6-Chloro-1,3-dimethyluracil (CAS No. 6972-27-6) is a high-purity pharmaceutical intermediate essential for the synthesis of critical cardiovascular medications. As a specialized pyrimidinedione derivative, it serves as a foundational building block in the production of Urapidil, a potent blood pressure-lowering agent, and Nifekalant, used in antiarrhythmic treatments, ensuring the efficacy and stability of the final medicinal products.
Our 6-Chloro-1,3-dimethyluracil is manufactured under rigorous quality control standards to meet the exacting requirements of the global pharmaceutical industry. With a purity level of 98% and a stable crystalline form, this intermediate supports the synthesis of drugs approved in over 30 countries for the treatment of primary renal hypertension, pheochromocytoma, and heart failure, providing a reliable supply chain solution for API manufacturers worldwide.
Detailed Parameters
| Product Name | 6-Chloro-1,3-dimethyluracil | CAS Number | 6972-27-6 |
|---|---|---|---|
| EINECS NO. | 230-205-2 | Molecular Formula | C6H7ClN2O2 |
| Molecular Weight | 174.585 | Purity | 98% |
| Appearance | Yellowish crystalline powder | Application | Pharmaceutical Intermediate |
| Standard Packing | 25kg/bag | Loading Capacity | 12mt per 20FCL (with pallets) |
Key Advantages
Premium Purity
Guaranteed 98% purity ensuring high yields and minimal impurities in the final API synthesis process.
Rapid Delivery
Efficient logistics system ensuring shipment within 10 days after payment confirmation.
Proven Experience
Over 20 years of expertise in the chemical industry with a robust quality control system.
Customizable Specs
Ability to customize quality specifications to meet your specific pharmaceutical requirements.
Full Documentation
Comprehensive technical support including TDS, MSDS, and third-party inspection reports.
Flexible MOQ
Accommodating a wide range of needs, with a low MOQ starting from just 1kg for testing.
Product Gallery
Management Platforms
Quality Control
Strict multi-stage testing and verification for every batch of pharmaceutical intermediates.
Synthesis Optimization
Advanced chemical processes to ensure the stability of 6-Chloro-1,3-dimethyluracil.
Supply Chain Management
Strategic partnerships with factories to ensure consistent volume and price stability.
Compliance Tracking
Adherence to international chemical transport and safety regulations for global export.
Inventory Logistics
Optimized palletization and 20FCL loading to maximize transport efficiency.
Technical Support
Dedicated technician teams available to analyze specs and customize product purity.
Investment Return Comparison
| Metric | Standard Grade | Our Premium Grade | Impact on ROI |
|---|---|---|---|
| Purity Level | 95-97% | 98%+ | Higher Final Yield |
| Impurity Profile | Moderate | Ultra-Low | Reduced Purification Cost |
| Lead Time | 15-30 Days | Within 10 Days | Faster Market Entry |
| Sample Availability | Paid | Free (Delivery Cost Only) | Lower R&D Risk |
| Documentation | Basic COA | TDS, MSDS, 3rd Party | Simplified Regulatory Approval |
Frequently Asked Questions
It is a critical intermediate used primarily for the synthesis of antihypertensive drugs like Urapidil and antiarrhythmic drugs such as Nifekalant.
Yes, we provide free samples for testing purposes. The customer is only responsible for the delivery shipping costs.
We provide a comprehensive technical data sheet (TDS), Material Safety Data Sheet (MSDS), and we accept third-party inspections upon request.
We accept a wide range of payment terms including L/C, T/T, Western Union, MoneyGram, and Paypal, depending on the destination country.
The standard packing is 25kg per bag. For full container loads, a 20FCL can accommodate approximately 12mt when shipped with pallets.
Yes, if you provide your specific requirements, our technical team will verify the feasibility and can customize the product to meet your needs.
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