Dapoxetine Hydrochloride | CAS 119356-77-3 | Pharma-Grade SSRI
Governed by our British technical headquarters and produced via our Strategic Supply Chain Alliance, every batch is refined to ensure ultra-low residual solvent profiles (≤ 500 ppm) and absolute chiral integrity.
We prioritize the needs of Small and Medium-sized Enterprises by providing first-hand access to production batches with full technical documentation (COA, MSDS, 1H-NMR). Secure your factory-direct supply today and accelerate your formulation pipelines with our rapid 24-hour quoting system.
Dapoxetine Hydrochloride (CAS 119356-77-3): The Molecular Standard for Rapid Serotonin Modulation
"In the complex landscape of Pharmaceutical APIs
, Blue Eye Bio defines the benchmark for Dapoxetine Hydrochloride. Leveraging our Asia-based manufacturing hub under British technical governance, we deliver a purely defined SSRI compound characterized by its optimized pharmacokinetic profile and crystalline integrity."
1.
Pharma-Grade Matrix
Technical Parameter | Industry Standard | Blue Eye Bio Premium |
Assay (HPLC) | ≥ 98.0% | ≥ 99.5% (High Precision) |
Residual Solvents | ≤ 5000 ppm | ≤ 500 ppm (Ultra-Low Trace) |
Particle Size | Variable | Uniform Micro-Crystalline |
Tmax (Absorption) | Standard | Fast-acting Kinetic Profile |
Isomer Purity | Standard | Chiral Integrity Verified |
2.Why is Dapoxetine a "Companion API"?
"Dapoxetine HCl is uniquely positioned as the premier Companion API in the global wellness industry. Due to its rapid elimation half-life, it is the preferred choice for laboratories researching Dual-Action Formulations. We support Small and Medium-sized Enterprises by providing the technical stability data needed to pair Dapoxetine with PDE5 inhibitors like Sildenafil and Tadalafil."
3.Why choose Blue Eye Bio for Dapoxetine HCl?
Optimized for Synergistic Research (复配研发优化):
As the leading Companion API specialist, our Dapoxetine HCl is refined to be highly compatible with PDE5 inhibitors (like Sildenafil). We provide the Drug-Drug Interaction (DDI) baseline data to help your R&D team optimize combination delivery systems. Ultra-Low Residual Solvent Profile: Using our Unified QC Standard (UQS), we strictly control the residual levels of ethanol and ethyl acetate, ensuring your final product meets the most stringent USP/EP pharmaceutical benchmarks. First-hand Strategic Sourcing: By managing our Asia-based manufacturing hub through our UK headquarters, we eliminate trading markups. We provide Small and Medium-sized Enterprises with factory-direct pricing and technical dossiers (COA, MSDS, 1H-NMR) within 24 hours. First-hand Sourcing: Eliminating intermediaries, we ship directly from our Strategic Supply Chain Alliance, offering the most competitive bulk dapoxetine prices.
Technical Integrity: Every batch is regulated by the Unified QC Standard (UQS), providing raw 1H-NMR, LC-MS, and HPLC spectra to ensure 100% authentic molecular characteristics.
Commonly researched alongside our [Sildenafil Citrate] and [Tadalafil API] for synergistic formulations.
Q: Why is residual solvent control so important for Dapoxetine HCl?
A: High levels of solvents like ethanol or methanol can affect the crystalline stability and safety of the final tablet. Blue Eye Bio uses vacuum-distillation technology to ensure our Pharma-grade Dapoxetine features the lowest solvent profile in the market.
Q: Do you offer trial quantities for Small and Medium-sized Enterprises? A: Yes. We prioritize the growth of Small and Medium-sized Enterprises by offering flexible industrial MOQs (starting at 1kg) and rapid 24-hour technical documentation delivery.
Compliance & Support
