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HS Code |
661128 |
| Chemicalname | 2-Amino-6-Methoxy-3-Nitropyridine |
| Molecularformula | C6H7N3O3 |
| Molecularweight | 169.14 g/mol |
| Casnumber | 22483-09-6 |
| Appearance | Yellow solid |
| Meltingpoint | 152-154 °C |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Smiles | COC1=CC(=NC=C1[N+](=O)[O-])N |
| Inchi | InChI=1S/C6H7N3O3/c1-12-5-3-4(7)8-2-6(5)9(10)11/h2-3H,7H2,1H3 |
As an accredited 2-Amino-6-Methoxy-3-Nitropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed 25g amber glass bottle, white screw cap, chemical label displaying: "2-Amino-6-Methoxy-3-Nitropyridine," CAS number, safety symbols. |
| Shipping | 2-Amino-6-Methoxy-3-Nitropyridine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported in compliance with chemical safety regulations, often as a non-hazardous substance, but appropriate labeling, documentation, and handling precautions are observed to ensure safe and secure delivery. |
| Storage | Store 2-Amino-6-methoxy-3-nitropyridine in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat, and sources of ignition. Protect from direct sunlight and incompatible substances such as strong acids and oxidizers. Label the container clearly, and avoid prolonged exposure to air. Use proper personal protective equipment when handling the compound. |
Applications of 2-Amino-6-Methoxy-3-Nitropyridine in Industrial Manufacturing2-Amino-6-Methoxy-3-Nitropyridine serves as a critical raw material for advanced chemical syntheses in several specialized downstream industries. As the original manufacturer, we support customers worldwide in delivering demanding application results, from niche pharmaceutical intermediates to high-performance agrochemical ingredient synthesis. The following sections detail prevalent application scenarios based on extensive supplier-consumer collaboration, process technology feedback, and international regulatory requirements. 1. Pharmaceutical API Intermediate: Third-Generation Kinase Inhibitor SynthesisLeading pharmaceutical manufacturers integrate this compound at early-stage synthesis of kinase inhibitor drug substances, leveraging its electron-rich and substituted pyridine ring for highly specific heterocyclic scaffolds. Custom process development requires rigorous handling from GMP-grade sourcing through to late-phase impurity control, particularly for active pharmaceutical ingredient (API) production targeting global oncology markets. Industry compliance standards
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2. Agrochemical Active Ingredient Synthesis: Selective Herbicide ScaffoldingMajor agrochemical firms utilize this nitropyridine derivative in the synthesis of novel selective herbicides, taking advantage of its methoxylated and amino-substituted framework for structure-activity optimization in pyridinyl urea or triazine herbicidal scaffolds. Downstream process engineers emphasize integration into fully compliant, large-scale continuous production routes. Industry compliance standards
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3. Specialty Dye and Pigment Precursor: Heterocyclic Azo DyesSelective dye and pigment manufacturers leverage the unique substitution pattern of this pyridine for synthesizing high-purity heterocyclic azo dyes, especially those requiring electron-donating and -withdrawing groups to engineer spectral properties critical for high-value textiles and plastics. Industry compliance standards
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4. Electronic Materials: Building Block for OLED and Liquid Crystal IntermediatesProducers of organic electronic and display materials harness the capability of this nitropyridine in assembling advanced intermediates for OLED emitting layers and specialized liquid crystal compounds, where strict electronics-grade purity and batch traceability are mission-critical. Industry compliance standards
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Daily work in our reactors tells a different story from that of traders or catalog vendors. We’ve produced 2-Amino-6-Methoxy-3-Nitropyridine for years, so the character of this compound is no mystery in our shop. The molecule may sound like a handful, but as a chemical manufacturer, we see it simply as a dependable intermediate in pharmaceutical and agrochemical synthesis. Reliable performance starts in the raw materials, and the entire workflow plays a part—from the gentle feeding of methoxypyridine into the reactor, to the final careful crystallization step and repeated purifications. Each batch brings its own challenges and learning curves, and what people often overlook about this molecule is that subtle inconsistencies—even with a stable process—can alter downstream use in unexpected ways.
Our model for 2-Amino-6-Methoxy-3-Nitropyridine centers on careful, reproducible nitration and amination sequences. The final product forms a pale-yellow crystalline powder with a defined melting point. As chemists, we watch for moisture levels, particle size, and trace impurities—the stuff that nobody lists in their glossy catalogues—because customers in the pharma sector in particular never want these surprises. Consistency doesn’t happen automatically; it is earned by attention to detail at every stage, from vacuum drying to sealed-packaging so that air or humidity won’t cause clumping.
Lots of documentation exists on 2-Amino-6-Methoxy-3-Nitropyridine, but what matters most in our own quality control lab often differs from simple purity numbers. For us, each batch goes through HPLC, NMR, and moisture analysis. Color, flowability, and absence of residual organic solvents can influence its real-world handling. Even tiny traces of related pyridine derivatives sometimes pop up if the raw material contains hidden contaminants. We invested years in process tweaks to avoid such surprises.
