Oxacillin Impurity 20 HCI CAS CATO-C4X-232120

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-232120
Molecular FormulaC18H21N3O4S
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Oxacillin Impurity 20 HCI CAS CATO-C4X-232120 chemical structure

Description

CATO manufactures Oxacillin Impurity 20 HCI 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.

CATO supplies Oxacillin Impurity 20 HCI (CAS CATO-C4X-232120), a pharmacopoeial impurity reference standard (molecular formula C18H21N3O4SHCl, MW 411.90 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C18H21N3O4SHCl, Oxacillin Impurity 20 HCI contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 411.90 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. 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 FormulaC18H21N3O4S HCl
Molecular Weight411.90 g/mol
Purity>95%
StorageStore in a cool place (≤25°C), protect from light, keep sealed and dry
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light; Hygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)9.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentCl-containing
Nitrogen Atoms3
Sulfur Atoms1

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