Description

Omaciclovir is a potent antiviral nucleoside analogue with significant therapeutic potential. This high-purity active pharmaceutical ingredient (API) is critical for the development and manufacturing of antiviral medications targeting herpesviruses and other viral infections. It is primarily utilized by pharmaceutical companies and research institutions engaged in antiviral drug discovery, formulation, and production.

Application

• Pharmaceutical API: Primary active ingredient in the formulation of antiviral prescription drugs.
• Antiviral Research: Key reference standard and investigational compound in virology and drug discovery programs.
• Generic Drug Manufacturing: Sourcing for the production of generic antiviral medications following patent expiry.
• Clinical Trial Material: Supply of cGMP-grade material for Phase I-III clinical studies.
• Biochemical Research: Used in studies of viral replication mechanisms and enzyme inhibition.
• Veterinary Pharmaceuticals: Potential application in developing antiviral treatments for animals.

Basic Information

Item	Detail
Product Name	Omaciclovir
CAS No.	124265-89-0
Molecular Formula	C8H11N5O3
Molecular Weight	225.21 g/mol
Synonyms	9-[(2-Hydroxyethoxy)methyl]guanine; H2G; A-5021; BWB 759U; 2-Amino-1,9-dihydro-9-[(2-hydroxyethoxy)methyl]-6H-purin-6-one; 2-Amino-9-[(2-hydroxyethoxy)methyl]-1,9-dihydro-6H-purin-6-one; Acyclovir analogue; Antiviral nucleoside
EINECS	Contact for details

Quality Control

Our Omaciclovir is manufactured under strict quality management systems. We provide material that meets or exceeds relevant pharmacopeial standards for active pharmaceutical ingredients. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles, ensuring traceability and compliance for regulatory submissions.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption and degradation.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.5%
Related Substances (HPLC)	Total impurities ≤ 1.5% Any single unknown impurity ≤ 0.5%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.