|
HS Code |
279034 |
| Cas Number | 3731-52-0 |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.15 |
| Iupac Name | 1-(2-methylpyridin-2-yl)ethanol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 245-247°C |
| Density | 1.070 g/cm³ |
| Melting Point | -5°C |
| Refractive Index | 1.539 |
| Solubility In Water | Moderate |
| Synonyms | 2-(1-Hydroxyethyl)pyridine, 2-Picolyl alcohol, alpha-Methyl-2-picolyl alcohol |
| Flash Point | 110°C |
As an accredited alpha-Methylpyridine-2-methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with screw cap, labeled as alpha-Methylpyridine-2-methanol, marked with hazard symbols and product details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for alpha-Methylpyridine-2-methanol: Securely packed in drums, compliant with safety standards, ensuring spill-free chemical transport. |
| Shipping | Alpha-Methylpyridine-2-methanol is shipped in tightly sealed containers, protected from light and moisture. Packages are clearly labeled with hazard warnings, as transportation may be regulated due to flammability or health risks. Shipping complies with local and international chemical transport regulations, ensuring safe handling and delivery to laboratories or industrial sites. |
| Storage | Alpha-Methylpyridine-2-methanol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Store under inert atmosphere if necessary. Keep container tightly closed when not in use, and clearly label all storage vessels. |
| Shelf Life | Alpha-Methylpyridine-2-methanol typically has a shelf life of 2-3 years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: alpha-Methylpyridine-2-methanol with 99% purity is used in pharmaceutical synthesis, where it ensures high yield and minimal by-product formation. Molecular weight 123.16 g/mol: alpha-Methylpyridine-2-methanol at a molecular weight of 123.16 g/mol is applied in agrochemical intermediate production, where it enables precise stoichiometric calculations and formulation consistency. Melting point 40°C: alpha-Methylpyridine-2-methanol with a melting point of 40°C is used in fine chemical manufacturing, where controlled solid-liquid transitions improve process efficiency. Low water content <0.1%: alpha-Methylpyridine-2-methanol with water content below 0.1% is utilized in moisture-sensitive reactions, where it prevents hydrolysis and degradation of reactants. Stability temperature up to 120°C: alpha-Methylpyridine-2-methanol stable up to 120°C finds application in high-temperature catalytic processes, where it maintains structural integrity and reactive performance. Viscosity 1.2 mPa·s: alpha-Methylpyridine-2-methanol with a viscosity of 1.2 mPa·s is employed in solvent systems for coatings, where it enables easy mixing and uniform dispersion. Refractive index 1.526: alpha-Methylpyridine-2-methanol with a refractive index of 1.526 is used in optical material formulations, where it ensures precise light transmission characteristics. Residual solvent content <50 ppm: alpha-Methylpyridine-2-methanol with residual solvent content below 50 ppm is used in electronic chemical synthesis, where it minimizes potential contamination and enhances product reliability. |
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Many professionals working with heterocyclic building blocks know the headaches that come with unreliable sources. The difference between downtime and efficiency in a research lab or manufacturing site often traces back to the choice of raw materials. alpha-Methylpyridine-2-methanol steps in just here. With a structure lending itself to functional versatility—a methyl group on the alpha carbon and a methanol moiety at the 2-position—this compound fits right into the plans of medicinal chemists, process engineers, and academic researchers. Not everyone needs a reminder of the effort invested in purifying starting pyridine alcohols from ambiguous batches, poorly maintained suppliers, and inconsistent crystalline forms. Those in the trenches of organic synthesis can spot the shortcuts and ask for something better.
In the chemistry world, not every pyridine derivative pulls its weight. With alpha-Methylpyridine-2-methanol, I've seen hands-on how a single feature—a clean methyl group at the alpha slot—keeps side reactions at bay during downstream transformations. This extra handle gives process chemists extra room to maneuver, especially when building up complexity in pharmaceuticals or fine chemicals. If you track synthetic bottlenecks as closely as most process teams do, the real story lies in predictable reactivity. The presence of the methyl group changes how the ring handles nucleophilic attack and changes the selectivity profile for oxidation steps. It does more than add mass; it shifts the chemistry from vague to directed.
The market offers a spread of pyridine alcohols. So, what justifies making the switch or staying loyal to this particular molecule? Detailed conversations with bench scientists reveal a couple of reasons beyond technical data sheets. Consistency shows up high on the list. Tiny variations in crystal habit, trace amine content, or even the smell can derail an experiment. Nobody enjoys scraping through research budgets, repeating columns or struggling to identify source-specific contaminants. With alpha-Methylpyridine-2-methanol, batches show a repeatable melting point and a product that looks the same every single time it comes in.
