Ganciclovir Mono-O-Acetate CAS: 88110-89-8
| Product Parameters | |
|---|---|
| Catalog No. | BK0C01 |
| CAS.RN | 88110-89-8 |
| Molecular Formula | C11H15N5O5 |
| Molecular Weight | 297.27 g/mol |
| Purity | NLT 98% |
| Synonyms | [2-[(2-amino-6-oxo-1H-purin-9-yl)methoxy]-3-hydroxypropyl] acetate |
Product Overview
O-Monoacetylganciclovir is an important pharmaceutical intermediate for ganciclovir, primarily used in the synthesis of antiviral drugs. As a key precursor, it is widely used in the research and development and production of nucleoside antiviral drugs. This product is suitable for compound screening, small-scale preparation, pilot-scale amplification, and commercial production during the research and development stage. It exhibits good chemical stability and reactivity, providing customers with high-quality, high-purity raw material support to accelerate new drug development, improve process efficiency, and enhance product quality.
Applications
- Antiviral drug synthesis raw materials
- Nucleoside analogue intermediate development
- Ganciclovir formulation process optimization
- Custom pharmaceutical synthesis projects
- Drug metabolism research and analysis
Quality & Supply Capability
English Name: Ganciclovir Mono-O-Acetate Properties: This product is a white to off-white crystalline powder, readily soluble in organic solvents, possessing a stable ester structure, suitable for various synthetic routes, and exhibiting good reaction compatibility and storage stability. Storage Recommendations: Store in a sealed, light-protected, and dry place, referring to the COA/MSDS for specific details. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging Documentation Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from laboratory sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust purity standards, impurity control schemes, packaging specifications, and delivery cycles according to customer needs, while providing complete quality documentation support to ensure product compliance with GMP and ICH requirements. We also provide technical support from R&D to scale-up, helping customers achieve process optimization and project transformation, ensuring an efficient and compliant supply chain system.
Why Choose Bioncan
Focused on pharmaceutical nucleoside intermediates, possessing extensive industry experience. Full-scale supply capabilities, covering needs from laboratory to commercial production. Provides complete quality control documentation to meet domestic and international regulatory requirements. Customized synthesis and packaging design available to meet client needs. Supporting process optimization and scale-up technologies to help clients quickly implement their projects.
Customers are responsible for ensuring compliance with applicable patent, regulatory, and import/export requirements in their respective jurisdictions.
Online Consulting
For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 88110-89-8, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.
