6-Amino-1,3-dimethyluracil is a high-purity pharmaceutical intermediate critical for the synthesis of xanthine derivatives. As a versatile building block in the pharmaceutical manufacturing industry, it serves as a foundational component in the production of essential medications, ensuring high yield and chemical stability during complex synthesis processes.
Beyond its primary role in medicine, this compound is strategically utilized in the production of Caffeine, Theophylline, and Aminophylline. Additionally, its unique chemical properties make it an effective additive for PVC applications, demonstrating a diverse utility range from life-saving healthcare products to advanced industrial plastic materials.
Detailed Parameters
| Chemical Name | 6-Amino-1,3-dimethyluracil | CAS RN | 6642-31-5 |
|---|---|---|---|
| EINECS RN | 229-662-0 | Molecular Formula | C6H9N3O2 |
| Molecular Weight | 155.1546 | Product Category | Pharmaceutical Intermediates |
| Main Application | Caffeine & Theophylline Synthesis | Industrial Use | PVC Additive |
| Purity Grade | Pharmaceutical Grade | Physical State | Crystalline Powder |
Key Advantages
High Chemical Purity
Rigorous purification processes ensure a high-grade intermediate that minimizes side reactions in drug synthesis.
Optimized Reaction Time
Enhanced reactivity allows for faster conversion rates when synthesizing theophylline and caffeine.
Versatile Utility
Dual-purpose application in both pharmaceutical API production and specialized PVC plastic additives.
Stable Shelf Life
Excellent chemical stability under standard storage conditions, reducing waste and inventory loss.
Strict Quality Control
Each batch is tested against international standards to ensure consistency and regulatory compliance.
Efficient Supply Chain
Streamlined logistics for pharmaceutical intermediates ensuring timely delivery to global laboratories.
Product Gallery
Management Platforms
Inventory Tracking
Real-time monitoring of raw material stocks to prevent production downtime.
Process Optimization
Continuous refinement of synthesis pathways to increase overall purity levels.
Quality Alerts
Automated notification system for batch testing results and quality deviations.
Compliance Monitoring
Strict adherence to pharmaceutical manufacturing regulations and safety standards.
Logistics Integration
End-to-end tracking from the production facility to the final pharmaceutical client.
R&D Collaboration
Dedicated platforms for custom synthesis and technical support for new drug research.
Investment Return Comparison
| Metric | Standard Grade | Premium Grade (Our Product) |
|---|---|---|
| Synthesis Yield | 75-82% | 92-98% |
| Impurity Level | Moderate | Ultra-Low |
| Process Stability | Variable | Highly Consistent |
| Production Cycle | Standard | Accelerated |
| Cost Efficiency | Baseline | High (Due to Yield) |
Frequently Asked Questions
It is primarily used as a key intermediate in the synthesis of xanthine-based drugs, including Caffeine, Theophylline, and Aminophylline.
Yes, it is also utilized as a specialized additive in the production of PVC plastics to enhance specific material properties.
Higher purity intermediates reduce the formation of unwanted by-products, simplifying the purification process of the final Active Pharmaceutical Ingredient (API).
It should be stored in a cool, dry, and well-ventilated area, away from incompatible substances and strong oxidizing agents.
Our products are manufactured under strict quality management systems to meet the rigorous requirements of the pharmaceutical intermediates industry.
Yes, we provide a comprehensive Certificate of Analysis (COA) and Technical Data Sheets for every shipment to ensure full traceability.
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