Description

5α-Olean-12-Ene-3β,16α,21β,22α,23,23,28-Heptol Heptaacetate is a high-purity, multi-functional triterpenoid derivative, valued for its role as a critical intermediate in advanced organic synthesis and pharmaceutical research. This compound offers a structurally defined scaffold for developing novel bioactive molecules, ensuring precise and reproducible chemical transformations. It is primarily sought by research institutions and manufacturers in the pharmaceutical, agrochemical, and fine chemical sectors for applications in drug discovery and process development.

Application

• Pharmaceutical Intermediate: Serves as a key synthetic precursor for the development of novel triterpenoid-based therapeutics and active pharmaceutical ingredients (APIs).
• Biochemical Research: Used as a reference standard or probe in studies investigating structure-activity relationships (SAR) and biological pathways.
• Fine Chemical Synthesis: Acts as a versatile building block for the preparation of complex natural product analogs and specialty chemicals.
• Agrochemical Development: Employed in the research and synthesis of new plant growth regulators or bioactive agrochemical agents.
• Academic & Industrial R&D: Essential for exploratory chemistry in university laboratories and corporate R&D centers focused on organic and medicinal chemistry.

Basic Information

Product Name	5α-Olean-12-Ene-3β,16α,21β,22α,23,23,28-Heptol Heptaacetate
CAS No.	25122-89-8
Molecular Formula	C44H64O14
Molecular Weight	816.97 g/mol
Synonyms	Oleanolic Acid Heptaacetate; 3β,16α,21β,22α,23,23,28-Heptahydroxyolean-12-en-5α-yl Heptaacetate; 5α-Olean-12-ene-3β,16α,21β,22α,23,23,28-heptol, heptaacetate; Heptaacetyloleanolic Acid; Olean-12-ene-3,16,21,22,23,28-heptol, 3,16,21,22,23,28-heptaacetate, (3β,5α,16α,21β,22α)-; 25122-89-8; Oleanolic Acid, peracetate
EINECS	Contact for details

Quality Control

Our 5α-Olean-12-Ene-3β,16α,21β,22α,23,23,28-Heptol Heptaacetate is manufactured 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) are provided with every shipment, detailing all relevant specifications. We adhere to cGMP principles for pharmaceutical intermediates to support our clients' regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). The compound should be kept under an inert atmosphere for long-term storage to maintain stability. Keep away from strong oxidizing agents.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Conforms to reference standard
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 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.