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HS Code |
983780 |
| Chemical Name | 5,5-Dimethyl-1-Pyrroline N-Oxide |
| Cas Number | 3317-61-1 |
| Molecular Formula | C6H11NO |
| Molecular Weight | 113.16 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 91-93°C |
| Boiling Point | 265°C at 760 mmHg |
| Solubility | Soluble in water, ethanol, and methanol |
| Density | 1.07 g/cm³ |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
| Synonyms | DMPO; 2,2-Dimethyl-3,4-dihydro-2H-pyrrole 1-oxide |
| Application | Spin trapping agent for detecting free radicals |
| Ph | Neutral to slightly basic in aqueous solution |
| Hazard Class | Irritant |
As an accredited 5,5-Dimethyl-1-Pyrroline N-Oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 5,5-Dimethyl-1-Pyrroline N-Oxide, with tamper-evident cap and hazard labeling. |
| Shipping | 5,5-Dimethyl-1-Pyrroline N-Oxide (DMPO) is shipped in tightly sealed containers under cool, dry conditions to prevent degradation. It should be protected from light and moisture. The packaging follows regulations for chemical safety, labeling, and handling. Transport must comply with local and international hazardous materials guidelines, if applicable. |
| Storage | 5,5-Dimethyl-1-Pyrroline N-Oxide (DMPO) should be stored tightly sealed in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. It is recommended to store DMPO at 2–8 °C (refrigerated) and protect it from moisture. Ensure the container is clearly labeled and only accessible to trained personnel. |
Applications of 5,5-Dimethyl-1-Pyrroline N-Oxide in Industrial ManufacturingAs a direct manufacturer of 5,5-Dimethyl-1-Pyrroline N-Oxide (DMPO), we support industrial customers across specialized scientific and technical domains, focusing on advanced analytical detection, biotechnological production, and food quality assessment. Each downstream segment detailed below reflects routine commercial deployment, precise handling protocols, and integration into validated manufacturing processes. 1. Electron Paramagnetic Resonance (EPR) Spin Trapping for Free Radical DetectionEPR-based detection workflows rely on DMPO as a nitrone-based spin trap for quantifying short-lived radical intermediates in environmental, pharmaceutical, and material science research. Instrument labs and QC departments formulate EPR reagents with defined concentrations of DMPO to reliably capture reactive oxygen and nitrogen species in aqueous, lipid, or complex matrices. Batch consistency and purity are critical, as even trace contaminants can alter radical adduct formation and compromise analytical reproducibility. For process reliability, users add DMPO directly to reaction solutions immediately prior to EPR measurement, minimizing decomposition and ensuring data integrity for routine industrial free radical monitoring. Industry compliance standards
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2. Pharmaceutical Reactive Oxygen Species (ROS) Detection AssaysPharmaceutical manufacturers leverage DMPO in ROS detection assays for oxidative stress evaluation during preclinical research, formulation stability testing, and biologic lot release. Process engineers add DMPO into in vitro antioxidant assays and forced degradation studies, enabling accurate quantitation of superoxide and hydroxyl radicals formed in active pharmaceutical ingredient (API) synthesis or finished product storage. The downstream application requires strict adherence to pharmacopeial references for analytical reagents and integration with high-throughput platforms that demand batch-specific documentation to satisfy regulatory scrutiny. Industry compliance standards
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3. Biotechnological Enzyme Reaction Mechanism StudiesBiotech companies employ DMPO to investigate enzymatic redox pathways, specifically in the characterization of oxidoreductases, monooxygenases, and peroxidases. DMPO is introduced to intercept highly transient enzymatic radicals during scale-up of biocatalytic reactions or protein engineering programs. The formulation of reaction mixtures with controlled DMPO concentration allows process scientists to assign mechanistic steps and verify enzyme activity profiles. Resulting adducts facilitate downstream data interpretation critical to QbD (Quality by Design) approaches and new bioprocess route qualification. Industry compliance standards
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4. Food and Beverage Oxidative Spoilage AssessmentFood quality control labs utilize DMPO for monitoring oxidative spoilage in oils, dairy, meats, and beverages, supporting both in-house QA protocols and third-party certification for shelf life claims. By spin trapping reactive radicals formed during processing, packaging, or storage, food scientists can trace oxidative pathways underlying off-flavor or shelf-life reduction. Analysts incorporate DMPO into validated extraction workflows, tailoring addition levels to fat content or product matrix to maximize detection of specific radical species. Measurement results inform production process adjustments, packaging design, and hazard analysis in compliance with food safety certification. Industry compliance standards
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Our work with 5,5-Dimethyl-1-Pyrroline N-Oxide (commonly known as DMPO) started decades ago, in a small lab that has grown into the production line we operate today. This molecule, which carries the formula C6H11NO, plays a particular role in free radical detection, something that draws attention from researchers in life sciences and analytical chemistry. For us, DMPO has never been just another chemical shipped in barrels or jars; it’s grown into a flagship product that sparks real change for customers who depend on reliability in their electron spin resonance (ESR) experiments.
