Methyl 4-((5-(aminomethyl)pyridin-2-yl)oxy)benzoate CAS 288588-40-9

Purity 97%+In StockPharmaceutical Standards
CAS No.288588-40-9
Molecular FormulaC14H14N2O3
Molecular Weight258.27 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Methyl 4-((5-(aminomethyl)pyridin-2-yl)oxy)benzoate CAS 288588-40-9 chemical structure

Description

The molecular framework of Methyl 4-((5-(aminomethyl)pyridin-2-yl)oxy)benzoate (C14H14N2O3) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies Methyl 4-((5-(aminomethyl)pyridin-2-yl)oxy)benzoate (CAS 288588-40-9), a certified reference material (molecular formula C14H14N2O3, MW 258.27 g/mol) for analytical method development and quality control.

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 Methyl 4-((5-(aminomethyl)pyridin-2-yl)oxy)benzoate 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 FormulaC14H14N2O3
Molecular Weight258.27 g/mol
AppearancePale yellow to yellow crystalline powder
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)2025
Nitrogen Atoms2

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