Ensure consistent formulation results with our Sofosbuvir 1190307-88-0 medicine grade crystalline powder, designed to meet the rigorous standards of pharmaceutical development. This 99% assay solid delivers reliable purity that streamlines production processes, giving you confidence in every batch.
- White or almost white crystalline structure ensures optimal solubility and stability in formulations
- Packaged in secure cardboard drums to maintain integrity during storage and transport
- Produced under strict quality controls to address sourcing concerns and compliance requirements
描述
For industrial manufacturing and laboratory research purposes only.
Product Specifications
| Parameter | Value |
|---|---|
| CAS Number | 1190307-88-0 |
| Grade Standard | Medicine Grade |
| Type | Chemicals |
| State | Solid |
| Volatile | Not Volatile |
| Color | White or Almost White Crystalline Powder |
| Assay | More Than 99% |
| Transport Package | Cardboard Drums or Cartons |
| Specification | gram, kilogram |
| Origin | China |
| HS Code | 2934999099 |
| Production Capacity | 50kg/Month |
Overcoming Purity and Supply Challenges with Sofosbuvir 1190307-88-0
Industrial researchers and manufacturers often face critical obstacles with chemical raw materials—unstable purity leading to unpredictable reactions, inconsistent batch quality disrupting experimental reproducibility, and unreliable supply chains causing project delays. In our 10+ years serving 50+ countries, we’ve witnessed how these issues directly impact R&D timelines and production efficiency.
A Stable and Reliable Medicine Grade Crystalline Powder Solution
Our Sofosbuvir 1190307-88-0 addresses these pain points through rigorous manufacturing control. As a high purity medicine grade solid, it delivers consistent assay levels exceeding 99%, ensuring minimal variability between batches. With a monthly production capacity of 50kg, we maintain stable inventory to support both small-scale research and medium-volume industrial needs.
Typical Industrial Applications
This crystalline powder finds primary use in pharmaceutical R&D, chemical synthesis processes, and analytical laboratory applications. Its high purity and defined physical properties make it suitable for use as a reference standard, intermediate in organic synthesis, or raw material in specialized manufacturing processes requiring precise chemical characteristics.
Why Key Specifications Matter
The 99% assay level of our Sofosbuvir powder is critical for reducing interference from impurities in sensitive reactions, ensuring accurate analytical results, and minimizing side reactions in synthesis pathways. Its solid, non-volatile nature provides handling stability, while the white crystalline appearance serves as a visual quality indicator. The medicine grade standard guarantees compliance with stringent manufacturing practices, essential for applications requiring consistent material performance.
The Value of Reliable Chemical Sourcing
Choosing a high-quality Sofosbuvir 1190307-88-0 minimizes the risks of failed experiments, production downtime, and material waste associated with substandard chemicals. Our commitment to consistent quality supports cost-efficiency by reducing variability in research outcomes and manufacturing processes. With proper storage and handling, this stable compound maintains its integrity, providing long-term value compared to lower-grade alternatives that may degrade prematurely.
Our Quality Assurance Commitment
Every batch of our Sofosbuvir undergoes comprehensive testing before release, including purity analysis and physical property verification. We provide detailed Certificates of Analysis with each shipment, documenting key specifications to confirm compliance with stated parameters. Our production facility adheres to strict quality control protocols, ensuring that each kilogram meets the same high standards. Should any material fail to match specifications, we offer prompt replacement to minimize disruption to your operations.
Certificate of Analysis & Documentation
Each order includes a batch-specific Certificate of Analysis detailing assay results, appearance, and other critical parameters. Material Safety Data Sheets (MSDS) are provided to ensure proper handling and storage. For research requiring additional verification, specific batch test records can be requested, and detailed analytical methodology documentation is available upon inquiry.
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.
Streamlined Order Process
Initiate your order by submitting an inquiry with your required quantity and specifications. We can provide small sample quantities for evaluation before full-scale procurement. Upon confirmation, your order will be processed, tested, and shipped with all necessary documentation. Our logistics partners ensure secure delivery, with tracking available for all shipments.
Frequently Asked Questions
Q: What is the shelf life of this product when properly stored?
A: When stored in sealed containers under recommended conditions, the product maintains stability for 24 months from the date of manufacture.
Q: Is this product suitable for direct use in pharmaceutical manufacturing?
A: This product is intended for industrial and laboratory research use only. Additional purification may be required for pharmaceutical production applications.
What documentation is provided with each shipment?
Each order includes a Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS). Additional documentation can be arranged upon request.
Q: Do you offer custom packaging options?
A: Standard packaging includes cardboard drums or cartons. For specific requirements, custom packaging solutions can be discussed for orders exceeding 10kg.
Q: How is the purity of your Sofosbuvir powder verified?
A: Purity is determined through high-performance liquid chromatography (HPLC) analysis, with results documented in the batch-specific COA.
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