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Entecavir EP Impurity F

N° de SZ CAT:SZ-E014007
Número CAS649761-24-0
Mol.F.C27H31N5O2Si
Peso Molecular485.7
Status de FaturaSynthesis on demand
Rel. CAS No701278-11-7 (HCl salt)
Shipping Condition Ambient Temperature

Nome Químico: 2-Amino-9-[(1S,3R,4S)-3-[(benzyloxy)methyl]-4-[dimethyl(phenyl)silyl]-2-methylidenecyclopentyl]-1,9-dihydro-6H-purin-6-one (as per EP) ; 9-[(1S,3R,4S)-4-Dimethylphenylsilyl-3-(benzyloxymethyl)-2-methylenecyclopentyl]guanine (as per USP)

Sinônimo: Entecavir USP Related Compound A ;

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C1C2=C(N([C@]3(C[C@@]([Si](C)(C4=CC=CC=C4)C)([H])[C@@]([H])(COCC5=CC=CC=C5)C3=C)[H])C=N2)N=C(N)N1

Entecavir EP Impurity F is chemically 2-Amino-9-[(1S,3R,4S)-3-[(benzyloxy)methyl]-4-[dimethyl(phenyl)silyl]-2-methylidenecyclopentyl]-1,9-dihydro-6H-purin-6-one (as per EP) ; 9-[(1S,3R,4S)-4-Dimethylphenylsilyl-3-(benzyloxymethyl)-2-methylenecyclopentyl]guanine (as per USP). It is also known as Entecavir USP Related Compound A ; . Entecavir EP Impurity F is supplied with detailed characterization data compliant with regulatory guideline. Entecavir EP Impurity F 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 Entecavir.

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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