Brexpiprazole Impurity 32 CAS 5118-13-8

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.5118-13-8
Molecular FormulaC8H5BrS
Molecular Weight213.09 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Brexpiprazole Impurity 32 CAS 5118-13-8 chemical structure

Description

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.

Brexpiprazole Impurity 32 (CAS 5118-13-8) is a certified pharmaceutical impurity reference standard with the molecular formula C8H5BrS and a molecular weight of 213.09 g/mol.

Brexpiprazole Impurity 32 (C8H5BrS) contains sulfur-containing functionality, bromine substitution, an aromatic ring system. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. 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).

CATO manufactures Brexpiprazole Impurity 32 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 FormulaC8H5BrS
Molecular Weight213.09 g/mol
Purity>95%
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)6.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1958
Halogen ContentBr-containing
Sulfur Atoms1

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