Consistency matters in synthesis. Our batch-to-batch quality comes from in-house process development and strict raw materials selection. Each time we produce DMPO, purity checks sit at the core of our routine, not as an afterthought but as a reflection of the responsibility we feel toward the scientists using the material. Our DMPO typically exceeds 98% purity, with trace moisture and peroxide content capped well below the levels that would interfere with sensitive radical trapping applications. We package the product immediately to limit environmental exposure that may degrade its performance before use.
Most of the people who call us about DMPO already know about its use as a spin trap for detecting free radicals. What often surprises newer researchers is how crucial small impurities can be, particularly those with similar structures or oxidation states. We’ve learned this lesson through dialogue with our clients, after more than one project stalled on unexpected ESR background signals. We shape our own analytical methods around this reality. Each lot of DMPO we sell ships with full traceability and supporting chromatographic data, not just a boilerplate certificate. DMPO’s melting point lands in the low 70s Celsius range, solubility sits high in water, methanol, and DMSO, and both physical and chemical stability remain strong when the material’s kept cool and dry.
Compared with lower-cost spin traps that crop up in catalogs, DMPO stands out. We see some chemistries that use PBN or MNP, both familiar N-oxide spin traps, but anyone who has run head-to-head ESR tests can tell the differences in signal strength and clarity. DMPO offers better kinetic performance for trapping hydroxyl and superoxide radicals due to the way its ring structure reacts, resulting in more stable adducts and higher detection sensitivity. This means ESR spectra are cleaner, easier to interpret, and less likely to mask the real data with excess noise.
Cutting corners doesn’t end well. We’ve encountered competitors cutting purity below 95% to shave pricing. In daily use, those percent points matter more than sales pitches would suggest. A contaminated DMPO batch throws off entire radical quantification studies, sometimes ruining months of grad student labor. We've worked shoulder to shoulder with researchers rerunning data after poor results linked back to material purity. Based on years of this experience, we maintain our in-process controls, using HPLC and GC-MS to hunt for byproducts that some manufacturers might leave behind. Every batch comes from our own plant, never from intermediaries or relabeled stock. If a customer brings a concern, we answer directly, drawing on logs from the very chemists who made the lot, not from a customer service script.
Storage also defines success. From the production floor to the client’s shelf, we avoid excess light and oxygen, two enemies of DMPO stability. That means amber glass packaging, inert gas purging, and minimal headspace in every bottle. These steps are not shortcuts or marginal improvements; they prevent autoxidation, peroxide formation, and the slow conversion of active DMPO to less-reactive byproducts. In our facility, we check storage spaces and regularly refresh our inventory to deliver material with maximum shelf life and minimal decomposition.
Every lab’s needs look different. Projects tracking ROS formation in mammalian cells, mapping environmental pollutant impacts, or running plant stress assays all come to DMPO with unique challenges. The common thread is the demand for certainty—a confidence that the spin trap won’t introduce artifacts or disappear before the critical reaction completes. In our production, we’ve built in feedback from years of direct customer dialogue: requests for bulk packaging, special documentation for regulated audits, and advice on sample preparation. We draw on our own laboratory experience with ESR techniques, sharing technical guidance on handling and dilution that stems from running hundreds of spin trapping assays, not just reading the literature.
