2-(4-Chlorophenyl)piperidinehydrochloride CAS 1172776-65-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1172776-65-6
Molecular FormulaC11H14ClN
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(4-Chlorophenyl)piperidinehydrochloride CAS 1172776-65-6 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 232.15 g/mol gives 2-(4-Chlorophenyl)piperidinehydrochloride distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-(4-Chlorophenyl)piperidinehydrochloride (CAS 1172776-65-6), a certified reference material (molecular formula C11H14ClNHCl, MW 232.15 g/mol) for analytical method development and quality control.

The molecular framework of 2-(4-Chlorophenyl)piperidinehydrochloride (C11H14ClNHCl) 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. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

As a certified reference material (CRM), 2-(4-Chlorophenyl)piperidinehydrochloride 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 FormulaC11H14ClN HCl
Molecular Weight232.15 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.)1989
Halogen ContentCl-containing
Nitrogen Atoms1

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