5-(Trifluoromethyl)uracil
- CAS No.54-20-6
- GradeIndustrial / Pharmaceutical
- Availability● In Stock
High-purity 5-(Trifluoromethyl)uracil (CAS 54-20-6) designed for pharmaceutical synthesis. Reliable supply with strict quality control.
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Product Overview
5-(Trifluoromethyl)uracil, commonly known as Trifluorothymine, is a critical fluorinated pyrimidine derivative widely utilized in the pharmaceutical and fine chemical industries. As a key building block, this compound plays an essential role in the synthesis of nucleoside analogs and various therapeutic agents. The introduction of the trifluoromethyl group enhances the metabolic stability and lipophilicity of the resulting molecules, making it a preferred choice for modern drug discovery and development programs.
Our facility specializes in the production of high-quality fluorinated intermediates. We adhere to stringent manufacturing protocols to ensure that every batch of 5-(Trifluoromethyl)uracil meets or exceeds international standards. This product is particularly valued for its consistency and reliability in complex organic synthesis routes.
Key Specifications
| Parameter | Specification |
|---|---|
| CAS Number | 54-20-6 |
| Molecular Formula | C5H3F3N2O2 |
| Molecular Weight | 180.085 |
| Appearance | White to off-white powder |
| Assay | ≥98.0% |
| Loss on Drying | ≤0.5% |
| Residue on Ignition | ≤0.5% |
| Single Impurity | ≤0.1% |
| Total Impurity | ≤0.3% |
| Melting Point | 245-246 °C |
Industrial Applications
This fluorinated uracil derivative serves as a versatile intermediate in the manufacture of antiviral and anticancer pharmaceuticals. Its robust chemical structure allows it to withstand various reaction conditions, making it suitable for multi-step synthesis processes. Researchers and production managers rely on this material for developing new medicinal compounds where fluorine substitution is required to improve bioavailability.
- Pharmaceutical intermediate for nucleoside analog synthesis
- Building block for fluorinated drug candidates
- Reagent for organic chemistry research and development
- Component in the production of advanced therapeutic materials
Quality Assurance and Packaging
Quality control is paramount in our production process. Each batch undergoes rigorous testing using advanced analytical techniques such as HPLC and NMR to verify purity and structural integrity. We provide a comprehensive Certificate of Analysis (COA) with every shipment to ensure transparency and compliance with your quality requirements.
The product is typically packaged in 25 kg drums, ensuring safe transport and storage. Custom packaging solutions are available upon request to meet specific logistical needs. We recommend storing the material in a cool, ventilated area away from direct sunlight and moisture to maintain optimal stability. Our commitment extends beyond production; we strive to offer a complete service platform including technical support and reliable global logistics.
