Levetiracetam EP Impurity B

N° de SZ CAT:	SZ-L001003
Número CAS	358629-47-7
Mol.F.	C8H12N2O2
Peso Molecular	168.2
Status de Fatura	In Stock

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Nome Químico: (2Z)-2-(2-Oxopyrrolidin-1-yl)but-2-enamide

Sinônimo: Levetiracetam Crotonamide (USP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: C/C=C(N1C(CCC1)=O)/C(N)=O

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 B is chemically (2Z)-2-(2-Oxopyrrolidin-1-yl)but-2-enamide . It is also known as Levetiracetam Crotonamide (USP). Levetiracetam EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Levetiracetam EP Impurity B 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 B

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Peso Molecular	: 171.2
Status de Fatura	: Out of Stock, Custom Synthesis

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Número CAS	: 358629-47-7
Mol.F.	: C8H12N2O2
Peso Molecular	: 168.2
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Status de Fatura	: Custom Synthesis

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