Ivermectin EP Impurity F CAS CATO-C4X-198213

Purity >90%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-198213
Molecular FormulaC48H74O14
Molecular Weight875.09 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Ivermectin EP Impurity F CAS CATO-C4X-198213 chemical structure

Description

As a certified reference material (CRM), Ivermectin 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.

CATO supplies Ivermectin EP Impurity F (CAS CATO-C4X-198213), a pharmacopoeial impurity reference standard (molecular formula C48H74O14, MW 875.09 g/mol) used for the identification and quantification of trace impurities in APIs.

Based on its molecular formula C48H74O14, Ivermectin EP Impurity F contains a carboxylic acid group, a hydroxyl group, an ether linkage, a polycyclic aromatic system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 875.09 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).

This reference standard supports related-substances testing and method development in line with ICH Q3A/Q3B guidance on impurity control, and is suitable for system suitability testing and forced-degradation studies.

Physical & Chemical Properties

Molecular FormulaC48H74O14
Molecular Weight875.09 g/mol
Purity>90%
StorageStore at room temperature, protect from light, keep sealed and dry
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)12.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present

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