|
HS Code |
114298 |
| Product Name | 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide |
| Molecular Formula | C7H8ClNO2 |
| Molecular Weight | 173.60 g/mol |
| Cas Number | 1166824-38-5 |
| Appearance | Solid, color varies |
| Solubility | Soluble in organic solvents |
| Purity | Typically ≥ 95% |
| Structure | Pyridine N-oxide core with 4-chloro, 3-methoxy, and 2-methyl substitutions |
| Smiles | CC1=NC(=C(C=C1OC)Cl)[N+](=O)[O-] |
| Inchi | InChI=1S/C7H8ClNO2/c1-5-7(11-2)3-4-6(8)9(5)10/h3-4H,1-2H3 |
| Synonyms | 4-Chloro-3-methoxy-2-methylpyridine oxide |
As an accredited 4-Chloro-3-Methoxy-2-Methylpyridine 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 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide, tightly sealed with tamper-evident cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide: 10MT packed in 200kg HDPE drums, securely palletized. |
| Shipping | 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide should be shipped in tightly sealed containers, protected from light, moisture, and extreme temperatures. Follow all applicable regulations for chemical transport. Include appropriate hazard labeling and ensure material safety data sheets (MSDS) accompany the shipment. Handle and store in accordance with standard laboratory safety guidelines. |
| Storage | 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat, and sources of ignition. Keep away from incompatible substances such as strong acids, bases, and oxidizing agents. Ensure proper labeling and avoid moisture exposure to maintain chemical stability and purity. |
| Shelf Life | Shelf life: Store in a cool, dry place; typically stable for at least 2 years if tightly sealed and protected from light. |
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Purity 98%: 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal impurities. Melting Point 82°C: 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide with a melting point of 82°C is used in solid-phase peptide synthesis, where controlled melting allows precise formulation blending. Moisture Content <0.2%: 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide with moisture content below 0.2% is used in agrochemical manufacturing, where low water content prevents hydrolysis and degradation during processing. Particle Size D90 <50 µm: 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide of particle size D90 less than 50 µm is used in catalyst preparation, where fine granularity enhances reactivity and dispersion. Stability Temperature 150°C: 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide stable up to 150°C is used in high-temperature organic syntheses, where thermal stability prevents decomposition and side reactions. |
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Our facility began producing 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide long before it became a commonly referenced intermediate in modern agrochemical labs. Over the years, requests for this compound have increased, which demonstrates a broader recognition from both synthetic chemists and industrial researchers. Keen interest has come from sectors focused on pharmaceutical development, crop protection, and custom synthesis, where nuanced N-oxide chemistry often sets the groundwork for further functionalization.
The production process demands both consistency and know-how. Experienced technicians run every batch using strictly controlled conditions—to us, tight temperature monitoring and careful solvent handling make the difference between a batch that passes strict purity benchmarks and one that lands in the waste drum. From its unique structure, the molecule presents a subtle challenge: the oxygen atom bonded to the nitrogen on the pyridine ring boosts the electron density, supporting specific oxidative transformations that conventional pyridines can’t reproduce.
Within this compound, the 4-chloro and 3-methoxy groups play a clear role. Chloro-substitution offers a balance between reactivity and selectivity in downstream reactions, limiting unwanted side-products. Methoxy substitution brings a mild electron-donating property, which stabilizes intermediates during multi-step synthesis. The methyl group at the 2-position adds bulk without wrecking the aromaticity that makes pyridine derivatives so versatile.
The presence of the N-oxide function means researchers gain a reactive site for nucleophilic substitutions or reduction to the parent pyridine, but with access to different reactivity than those working with unoxidized pyridines. Through the years, chemists have come to us with frameworks that demand regioselective transformations difficult to achieve by direct halogenation or alkylation alone. The N-oxide route solves problems that would stymie a traditional pyridine, providing chemoselectivity and protecting the ring during tricky oxidations.
Our technical team aims for a purity above 98%. Every batch faces a robust quality control protocol: proton NMR confirms the presence and placement of the functional groups, while HPLC guarantees the absence of key impurities. Moisture control matters here. Even less than one percent residual water or alcohol sometimes disrupts later transformations—sensitivity we’ve learned about the hard way, through customer feedback and tough troubleshooting calls. Long discussions with end users of our material led us to find packaging materials that don’t leach or react with the N-oxide, something that rarely appears on spec sheets but often shakes out in practice.
