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Estradiol 17-Acetate CAS NO 6045-67-6
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CAS No.:6045-67-6
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Estradiol 17-Acetate is a synthetic ester derivative of the primary female sex hormone, estradiol. This compound is a crucial pharmaceutical intermediate and reference standard in the development and quality control of steroidal medications. It is primarily utilized by manufacturers and research institutions in the pharmaceutical, biotechnology, and life sciences sectors for the synthesis of more complex hormone therapies and for analytical purposes.
Application
- Pharmaceutical Intermediate: A key building block in the synthesis of more complex steroidal drugs and hormone replacement therapies (HRT).
- Reference Standard: Used in analytical laboratories for method development, validation, and quality control testing of estradiol-based products via HPLC, GC, or MS.
- Biochemical Research: Employed in preclinical and clinical studies to investigate estrogen receptor binding, metabolic pathways, and endocrine system functions.
- Veterinary Medicine: Utilized in the formulation of hormonal treatments for animals.
- Cosmeceutical R&D: Investigated for potential applications in advanced dermatological and anti-aging formulations.
Basic Information
| Product Name | Estradiol 17-Acetate |
| CAS No. | 6045-67-6 |
| Molecular Formula | C20H26O3 |
| Molecular Weight | 314.42 g/mol |
| Synonyms | Estradiol 17-Acetate; 17β-Estradiol 17-acetate; Estra-1,3,5(10)-triene-3,17β-diol 17-acetate; 3,17β-Dihydroxyestra-1,3,5(10)-trien-17-yl acetate; NSC 9895; 17β-O-Acetylestradiol; Estradiol acetate (17-) |
| EINECS | 227-947-5 |
Quality Control
Our Estradiol 17-Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide Certificates of Analysis (COA) with detailed results for parameters including assay, related substances, and residual solvents. Our quality commitment aligns with cGMP principles for pharmaceutical intermediates, ensuring reliability for your critical applications.
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); ensure the container is sealed tightly after each use to prevent degradation from atmospheric moisture.
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% |
| 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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Rigorous Quality Assurance
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.






