Everolimus Impurity N1 CAS 164162-36-1

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.164162-36-1
Molecular FormulaC9H19F3O4SSi
Molecular Weight308.39 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Everolimus Impurity N1 CAS 164162-36-1 chemical structure

Description

The molecular framework of Everolimus Impurity N1 (C9H19F3O4SSi) is characterized by a sulfone group, a carboxylic acid group, a hydroxyl group, an ether linkage, fluorine substitution. In reversed-phase chromatography, its retention is governed primarily by the polarity and ionization state of its functional groups, which provides a practical basis for HPLC-UV/DAD or LC-MS method development. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

CATO supplies Everolimus Impurity N1 (CAS 164162-36-1), a pharmacopoeial impurity reference standard (molecular formula C9H19F3O4SSi, MW 308.39 g/mol) used for the identification and quantification of trace impurities in APIs.

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.

As a certified reference material (CRM), Everolimus Impurity N1 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 FormulaC9H19F3O4SSi
Molecular Weight308.39 g/mol
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityHygroscopic; reseal immediately after opening; Contains ester bond; hydrolyzes under strong alkaline conditions
Degree of Unsaturation (DBE)-1.0
CAS Registry Year (est.)2003
Halogen ContentF-containing
Sulfur Atoms1

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