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HS Code |
736127 |
| Name | Ebselen |
| Chemical Formula | C13H9NOSe |
| Cas Number | 60940-34-3 |
| Appearance | White to off-white solid |
| Solubility In Water | Poor |
| Melting Point | 186-193°C |
| Synonyms | PZ51; SPI-1005 |
| Iupac Name | 2-phenyl-1,2-benzoselenazol-3(2H)-one |
| Storage Conditions | Store at 2-8°C, protected from light |
| Logp | 2.65 |
| Pubchem Cid | 3194 |
As an accredited Ebselen factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ebselen is supplied in a 1-gram amber glass vial, sealed with a screw cap and labeled with chemical details and safety information. |
| Shipping | Ebselen is shipped in tightly sealed containers to prevent exposure to air and moisture. It should be kept in a cool, dry, and well-ventilated place, away from incompatible substances. Appropriate labeling and hazard documentation are provided according to regulations. Handling by trained personnel using suitable protective equipment is recommended. |
| Storage | Ebselen should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to incompatible substances such as strong oxidizers. Proper labeling and secure storage are essential to prevent accidental exposure or environmental contamination. Always follow institutional and regulatory guidelines for chemical storage. |
Applications of Ebselen in Industrial ManufacturingEbselen, an organoselenium compound, supports advanced synthesis and process safety in pharmaceutical and specialty chemicals industries. As the original manufacturer, we supply this material to sectors where its antioxidant, catalytic, and protective functions deliver manufacturing and end-product value. The following application scenarios illustrate where our product enters industrial formulations, batch processes, and downstream supply chains. 1. Active Pharmaceutical Ingredient SynthesisLeading pharmaceutical companies utilize our raw material as an intermediate or a final API for oxidative stress-related drug research. Manufacturers integrate it at key stages in the pipeline of neurology and hepatology-focused drugs, using GMP-controlled reactors and purification lines. Integration occurs post-esterification or amidation, immediately before crystallization and isolation. Downstream, rigorous QC ensures trace-level selenium impurity management in alignment with ICH Q3D guidelines. Finished products proceed through clinical trial material (CTM) supply, often as tablets or capsules for indications such as stroke adjunct therapy or bipolar disorder. Industry compliance standards
Typical usage ratio
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2. Polymer Stabilizer in Specialty CoatingsProduction teams in advanced polymer and film manufacturing employ our material as an oxidative degradation inhibitor. It enters at the compounding and extrusion phases of acrylic, polyurethane, and PVDC-based films for electronics and medical device packaging. Technical managers set process parameters to minimize free radical formation, extending finished product shelf life. Integration is tightly regulated, and extruder line QC samples are analyzed for selenium migration using ISO/IEC 17025 methods. Industry compliance standards
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3. Electrochemical Catalyst for Hydrogen Peroxide ProductionSpecialty industrial chemical plants incorporate our material as a heterogeneous catalyst in electrochemical cells for green synthesis of hydrogen peroxide. High selectivity toward two-electron oxygen reduction enhances productivity at moderate voltages, facilitating safer, scalable, and lower-waste production compared to anthraquinone methods. Process operators monitor catalyst loading and cell voltage drop via automated feedback controls, while product purity is validated for residual selenium according to EPA standards. Industry compliance standards
Typical usage ratio
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4. Antimicrobial Agent for Medical Device CoatingsRegulated device manufacturers blend our compound into antimicrobial coatings for hospital and critical care devices. It enters at the final surface treatment process: after sterilizable base polymers form, engineers apply it via dip, spray, or plasma deposition. Its inclusion targets biofilm suppression and durable surface protection. Compliant companies file technical dossiers with real-time leaching and cytotoxicity profiles as per medical device directives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Research Reagent for Cellular Oxidative Stress ModelsAcademic and contract research laboratories purchase our material as a reference compound for cell-culture oxidative stress assessment and high-throughput screening. Lab staff prepare stock solutions in DMSO or ethanol and introduce them at defined stages during cell viability and ROS measurement assays. Adjustments are made according to species and assay system, as documented in validated protocols and experimental reports. Quality assurance includes CoA review and in-house batch analytical confirmation. Industry compliance standards
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Turning raw materials into molecules that make a difference—this is the challenge and promise behind every product we scale. Among organoselenium compounds, Ebselen stands out for chemists who value innovation and reliability. Traditionally, our focus has always rested on safety, purity, and reproducibility. Over the past decade, we have made numerous improvements in our Ebselen processes to serve the growing interest from both research and industry. Here’s why Ebselen gets a page of its own on our product roster and how its distinctive chemistry shapes its present and future applications.
Ebselen, structurally known as 2-Phenyl-1,2-benzisoselenazol-3(2H)-one, brings a rare set of characteristics among organoselenium compounds. Most of our synthetic catalog includes sulfur- or oxygen-based functional molecules, but selenium, set right in the chalcogen family, offers reactivity and selectivity that few others can match. Selenium’s atomic properties give rise to antioxidant activities that sulfur and oxygen analogs simply cannot replicate, especially when targeting biological free radicals.
