2-Chloro-3-hydroxy-1-methylpyridin-1-ium 4-methylbenzenesulfonate CAS 73059-19-5

Purity 97%+In StockPharmaceutical Standards
CAS No.73059-19-5
Molecular FormulaC7H7O3S
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-Chloro-3-hydroxy-1-methylpyridin-1-ium 4-methylbenzenesulfonate CAS 73059-19-5 chemical structure

Description

As a certified reference material (CRM), 2-Chloro-3-hydroxy-1-methylpyridin-1-ium 4-methylbenzenesulfonate 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.

2-Chloro-3-hydroxy-1-methylpyridin-1-ium 4-methylbenzenesulfonate (CAS 73059-19-5), molecular formula C7H7O3SC6H7ClNO and molecular weight 315.77 g/mol, is a CATO reference standard with documented purity and traceability.

The molecular framework of 2-Chloro-3-hydroxy-1-methylpyridin-1-ium 4-methylbenzenesulfonate (C7H7O3SC6H7ClNO) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution. 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 presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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.

Physical & Chemical Properties

Molecular FormulaC7H7O3S C6H7ClNO
Molecular Weight315.77 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
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)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1977
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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