phenylethyl)-4-piperidone 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 FormulaC14H19NO
Molecular Weight217.31 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1993
Nitrogen Atoms1

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