Chemists typically ask about assay by HPLC, water content by Karl Fischer titration, and melting point. Our material shows purity levels consistently above 98%, with water content tightly controlled below 0.5%. An uncontaminated profile helps research and commercial users sidestep headaches in scale-up steps, whether you’re preparing new drug candidates or specialty dyes. The molecule’s crystalline nature helps prevent dusting—a common annoyance in the lab—and the clear-cut melting range gives additional confidence in the integrity batch after batch. We store this product in tight containers in a cool, low-humidity warehouse, minimizing the chances of caking or slow degradation.
The heart of our customer base relies on 2-Amino-6-Methoxy-3-Nitropyridine as a key intermediate rather than a final ingredient. Most work with advanced intermediates or active pharmaceutical ingredients (APIs). For united labs, university researchers, and well-funded pharma companies, this molecule serves as a launching point for synthesizing more complex heterocyclic structures—especially in lead optimization where the pyridine core offers flexibility for further derivatization. Many antineoplastic, anti-infective, and CNS-active drug candidates use this scaffold, sometimes incorporating fluorine or halogen substitutions in adjacent rings. We see its popularity grow in medicinal chemistry as researchers hunt for molecules with improved solubility or better metabolic profiles, features that the methoxy and amino groups help influence.
Demand spikes occasionally from agrochemical development, as this compound has made appearances in synthesis protocols for insecticides and herbicides. The nature of the nitro group, right at position 3, lends itself to further reduction or cyclization chemistry in many patent filings. Sometimes, dye chemists visit us for samples because the pyridine ring can serve as an anchor for highly chromatic molecules. These are not theoretical uses—they drive real production volumes and process improvements at our plant. Every order brings a story, and every feedback loop sharpens our own process—whether a customer is scaling for clinical trials or testing a totally novel crop protection agent.
Working hands-on, we see marked differences between 2-Amino-6-Methoxy-3-Nitropyridine and its relatives. Compare to 2-Amino-6-Chloro-3-Nitropyridine, for example. The methoxy substituent changes solubility and reactivity in subtle ways. Methoxy brings more electronic richness to the ring, affecting how the molecule participates in nucleophilic substitution or metal-catalyzed cross-coupling. Chloro- or fluoro- analogues often create bottlenecks in downstream chemistry because of their electron-withdrawing power.
Ordinary 3-Nitropyridine lacks the functional handles for further elaboration—no amino group for coupling, no methoxy for polar interactions. Multi-step synthetic campaigns often skip the “vanilla” pyridines and go straight for substituted versions like ours, as they cut out extra steps. We’ve seen projects stall when the wrong intermediate is chosen early on, simply because someone didn’t appreciate nuances in substitution pattern. Direct access to the methoxy- and amino- positions turns out to be a make-or-break factor for timelines in real medicinal chemistry labs.
Years of producing this molecule have taught us that the devil hides in the details. Nitration always looks simple on paper, but temperature control makes or breaks the process. Go too warm, and you risk over-nitration or tarring. Too cool, and the yield tanks. Early in our scale-up journey, we learned to automate temperature ramps—data logging thermocouples at multiple points in the reactor, not just at the jacket. These investments came directly from real-world batch failures and the headaches they caused.
Post-reaction workup demands even more attention. Ammonia addition should be slow and controlled—dump it in too fast, and you’ll end up with uneven product or side reactions that are hard to separate. Filtration can clog if particle size goes awry; drying takes care because the finished crystals will cake if even a little moisture remains. We hand over only well-dried, free-flowing product. Process monitoring matters at each stage, and sometimes that means waking up at odd hours to collect a time-point sample or adjust a pump.
Process innovation doesn’t stop just because you’ve operated for years. We experiment with alternative solvents. Some batches use less chlorinated waste because we tested new green solvents and adjusted to improve batch-to-batch repeatability. Our pilot plant trials feed directly into routine production. If a chemist downstream suggests a change—maybe a narrower particle size for better suspensions in their reactor—we incorporate that feedback into the next run. Every tweak changes the process envelope, but as the actual manufacturers, we make sure each modification translates into improved yield or cleaner product, not just a write-up in the lab notebook.
When researchers run into trouble downstream, they often call us before reaching for the next bottle. A common question: does a minor impurity profile affect hydrogenations, oxidations, or cross-couplings? We check stability under the customer’s planned conditions before a new process scale-up. Some users need lower particle sizes for slurry preparations, others request a specific drying regime to minimize decomposition. Nobody gets a “stock” response—we address each query with direct input from our own synthesis team.
Over the years, we’ve seen how using a poorly made intermediate affects critical steps later: one missed purification can foul a column and stall scale-up for weeks. Researchers sometimes switch to us after running into reproducibility issues with intermediates sourced from less careful suppliers. Our approach has always been to ask about end-use and then suggest packaging, particle sizing, and even different crystallization steps to help, not just ship drums and move on. Sometimes, that means custom milling or re-drying prior to dispatch.