Processing Ebselen shows us the delicate balance needed between yield, safety, and cleanup. Selenium’s reactivity demands careful handling: our years refining reactor controls, solvent selections, and crystallization steps pay off in batch-to-batch consistency. This reliability encourages academic labs and pharmaceutical partners to return for each phase of their research.
In the plant, Ebselen consistently forms as pale or off-white crystalline solids—soluble in a host of organic solvents but difficult to hydrolyze or oxidize under ambient conditions. Typical molecular weight falls at 274.16 g/mol. Our standard batches trend at a minimum 99% purity by HPLC, which supports applications ranging from in vitro screens to in vivo studies.
We optimize particle size by careful control of precipitation and drying, since excessive grinding can generate fines that complicate handling or filtration. Some customers request particular crystal size fractions, especially for pharmacokinetic work. For most, our default is a moderate particle size that balances dissolution speed and bulk stability.
Quality control spotlights residual solvent content, selenium speciation, and crystalline phase identity. Nothing leaves our site without inspection by X-ray diffraction and NMR. Chemists on our team keep a close eye on residual trace metals—something that matters when selenium moves through biological testing.
Ebselen belongs to a tight group of benzisoselenazolone compounds. What sets it apart among them is its stability as both a powder and in formulated mixtures. Compared to open-chain organoselenium molecules, Ebselen resists air oxidation, sidesteps unwanted side reactions, and stores well for long periods. This stability pays dividends for logistics and end users; materials do not break down in transit or storage if kept dry.
Other selenium reagents, such as selenocystine and sodium selenite, offer less selectivity and often pose additional safety hazards. Ebselen’s aromatic backbone, coupled with its cyclic structure, tames selenium’s innate reactivity and gives it advantages in handling and dosage comparisons. Bench chemists appreciate not having to contend with pungent odors or excessive toxicity—both issues that can slow down research.
Our team recognizes Ebselen’s first major draw: its role as a glutathione peroxidase (GPx) mimic. This activity underpins its work as an antioxidant, protecting cells against damage by hydrogen peroxide and organic peroxides. Medical researchers prize this action when studying neurodegenerative disease models or examining oxidative stress in cardiovascular medicine.
Production scale matters here. Many organoselenium products never make it out of the pilot lab, as synthesizing even a kilogram can pose outsized risks. Through repeated scale-ups, we have found pressure points in crystallization, solvent recovery, and waste handling that allow us to supply Ebselen in both research and preclinical quantities. Such vertical integration gives customers peace of mind that safety, compliance, and batch history all tie back to a single process.
Beyond medicine, Ebselen has captured attention in environmental monitoring. Its ability to remove heavy metals from wastewater by forming stable complexes gives analytical chemists an edge when they need to clean up industrial effluents. We ship standard and custom formats for these users, adjusting packaging and labeling to fit regulatory requirements.
Chemistry always comes down to tradeoffs. No single molecule fits every use case. Still, Ebselen bridges gaps that many other selenium products leave wide open. While sodium selenite and selenomethionine showcase roles in nutrition and supplementation, they lack Ebselen’s selective enzyme mimicry and resistance to random reduction or oxidation. Selenocysteine, for example, breaks down quickly in storage or when exposed to air—an issue neither bench chemists nor quality assurance can ignore for high-value programs.
In the matter of toxicity and environmental footprint, Ebselen wins out over open-chain selenium carriers. Handling procedures for open-chain or ionic selenium include strict ventilation and mitigation plans—our improved Ebselen batches fall well within accepted exposure limits for lab and pilot users. A robust safety profile not only streamlines logistics; it builds confidence for clients scaling from trial studies to larger campaigns.
Synthetic analogs also compete in the antioxidant and anti-inflammatory arenas. Yet, our feedback from collaborative research reports underscores how rapidly Ebselen integrates into pharmacology pipelines, compared to less stable or less selective selenium scaffolds. Preclinical studies from several partners emphasize its rapid clearance and consistent metabolism—properties that rival or surpass more traditional antioxidants.
From day one, we approached Ebselen synthesis with attention to downstream predictability. Organic selenium synthesis, whether for academic or industrial projects, often hits obstacles with heavy metal contaminants. Instead of hand-waving this challenge, we direct considerable resources to stepwise purification at intermediate and final stages.
Our staff hands-on experience led to transitioning away from older, high-volume solvent processes, favoring recyclable systems wherever possible. Spent solvents and residual selenium burdens undergo closed-loop recovery, reducing both disposal volume and trace emissions. What matters to us—beyond the balance sheet—are the operating lives of our reactors and the long-term safety of our teams.
Some chemists may take for granted the subtleties in selenium reactivity. Our years with Ebselen remind us that uncontrolled oxidant addition turns a safe batch into an unpredictable, exothermic challenge. We stabilize these risks through slow addition protocols, continuous parameter monitoring, and staged heat exchange—bypassing the shortcuts that trip up less-experienced processors.
