Description

[(3β)-17-Carboxy-28-Norolean-12-En-3-Yl]3-o-β-D-Glucopyranosyl-β-D-Glucopyranosiduronic Acid is a high-purity, structurally defined triterpenoid saponin derivative. 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 primarily sought by pharmaceutical, nutraceutical, and advanced material research sectors for its specific biological activity and structural properties.

Application

• Pharmaceutical Reference Standard: Used for the qualitative and quantitative analysis of herbal extracts and finished drug products in quality control laboratories.
• Active Pharmaceutical Ingredient (API) Intermediate: Serves as a key building block in the synthesis of novel therapeutic agents targeting inflammation and metabolic disorders.
• Nutraceutical & Cosmetic Research: Investigated for its potential bioactive properties in the formulation of high-end dietary supplements and skincare products.
• Biochemical Research: Employed in enzymatic studies and as a probe for understanding saponin-mediated biological pathways and membrane interactions.
• Herbal Medicine Standardization: Essential for standardizing extracts from plants like Glycyrrhiza glabra (licorice) to ensure consistent potency and efficacy.

Basic Information

Product Name	[(3β)-17-Carboxy-28-Norolean-12-En-3-Yl]3-o-β-D-Glucopyranosyl-β-D-Glucopyranosiduronic Acid
CAS No.	25406-56-8
Molecular Formula	C48H74O19
Molecular Weight	931.1 g/mol
Synonyms	Glycyrrhizic Acid; Glycyrrhizin; Glycyrrhizinic Acid; Enoxolone; Glycyrrhizic acid ammonium salt (related); 3β-[(2-O-β-D-Glucopyranuronosyl-β-D-glucopyranuronosyl)oxy]-11-oxoolean-12-en-30-oic acid; Uralenic acid glycoside; Liquorice saponin G2
EINECS	Contact for details

Quality Control

Our [(3β)-17-Carboxy-28-Norolean-12-En-3-Yl]3-o-β-D-Glucopyranosyl-β-D-Glucopyranosiduronic Acid is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including HPLC, NMR, and MS, to ensure identity, purity, and consistency. Certificates of Analysis (COA) detailing all specifications are provided with every shipment. We support compliance with cGMP, ICH guidelines, and relevant pharmacopoeial standards (USP, EP) for pharmaceutical 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). This product is hygroscopic (moisture-sensitive) and should be handled in a low-humidity environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms to reference standard
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 95.0%
Loss on Drying	≤ 5.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Specific Rotation	Contact for details

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