Description

Majoroside F6 is a high-purity, standardized phytochemical reference standard derived from natural sources. This compound is of significant interest for its role in advanced research and quality control within the pharmaceutical and nutraceutical industries. It serves as a critical analytical standard for the identification and quantification of bioactive saponins in complex botanical extracts. Key users include analytical laboratories, R&D departments, and manufacturers requiring precise standardization for product development and regulatory compliance.

Application

• Pharmaceutical Reference Standard: Used as a primary standard for the assay and purity testing of saponin-containing drugs and herbal preparations.
• Bioactivity Research: Employed in in vitro and in vivo studies to investigate potential anti-inflammatory, neuroprotective, or metabolic effects.
• Nutraceutical Quality Control: Essential for the standardization and authentication of botanical dietary supplements, ensuring consistent potency and safety.
• Analytical Method Development: Serves as a key component in developing and validating HPLC, LC-MS, and other chromatographic methods for saponin analysis.
• Chemical Synthesis Intermediate: Acts as a starting material or intermediate for the semi-synthesis of novel glycosidic compounds with modified biological activity.

Basic Information

Product Name	Majoroside F6
CAS No.	125310-00-1
Molecular Formula	C58H94O27
Molecular Weight	1223.34 g/mol
Synonyms	3-O-[α-L-Rhamnopyranosyl-(1→2)-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl] oleanolic acid 28-O-β-D-glucopyranosyl ester; (3β)-3-[[2-O-(6-Deoxy-α-L-mannopyranosyl)-β-D-glucopyranosyl]oxy]olean-12-en-28-oic acid β-D-glucopyranosyl ester; Timosaponin F6; Anemarrhenasaponin F6; Sarsasapogenin glycoside F6
EINECS	Contact for details

Quality Control

Our Majoroside F6 is produced under strict quality management protocols. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and residual solvent analysis. We provide a detailed Certificate of Analysis (COA) with every shipment, ensuring traceability and compliance with your internal specifications and relevant pharmacopeial guidelines for reference standards.

Storage

Preserve in a tightly closed container, protected from light. Store at 2-8°C in a dry environment. This product is hygroscopic (moisture-sensitive). For long-term storage, consider desiccant use and storage under inert atmosphere to maintain stability.

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%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm

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