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17,21-Dihydroxypregna-1,4-Diene-3,11,20-Trione 21-Heptanoate CAS NO 85959-59-7
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CAS No.:85959-59-7
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
17,21-Dihydroxypregna-1,4-Diene-3,11,20-Trione 21-Heptanoate is a synthetic steroid derivative, specifically a heptanoate ester of a dihydroxypregnadienetrione. This compound is a critical pharmaceutical intermediate used in the synthesis of more complex steroid-based active pharmaceutical ingredients (APIs). Its precise chemical structure allows for targeted modifications, making it essential for research and development in steroid chemistry. This high-purity intermediate is primarily required by manufacturers in the pharmaceutical and advanced fine chemical sectors.
Application
- Pharmaceutical Intermediate: Key building block in the multi-step synthesis of corticosteroid and other steroid-based APIs.
- Research & Development: Used in medicinal chemistry for the discovery and structural optimization of new steroid drug candidates.
- Process Chemistry: Serves as a defined starting material or intermediate in scale-up and process optimization for commercial drug manufacturing.
- Reference Standard: Can be utilized as an analytical standard for quality control and method development in pharmaceutical analysis.
- Biochemical Research: Employed in studies investigating steroid hormone pathways, receptor interactions, and metabolic processes.
Basic Information
| Product Name | 17,21-Dihydroxypregna-1,4-Diene-3,11,20-Trione 21-Heptanoate |
| CAS No. | 85959-59-7 |
| Molecular Formula | C28H38O7 |
| Molecular Weight | 486.60 g/mol |
| Synonyms | Pregna-1,4-diene-3,11,20-trione, 17,21-dihydroxy-, 21-heptanoate; 21-Heptanoyloxy-17-hydroxypregna-1,4-diene-3,11,20-trione; Cortienic Acid Heptanoate Ester; 17,21-Dihydroxypregnadienetrione 21-Heptanoate; 1,4-Pregnadiene-17,21-diol-3,11,20-trione 21-heptanoate |
| EINECS | Contact for details |
Quality Control
Our 17,21-Dihydroxypregna-1,4-Diene-3,11,20-Trione 21-Heptanoate is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure high purity and consistency, meeting the stringent requirements for pharmaceutical intermediates. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to support your quality assurance protocols.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain product integrity.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% |
| Loss on Drying | ≤ 0.5% |
| 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.






