5-Fluoropyridin-2-yl trifluoromethanesulfonate CAS 1310559-95-5

Purity 97%+In StockPharmaceutical Standards
CAS No.1310559-95-5
Molecular FormulaC6H3F4NO3S
Molecular Weight245.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-Fluoropyridin-2-yl trifluoromethanesulfonate CAS 1310559-95-5 chemical structure

Description

The molecular framework of 5-Fluoropyridin-2-yl trifluoromethanesulfonate (C6H3F4NO3S) is characterized by an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the protonation state of its nitrogen-containing groups, 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).

5-Fluoropyridin-2-yl trifluoromethanesulfonate (CAS 1310559-95-5) is a high-purity analytical reference standard with the molecular formula C6H3F4NO3S and a molecular weight of 245.15 g/mol.

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), 5-Fluoropyridin-2-yl trifluoromethanesulfonate 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 FormulaC6H3F4NO3S
Molecular Weight245.15 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO, water
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentF-containing
Nitrogen Atoms1
Sulfur Atoms1

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