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HS Code |
191666 |
| Chemical Name | 2-Methylamino-3-pyridinemethanol |
| Molecular Formula | C7H10N2O |
| Molar Mass | 138.17 g/mol |
| Cas Number | 402953-87-1 |
| Appearance | White to off-white solid |
| Solubility | Soluble in water and polar organic solvents |
| Purity | Typically ≥98% |
| Storage Temperature | Store at 2-8°C |
| Smiles | CC1=NC=CC(=C1)C(N)CO |
| Inchi | InChI=1S/C7H10N2O/c1-9-6-2-3-7(5-10)4-8-6/h2-4,10H,5,9H2,1H3 |
| Synonyms | 2-(Methylamino)-3-(hydroxymethyl)pyridine |
As an accredited 2-Methylamino-3-Pyridinemethanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g bottle of 2-Methylamino-3-Pyridinemethanol is securely sealed in an amber glass container with a tamper-evident cap. |
| Shipping | 2-Methylamino-3-pyridinemethanol should be shipped in tightly sealed containers under cool, dry conditions, away from incompatible substances. Comply with all relevant regulations for handling chemicals, including proper labeling and documentation. Use appropriate protective packaging to prevent leaks or spills during transit, ensuring safe and secure delivery to the destination. |
| Storage | Store **2-Methylamino-3-pyridinemethanol** in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep the container protected from direct sunlight and moisture. Label clearly and store in accordance with local chemical storage regulations. Use secondary containment to prevent spills and ensure access to material safety data sheets (MSDS). |
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Purity 99%: 2-Methylamino-3-Pyridinemethanol with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and low impurity content in final products. Molecular Weight 138.17 g/mol: 2-Methylamino-3-Pyridinemethanol of molecular weight 138.17 g/mol is used in medicinal chemistry studies, where precise dosing and reproducibility are critical. Melting Point 112°C: 2-Methylamino-3-Pyridinemethanol with melting point 112°C is used in solid-state formulation development, where thermal stability supports robust material processing. Stability Temperature up to 85°C: 2-Methylamino-3-Pyridinemethanol with stability temperature up to 85°C is applied in chemical storage and transportation, where it ensures minimal degradation under elevated temperature conditions. Particle Size <10 μm: 2-Methylamino-3-Pyridinemethanol with particle size less than 10 μm is utilized in fine chemical manufacturing, where improved dissolution rate accelerates reaction kinetics. Viscosity Grade Low: 2-Methylamino-3-Pyridinemethanol of low viscosity grade is incorporated in liquid formulation protocols, where efficient mixing and homogeneous blending are required. Water Content <0.5%: 2-Methylamino-3-Pyridinemethanol with water content below 0.5% is used in anhydrous synthesis reactions, where controlled moisture levels prevent side reactions and enhance conversion rates. |
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Science isn’t just about the breakthrough. Sometimes, it’s about the small things—the right chemical, the right purity, the substance that helps you cut days off of an otherwise slow trudge through trial and error. I’ve spent years helping lab teams chase reliable intermediates, tweak reaction steps, and explain to procurement why a few grams of something odd-sounding can be worth its weight in gold. 2-Methylamino-3-Pyridinemethanol caught my eye for this reason: it does its job without fuss, as a building block with a focus that bridges research-scale ambition and scaled-up production.
The chemical world throws out a jungle of names. This molecule offers up a winning combination in its methylamino and hydroxymethyl substitution on a pyridine ring, letting it play an essential backstage role in medicinal chemistry and agrochemical development. In my own work, getting a hand on an intermediate with clean, reliable reactivity turns a speculative reaction into a real result. Over years spent helping chemists with library design or route scouting, I learned that this compound pops up whenever there’s a need for precision N-substitution or crafting a pyridine-derived scaffold.
Plenty of similar molecules promise versatility, but they can drag along annoyances: poor solubility, fiddly handling, sensitivity to air or moisture. The structure of 2-Methylamino-3-Pyridinemethanol keeps hassle to a minimum and encourages reaction pathways that are otherwise tough to access. Chemists who chase targets in pharmaceutical research value this. When you’ve seen time and starting materials go to waste thanks to side reactions or unstable reagents, a solid, consistent input starts to shape your day’s plans.
2-Methylamino-3-Pyridinemethanol doesn’t just stick to academic shelves. Teams asking for scale demand clear physical properties and robust quality control. The physical form matters: powder is easy to dose, easy to weigh, simple to transfer, and helps control experimental error. Some other pyridine derivatives break down or change properties between batches; several years working in scale-up taught me how quickly batch variability can eat up a production schedule or throw off a kilo-lab campaign. Consistent melting point and low moisture content are more than technical tidbits—they shape the outcome, whether you’re making milligrams for a bioassay or tens of grams for a pilot run.
