2,3,5,6-Tetramethylbenzenesulfonyl chloride CAS 60706-63-0

Purity 97%+In StockPharmaceutical Standards
CAS No.60706-63-0
Molecular FormulaC10H13ClO2S
Molecular Weight232.73 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

2,3,5,6-Tetramethylbenzenesulfonyl chloride CAS 60706-63-0 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including 2,3,5,6-Tetramethylbenzenesulfonyl chloride.

CATO supplies 2,3,5,6-Tetramethylbenzenesulfonyl chloride (CAS 60706-63-0), a certified reference material (molecular formula C10H13ClO2S, MW 232.73 g/mol) for analytical method development and quality control.

Structurally, 2,3,5,6-Tetramethylbenzenesulfonyl chloride (C10H13ClO2S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, chlorine substitution, an aromatic ring system. 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 232.73 g/mol, it falls into the medium-molecular-weight range. The presence of an aromatic ring or conjugated system gives the compound characteristic absorption bands in the UV-Vis region, making it well suited to UV or diode-array detection (DAD).

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), 2,3,5,6-Tetramethylbenzenesulfonyl 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 FormulaC10H13ClO2S
Molecular Weight232.73 g/mol
Purity97%+
StorageStore at room temperature, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1974
Halogen ContentCl-containing
Sulfur Atoms1

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