N,N-Dinitroso Levofloxacin EP Impurity G

N° de SZ CAT:	SZ-L020033
Número CAS	NA
Mol.F.	C16H16FN5O6
Peso Molecular	393.3
Status de Fatura	In Stock

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SynZeal will update these details as per new development or finding in product specification without further noticed.

Nome Químico: (S)-9-Fluoro-3-methyl-10-((2-(methyl(nitroso)amino)ethyl)(nitroso)amino)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C(C1=CN2C3=C(C=C(F)C(N(CCN(C)N=O)N=O)=C3OC[C@@H]2C)C1=O)O

In silico and in vitro genotoxicity evaluation of levofloxacin n-oxide, an impurity in levofloxacin
Qingfen Zhu1,2, Tao Li2 , Jun Li2 , Ming Guo2 , Weijian Wang2 , and Xiumei Zhang
Toxicology Mechanisms and Methods, 2012; 22(3): 225–230

Identification, Isolation and Characterization of New Process-related Impurities in Levofloxacin
Kishor More* , Leena Gupta, Brajesh Sharma, Prashant Patil, Dattatray Govare
Der Pharma Chemica, 2017, 9(12):7-13

An integrated approach for detection and characterization of the trace impurities in levofloxacin using liquid chromatography– tandem mass spectrometry
Ya-Jie Zheng1 , Jiu-Ming He1 , Rui-Ping Zhang1 , Yu-Cheng Wang2 , Ju-Xian Wang2 , Hui-Qing Wang1 , Yan Wu1 , Wen-Yi He1 and Zeper Abliz
Rapid Commun. Mass Spectrom. 2014, 28, 1164–1174

Analyses of Levofloxacin Adsorption on Pretreated Barley Straw with Respect to Temperature: Kinetics, π–π Electron-Donor–Acceptor Interaction and Site Energy Distribution
Bei Yan, Catherine Hui Niu, and Jian Wang
Environ. Sci. Technol. 2017, 51, 14, 8048–8056

Rapid chiral separation and impurity determination of levofloxacin by ligand-exchange chromatography
Hongyuan Yan, Kyung Ho Row
Analytica Chimica Acta 584 (2007) 160–165

N,N-Dinitroso Levofloxacin EP Impurity G is chemically (S)-9-Fluoro-3-methyl-10-((2-(methyl(nitroso)amino)ethyl)(nitroso)amino)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid. N,N-Dinitroso Levofloxacin EP Impurity G is supplied with detailed characterization data compliant with regulatory guideline. N,N-Dinitroso Levofloxacin 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 Levofloxacin.

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.

N,N-Dinitroso Levofloxacin EP Impurity G

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