|
HS Code |
649823 |
| Name | 2-Methoxy-6-methylpyridine |
| Cas Number | 18368-63-3 |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.15 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point Celsius | 176-178 |
| Melting Point Celsius | -12 |
| Density G Per Cm3 | 1.045 |
| Refractive Index N20 | 1.523 |
| Flash Point Celsius | 62 |
As an accredited 2-Methoxy-6-methyl pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Methoxy-6-methyl pyridine, securely sealed with a screw cap and labeled for laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Methoxy-6-methyl pyridine ensures safe, efficient bulk shipment, maximizing space, and minimizing contamination risks. |
| Shipping | 2-Methoxy-6-methyl pyridine is shipped in tightly sealed containers, protected from light and moisture. The chemical should be handled following standard hazardous materials regulations, including appropriate labeling and documentation. Transport should occur at ambient temperature, with care to prevent leaks or spills, according to local, national, and international chemical shipping guidelines. |
| Storage | 2-Methoxy-6-methylpyridine should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep the chemical away from direct sunlight and moisture. Ensure proper labelling and store at temperatures recommended by the manufacturer, typically at room temperature. Use appropriate secondary containment to prevent spills. |
| Shelf Life | 2-Methoxy-6-methyl pyridine typically has a shelf life of 2 years when stored in a cool, dry, and tightly sealed container. |
|
Purity 99.0%: 2-Methoxy-6-methyl pyridine with purity 99.0% is used in pharmaceutical intermediate synthesis, where high product yield and minimal impurities are achieved. Boiling point 183°C: 2-Methoxy-6-methyl pyridine with a boiling point of 183°C is used in solvent systems for organic reactions, where enhanced thermal processing stability is ensured. Low water content <0.2%: 2-Methoxy-6-methyl pyridine with low water content <0.2% is applied in agrochemical formulation, where optimal chemical reactivity and shelf life are attained. Density 1.013 g/cm³: 2-Methoxy-6-methyl pyridine with density 1.013 g/cm³ is utilized in analytical reagent preparation, where consistent volumetric measurements improve assay reproducibility. Melting point -5°C: 2-Methoxy-6-methyl pyridine with melting point -5°C is used in low-temperature synthesis protocols, where liquid handling performance is optimized. GC Assay ≥98%: 2-Methoxy-6-methyl pyridine with GC assay of ≥98% is applied in high-purity catalyst systems, where controlled reaction selectivity is maintained. Stable up to 120°C: 2-Methoxy-6-methyl pyridine stable up to 120°C is utilized in industrial polymerization processes, where decomposition risks are minimized. |
Competitive 2-Methoxy-6-methyl 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!
The world of fine chemicals brims with options, each offering a unique spin on utility and precision. Among these, 2-Methoxy-6-methyl pyridine has started to stand out for chemists and researchers looking to push boundaries in synthesis and formulation. It’s always interesting to pick up a new bottle and immediately notice what sets it apart—this product makes an impression even before it breaks seal. Sometimes the most valuable compounds don’t come with the flashiest introductions, but grow their reputation thanks to how they behave on the workbench.
2-Methoxy-6-methyl pyridine, known to many by its structural shorthand (with the methoxy group attached to the second carbon and the methyl at the sixth), doesn’t get lost in a crowd of generic pyridines. The compound’s molecular structure influences everything from its physical properties to its reaction tendencies. It registers as a light to medium-weight aromatic, often sporting a clear to pale yellow appearance. Its formula—C7H9NO for those keeping count—gives it a portable presence in the lab. Lab veterans learn the feel of it quickly. It resists unnecessary fuss, dissolving efficiently in a range of solvents and making itself useful even before an experiment kicks off.
On the shelf, you’ll spot it typically offered in precise purities, making it suitable for both research-grade discovery and consistent industrial work. Reliable supply matters; a well-purified bottle saves time. No one wants to troubleshoot an entire reaction pathway just because they accepted a batch with noisy contaminants.
Every synthetic chemist chases efficiency. The arrival of 2-Methoxy-6-methyl pyridine has broadened the toolkit, particularly for people working in medicinal chemistry or building next-generation materials. Consider the common hurdles: fine-tuning selectivity in reactions, controlling byproduct profiles, and getting clean, sharp yields with less post-reaction cleanup. This molecule’s carefully balanced electronic environment often delivers one or more of those solutions.
