[2-(benzyloxy)pyridin-4-yl]methanamine CAS 869293-84-5

Purity 97%+In StockPharmaceutical Standards
CAS No.869293-84-5
Molecular FormulaC13H14N2O
Molecular Weight214.26 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

[2-(benzyloxy)pyridin-4-yl]methanamine CAS 869293-84-5 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 [2-(benzyloxy)pyridin-4-yl]methanamine.

CATO supplies [2-(benzyloxy)pyridin-4-yl]methanamine (CAS 869293-84-5), a certified reference material (molecular formula C13H14N2O, MW 214.26 g/mol) for analytical method development and quality control.

Structurally, [2-(benzyloxy)pyridin-4-yl]methanamine (C13H14N2O) contains a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. The molecule exhibits a degree of unsaturation (DBE) of 8.0, corresponding to approximately 8 ring(s) or double-bond equivalent(s). With a molecular weight of 214.26 g/mol, it falls into the medium-molecular-weight range. 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.

CATO manufactures [2-(benzyloxy)pyridin-4-yl]methanamine 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 FormulaC13H14N2O
Molecular Weight214.26 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1987
Nitrogen Atoms2

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