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HS Code |
268461 |
| Product Name | 6-Methyl-2-pyridinemethanol |
| Cas Number | 3731-51-9 |
| Molecular Formula | C7H9NO |
| Molar Mass | 123.15 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 48-52°C |
| Boiling Point | 273°C (estimated) |
| Density | 1.113 g/cm3 (at 25°C, estimated) |
| Solubility In Water | Moderately soluble |
| Smiles | CC1=NC=CC(CO)=C1 |
| Inchi Key | VIJIYJMYKZPLJX-UHFFFAOYSA-N |
As an accredited 6-METHYL-2-PYRIDINEMETHANOL factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 6-METHYL-2-PYRIDINEMETHANOL is supplied in a tightly sealed amber glass bottle with a printed safety-label. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 6-METHYL-2-PYRIDINEMETHANOL: Securely packed in drums or IBCs, properly labeled, maximizing container space efficiency. |
| Shipping | 6-METHYL-2-PYRIDINEMETHANOL should be shipped in tightly sealed containers, protected from light and moisture. Transport under cool, dry conditions, adhering to applicable local, national, and international regulations for handling and shipping chemicals. Proper labeling, documentation, and hazard communication must be ensured throughout transit to guarantee safety and regulatory compliance. |
| Storage | 6-Methyl-2-pyridinemethanol 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 the chemical from moisture and direct sunlight. Ensure appropriate labeling, and access should be restricted to trained personnel. Wear suitable personal protective equipment when handling the compound. |
| Shelf Life | 6-METHYL-2-PYRIDINEMETHANOL typically has a shelf life of 2–3 years when stored in a cool, dry, tightly sealed container. |
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Purity 99%: 6-METHYL-2-PYRIDINEMETHANOL with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical yield and minimized impurity content are ensured. Melting Point 93°C: 6-METHYL-2-PYRIDINEMETHANOL with melting point 93°C is used in fine chemical manufacturing, where controlled phase transition enhances formulation stability. Molecular Weight 137.17 g/mol: 6-METHYL-2-PYRIDINEMETHANOL at molecular weight 137.17 g/mol is used in agrochemical product development, where precise dosing and consistent active content are critical for performance. Water Content ≤ 0.2%: 6-METHYL-2-PYRIDINEMETHANOL with water content ≤ 0.2% is used in catalyst preparation, where low moisture levels prevent unwanted side reactions. Stability Temperature up to 150°C: 6-METHYL-2-PYRIDINEMETHANOL with stability temperature up to 150°C is used in high-temperature organic synthesis, where thermal integrity maintains product reliability. Viscosity 4.6 mPa·s (at 25°C): 6-METHYL-2-PYRIDINEMETHANOL with viscosity 4.6 mPa·s (at 25°C) is used in resin formulation, where controlled flow properties facilitate uniform blending and processing. |
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Working in a lab means constantly dealing with a mountain of chemical options, many of which sound similar at first glance. Take 6-METHYL-2-PYRIDINEMETHANOL, for example. At a glance, its name seems like any other pyridine derivative, but those who work with it know the subtle changes in its structure bring tangible benefits to the table. Chemists and chemical engineers use products like this to get reliable results, keep projects moving, and avoid frustrating dead ends. Over the years, this compound has shown up in both academic and industrial labs, making it worth a deeper look.
6-METHYL-2-PYRIDINEMETHANOL starts with a simple pyridine ring. Add a methyl group at the 6-position and a hydroxymethyl group at the 2-position and you get a molecule with a different set of reactivity and solubility profiles than its cousins. That tweak turns out to be useful in real-world synthesis, especially when selectivity matters or solubility can’t be left to chance. If you’ve ever watched a reaction sputter out for lack of a good intermediate, you know the value of reliable inputs. This compound shows up in the toolbox for exactly that reason—it’s dependable and adaptable.
Having used 6-METHYL-2-PYRIDINEMETHANOL in organic transformations, I’ve seen firsthand how even small changes in ring substitution can tilt outcomes in your favor. The performance difference may not be obvious on paper, but in a lab notebook, successful reactions make their mark. People talk a lot about high yields and fast reactions, but what matters is the actual ability to complete synthesis steps without wandering into side reactions. This pyridine derivative sticks to the plan more often than not, so long as the method isn’t outside of published boundaries.
Each project brings its own requirements for reagent purity and form. For batches where trace impurities could trip things up—say, in pharmaceutical intermediates or electronic materials—purity levels over 98 percent start to matter. It’s reassuring when suppliers offer 6-METHYL-2-PYRIDINEMETHANOL at high purity, because you avoid wasting time troubleshooting unknown contaminants. Most manufacturers sell this chemical in crystalline or liquid form, depending on your temperature and solvent needs. Keeping an eye on melting point, moisture levels, and storage conditions helps preserve quality; as with many organics, a cool, dry shelf beats a lab bench any day. Stability isn’t usually a headache, though always watch for slow air oxidation or light sensitivity over long storage.
