Bupropion Impurity 15 CAS 92821-91-5

Description

Compared with other compounds in its class, the molecular weight of 281.96 g/mol gives Bupropion Impurity 15 distinctive chromatographic separation conditions and mass-spectrometry parameter settings.

Bupropion Impurity 15 (CAS 92821-91-5) is a certified pharmaceutical impurity reference standard with the molecular formula C9H7BrCl2O and a molecular weight of 281.96 g/mol.

Owing to a hydroxyl group, an ether linkage, chlorine/bromine substitution, an aromatic ring system, Bupropion Impurity 15 is typically off-white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 281.96 g/mol — guide the selection of appropriate sample preparation and analytical techniques. 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 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 Bupropion Impurity 15 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

Why CATO?

• ISO 17034 accredited reference material producer (CNAS + ANAB dual accreditation)
• 130,000+ catalog items in stock, COA supplied with every batch
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