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HS Code |
950006 |
| Chemical Name | N-Methyl-2-pyridineethanamine |
| Molecular Formula | C8H12N2 |
| Molar Mass | 136.19 g/mol |
| Cas Number | 42142-52-9 |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 230-232 °C |
| Density | 0.995 g/mL at 25 °C |
| Solubility | Soluble in water and common organic solvents |
| Smiles | CNCCc1ccccn1 |
| Inchi | InChI=1S/C8H12N2/c1-9-6-7-8-4-2-3-5-10-8/h2-5,9H,6-7H2,1H3 |
| Pka | Approx. 9.6 (for the amine group) |
| Storage Temperature | Store at 2-8 °C |
As an accredited N-Methyl-2-pyridineethanamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of N-Methyl-2-pyridineethanamine supplied in a tightly sealed amber glass bottle with a tamper-proof cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Typically 80–100 drums, each 200 kg, secured and palletized, total net weight 16–20 metric tons. |
| Shipping | N-Methyl-2-pyridineethanamine should be shipped in tightly sealed containers, protected from light and moisture. It must be packaged according to regulations for hazardous chemicals, with proper labeling and documentation. During transport, temperature should be controlled as recommended in the safety data sheet (SDS), and spill response materials should be available. |
| Storage | N-Methyl-2-pyridineethanamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from heat, moisture, and direct sunlight. Use proper chemical storage cabinet if possible. Clearly label containers, and follow all standard laboratory chemical storage protocols to ensure safety and prevent contamination. |
| Shelf Life | N-Methyl-2-pyridineethanamine typically has a shelf life of 2 years when stored in a cool, dry, and tightly sealed container. |
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Purity 99%: N-Methyl-2-pyridineethanamine with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal impurity formation. Melting Point 56°C: N-Methyl-2-pyridineethanamine with a melting point of 56°C is used in fine chemical manufacturing, where it enables precise crystallization and easy purification. Molecular Weight 136.20 g/mol: N-Methyl-2-pyridineethanamine at a molecular weight of 136.20 g/mol is used in analytical reagent preparation, where it provides accurate quantitative measurements. Stability Temperature up to 80°C: N-Methyl-2-pyridineethanamine with stability up to 80°C is used in high-temperature organic reactions, where it maintains chemical integrity and consistent performance. Viscosity 1.05 cP: N-Methyl-2-pyridineethanamine at a viscosity of 1.05 cP is used in automated dosing systems, where it allows for precise liquid handling and reproducible process control. Water Content <0.2%: N-Methyl-2-pyridineethanamine with water content below 0.2% is used in moisture-sensitive synthesis, where it prevents hydrolysis and ensures product stability. Boiling Point 208°C: N-Methyl-2-pyridineethanamine with a boiling point of 208°C is used in solvent extraction methods, where it provides efficient separation and minimal loss due to evaporation. Shelf Life 24 months: N-Methyl-2-pyridineethanamine with a shelf life of 24 months is used in bulk chemical storage, where it guarantees long-term usability and reduces inventory turnover. |
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In research labs and advanced manufacturing, there aren’t many compounds that catch as much attention as N-Methyl-2-pyridineethanamine. So many of the conversations I’ve had with colleagues eventually circle back to this molecule due to its flexible structure and reliable behavior in synthesis. From what I’ve seen, its main draw lies not only in its reactivity but in how it navigates specific reactions that stymie simpler amines. Pure, clear to pale yellow, and carrying a molecular formula of C8H12N2, this amine stands out for chemists seeking both stability and unique reactivity.
Most of us working with this compound appreciate the confidence it brings to sensitive batch runs and pilot projects. Its molecular weight sits at 136.19 g/mol, and what grabs me most is the way its structure enables streamlined alkylation and acylation steps. Peers often highlight how that methyl group tweaks electron density enough to open up new possible functionalizations that older pyridine analogs just couldn’t offer.
I remember the first time I handled N-Methyl-2-pyridineethanamine in an industrial pilot line. Its purity allowed me to get accurate, predictable yields during each run—no odd peaks when scanned by NMR or GC. Consistency like that matters when you’re scaling from milligrams to kilos. In the fast-moving pharmaceutical world, small unpredictable behaviors can mean delays or scrapped lots. Here, that sort of peace of mind transforms productivity.
Chemical manufacturers with years of experience often reach for this compound when building more complex scaffoldings for drug candidates. Its structure suits various customizations, from basic salt formation to preparation of intermediate building blocks. Many have found that it plays well with both strong and mild reagents, which keeps reaction times short and waste generation minimal. You won’t find yourself wrestling with byproducts or hunting down obscure purification strategies.
