Levetiracetam EP Impurity G

N° de SZ CAT:	SZ-L001008
Número CAS	7682-20-4
Mol.F.	C4H10N2O : HCl
Peso Molecular	102.1 : 36.5
Status de Fatura	In Stock
Rel. CAS No	7324-11-0 (free base)
Shipping Condition	Ambient Temperature

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Nome Químico: (S)-2-Aminobutanamide hydrochloride

Sinônimo: Levetiracetam USP Related Compound B

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: CC[C@H](N)C(N)=O.Cl

Enantiomeric impurity determination of levetiracetam using capillary electrochromatography
Debby Mangelings1 Jan Saevels2 Yvan Vander Heyden
J. Sep. Sci. 2006, 29, 2827 – 2836

separation and estimation of process related impurities and degradation products of levetiracetam in solid pharmaceutical formulation using ion-pair chromatography
Navneet Kumar1,2 and D. Sangeetha
Journal of Liquid Chromatography & Related Technologies, 36:1835–1848, 2013

Simple GC-MS Method for Analysis of Levetiracetam and ProcessRelated Toxic Impurity
Hazim M. Ali1,2 , Mohammed Gamal* 3,4 , Nada S. Abdelwahab4 , Nehal F. Farid
Microchemical Journal Volume 146, May 2019, Pages 1236-1240

Levetiracetam EP Impurity G is chemically (S)-2-Aminobutanamide hydrochloride . It is also known as Levetiracetam USP Related Compound B . Levetiracetam EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. Levetiracetam EP Impurity G can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Levetiracetam.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

Levetiracetam EP Impurity G

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