Description

6α,17β-Dihydroxy-5β-Androstan-3-One is a high-purity steroid intermediate of significant importance in pharmaceutical synthesis. This compound serves as a critical building block for the development of steroidal drugs and active pharmaceutical ingredients (APIs). It is primarily required by research institutions and manufacturers in the pharmaceutical and biotechnology sectors for the production of specialized therapeutics.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of steroidal hormones and other therapeutic agents.
• Research & Development: Used in biochemical research to study steroid metabolism and receptor interactions.
• API Synthesis: Employed in the multi-step synthesis of complex Active Pharmaceutical Ingredients (APIs).
• Reference Standard: Serves as a high-purity analytical standard for quality control and method validation in laboratories.
• Biochemical Studies: Utilized in metabolic pathway research and enzyme inhibition studies.

Basic Information

Product Name	6α,17β-Dihydroxy-5β-Androstan-3-One
CAS No.	51467-36-8
Molecular Formula	C19H30O3
Molecular Weight	306.44 g/mol
Synonyms	5β-Androstane-3-one, 6α,17β-dihydroxy-; 6α,17β-Dihydroxy-5β-androstan-3-one; 3-Oxo-5β-androstane-6α,17β-diol; 5β-Androstane-6α,17β-diol-3-one; 6α,17β-Dihydroxyetioallocholan-3-one
EINECS	Contact for details

Quality Control

Our 6α,17β-Dihydroxy-5β-Androstan-3-One is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation, to ensure it meets the high standards required for pharmaceutical intermediates. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its sensitivity, the product should be stored under an inert atmosphere to prevent oxidation. Keep away from heat and incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Single Unknown Impurity (HPLC)	≤ 0.5%
Total Impurities (HPLC)	≤ 2.0%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.