Acyclovir sodium

阿昔洛韦钠

Also known as: ACYCLOVIR SODIUM, Acyclovir sodium, Sodium 2-((2-amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethanolate, aciclovir sodium, acycloguanosine sodium, acycloguanosinesodium(obs.), acyclovirsodiumsalt, sodiumacyclovir, zovirax, zoviraxsodium

Acyclovir sodium (CAS 69657-51-8) is a compound in the Organic Compounds category listed in the Jingsj chemical database. It has the molecular formula C8H10N5NaO3 and a molecular weight of 247.18600 g/mol. It is also known as ACYCLOVIR SODIUM, Sodium 2-((2-amino-6-oxo-1H-purin-9(6H)-yl)methoxy)ethanolate and aciclovir sodium. Key property: a boiling point of 613.1ºC at 760 mmHg. No supplier offers are currently listed; request a quote. Record last updated Aug 21, 2026.

CAS No.: 69657-51-8
Jingsj CID: J-1983372-3
Molecular Formula: C₈H₁₀N₅NaO₃
Chinese Name: 阿昔洛韦钠
Molecular Weight: 247.18600 g/mol
Category: Organic Compounds
Last updated: 8/21/2026

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Physicochemical Properties

Boiling Point	613.1ºC at 760 mmHg
Exact Mass	247.06800
PSA	122.14000
LogP	0.09990

Activity & Biological Data

Target	HSV-1:0.85 μM (IC50) HSV-2:0.86 μM (IC50)
Additional Information	[1]. Benedetti S, et, al. Acyclovir induces cell cycle perturbation and apoptosis in Jurkat leukemia cells, and enhances chemotherapeutic drug cytotoxicity. Life Sci. 2018 Dec 15;215:80-85. [2]. Suzuki M, et, al. Synergistic antiviral activity of acyclovir and vidarabine against herpes simplex virus types 1 and 2 and varicella-zoster virus. Antiviral Res. 2006 Nov;72(2):157-61. [3]. Li Z, et, al. Acyclovir treatment of skin lesions results in immune deviation in mice infected cutaneously with herpes simplex virus. Antivir Chem Chemother. 1999 Sep;10(5):251-7. [4]. Lönnqvist B, et, al. Oral acyclovir as prophylaxis for bacterial infections during induction therapy for acute leukaemia in adults. The Leukemia Group of Middle Sweden. Support Care Cancer. 1993 May;1(3):139-44.

Target

HSV-1:0.85 μM (IC50) HSV-2:0.86 μM (IC50)

Additional Information

[1]. Benedetti S, et, al. Acyclovir induces cell cycle perturbation and apoptosis in Jurkat leukemia cells, and enhances chemotherapeutic drug cytotoxicity. Life Sci. 2018 Dec 15;215:80-85. [2]. Suzuki M, et, al. Synergistic antiviral activity of acyclovir and vidarabine against herpes simplex virus types 1 and 2 and varicella-zoster virus. Antiviral Res. 2006 Nov;72(2):157-61. [3]. Li Z, et, al. Acyclovir treatment of skin lesions results in immune deviation in mice infected cutaneously with herpes simplex virus. Antivir Chem Chemother. 1999 Sep;10(5):251-7. [4]. Lönnqvist B, et, al. Oral acyclovir as prophylaxis for bacterial infections during induction therapy for acute leukaemia in adults. The Leukemia Group of Middle Sweden. Support Care Cancer. 1993 May;1(3):139-44.

Customs & Trade Information

HS Code	2933990090
Summary	2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Frequently Asked Questions

What is the CAS number of Acyclovir sodium?

The CAS number of Acyclovir sodium is 69657-51-8.

What are the molecular formula and molecular weight of Acyclovir sodium?

Acyclovir sodium has molecular formula C8H10N5NaO3 and molecular weight 247.18600 g/mol.

Data compiled from public chemical databases and supplier catalogs; supplier offers are provided by suppliers.

Last updated: 8/21/2026

How to cite: Jingsj. "Acyclovir sodium (CAS 69657-51-8)". Jingsj Chemical Database. https://www.jingsj.com/compound/J-1983372-3 (accessed 2026-10-28).

Data for reference only; verify specifications, grades and regulatory status with suppliers before purchase.