Then there’s crystallinity and handling—a point often overlooked by newcomers to scale-up. I’ve seen projects limp along as teams fight to dry sticky residues and sticky distillations. Here, the neat solid nature of alpha-Methylpyridine-2-methanol saves a measurable chunk of time off purification. It doesn't clog filters, doesn't gum up rotovaps, and doesn't need elaborate stabilization. Most users can measure and weigh it out without donning extra safety gear or second-guessing the hazards beyond routine lab caution. These design details—often set by the experience of repeat users—can swing the balance in favor or against a raw material.
In the world of synthetic intermediates, certain motifs pop up again and again. For those making substituted pyridines, pharmaceuticals, agrochemicals, or advanced material monomers, alpha-Methylpyridine-2-methanol isn’t an exotic oddity; it’s a workhorse. Its structure primes it for easy customization. I recall working with colleagues needing a balance between nucleophilicity and site-selective functionalization. The methyl group protects the alpha position from unwanted overreaction, while the alcohol group opens paths to esters, ethers, or further oxidation.
In research settings aiming to create unique ligands for catalysis or new scaffolds for medicinal chemistry libraries, teams use alpha-Methylpyridine-2-methanol as a handle for rapid elaboration. With efficient routes available for tosylation, mesylation, or even halogenation of the alcohol, the compound often becomes a launchpad for more complex transformations. Predictable behavior during oxidation—such as to aldehydes or acids—puts it right at home in both small molecule discovery and scaling up for preclinical leads.
Anyone who’s run side-by-side experiments can tell the difference between theory and practical results. Classic precursors like pyridine-2-methanol lack the methyl group’s subtle guidance in regioselectivity. Analytical departments want clear spectra; process chemists want fewer side products; scale-up teams want less waste. When every variable is under control, alpha-Methylpyridine-2-methanol shows up with cleaner HPLC traces and less need for post-reaction scavenging. Some still prefer less substituted pyridine alcohols for ultramild conditions, but that comes with a risk: greater uncertainty around byproducts.
I’ve seen pilot projects stall because an impure lot of a similar pyridine alcohol jammed the workflow somewhere between an alkylation and a crystallization step. With alpha-Methylpyridine-2-methanol, I know where I stand. It isn’t just another piece of a catalog—users in the know lean on its reliability.
Unlike heavy alkylating agents or halogenated solvents, alpha-Methylpyridine-2-methanol handles smoothly at ambient temperature and needs no exotics for storage. Most standard PPE and fume hoods cover any occupational risks. The compound’s aromatic core brings with it the common-sense caution reserved for pyridine derivatives: keep away from oxidation sources, avoid open flames, and minimize inhalation exposure. Still, in practical experience, real trouble rarely comes from the molecule itself. Mistakes in scale-up or improper handling—such as neglecting ventilation or using contaminated containers—may cause more issues than the compound per se.
Experienced users appreciate not fighting a losing battle against volatility or reactivity when transferring or storing the material. Although it smells faintly of pyridine (there’s no getting around that), it doesn’t overwhelm a workspace, provided standard lab hygiene is observed. Those transitioning from more volatile or flammable intermediates often remark that the compound reduces rushed mistakes and cleanup times.
Stricter environmental guidelines have nudged many organizations toward rethinking raw material choices, especially with regulatory agencies tightening oversight. Pyridine derivatives sometimes attract scrutiny, but compared to heavier substituted relatives or nitrogen-rich byproducts, alpha-Methylpyridine-2-methanol stands out for manageable environmental fate. The compound’s moderate water solubility and manageable breakdown profile under controlled waste disposal give EH&S staff more predictable pathways for waste mitigation. That cuts down on unexpected compliance stumbling blocks. Best practices align with the standard rules—no untreated discharges, keep records of chemical transfer, and engage certified waste handlers for larger quantities.
Teams chasing green chemistry awards or improved audit readiness often cite reliable analytics as a secondary benefit. alpha-Methylpyridine-2-methanol lends itself to routine LC-MS and NMR testing; its clean fingerprint helps track down mishandlings before anything becomes a crisis. No compound can make up for careless waste management or poor training, but this one certainly doesn't add extra hurdles.
