Description

6 α-Methyl-17 α-Hydroxy-11-Deoxy-Corticosterone-21-Acetate is a synthetic steroid derivative of significant interest in pharmaceutical research and development. This compound serves as a key intermediate in the synthesis of more complex steroid-based active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of novel therapeutic agents, particularly within the fields of endocrinology and anti-inflammatory drug discovery.

Application

• Pharmaceutical Intermediate: A crucial building block in the multi-step synthesis of advanced corticosteroid analogs and other steroid-based drugs.
• Research & Development: Used in academic and industrial laboratories for studying steroid metabolism, receptor binding, and structure-activity relationships (SAR).
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical analysis using techniques like HPLC and LC-MS.
• Precursor for API Synthesis: Employed in the production pathway for potential anti-inflammatory or hormonal therapeutic agents under investigation.
• Biochemical Research: Utilized in studies exploring enzyme inhibition and the biochemical pathways of steroid hormones.

Basic Information

Product Name	6 α-Methyl-17 α-Hydroxy-11-Deoxy-Corticosterone-21-Acetate
CAS No.	3386-03-6
Molecular Formula	C24H36O5
Molecular Weight	404.54 g/mol
Synonyms	6α-Methyl-17α-hydroxy-11-deoxycorticosterone 21-acetate; 6α-Methyl-17α-hydroxypregn-4-ene-3,20-dione 21-acetate; 21-Acetoxy-6α-methyl-17α-hydroxypregn-4-ene-3,20-dione; 6α-Methyl-17α-hydroxyprogesterone 21-acetate; Medroxyprogesterone acetate intermediate; 6α-Methyl-11-deoxycorticosterone acetate
EINECS	Contact for details

Quality Control

Our 6 α-Methyl-17 α-Hydroxy-11-Deoxy-Corticosterone-21-Acetate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency. We provide full traceability and Certificates of Analysis (COA) are available for all shipments, detailing key parameters such as assay and impurity profiles. Our quality commitment aligns with standards expected for pharmaceutical intermediates used in GMP environments.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). The product is light-sensitive and should be handled accordingly to maintain stability.

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.