A lot of the chemistry literature describes N-Methyl-2-pyridineethanamine as a starting material for preparing diverse functional groups. The truth is I’ve watched whole teams switch from classic 2-pyridylethanamines, puzzled by inconsistencies, to this methylated version and finally breathe easier. The methyl group on the nitrogen atom nudges the molecule’s reactivity in ways that favor site-selective modifications. This detail lets researchers plan transformations for libraries of products without constantly recalculating reaction conditions.
Where 2-pyridineethanamine sometimes brought up difficulties in amide coupling or reductive amination due to over-alkylation, this methylated form limits extraneous side reactions. That factor matters for researchers needing high selectivity to push drug discovery forward. In addition, the methylation offers a subtle but welcome boost in basicity, helping the compound perform well under both neutral and mildly acidic conditions. That flexibility keeps your workflow smooth if small shifts in pH happen during processing.
A lot of folks entering the chemical industry are eager to minimize the number of reagents on their shelves. At first, it seems sensible to just buy one simple amine and stretch it for every use. The trouble is, generic ethylamines often show up short either in stability or versatility. N-Methyl-2-pyridineethanamine stands apart due the way it balances nucleophilicity and steric accessibility. From what I’ve seen, when you match it against an unmethylated version for a cyclization or a ring-opening sequence, yields spike and purifications get easier.
While some other functionalized amines show stubborn volatility or degrade during storage, this compound keeps its integrity for far longer under standard lab conditions. Trade journals have reported that, for multi-step syntheses, researchers revisit their blueprints to swap out traditional alkylamines for N-Methyl-2-pyridineethanamine to reduce unwanted polymerization steps. Teams outputting new agrochemicals, advanced dyes, and even specialty battery additives all report higher throughput after switching.
Big breakthroughs in modern pharmaceuticals don’t just come from blockbuster drugs. It’s easy to forget that often success rides on a reliable intermediate making the rest of synthesis viable, fast, and cost-effective. N-Methyl-2-pyridineethanamine powers this behind-the-scenes progress. In small molecule synthesis, it helps introduce methyl groups with predictable site selectivity, making it possible to build out diverse candidate series. That trait matters when companies race to develop and patent new lead compounds.
Many material science programs have adopted this molecule for the tailored ligand design that supports innovative catalysts, metal-organic frameworks, or even optoelectronic components. By bringing both nucleophilic amine and electron-rich pyridine characters together in compact form, N-Methyl-2-pyridineethanamine unlocks complexity in fewer synthetic steps than bulkier or less-reactive analogs.
There are secondary benefits you don’t always notice until months after switching to a compound like this one. I’ve rotated between big research institutions and smaller contract labs, and a recurring theme is the stress around storage, stability losses, and disposal. Some amines pick up moisture quickly or need refrigeration. With this methylated amine, most everyday lab storage suffices: standard ventilated shelving in a dry place, away from strong acids or oxidizers. Labs have reported reduced lost inventory from spoilage, with containers often remaining usable well past initial purchase.
Waste streams shrink, too, since fewer purification passes mean less solvent consumption. I’ve appreciated how less time spent recoiling from stubborn, decomposing amines lets me concentrate on core synthesis. Spills and off-gassing risks stay low due to its manageable volatility and well-documented hazards—no guessing needed.
Fast-moving companies developing new flavors, fragrances, or specialty chemicals don’t get second chances to deliver consistent product. My time supporting custom synthesis taught me that N-Methyl-2-pyridineethanamine responds predictably to scaling, even outside of pharmaceutical settings. The consistency in both small-batch and larger pilot plant operations means repeating an order a year later brings the same results.
Technicians and process chemists report easier time with analytical tracking. Clear, well-separated NMR and GC signals translate into precise quantification—no vague peaks or interference from closely related impurities. That clarity saves hours of repeat runs and insulates teams from ambiguous regulatory findings down the line.
Trust in a specialty chemical boils down to having real-world data to back up every claim. The run-of-the-mill compounds on the market may come with sparse analytical support, but high-quality suppliers make sure documentation for N-Methyl-2-pyridineethanamine is comprehensive. Users can reference detailed spectral data and chromatographic purity records without combing through gray literature.
Health and safety professionals have established straightforward procedures for handling, inhalation, and spill response. Labs appreciate clear hazard identification with matching pictograms and phrase standards, which streamlines training for interns and new hires. I’ve seen that, with this compound, onboarding documentation comes together in less than a morning. The value in a product with low ambiguity and ample third-party documentation can’t be overstated when compliance deadlines loom.
Over the last few years, research into energetic materials, advanced polymerization, and even directed enzyme evolution has drawn on building blocks once considered niche. N-Methyl-2-pyridineethanamine finds its way into protocols as a flexible linker or as a secondary amine reactant. The chemical’s unique scaffold, with methylation next to the pyridine ring, enables cross-coupling techniques that move beyond what standard amines allow.
