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Eplivanserin Mixture CAS NO 130581-13-4
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CAS No.:130581-13-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Eplivanserin Mixture CAS NO 130581-13-4 is a key chemical intermediate of significant interest in advanced pharmaceutical research and development. This compound is valued for its role in the synthesis pathway of active pharmaceutical ingredients (APIs) targeting specific neurological pathways. It is primarily utilized by research institutions, contract development and manufacturing organizations (CDMOs), and pharmaceutical companies engaged in the development of novel therapeutic agents.
Application
- Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of complex active pharmaceutical ingredients (APIs).
- Neurological Research: Used in preclinical and research settings for the development of compounds targeting specific receptor systems.
- Process Development: Employed by CDMOs for route scouting, optimization, and scale-up studies for new drug candidates.
- Reference Standard: Can be utilized as a qualitative or quantitative analytical standard in method development and quality control laboratories.
- Chemical Synthesis: Acts as a specialized synthon in organic chemistry for constructing complex molecular architectures in medicinal chemistry programs.
Basic Information
| Product Name | Eplivanserin Mixture |
| CAS No. | 130581-13-4 |
| Molecular Formula | Contact for details |
| Molecular Weight | Contact for details |
| Synonyms | Eplivanserin; Eplivanserin fumarate intermediate; 4-(2-Fluorophenyl)-6-methyl-2-piperazin-1-yl-thieno[2,3-d]pyrimidine mixture; SR 46349 mixture; SR-46349 mixture; Thienopyrimidine derivative mixture; 6-Methyl-4-(2-fluorophenyl)-2-(1-piperazinyl)thieno[2,3-d]pyrimidine mixture |
| EINECS | Contact for details |
Quality Control
Our Eplivanserin Mixture is produced and handled under a strict quality management system. Each batch undergoes comprehensive analytical testing, including identity confirmation and purity assessment, to ensure it meets the stringent requirements for pharmaceutical R&D. A Certificate of Analysis (COA) detailing specific test results is provided with every shipment to guarantee traceability and compliance.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature. Keep away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | Off-white to light yellow solid/powder |
| Identification (HPLC/IR) | Conforms to reference standard |
| Assay (HPLC) | ≥ 95.0% |
| Related Substances (HPLC) | Individual impurity ≤ 1.0%; Total impurities ≤ 3.0% |
| Residual Solvents (GC) | Complies with ICH guidelines |
| Loss on Drying | ≤ 1.0% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Trusted Manufacturer
With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