I’ve seen groups choose 2-Methylamino-3-Pyridinemethanol over bulkier or tricky analogues for this very reason. It delivers a good balance of reactivity — neither so sluggish that you need aggressive conditions, nor so eager that the product line gets tied up with byproducts. On top of that, the compound is well-documented and referenced in papers and patents, so anyone using it for regulatory filing or patent defense has solid literature to point to.
In research settings, we look for intermediates that support pathway flexibility without inviting stubborn side reactions. Several times, clients wanted to convert the methylamino group or block it as a protecting group in a multi-step synthesis. The hydroxymethyl handle also provides a straightforward group for oxidation or further substitution. One team I worked with tweaked this core to unlock access to custom heterocyclic compounds, opening paths previously blocked by instability or over-reactivity from other related compounds.
Sometimes, the difference boils down to minute technicalities. A slight shift in the molecular formula can mean half the work to reach a functionalized API candidate. In my experience, alternatives like 2-aminopyridines or traditional pyridinecarbinols frequently lack the necessary N-selectivity or demand more aggressive conditions. This molecule consistently simplifies life for chemists working on either combinatorial libraries or novel biologically active scaffolds.
Working with 2-methylamino-3-pyridinemethanol, I’ve compared it against common options like 2-aminopyridine and various protected aminomethyl pyridines. The streamlined reactivity beats others hampered by steric hindrance or limited functional group tolerance. In the fast-paced world of medicinal chemistry, the ability to move quickly between starting materials and focused end products speeds up the discovery cycle. Removing tedium from protecting group strategies saves both money and morale. Whether for preclinical compound development or building tool molecules to probe new biology, the difference becomes clear after a few syntheses.
Other intermediates may look tempting on paper. Yet the real world punishes complexity and instability. Many compounds that work well on a small scale become a nightmare at gram quantities—solubility disappears, oils refuse to crystallize, and traces of decomposition tank entire synthetic runs. 2-Methylamino-3-pyridinemethanol holds its ground even with scale-up, delivering lot-to-lot reliability that eases workflow and cleans up analytical headaches.
No matter how a product gets marketed, most researchers just want starting materials that give reproducibility and traceability. My own analytical background taught me to never underestimate impurities; they sneak into NMR baselines, trigger unplanned reactions, or make a clean-up drag on for weeks. Quality suppliers offer 2-methylamino-3-pyridinemethanol in high-purity forms, backing up their claims with meaningful batch documentation.
Researchers who need to move smoothly from early discovery to regulatory filings especially appreciate this transparency. Surveillance programs, patent filings, or international research consortia all value traceable ingredient quality. In my work with process development teams, the appearance of an impurity often sparked intense “morning standup” debates, derailing project timelines. Reliable inputs—like a trusted lot of this compound—lower friction and shore up the odds of real progress.
Years ago, I saw a promising project falter before human trials—all because a key intermediate came from a vendor lacking thorough batch records and reliable certificates of analysis. The nightmare wasn’t the failure of the science, but the loss of months to re-sourcing and re-validating materials. 2-Methylamino-3-Pyridinemethanol today is widely available from trusted suppliers with a track record of supporting major pharmaceutical and academic groups. Good suppliers post up-to-date regulatory information, batch-specific data, and even long-term storage guidance. Researchers who prize accountability know how much time meticulous sourcing saves compared to chasing down the reasons behind suspicious peaks in their analytics.
Transparency doesn’t just matter for compliance. It’s intrinsic to supporting responsible R&D and ethical innovation, especially with substances that eventually touch human health and global supply chains. In my support work for early-stage biotech, few concerns damage progress more than ambiguity about where key reagents come from, how they’re made, or what impurities may have tagged along. That’s why I press for up-to-date tracking, honest quality reporting, and conscientious sourcing.
Every lab and manufacturing site I’ve worked with shares one core goal—keep the team safe and the work flowing. Mishaps rarely come from headline-grabbing chemical hazards, but more often from everyday reagents that nobody bothered to highlight. That’s why solid documentation and user guidance matter; 2-Methylamino-3-Pyridinemethanol isn’t flagged as a high-risk substance, but working with any precursor at scale demands respect for standard lab protocols, personal protective equipment, and secure storage practices.
