2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine CAS 1111110-54-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1111110-54-3
Molecular FormulaC12H8F3NO
Molecular Weight239.19 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine CAS 1111110-54-3 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-Hydroxy-6-(4-trifluoromethylphenyl)pyridine.

2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine (CAS 1111110-54-3) is a high-purity analytical reference standard with the molecular formula C12H8F3NO and a molecular weight of 239.19 g/mol.

The molecular framework of 2-Hydroxy-6-(4-trifluoromethylphenyl)pyridine (C12H8F3NO) 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. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

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.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC12H8F3NO
Molecular Weight239.19 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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.)1989
Halogen ContentF-containing
Nitrogen Atoms1

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