Bis(3,4-dichlorophenyl)iodonium chloride CAS 50848-00-5

Purity 97%+In StockPharmaceutical Standards
CAS No.50848-00-5
Molecular FormulaC12H6Cl4I
Molecular WeightN/A
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

Bis(3,4-dichlorophenyl)iodonium chloride CAS 50848-00-5 chemical structure

Description

The occurrence of Bis(3,4-dichlorophenyl)iodonium chloride is closely related to chlorine/iodine substitution, an aromatic ring system in its molecular formula, which determines its behaviour during synthesis, purification, or degradation.

Bis(3,4-dichlorophenyl)iodonium chloride (CAS 50848-00-5), molecular formula C12H6Cl4IHCl and molecular weight 455.34 g/mol, is a CATO reference standard with documented purity and traceability.

Bis(3,4-dichlorophenyl)iodonium chloride (C12H6Cl4IHCl) contains chlorine/iodine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point, its high carbon-to-hydrogen ratio confers good lipid solubility; these physicochemical properties determine the optimal preparation and storage of its standard solutions. The high carbon-to-hydrogen ratio imparts good lipophilicity, allowing liquid-liquid extraction with non-polar solvents such as n-hexane or ethyl acetate.

Recommended for analytical method development and validation; each product is supplied with a full Certificate of Analysis (COA) ensuring ISO 17034 metrological traceability.

As a certified reference material (CRM), Bis(3,4-dichlorophenyl)iodonium chloride 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 FormulaC12H6Cl4I HCl
Molecular Weight455.34 g/mol
AppearanceOff-white to pale yellow crystalline powder. (slight halide-like odor, low volatility)
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.5
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1971
Halogen ContentCl/I-containing

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Why CATO?