1-{[4-(chloromethyl)phenyl]methyl}piperidine hydrochloride CAS 1909337-89-8

Purity 97%+In StockPharmaceutical Standards
CAS No.1909337-89-8
Molecular FormulaC13H18ClN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-{[4-(chloromethyl)phenyl]methyl}piperidine hydrochloride CAS 1909337-89-8 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.

1-{[4-(chloromethyl)phenyl]methyl}piperidine hydrochloride (CAS 1909337-89-8), molecular formula C13H18ClNHCl and molecular weight 260.20 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 1-{[4-(chloromethyl)phenyl]methyl}piperidine hydrochloride (C13H18ClNHCl) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, chlorine substitution. 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).

CATO manufactures 1-{[4-(chloromethyl)phenyl]methyl}piperidine 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 FormulaC13H18ClN HCl
Molecular Weight260.20 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)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentCl-containing
Nitrogen Atoms1

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