Levocarnitine Impurity 10 CAS CATO-C4X-129210

Purity 97%+In StockPharmacopoeial Impurity Standards
CAS No.CATO-C4X-129210
Molecular FormulaC6H15ClNO
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Levocarnitine Impurity 10 CAS CATO-C4X-129210 chemical structure

Description

As a certified reference material (CRM), Levocarnitine Impurity 10 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.

As a process- or degradation-related impurity, Levocarnitine Impurity 10 (CAS CATO-C4X-129210, C6H15ClNOCl) is essential for impurity profiling, related-substances testing, and forced-degradation studies in pharmaceutical development.

Based on its molecular formula C6H15ClNOCl, Levocarnitine Impurity 10 contains an amide group, a hydroxyl group, an ether linkage, chlorine substitution; these features give the compound characteristic functional-group stretching vibrations in infrared spectroscopy. The molecular weight of 188.09 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

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.

Physical & Chemical Properties

Molecular FormulaC6H15ClNO Cl
Molecular Weight188.09 g/mol
Purity97%+
StorageStore at 2-8°C, protect from light, keep tightly closed to prevent evaporation
Solubility (reference)Soluble in methanol, acetonitrile, DMSO, water (slightly soluble)
StabilityLight-sensitive; avoid direct strong light
Degree of Unsaturation (DBE)-1.0
Halogen ContentCl-containing
Nitrogen Atoms1

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