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Cefepime EP Impurity E (Cl)

N° de SZ CAT:SZ-C085006
Número CAS103121-85-3
Mol.F.C13H20N3O3S : Cl
Peso Molecular298.4 : 35.5
Status de FaturaIn Stock
Rel. CAS No110026-16-9 (free base)
Shipping Condition Ambient Temperature

Nome Químico: (6R,7R)-7-Amino-3-[(1-methylpyrrolidinio)methyl]-8-oxo-5-thia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxylate chloride (as per EP); 1-{[(6R,7R)-7-Amino-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-1-methylpyrrolidin-1-ium chloride (as per USP)

Sinônimo: Cefepime USP Related Compound E ; Cefepime Amine Derivative (USP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: OC(C(N1[C@@]2([H])[C@H](N)C1=O)=C(CS2)C[N+]3(CCCC3)C)=O.[Cl-]

Cefepime EP Impurity E (Cl) is chemically (6R,7R)-7-Amino-3-[(1-methylpyrrolidinio)methyl]-8-oxo-5-thia-1-azabicyclo [4.2.0]oct-2-ene-2-carboxylate chloride (as per EP); 1-{[(6R,7R)-7-Amino-2-carboxy-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-3-yl]methyl}-1-methylpyrrolidin-1-ium chloride (as per USP). It is also known as Cefepime USP Related Compound E ; Cefepime Amine Derivative (USP). Cefepime EP Impurity E (Cl) is supplied with detailed characterization data compliant with regulatory guideline. Cefepime EP Impurity E (Cl) 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 Cefepime.

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.

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