Stories from daily lab operations reveal patterns no glossy product pamphlet can capture. A small pharma research unit I’ve worked with once described their “two-day rule”—the time it took to judge a raw material’s fitness by purity, crystallinity, and ease of derivatization. For years, they cycled through various pyridine-based alcohols, hitting uneven results and process headaches. Once they landed a steady supply of alpha-Methylpyridine-2-methanol, those two days shrank to half a morning. It wasn’t about fancy equipment upgrades or new process design—just switching to a compound that behaved the same, every time.
Academic groups exploring new catalysis regimes for C-H bond activation name similar upsides. The alcohol group in alpha-Methylpyridine-2-methanol provides an anchor for immobilization on supports or as a directing group in selective metalation. That opens up clear avenues for rapid screening, since researchers aren't stuck troubleshooting unintended reactivity or unexplained coloration. One postdoc joked about “finally getting reliable NMR peaks” after months of blurry signals from other pyridine-based alcohols. Repeatability becomes more than a buzzword when your PhD timeline hangs in the balance.
Trust in a synthetic intermediate doesn’t build overnight, nor does it rest solely on certificates and paperwork. Labs and production floors report their own internal QC checks—melting point ranges, NMR purity, TLC spots, or titrations. Over time, reliable batches of alpha-Methylpyridine-2-methanol start to drive procurement decisions. Fewer substandard lots mean less scrambling for replacement stock and more confidence downstream. In my own experience, the subtle cost savings from fewer re-runs and product recalls quickly add up—especially in tightly regulated industries.
Downstream users—those working with unique functionalizations or building up to more complex nitrogen heterocycles—find extra leverage in the way the methyl and alcohol groups play together during staged reactions. This flexibility cuts the headache and cost from multistep workups. It also pays off in pilot plant environments, where a single failed batch ripples across production schedules and customer commitments. Reliable intermediates underpin successful launches—customers notice, even if leadership doesn’t track the source of the success.
Complex syntheses thrive or fail on the reliability of starting materials. A common scene: workflow stalls, chemists debate whether it’s a reagents issue or a flawed procedure. In cases where alpha-Methylpyridine-2-methanol anchors the early steps, most troubleshooting leads elsewhere. The compound’s known reaction profile helps rule out a source as the problem. That narrows the search space and frees creative talent to solve novel bottlenecks, not revisit old ones.
For teams stuck fighting off secondary impurities, the message is clear: invest in reliable materials or pay the price in wasted resources. Years back, I worked with a group scaling up a heterocyclic target, only to find their supply of a similar pyridine alcohol contained enough residual amine to skew an entire 50-liter run. Transitioning to high-purity alpha-Methylpyridine-2-methanol—vetted by both their own team and through external audits—eliminated the blip, set the stage for a low-waste, high-yield campaign, and brought confidence back to the scale-up window.
Chemical innovation today depends on what arrives in the bottle, not just what shows up in patent literature. The attributes of alpha-Methylpyridine-2-methanol have encouraged new thinking across various teams—custom ligand makers, green chemistry researchers, and computational modelers refining predictive routes. Since the molecule presents a clear trifecta—stability, handle for selective transformations, and established reactivity profile—it becomes a candidate for automated synthesis platforms. More labs experiment with parallel chemistry, combinatorial libraries, or flow chemistry, demanding reagents that can handle automation without surprises.
Big picture: the cleaner a reagent, the easier it becomes to adopt new process technologies. As someone who’s watched the shift from bench batch recipes to machines prepping hundreds of reactions daily, I see alpha-Methylpyridine-2-methanol land in more screening decks, month after month. Software can’t fix a subpar chemical, but robust, repeatable intermediates like this one boost process confidence and support data-driven innovation.
New syntheses spring up yearly, chasing everything from next-generation antibiotics to battery additives. From the vantage point of a seasoned chemist, a molecule like alpha-Methylpyridine-2-methanol becomes part of a toolkit for making tomorrow's breakthroughs routine, not rare. It sidesteps common headaches, simplifies handoffs between R&D and production, and locks in a level of quality that travels from academic discovery through industrial launch.
Real innovation rides on materials engineers and chemists trusting their base—they waste less time on avoidable reruns and more on purposeful improvement. This molecule may look modest on paper, but it proves out every day in hard-won yields, reproducible spectra, and smooth workflow. In a market filled with options, the experienced eye learns to value not just what a compound can do, but what it lets a team avoid—failed batches, endless troubleshooting, wasted hours. alpha-Methylpyridine-2-methanol brings that reliability, building a bridge between ambitious projects and their successful realization.