|
HS Code |
435339 |
| Product Name | 5-Nitro-2-Methoxy Pyridine |
| Cas Number | 51938-33-5 |
| Molecular Formula | C6H6N2O3 |
| Molecular Weight | 154.12 g/mol |
| Appearance | Yellow to brown crystalline powder |
| Melting Point | 73-75°C |
| Boiling Point | 341.5°C at 760 mmHg |
| Solubility | Soluble in organic solvents like ethanol, DMSO |
| Purity | Typically ≥98% |
| Density | 1.36 g/cm³ |
| Synonyms | 2-Methoxy-5-nitropyridine |
| Smiles | COC1=NC=C(C=C1)[N+](=O)[O-] |
As an accredited 5-NITRO-2-METHOXY PYRIDINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 5-Nitro-2-methoxy pyridine (10g) is a sealed amber glass bottle with a tamper-evident cap and hazard labeling. |
| Container Loading (20′ FCL) | 20′ FCL container loading for 5-NITRO-2-METHOXY PYRIDINE ensures secure, moisture-free, bulk packaging for efficient global chemical transport. |
| Shipping | 5-Nitro-2-methoxy pyridine is shipped in compliance with all relevant safety regulations. It is securely packaged in airtight, chemical-resistant containers to prevent leaks or contamination, and clearly labeled. The package includes necessary hazard information, and is transported under suitable conditions to avoid extreme temperatures, moisture, and physical damage during transit. |
| Storage | 5-Nitro-2-methoxy pyridine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Keep the container tightly closed and protected from light and moisture. Store in a secure chemical storage cabinet, labeled clearly, and follow all appropriate safety protocols for handling hazardous chemicals. |
| Shelf Life | 5-Nitro-2-methoxy pyridine should be stored in a cool, dry place; shelf life is typically 2–3 years if unopened. |
|
Purity 98%: 5-NITRO-2-METHOXY PYRIDINE with a purity of 98% is used in pharmaceutical intermediate synthesis, where high chemical yield and purity are achieved. Melting Point 72°C: 5-NITRO-2-METHOXY PYRIDINE with a melting point of 72°C is used in controlled crystallization processes, where consistent solid formation and product reproducibility are ensured. Molecular Weight 154.12 g/mol: 5-NITRO-2-METHOXY PYRIDINE with a molecular weight of 154.12 g/mol is used in fine chemical formulation, where precise stoichiometric calculations enhance reaction efficiency. Particle Size <50 µm: 5-NITRO-2-METHOXY PYRIDINE with a particle size less than 50 µm is used in tablet manufacturing, where uniform dispersion and homogeneous mixing are achieved. Stability Temperature 40°C: 5-NITRO-2-METHOXY PYRIDINE stable at 40°C is used in long-term storage of active pharmaceutical ingredients, where product integrity and shelf life are prolonged. |
Competitive 5-NITRO-2-METHOXY PYRIDINE prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
In the world of organic chemistry, pyridine rings have opened doors to a surprising range of innovations. One of the lesser-known but highly practical molecules in this category is 5-Nitro-2-Methoxy Pyridine. Over the years, my own experience working in lab environments and with pharmaceutical partners has highlighted how compounds like this quietly keep research and industry on their feet. Unlike standard pyridine derivatives, which tend to disappear into bulk commodity catalogs, 5-Nitro-2-Methoxy Pyridine stands out for several reasons—reactivity, reliability, and its sweet spot for particular synthetic hurdles.
Those unfamiliar with this molecule tend to ask about the difference a nitro group and a methoxy group make. The simple change at the 2- and 5-positions transforms this pyridine from just another ring structure to a highly sought-after reagent. I’ve watched research groups wrestle with substitutions that require both activation and guidance on an aromatic system. The nitro group at the 5-position fundamentally alters the electron density of the ring, opening the door for specific nucleophilic and electrophilic substitutions. In pharmaceutical chemistry, specificity like this often means trimming weeks off research cycles.
Let’s talk about the main difference between this compound and others that show up in synthetic toolkits. Most pyridine derivatives can serve as basic aromatic scaffolds, but they either react too slowly, too unpredictably, or create downstream purification messes. With 5-Nitro-2-Methoxy Pyridine, the substitution pattern fine-tunes reactivity without over-sensitizing the molecule. Chemists notice this benefit most on the bench: product yields become more consistent, and by-products are easier to separate. The methoxy group helps with solubility in both polar and non-polar solvents, which counts for a lot when switching between reactions or scaling up. There’s less need to thread the needle between too much reactivity and not enough.