In my own experience, introducing this compound to a challenging alkylation reaction brought a noticeable jump in selectivity, especially where similar pyridines would encourage unwanted side routes or double additions. One of the keys lies in the way the methoxy and methyl groups work together to modulate both electron density and steric effects around the aromatic ring. The result often involves a smoother path from reactant to product, fewer purification headaches, and—if you track your yields closely—a bump in recovered final product.
Traditionally, many in the field reach for 2-methylpyridine or 2-methoxypyridine when a bit of aromatic finesse is required. These stalwarts certainly have their place, but 2-Methoxy-6-methyl pyridine invites closer inspection. Unlike the bare 2-methyl version, this molecule carries a methoxy group that introduces greater electron-donating effect, giving it the ability to actively steer reactions in new directions. The methyl group, tucked away at the sixth position, subtly adjusts reactivity without the brute force seen in some more heavily substituted rings.
For those invested in organic electronic materials, the compound’s aromatic properties and functional group layout open doors to novel building blocks for organic LEDs or small-molecule semiconductors. Tinkering with its isomers revealed just how much difference a single substituent can make. In contrast to its more common relatives, 2-Methoxy-6-methyl pyridine often produces crisper, more reliable reactions for cross-coupling and Suzuki-Miyaura chemistry. Personal trials with this in carbon-carbon bond-forming processes turned up fewer side products than expected, suggesting that this pyridine could help raise the standard for routine syntheses.
Industry moves rapidly, and academic labs run on slim budgets and pressing timelines. Anything that smooths out the workflow has value beyond numbers in a catalog. 2-Methoxy-6-methyl pyridine's stable handling characteristics and predictable reactivity have helped cut down on experimental uncertainty. Few things compare to the relief of seeing sharp, single-peak chromatograms after a day’s work, especially after struggling with messier analogs in previous projects.
Downstream, this purity translates into safer scale-up, clearer regulatory paperwork, and fewer environmental headaches. Anyone aiming to balance sustainable practices with ambitious research targets should pay attention here. I’ve watched chemists sink countless hours into cleaning up after harsh, less discriminating pyridines. Using a compound with cleaner exits simply makes life easier.
Assuming all pyridines act the same misses out on the nuances that drive innovation. The specific interplay of methoxy and methyl groups changes more than just naming conventions—it allows users to explore new chemistry. For example, in heterocyclic synthesis where regioselectivity means everything, this molecule consistently shows an ability to direct functionalization to the right positions. As reaction plans grow more advanced, that kind of built-in guidance offers real advantages.
In academic groups exploring asymmetric synthesis, the compound lends itself to applications where chiral outcomes or harnessing subtle differences in polarity truly matter. A shift of a single substituent can tip a process from broad-spectrum utility into one favored by specialists working at the edge of the field.
It’s not all smooth sailing—the usual precautions still apply. Storage conditions and ventilation remain key, as pyridines can still boast a stubbornly pungent odor if mishandled. While the chemical behaves reliably, its relatively low profile in commercial settings means it’s sometimes overlooked during initial project planning. I’ve had colleagues regret not exploring it earlier, through habit or simple lack of awareness.
One way to improve adoption involves more direct communication between researchers and suppliers. Open sharing of case studies, especially unexpected highlights, often leads new users to reconsider their reaction design. Communities built around specific types of chemistry—say, those focusing on heterocycle modification or fine-tuning of pharmaceutical candidates—could benefit from pooling this kind of wisdom. After seeing adoption snowball in related pyridine derivatives, there’s every reason to expect a broader following for this variant.
What stands out about 2-Methoxy-6-methyl pyridine is how it makes established processes just a little bit sharper. In chromatographic separations, the compound’s volatility and polarity line up in a way that often shortens run times or reduces the need for elaborate eluent systems. Working with material that behaves well in both analytical and preparative applications gives labs much-needed flexibility, and over time, those small advantages stack up.
Learning from the field, some teams have successfully introduced 2-Methoxy-6-methyl pyridine into parallel synthesis campaigns. Perhaps the most interesting result comes from cases where the compound boosted reaction reproducibility. Colleagues reported less batch-to-batch variation, saving time on re-validating procedures. Given the rising pressure to document and maintain robust quality standards, this reliability becomes a practical selling point.
