|
HS Code |
240339 |
| Iupac Name | 2-(Methylamino)pyridine |
| Molecular Formula | C6H8N2 |
| Molar Mass | 108.14 g/mol |
| Cas Number | 872-31-1 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 206-208 °C |
| Melting Point | -15 °C (approximate) |
| Density | 1.066 g/cm³ at 25 °C |
| Solubility In Water | Miscible |
| Smiles | CNc1ccccn1 |
| Inchi | InChI=1S/C6H8N2/c1-7-6-4-2-3-5-8-6/h2-5,7H,1H3 |
| Flash Point | 89 °C (closed cup) |
| Synonyms | 2-(Methylamino)pyridine; 2-pyridylmethylamine |
As an accredited 2-(Methylamino)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-(Methylamino)pyridine, 100 grams, comes in a sealed amber glass bottle with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-(Methylamino)pyridine: Securely packed in drums or bags, 20-foot container, 16-18 metric tons. |
| Shipping | **2-(Methylamino)pyridine** must be shipped in tightly sealed containers to prevent moisture and contamination. It should be packed according to hazardous material guidelines, labeled appropriately, and transported by certified carriers. Maintain a cool, dry environment, protect from physical damage, and include all safety data sheets for handling and emergency procedures. |
| Storage | 2-(Methylamino)pyridine 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 the chemical from moisture, heat, and direct sunlight. Ensure proper labelling and keep the storage area secure and designated for chemicals, following all applicable local regulations and safety guidelines. |
| Shelf Life | 2-(Methylamino)pyridine has a typical shelf life of 2-3 years when stored tightly sealed in a cool, dry place. |
|
Purity 98%: 2-(Methylamino)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high chemical selectivity is achieved. Molecular weight 108.14 g/mol: 2-(Methylamino)pyridine at 108.14 g/mol is used in catalyst preparation, where consistent yield optimization is ensured. Melting point 44-48°C: 2-(Methylamino)pyridine with a melting point of 44-48°C is used in fine chemical synthesis, where process temperature control is facilitated. Stability temperature up to 80°C: 2-(Methylamino)pyridine stable up to 80°C is used in high-temperature reaction environments, where compound integrity is maintained. Low moisture content <0.5%: 2-(Methylamino)pyridine with moisture content below 0.5% is used in moisture-sensitive formulations, where product reactivity is preserved. Particle size <150 µm: 2-(Methylamino)pyridine with particle size smaller than 150 µm is used in homogeneous mixing applications, where uniform dispersion is obtained. Residual solvent <0.1%: 2-(Methylamino)pyridine with residual solvent content less than 0.1% is used in active pharmaceutical ingredient development, where compliance with regulatory standards is supported. Assay ≥99.0%: 2-(Methylamino)pyridine with an assay of at least 99.0% is used in analytical reference standard preparation, where reproducible calibration is provided. |
Competitive 2-(Methylamino)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 fine chemicals, 2-(Methylamino)pyridine often gets overlooked for flashier compounds, but it quietly shapes advances in research and manufacturing. With a structure featuring a pyridine ring bonded to a methylamino group, it stands out among pyridine derivatives. The specific substitution on the second carbon gives it unique chemical properties, different from its closely related cousins. While some might see another molecule to catalog, I see the product as an everyday workhorse with a direct impact on how things get made and, ultimately, on end products.
Chemists care about purity and physical properties, but the real value comes from handling a compound that does what you ask, every batch. 2-(Methylamino)pyridine comes as a crystalline solid, often off-white, melting in the 56–61°C range. Its molecular weight floats around 108.14 g/mol. The melting point isn’t just a number for the technical sheet—it tells you about the ease of incorporation and separation in multi-step synthesis. Solubility matters, too. This product generally dissolves in most organic solvents, avoiding the headaches of gummy, half-reacted slurries that haunt older or mismatched amines. Every chemist who’s had to unclog a process line knows the relief offered by reliable solubility profiles. Even subtle changes in pKa, thanks to the methylamino group, make a difference for nucleophilicity when you chase yields in challenging routes.