Anyone who’s dealt with late-stage pharmaceutical intermediates knows how hard it is to hit that sweet spot. Changing position or the nature of a substituent leads to frustrating trial and error in pathway optimization. Repeating experiments to chase after poorly-behaved analogues costs money and time. 5-Nitro-2-Methoxy Pyridine’s track record in heterocyclic synthesis makes it a go-to option in medicinal chemistry programs. The results don’t lie—I’ve seen teams switch to this compound after months of setbacks and suddenly find themselves able to push forward in synthesis or library expansion.
Besides its value in laboratory research, this molecule shows up in industrial settings where intermediate stability matters. The combination of the nitro and methoxy substitutions makes this compound a useful choice when synthesizing more elaborate nitrogen-containing heterocycles. These are structures at the heart of countless pharmaceutical agents, agrochemicals, and diagnostic probes. One notable application lies in the route to anti-cancer and anti-viral agents, where even the smallest tweak in structure can mean the difference between activity and inactivity. Facing hurdles with uncooperative reactants or undesired by-products, chemists often pick this compound because of its unique electronic profile.
Many production chemists rely on 5-Nitro-2-Methoxy Pyridine as a building block for cross-coupling and nucleophilic substitution reactions. Its increased reactivity compared to unsubstituted pyridine stems not just from the electron-withdrawing nitro group but also from the resonance effects of the methoxy group—something you only appreciate after running a variety of reactions and seeing the real-world yields. Coupling this compound with a wide range of metals or catalytic systems leads to robust, scalable processes. In the world of fine chemicals, this can mean a more secure supply chain and fewer headaches with process validation.
I’ve watched students and postdocs try to cut corners with cheaper or more familiar pyridine derivatives. There’s always skepticism about swapping a core scaffold, given the risk of losing time to unexplained failures. Those who give 5-Nitro-2-Methoxy Pyridine an honest chance see a payoff in reaction times and work-up efficiency. Compared to alternatives like 3-nitro or 2-chloro pyridines, separating pure product gets less messy—fewer rounds of chromatography, less wasted effort. You notice fewer side products clogging up NMR spectra or complicating final isolation steps.
Some skeptics worry about cost or availability, yet the value comes from what you save downstream. For one synthesis in a project focused on kinase inhibitors, routine 2-substituted pyridines led to low conversion, tarring, and headaches at scale. Swapping to this compound, the process not only became manageable but avoided hours of post-reaction cleanup. Raw material price and lead time matter, but downstream labor and plant time are bigger line items in most budgets.
One of the big questions lately is how specialty reagents affect environmental footprints. As more labs and companies aim for greener processes, choosing building blocks that move reactions toward higher selectivity and less waste is essential. Many standard pyridines create more side streams—something that causes problems in waste treatment and downstream solvent recovery. This compound’s selective reactivity and consistent yields often cut the load of purification and reduce the amount of hazardous waste. Better selectivity means smaller solvent volumes and fewer halogenated solvents—two metrics that directly tie into sustainability performance.
Safety is another major topic. Like a lot of nitroaromatics, this compound requires the usual lab sense: good ventilation, gloves, and properly calibrated balances. In my experience, articulated handling procedures and real-world training matter most. Workers who are trained to check MSDS guidance, handle potential dust, and avoid open flames see almost no incidents. The molecule’s solid-state characteristics help reduce airborne risk compared to some fine powders that lead to static accumulation or inhalation hazards.
On paper, you’ll see 5-Nitro-2-Methoxy Pyridine presented with a defined melting point, molecular weight, and high purity—typically exceeding 98 percent by most analytical standards. These specs matter not just for regulatory compliance, but for practical performance. Lower impurity levels mean fewer surprise peaks in LC-MS or GC-MS analyses. Unlike some less stable nitro compounds, this molecule keeps its integrity when stored at room temperature in a dry, closed vessel. As with any specialty chemical, open packages before use and always document batch numbers for traceability. Labs aiming for GMP-grade output appreciate how this consistency translates into easier validation runs and audit trails.
From a bench chemist’s perspective, not all pyridines are interchangeable. Each substitution pattern brings out different reactivity trends, solubility profiles, and stability considerations. The 5-nitro-2-methoxy pattern delivers a combination of mild electron withdrawal and moderate electron donation, striking a balance that accelerates many targeted reactions without promoting destructive over-reactivity. Working with similar compounds—such as 2-methoxypyridine or 3-nitropyridine—can highlight why this balance matters. In my own projects, changes in yield or purity after these swaps became immediately obvious. Tweaking the position of substituents often slowed down key steps or forced changes to purification protocols.
Quality control teams notice the difference too. The solid form allows for easy sampling and accurate weighing without the clumping issues seen in some more hygroscopic pyridines. Analytical groups can count on reliable reference spectra, making it easier to spot adulteration or off-spec lots. When a project depends on reproducibility, picking a compound with a clear track record of performance protects both timelines and budgets.
