3,4-Dichloroisothiazole-5-carboxylic acid CAS 18480-53-0

Purity >95%In StockPharmaceutical Standards
CAS No.18480-53-0
Molecular FormulaC4HCl2NO2S
Molecular Weight198.03 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3,4-Dichloroisothiazole-5-carboxylic acid CAS 18480-53-0 chemical structure

Description

CATO supplies 3,4-Dichloroisothiazole-5-carboxylic acid (CAS 18480-53-0), a certified reference material (molecular formula C4HCl2NO2S, MW 198.03 g/mol) for analytical method development and quality control.

Structurally, 3,4-Dichloroisothiazole-5-carboxylic acid (C4HCl2NO2S) contains an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution. The molecule exhibits a degree of unsaturation (DBE) of 4.0, corresponding to approximately 4 ring(s) or double-bond equivalent(s). With a molecular weight of 198.03 g/mol, it falls into the medium-molecular-weight range. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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), 3,4-Dichloroisothiazole-5-carboxylic 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 FormulaC4HCl2NO2S
Molecular Weight198.03 g/mol
Purity>95%
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
CAS Registry Year (est.)1962
Halogen ContentCl-containing
Nitrogen Atoms1
Sulfur Atoms1

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