N-Nitroso Flucloxacillin Impurity 22 CAS CATO-C4X-164722

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-164722
Molecular FormulaC19H18ClFN4O7S
Molecular Weight500.89 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

N-Nitroso Flucloxacillin Impurity 22 CAS CATO-C4X-164722 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.

CATO supplies N-Nitroso Flucloxacillin Impurity 22 (CAS CATO-C4X-164722), a pharmacopoeial impurity reference standard (molecular formula C19H18ClFN4O7S, MW 500.89 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C19H18ClFN4O7S, N-Nitroso Flucloxacillin Impurity 22 contains a flavonoid core, an amide group, a sulfone group, a hydroxyl group, an ether linkage, fluorine/chlorine substitution; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 500.89 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

As a certified reference material (CRM), N-Nitroso Flucloxacillin Impurity 22 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.

Physical & Chemical Properties

Molecular FormulaC19H18ClFN4O7S
Molecular Weight500.89 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)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Halogen ContentF/Cl-containing
Nitrogen Atoms4
Sulfur Atoms1

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