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Mexiprostil CAS NO 88980-20-5
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CAS No.:88980-20-5
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Mexiprostil is a synthetic prostaglandin analog, a high-purity active pharmaceutical ingredient (API) with significant therapeutic potential. Its primary value lies in its potent biological activity, which makes it a critical intermediate for advanced pharmaceutical research and development. This compound is essential for researchers and manufacturers in the pharmaceutical industry, particularly those developing treatments in areas such as gastroenterology and reproductive health. The product, identified as CAS NO 88980-20-5, is supplied under stringent quality controls to ensure reliability for sensitive applications.
Application
- Pharmaceutical Intermediate: Serves as a key building block in the synthesis of novel prostaglandin-based therapeutics.
- Gastrointestinal Research: Investigated for potential cytoprotective and anti-ulcer properties in preclinical and clinical studies.
- Reproductive Health R&D: Used in research related to fertility treatments and the modulation of reproductive system functions.
- Biochemical Standard: Acts as a reference standard in analytical laboratories for method development and quality control of related compounds.
- Mechanistic Studies: Employed in pharmacological research to study prostaglandin receptor interactions and signaling pathways.
Basic Information
| Product Name | Mexiprostil |
| CAS No. | 88980-20-5 |
| Molecular Formula | C₂₃H₃₈O₅ |
| Molecular Weight | 394.55 g/mol |
| Synonyms | 9-Deoxo-9-methylene-16,16-dimethyl PGE2; 9-Deoxo-9-methylene-16,16-dimethylprostaglandin E2; 16,16-Dimethyl-9-deoxo-9-methylene PGE2; CL 115,347; CL-115,347; Mexiprostilum; (11α,13E,15S)-11,15-Dihydroxy-16,16-dimethyl-9-oxoprost-13-en-1-oic acid |
| EINECS | Contact for details |
Quality Control
Mexiprostil is manufactured and tested to meet high-purity standards suitable for pharmaceutical research. Our quality assurance protocol includes rigorous analytical testing to confirm identity, purity, and potency. A comprehensive Certificate of Analysis (COA) is provided with each batch, detailing results from tests such as HPLC assay, related substances, and residual solvents. We adhere to cGMP principles where applicable to ensure batch-to-batch consistency and traceability for our global B2B clients.
Storage
Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen) at controlled room temperature (15-25°C) to minimize oxidation and degradation. The container should be kept in a cool, dry, and well-ventilated area, away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time corresponds to reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any single impurity ≤ 1.0% |
| Loss on Drying | ≤ 0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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