Bacampicillin EP Impurity F CAS 52-66-4

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.52-66-4
Molecular FormulaC5H11NO2S
Molecular Weight149.21 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Bacampicillin EP Impurity F CAS 52-66-4 chemical structure

Description

As a certified reference material (CRM), Bacampicillin EP Impurity F 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, Bacampicillin EP Impurity F (CAS 52-66-4, C5H11NO2S) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Owing to an amide group, a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, Bacampicillin EP Impurity F is typically white to off-white liquid. Its solid-state physicochemical attributes — including a molecular weight of 149.21 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 FormulaC5H11NO2S
Molecular Weight149.21 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)1.0
CAS Registry Year (est.)1957
Nitrogen Atoms1
Sulfur Atoms1

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