There’s something practical about the way this molecule fits into existing synthesis workflows. Its moderate polarity and manageable size let it blend well with common organic solvents. Some derivatives struggle in water or non-polar environments; 6-METHYL-2-PYRIDINEMETHANOL rarely gives you trouble dissolving or mixing, which spares a lot of wasted time prepping obscure solutions. You know something has found a regular place in labs when everyone keeps a bottle ready to hand instead of chasing down special order forms.
People often compare 6-METHYL-2-PYRIDINEMETHANOL to run-of-the-mill pyridinemethanols or plain pyridines. The extra methyl group seems modest, but that change creates differences in electron distribution and sterics. Reactions with strong electrophiles or transition-metal catalysts can show a noticeable boost in selectivity. I’ve been through projects where the methyl group steered outcomes toward the main product, letting us skip extra purification steps. Nobody wants to spend hours cleaning up a reaction mix when a better reagent does the work upfront.
The physical properties shift enough that you can sometimes drop an extra step in the synthetic sequence. Higher boiling points help with distillations, and altered polarity occasionally solves stubborn solubility challenges. In my work with nitrogen-containing heterocycles, some analogs proved too greasy or uncooperative in water, but 6-METHYL-2-PYRIDINEMETHANOL handled extractions and washes with less fuss. These advantages might sound small, but strung together in a multi-step synthesis, they save weeks at the bench.
Across pharmaceutical, agrochemical, and materials science fields, pyridine derivatives get called on for more jobs than people outside the field might guess. Researchers look for new ligands, intermediates, or pharmacophores with every project cycle, so a molecule that keeps showing up through patents, papers, and patents has already proven its worth. With reference literature reporting uses of 6-METHYL-2-PYRIDINEMETHANOL as both a building block and a fine-tuner of reactivity, it’s earned its reputation by showing up where other alternatives falter. Sourcing reliable chemical inputs shouldn't slow down progress—and this compound delivers just that steadiness.
If the end goal involves exploring new reaction pathways, this compound’s reactivity profile opens up options. You can attach a diverse array of substituents on the methyl or hydroxymethyl group, setting yourself up for reduced trial-and-error. In one research stint, our team needed a scaffold stable to both mild oxidants and reductants. Many pyridinemethanol derivatives gave ambiguous results, but the 6-methyl variant stood out for its resilience under a variety of conditions. That translated directly to less wasted reagent and faster troubleshooting.
Lab supply chains have seen disruptions lately, whether from upstream raw materials, freight costs, or shifts in manufacturing centers. A responsible approach to sourcing and sustainability involves tracking where and how chemicals like 6-METHYL-2-PYRIDINEMETHANOL are produced. If you care about the full lifecycle, it makes sense to choose vendors investing in safe, low-waste processing routes. Observing ISO standards or similar certifications for traceability shows commitment beyond quick profit. Most well-established chemical companies publish enough information about their manufacturing controls to help researchers stay on the right side of environmental responsibility.
I’ve seen both positive and negative impacts based on upstream supply choices. Labs that take the time to verify origin and purity usually face fewer surprises, such as inconsistent yields or difficult waste management after synthesis. Choosing a high-quality supplier doesn’t cost much more in the grand scheme but delivers savings in repeatability and reduced troubleshooting. For those working in regulated industries—where every batch counts—consistent quality can mean the difference between a fast project and a flurry of corrective paperwork.
No chemical is perfect, and 6-METHYL-2-PYRIDINEMETHANOL has its quirks. Not every reaction benefits from that methyl tweak. There will always be a trade-off when tuning electronic or steric profiles, so careful literature review or small-scale pilot reactions can keep avoidable problems at bay. Some projects, especially those focusing on narrow selectivity or stringent environmental criteria, may still need to customize protocols to keep results on track. Awareness of how side-reactivity or minor impurities show up matters more with sensitive downstream reactions, especially in pharmaceutical contexts.
At the same time, the diversity of research into new synthetic methods, including greener catalytic processes or more straightforward routes to targeted molecules, opens new uses for this compound. I’ve seen groups experiment with 6-METHYL-2-PYRIDINEMETHANOL as a ligand in palladium- or copper-catalyzed couplings, opening up new scaffold-building routes. Interdisciplinary work benefits from this kind of reliable input—reducing embarrassing mid-project pivots when traditional pyridine derivatives underperform.
Chemistry isn’t all about theory. Much of what happens in the lab comes down to practical experience. I’ve worked on projects where getting a high-quality intermediate on time meant keeping a well-stocked shelf. When we had trusted sources for compounds like 6-METHYL-2-PYRIDINEMETHANOL, we could run parallel reactions, test new methods, and push past dead-ends that stymied other groups. Fewer delays meant more cycles of hypothesis and data, directly translating into faster discoveries.
Having watched less experienced colleagues try to cut costs using lesser-known suppliers, I’ve seen the trouble that follows: low purity, unexpected side-reactions, days spent calling customer service with batch numbers in hand. Getting a recognizable, well-characterized lot from a reputable source protected against those headaches. After one too many wasted afternoons troubleshooting, the lesson stuck—an investment in quality inputs is foundational, regardless of the flashiness of the final application.
