Vincristine EP Impurity B CAS CATO-C4X-208912

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-208912
Molecular FormulaC46H56N4O9
Molecular Weight808.96 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Vincristine EP Impurity B CAS CATO-C4X-208912 chemical structure

Description

Owing to a nitrogen-containing heterocyclic scaffold, an amide group, a hydroxyl group, an ether linkage, Vincristine EP Impurity B is typically pale yellow to yellow amorphous powder. Its solid-state physicochemical attributes — including a molecular weight of 808.96 g/mol — guide the selection of appropriate sample preparation and analytical techniques. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

Vincristine EP Impurity B (CAS CATO-C4X-208912) is a certified pharmaceutical impurity reference standard with the molecular formula C46H56N4O9 and a molecular weight of 808.96 g/mol.

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.

CATO manufactures Vincristine EP Impurity B 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.

Physical & Chemical Properties

Molecular FormulaC46H56N4O9
Molecular Weight808.96 g/mol
Purity97%+
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
Degree of Unsaturation (DBE)21.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
Nitrogen Atoms4

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