|
HS Code |
238480 |
| Iupac Name | 2-(Hydroxymethyl)-1-methylpyridine |
| Common Name | α-methylpyridine-2-methanol |
| Molecular Formula | C7H9NO |
| Molar Mass | 123.15 g/mol |
| Cas Number | 3731-51-9 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 244 °C |
| Density | 1.080 g/cm³ |
| Solubility In Water | Moderate |
| Smiles | CC1=CC=CC=N1CO |
| Inchi | InChI=1S/C7H9NO/c1-6-3-2-4-8-7(6)5-9/h2-4,9H,5H2,1H3 |
As an accredited α-methylpyridine-2-methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with tamper-evident cap, labeled with chemical name, 99% purity, hazard symbols, and manufacturer details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): α-Methylpyridine-2-methanol packed in 200 kg drums, totaling 80 drums (16 MT net) per container. |
| Shipping | α-Methylpyridine-2-methanol is shipped in tightly sealed containers, protected from light and moisture. Ensured under standard chemical transport regulations, it should be labeled as a hazardous material. The package must be handled with care, ensuring ventilation, and kept away from incompatible substances during transit. Safety data sheets accompany the shipment. |
| Storage | **α-Methylpyridine-2-methanol** should be stored in a cool, dry, and well-ventilated area, away from sources of heat and ignition. Keep the container tightly closed and protected from light. Store separately from oxidizers and acids. Use appropriate, labeled containers made of compatible materials. Ensure access to spill control materials and proper ventilation to minimize inhalation risks. |
| Shelf Life | α-Methylpyridine-2-methanol typically has a shelf life of 2 years when stored tightly sealed, protected from light, moisture, and air. |
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Purity 99.5%: α-methylpyridine-2-methanol with purity 99.5% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized impurity formation. Melting point 41°C: α-methylpyridine-2-methanol with melting point 41°C is used in fine chemical manufacturing, where controlled phase transitions enhance process scalability. Molecular weight 123.16 g/mol: α-methylpyridine-2-methanol with molecular weight 123.16 g/mol is used in catalyst preparation, where precise stoichiometry improves catalytic efficiency. Stability up to 120°C: α-methylpyridine-2-methanol with stability up to 120°C is used in high-temperature reaction processes, where it maintains structural integrity and consistent reactivity. Water content <0.2%: α-methylpyridine-2-methanol with water content <0.2% is used in moisture-sensitive organic syntheses, where reduced hydrolysis risk preserves product integrity. Viscosity 8.5 mPa∙s: α-methylpyridine-2-methanol with viscosity 8.5 mPa∙s is used in specialty coating formulations, where optimized flow properties promote uniform film application. Density 1.07 g/cm³: α-methylpyridine-2-methanol with density 1.07 g/cm³ is used in laboratory reagent preparations, where accurate volumetric measurements ensure experimental reproducibility. Storage temperature 2–8°C: α-methylpyridine-2-methanol with storage temperature 2–8°C is used in analytical sample storage, where low-temperature stability prevents degradation. |
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Most folks working in chemical synthesis chase after reliability and consistency. Finding a product that handles the unpredictable demands of lab and plant work takes patience. I’ve seen chemists stop mid-experiment and grumble about a bad batch of a core building block—sometimes the answer lies in selecting a better source material from the start. α-Methylpyridine-2-methanol is one of those raw chemicals that shows its worth across different situations, and I say this from the experience of folks who rely on each step running right.
α-Methylpyridine-2-methanol sometimes pops up under alternative names—2-hydroxymethyl-α-picoline, for example, but the end result is always the same: a white-to-off-white crystalline compound with a unique mix of volatility and stability. Most labs getting it by the kilogram can count on purity levels above 98%. What’s more, reputable suppliers measure moisture content, check for trace heavy metals, and stress-test the batch for breakdown during normal shelf life. From my experience working in university labs, unchecked moisture creeps into reactions and throws off results. So it makes sense to track the water content and insist on fresh product, not leftovers from a dusty storeroom.
