Orlistat Impurity 20(3S,4S,6R) CAS 104801-96-9

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.104801-96-9
Molecular FormulaC22H42O3
Molecular Weight354.57 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Orlistat Impurity 20(3S,4S,6R) CAS 104801-96-9 chemical structure

Description

Orlistat Impurity 20(3S,4S,6R) (CAS 104801-96-9) is a certified pharmaceutical impurity reference standard with the molecular formula C22H42O3 and a molecular weight of 354.57 g/mol.

Owing to a carboxylic acid group, a hydroxyl group, an ether linkage, Orlistat Impurity 20(3S,4S,6R) is typically white to off-white crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 354.57 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 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.

CATO manufactures Orlistat Impurity 20(3S,4S,6R) 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 FormulaC22H42O3
Molecular Weight354.57 g/mol
Purity>95%
StorageStore at room temperature, keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityStable under recommended storage conditions
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1986

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