Description

(2B,3A,5A,16B,17B)-17-Acetoxy-3-Hydroxy-2-(4-Morpholinyl)-16-(1-Pyrrolidinyl)Androstane is a high-purity, synthetically modified steroid derivative of significant interest in advanced pharmaceutical research and development. This compound matters as a sophisticated chemical intermediate, offering a unique structural framework for creating novel therapeutic agents targeting specific hormonal pathways. It is primarily needed by R&D laboratories and pharmaceutical manufacturers focused on developing next-generation treatments in endocrinology, oncology, and metabolic disorders.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of novel steroidal drugs and active pharmaceutical ingredients (APIs).
• Research & Development: Used in academic and industrial laboratories for studying steroid receptor interactions and metabolic pathways.
• Hormone Analog Development: Acts as a precursor for creating targeted hormone analogs with potential therapeutic applications.
• Biochemical Probe: Utilized as a specialized tool compound in biochemical assays to investigate enzyme inhibition or receptor binding.
• Process Chemistry: Employed in scale-up and process optimization studies for new chemical entities (NCEs).

Basic Information

Item	Details
Product Name	(2B,3A,5A,16B,17B)-17-Acetoxy-3-Hydroxy-2-(4-Morpholinyl)-16-(1-Pyrrolidinyl)Androstane
CAS No.	119302-24-8
Molecular Formula	C29H46N2O4
Molecular Weight	486.70 g/mol
Synonyms	17β-Acetoxy-3β-hydroxy-2β-(morpholin-4-yl)-16β-(pyrrolidin-1-yl)androstane; 2β-(Morpholin-4-yl)-16β-(pyrrolidin-1-yl)-3β,17β-dihydroxyandrostane 17-acetate; (2β,3β,5α,16β,17β)-17-(Acetyloxy)-3-hydroxy-2-(4-morpholinyl)-16-(1-pyrrolidinyl)androstane; 119302-24-8; Steroid Morpholine Pyrrolidine Derivative
EINECS	Contact for details

Quality Control

Our (2B,3A,5A,16B,17B)-17-Acetoxy-3-Hydroxy-2-(4-Morpholinyl)-16-(1-Pyrrolidinyl)Androstane is produced under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. Certificates of Analysis (COA) documenting full specifications are available upon request, 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). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption. For long-term storage, consider using desiccants.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
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.