Lab-scale batches introduce few surprises. The real differences emerge at pilot and kilo scales, where heat and mass transfer jump out as problems at every corner. The exothermicity of nitration reactions shows itself more forcefully in larger reactors. Our process team watched for these pitfalls carefully, investing in real-time temperature and pressure controls. Switching mixing paddles, adjusting agitation speeds, and carefully sequencing addition points make a dramatic difference. What works in glassware does not always work in 500-liter reactors.
Product washing takes more than a swirl and filter. You find manageable techniques work smoothly in ten-liter glass, but sticky residues, poor washing efficiency, and clumping become real pain points when drums replace flasks. We design our process with future users in mind—minimizing water usage, ensuring waste streams are easy to manage, and making sure that delivery fits into gloveboxes, isolators, or open bench settings. We also clean and test reactors between campaigns to prevent contamination crossing over to other products.
We run more than the basic COA for every batch. NMR checks for aromatic region clarity—no lurking byproducts hiding under main peaks. HPLC covers quantification and helps flag any persistent unknowns. Moisture, unreacted starting material, trace metals, and color all catch our eye. Some end-users need more: residual solvent testing by GC, expanded impurity analysis, and custom reporting. Our philosophy is straightforward: if the data can help avoid surprises downstream, we collect and share it. Customers counting on our batch for clinical candidate synthesis never want to learn about a new impurity halfway through a sixteen-step sequence.
We maintain long-term sample retention, with previous batch reference spectra available if a user has questions about consistency. Open, fast communication with users—sharing analytical traces instead of just purity numbers—helps our partners design better processes and reduces downtime. Unexamined material often leads to months-long headaches; a quick analytical cross-check up front can save whole projects.
Powders like 2-Amino-6-Methoxy-3-Nitropyridine demand more than just dry storage. We learned that even warehouse humidity changes between seasons can impact caking and product flow. Each drum gets an inner polyethylene liner and secondary sealing before shipping. There’s no substitute for checking every container as it leaves the plant—if a bag feels off, we open and inspect rather than risk complaints down the line. Chemists in process labs appreciate little things: easy-pour containers, antistatic packaging, clear labeling, and documentation organized for quick QC checks.
Some partners order in laboratory amber glass, others want bulk in fiber drums. We’ve even dispatched single-dose vials when stability or contamination concerns come to the front. On large orders, we work closely with shippers to shorten time in uncontrolled environments, as temperature spikes in summer can change the behavior of even stable compounds. Documentation travels with every shipment—not just MSDS and COA, but also shipping labels, raw material traceability, and batch photos if requested.
Synthetics routines for compounds like 2-Amino-6-Methoxy-3-Nitropyridine come with substantial waste streams. We capture spent acids and bases, treat them on-site, and neutralize or recycle where possible. Team members operate under strict procedural checklists, with PPE at every stage—goggles, gloves, chemistry-grade ventilation, and regular monitoring for vapor releases. Watching for residual nitroaromatics in our waste water is a constant part of the routine. Our goal is nonstop safety—protecting our people, the community, and everyone in between.
We regularly update process hazard analyses, train staff on emergency scenarios, and audit third-party waste handlers to make sure our standards hold. Every incident—no matter how minor—feeds into our improvement cycle. Beyond compliance, our approach aims for best-in-class safety, not just “good enough for today.” Downstream users always ask about handling guidance; our experience means we can offer more than stock phrases—what to avoid, how to store long term, and what to do in case of a spill or accident. We keep our lines open for post-shipment technical support, because safe use starts with honest information from the maker.
We watch the literature and patent filings steadily. Year by year, the use of 2-Amino-6-Methoxy-3-Nitropyridine grows, finding space in ever-expanding classes of advanced pharmaceutical agents. Medicinal chemists increasingly rely on the “privileged” methoxy- and amino-functionalized pyridine scaffold to introduce targeted changes in pharmacokinetics and metabolic stability. Recent years show more demand for enantiomerically pure derivatives, prompting us to explore chiral resolution steps and asymmetric synthesis for select projects.
Demand from agrochemical innovators and materials scientists continues as well—pyridine derivatives underpin color-stable dyes, new pesticides, and sometimes polymer additives with unique electron-donating properties. Each new inquiry challenges us to examine subtle differences in the molecule’s reactivity, thermal behavior, and compatibility with additives or stabilizers. Keeping up with applications lets our internal R&D group work closely with users—sometimes custom-tailoring next-generation intermediates that cut extra synthetic steps or boost downstream activity.
No two batches turn out identical, and every run teaches us something. Demand for 2-Amino-6-Methoxy-3-Nitropyridine continues to grow—not from advertisements, but from word of mouth between working chemists. The punchline is simple: dependable materials, made and backed by producers who answer the phone, bring more long-term value than any online catalog. Ongoing investment in clean chemistry, analytical controls, packaging, and environmental safety make this process a living practice, not a one-time effort. Trusted supply lines hinge on more than price or paperwork—they rest on people willing to listen, adapt, and support downstream science with every drum delivered.