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Periplocogenin CAS NO 112899-63-5
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CAS No.:112899-63-5
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Periplocogenin is a specialized steroidal sapogenin compound of significant interest in advanced pharmaceutical and biochemical research. Its unique structure makes it a valuable intermediate and reference standard for the development of novel therapeutic agents and analytical methods. This high-purity compound is essential for researchers and manufacturers in the pharmaceutical, biotechnology, and fine chemical sectors who require reliable, well-characterized building blocks for synthesis and quality control.
Application
- Pharmaceutical Intermediate: A key starting material or intermediate in the synthesis of steroidal drugs and bioactive molecules.
- Reference Standard: Used as a high-purity analytical standard in HPLC, LC-MS, and other chromatographic methods for quality control and research.
- Biochemical Research: Employed in studies investigating enzyme inhibition, receptor binding, and other cellular mechanisms due to its specific steroidal framework.
- Natural Product Isolation & Analysis: Serves as a benchmark compound for the identification and quantification of related sapogenins in plant extracts and herbal formulations.
- Academic & R&D Laboratories: Utilized in universities and research institutions for synthetic chemistry projects and pharmacological studies.
Basic Information
| Product Name | Periplocogenin |
| CAS No. | 112899-63-5 |
| Molecular Formula | C27H42O4 |
| Molecular Weight | 430.62 g/mol |
| Synonyms | (20S,22R)-3β,14β,17β-Trihydroxy-5α-pregn-8-en-11,15-dione; 3β,14β,17β-Trihydroxy-5α-card-8-en-11,15-dione; Periplogenin; Periplocosides aglycone; NSC 404996; 5α-Card-8-enolide-3β,14β,17β-triol-11,15-dione |
| EINECS | Contact for details |
Quality Control
Our Periplocogenin is manufactured under strict quality management protocols to ensure batch-to-batch consistency and high purity. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles as determined by advanced analytical techniques including HPLC, NMR, and MS. We are committed to meeting the stringent requirements of research and development, with specifications that can align with cGMP standards for pharmaceutical intermediates upon request.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.0% |
| Loss on Drying | ≤ 1.0% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 10 ppm |
| Related Substances (HPLC) | Individual impurity ≤ 0.5%; Total impurities ≤ 2.0% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






