Description

(24R)-5α-Dammara-20-Ene-3β,24,25-Triol CAS NO 55050-69-6 is a high-purity, specific stereoisomer of a dammarane-type triterpenoid triol, valued for its defined molecular structure and biological relevance. This compound serves as a critical reference standard and a versatile pharmaceutical intermediate in advanced research and development. It is primarily sought by the pharmaceutical, nutraceutical, and cosmeceutical industries for applications in drug discovery, metabolic studies, and the formulation of bioactive products.

Application

• Pharmaceutical Reference Standard: Used for the identification, purity testing, and quantification of dammarane derivatives in analytical methods like HPLC and LC-MS.
• Drug Discovery Intermediate: Serves as a key chiral building block or precursor in the synthesis of novel therapeutic agents targeting metabolic and inflammatory pathways.
• Nutraceutical Research: Investigated for its potential bioactive properties in dietary supplements and functional food formulations.
• Cosmeceutical Actives: Explored as a potential active ingredient in high-end skincare products for its purported anti-aging or skin-rejuvenating effects.
• Biochemical Research: Utilized in metabolic and enzymatic studies to understand the biological activity and pathways of triterpenoids.
• Natural Product Isolation & Synthesis: Acts as a benchmark compound for the isolation, characterization, or semi-synthesis of related natural products from plant sources like ginseng.

Basic Information

Product Name	(24R)-5α-Dammara-20-Ene-3β,24,25-Triol
CAS No.	55050-69-6
Molecular Formula	C30H52O3
Molecular Weight	460.73 g/mol
Synonyms	(24R)-Dammara-20-ene-3β,24,25-triol; 3β,24,25-Trihydroxydammar-20-ene; 24(R)-Hydroxydammarenediol II; Dammar-20-ene-3β,24,25-triol, (24R)-; 24-Epidammar-20-ene-3β,24,25-triol; Ginsenoside precursor; Dammarane triol derivative
EINECS	Contact for details

Quality Control

Our (24R)-5α-Dammara-20-Ene-3β,24,25-Triol is manufactured under strict quality systems to ensure batch-to-batch consistency and high purity. Each lot is supported by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to relevant GMP guidelines for pharmaceutical intermediates, and specifications can be tailored to meet specific research or regulatory requirements.

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 desiccants or inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Specific Rotation	Contact for details
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

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