Pyrroloquinoline Quinone Disodium Salt, commonly known as PQQ Disodium, is a high-purity pharmaceutical intermediate and nutritional supplement component. As a redox cofactor found in various organisms, this disodium salt formulation is engineered for enhanced stability and solubility, making it an essential raw material for the synthesis of advanced pharmaceutical agents and premium health formulations.
Our PQQ Disodium Salt is produced under rigorous quality control standards, ensuring strict adherence to the chemical specifications required for pharmaceutical intermediates. By leveraging precision synthesis and purification processes, we provide a consistent, high-grade product designed to meet the demanding requirements of global pharmaceutical and biotech manufacturers.
Detailed Parameters
| Product Name | Pyrroloquinoline Quinone Disodium Salt | Common Alias | PQQ Disodium / Methoxatin |
|---|---|---|---|
| Chemical Formula | C14H6Na2N1O8 | CAS Number | 124635-44-8 |
| Molecular Weight | 363.18 g/mol | Physical State | Crystalline Powder |
| Purity Level | ≥ 98% (HPLC) | Solubility | Highly Soluble in Water |
| Storage Condition | Store in cool, dry place | Application | Pharmaceutical Intermediate / API |
Key Advantages
Ultra-High Purity
Strict purification processes ensure minimal impurities, meeting pharmaceutical grade requirements.
Enhanced Stability
The disodium salt form provides superior chemical stability compared to the free acid form.
Optimal Solubility
Excellent aqueous solubility allows for efficient formulation in various liquid delivery systems.
Consistent Batch Quality
Standardized manufacturing ensures batch-to-batch consistency for large-scale industrial use.
Rigorous Testing
Every shipment is accompanied by a comprehensive COA and HPLC analysis report.
Global Compliance
Produced according to international chemical manufacturing safety and quality guidelines.
Product Gallery
Management Platforms
Inventory Tracking
Real-time monitoring of raw material stocks to ensure uninterrupted supply chains.
Quality Assurance
Integrated QC platform tracking every synthesis step from precursors to final salt.
Order Notification
Automated alerts for shipment status and delivery timelines for global logistics.
Compliance Monitoring
Digital documentation of safety data sheets (SDS) and regulatory certifications.
Cold Chain Logic
Specialized logistics management for temperature-sensitive pharmaceutical chemical shipments.
Synthesis Optimization
Continuous process improvement using data-driven chemical yield analysis.
Investment Return Comparison
| Feature Metric | Standard Grade PQQ | Our Pharma Grade PQQ | Competitive Edge |
|---|---|---|---|
| Purity Level | 95% - 97% | ≥ 98% - 99% | Higher Bio-activity |
| Solubility Rate | Moderate | Instant/High | Easier Formulation |
| Shelf Life | 12 Months | 24 Months | Reduced Waste |
| Impurity Profile | Generic | Ultra-Low/Controlled | Higher Safety Margin |
| Supply Stability | Variable | Guaranteed/Contractual | Operational Security |
Frequently Asked Questions
It serves as a critical pharmaceutical intermediate and API component, primarily used in the development of neuroprotective agents and metabolic enhancers due to its role as a redox cofactor.
The disodium salt form significantly increases water solubility and chemical stability, making it much more suitable for pharmaceutical formulations and industrial processing.
Each batch is supplied with a Certificate of Analysis (COA), HPLC purity reports, and a Material Safety Data Sheet (MSDS) to ensure full regulatory compliance.
Yes, our high-purity PQQ Disodium Salt is suitable for veterinary pharmaceutical applications, particularly in products targeting oxidative stress and cognitive health in animals.
It should be stored in a tightly sealed container, protected from light, and kept in a cool, dry environment to prevent degradation and maintain its high purity level.
Yes, we provide various packaging solutions ranging from small laboratory vials to large industrial stainless steel drums, depending on the client's volume and stability requirements.
Request a Professional Quotation for PQQ Disodium Salt
Contact UsRead Our Latest News
Jun.13,2026
What Does api stand for in pharmaceutical analysis Guide
What Does API Stand For in Pharmaceutical Analysis? In the complex world of drug development and quality control, understanding technical terminology is essential for ensuring patient safety and product efficacy. If you have ever wondered what api stand for in pharmaceutical analysis , the answer is Active Pharmaceutical Ingredient . An API is the biologically active component of a drug product that produces the intended health effect. While a pill may contain various fillers and binders, it is the API that does the actual work in the body.
Read More
Jun.11,2026
Strategic Guide to Optimize API Sales Pharma and Sourcing
Optimizing API Sales Pharma: A Strategic Guide to Pharmaceutical Ingredient Sourcing In the highly regulated world of pharmaceutical manufacturing, the efficiency of api sales pharma operations determines the speed at which life-saving medications reach patients. Active Pharmaceutical Ingredients APIs are the primary biological components of a drug, and sourcing them requires a delicate balance of purity, regulatory compliance, and cost-effectiveness. For procurement managers and pharmaceutical companies, navigating the global supply chain involves understanding the nuances of quality standards and supplier reliability. This guide explores how to optimize the sourcing process to ensure stability and excellence in drug production.
Read More
Jun.09,2026
High Quality API Products Pharma for Modern Medicine Safety
Understanding the Role of API Products Pharma in Modern Medicine In the complex world of drug development, the foundation of every medication lies in its Active Pharmaceutical Ingredient API. The demand for high-quality api products pharma is critical for ensuring the efficacy, safety, and stability of the final pharmaceutical dosage form. Whether it is a simple analgesic or a complex biologic, the API is the component directly responsible for the therapeutic effect on the patient. For pharmaceutical manufacturers, sourcing these components from reputable suppliers is not just a matter of business, but a matter of public health and regulatory compliance.
Read More
