Description

18-Acetoxy-7α,20-Epoxy-6β,7-Dihydroxykaur-16-En-15-One is a highly functionalized diterpenoid derivative, a key intermediate in the synthesis of complex natural products and pharmaceuticals. Its intricate molecular architecture, featuring multiple oxygenated functional groups, makes it a valuable scaffold for medicinal chemistry research and the development of novel bioactive compounds. This compound is essential for researchers and manufacturers in the pharmaceutical, agrochemical, and fine chemical sectors who require high-purity, structurally defined intermediates for advanced synthesis.

Application

• Pharmaceutical Intermediate: A critical building block for the synthesis of diterpenoid-based drugs and active pharmaceutical ingredients (APIs).
• Medicinal Chemistry Research: Used as a core scaffold for structure-activity relationship (SAR) studies and the discovery of new therapeutic agents.
• Natural Product Synthesis: Serves as a key intermediate in the total or semi-synthesis of complex natural products with kaurane or related diterpenoid skeletons.
• Biochemical Research: Potential use as a probe or standard in studying biological pathways involving diterpenoid metabolism.
• Fine Chemical Production: Employed in the manufacture of specialty chemicals requiring specific stereochemistry and functionalization.
• Reference Standard: Used as a high-purity analytical standard for quality control and method development in analytical laboratories.

Basic Information

Item	Detail
Product Name	18-Acetoxy-7α,20-Epoxy-6β,7-Dihydroxykaur-16-En-15-One
CAS No.	77284-05-0
Molecular Formula	C22H30O7
Molecular Weight	406.47 g/mol
Synonyms	7α,20-Epoxy-6β,7-dihydroxy-18-acetoxykaur-16-en-15-one; 18-Acetoxy-7α,20-epoxy-6β,7-dihydroxykaur-16-en-15-one; Kaur-16-en-15-one, 18-(acetyloxy)-7,20-epoxy-6,7-dihydroxy-, (6β,7α)-; (6β,7α)-18-(Acetyloxy)-7,20-epoxy-6,7-dihydroxykaur-16-en-15-one
EINECS	Contact for details

Quality Control

Our 18-Acetoxy-7α,20-Epoxy-6β,7-Dihydroxykaur-16-En-15-One is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC, NMR, and MS, to ensure high chemical purity and structural identity. Certificates of Analysis (COA) detailing all specifications are provided with every shipment. We adhere to cGMP principles for pharmaceutical intermediates, ensuring traceability and batch-to-batch consistency for critical research and development applications.

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 compound may be hygroscopic; therefore, containers should be kept tightly sealed in a dry environment to prevent moisture uptake. For long-term storage, consider inert atmosphere conditions.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (HPLC)	Conforms to reference standard
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 95.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm

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