3-Methylsulfonyl-2,2',3',4',5,5'-hexachlorobiphenyl CAS 104086-18-2

Purity 97%+In StockPharmaceutical Standards
CAS No.104086-18-2
Molecular FormulaC13H6Cl6O2S
Molecular Weight438.97 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

3-Methylsulfonyl-2,2',3',4',5,5'-hexachlorobiphenyl CAS 104086-18-2 chemical structure

Description

Owing to a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system, 3-Methylsulfonyl-2,2',3',4',5,5'-hexachlorobiphenyl is typically pale yellow to yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 438.97 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 3-Methylsulfonyl-2,2',3',4',5,5'-hexachlorobiphenyl (CAS 104086-18-2), a certified reference material (molecular formula C13H6Cl6O2S, MW 438.97 g/mol) for analytical method development and quality control.

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

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.

Physical & Chemical Properties

Molecular FormulaC13H6Cl6O2S
Molecular Weight438.97 g/mol
Purity97%+
StorageStore at room temperature, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
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)8.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1986
Halogen ContentCl-containing
Sulfur Atoms1

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