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Olmesartan Medoxomil EP Impurity B

N° de SZ CAT:SZ-O006003
Número CAS849206-43-5
Mol.F.C24H24N6O2
Peso Molecular428.5
Status de FaturaIn Stock
Shipping Condition Ambient Temperature

Nome Químico: 6,6-Dimethyl-2-propyl-3-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-3,6-dihydro-4H-furo[3,4-d]imidazol-4-one

Sinônimo: Olmesartan USP Related Compound A ; Olmesartan gama-Lactone ; Olmesartan Lactone

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C1OC(C)(C)C2=C1N(CC3=CC=C(C4=CC=CC=C4C5=NNN=N5)C=C3)C(CCC)=N2

Olmesartan Medoxomil EP Impurity B is chemically 6,6-Dimethyl-2-propyl-3-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-3,6-dihydro-4H-furo[3,4-d]imidazol-4-one. It is also known as Olmesartan USP Related Compound A ; Olmesartan gama-Lactone ; Olmesartan Lactone. Olmesartan Medoxomil EP Impurity B is supplied with detailed characterization data compliant with regulatory guideline. Olmesartan Medoxomil 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 Olmesartan.

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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