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HS Code |
643634 |
| Chemical Name | 2,3-Dimethoxypyridine |
| Cas Number | 12800-19-0 |
| Molecular Formula | C7H9NO2 |
| Molecular Weight | 139.15 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 210-212 °C |
| Melting Point | -20 °C (approximate) |
| Density | 1.091 g/cm3 |
| Refractive Index | 1.511 |
| Solubility In Water | Slightly soluble |
| Flash Point | 101 °C |
| Smiles | COC1=NC=CC(=C1)OC |
| Iupac Name | 2,3-dimethoxypyridine |
As an accredited 2,3-Dimethoxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle with a screw cap, labeled "2,3-Dimethoxypyridine," features hazard symbols and product information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2,3-Dimethoxypyridine: 12 metric tons (drums on pallets), safely packed for secure international shipment. |
| Shipping | 2,3-Dimethoxypyridine is shipped in tightly sealed containers under ambient conditions. It is typically packed in glass or HDPE bottles, protected against moisture and direct sunlight. Proper labeling, including hazard information, accompanies the shipment. Standard chemical transport precautions and relevant regulatory guidelines for non-hazardous organic compounds are observed during shipping. |
| Storage | 2,3-Dimethoxypyridine should be stored in a tightly sealed container, away from moisture, heat, and sources of ignition. Keep it in a cool, dry, well-ventilated area and protect it from direct sunlight. Store separately from incompatible substances such as strong oxidizers and acids. Properly label the container and follow all relevant safety guidelines for chemical storage. |
| Shelf Life | 2,3-Dimethoxypyridine has a shelf life of at least 2 years when stored tightly sealed, cool, dry, and protected from light. |
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Purity 99%: 2,3-Dimethoxypyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and product consistency. Molecular Weight 139.15 g/mol: 2,3-Dimethoxypyridine with a molecular weight of 139.15 g/mol is used in heterocyclic compound development, where it facilitates precise stoichiometric calculations. Stability Temperature 120°C: 2,3-Dimethoxypyridine with stability temperature of 120°C is used in high-temperature organic reactions, where it maintains molecular integrity. Melting Point 48-51°C: 2,3-Dimethoxypyridine with a melting point of 48-51°C is used in controlled crystallization processes, where it enables reproducible solid-state properties. Particle Size <50 µm: 2,3-Dimethoxypyridine with particle size less than 50 µm is used in formulation of fine chemical blends, where it improves homogeneity and dispersion. Water Content <0.5%: 2,3-Dimethoxypyridine with water content below 0.5% is used in moisture-sensitive syntheses, where it minimizes hydrolysis risk and enhances product stability. |
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In laboratories where the margin for error is slim and expectations run high, reliable tools and quality materials make all the difference. More people recognize that subtle choices in raw materials shape scientific progress. 2,3-Dimethoxypyridine stands as a chemistry workhorse, not because it trends on sales charts, but because it does a quiet job well and fills an important space on the shelf. For those who spend long hours exploring heterocyclic chemistry, this compound draws attention with its performance and flexibility.
Anyone who has handled nitrogen-containing aromatic compounds knows their role stretches far. 2,3-Dimethoxypyridine usually turns up as a free-flowing solid. With a defined structure—methoxy groups at positions two and three on the pyridine ring—it lends itself to specialized reactions. Many chemists value this placement, as these methoxy groups protect against unwanted side reactions and promote reactivity where needed.
Most commercially available 2,3-Dimethoxypyridine offers high purity, supporting both research and process applications. Color remains a simple but telling indicator—good batches typically show a faint yellow hue, signaling purity without the fuss. In terms of stability, this compound does well in standard laboratory storage conditions, holding up under moderate temperatures without requiring elaborate care routines. Its molecular weight and formula match expectations for derivatives in its class.
Daily use builds a kind of trust in a reagent, the kind that comes only after seeing a product perform repeatedly in sensitive syntheses. One feature standing out with 2,3-Dimethoxypyridine is the reproducibility it delivers. I remember running Pd-catalyzed cross-coupling reactions, where uncertainty over starting materials brought unnecessary stress. Swapping out lower grade pyridines for a pure sample of 2,3-Dimethoxypyridine improved yields, especially in Suzuki-Miyaura couplings involving complex boronates. This speaks not only to the compound’s compatibility with modern catalysts, but also to its clean reaction profile—a concern for anyone chasing the last few percent in product yield.