As new uses emerge and regulations evolve, we adjust specifications and support for various sectors. For researchers exploring pharmaceuticals, our team offers deeper quality documentation—supplying spectral data, heavy metal reports, and compliance records. Drug discovery clients frequently work with our R&D liaison to ensure every batch aligns with submission-ready standards.
Some industrial users need bulk packaging with tamper-evident seals, while academic labs often prefer smaller, sealed glass containers for stability and easier sub-division. We have gained plenty of insight listening to users who found out the hard way that poor packaging leads to moisture ingress, which in turn, dulls Ebselen’s performance.
Our records highlight the diversity among application protocols. High-throughput screens for biological activity typically require ready-to-use concentrations in DMSO or ethanol. Understanding the solubility margin and solvent compatibility allows us to recommend suitable stock solutions that streamline end-user workflows, eliminating the scramble to troubleshoot lumpy suspensions or solution artifacts.
Governance around selenium compounds keeps shifting, demanding vigilance. For example, we proactively audit compliance documentation, so that every shipment of Ebselen travels with up-to-date safety data and full traceability. Our history of cooperation with regulatory agencies enables us to stay ahead of changing guidance around transport, storage, and labeling.
Customers regularly seek assurance about batch-to-batch reproducibility for selenium content and impurity profiles. In our experience, cut-rate materials often arrive with ambiguous labeling or incomplete testing. Every drum and bottle we dispatch receives a unique identifier, tied directly to QC records and batch synthesis logs. This policy gives both our clients and our internal audit team a full view of every material movement and origin.
Disruptions in the global supply chain affect logistics and timelines. We mitigate this by holding safety stock on popular intermediates, forging direct relationships with approved raw material suppliers, and investing in local warehousing when demand justifies it. Over the past five years, this forward planning has prevented delays, even as demand spikes during global health emergencies or industry upswings.
We measure Ebselen’s value not only by volume moved, but by its impact on discovery. Recent publications highlight Ebselen’s promise across a spectrum of therapeutic targets—neuroprotection, antiviral action, and anti-inflammatory activity. Some researchers also study it as a potential adjunct in COVID-19 investigations, pointing to its ability to interfere with viral enzymes. The drive to unlock new science pushes us to provide samples for pilot studies and custom syntheses for non-commercial inquiries.
Having worked directly with multiple biotech partners, we have received thorough feedback on technical documentation, analytical results, and presentation. These exchanges sharpen our knowledge, as nuanced application demands shape our process refinements and information sharing. Instead of generic datasheets, we share method development guidance, recommendations for storage, and details about stability under real lab conditions.
For ongoing research contracts, we occasionally collaborate on customizing synthesis—tweaking starting materials, handling isotopic variants, or preparing specialized crystalline forms. Additional analytical support, such as detailed impurity mapping, often arises from these partnerships.
Selenium, with all its promise, remains a double-edged sword if mishandled. Our process engineers pay close attention to air monitoring, staff training, and waste neutralization. Years of adherence to best practices limit selenium dust escape, ensure wipe-down at critical transfer points, and make sure the same safety values get passed along to our customers. Wastewater from cleaning and process carry-over passes through multi-step selenium recovery, with trace selenium content documented to the decimal.
Beyond our doors, we recommend downstream users adopt similar safeguards. Our shipping paperwork includes safe handling and Emergency Response Guide codes, not just because it is required, but because we know downstream risks can arise. Outreach through technical bulletins or webinars forms part of our commitment—bridging the gap between production know-how and field application.
Despite all Ebselen’s promise, reaching high-volume, low-cost production remains a challenge. Raw selenium pricing fluctuates, driven in part by the global metal market. Demand surges create short-term pressure on intermediate availability. Recognizing this, we continually revisit sourcing agreements and substitute synthetic routes when volatility hits. Whenever new supplier options appear or technology opens up a safer, more efficient transformation, process engineers trial alternatives in pilot campaigns prior to full-scale transition.
Continuous improvement in analytical and process monitoring brings us closer to eliminating batch deviations. Historically, selenium chemistry has frustrated many would-be manufacturers with subtle side reactions and color contaminants. Our advances in real-time NMR and UV-Vis monitoring allow us to step in before these side reactions sap product quality. Instead of writing off off-spec batches, we have developed methods to rework these, reducing waste and capturing more value.
Even as new selenium analogs appear in the literature, Ebselen holds a unique place through the synergy of stability, selectivity, and manageable toxicity. Its use continues to climb in oxidative stress assays, clinical research, and environmental applications. Engineers at our plant know innovation comes not just in designing a molecule, but in how teams scale, protect, and deliver it worldwide.
By anchoring operations on safety, transparency, and technical dialogue, we strive to demystify the pathway from raw selenium to deployed chemicals. Our perspective—learned from hands-on synthesis, process troubleshooting, and user feedback—reminds us that real value in chemistry lies in keeping promises batch after batch, study after study.
For users considering Ebselen, the most compelling evidence of reliability comes not from marketing, but from the miles of stainless pipe, the refinement of protocols, and the challenge of meeting exacting standards over time. The real story of Ebselen is still taking shape in labs around the world, and we are proud every day to contribute to that evolution.