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Clevudine CAS NO 172494-45-0
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CAS No.:172494-45-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Clevudine is a synthetic nucleoside analogue with potent antiviral activity. It is a critical active pharmaceutical ingredient (API) primarily valued for its targeted mechanism of action against viral replication. This compound is essential for pharmaceutical manufacturers and research institutions developing antiviral therapies. Its specific activity profile makes it a key component in advanced therapeutic formulations.
Application
- Antiviral Drug Synthesis: Primary use as an Active Pharmaceutical Ingredient (API) in the manufacture of antiviral medications.
- Hepatitis B Virus (HBV) Research: A vital reference standard and investigational compound in virology and antiviral drug discovery programs targeting HBV.
- Pharmaceutical Intermediates: Serves as a key building block in the multi-step synthesis of more complex nucleoside-based therapeutics.
- Biochemical Research: Used in enzymatic studies and as a probe to understand nucleoside metabolism and viral polymerase inhibition mechanisms.
- Formulation Development: Employed in the R&D of solid dosage forms (tablets, capsules) and other drug delivery systems.
- Reference Standard: Utilized as a high-purity certified reference material (CRM) for quality control and analytical method development in QC laboratories.
Basic Information
| Product Name | Clevudine |
| CAS No. | 172494-45-0 |
| Molecular Formula | C10H13FN2O5 |
| Molecular Weight | 260.22 g/mol |
| Synonyms | 1-(2-Deoxy-2-fluoro-β-L-arabinofuranosyl)-5-methyluracil; L-FMAU; 2'-Fluoro-5-methyl-β-L-arabinofuranosyluracil; FMAU; Clevudine; L-Fd4C; Reverset (developmental code name); L-2'-Fd4C |
| EINECS | Contact for details |
Quality Control
Our Clevudine is manufactured under strict quality management systems. It undergoes rigorous analytical testing to ensure it meets high-purity standards suitable for pharmaceutical research and development. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with each batch. We can support compliance with relevant pharmacopeial guidelines (e.g., USP, EP) for API specifications upon request.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere conditions.
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) | ≥98.0% |
| Related Substances (HPLC) | Total impurities ≤2.0% |
| 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.
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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






