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HS Code |
112015 |
| Productname | 3,5-Dimethyl-4-Nitropyridine 1-Oxide |
| Casnumber | 36839-90-2 |
| Molecularformula | C7H8N2O3 |
| Molecularweight | 168.15 g/mol |
| Appearance | Yellow to orange crystalline solid |
| Meltingpoint | 151-154°C |
| Solubility | Soluble in organic solvents such as ethanol and DMSO |
| Purity | Typically ≥98% |
| Synonyms | 4-Nitro-3,5-dimethylpyridine N-oxide |
| Storageconditions | Store at room temperature, in a cool, dry place |
| Smiles | CC1=CN(C=C(C1)[N+](=O)[O-])N=O |
| Inchi | InChI=1S/C7H8N2O3/c1-5-3-7(10(12)13)6(2)4-8(5)11/h3-4H,1-2H3 |
As an accredited 3,5-Dimethyl-4-Nitropyridine 1-Oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, with tightly sealed cap, labeled “3,5-Dimethyl-4-Nitropyridine 1-Oxide,” hazard symbols, and handling instructions. |
| Container Loading (20′ FCL) | 3,5-Dimethyl-4-Nitropyridine 1-Oxide is loaded in 20′ FCLs, securely packed in drums or cartons for safe transport. |
| Shipping | **Shipping Description:** 3,5-Dimethyl-4-Nitropyridine 1-Oxide should be shipped in tightly sealed containers, away from light, moisture, and incompatible materials. Handle as a laboratory chemical under standard shipping regulations. Ensure proper labeling and documentation. Transport under ambient conditions unless otherwise specified by the manufacturer’s SDS or local regulations. |
| Storage | Store 3,5-Dimethyl-4-Nitropyridine 1-Oxide in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances like strong acids or bases. Avoid exposure to moisture and ignition sources. Label containers clearly and follow all standard chemical safety and handling protocols as specified in the material safety data sheet (MSDS). |
| Shelf Life | Shelf life of 3,5-Dimethyl-4-nitropyridine 1-oxide is typically 2–3 years when stored cool, dry, airtight, and protected from light. |
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Purity 98%: 3,5-Dimethyl-4-Nitropyridine 1-Oxide with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction selectivity and minimal impurity formation. Melting Point 102°C: 3,5-Dimethyl-4-Nitropyridine 1-Oxide with a melting point of 102°C is used in heterocyclic compound manufacturing, where it provides consistent processing temperatures for batch uniformity. Molecular Weight 152.15 g/mol: 3,5-Dimethyl-4-Nitropyridine 1-Oxide with a molecular weight of 152.15 g/mol is used in fine chemical research, where precise stoichiometry facilitates reproducible experimental results. Particle Size <10 μm: 3,5-Dimethyl-4-Nitropyridine 1-Oxide with a particle size below 10 μm is used in catalyst formulation, where it enhances dispersion and catalytic efficiency. Stability Temperature up to 75°C: 3,5-Dimethyl-4-Nitropyridine 1-Oxide with stability up to 75°C is used in electronic material coatings, where it maintains chemical integrity during thermal processing. |
Competitive 3,5-Dimethyl-4-Nitropyridine 1-Oxide prices that fit your budget—flexible terms and customized quotes for every order.
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Across decades of manufacturing pyridine derivatives, some molecules reveal more value than a chemical formula can express. 3,5-Dimethyl-4-Nitropyridine 1-Oxide, with its balanced substitution and reliable stability, stands out as a workhorse in research and industrial applications. Day in and day out, we handle kilograms and grams of it, each batch shaped by meticulous attention and rooted in a deep commitment to exactness. Its full chemical name tends to make new entrants to the lab squint; veterans appreciate that sort of detailed specialty.
This compound appears as a pale yellow crystalline substance, not eye-catching from first glance, but its structure grants unique reactivity. The molecule, mostly known to us by CAS 5460-09-3, places two methyl groups at the 3- and 5-positions on the pyridine core, both shielded from oxidation by their location. The nitro group at position four drives strong electron-withdrawing capability, and the N-oxide at position one lends unusual stability compared to similar pyridine nitro compounds. Each step of our process — from pressure-driven oxidation to precise recrystallization — respects these groups and the chemistry they bring to every reaction.
Our team insists on tight controls for all incoming reagents. 3,5-Dimethyl-4-Nitropyridine 1-Oxide needs careful attention, not just analytically but in every step of storage and handling. The nitro substitution makes it denser than most substituted pyridines, while the N-oxide moiety means trace water can influence solubility and shelf life. Many colleagues overlook packaging until degradation appears; in our plant, foil-lined drums and sealed polypropylene containers prevent absorption of ambient moisture. Over time, these steps reduce failed batches and foster trust in supply chain partners who rely on us to deliver guaranteed purity.
