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Losartan EP Impurity J

N° de SZ CAT:SZ-L028011
Número CAS1006062-27-6
Mol.F.C24H25ClN6O2
Peso Molecular465.0
Status de FaturaIn Stock

Nome Químico: [2-Butyl-4-chloro-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-imidazol-5-yl]methyl acetate (as per EP & USP)

Sinônimo: Losartan USP Related Compound B ; O-Acetyl Losartan ; Losartan Acetate

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: CC(OCC1=C(Cl)N=C(CCCC)N1CC2=CC=C(C3=CC=CC=C3C4=NN=NN4)C=C2)=O

Losartan EP Impurity J is chemically [2-Butyl-4-chloro-1-[[2′-(1H-tetrazol-5-yl)biphenyl-4-yl]methyl]-1H-imidazol-5-yl]methyl acetate (as per EP & USP). It is also known as Losartan USP Related Compound B ; O-Acetyl Losartan ; Losartan Acetate. Losartan EP Impurity J is supplied with detailed characterization data compliant with regulatory guideline. Losartan EP Impurity J 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 Losartan.

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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