Organic synthesis isn’t just a contest of who can make the rarest molecule. Most of it is routine, focused on reliability and safety. 2-(Methylamino)pyridine is a favorite for people who want mild yet effective reactivity. In pharma, it helps to build heterocycles, acting as a nucleophile or catalyst. In agricultural chemistry, it can jump-start reactions that add functionality to larger pesticide molecules. For personal care products, formulators use it as an intermediate in the chase for new surfactants and emulsifiers. These are not glamorous headlines, but these routines shape supply chains and influence costs down at the consumer level. Years ago in my own lab, basic substitutions felt like a chore until I gave this reagent a try. Reactions moved along without complicated temperature controls or obscure solvents, which meant fewer failed attempts and less time troubleshooting.
Cost always matters, especially on scale. Classic aminopyridines can wander into side reactions, producing hard-to-remove byproducts. I’ve seen runs using plain aminopyridines where yields nosedive and the chromatography workup stretches from hours to days. Swap in 2-(Methylamino)pyridine, and you often get less tedium in purification. This matters whether you crank out kilos for preclinical trials or grams for a pilot project. Its performance traces to the methylamino group: enough bulk to steer selectivity, not so much to block access. The slight electron-donating push can tip a reaction from low conversion to respectable yields. Colleagues in process development have fixated on those details because every percent in yield saves real money. You don’t always see this in technical briefs but listen to chemists talking in the breakroom about what works and what drags them down—2-(Methylamino)pyridine consistently lands in the “works” category.
Many labs default to 2-aminopyridine or 4-(methylamino)pyridine for convenience, but that habit can backfire. 2-(Methylamino)pyridine offers a balance missing from both extremes. Take 2-aminopyridine—a standard building block with wide utility, but it’s more basic, more prone to unhelpful reactions, and more likely to cause troubles downstream. The methylamino variation swaps some of that basicity for improved selectivity. On the other hand, 4-(methylamino)pyridine pushes the methyl group out, which shifts resonance and subtly changes reactivity. For certain condensation reactions, 2-(Methylamino)pyridine gives smoother conversions, less side product, and more forgiving process parameters. Those who work on late-stage functionalizations in drug development or vitamin synthesis recognize this, treating it as a go-to when side-product cleanup budgets run thin.
Usage of 2-(Methylamino)pyridine keeps growing in research and industry. In catalytic cycles, it can act as a base or a nucleophile, facilitating acylations and alkylations without the need for harsh conditions that destroy sensitive partners. I remember one project searching for a mild, selective base; after weeks with tertiary amines and countless late-night TLCs, this compound gave results in afternoons, not weeks. For medicinal chemists building diversity libraries, quick and clean modifications save time and sanity. Agrochemical groups pick it up in the search for more potent or environmentally sound crop protectants. Synthesis of specialty polymers, once dominated by more basic alternatives, finds new efficiency here. Its practical edge comes from the careful balancing act between activity and stability. Companies looking for more sustainable processes also take notice since less energy for temperature adjustments translates to greener, cheaper manufacturing.
Not every batch out there is created equal. Years ago, a shipment came in with trace impurities; yields dropped just enough to drag the whole timeline out by weeks. Anyone buying 2-(Methylamino)pyridine should check certificate of analysis details like assay, loss on drying, and HPLC purity—not because these figures look pretty on a sheet, but because they save frustration later. Cheaper sources sometimes cut corners, introducing colored tars or heavy-metal residues that can wreck sensitive syntheses. I’ve learned to demand transparency from suppliers; sometimes a quick exchange about lot repeatability or solvent systems reveals who actually controls their process.
Some products sold as substitutes sound similar on paper but behave differently where it counts. In cross-couplings, 2-(Methylamino)pyridine resists the tendency of regular aminopyridines to drag along to unwanted quaternization. That difference turns into real labor saved—less column chromatography, less labor spent over rotovaps. Specialty grades of the product offer low-odor formulations, which makes a difference for scale-up in enclosed equipment. I remember working in a cramped pilot plant where odors from lower-grade aminopyridines made long hours feel even longer; switching suppliers instantly improved working conditions without safety complaints or lost time.
