Acyclovir EP Impurity I
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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.

1797832-75-7Acyclovir EP Impurity I

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Catalogue No.:VL13020
CAS No.:1797832-75-7
Mol. Formula:C14H16N10O4
Mol. Weight:388.34 g/mol

Additional information on CAS 1797832-75-7

Parent drug

Acyclovir

IUPAC Name

2-Amino-7-[[2-[(2-amino-6-oxo-1,6-dihydro-9H-purin-9- yl)methoxy]ethoxy] methyl]-1,7-dihydro-6H-purin-6-one

Pharmacopoeial Synonyms

N/A

Other Synonyms

Acyclovir 7,9 Diguanyl Analog; O-[(Guanin-7-yl)methyl] Acyclovir; O-[(Guanin-7-yl)methyl] Acyclovir; 7,9′-(ETHYLENEBIS(OXYMETHYLENE))DIGUANINE; (7,9′-(ETHYLENEBIS(OXYMETHYLENE))DIGUANINE); 2-Amino-9-((2-((2-amino-6-oxo-3,6-dihydro-7H-purin-7-yl)methoxy)ethoxy)methyl)-3,9-dihydro-6H-purin-6-one

Smiles

C1=NC2=C(N1COCCOCN3C=NC4=C3C(=O)NC(=N4)N)N=C(NC2=O)N

InChI

InChI=1S/C14H16N10O4/c15-13-19-9-8(12(26)22-13)23(4-18-9)5-27-1-2-28-6-24-3-17-7-10(24)20-14(16)21-11(7)25/h3-4H,1-2,5-6H2,(H3,15,19,22,26)(H3,16,20,21,25)

Description

Acyclovir EP Impurity I is a meticulously characterized reference material that complies with rigorous regulatory requirements, including those defined by USP, EMA, JP, and BP. This product plays a crucial role in Abbreviated New Drug Applications (ANDA), New Drug Applications (NDA), and the commercial manufacturing of Acyclovir. It is further supported by a detailed Structure Elucidation Report (SER), ensuring high accuracy and reliability across a broad range of analytical applications.

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.

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