Description

Ganolucidic Acid A CAS NO 98665-21-5 is a bioactive triterpenoid compound isolated from the medicinal mushroom *Ganoderma lucidum* (Reishi). This high-purity reference standard is critical for research and development in the pharmaceutical and nutraceutical sectors, where precise quantification and biological activity studies are paramount. It is primarily sought by scientists and quality control professionals for applications in analytical method development, pharmacological research, and the standardization of herbal extracts.

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for the identification, assay, and impurity profiling of Ganoderma-based products in HPLC and LC-MS analysis.
• Bioactivity Research: Serves as a key investigational compound in pharmacological studies targeting anti-inflammatory, hepatoprotective, and anti-tumor activities.
• Nutraceutical Quality Control: Essential for the standardization and potency verification of Reishi mushroom extracts in dietary supplement manufacturing.
• Academic Research: A vital tool for universities and research institutes studying the chemistry and therapeutic potential of triterpenoids.
• Method Development & Validation: Used to develop and validate analytical methods in compliance with ICH and pharmacopoeial guidelines (e.g., USP, EP).
• Cosmeceutical Ingredient Research: Investigated for potential applications in skincare formulations due to its bioactive properties.

Basic Information

Product Name	Ganolucidic Acid A
CAS No.	98665-21-5
Molecular Formula	C30H46O7
Molecular Weight	518.68 g/mol
Synonyms	Ganolucidic Acid; Ganoderic acid variant A; (3β,12β,15α,25R)-3,12,15,25-Tetrahydroxy-7,11,23-trioxolanost-8-en-26-oic Acid; Reishi Triterpenoid A; Ganoderma Triterpene A; Lucidenic acid analogue; 98665-21-5
EINECS	Contact for details

Quality Control

Our Ganolucidic Acid A is produced under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and residual solvent analysis. We provide Certificates of Analysis (COA) with detailed chromatographic data, ensuring traceability and compliance with research-grade standards. Specifications are designed to meet the rigorous demands of analytical and pharmacological applications.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry environment. For long-term storage, consider keeping the material at 2-8°C. The compound is light-sensitive; prolonged exposure to light should be avoided to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.2%
Heavy Metals	≤ 20 ppm
Residual Solvents	Complies with ICH guidelines

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