Researchers sometimes want DMPO in forms or concentrations tailored for their specific workflow. While smaller operations and traders often buy blended or diluted products from upstream sources, we offer the original, fully characterized compound as a solid. From there, users prepare stock solutions in house, controlling solvent quality and dilution accuracy. This saves cost in the long run, reduces variability in repeated experiments, and protects scientific credibility when peer review pushes for rigorous control experiments.
DMPO’s application field has widened over time. Biomedical scientists use the compound to study oxidative stress in heart, brain, and immune tissues. Its ability to stably trap and identify short-lived oxygen-centered radicals provides a key advantage over chemical probes that lack specificity or generate false-positive data. Physical chemists investigating the effect of antioxidants in foods and pharmaceuticals depend on DMPO to produce interpretable spin adducts, which then reveal subtle reaction mechanisms. Environmental scientists, studying atmospheric chemistry or bio-remediation, use it to map how radicals transform pollutants before they reach people or ecosystems. Each field leans on DMPO’s performance, and each has specific stories of the compound turning confusion into clear, publishable results.
One researcher shared with us how small stability improvements to our DMPO lot allowed for the detection of hydroxyl radicals in transient cellular events. Another group working in marine chemistry credited the lack of trace oxidants in our product with minimizing interference in metal-catalyzed radical reactions. These accounts aren’t isolated. Year after year, we collect—often via late-night emails—accounts of DMPO enabling results that shape grant proposals and drive the boundaries of free radical science. These experiences drive us to sharpen every synthesis and QC step.
At a glance, DMPO sits alongside several other N-oxide structures widely used for radical trapping. The detail is in how its methyl groups and five-membered ring combine. The electron distribution of DMPO leads to formation of ESR-active adducts with sharper, more informative hyperfine splitting. Compared to PBN (N-tert-butyl-alpha-phenylnitrone), DMPO binds oxygen-centered radicals more quickly and produces less background interference. MNP (2-methyl-2-nitrosopropane) can trap some radicals rapidly, but its adducts decay faster and narrow the practical window for detection.
As a supplier, we pay close attention to these distinctions. In our own tests, DMPO provides stronger, more reproducible ESR signals when probing superoxide and hydroxyl radicals. Clients performing in vitro or in vivo work have told us about the improved clarity of spectra obtained with DMPO compared to other spin traps. Its compatibility with aqueous biological media opens possibilities not available with less soluble or less stable analogs. This performance edge is the outcome of both the material chemistry and the attention given to purity and handling.
Researchers seeking to compare products are often met with simplified tables or marketing blurbs describing “broad radical detection.” Experience shows the limitations. Slight changes in impurity profile, storage method, or packaging can derail a finely tuned experiment. Some labs report unsuccessful radical trapping with generic DMPO sourced from low-cost traders, often traced back to suboptimal handling from the time of production to the arrival on the researcher’s bench. Our in-house synthesis, performed under monitored conditions, is about delivering control—not taking chances with someone else’s supply chain mistakes.
Over the years, we have learned that good lab chemistry translates poorly to large-scale production without real process understanding. Scale brings its own risks: uneven mixing hills, slow reaction initiation, or incomplete removal of side products. We design our DMPO processes with redundant monitoring, including in-line sensors for temperature and pressure, and periodic manual sampling for off-line GC and HPLC analysis. Every operator on our line receives hands-on training. We believe people, not just instrumentation, keep problems from growing into product failures.
We have built relationships with academic collaborators, not just as suppliers but as partners. They invite us to audit their finished experiments and offer honest feedback on our product’s impact in practice. This culture of transparency shapes quality improvements not forced by regulation, but by our own pride in seeing published data linked to our material. We have upgraded our dryers, added additional packaging automation, and adjusted our reagent sourcing to keep up with evolving customer needs—all from this feedback loop. Accreditation and audits from regulators and customers add outside scrutiny, but our own standards always exceed the minimum.