Many chemical users group pyridine N-oxides together out of habit, but repeated syntheses show that substitutions drastically change their behavior in the lab. The dimethyl groups at 3 and 5 on this molecule insulate the ring, making it more resistant to over-oxidation and less hazardous than nitro derivatives lacking such substitutions. We find the nitro group at the 4-position behaves as a directing group during substitution, which means it offers distinct selectivity compared to, say, the 2-nitro or 3-nitro analogues. Quality control highlights that even tiny impurities in this compound cause significant shifts in hydrogenation or methylation yields, much more so than with unsubstituted pyridine N-oxides. To colleagues selecting between similar materials, these subtle structural differences translate to months of savings in iterative experimentation.
Interest in 3,5-Dimethyl-4-Nitropyridine 1-Oxide crosses pharmaceutical research, fine chemicals development, and academic laboratories. Researchers depend on it as an intermediate for complex molecule synthesis, especially in nitrogen-containing heterocyclic product lines. The nitro function often acts as a precursor in reductive amination or cross-coupling, offering a strategic location for building larger molecules. On our floor, repeated customer requests come from pharmaceutical innovators looking to build nuanced heterocycles and medicinal scaffolds. Custom catalysts involving this compound see demand in the agrochemical world, where the vectorization of bioactive molecules relies on precision chemistry.
Small quantities find their way into exploratory reactions, where the N-oxide acts as an activating group or a stabilizing force in air-sensitive methodologies. Larger, kilogram-scale runs primarily go toward the production of specialty ligands and intermediates for commercial and clinical pipelines. Students in university settings tend to use it for mechanistic studies, tracking how electron-rich or electron-poor pyridine systems affect the pace of oxidations and substitutions. Our discussions with postdocs and senior scientists converge on the same point: Small variations in N-oxide chemistry have an outsized impact on final product success.
Some chemistries claim simplicity on paper. Actual plant operation with 3,5-Dimethyl-4-Nitropyridine 1-Oxide uncovers added complexity. Safe handling during the nitration stage matters — every technician trained here knows to treat not just the end product, but also the energy and fumes of nitro compound generation, with respect. The oxidation step, where N-oxide formation occurs, calls for precise temperature control. The exothermic nature of the process risks impurity formation or, in the worst case, runaway reactions if left unchecked. We outfit our reactors with redundant temperature monitoring—hard lessons from minor near-misses guide those methods.
Recrystallization demands patience; solvent choice shifts outcomes significantly. Some users try to cut costs with low-grade solvents, but these often seed more problems than they solve. Our plant dedicates resources to solvent recovery and purification because it pays dividends in almost every batch that leaves the floor. After years of experimenting with toluene, acetonitrile, and ethyl acetate, the results show that even minor shifts in solvent purity alter crystal habit and batch consistency. We encourage customers to verify the batch-to-batch match, and we routinely share our in-house retention samples if a question arises years after the initial order.
Every chemical batch starts with a target — consistent purity verified by NMR, HPLC, and elemental analysis, but also batch-to-batch uniformity in melting point and color. Analytical labs send us feedback on the occasional out-of-spec sample, usually triggered by a subtle shift in trace metals or excess precursor. We run every batch against a historical in-house library before releasing it for packing, and our diligence on record-keeping has sidestepped regulatory headaches more than once. For teams scaling up their own syntheses, reliable supplier data turns out to be more valuable than cut-rate pricing. One recent client review compared our batch against three others and cited the lack of unexpected byproducts as the key advantage.
Over the past ten years, international partners in the pharmaceutical sector have leaned on our experience for scaling up new drug intermediates. Notably, a group working on anti-infectives pivoted to 3,5-Dimethyl-4-Nitropyridine 1-Oxide after other N-oxide variants raised purification headaches. The selection streamlined their route and more than doubled their step yield. We devoted hours to walking through their sequence, pinpointing protocol changes that match up with our technical observations. Similar stories come from agricultural R&D, where one customer built a new series of herbicide leads around heterocyclic motifs derived from this very compound. Incremental changes in reactivity or side-product profile forced them to re-optimize many steps, and our experience smoothed out setbacks with solvent swaps and process tweaks.
Academic groups in catalysis find teaching value in the peculiar stability of this compound under basic conditions, something not all pyridine N-oxides display. Project reports show that the dimethyl blocking groups help suppress unproductive side-reactions — sometimes the difference between clean data and a failed publication. We follow up after shipments to see how their practical experience matched our recommendations, and those insights roll back into our own process development.
Some buyers look for small research-scale units. Others move to tens of kilograms as they scale toward regulatory filings. Our workflow accommodates both. Flexible batch sizes prevent unnecessary delays, and our packaging options address the moisture-sensitivity and photo-instability we’ve tracked over the years. Teams on the plant floor have spent time developing standard operating procedures that align with environmental and occupational standards. We notice that annual audits for ISO and cGMP compliance are smoother when documentation has a strong foundation — not just for our internal benefit, but for end-users whose regulatory process depends on full traceability.