In my interactions with contract manufacturers and process development teams, the top selection criteria include reliability, selectivity, and compliant supply chains. Standard pyridines sometimes fall short, especially when a project transitions from milligram scale in research to multi-kilogram pilot runs. 5-Nitro-2-Methoxy Pyridine consistently finds favor in scaling because the same substitution pattern that aids synthetic routes in small batches also works at production scale.
The pharmaceutical industry, in particular, values building blocks that preserve chirality, avoid contamination, and simplify downstream purification. No one wants to babysit columns all night or dispose of dozens of gallons of solvent from a single batch. Using building blocks like this pyridine derivative means fewer surprises and fewer workarounds. Over time, these practical factors compound—helping projects move faster and budgets stretch further.
While this compound delivers on many fronts, there are still some hurdles. Price and lead time can become critical issues for tight budgets or fast-moving timelines. Some companies are reluctant to commit to single-source supply, especially with shifting global regulations or raw material markets. In my own project management work, partnering with suppliers who invest in forward inventory, reliable delivery schedules, and transparent documentation protects against most disruptions. For organizations worried about long-term supply, diversifying sources and building strategic reserves can smooth out most procurement bumps.
Regulation in the specialty chemical sector continues to evolve. Certain jurisdictions have tightened rules on nitroaromatics, both to improve workplace safety and to reduce environmental risk. Proactive companies openly share safety data, invest in better handling facilities, and train staff thoroughly. For labs and plants with newer staff, investing in ongoing safety education makes a real difference in incident rates. In practice, clear documentation, labeling, and robust control processes keep adoption straightforward—even for facilities less familiar with nitroaromatics.
Large-scale medicinal chemistry projects rely more than ever on high-performance building blocks. 5-Nitro-2-Methoxy Pyridine supports rapid lead optimization, allowing new analogues to be synthesized without reinvention at every step. Activity screens become easier to interpret when feedstock purity stays high and by-product levels remain consistent run to run. For life science companies chasing the next blockbuster or critical diagnostic, building on a reliable foundation can mean getting to the next milestone months ahead of lagging competition.
Academic researchers, focused on heterocycle modification or novel drug pathways, benefit from easier fragment couplings and fewer synthetic detours. Student projects or grant-funded research can stretch further when failed syntheses drop away, freeing up time for actual discovery and exploration. Graduate seminars and collaborative workshops often feature real-world case studies of successful substitution patterns—many highlighting the consistent performance of this molecule in comparative trials.
In facilities that make fine and specialty chemicals, efficiency and reproducibility take priority every day. Products like 5-Nitro-2-Methoxy Pyridine don’t just solve a single bottleneck—they often allow for new processes altogether. During a shift on the production floor, operators appreciate how easily this solid can be weighed, mixed, and stored. Losses to static or atmospheric absorption drop compared to more volatile or hydroscopic analogues. Down the line, maintenance and cleaning schedules stay on track because fewer by-products end up clogging filters or corroding pipes.
Supervisors and plant managers often cite faster changeovers and simpler product switches as economic benefits. When processes produce less waste and run closer to their theoretical maximum yields, the whole organization wins. Process validation engineers, auditors, and quality inspectors see fewer deviations on batch records—another marker of steady, dependable performance in day-to-day operations.
Over the last decade, demand for smart building blocks has only grown. Customers want purity, reliability, and traceability, especially as cross-border regulations get stricter. Environmental, social, and governance (ESG) goals are also shifting upstream, driving suppliers and manufacturers to invest in greener processes and more efficient supply chains. Products that fit cleanly into these efforts, without extra documentation or risk mitigation, score highest among procurement and compliance teams.
Ongoing research in green chemistry hints at even more reasons to value compounds like this. Catalytic methods keep improving, making use of electron-rich and electron-deficient building blocks to streamline synthesis. As process chemistry gets more sophisticated, products once considered too niche now become standard choices for complex pharmaceutical, imaging, or specialty material projects.
Teams aiming for greater efficiency in research and scale-up projects can evaluate partnership with established suppliers. Look for vendors known for transparent documentation, proven logistics, and routine third-party testing. For lab managers, keeping on top of internal training around safe handling and waste management goes a long way in sustaining adoption over time. Regularly checking inventory, rotating stock, and tracking batch histories prevent most supply chain headaches.
Process engineers and technical directors should work closely with quality assurance units to validate supplier certifications and implement clear change notification pathways. Early-stage risk management—looking at both upstream and downstream vulnerabilities—sets the stage for smoother production runs and less downtime across the plant.
Looking across the many sectors that rely on pyridine derivatives, this compound delivers a blend of reactivity and reliability seldom matched elsewhere. From my vantage point working with early-career chemists, process engineers, and supply chain managers, its unique substitution pattern continues to deliver cost and time savings across research and industry settings. By focusing on well-understood, high-purity building blocks, organizations don’t just make chemistry easier—they free up resources for more important scientific discovery, application development, and innovation.