Oxaliplatin Impurity 11 CAS 61848-66-6

Purity 95%In StockPharmacopoeial Impurity Standards
CAS No.61848-66-6
Molecular FormulaC6H12Cl2N2Pt
Molecular Weight378.16 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Oxaliplatin Impurity 11 CAS 61848-66-6 chemical structure

Description

Under current pharmacopoeial and regulatory frameworks, quality-control requirements for this class of reference material explicitly involve the control of targets including Oxaliplatin Impurity 11.

CATO supplies Oxaliplatin Impurity 11 (CAS 61848-66-6), a pharmacopoeial impurity reference standard (molecular formula C6H12Cl2N2Pt, MW 378.16 g/mol) used for the identification and quantification of trace impurities in APIs.

Oxaliplatin Impurity 11 (C6H12Cl2N2Pt) contains chlorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

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 Oxaliplatin Impurity 11 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 FormulaC6H12Cl2N2Pt
Molecular Weight378.16 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)1.0
CAS Registry Year (est.)1974
Halogen ContentCl-containing
Nitrogen Atoms2

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