Sodium Valproate Impurity 14 CAS 1636-27-7

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.1636-27-7
Molecular FormulaC9H16O4
Molecular Weight188.22 g/mol
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Sodium Valproate Impurity 14 CAS 1636-27-7 chemical structure

Description

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 supplies Sodium Valproate Impurity 14 (CAS 1636-27-7), a pharmacopoeial impurity reference standard (molecular formula C9H16O4, MW 188.22 g/mol) used for the identification and quantification of trace impurities in APIs.

The molecular framework of Sodium Valproate Impurity 14 (C9H16O4) is characterized by a carboxylic acid group, a hydroxyl group, an ether linkage. 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.

As a certified reference material (CRM), Sodium Valproate Impurity 14 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 FormulaC9H16O4
Molecular Weight188.22 g/mol
Purity>95%
StorageStore at 2-8°C, keep sealed and dry
Solubility (reference)Soluble in methanol, ethanol, DMSO
StabilityHygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)2.0
CAS Registry Year (est.)1957

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