Ozanimod Impurity 25 CAS CATO-C4X-290225

Purity 95%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-290225
Molecular FormulaC14H18N2OS
Molecular Weight262.37 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Ozanimod Impurity 25 CAS CATO-C4X-290225 chemical structure

Description

The molecular framework of Ozanimod Impurity 25 (C14H18N2OS) is characterized by a nitrogen-containing heterocyclic scaffold, an amide group, sulfur-containing functionality, a hydroxyl group, an ether linkage. In reversed-phase chromatography, its retention is governed primarily by its high hydrophobicity (logP), which provides a practical basis for HPLC-UV/DAD or LC-MS method development. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Ozanimod Impurity 25 (CAS CATO-C4X-290225) is a certified pharmaceutical impurity reference standard with the molecular formula C14H18N2OS and a molecular weight of 262.37 g/mol.

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.

As a certified reference material (CRM), Ozanimod Impurity 25 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 FormulaC14H18N2OS
Molecular Weight262.37 g/mol
Purity95%
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in DMSO, DMF, methanol
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)7.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms2
Sulfur Atoms1

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