Vardenafil 224789-15-5 is used to treat male erectile dysfunction. This product must exert its effect under conditions of sexual stimulation by inhibiting PDE5 enzyme activity, reducing the degradation of cyclic guanosine monophosphate (cGMP), relaxing the smooth muscle of the penile corpus cavernosum, dilating cavernous blood vessels, and increasing local blood flow to help obtain and maintain an erection of sufficient hardness. This raw material has high selectivity for PDE5, has smaller effects on ocular PDE6, and has a relatively lower incidence of visual adverse reactions. The recommended starting dose for adult oral administration is 10mg, once daily, taken 25 to 60 minutes before sexual activity. According to efficacy and tolerability, the dose can be adjusted to 5mg or 20mg. The maximum recommended dose is 20mg per day.
Product Description & Parameters

The appearance of Vardenafil is a white or off-white crystalline powder. Under sexual stimulation, this product can inhibit PDE5 enzyme activity, reduce cyclic guanosine monophosphate degradation, relax penile corpus cavernosum smooth muscle, dilate blood vessels, increase local blood flow, and help improve male erectile dysfunction. This product has high selectivity, minimal effects on ocular-related enzymes, and relatively fewer visual adverse reactions. The raw material has high purity and strict impurity control, and a COA quality inspection report can be provided for each batch with stable quality. It can be used for tablet formulation production, pharmaceutical scientific research, reference standard testing, generic drug R&D, and API import and export business. The raw material is sealed and stored in a cool, dry, and light-protected environment, packaged in fiber drums or aluminum foil vacuum bags, and supports supply for both domestic and foreign orders.
Parameters
| Name | Vardenafil |
| Aliases | Vardenafil dihydrochloride |
| CAS No. | 224789-15-5 |
| Molecular Formula | C29H40N6O11S |
| Molecular Weight | 680.726 |
| Exact Mass | 680.248 |
| PSA | 253.41 |
| LogP | 1.7785 |
| Appearance | White powder |
| Testing Method | Liquid chromatography spectrum testing, third-party institution testing |
| Shelf Life | 24 months |
| Storage Method | Protect from light; store in a cool, dry place |
What is the Main Effect of Vardenafil?
This drug is a phosphodiesterase type 5 (PDE5) inhibitor. Oral administration of this drug can effectively improve erection quality and duration, increasing the sexual success rate of male patients with erectile dysfunction. The initiation and maintenance of penile erection are related to the relaxation of corpus cavernosum smooth muscle cells, and cyclic guanosine monophosphate (cGMP) is the mediator causing the relaxation of corpus cavernosum smooth muscle cells. This drug prevents cGMP breakdown by inhibiting phosphodiesterase type 5, thereby causing cGMP accumulation, corpus cavernosum smooth muscle relaxation, and penile erection. Compared with phosphodiesterase isoenzymes 1, 2, 3, 4, and 6, this drug has very high selectivity for phosphodiesterase type 5. Data show that its selectivity and inhibitory effect on phosphodiesterase type 5 are superior to those of other phosphodiesterase type 5 inhibitors, suggesting that this selectivity may make the cardiovascular and visual adverse reactions of this drug less than those of other phosphodiesterase type 5 inhibitors.


Product Application Fields
Pharmaceutical Formulation Production
Used to prepare Vardenafil hydrochloride tablets and develop formulations for the treatment of male erectile dysfunction.
Pharmaceutical Scientific Research Projects
Used as experimental raw materials to carry out in vitro and in vivo experimental research related to pharmacology and toxicology.
Laboratory Testing Calibration
Used as reference standards for raw material content and related substance analysis testing.
Generic Drug R&D Projects
Used for prescription screening, process optimization, and stability study trials.
API Import and Export Trade
Supplying domestic and overseas pharmaceutical enterprises to meet raw material procurement needs.
Innovative Dosage Form Development
Used for formula research of new oral formulations such as orally disintegrating tablets.
Product Content
1.The main content of Vardenafil API raw material is ≥99.0%, tested by High-Performance Liquid Chromatography (HPLC), with stable and reliable data.
2.Individual impurities are strictly controlled and kept at low limits, complying with pharmaceutical raw material standards.
3.Total impurities are strictly managed with a low total impurity amount, guaranteeing the safety of raw materials used in formulation production.
4.Physical and chemical indicators such as water content, heavy metals, and residue on ignition are tested synchronously, all meeting quality requirements.
5.Each batch of products is accompanied by a COA quality inspection report upon shipment, with complete content and impurity data available for verification.
6.Content fluctuation between product batches is small, with good quality consistency, suitable for long-term formulation R&D and production.
Packaging Methods and Logistics
1.Samples are vacuum-sealed using thickened aluminum foil vacuum bags to isolate oxygen and ensure the long-term stable storage of small samples.
2.Outer packaging drums clearly print the product name, batch number, and specification information, and sub-packaging can be customized according to customer needs.
3.Outer packaging is reinforced with protective treatment before goods leave the warehouse to reduce transport collisions and lower the risk of damage.
4.Domestic orders select room-temperature chemical dedicated-line freight transport, with full protection against rain and sun exposure, and transport trajectories can be queried in real time.
5.Foreign trade orders support sea freight and air freight, equipped with complete customs declaration documents to assist customers in overseas customs clearance.
6.Orders are quickly scheduled for production and outbound upon confirmation, with logistics information pushed promptly to help customers grasp cargo flow dynamics.
7.Batch numbers and quantities are carefully checked before shipment, confirming that product specifications are correct before delivery for transport.
Product After-Sales Service
Our company has established a mature and complete after-sales service system. All Vardenafil raw materials undergo strict inspection before leaving the warehouse, accompanied by a complete COA quality inspection report, with all test data true and verifiable. After customers receive goods, if they have any questions regarding product quality, appearance, packaging, or batch indicators, they can contact us at any time, and we will respond quickly to check the batch testing data at the first opportunity and patiently answer questions. A professional technical team can provide raw material-related technical consultations, assisting in solving various technical difficulties such as prescription screening and testing methods. If goods experience abnormal situations such as damage or leakage during transport, after customers provide relevant proof such as photos, we will communicate promptly and quickly negotiate a reasonable handling solution. Orders are followed up by dedicated personnel throughout the process, synchronizing production progress and logistics information in real time to help customers grasp cargo conditions. We adhere to the concept of honest management, value every customer's needs, earnestly protect customers' procurement rights and interests, and strive for mutual benefit and win-win outcomes.
FAQ
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