Our crystalline material forms in free-flowing powder, facilitating accurate dosing at both lab and kilo scale. Over time, we’ve seen that some clients favor this morphology for ease of handling and reliable dissolution, especially compared to certain sticky, hygroscopic analogs. We keep a close watch on color and trace side product levels, as both subtly indicate batch-to-batch consistency. From an operational perspective, storing the product in sealed, amber glass containers extends shelf life, as the N-oxide is prone to degradation if exposed to sustained light or humidity.
Comparing 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide with other pyridine N-oxides reveals both overlapping and distinct utility. We’ve handled close analogs—parent pyridine N-oxides, or those bearing bromo or trifluoromethyl groups at different positions. While these compounds can substitute in some reactions, our 4-chloro-3-methoxy-2-methyl version hits a particular sweet spot for chemists chasing selective transformations and improved yields.
For example, unmodified pyridine N-oxide serves many catalytic oxidation reactions, yet lacks the targeted reactivity needed for stepwise pharmaceutical intermediates. The balance in electron-withdrawing and electron-donating groups in this molecule shifts reactivity toward pathways unavailable to the parent ring. Discussing specifics, when our partners need to introduce complexity or block unwanted pathways, they switch to this compound rather than retrofitting simpler pyridine N-oxides with additional synthetic steps.
Working with this N-oxide unlocks more than just chemical flexibility—it influences efficiency on the bench and at scale. Customers in medicinal chemistry often highlight time savings: using this intermediate cuts out an entire step of functional group exchange, one that usually requires hazardous oxidants or tricky chlorination. Agrochemical developers appreciate that the compound remains stable under mild conditions yet activates in the presence of specific catalysts, streamlining late-stage modifications.
Real-life feedback has driven us to refine crystallization and drying steps. In some early batches, we noticed trace acid impurities triggered side reactions later in the synthesis pipeline. Our analytical team partnered with process chemists to tweak washing protocols, nearly eradicating the problem. Ongoing conversation with end users continues to shape what quality means on the ground, as precise needs shift between drug synthesis and agrochemical discovery.
Increasingly, our partners request insight into safety, waste, and environmental profile. The N-oxide route brings up specific handling points: While this compound avoids some of the worst hazards of strong oxidants or halogen carriers, it calls for respect regarding dust control and the potential for exothermic decomposition. For us, small details count. Dedicated workstations, careful weighing, and filtered exhaust keep our team safe and the product pure.
On the environmental front, we’ve taken steps to recycle and neutralize byproducts. Solvent management systems recapture and purify major solvents, lowering our waste output and reducing emissions. After years of running the same process, we reduced process water requirements by sampling in process rather than post-production. Not every competitor prioritizes these controls, but our experience tells us that small refinements pay off—not just in compliance, but in real risk reduction and cost control.
We draw much of our product insight directly from conversations with those who use it in the lab or at scale. N-oxide intermediates present a specialized set of handling and reactivity features—meaning researchers often benefit from experience shared by those who have seen a spectrum of issues. Over the years, we’ve seen researchers unlock catalytic cycles or streamline difficult syntheses by leveraging the features unique to 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide. In one memorable project, a pharmaceutical client reported a double-digit yield bump simply by switching from a less robust pyridine intermediate to our N-oxide version. The switch also dropped their overall reaction time and removed the need for a redundant workup step.
Field experience continually shapes how we approach both product development and customer support. We’ve supported pilot-scale campaigns where kilogram lots carried strict purity, particle size, and dry-down requirements. Frequent batch-to-batch analytical confirmation and hands-on customer dialogue prevent hiccups. Operational feedback from researchers has told us which impurity traces are most disruptive, which packaging formats survive cold shipping, and what minor additives to avoid for downstream compatibility.
Our quality controls did not emerge overnight. Ten years ago, trace residual solvents once went unnoticed until a client’s reaction seized up during scale-up. Since then, we doubled down on cross-checks, expanded GC-MS screening, and introduced release protocols for every package leaving our facility. Our customers count on this diligence, and we count on theirs to call out even minor quality flaws. Sometimes, one analyst’s sharp eye has prevented a downstream failure that would have burned days of lab time.
We prefer sharing analytical results and process changes openly. If a synthetic route shifts—due to a raw material change, a new regulatory guideline, or basic supply chain realities—we update end users promptly. This transparency keeps everyone on the same page, even as technical needs evolve.
