Levocarnitine Impurity N29 CAS 101396-91-2

Purity >95%In StockPharmacopoeial Impurity Standards
CAS No.101396-91-2
Molecular FormulaC6H15ClNO
Molecular WeightN/A
CategoryPharmacopoeial Impurity Standards / EP Impurities
AvailabilityIn Stock

Chemical Structure

Levocarnitine Impurity N29 CAS 101396-91-2 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.

CATO supplies Levocarnitine Impurity N29 (CAS 101396-91-2), a pharmacopoeial impurity reference standard (molecular formula C6H15ClNOCl, MW 188.09 g/mol) used for the identification and quantification of trace impurities in APIs.

Levocarnitine Impurity N29 (C6H15ClNOCl) contains an amide group, a hydroxyl group, an ether linkage, chlorine substitution. Halogen substitution raises its density and boiling point; these physicochemical properties determine the optimal preparation and storage of its standard solutions. Halogen substitution (F/Cl/Br/I) produces a distinctive isotope pattern in mass spectrometry, a valuable aid for qualitative confirmation.

As a certified reference material (CRM), Levocarnitine Impurity N29 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 FormulaC6H15ClNO Cl
Molecular Weight188.09 g/mol
Purity>95%
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
CAS Registry Year (est.)1985
Halogen ContentCl-containing
Nitrogen Atoms1

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