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Ledipasvir Diacetone CAS NO 1502655-48-2
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CAS No.:1502655-48-2
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Ledipasvir Diacetone CAS NO 1502655-48-2 is a key pharmaceutical intermediate, specifically a protected form of the active pharmaceutical ingredient Ledipasvir. This compound is of critical importance in the synthesis of modern antiviral medications. It is primarily required by pharmaceutical manufacturers and advanced research institutions engaged in the development and production of treatments for hepatitis C virus (HCV) infection.
Application
- Primary Intermediate in the synthesis of Ledipasvir, a direct-acting antiviral (DAA) agent.
- Active Pharmaceutical Ingredient (API) Manufacturing for HCV combination therapies.
- Pharmaceutical Research & Development for novel antiviral drug candidates.
- Process Chemistry & Scale-Up studies in contract development and manufacturing organizations (CDMOs).
- Reference Standard for quality control and analytical method development in pharmaceutical labs.
- Academic Research in virology and medicinal chemistry programs.
Basic Information
| Product Name | Ledipasvir Diacetone |
| CAS No. | 1502655-48-2 |
| Molecular Formula | C56H66F2N8O8 |
| Molecular Weight | 993.18 g/mol |
| Synonyms | Ledipasvir Diacetone; Ledipasvir Acetone Adduct; GS-5885 Acetone Adduct; (2R,5S,13aR)-8-Methoxy-7,9-dioxo-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxylic acid, 1,1-dimethylethyl ester, compound with acetone (1:2); Ledipasvir Acetone Solvate; GS-5885 Diacetone Solvate |
| EINECS | Contact for details |
Quality Control
Our Ledipasvir Diacetone is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identification by spectroscopic methods (IR, NMR), and control of residual solvents and related substances. We provide full traceability and Certificates of Analysis (COA) are available for every shipment, ensuring compliance with cGMP guidelines for pharmaceutical intermediates.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment. For long-term storage, consider using desiccants.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white 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% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
| Water Content (KF) | ≤ 1.0% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Why choose US
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.






