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化学名称: 2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl acetate (as per EP & USP)
异名: O-Acetylacyclovir ; Valaciclovir EP Impurity I ; Acyclovir USP Related Compound A ; Valaciclovir USP Related Compound I
Shipping Temperature: Ambient
HSN Code: 38229010
Country of Origin: India
微笑: CC(OCCOCN1C=NC2=C1N=C(N)NC2=O)=O
Aciclovir EP Impurity A is chemically 2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl acetate (as per EP & USP). It is also known as O-Acetylacyclovir ; Valaciclovir EP Impurity I ; Acyclovir USP Related Compound A ; Valaciclovir USP Related Compound I . Aciclovir EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Aciclovir EP Impurity A 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 Aciclovir.
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.
Compatible stability of vidarabine monophosphate for injection and aciclovir injection
By Liu, Yuelin
From Zhongguo Yaofang (2016), 27(5), 616-618
Determination of aciclovir and ganciclovir in human plasma by liquid chromatography-spectrofluorimetric detection and stability studies in blood samples
By Perrottet, N.; Beguin, A.; Meylan, P.; Pascual, M.; Manuel, O.; Buclin, T.; Biollaz, J.; Decosterd, L. A.
From Journal of Chromatography B: Analytical Technologies in the Biomedical and Life Sciences (2007), 852(1-2), 420-429