2-(1-Phenylimidazo[1,5-a]pyridin-3-yl)ethan-1-amine CAS 724438-59-9

Purity 97%+In StockPharmaceutical Standards
CAS No.724438-59-9
Molecular FormulaC15H15N3
Molecular Weight237.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(1-Phenylimidazo[1,5-a]pyridin-3-yl)ethan-1-amine CAS 724438-59-9 chemical structure

Description

The occurrence of 2-(1-Phenylimidazo[1,5-a]pyridin-3-yl)ethan-1-amine 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.

2-(1-Phenylimidazo[1,5-a]pyridin-3-yl)ethan-1-amine (CAS 724438-59-9), molecular formula C15H15N3 and molecular weight 237.30 g/mol, is a CATO reference standard with documented purity and traceability.

2-(1-Phenylimidazo[1,5-a]pyridin-3-yl)ethan-1-amine (C15H15N3) 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 2-(1-Phenylimidazo[1,5-a]pyridin-3-yl)ethan-1-amine 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 FormulaC15H15N3
Molecular Weight237.30 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)10.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Nitrogen Atoms3

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