The model folks choose for their synthesis makes a difference. Many labs stick to well-documented variants with a clear lot history, which helps cross-check reactivity from batch to batch. Having physicochemical data on hand—like melting point, refractive index, or high-performance liquid chromatography traces—backs up your purchase. This transparency isn’t just about nerdy recordkeeping; it streamlines approvals, makes reports easier, and helps everyone trust data over guesswork.
You won’t find α-methylpyridine-2-methanol in drugstore aisles or supermarket shelves, but step inside a research lab or pharma plant, and it’s a familiar name. This compound acts as a vital intermediate. Medicinal chemistry teams reaching into the toolbox for heterocyclic scaffolds, especially those with specialized pyridine rings, know the value of that α-methyl group and hydroxymethyl side. It can get transformed into more reactive alcohols, oxidized to aldehydes, or linked to other pharmacophores to build bigger, more complex molecules that end up as medicines, herbicides, or other high-value products.
I recall a colleague in the agrochemical sector who needed a methyl-substituted pyridine derivative that wouldn’t poison downstream coupling or lead to tars during scale-up. Most other options would cough up residues or make purification a nightmare. α-Methylpyridine-2-methanol clicked into the synthetic route, with the extra methyl leaning just far enough from the nitrogen ring to support regioselective reactions. With a wide range of applications in solvent production, resin modification, and even some niche flavors with deep chemical tweaks, this compound leaves laboratories plenty of room to experiment.
Many pyridine-based alcohols can pinch-hit for one another. But the two-position methyl on the ring and the placement of its alcohol group swap the reactivity, solubility, and even safety profile, setting α-methylpyridine-2-methanol apart from the more common 2-pyridinemethanol or plain α-methylpyridine. I’ve seen some researchers try to economize by using more generic compounds, only to fight off low yields, unexpected side reactions, or persistent off-odors in the end product. The extra methyl group here changes the electron cloud over the ring, moderates how the molecule fits into larger frameworks, and often makes a tough reaction easier by guiding selectivity.
A practical difference shows up in scale-up, and few people talk about it until they hit that wall. α-Methylpyridine-2-methanol resists oxidation well enough during storage, something that can’t always be said for other alcohol-bearing pyridines. This means you spend less time reworking process controls or treating offspec materials. I once worked on a pilot project where an alternative pyridyl alcohol routinely browned or developed odd peaks during gas chromatography, forcing a full repurchase. α-Methylpyridine-2-methanol proved steadier, saving time, headaches, and money.
A lot of folks outside chemical research might not notice lab life changing from one white powder to another, but inside the industry, those small tweaks make or break projects. Health authorities and regulators demand robust evidence that your synthesis doesn’t just work, but that it’s consistent, minimizes hazardous byproducts, and stands up over time. If you swap in a compound with unpredictable impurities or poor documentation, you risk more than a failed experiment—you could lose a quarter’s work or endanger a product line. α-Methylpyridine-2-methanol, with provenance from a trusted supplier, simplifies audits and puts those worries to rest.
Beyond routine compliance, toxicity and workplace safety get a nod here, too. Pyridine derivatives deserve respect in handling. Some analogues can release strong, persistent odors or hold on to residual solvents that linger in production areas for days. My own trial-and-error with exhaust hood airflow and personal protective equipment taught me to prefer batches with cleaner specs, lower offgassing, and reliable safety sheets. α-Methylpyridine-2-methanol, as supplied by major chemical manufacturers, typically lands well within occupational guidelines when handled with common sense and standard gear.
Every chemical, no matter how tried and true, brings a few headaches. For α-methylpyridine-2-methanol, the main trouble comes from inconsistent quality, supply interruptions, and occasional changes in regulatory status. A few pharmacopoeias update their monographs, making yesterday’s certificate of analysis out of date with new impurity thresholds. Lab managers have complained to me about finding “surprise” trace impurities only after scaling up an order—costly, especially when downstream processing depends on a clean slate.
