Valganciclovir EP Impurity L

N° de SZ CAT:	SZ-V014044
Número CAS	NA
Mol.F.	C29H44N12O10
Peso Molecular	720.7
Status de Fatura	Custom Synthesis

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Nome Químico: (2R)-3-hydroxy-2-[[2-[[[[9-[[[(2S)-1-hydroxy-3-(L-valyloxy)propan-2-yl]oxy]methyl]-6-oxo-1,6-dihydro-9H-purin-2-yl]amino]methyl]amino]-6-oxo-1,6-dihydro-9H-purin-9-yl]methoxy]propyl L-valinate (as per EP)

Shipping Temperature: Ambient

HSN Code: 38229010

Country of Origin: India

Sorrisos: O=C(N1)C2=C(N(CO[C@@](CO)([H])COC([C@](N)([H])C(C)C)=O)C=N2)N=C1NCNC3=NC(N(CO[C@@]([H])(CO)COC([C@](N)([H])C(C)C)=O)C=N4)=C4C(N3)=O

Valganciclovir EP Impurity L is chemically (2R)-3-hydroxy-2-[[2-[[[[9-[[[(2S)-1-hydroxy-3-(L-valyloxy)propan-2-yl]oxy]methyl]-6-oxo-1,6-dihydro-9H-purin-2-yl]amino]methyl]amino]-6-oxo-1,6-dihydro-9H-purin-9-yl]methoxy]propyl L-valinate (as per EP). Valganciclovir EP Impurity L is supplied with detailed characterization data compliant with regulatory guideline. Valganciclovir EP Impurity L 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 Valganciclovir.

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.

Valganciclovir EP Impurity L

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