5-(chlorosulfonyl)-3-fluoro-2-methylbenzoic acid CAS 1909326-68-6

Purity 97%+In StockPharmaceutical Standards
CAS No.1909326-68-6
Molecular FormulaC8H6ClFO4S
Molecular Weight252.65 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

5-(chlorosulfonyl)-3-fluoro-2-methylbenzoic acid CAS 1909326-68-6 chemical structure

Description

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.

5-(chlorosulfonyl)-3-fluoro-2-methylbenzoic acid (CAS 1909326-68-6) is a high-purity analytical reference standard with the molecular formula C8H6ClFO4S and a molecular weight of 252.65 g/mol.

The molecular framework of 5-(chlorosulfonyl)-3-fluoro-2-methylbenzoic acid (C8H6ClFO4S) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution, an aromatic ring system. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional 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).

As a certified reference material (CRM), 5-(chlorosulfonyl)-3-fluoro-2-methylbenzoic acid 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 FormulaC8H6ClFO4S
Molecular Weight252.65 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1995
Halogen ContentF/Cl-containing
Sulfur Atoms1

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