Handling also sets this compound apart. No unusual odors linger once opened, and if you’re weighing out small quantities, the powder doesn’t clump up in humid weather. In a busy lab, ease of pouring and accurate measuring cut down on small annoyances that add up over the course of a long week.
Medicinal chemistry tends to grab headlines, but the story of 2,3-Dimethoxypyridine stretches further. Pharmaceutical researchers use it for building complex scaffolds in drug development, synthesizing key intermediates that carry methoxy substitutions onto future active molecules. Its role doesn’t end there. Agrochemical producers incorporate it when designing new candidates in crop science. Beyond bench-scale discovery, this pyridine derivative finds its place in pilot projects for specialty chemicals—demonstrating a relevance that extends from molecule design to intermediate manufacture.
During synthesis, the methoxy group arrangement opens doors for selective transformations. This is crucial for teams designing next-generation ligands or heterocycle-based frameworks. Some teams rely on its ability to activate specific ring positions while protecting others—something not every substituted pyridine achieves so cleanly. Several published syntheses showcase it as a building block for anti-infective agents, further cementing its reputation among those who follow trends in chemical biology.
With the sheer number of pyridine derivatives on the market, picking the right one depends on experience and understanding. I recall a few projects where the choice boiled down to 2,3-Dimethoxypyridine versus cousins like its 2,4- or 3,5-substituted relatives. The differences might sound subtle, but reaction leads often hinge on reactivity and selectivity—two qualities strongly influenced by substitution pattern.
In direct cross-coupling, the 2,3-variant often helps avert unwanted rearrangement or over-reaction seen with other isomers. Compared to unsubstituted pyridine, this compound blocks certain side pathways, ensuring a cleaner, more reliable synthesis. When compared to 2,6- or 3,5-dimethoxypyridine, the 2,3-pattern emerges as a better fit for reactions that want both electron-donating effects and precise positional activation. This means less troubleshooting on purification steps and more focus on innovation.
Chemists often overlook environmental considerations until facing regulations or budget reviews. I grew to appreciate starting materials that reduce the need for rework and minimize side waste streams. 2,3-Dimethoxypyridine helps in this respect. High performance and purity lower the need for repeated runs, translating to less energy and solvent waste. For teams tasked with greener chemistry initiatives, every reliable product means a real reduction in environmental footprint.
A few years back, I worked on a process optimization project aiming to streamline an aromatic amination step. Switching to this dimethoxy-pyridine dropped solvent use by nearly twenty percent, because cleaner starting material minimized purification overhead. That sort of result opens up possibilities—not just for private labs, but for organizations working towards compliance with industry-wide environmental guidelines.
People in procurement look beyond purity, focusing on long-term availability and cost stability. In recent years, specialty pyridines sometimes caused unpredictability in project budgets. 2,3-Dimethoxypyridine, though it remains a niche product, benefits from improved synthetic routes that keep supply steady. Scale-up from gram to multi-kilogram batches seldom brings hiccups, mainly because the starting raw materials for this compound show good availability. This lowers stress for managers concerned about project delays or spiraling costs.
Developers working in custom synthesis also appreciate price transparency. The absence of supply bottlenecks, as expected with more exotics, lets labs plan multiple months ahead. For graduate students and principal investigators alike, this means project timelines stay reliable and proposals don’t stall due to unexpected shortages. In a small way, that predictability takes a load off everyone’s mind.
Most routine chemicals deserve respect and careful use—2,3-Dimethoxypyridine proves to be no exception. In practice, seasoned chemists favor compounds that align with common lab safety protocols and don’t call for extra personal protective equipment beyond gloves and goggles. During years spent in shared workspaces, I rarely saw incident reports linked to this compound. Properly stored, it doesn’t degrade quickly or release hazardous volatiles under normal conditions. For learners just starting out, having a material that doesn’t challenge familiar handling routines matters more than marketing claims or bold hazard statements.
From a waste management perspective, used purification media and solutions containing this pyridine can enter standard organic waste streams, provided labs operate under standard international regulations. This removes headaches for safety officers and keeps workflow predictable. For anyone evaluating a chemical for both experimental utility and risk, this balance tends to tip the scales in its favor.
Years ago, some labs faced uneven quality across pyridine derivatives. Today, demands from regulatory audits and end users push for tighter specifications. Producers now provide 2,3-Dimethoxypyridine with certificates of analysis covering everything from assay percentage to trace impurity levels. This shift lets purchasing agents and researchers trust that each bottle performs like the last. Batch-to-batch uniformity means fewer surprises, faster troubleshooting, and easier fulfillment of good manufacturing practice requirements.
