Lurasidone Impurity 21 CAS 14100-97-1

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.14100-97-1
Molecular FormulaC8H16O3S
Molecular Weight192.28 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Lurasidone Impurity 21 CAS 14100-97-1 chemical structure

Description

As a certified reference material (CRM), Lurasidone Impurity 21 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.

As a process- or degradation-related impurity, Lurasidone Impurity 21 (CAS 14100-97-1, C8H16O3S) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Lurasidone Impurity 21 (C8H16O3S) contains a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage. It is notably hygroscopic, the carboxyl group imparts weak acidity; these physicochemical properties determine the optimal preparation and storage of its standard solutions.

Recommended for quantitative analysis by HPLC, GC, LC-MS/MS, or GC-MS as an external calibration standard; it can also be used for spiked-recovery experiments, LOD/LOQ determination, and LC-MS/MS multiple-reaction-monitoring (MRM) calibration.

Physical & Chemical Properties

Molecular FormulaC8H16O3S
Molecular Weight192.28 g/mol
Purity97%+
StorageStore at 2-8°C, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityHygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)1.0
CAS Registry Year (est.)1961
Sulfur Atoms1

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