3-Iodo-2-phenoxypyridine CAS 754214-57-8

Purity 97%+In StockPharmaceutical Standards
CAS No.754214-57-8
Molecular FormulaC11H8INO
Molecular Weight297.09 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Iodo-2-phenoxypyridine CAS 754214-57-8 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 297.09 g/mol gives 3-Iodo-2-phenoxypyridine distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

3-Iodo-2-phenoxypyridine (CAS 754214-57-8) is a high-purity analytical reference standard with the molecular formula C11H8INO and a molecular weight of 297.09 g/mol.

The molecular framework of 3-Iodo-2-phenoxypyridine (C11H8INO) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, iodine 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.

As a certified reference material (CRM), 3-Iodo-2-phenoxypyridine 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 FormulaC11H8INO
Molecular Weight297.09 g/mol
AppearancePale yellow to yellow crystalline powder. (slight halide-like odor)
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.)1986
Halogen ContentI-containing
Nitrogen Atoms1

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