Researchers working on clinical-stage synthesis value this consistency. Strict purity benchmarks now directly influence regulatory submissions. In one project, our team documented this compound’s impurity profile as part of a file for a potential therapeutic. This transparency supported our application and proved to reviewers that we understood every step of our process, from bench scale to kilogram campaigns.
Broad relevance sets some chemicals apart from others that might appear functionally similar. 2,3-Dimethoxypyridine turns up anywhere from advanced materials science to teaching laboratories. Synthetic chemists use it as a shortcut for varied substitution patterns on the pyridine ring, leading to innovative research on new catalysts. Teams working on organic electronics appreciate its utility while assembling heteroaromatic backbones for high-performance materials. Even those developing sensors draw on its core structure.
Biotech companies exploring enzyme inhibition benefit from the methoxy group’s electron-donating qualities, influencing the binding characteristics of final compounds. It might not carry the name recognition of other building blocks, but anyone aiming to break new ground finds it worth including in the toolbox. Drawing from my own stint in academic research, I recall how quickly screen results could improve after introducing this compound into candidate libraries. Each small improvement built momentum for the next step in discovery.
Every useful reagent shows limits. For this compound, solubility in some non-polar solvents doesn’t match everyone’s requirements. Paradoxically, this serves as a built-in safety net for labs looking to control volatile emissions, but those running reactions under strictly anhydrous or harshly basic conditions should check compatibility in advance. Working around these limits, researchers adjust solvent mixtures and reaction conditions, proving flexibility trumps raw performance in many cases.
Alternative approaches to storage or packaging offer another area for improvement. With the surge in online procurement, some users notice variation in container types, from screw-top jars to sealed ampoules. Each has pros and cons. Air- and moisture-sensitive applications benefit from sealed packaging, while everyday preparation moves quicker with easy-access containers. Feedback from the field encourages suppliers to strike a balance, reducing both costs and delays from broken packages or missed shipments.
Trust grows slowly, experiment by experiment. Reliable batches of 2,3-Dimethoxypyridine keep projects on track through all stages of product development. I’ve seen teams regain lost time after switching to a better supply, with the results spreading from one department to the next as word got out. It comes down to consistency—erratic results threaten research timelines and discourage younger chemists. With a dependable product, teams shift focus back to design and hypothesis testing, instead of chasing down mysterious side reactions or failed runs.
Those of us who’ve trained new scientists know the value of products that do their job without fuss. Small improvements to workflow—shorter weighing times, quicker dissolving, easier filtration—translate to real savings and higher morale. In pharmaceutical innovation and basic research alike, these benefits move work ahead measurably.
Making smart choices about chemical sourcing reflects a growing sense of responsibility for both science and the wider world. Companies supplying 2,3-Dimethoxypyridine face increased pressure to document sourcing, production standards, and labor practices. Many researchers now seek transparency not only for regulatory compliance, but also to meet internal ethical commitments. The market has shifted—labs notice when suppliers commit to sustainable, responsible practices.
Those managing lab budgets combine price, reliability, and ethics into purchasing decisions. Open discussion about production practices inspires trust and supports a healthier scientific ecosystem. When choosing between functionally similar products, a record of ethical sourcing often closes the deal.
Chemistry keeps advancing, sometimes in small steps, sometimes by leaps. 2,3-Dimethoxypyridine’s role remains secure, thanks to its balance of reactivity, reliability, and broad utility. Research into synthetic methods, catalytic cycles, and structure-activity relationships continues to unlock new applications. As fields like medicinal chemistry demand more complex scaffolds and as green chemistry initiatives push for cleaner processes, this compound stands ready for evolving challenges.
Ongoing collaboration between chemists, procurement specialists, and suppliers ensures that future batches meet not just current, but also emerging demands. It takes feedback from the lab bench and the boardroom to keep refining both the compound and its role in discovery and production. Looking ahead, greater integration with digital inventory systems and direct feedback on product performance may refine shipping, storage, and application even further.
After years spent working with a wide palette of reagents, I’ve seen how often progress comes from familiar, trusted tools. 2,3-Dimethoxypyridine fits this pattern. Reliable, versatile, and responsive to the real needs of practicing chemists, it deserves its spot in the limelight. Finding quality starting materials shortens the distance to the finish line—every researcher, from graduate student to industrial project lead, benefits from products that work as expected and support innovation instead of slowing it. Spending less time troubleshooting and more time building new science makes all the difference, and this compound plays its part quietly, but effectively, day in and day out.