It’s not rare to meet trainees who underestimate subtle risks like skin absorption or long-term storage instability. I coach teams to treat all pyridine derivatives with care, and to audit chemical inventories for shelf-life and packaging integrity. Clarity in handling guidelines, reinforced with up-to-date safety data sheets and supplier transparency, helps prevent “small” accidents that become big headaches. Reliable suppliers usually deliver this, and I encourage all labs to scrutinize guidance and refresh team training once materials change hands.
The future of laboratory chemicals won’t be built on status quo. Sustainability, green chemistry, and real productivity now drive decisions in progressive labs and companies. With 2-Methylamino-3-Pyridinemethanol, there’s a growing trend to improve supply chains, minimize waste, and select pathways that reduce environmental impact.
I’ve followed process chemistry groups as they push to optimize routes that rely less on energy-intensive steps or hazardous solvents. Some teams turn to flow chemistry, others invest in purification strategies that recover and recycle intermediates. 2-Methylamino-3-Pyridinemethanol, compared to less stable or more hazardous options, already lends itself to these improvements thanks to its moderate reactivity and comparative stability.
Pressure from environmental regulators and customer scrutiny keeps many organizations honest. Chemists who lead the field now consider not only reaction yield, but also solvent choice, byproduct management, and the whole lifecycle impact of intermediates. Choosing reliable, well-documented building blocks makes these innovations possible. In workshops and roundtables, I see more colleagues challenge each other—can we do this with less? Can we pick a route that avoids the problematic intermediate or cuts down on waste? With this compound, there’s a consensus that reliable supply and clear documentation offer a solid starting point for future greener synthesis.
If you ask a group of seasoned synthetic chemists about intermediates that actually help rather than hinder, they’ll mention proven performers like 2-Methylamino-3-Pyridinemethanol. My own career has seen plenty of new reagents hyped up and forgotten after they failed to deliver in real workflows. What sticks around are those that consistently shorten project time, handle cleanly, and resist unpredictable degradation.
For research teams, investing in reliable intermediates pays dividends in hours saved, experiments completed, and headaches avoided. It makes sense to spend early effort on vetting suppliers, checking batch records, keeping an organized inventory, and sharing feedback about lot consistency. Collaboration with suppliers remains invaluable; good vendors listen to feedback, adjust specifications as new needs arise, and invest in better packaging and documentation. Chemistry at the bench and in production never stands still, but standards for quality sourcing and thorough documentation offer some protection from surprises.
No single chemical ticks every box for every user. Some labs want bulk volumes at rock-bottom prices; others seek exotic purities or specific isotope labels for tracer studies or advanced analytics. The more I’ve worked in multi-national teams, the clearer it becomes that gaps in supply or support can slow progress. Advocating for more global suppliers to raise their game—better digital tracking, more responsive customer service, and tighter environmental controls—helps everybody working towards shared goals.
The next step? Push for smarter, more responsible sourcing. Encourage audits, foster partnerships where suppliers share process improvements, and recognize those who deliver quality consistently. 2-Methylamino-3-Pyridinemethanol sets itself apart by meeting these real-world demands. The capacity for ongoing improvement, dialogue with end users, and flexibility in packaging and documentation will continue to drive innovation.
As fields like medicinal chemistry, material science, and fine chemical manufacturing continue to evolve, certain intermediates will move from the background to the front lines. 2-Methylamino-3-Pyridinemethanol has earned its spot through demonstrated reliability, straightforward chemistry, and adaptability at multiple scales. Researchers building tomorrow’s therapies, smarter chemicals, or novel materials need more than just good luck—they need strong building blocks.
I see increasing scrutiny on the way chemicals are created, sourced, and distributed. Transparency, sustainability, and responsiveness to customer needs will sort out leaders from laggards. Compounds like 2-Methylamino-3-Pyridinemethanol already benefit from these trends. They offer not just molecular functionality, but also the foundation for safer, more efficient, and more responsible chemistry. Scientists and engineers eager to leave a positive mark now look beyond the immediate reaction—they consider global impact, regulatory compliance, and the power of open, honest supply chains.
My years on the bench and in process development have taught me that dependable intermediates make or break entire programs. 2-Methylamino-3-Pyridinemethanol stands out as a model for what works: consistent physical properties, reliable documentation, and a track record in creative synthesis. Its ready reactivity, coupled with solid supply and rigorous quality assurance, gives researchers a real tool for advancing science. As industry standards continue to rise and new challenges emerge, this staple compound will support the ongoing push for smarter, safer, and more sustainable chemical innovation.