Every synthetic chemist eventually settles into a set of reliable materials. 6-METHYL-2-PYRIDINEMETHANOL earns its place in that circle because it shows up, does its job, and keeps the wheels turning. For large industrial teams, that consistency scales up; for small academic groups, that means less budget spent fixing preventable problems. The introduction of this compound to a project rarely requires major adjustments—common work-up techniques, easy solvent options, and straightforward handling mean new users don’t spend weeks learning the ropes.
I’ve come to appreciate compounds that cut down on wasted time and enable genuine progress. With years spent working side-by-side with ambitious grad students and tenured faculty, I’ve noticed the seasoned researchers reach for 6-METHYL-2-PYRIDINEMETHANOL when other options create uncertainty or inefficiency. They remember the cost of experiments that worked in theory, but not in practice. This molecule keeps the focus on making advances, not circling back to solve basic supply problems.
Anyone new to the world of multistep organic synthesis benefits from working with materials that won’t spring unwelcome surprises. As with any chemical, reading up on published protocols, double-checking purity specs, and setting aside time for small-scale tests goes a long way. Take note of how 6-METHYL-2-PYRIDINEMETHANOL’s properties line up with your project goals; sometimes its strengths only show up in side-by-side comparisons. Don’t be afraid to document unexpected results—it’s often the small, initially confusing observations that point to new solutions.
Consulting with more experienced researchers pays dividends too. I remember being encouraged to set up parallel reactions with both standard pyridinemethanol and the 6-methyl variant. Only after running both did the differences become clear: less separation time, higher yields, cleaner spectra. Guidance from those who’ve run dozens of similar syntheses made all the difference, as did comparing data to research articles from reliable journals and trade groups.
Emerging synthetic methods make clever use of existing building blocks, and 6-METHYL-2-PYRIDINEMETHANOL stands to benefit from these innovations. As chemistry continues looking for more sustainable or selective ways to construct useful molecules, this compound provides a strong base for ligand design, pharmaceutical intermediates, and fine chemicals. Researchers investigating new catalysts or greener reaction media have found the predictable properties of this molecule reduce variables, making scale-up less fraught with uncertainty.
Its versatility comes out most when research moves beyond the textbook into application. Whether in medicinal chemistry, where subtle changes make a difference in biological properties, or in polymer science, where stability and reactivity need careful balance, 6-METHYL-2-PYRIDINEMETHANOL supports creative approaches. The next decade will likely see more uses for this compound as new areas of chemical synthesis demand reliable, adaptable reagents that don’t bring hidden complications.
No discussion about laboratory chemicals would be complete without a nod to safety and smart handling. While 6-METHYL-2-PYRIDINEMETHANOL doesn’t pose outsized risks compared to related compounds, labeling containers, managing exposure, and disposing of waste responsibly remain basic best practices. Relying on up-to-date safety data sheets and local lab protocols keeps everyone on the right side of regulations while safeguarding personal health. Good organization is a quiet asset in the lab—it’s rare you see accidents in well-run, orderly setups, especially with common chemicals like this on hand.
Planning for reproducibility means keeping a careful record of reagent batches and preparation steps. Skilled chemists know that a clean work area and detailed notes prevent mistakes, especially when switching among different suppliers or experimenting with alternative synthetic routes. Awareness of typical byproducts during synthesis or decomposition prepares users for small surprises rather than sudden disasters. Investing a little time up front pays back in reliable results and greater professional credibility down the line.
Science grows best through collaboration. Those who use 6-METHYL-2-PYRIDINEMETHANOL regularly often share their findings at conferences, through open lab notebooks, or in published journal articles. Online forums and professional societies build up a living record of practical tips, troubleshooting advice, and suggested alternatives. Creative workarounds—mixing solvents, optimizing reaction conditions, or swapping catalysts—move from rumor to standard practice because people take the time to learn from one another’s experience. The collective wisdom that grows around familiar chemicals, passed from postdoc to postdoc or handed down in lab meetings, can carry as much weight as suppliers’ technical notes.
The accessibility of this shared knowledge makes it possible for labs of every size to benefit from hard-won insights. That’s a powerful tool for academic groups operating with lean resources or industry teams trying to build know-how without reinventing the wheel. Reproducibility, reliability, and scalability all spring from communities that share what actually works, and 6-METHYL-2-PYRIDINEMETHANOL’s track record keeps expanding thanks to that culture.
Everyday lab work relies on reagents that behave as expected. In my experience and judging from the literature, 6-METHYL-2-PYRIDINEMETHANOL stands out in crowded shelves for its blend of reliability, manageable handling, and adaptability across several fields. Whether used on the milligram or kilogram scale, teams that make a habit of selecting dependable inputs rarely regret the choice. Choosing this compound reflects a commitment to high standards, smoother project flow, and respect for the time and energy of everyone involved.
As the chemical sciences push toward more efficient, sustainable, and integrated approaches, dependable tools make innovation possible. The story of 6-METHYL-2-PYRIDINEMETHANOL is one of small changes that make a big impact—in better yields, fewer side reactions, and simpler workflows. In a world that sometimes overcomplicates progress, sticking with what works can offer the surest path to discovery.