Description

Quasipanaxatriol CAS NO 171903-78-9 is a high-purity, specialized triterpenoid compound derived from ginseng species. This compound is valued for its role as a critical reference standard and active pharmaceutical ingredient (API) intermediate in advanced research and development. It is essential for pharmaceutical, nutraceutical, and academic laboratories focused on metabolic, neurological, and anti-inflammatory studies. Our supply ensures consistent quality and reliable availability for your most demanding projects.

Application

• Pharmaceutical Reference Standard: Used for the qualitative and quantitative analysis of ginseng-derived products in pharmacopoeial testing (e.g., USP, EP).
• Active Pharmaceutical Ingredient (API) Intermediate: Serves as a key building block in the synthesis of novel therapeutic agents targeting metabolic and neurological pathways.
• Nutraceutical & Dietary Supplement Research: Employed in the standardization and efficacy studies of high-end ginseng extracts and herbal formulations.
• Academic & Biomedical Research: A vital tool for investigating the mechanisms of action, pharmacokinetics, and bioactivity of triterpenoids in vitro and in vivo.
• Quality Control & Method Development: Essential for developing and validating analytical methods (HPLC, LC-MS) in quality assurance laboratories.
• Cosmeceutical Development: Explored for potential applications in advanced skincare formulations due to its bioactive properties.

Basic Information

Product Name	Quasipanaxatriol
CAS No.	171903-78-9
Molecular Formula	C30H52O4
Molecular Weight	476.7 g/mol
Synonyms	(20S)-Dammarane-3β,6α,12β,20,25-pentol; 25-Hydroxydammarane-3,6,12,20-tetrol; Quasipanaxatriol A; Ginsenoside aglycone; Dammarane pentol; Panaxatriol derivative; 3β,6α,12β,20S,25-Pentahydroxydammarane
EINECS	Contact for details

Quality Control

Every batch of Quasipanaxatriol is manufactured and analyzed under strict quality management systems. We provide comprehensive analytical data to ensure the identity, purity, and consistency of the product meet the exacting requirements for research and pharmaceutical applications. A detailed Certificate of Analysis (COA) including results for assay, related substances, and residual solvents is supplied with each shipment. Our quality protocols are designed to support compliance with cGMP and ICH guidelines where applicable.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0% Any single impurity ≤0.5%
Loss on Drying	≤1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤20 ppm

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