1-(2-Iodobenzyl)piperidine CAS 76464-88-5

Purity 97%+In StockPharmaceutical Standards
CAS No.76464-88-5
Molecular FormulaC12H16IN
Molecular Weight301.17 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

1-(2-Iodobenzyl)piperidine CAS 76464-88-5 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 1-(2-Iodobenzyl)piperidine.

1-(2-Iodobenzyl)piperidine (CAS 76464-88-5), molecular formula C12H16IN and molecular weight 301.17 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 1-(2-Iodobenzyl)piperidine (C12H16IN) is characterized by a nitrogen-containing heterocyclic scaffold, a nitrile group, iodine 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.

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

CATO manufactures 1-(2-Iodobenzyl)piperidine 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 FormulaC12H16IN
Molecular Weight301.17 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor)
Purity97%+
StorageStore at 2-8°C, protect from light
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1978
Halogen ContentI-containing
Nitrogen Atoms1

Related Iodobenzyl Standards

Recommended Standards

Why CATO?