Chemicals

Pseudoginsenoside F11 CAS 69884000 High Purity China Suppliers Factory

Looking for high-purity Pseudoginsenoside F11? As leading China suppliers and a professional factory, we provide this essential ocotillol-type triterpene saponin from American ginseng for botanical authentication and neuroprotective research. Our pharmaceutical grade compound ensures precise results for pharmacologists and quality control analysts worldwide.

SupplierGlobal Technology Co., Ltd.www.hqtechtirz.com
Source categories

About this product

Product information from the supplier.

Pseudoginsenoside F11 (CAS NO.69884-00-0) is a high-purity botanical reference standard and research chemical derived from Panax species. As a potent Ocotillol-type ginsenoside, it is widely utilized in pharmaceutical R&D for its significant neuroprotective and anti-inflammatory properties, serving as a critical tool for identifying and quantifying active compounds in American ginseng materials.

Engineered for precision, Pseudoginsenoside F11 acts as a partial PPARγ agonist and a TLR4 inhibitor, targeting critical signaling pathways to alleviate neuroinflammation and restore autophagic flux in neurons. This makes it an indispensable lead compound for scientists researching interventions for Alzheimer’s disease, Parkinson’s disease, and ischemic stroke in preclinical models.

Detailed Parameters

Product NamePseudoginsenoside F11 CAS NO.69884-00-0
Molecular FormulaC42H72O14 Molecular Weight801.01 g/mol
AppearanceWhite to off-white crystalline powder Purity (RP-HPLC)≥98%
SolubilityWater, methanol, ethanol Endotoxin≤10 EU/mg
Storage-20°C, protected from light MOQ1g

Key Advantages

Ultra-High Purity

RP-HPLC verified purity of ≥98% ensures precise results in quantitative analysis and pharmacological research.

Neuroprotective Potency

Proven attenuation of cerebral ischemic injury and reduction of cognitive deficits in preclinical models.

Multi-Target Action

Dual action as a PPARγ agonist and TLR4 inhibitor to modulate inflammatory cascades effectively.

Standardized Quality

Strict compliance with pharmacopoeial standards, ideal for botanical identification and reference.

Low Endotoxin Levels

Maintained at ≤10 EU/mg, making it suitable for sensitive in vitro and in vivo cellular assays.

Full Documentation

Each batch is accompanied by COA, HPLC reports, and MS chromatograms for complete traceability.

Product Gallery

Management Platforms

GMP Production

Manufacturing partners utilize GMP-compliant systems for synthesis and purification.

Quality Control

Standardized QC processes covering raw materials through to final packaging.

Batch Traceability

Rigorous management ensuring every batch has stable performance and documented history.

Global Logistics

Secure shipping via DHL, FedEx, and UPS with specialized temperature-controlled packaging.

Scale Flexibility

Capable of supplying research needs from gram-level to ton-level quantities.

Regulatory Compliance

Strict adherence to international trade standards and pharmaceutical API guidelines.

Investment Return Comparison

FeatureStandard GradeGlobalTech High-Purity
Chemical Purity<95%≥98% (RP-HPLC)
Endotoxin LevelUnspecified≤10 EU/mg
DocumentationBasic COAFull COA, HPLC, MS Reports
StabilityVariableVerified -20°C Stability
Delivery SpeedStandard FreightPriority Air Freight (DHL/FedEx)

Frequently Asked Questions

Q: What is the primary application of Pseudoginsenoside F11 in research?

It is primarily used as a chemical reference standard for Panax species identification and as a lead compound in preclinical studies for neurodegenerative diseases and stroke.

Q: How should Pseudoginsenoside F11 be stored to maintain stability?

The product should be stored at -20°C, protected from light, and kept in a dry, sealed container to ensure long-term stability.

Q: Can this product be used for clinical treatment in humans?

No, Pseudoginsenoside F11 is strictly indicated for non-clinical laboratory research and is not approved for human or animal therapeutic administration.

Q: What quality certifications accompany the pharmaceutical intermediates?

Our production partners adhere to GMP-compliant systems. Each batch includes a Certificate of Analysis (COA), HPLC purity report, and MS chromatograms.

Q: What is the shipping method for these chemical compounds?

We utilize International Air Freight via DHL, FedEx, UPS, and TNT to ensure the fastest transit time and maintain product integrity.

Q: Does the company support custom packaging requirements?

Yes, we can customize packaging according to customer needs to ensure maximum stability and compliance with specific laboratory requirements.

Ready to Advance Your Research with High-Purity Reference Standards?

Contact Us