This Avanafil raw material powder is a high-purity, pharmaceutical-grade Active Pharmaceutical Ingredient (API) and serves as the core raw material for a new generation of selective PDE5 inhibitors. It is refined using modern fine chemical synthesis processes and multi-stage recrystallization purification techniques. The powder is white, fine-textured, and free-flowing, with highly consistent specifications-including potency, impurity levels, and particle size-across batches, meeting international standards for pharmaceutical raw materials. Compared to similar PDE5 inhibitor raw materials, Avanafil is distinguished by its rapid onset of action, quick metabolism, low potential for accumulation in the body, and superior selectivity; finished products formulated with it offer a favorable tolerability profile, making it a highly sought-after core ingredient for compliant pharmaceutical formulations and R&D projects worldwide. We support everything from small-scale sample testing to stable, large-volume supply. We provide comprehensive export documentation-including batch-specific Certificates of Analysis (CoA) and HPLC chromatograms-and utilize neutral, sealed export packaging suitable for sea and air freight. We offer long-term, stable supply partnerships to pharmaceutical companies and research institutions across the globe.
Basic Product Specifications
| Name | Avanafil Powder |
| CAS No. | 330784-47-9 |
| Appearance | White to off-white fine crystalline powder |
| Purity | ≥99.0% (by HPLC) |
| Solubility | Sparingly soluble in water; readily soluble in organic solvents such as methanol, ethanol, and DMSO |
| Storage Conditions | Store in a sealed container in a cool, dry place, protected from light |
| Shelf Life | 24 months (under standard storage conditions) |
| Packaging | Aluminum foil bags for samples; fiber drums for bulk orders; neutral English export packaging available |
Key Product Features
High-purity powder with excellent processing compatibility
A fine, white crystalline powder featuring good dispersibility, resistance to caking, and superior flowability. It is compatible with various pharmaceutical processing methods-such as tablet compression, solvent blending, and laboratory formulation development-ensuring smooth downstream production and effectively minimizing manufacturing losses.
Strict quality control ensuring batch-to-batch consistency
Produced in standardized cleanroom facilities with comprehensive monitoring of impurities such as moisture, heavy metals, residual solvents, and related substances. Each batch undergoes independent HPLC testing and documentation; minimal variations in potency, color, and particle size between batches guarantee the stability of mass-produced finished products.
Stable physicochemical properties suitable for cross-border logistics
The raw material maintains chemical stability at room temperature and is resistant to moisture-induced degradation. It withstands the temperature and humidity fluctuations associated with long-distance sea and air transport; combined with sealed, moisture-proof packaging, this significantly reduces losses during cross-border shipping.
Excellent solubility
Dissolves rapidly in common pharmaceutical organic solvents, yielding clear solutions free from visible sediment or suspended matter. It meets the rigorous requirements for high-end formulation development and precision laboratory testing.
Core Product Advantages
Distinctive Raw Material Characteristics
Compared to similar active pharmaceutical ingredients (APIs) such as sildenafil, tadalafil, and vardenafil, avanafil offers the advantages of rapid onset of action, fast metabolic clearance, and low drug accumulation. These properties make it ideal for developing compliant, short-acting pharmaceutical formulations with a favorable safety profile, creating a competitive edge in the finished product market.
Flexible Supply Model for Various Procurement Stages
We maintain ready stock to support early-stage experimental prototyping with small samples and ensure stable production scheduling for large-volume orders. We also accommodate long-term annual framework agreements for overseas clients, flexibly meeting procurement needs across trial and mass production phases.
Comprehensive Export Documentation for Hassle-Free Customs Clearance
Each batch comes with essential documentation, including Certificates of Analysis (CoA) and HPLC chromatograms. These documents meet customs clearance requirements in multiple countries and satisfy pharmaceutical companies' supplier qualification audits, thereby saving time on compliance reviews and reducing procurement risks.
One-Stop Foreign Trade Support Services
We offer customization for packaging specifications and foreign-language labeling. A dedicated foreign trade team provides one-on-one order management, handling the entire process-from initial inquiry, quotation, and production scheduling to shipment and after-sales service-ensuring efficient responses and a seamless partnership experience.
Scope of Compliance Application
This product is a pharmaceutical-grade Active Pharmaceutical Ingredient (API). It is supplied exclusively to pharmaceutical enterprises holding valid manufacturing licenses and to legitimate pharmaceutical research institutions for use in compliant pharmaceutical formulation development and scientific research.
Illegal addition of this product to ordinary consumer goods-such as foods, health products, or dietary supplements-is prohibited. Private repackaging, compounding, or processing into finished products for sale by individuals is strictly forbidden. The import, export, and use of this product must strictly comply with all applicable local pharmaceutical laws and regulations.



Please feel free to contact us for samples, detailed quality inspection reports, or the latest price quotes; we look forward to establishing long-term, mutually beneficial partnerships with compliant partners worldwide.
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