DMPO’s cost structure leaves little room for shortcuts. The price of high-purity precursors, energy demands in recrystallization, and the ongoing validation of analytical methods are not hidden fees but the building blocks of trustworthy product. We educate new buyers about these realities to set expectations and cut through the illusion that all “chemical X” options match up once inside a reaction vessel. There are cheaper options, and for some low-sensitivity applications, those may suffice. For precision ESR work and sensitive biological applications, performance differences quickly show.
Global supply chain disruptions—spanning from solvent shortages to delays in freight transit—have threatened consistency in recent years. We respond by overstocking key precursors, qualifying multiple supply routes, and maintaining a rolling, six-month production forecast tied to real sales trends and repeat customer orders. Our investment in local infrastructure cushions against sudden shifts. Each order is filled directly from our main facility, not from warehoused third-party intermediaries. If something goes off track, our production managers call affected clients, share real-time updates, and propose workable solutions, not just apologies.
Looking forward, we see DMPO’s uses broadening as the tools of chemical biology and environmental science advance. Real-time, in-cell ESR work, new in vitro model systems, and the increasing complexity of free radical detection demand spin traps with stability, selectivity, and clear documentation. We lean into these needs by collaborating with research consortia, funding new stability testing on tissue panels, and supporting method validation studies that help expand DMPO’s application range. Our chemists attend workshops, field direct technical questions, and offer visit days for partner labs. We see the best improvements come not from just chemistry, but from the relationships built around listening and adapting to real-world research obstacles.
Changes in regulatory landscapes, particularly regarding hazardous packaging and chemical tracking, prompt process updates on our side. We review each development, not for bare compliance but for the chance to set higher safety benchmarks. Our packaging lines use tamper-evident seals and traceable lot numbers, so that every customer—regardless of scale—knows exactly what they’re working with, when it was produced, and how it was shipped.
We built our business on direct communication. Customers contact us for clarity about DMPO lot specifications, and our technical teams respond based on laboratory records, not sales scripts. We believe this directness builds trust, especially for new research projects where uncertainty overreaches theory. We get on calls with principal investigators, arrange joint troubleshooting sessions, and share published and unpublished analytical data when warranted. Through these relationships, we have seen new uses for DMPO emerge—including in real-time live cell imaging, combinatorial antioxidant screening, and atmospheric radical detection at remote field sites.
We also welcome conversations about improvements; nothing in chemical manufacturing stands still. Our flexibility in special packaging, custom documentation, or short lead times often starts from customer requests. Our workforce includes former academic researchers, regulatory specialists, and experienced plant operators, each adding their own view on what makes for a solid, dependable product.
Many ask if our DMPO will address all challenges in free radical detection. We know it has limits—some radicals evade spin trapping, certain biological systems present confounding factors, and analytical hardware still sets ultimate limits. The lessons from our years of production have focused on removing the avoidable errors—the ones traceable to inconsistent quality, careless packaging, or incomplete data rather than the inherent hurdles of spin trapping chemistry. Keeping our own feedback loop active, bridging our expertise with that from our user base, keeps the material most relevant where it matters.
As we refine our process, we document every deviation and corrective action, not to fill a binder for inspection, but to keep alive a living record of how the molecule performs under different conditions. We have solved crystallization problems by temperature tweaking and responded to customer findings on lot-dependent stability with deeper impurity profiling. Every anomaly becomes part of the learning curve, feeding back into our control plan for upcoming batches.
As the direct manufacturer of DMPO, we take pride in each container that leaves our plant, knowing it supports serious science and real-world discovery. The difference—seen in purity, analytical backing, transparent sourcing, and the quality of packaging—arises from the culture inside our walls. Our chemists view each feedback thread as another chance to improve. Our clients’ breakthroughs become proof that details in production matter. We aim not to sell just any chemical, but to offer a tool whose reliability stands behind the progress of those working to map the invisible dynamics of free radicals.
Our team stands ready for the questions, challenges, and ideas that keep science moving. DMPO will remain a cornerstone in the pursuit of understanding free radical dynamics, and our pledge is to sustain that reputation through grounded, responsive manufacturing and a culture of relentless improvement.