Ensure consistent formulation quality with our Sofosbuvir API, a medicine grade white powder designed to meet the stringent standards of pharmaceutical production. With an assay of ≥99%, this solid API powder delivers reliable performance, supporting precise dosing and batch-to-batch uniformity in your manufacturing process.
- Produced under strict quality control measures, ensuring compliance with global pharmaceutical standards
- Available in flexible packaging options (cardboard drums or cartons) to suit your production scale, with a monthly capacity of 200kg to meet steady demand
- Non-volatile solid form ensures stability during storage and transportation, reducing risk of degradation
描述
For industrial manufacturing and laboratory research purposes only.
Product Specifications
| Parameter | Value |
|---|---|
| Product Name | Sofosbuvir |
| CAS Number | 1190307-88-0 |
| Grade Standard | Medicine Grade |
| Physical State | Solid |
| Appearance | White or off-White Powder |
| Assay | More Than 99% |
| Volatility | Not Volatile |
| Packaging | Cardboard Drums or Cartons |
| Specification | gram, kilogram |
| Origin | China |
| HS Code | 2934999099 |
| Production Capacity | 200kg/Month |
Addressing Purity and Supply Challenges with Sofosbuvir 1190307-88-0 API
Industrial researchers and manufacturers often face critical hurdles with chemical raw materials—unstable purity leading to inconsistent reactions, batch-to-batch variations that compromise experimental reproducibility, and unreliable supply chains causing costly production delays. Over our 10+ years serving global industrial clients, we’ve witnessed how these issues directly impact R&D timelines and manufacturing efficiency, especially for high-specification chemical APIs.
A Stable and Reliable Chemical Supply Solution
Our Sofosbuvir API addresses these challenges through stringent quality control and consistent production processes. As a 99% assay white powder API, it delivers the high purity required for precise industrial applications, while our monthly 200kg production capacity ensures stable supply even for large-scale manufacturing needs. This combination of quality and reliability supports seamless operations for both research institutions and industrial producers across 50+ countries.
Typical Industrial Applications
Sofosbuvir 1190307-88-0 serves as a key intermediate in specialty chemical synthesis and laboratory research programs. Its high-purity solid form makes it suitable for controlled reactions requiring precise dosing and minimal impurities. Common applications include pharmaceutical intermediate development, chemical process optimization studies, and analytical standard preparation—strictly for industrial and research contexts.
Why Key Specifications Matter
The ≥99% assay of our Sofosbuvir API is critical for reducing side reactions and ensuring consistent experimental outcomes, as even minor impurities can alter reaction pathways in sensitive industrial processes. Its solid, non-volatile nature enhances storage stability and handling safety, minimizing degradation risks during transportation and shelf life. The white to off-white powder appearance also provides a visual quality check, with consistent coloration indicating batch uniformity—an essential factor for scaling up manufacturing processes.
What You Gain With Our Product
Choosing our high purity Sofosbuvir means avoiding the hidden costs of substandard materials: failed experiments due to impurity interference, production shutdowns from supply disruptions, and compliance issues with regulatory standards. Our commitment to consistent quality aligns with global industrial expectations, while our established supply chain ensures cost efficiency through stable pricing and reliable delivery schedules—critical factors for long-term manufacturing planning.
Why You Can Trust Us
Our quality assurance process begins with raw material screening and continues through every production stage, including HPLC purity testing for each batch. Every shipment includes a Certificate of Analysis (COA) with detailed test results, providing verifiable documentation of product specifications. We maintain full traceability from synthesis to delivery, and offer technical support to address application-specific questions. With 10000+ satisfied industrial clients, our track record demonstrates a commitment to transparency and reliability in chemical supply.
Certificate of Analysis & Documentation
Each order of Sofosbuvir 1190307-88-0 is accompanied by a batch-specific COA and MSDS, containing comprehensive testing data including assay results, appearance, and physical properties. For specialized research needs, additional analytical documentation can be provided upon request, ensuring full compliance with your quality control protocols.
Storage & Handling
- Store in a cool, dry, well-ventilated area, sealed and away from direct sunlight.
- Keep away from incompatible materials, food and feed sources.
- Handle with appropriate personal protective equipment (gloves, goggles, lab coat).
- Follow good industrial hygiene practices. Avoid inhalation and skin contact.
- Refer to MSDS for detailed storage and safety instructions.
How to Place Your Order
Initiate your procurement by contacting our sales team with your specific requirements, including quantity and packaging preferences. We can provide samples for qualification testing prior to full-scale orders, ensuring the product meets your application needs. Once specifications are confirmed, we’ll arrange production and delivery with full documentation, supporting a streamlined transition from evaluation to manufacturing.
Frequently Asked Questions
Q: What is the shelf life of Sofosbuvir API when stored properly?
A: When stored in sealed containers under recommended conditions, the product maintains stability for 24 months from the manufacturing date, as verified by accelerated stability testing.
Q: Can this product be used directly in pharmaceutical production for human consumption?
A: No. This product is supplied exclusively FOR INDUSTRIAL AND LABORATORY RESEARCH USE ONLY. It is not intended for direct human consumption, therapeutic, or household use.
What documentation is provided with each shipment?
A: Every order includes a Certificate of Analysis (COA) with batch-specific test results and a Material Safety Data Sheet (MSDS) containing handling and safety information.
Q: Do you offer custom packaging options?
A: Yes, we can provide packaging in various sizes beyond standard gram and kilogram specifications to meet specific industrial requirements. Contact our sales team for details.
Q: How is the purity of your Sofosbuvir API verified?
A: Purity is determined using High-Performance Liquid Chromatography (HPLC) analysis, with results ≥99% as stated in the product specifications and confirmed in each batch’s COA.
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