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Artemisinic Alcohol Impurity CAS NO 125184-95-4
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CAS No.:125184-95-4
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Artemisinic Alcohol Impurity is a high-purity chemical reference standard used for analytical and research purposes. This compound is critical for quality control and method development in the pharmaceutical industry, particularly in the synthesis and analysis of artemisinin-derived antimalarial drugs. It is essential for researchers, analytical laboratories, and manufacturers requiring precise impurity profiling and regulatory compliance.
Application
- Pharmaceutical Reference Standard: Used as a certified impurity standard for HPLC, GC, and LC-MS analysis in quality control laboratories.
- Method Development and Validation: Critical for developing and validating analytical methods for artemisinin and its derivatives.
- Process Chemistry Research: Employed in studying synthetic pathways, degradation routes, and stability profiling of artemisinin-based APIs.
- Regulatory Compliance & Documentation: Supports regulatory filings (e.g., FDA, EMA) by providing identified impurity data for drug master files.
- Academic and Clinical Research: Facilitates studies on the metabolism, pharmacokinetics, and impurity toxicity of artemisinin compounds.
Basic Information
| Product Name | Artemisinic Alcohol Impurity |
| CAS No. | 125184-95-4 |
| Molecular Formula | C15H24O |
| Molecular Weight | 220.35 g/mol |
| Synonyms | Artemisinic Alcohol; (3R,5aS,6R,8aS,9R,10S,12R,12aR)-Decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-ol; Dihydroartemisinic Alcohol; Arteannuic Alcohol; Artemisia Alcohol Impurity; Artemisinin Alcohol Impurity; Artemisinin Related Compound |
| EINECS | Contact for details |
Quality Control
Our Artemisinic Alcohol Impurity is manufactured under strict quality systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation (IR, NMR), to ensure it meets the high standards required for pharmaceutical reference materials. A comprehensive Certificate of Analysis (COA) detailing purity, assay, and impurity profile is provided with every shipment.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white solid |
| Identification (IR) | Conforms to reference spectrum |
| Purity (HPLC) | ≥ 95.0% |
| Assay | 90.0% - 110.0% |
| Water Content | ≤ 5.0% |
| 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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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.