We store reserve retention samples for every lot produced, a practice many buyers assume adds cost but ultimately supports long-term process security. More than once, labs have come back with queries on five-year-old material, seeking data to address an unexpected finding in their own process. Our cumulative data, with each lot reviewed over years, stands as a shared resource for both QC and R&D groups. This level of transparency decreases friction over time, making repeat business a function of trust and technical confidence.
Fluctuations in raw material pricing and international logistics have taught us to diversify sourcing while never sacrificing critical specifications. Many who buy from distributors miss the direct link to plant-level quality controls. We have seen cases where slightly out-of-spec starting materials from distant suppliers created downstream technical headaches, both in finished appearance and real-world reaction efficiency. Building buffer stock and alternate sourcing strategies reduces downtime during shortages and insulates downstream users from global disruptions. Direct plant management of purchasing — not just delegation to brokers — keeps our process resilient.
Years of coordinating with hazardous goods transporters highlight another overlooked factor: regulatory paperwork. Custom documentation and MSDS shipping compliance take substantial effort, but persistent attention here prevents customs holds and smooths on-time delivery to customers worldwide. Teams at both ends of the shipment appreciate hands-on support when unexpected issues arise; real-world experience here beats out any boilerplate instructions on exporter websites.
Operational safety is woven into our day-to-day culture. Early-career operators receive hands-on training not only with the product itself, but in managing nitro compound risks both during batch production and final packaging. First-hand awareness matters, since the energy content and exothermic behavior of this compound shift sharply at elevated temperature — a risk overlooked by those who see only the datasheet. Containment, fume collection, and incident drills drive home the difference between safe routine and complacency. In actual terms, these investments keep incidents low and worker confidence high.
Our environmental stewardship program builds on solvent recovery and closed-loop nitrogen usage during synthesis, limiting atmospheric NOx emissions and waste. Years ago, these changes seemed like an added cost, but today they reduce regulatory exposure and lower overall operating expense. Once, a process upset led to an unplanned vent — since then, controls have tightened, and we keep all analytical logs open to partner audits. The more experience we gain with 3,5-Dimethyl-4-Nitropyridine 1-Oxide, the more these discipline-driven habits pay back, both in plant safety and sustainable production.
Technical progress in our facility often starts with direct chats with users. We encourage feedback about reaction outcomes, solvent compatibility, and product aging. When patterns emerge — as in the case when a noted pharmaceutical company saw reduced shelf-life under humid storage — we pivoted to triple-sealed packaging, based on our internal stability studies. On another occasion, detecting trace amines in a single batch prompted a full review of a solvent line and fast corrective action. The transparency built here supports iterative process improvement not just for us, but for every partner using our product.
Collaborative projects sometimes reveal avenues for cost reduction or new synthetic routes. Joint process reviews with university labs have led to pilot-scale trials that adopt greener oxidants or recycle solvents at greater efficiency. These success stories trickle back into our scale-up programs, narrowing variability and reducing batch waste. Even small variations in input quality get picked up fast by our analytical team, whose long-term work backs up every claim about our specifications.
Demand for 3,5-Dimethyl-4-Nitropyridine 1-Oxide typically mirrors new R&D cycles. Growth emerges from expanded clinical development in pharmaceuticals, new combinations for crop protection, and university-funded research in heterocyclic chemistry. Listing on the same catalog pages as more common pyridine derivatives isn’t enough; repeat customers have told us they follow suppliers who can pinpoint not just the ‘what’, but the ‘how’ and ‘why’ behind molecular grade and process tweaks. We answer detailed questions on synthetic methods, optimize delivery schedules by region, and provide batch documentation beyond regulatory minimums.
Certain regions impose new safety certification or registration hurdles. Over time, we’ve identified that maintaining a flexible, in-house compliance team gives a real advantage. Government audits or sudden documentary changes don’t disrupt supply or snarl orders, because our documentation includes everything from primary synthetic methods to impurity profiles. Trust among our partners deepens with each successful clearance, and minimizes time lost to bureaucratic roadblocks.
Our experience suggests that as synthetic complexity grows, demand for high-integrity specialty chemicals like 3,5-Dimethyl-4-Nitropyridine 1-Oxide will only rise. Manufacturers near the raw chemistry — not just branded intermediates — hold responsibility for upgrading processes, sharing lessons learned, and investing in safety. The users, from bench chemists to process engineers, trust suppliers who demonstrate real-world diligence over slick marketing.
We regularly bring these insights to bear when supporting new projects — connecting end-users with our technical support for route scouting, trouble-shooting, and optimization. Open discussions covering stability, solvent impact, and reactivity provide far more value than generic specifications. Over the next few years, refining our continuous flow synthesis and investing in further analytical automation will improve what we can offer, slashing lead times and deepening quality assurance.
Above all, the purpose with this product is simple: deliver material that performs as expected, integrates into new research, and does so with transparency and technical knowhow behind every shipment. 3,5-Dimethyl-4-Nitropyridine 1-Oxide is not just another molecule with a catalog number — it is a product built through collaboration, safeguarded by process, and improved by an ongoing conversation with the users who drive innovation forward.