One application that keeps cropping up is in green chemistry initiatives, where anyone interested in safer, cleaner runs prizes amines that don’t throw off excess byproducts or demand hazardous purifications. Recent literature includes protocols where solvent reduction, minimized waste, and safer scale-up go hand-in-hand with this particular reagent. In that sense, the molecule supports research that doesn’t just target speed or cost, but genuine sustainability in large-scale manufacturing.
Maybe it’s tempting to judge laboratory chemicals on a spreadsheet of specs. That kind of approach doesn’t capture the full experience though. Having worked shoulder-to-shoulder with teams handling everything from combinatorial chemistry to petrochemical research, I’ve noticed the best tools in the lab build trust through reliability over thousands of runs. N-Methyl-2-pyridineethanamine wins favor in part because it behaves as expected—batch after batch, year after year.
Teams in different cities or research areas swap notes and find nearly identical outcomes, no matter the workflow or application. With other amines, I’ve fielded calls on late-night troubleshooting sessions, prodding at unexplained failures. With this molecule, those kinds of setbacks mostly just don’t happen. The value in reduced downtime, fewer failed assays, and reliable documentation stacks up. This is the kind of unseen advantage that lets teams advance discoveries quickly, without pausing on yet another investigation into some erratic impurity.
Pricing and supply chain issues hit everyone. I remember stretches where certain specialty reagents shot up in cost or vanished from usual suppliers. The widespread adoption of N-Methyl-2-pyridineethanamine brought more active manufacturing lines and steadier inventories than many alternatives. Since it plugs into various downstream applications—whether in pharmaceuticals, electronics, or agriculture—distributors have responded by expanding both on-hand stock and delivery options.
A reliable supply means fewer delays and better contract fulfillment. Over time, that stability translates into real dollars saved and fewer client complaints. Labs balancing budgets have been able to switch without retraining staff or rewriting SOPs. For large companies, switching out less robust amine reagents has gradually streamlined procurement and brought greater negotiating power with bulk suppliers.
New technologies often require new building blocks. I’ve been part of meetings with teams looking at everything from personalized therapeutics to conductive polymers, and the questions often come back to versatile, well-understood reagents. Here, the modest-sized N-Methyl-2-pyridineethanamine does a lot of heavy lifting. Medicinal chemists, for example, take advantage of its structure to install subtle modifications at a late synthesis stage, opening up families of analogs that would otherwise be much harder to access.
Teams in electrochemical and green energy research also favor this molecule for its clean breakdown profile and minimal off-target reactivity. Its role in ligand design for next-gen catalysts keeps growing, especially as the electronics industry demands smaller, more agile batches of custom intermediates. From my experience, integrating this compound into new reaction workflows sparks creative combinations that weren’t possible with stiffer alternatives.
Even a well-loved compound has room for progress. With the rise of greener chemistry, the next wave of innovation lies in designing scalable reactions that use less solvent and cut emissions. I’ve seen leading-edge groups turn toward solid-supported reagents, and there’s strong promise in adapting N-Methyl-2-pyridineethanamine to such systems. Adoption of continuous-flow synthesis, paired with in-line purification, can help cut down on waste and lower energy loads.
Sourcing raw materials ethically remains a big challenge for the chemical industry. One clear step is driving suppliers to offer fully traceable N-Methyl-2-pyridineethanamine, encouraging renewable feedstocks and transparent data for customers. With regulatory standards getting tougher worldwide, future-ready labs will benefit from documentation showing green production routes and safe, closed-loop recycling or disposal methods.
No one researcher or chemist holds all the answers, and some of the most interesting developments around N-Methyl-2-pyridineethanamine come from crowd-sourced knowledge. Forums and conference panels continue to fill up with notes from newcomers and old hands alike: best practices for integration into existing runs, ideas for improving yield, anecdotes on safe scaling. The general consensus puts this reagent near the top for reliability, versatility, and manageable hazards.
Looking ahead, I see even more groups sharing protocols, troubleshooting tips, and hard data on this compound’s performance in both legacy and emerging applications. That information stream lifts the field, letting labs avoid repeating old mistakes and opening space for new creative uses. Students today learn on better, safer, more reproducible workflows because those ahead of them have already ironed out many kinks with compounds like this one.
Not all the progress in science comes from flashy new inventions—reliable workhorses like N-Methyl-2-pyridineethanamine empower scientists to push the edges of what’s possible. In day-to-day practice, the small things add up: cleaner reactions, shorter purification times, and a familiar, easy-to-manage hazard profile. Taken together, these benefits ripple outward, saving hours, reducing costs, and building confidence in each round of research or production.
Once teams integrate this molecule into their workflows, they rarely go back. Its effect on the industry can be measured not only by how often it’s ordered but by the projects it quietly enables—new medicines, safer materials, and faster research delivered to the world. For those aiming to work smarter, safer, and faster, N-Methyl-2-pyridineethanamine continues to prove why it earns a place in labs wherever precision and performance matter most.