4-(3-Chlorophenyl)-1,2,3-thiadiazole-5-carboxylic acid CAS 1083274-64-9

Purity 97%+In StockPharmaceutical Standards
CAS No.1083274-64-9
Molecular FormulaC9H5ClN2O2S
Molecular Weight240.67 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

4-(3-Chlorophenyl)-1,2,3-thiadiazole-5-carboxylic acid CAS 1083274-64-9 chemical structure

Description

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.

CATO supplies 4-(3-Chlorophenyl)-1,2,3-thiadiazole-5-carboxylic acid (CAS 1083274-64-9), a certified reference material (molecular formula C9H5ClN2O2S, MW 240.67 g/mol) for analytical method development and quality control.

The molecular framework of 4-(3-Chlorophenyl)-1,2,3-thiadiazole-5-carboxylic acid (C9H5ClN2O2S) 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 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.

Physical & Chemical Properties

Molecular FormulaC9H5ClN2O2S
Molecular Weight240.67 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 DMSO, DMF, methanol
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1989
Halogen ContentCl-containing
Nitrogen Atoms2
Sulfur Atoms1

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