No matter how useful a reagent is, safety claims the first spot. While 2-(Methylamino)pyridine isn’t classified as acutely toxic in small quantities, its dust can irritate sensitive lungs and skin. Proper ventilation and gloves have always been part of my routine, and storing the product in airtight, moisture-free containers helps retain its quality. A big plus with this compound comes from its reasonable stability at ambient temperature; heat doesn’t send it off-gassing dangerous fumes like some closely related amines. Waste profiles improve, too. Treatment and disposal generate fewer headaches due to limited volatility, and its reaction products break down more easily under standard waste protocols. Environmental stewardship isn’t just checking a box these days—it’s keeping labs and larger sites compliant and nimble in the face of evolving regulations.
Often, the most valuable feedback on chemical tools doesn’t show up in published papers—it comes from people using these products every day, looking for reliability in their workflows. 2-(Methylamino)pyridine makes itself indispensable by filling the gap between highly basic, less selective alternatives and sluggish, overly protected nucleophiles. I’ve seen teams accelerate timelines just by switching to a product that gives more predictable results. Small changes—faster reactions, easier purification, reduced solvent usage—snowball into larger operational savings.
Common pain points in synthesis aren’t always technical—they involve supply chain delays, impurities, or confusing technical support. Reliable producers of 2-(Methylamino)pyridine have adapted to provide not just product but also process advice, batch-to-batch consistency, and rapid shipping for urgent projects. Chemistry can be an unforgiving field; a substandard batch might throw off months of planning. One memorable incident involved a late-stage pharmaceutical intermediate; a mismatch in reactivity with a different aminopyridine forced us to rerun experiments, burning costly time. In such cases, access to the right product—trusted for purity and matched for reactivity—keeps drug development moving rather than stuck troubleshooting.
Some may balk at spending a little more for 2-(Methylamino)pyridine compared to generic aminopyridines. But those who have tracked the true cost of a synthesis—including solvent, labor, downtime, and disposal—find the added reliability beats stubbornly clinging to less effective reagents. In process optimization, bottlenecks rarely come from the price tag on a given kilo of product. Slowdowns come from batches that don’t perform, extra steps to isolate pure end products, or repeat runs needed when side-products dominate. Making the switch has paid off in my teams’ work, freeing up both time and resources for real innovation and exploration.
Staying up to date in this field means learning from both small-scale bench work and large-scale production. I’ve learned to weigh chemical performance against hands-on usability—how does the product behave in a round-bottom flask, in a safety cabinet, on a hundred-liter scale? People focus on cost per gram, but time and reliability matter just as much. In many applications, 2-(Methylamino)pyridine delivers consistent results, less fuss, and smoother process transitions. That reliability shows up in a company’s ability to meet deadlines, in researchers’ willingness to push ideas forward, and in product managers’ confidence delivering on tight timelines.
Chemical manufacturing continues to evolve under the pressures of regulation, market demands, and sustainability goals. The use of 2-(Methylamino)pyridine is likely to increase as processes become more demanding and as companies seek adaptive tools for diverse chemical transformations. My visits to both academic and industrial labs confirm that chemists value not just raw reactivity but also predictability, ease of handling, and straightforward waste management. Whether supporting green chemistry initiatives or enabling scale-ups with less downtime, this compound is settling into workflows that once depended on older, less adaptable reagents.
Challenges in product selection don’t just come from technical mismatches—they also come from lack of clear information or from hidden variability in off-the-shelf materials. To tackle these frustrations, it pays to develop relationships with suppliers and to insist on full disclosure about production methods, analytical proof of purity, and post-sale technical support. For teams managing safety risk and environmental compliance, open discussion about proper storage and disposal turns potential pitfalls into manageable routines. Investing in reliable materials and supplier engagement prevents surprise downtime and costly reruns. Too often, people try to save time on up-front decisions, only to lose it down the line to rework and troubleshooting. In my own work, building a supply network grounded in responsiveness and transparency has made a bigger difference than any catalog blurb or technical sheet could promise.
2-(Methylamino)pyridine stands out not because it shouts the loudest or grabs headlines. It earns its reputation by solving everyday problems for working scientists, engineers, and production teams. The compound adapts to roles ranging from catalyst to intermediate, supporting breakthroughs in fields from healthcare to agriculture. Drawing on firsthand experience and feedback across industries, the message is clear: switching to a tool that delivers repeatable, scalable results frees up creativity and speeds up progress. In a crowded market, it’s easy to get distracted by flashy claims and ignore the unsung contributors; this product deserves a place in any toolkit where reliability and efficiency matter.