4-((5-(Trifluoromethyl)pyridin-2-yl)oxy)aniline CAS 71422-81-6

Purity 97%+In StockPharmaceutical Standards
CAS No.71422-81-6
Molecular FormulaC12H9F3N2O
Molecular Weight254.21 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-((5-(Trifluoromethyl)pyridin-2-yl)oxy)aniline CAS 71422-81-6 chemical structure

Description

The molecular framework of 4-((5-(Trifluoromethyl)pyridin-2-yl)oxy)aniline (C12H9F3N2O) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

4-((5-(Trifluoromethyl)pyridin-2-yl)oxy)aniline (CAS 71422-81-6), molecular formula C12H9F3N2O and molecular weight 254.21 g/mol, is a CATO reference standard with documented purity and traceability.

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.

As a certified reference material (CRM), 4-((5-(Trifluoromethyl)pyridin-2-yl)oxy)aniline meets the metrological traceability requirements of ISO/IEC 17025 laboratories. Batch-to-batch consistency is monitored via control charts to guarantee comparable assigned values across lots.

Physical & Chemical Properties

Molecular FormulaC12H9F3N2O
Molecular Weight254.21 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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977
Halogen ContentF-containing
Nitrogen Atoms2

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