Description

(14α,15S,17Ar)-15-Methyl-15,17A:20,24-Diepoxy-25-Hydroxy-D-Homo-C,30-Dinor-13,17A-Secodammaran-3-One is a highly specialized, complex triterpenoid derivative with a unique secodammaran skeleton. This compound serves as a critical advanced pharmaceutical intermediate for the research and synthesis of novel therapeutic agents. It is primarily sought by pharmaceutical R&D laboratories and fine chemical manufacturers engaged in developing new drug candidates, particularly in areas like oncology and metabolic disease.

Application

• Pharmaceutical Intermediate: Key building block for the synthesis of novel triterpenoid-based drug candidates.
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies to explore new biological activities.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in pharmaceutical analysis.
• Biochemical Research: Investigated for its potential interactions with various enzymes and biological pathways.
• Process Chemistry Development: Utilized in scaling up synthetic routes for complex natural product derivatives.
• Academic Research: Employed in universities and research institutes for studies in organic synthesis and natural product chemistry.

Basic Information

Product Name	(14α,15S,17Ar)-15-Methyl-15,17A:20,24-Diepoxy-25-Hydroxy-D-Homo-C,30-Dinor-13,17A-Secodammaran-3-One
CAS No.	18524-62-4
Molecular Formula	C30H46O5
Molecular Weight	486.7 g/mol
Synonyms	15-Methyl-15,17A:20,24-diepoxy-25-hydroxy-D-homo-C,30-dinor-13,17A-secodammaran-3-one; Secodammaran-3-one derivative; D-Homo-C,30-Dinor-13,17A-secodammaran triterpenoid; 25-Hydroxy-15-methyl-secodammarane epoxide; (14α,15S,17αR)-15-Methyl-15,17α:20,24-diepoxy-25-hydroxy-D-homo-C,30-dinor-13,17α-secodammaran-3-one; Triterpenoid epoxide intermediate; 18524-62-4
EINECS	Contact for details

Quality Control

Our production of this high-value intermediate adheres to strict quality management systems. Each batch is characterized and tested using advanced analytical techniques including HPLC, GC-MS, and NMR to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical specifications. Our quality protocols are designed to meet the exacting standards required for pharmaceutical R&D and cGMP manufacturing.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry, well-ventilated area. This compound 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)	Retention time matches reference standard
Purity (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.