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Velnacrine CAS NO 104675-29-8
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CAS No.:104675-29-8
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Velnacrine is a synthetic organic compound of significant interest in pharmaceutical research and development. This compound is recognized for its potential as a key intermediate or active pharmaceutical ingredient (API) in the synthesis of advanced therapeutic agents. It is primarily utilized by research institutions, pharmaceutical manufacturers, and fine chemical suppliers engaged in the development of novel central nervous system (CNS) drugs. Our supply of Velnacrine CAS NO 104675-29-8 is characterized by high purity and consistent quality to meet the stringent demands of modern pharmaceutical applications.
Application
- Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of investigational cholinesterase inhibitors for neurological research.
- Active Pharmaceutical Ingredient (API) Development: Used in preclinical and clinical research for the formulation of potential treatments targeting cognitive disorders.
- Biochemical Research: Employed as a reference standard or tool compound in studies of acetylcholinesterase enzyme kinetics and mechanism of action.
- Fine Chemical Synthesis: Acts as a specialized intermediate for custom synthesis services catering to the life sciences sector.
- Academic Research: Utilized in university and institutional laboratories for medicinal chemistry projects and pharmacological studies.
Basic Information
| Item | Details |
|---|---|
| Product Name | Velnacrine |
| CAS No. | 104675-29-8 |
| Molecular Formula | C15H14N2O2 |
| Molecular Weight | 254.29 g/mol |
| Synonyms | 9-Amino-1,2,3,4-tetrahydroacridin-1-ol; (±)-9-Amino-1,2,3,4-tetrahydroacridin-1-ol; HP 029; 1,2,3,4-Tetrahydro-9-acridinamine, 1-hydroxy-; 9-Amino-1-hydroxy-1,2,3,4-tetrahydroacridine; Velnacrine base |
| EINECS | Contact for details |
Quality Control
Our Velnacrine is manufactured under a strict quality management system to ensure batch-to-batch consistency and high purity. Each lot is subjected to comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling. A Certificate of Analysis (COA) detailing all test results is provided with every shipment. Our quality standards are designed to support GMP (Good Manufacturing Practice) principles for pharmaceutical applications, and we comply with relevant global regulatory frameworks.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after each use to prevent degradation from atmospheric moisture. For long-term storage, consider using desiccants.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 1.0% |
| Loss on Drying | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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