2-(3-Iodophenyl)isothiazolidine 1,1-dioxide CAS 1228776-05-3

Purity 97%+In StockPharmaceutical Standards
CAS No.1228776-05-3
Molecular FormulaC9H10INO2S
Molecular Weight323.15 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2-(3-Iodophenyl)isothiazolidine 1,1-dioxide CAS 1228776-05-3 chemical structure

Description

Compared with other compounds in its class, the molecular weight of 323.15 g/mol gives 2-(3-Iodophenyl)isothiazolidine 1,1-dioxide distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

CATO supplies 2-(3-Iodophenyl)isothiazolidine 1,1-dioxide (CAS 1228776-05-3), a certified reference material (molecular formula C9H10INO2S, MW 323.15 g/mol) for analytical method development and quality control.

2-(3-Iodophenyl)isothiazolidine 1,1-dioxide (C9H10INO2S) contains a nitrogen-containing heterocyclic scaffold, an amide group, a sulfone group, a hydroxyl group, an ether linkage, iodine substitution. Halogen substitution raises its density and boiling point, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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.

CATO manufactures 2-(3-Iodophenyl)isothiazolidine 1,1-dioxide under ISO 17034:2016 accreditation with dual CNAS and ANAB accreditation. Each batch is characterized by orthogonal methods and supplied with a full Certificate of Analysis (COA), ensuring metrological traceability.

Physical & Chemical Properties

Molecular FormulaC9H10INO2S
Molecular Weight323.15 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
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)5.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1990
Halogen ContentI-containing
Nitrogen Atoms1
Sulfur Atoms1

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