Chemistry departments increasingly juggle multidisciplinary projects, bridging theoretical studies with translational research. Using a pyridine that stays versatile without sacrificing consistency supports that demand. Take drug metabolism studies, for example—an area rife with unpredictability. The subtlety introduced by both methyl and methoxy groups lends itself well to probing enzyme specificity, supporting the work that leads from a hit compound to an actual clinical candidate.
Routine doesn’t mean boring. Instead, it delivers a quiet confidence that routine tasks will progress as planned. Teamed up with careful lab management, access to compounds like 2-Methoxy-6-methyl pyridine sets the stage for larger, more ambitious projects. Researchers who value time often choose such compounds for their balance of function and dependability.
Success in chemical research often depends on connections between the university bench and the factory floor. 2-Methoxy-6-methyl pyridine helps close that gap. Its popularity among medicinal chemists stems from its straightforward incorporation into varied synthetic routes. On the industrial side, production engineers appreciate fewer surprises during scale-up. It melts and boils at temperatures that don’t cause logistical hurdles, and doesn’t clog up equipment—issues that can quietly drain budgets.
For quality control teams, the ability to quickly screen batches and manage trace impurities brings peace of mind, especially when compared to more flexible but unpredictable analogs. Decision-makers working to hit regulatory marks find fewer red flags in their documentation since this compound often leaves behind a tidier analytical trail.
Green chemistry no longer fits neatly into a box labeled ‘future concerns’—it’s an everyday necessity. By shifting to materials that cut down on hazardous byproducts and ease downstream filtration, labs can lighten their environmental load. 2-Methoxy-6-methyl pyridine provides a welcome alternative for teams aiming to comply with rising environmental standards, especially where cleaner burning or lower aquatic toxicity matter.
The compound’s leaner reaction profiles mean less solvent waste, shorter cleanups, and gentler emissions. For companies working to squeeze every last drop out of limited compliance budgets, this kind of upfront planning pays off.
Walking through project retrospectives, the compounds that get mentioned most often are those that rescued schedules, uncovered rare selectivities, or let researchers finish out a tough synthesis run without throwing away a weekend. As chemists grow familiar with 2-Methoxy-6-methyl pyridine, they find not just a niche, specialty reagent, but a new foundation for creativity.
We live in a time when breakthroughs often come from surprising places. The right synthetic partner amplifies that momentum. This isn’t a panacea, but in the hands of a diligent team, 2-Methoxy-6-methyl pyridine acts more as a catalyst for innovation than a mere tool of convenience.
Early adopters found value quickly, but widespread uptake remains a work in progress. Wider testing in pharmaceutical and agrochemical development will likely push its profile higher. For synthetic teams willing to invest a bit of time in adapting procedures, significant gains in reliability and clean-up are within reach.
Chemistry educators could introduce students to this molecule as an example of why structural nuances matter. Walking through synthesis assignments that swap this variant for a more common pyridine brings home just how small changes on paper play out in real glassware.
Supplier engagement plays a role here, too. With labs demanding ever higher purity, readily available technical support, and real-world application notes, companies that respond proactively see greater loyalty from dedicated researchers. It's remarkable how much difference direct communication between labs and suppliers brings to the overall experience.
Selecting chemicals has always involved balancing price, performance, and availability. The story shifts, though, once genuine productivity gains come into play. By keeping an eye on the way 2-Methoxy-6-methyl pyridine performs in real scenarios, practitioners can tweak protocols with fewer missteps. The shared experience of colleagues, published results, and personal bench trials will keep shaping best practices around this compound.
While major, headline-grabbing discoveries may take time, the everyday impact already shows up in labs that learn to trust what this molecule brings to the table. As synthesis needs grow more sophisticated and regulations demand higher standards, compounds like 2-Methoxy-6-methyl pyridine will likely anchor a new wave of smarter, leaner chemistry.
Trusted reagents don’t get that way overnight. The climb comes from repeated, real-world success. 2-Methoxy-6-methyl pyridine has started to earn its place not just as another trading card in the chemical catalog, but as a go-to solution for researchers aiming for clear results and less hassle. The more project teams share stories about unexpected improvements and easier separations, the quicker the word spreads. For those willing to step outside the familiar, this compound offers a fresh take on what careful molecular design brings to the unpredictable world of benchwork. In the long run, small shifts make the biggest difference, and 2-Methoxy-6-methyl pyridine brings enough practical advantages to keep forward-thinking chemists coming back for more.