Acyclovir EP Impurity A
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Documentation

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Includes: HPLC, MASS/LC-MS, 1H NMR, FT-IR, Potency, Structure Elucidation Report (SER), and additional analytical data depending on the product.

102728-64-3Acyclovir EP Impurity A

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Catalogue No.:VL13001
CAS No.:102728-64-3
Mol. Formula:C10H13N5O4
Mol. Weight:267.24 g/mol

Additional information on CAS 102728-64-3

Parent drug

Acyclovir / Valciclovir

IUPAC Name

2-[(2-Amino-6-oxo-1,6-dihydro-9H-purin-9-yl)methoxy]ethyl acetate

Pharmacopoeial Synonyms

Acyclovir Related Compound A; Valciclovir EP Impurity I

Other Synonyms

O-Acetyl Acyclovir; 9-(2-Acetoxyethoxymethyl)guanine; 6H-Purin-6-one, 9-[[2-(acetyloxy)ethoxy]methyl]-2-amino-1,9-dihydro-; 2-[(2-amino-6-oxo-3H-purin-9-yl)methoxy]ethyl acetate; 9-(2-acetoxyethoxy)methylguanine; 2-((2-Amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethylacetate

Smiles

CC(OCCOCN1C=NC2=C1N=C(N)NC2=O)=O

InChI

InChI=1S/C10H13N5O4/c1-6(16)19-3-2-18-5-15-4-12-7-8(15)13-10(11)14-9(7)17/h4H,2-3,5H2,1H3,(H3,11,13,14,17)

Description

Acyclovir EP Impurity A, also known as Acyclovir Related Compound A; Valciclovir EP Impurity I, in various pharmacopoeias, is a highly characterized standard. It meets strict regulatory requirements set by USP, EMA, JP, and BP, making it a crucial component in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial production of Acyclovir/ Valciclovir.

References

Huidobro, A. L., et al. “LC Methods for Acyclovir and Related Impurities Determination.” Journal of Pharmaceutical and Biomedical Analysis, vol. 37, no. 4, Apr. 2005, pp. 687–94, https://doi.org/10.1016/j.jpba.2004.11.039. Ilager, Davalasab, et al. “Synthesis of Ca-Doped ZnO Nanoparticles and Its Application as Highly Efficient Electrochemical Sensor for the Determination of Anti-Viral Drug, Acyclovir.” Journal of Molecular Liquids, vol. 322, Jan. 2021, p. 114552, https://d

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