Ensure pharmaceutical production consistency with our high-purity Ulipristal Acetate API, a critical raw material that meets stringent quality benchmarks for reliable formulation. Sourced from controlled manufacturing with a monthly production capacity of 50kg, this white or light yellow crystalline powder delivers assay levels exceeding 99%, minimizing batch variability and supporting compliance with global regulatory standards.
- Solid, non-volatile form ensures stable handling and storage, reducing formulation risks in pharmaceutical processes
- Packaged in secure cardboard drums or cartons to maintain integrity during transport and storage
- Backed by comprehensive quality documentation to streamline your procurement and testing workflows
描述
For industrial manufacturing and laboratory research purposes only.
Product Specifications
| Parameter | Value |
|---|---|
| Product Name | Ulipristal Acetate |
| CAS Number | 126784-99-4 |
| State | Solid |
| Volatility | Not Volatile |
| Color | White or Light Yellow Crystalline Powder |
| Assay | More Than 99% |
| Transport Package | Cardboard Drums or Cartons |
| Specification | gram, kilogram |
| Origin | China |
| HS Code | 2934999099 |
| Production Capacity | 50kg/Month |
Ulipristal Acetate 126784-99-4: Overcoming API Manufacturing Challenges with 99% Purity
For over a decade in pharmaceutical raw material supply, we’ve witnessed the critical impact of API purity on production outcomes. Researchers and manufacturers frequently face setbacks from inconsistent batch quality—fluctuating assay levels leading to failed reactions, uncertified materials causing compliance risks, and supply delays disrupting production timelines. These challenges not only increase R&D costs but also threaten project deadlines in pharmaceutical development.
A Stable and Reliable Pharmaceutical API Supply Solution
Our Ulipristal Acetate API addresses these pain points by delivering consistent ≥99% assay purity in solid powder form. Backed by 10+ years of fine chemical expertise, we’ve optimized production processes to ensure batch-to-batch uniformity, supporting seamless scale-up from laboratory research to industrial manufacturing. With a monthly capacity of 50kg, we provide stable supply to pharmaceutical and research institutions across 50+ countries.
Typical Industrial Applications
As a high-purity pharmaceutical raw material powder, Ulipristal Acetate serves as a key intermediate in pharmaceutical synthesis and analytical research. Its controlled physical and chemical properties make it suitable for laboratory-scale formulation development, process validation studies, and industrial manufacturing of pharmaceutical intermediates. All applications must adhere strictly to industrial and research use guidelines.
Why Key Specifications Matter in API Quality
The ≥99% assay purity of our Ulipristal Acetate minimizes impurity interference, ensuring reliable reaction outcomes in synthesis processes. Its non-volatile solid state enhances handling stability during manufacturing, reducing loss and contamination risks. The white or light yellow crystalline powder form allows for precise dosing, a critical factor in maintaining reaction stoichiometry. Additionally, our strict volatility control ensures product integrity during storage and transportation, preventing degradation that could compromise research results or production yields.
What You Gain With Our Pharmaceutical Raw Material Powder
Choosing our Ulipristal Acetate 99% powder for API applications means prioritizing quality that translates to tangible benefits: reduced rework from failed batches, streamlined regulatory compliance through comprehensive documentation, and optimized production efficiency. Unlike low-purity alternatives that introduce unknown variables, our consistent material quality lowers long-term costs by minimizing experimental errors and production delays. Every batch meets stringent industry standards, supporting your commitment to reliable manufacturing practices.
Why You Can Trust Our Ulipristal Acetate Supply
Our quality assurance process begins with raw material screening and continues through every production stage, utilizing advanced analytical techniques including HPLC and NMR for purity verification. Each shipment includes a detailed Certificate of Analysis (COA) with batch-specific test results. We maintain full traceability from production to delivery, and offer technical support to address application challenges. With a proven track record serving 10000+ industrial clients, our commitment to transparency means you receive exactly what’s specified—no surprises, just reliable pharmaceutical raw material you can depend on.
Certificate of Analysis & Documentation
Every order of Ulipristal Acetate includes a batch-specific COA detailing assay results, appearance, and physical properties. MSDS documents are provided to ensure safe handling and storage. For research institutions requiring additional verification, specific batch testing data can be requested using your order reference number, and complete analytical spectra are available upon request to support method validation and regulatory submissions.
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 for Ulipristal Acetate API
Initiate your order by contacting our technical sales team to confirm specifications and request a sample for evaluation. After sample approval, we’ll finalize your order details including quantity and delivery timeline. All shipments include complete documentation for customs clearance and quality verification. Our team remains available for technical support throughout your project, ensuring a smooth procurement experience from inquiry to delivery.
Frequently Asked Questions
Q: What is the shelf life of Ulipristal Acetate when stored properly?
A: When stored in sealed containers under recommended conditions (cool, dry, away from direct sunlight), the product maintains stability for 24 months from the date of manufacture.
Q: Can this product be used directly in pharmaceutical formulations for human consumption?
A: No. This product is supplied 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?
Each order includes a Certificate of Analysis (COA) with batch-specific test results and a Material Safety Data Sheet (MSDS) for safe handling.
Q: Do you offer custom packaging options?
A: Yes, we can provide packaging in various sizes beyond standard gram and kilogram specifications. Contact our sales team to discuss custom packaging requirements.
Q: How is the 99% assay purity verified?
A: Purity is determined using high-performance liquid chromatography (HPLC) as part of our comprehensive quality control process, with results documented in the batch-specific COA.
相关产品
-
Cabozantinib Malate 99% Assay Medicine Grade Solid for Oncology Research Treatment
阅读更多 -
Acyclovir 59277-89-3 Medicine Grade 99%+ Purity White Crystalline Powder for Pharma Ingredients
阅读更多 -
Apixaban 503612-47-3: 99% Purity Medicine Grade Solid Anticoagulant for Blood Thinning
阅读更多 -
Baloxavir Marboxil 1985606-14-1 Medicine Grade Solid Powder 99% Assay for Antiviral Use
阅读更多
