Valproate Impurity 65 CAS CATO-C4X-116665

Purity >90%In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-116665
Molecular FormulaC10H17NO2
Molecular Weight183.25 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Valproate Impurity 65 CAS CATO-C4X-116665 chemical structure

Description

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.

Valproate Impurity 65 (CAS CATO-C4X-116665) is a certified pharmaceutical impurity reference standard with the molecular formula C10H17NO2 and a molecular weight of 183.25 g/mol.

Owing to an amino-acid-derived structure, an amide group, a hydroxyl group, an ether linkage, Valproate Impurity 65 is typically white to pale yellow crystalline powder. Its solid-state physicochemical attributes — including a molecular weight of 183.25 g/mol — guide the selection of appropriate sample preparation and analytical techniques. Nitrogen-containing functional groups confer excellent ionization efficiency in positive-ion electrospray (ESI) mode, making the compound well suited to LC-MS/MS analysis.

CATO manufactures Valproate Impurity 65 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 FormulaC10H17NO2
Molecular Weight183.25 g/mol
AppearanceWhite to pale yellow crystalline powder. (faint amine-like odor)
Purity>90%
StorageStore at 2-8°C, protect from light
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Light-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)3.0
UV AbsorptionUV-absorbing
Nitrogen Atoms1

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