3-(Aminomethyl)-1-benzyl-1,2,5,6-tetrahydropyridine CAS 124257-63-2

Purity 97%+In StockPharmaceutical Standards
CAS No.124257-63-2
Molecular FormulaC13H18N2
Molecular Weight202.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-(Aminomethyl)-1-benzyl-1,2,5,6-tetrahydropyridine CAS 124257-63-2 chemical structure

Description

The occurrence of 3-(Aminomethyl)-1-benzyl-1,2,5,6-tetrahydropyridine is closely related to a nitrogen-containing heterocyclic scaffold, a nitrile group in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies 3-(Aminomethyl)-1-benzyl-1,2,5,6-tetrahydropyridine (CAS 124257-63-2), a certified reference material (molecular formula C13H18N2, MW 202.30 g/mol) for analytical method development and quality control.

3-(Aminomethyl)-1-benzyl-1,2,5,6-tetrahydropyridine (C13H18N2) contains a nitrogen-containing heterocyclic scaffold, a nitrile group. Its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

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.

CATO manufactures 3-(Aminomethyl)-1-benzyl-1,2,5,6-tetrahydropyridine 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 FormulaC13H18N2
Molecular Weight202.30 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Nitrogen Atoms2

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