To keep these surprises at bay, buyers get better results by working closely with suppliers on batch-level documentation. Request spectral data and impurity breakdowns, not just generic data sheets. In places like Europe and the United States, traceability isn’t just nice to have; it answers to regulators who increasingly want full disclosure. For teams needing a long-term supply, building partnerships with established chemical suppliers, and arranging supply chain audits, ensures fewer delays or recalls tied to changing specification requirements.
Another issue comes from mishandling. Some users leave the product exposed to air longer than necessary during transfers, thinking no harm will come. Pyridines can pick up moisture, affecting reactivity and risking unwanted byproducts, especially in moisture-sensitive syntheses. Training teams on simple precautions—tightly capping containers, working under inert atmosphere when possible, rotating stock—keeps quality up and losses down.
Disposal and environmental risks need attention, too. Pyridine derivatives aren’t benign; they demand proper neutralization before discarding waste. Some facilities pour spent reagents in standard solvent waste tanks, unaware of long-term build-up in shared tanks. Coordinating with environmental health and safety departments and running small-scale degradation tests prevents violations during audits and supports sustainable lab practice.
People sometimes wonder why not stick to 2-pyridinemethanol or just α-methylpyridine without the alcohol group. Simple answer: the chemistry changes. The methyl group shifts the electronic properties of the ring, alters metabolic profiles for pharma applications, and eases selective functionalization in synthetic routes. For some projects, using other analogues throws off reactivity, reduces end-product yields, or delivers the wrong physical properties, such as melting points or solubility.
From experience, the impurities that show up in related pyridines can differ. For instance, plain 2-pyridinemethanol may bring along higher UV-absorbing impurities, which complicate photochemical syntheses or spectroscopic analysis. α-Methylpyridine, lacking the methanol group, limits how you attach additional side chains or protective groups. Accurate selection at the beginning of a research project, based on route scouting and analytical screening, inevitably saves weeks or months chasing down problems later.
Some users with cost concerns may mix and match, but the gains rarely offset the unpredictability. More than one scale-up team I know slogged through solvent exchanges and extra recrystallizations after trying to cut corners. α-Methylpyridine-2-methanol usually costs a bit more up front, but the extra purity, reactivity, and documentation pay for themselves in reduced failure rates, less rework, and easier filings for process patents or regulatory submissions.
Standing inside a lab with shelves lined by carefully chosen chemicals, you learn that the small choices add up. Working with products like α-methylpyridine-2-methanol makes tough chemistry more reliable, supports cleaner workflows, and meets stricter regulatory environments year after year. Where some analysts see only another detail in a list of raw materials, chemists and engineers know that compound selection determines whether research moves forward or runs into dead ends.
The deeper value here comes from putting quality first, pushing for rigorous upfront documentation, and not cutting corners during procurement or handling. Listening to the experienced voices of safety professionals, bench chemists, and regulatory affairs people, trends point toward tighter supply controls, routine impurity testing, and better waste management. In my own work, putting these pieces in place takes effort, but it beats scrambling to redo weeks of painstaking syntheses or fielding last-minute audit findings.
Looking ahead, it pays to keep lines of communication open with suppliers and stay informed about shifts in global chemical markets. Regulatory harmonization across Asia, Europe, and the Americas changes specification thresholds for key substances, so sticking to old habits brings risky surprises. Training lab staff on smart storage and routine in-house quality testing arms you against new gaps in documentation.
Industry-wide, sharing more application notes, reaction schemes, and troubleshooting tips for α-methylpyridine-2-methanol puts valuable knowledge within reach. Networking at technical conferences or through online forums closes the information gap between researchers, regulatory specialists, and production managers. In the end, carving out a niche for this compound—treating it as a trustworthy building block instead of a simple catalog entry—prepares labs for tomorrow’s research questions and today’s daily challenges.
Each time a team invests in higher-quality inputs like α-methylpyridine-2-methanol, the ripple effect stretches through multiple stages of innovation. Well-documented, stable, and carefully handled reagents help turn complex chemical dreams into tangible products. The challenges along the way remind us that chemistry, in its practical day-to-day, rewards diligence, shared learning, and a refusal to settle for second-best when it comes to foundational materials.