N-(2-Fluoroethyl)pyridin-4-amine CAS 122974-87-2

Purity 97%+In StockPharmaceutical Standards
CAS No.122974-87-2
Molecular FormulaC7H9FN2
Molecular Weight140.16 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

N-(2-Fluoroethyl)pyridin-4-amine CAS 122974-87-2 chemical structure

Description

The occurrence of N-(2-Fluoroethyl)pyridin-4-amine is closely related to a nitrile group, fluorine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

CATO supplies N-(2-Fluoroethyl)pyridin-4-amine (CAS 122974-87-2), a certified reference material (molecular formula C7H9FN2, MW 140.16 g/mol) for analytical method development and quality control.

N-(2-Fluoroethyl)pyridin-4-amine (C7H9FN2) contains a nitrile group, fluorine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 N-(2-Fluoroethyl)pyridin-4-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 FormulaC7H9FN2
Molecular Weight140.16 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1992
Halogen ContentF-containing
Nitrogen Atoms2

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