The mainstay applications for 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide remain in chemical synthesis. Yet, we have observed new areas opening up. Heterocycle research continues to expand, with computational chemists flagging new N-oxide derivatives as promising scaffolds for future drugs or pesticides. Our R&D team tracks external research closely. In cases where our molecule’s electron profile has matched up to a prospective target, we offered pilot lots for custom evaluation. Some of these projects matured into full process support for larger manufacturing runs.
One less obvious area of research involves the molecule’s role as a modulator in catalytic cycles. Collaborators working on green chemistry have probed its ability to support milder, more energy-efficient transformations. This demand for lower environmental impact continues to shape not just our batch operations, but the direction our technical improvement takes.
Experience matters when troubleshooting. Early on, we lost product stability in storage simply by neglecting the impact of minimal air leaks. An opaque container swap alone stabilized the material, saving both replacement costs and trust with our customers. Another lesson emerged in scale-up; persistent trace alkali residues, practically silent on the small scale, jumped out during a multi-kilo batch run. Frequent collaboration with labs running application tests often heads off these issues. The best results come from pairing deep product knowledge with real-life user challenges.
Delivering the molecule at kilo scale bridges two realities: analytical consistency and industrial practicality. We sometimes field requests to tweak parameters others rarely measure—particle size, trace halide content, even bulk flow characteristics. Technical teams, both on our end and in client labs, have found that open data exchange shortens the distance between synthesis theory and usable product.
Reliable intermediates encourage exploration. Organic chemists continually push for higher selectivity and shorter syntheses, and every new data point on the stability or reactivity of 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide feeds back into process improvement. We’ve provided input for custom syntheses, set up ship-ready small batch production for startup ventures, and occasionally supported academic projects that cycle between bench and pilot scale with little warning. Each of these cases returns knowledge that hones our future production or packaging decisions.
Material quality means more than just hitting a number on an assay sheet. It tracks how smoothly labs run from receiving lot to sealed product, and whether researchers feel confident about reaction outcomes. Our production teams invest countless hours documenting process tweaks and supporting staff through new analytical instrumentation. We compare every new batch against long-running reference standards, cross-checking more than just purity—color, flow, and dissolution rate often reveal problems before a formal assay does.
4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide does not serve every possible transformation, but within its niche, it holds key advantages. The combination of functional groups supports targeted synthetic steps with minimized side reactions. We see that in client metrics: higher yields, crisper analytical profiles, reduced troubleshooting calls. The process stability grows out of daily, on-the-ground experience—small changes in drying method, periodic calibration of weighing stations, incremental improvement in solvent recovery policy.
In a competitive market, offerings multiply, and every compound fights for relevance. Ours earned its place not just through regular batch output, but by standing up to continuous testing and critique from skilled chemists in laboratories and pilot plants around the world. The dialogue between manufacturer and user shapes where the product lands in the real landscape of chemical manufacturing.
As chemical research pushes deeper into complex functionalizations and more precise molecule design, N-oxide intermediates stand as foundational materials. Our engagement with researchers and technical teams widens the scope for process optimization. We seldom stand still; each year brings requests for new batch sizes, new packaging formats, and ever-tighter specifications to suit novel applications.
Our on-site R&D team tests every improvement first in small-scale runs. They document process tweaks in detail, incrementally improving reaction times, reducing waste, and extending shelf life as discoveries permit. This forward-looking approach means each batch reflects both hard-won reliability and adaptive technical growth.
Our most valuable lessons arise in close collaboration. Researchers and technical specialists share concerns about trace impurities, or offer creative feedback on how a change in packing format could streamline their workflow. We field questions about light sensitivity or suggest shipment in nitrogen-flushed containers when high humidity looms. Each exchange tightens the margin of error.
Even now, we work with partners investigating next-generation green synthesis routes or deploying automated reactors. In these scenarios, robust, high-purity intermediates make all the difference—preventing pauses, troubleshooting, or costly reruns. We actively support those pursuing new frontiers with analytical support, historical batch data, and direct technical feedback.
The landscape for specialty pyridine N-oxides continues to evolve. Regulatory expectations, end-user demands, and shifts in market supply require continuous monitoring and adjustment. Our long-term relationships with academic labs, pharmaceutical companies, and fine chemical processors ground our sense of what’s next—not just what’s possible, but what’s demanded at scale.
We commit to sharing clear insights as our methods evolve and to bringing practical, accessible improvements to every customer batch. Our best results come when users share outcomes, flag roadblocks early, and engage in ongoing dialogue—building both compound reliability and community expertise around 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide.