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(13α)-3-Hydroxyestra-1,3,5(10)-Trien-17-One CAS NO 474-84-0
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CAS No.:474-84-0
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
(13α)-3-Hydroxyestra-1,3,5(10)-Trien-17-One CAS NO 474-84-0 is a high-purity steroid derivative, specifically an estrone-related compound. It serves as a critical intermediate in the synthesis of complex steroid hormones and active pharmaceutical ingredients (APIs). This compound is essential for pharmaceutical R&D, analytical reference standards, and fine chemical manufacturing. Its defined structure and purity make it a valuable building block for producing specialized therapeutic agents.
Application
- Pharmaceutical Intermediate: Key precursor in the synthesis of steroidal drugs, including hormone therapies and anti-inflammatory agents.
- Research & Development: Used as a reference standard and starting material in medicinal chemistry and biochemical research.
- Analytical Chemistry: Serves as a certified reference material (CRM) for method development, validation, and quality control in laboratories.
- Fine Chemical Synthesis: Building block for creating custom steroid derivatives and other high-value specialty chemicals.
- Biochemical Studies: Utilized in studies investigating estrogen receptor interactions and metabolic pathways.
Basic Information
| Product Name | (13α)-3-Hydroxyestra-1,3,5(10)-Trien-17-One |
| CAS No. | 474-84-0 |
| Molecular Formula | C18H22O2 |
| Molecular Weight | 270.37 g/mol |
| Synonyms | 13α-Hydroxyestra-1,3,5(10)-trien-17-one; 13α-Hydroxy-17-oxoestra-1,3,5(10)-triene; 13α-Hydroxyestrone; 13-epi-Estrone; 17-Oxo-13α-estra-1,3,5(10)-trien-3-ol; NSC 121773 |
| EINECS | 207-477-4 |
Quality Control
Our (13α)-3-Hydroxyestra-1,3,5(10)-Trien-17-One is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy. We provide Certificates of Analysis (COA) with detailed specifications for traceability and quality assurance, supporting compliance with cGMP and ICH guidelines for pharmaceutical intermediates.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). The product is light-sensitive and should be handled under appropriate conditions to maintain stability.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Conforms to reference |
| Purity (HPLC) | ≥ 98.0% |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
| Heavy Metals | ≤ 20 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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Why choose US
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.






