|
HS Code |
343120 |
| Compound Name | 6-Methylpyridine-3-methanol |
| Molecular Formula | C7H9NO |
| Molecular Weight | 123.15 g/mol |
| Cas Number | 23600-16-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 240-242 °C |
| Density | 1.087 g/cm3 |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.539 |
| Smiles | CC1=NC=CC(CO)=C1 |
| Inchi | InChI=1S/C7H9NO/c1-6-2-3-7(5-9)4-8-6/h2-4,9H,5H2,1H3 |
As an accredited 6-Methylpyridine-3-methanol 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 6-Methylpyridine-3-methanol, sealed with a screw cap and labeled with safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 6-Methylpyridine-3-methanol securely packed in drums, stacked efficiently to maximize 20-foot full container load capacity. |
| Shipping | 6-Methylpyridine-3-methanol is shipped in secure, airtight containers to prevent leakage and contamination. It must be stored away from heat, sparks, and open flames, in a cool, well-ventilated area. Proper hazard labeling and accompanying safety documentation (such as SDS) are provided, ensuring compliance with relevant chemical transportation regulations. |
| Storage | Store **6-Methylpyridine-3-methanol** in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight, sources of ignition, and incompatible substances such as strong oxidizers and acids. Ensure the storage area is equipped with proper spill containment and that the container is clearly labeled. Follow all relevant safety and regulatory guidelines for handling and storage. |
| Shelf Life | 6-Methylpyridine-3-methanol should be stored tightly sealed, away from light and moisture; typical shelf life is 2-3 years. |
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Purity 98%: 6-Methylpyridine-3-methanol with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation. Molecular Weight 123.16 g/mol: 6-Methylpyridine-3-methanol of molecular weight 123.16 g/mol is used in organic synthesis processes, where precise molecular incorporation guarantees consistent formulation quality. Melting Point 54°C: 6-Methylpyridine-3-methanol with a melting point of 54°C is applied in catalyst preparation, where it enables controlled melting for uniform mixing. Stability Temperature Up to 120°C: 6-Methylpyridine-3-methanol stable up to 120°C is used in high-temperature polymerization reactions, where it maintains chemical integrity during processing. Particle Size <10 μm: 6-Methylpyridine-3-methanol with particle size less than 10 μm is utilized in fine chemical manufacturing, where enhanced dispersion increases reaction efficiency. Viscosity 1.2 mPa·s: 6-Methylpyridine-3-methanol at viscosity 1.2 mPa·s is used in specialty coating formulations, where optimal flow properties improve surface uniformity. Refractive Index 1.506: 6-Methylpyridine-3-methanol with a refractive index of 1.506 is used in optical material synthesis, where it contributes to precision light transmission characteristics. Water Content <0.5%: 6-Methylpyridine-3-methanol with water content below 0.5% is used in moisture-sensitive reactions, where low water levels reduce side reactions and byproducts. Assay ≥99%: 6-Methylpyridine-3-methanol with assay not less than 99% is used in analytical reference standards, where high assay guarantees measurement accuracy. pH (5% Solution) 7.5: 6-Methylpyridine-3-methanol in a 5% solution at pH 7.5 is used in biochemical assay preparations, where neutral pH ensures compatibility with sensitive biological systems. |
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Over the years, chemistry has opened doors to thousands of compounds that keep the world of industry and research spinning. Among these, 6-Methylpyridine-3-methanol stands out as a dependable specialty chemical. This compound, bearing a distinctive pyridine ring with a methyl group and a methanol moiety, stands apart due to its balanced molecular profile and broad application range. Some might see it as just another laboratory reagent, yet its unique blend of structure and function places it on a higher tier for demanding processes in pharmaceuticals, fine chemicals, and advanced materials research.
Anyone with a background in synthetic organic chemistry recognizes the value of precision. 6-Methylpyridine-3-methanol answers those requirements by offering a composition that lends itself well to targeted transformations. Its chemical structure, where a methyl group perches on the six position of the pyridine ring while a hydroxymethyl arm extends from the three position, makes it more than a sum of its parts. This arrangement encourages selective reactivity, opening the way for chemists to design syntheses that lower unwanted side products. For me, as someone whose early lab days often lined up glassware with uncertain results, the benefit of a well-characterized intermediate like this is clear: less guesswork, more reproducibility. In my experience, compounds engineered with clear functionalization save both time and troubleshooting headaches.
Specifications matter too, and product consistency sits close to the top of any chemist’s wish list. 6-Methylpyridine-3-methanol can arrive in highly pure forms, supporting reliable batch-to-batch performance. Anyone managing the syntheses of active pharmaceutical ingredients knows the chaos that can result from impurities. Trace byproducts, even in minute levels, can sideline an entire project by complicating purification steps or, worse, triggering regulatory red flags. That’s why the documented chemical specifications—boiling point, melting point, and spectral purity—aren’t bureaucratic details for a safety sheet. They are assurances for anyone seeking high-fidelity results.
Compound libraries in pharmaceutical research expand rapidly, but finding the right building blocks is a careful balancing act. Medicinal chemists turn to 6-Methylpyridine-3-methanol when they want to diversify their molecular scaffolds without sacrificing predictability. It fits seamlessly into synthetic routes leading to drugs that require a robust, aromatic core, especially where pyridine derivatives have shown therapeutic promise. For anyone who has navigated the challenging path of hit-to-lead optimization in drug discovery, precise intermediates like this one feed the creative process while keeping a tight rein on unwanted complexity.
Beyond pharmaceuticals, fine chemical manufacturers have found value in leveraging this compound’s unique functional groups. Its dual composition—a nitrogenous heterocycle and an alcoholic group—supports a wide array of downstream modifications, such as esterifications or coupling reactions. It’s this versatility that keeps 6-Methylpyridine-3-methanol on the shortlist for those working in custom synthesis and process development environments. Years ago, I watched a team avoid weeks of failed experiments by shifting their starting material to one just like this—precision paid dividends then, and still does now.
The kingdom of pyridine derivatives is broad, with compounds like 4-methylpyridine and 3-hydroxymethylpyridine claiming their own slice of the chemistry world. Yet, 6-Methylpyridine-3-methanol offers something neither can fully replicate: a strategic placement of functional groups. While positional isomers may look similar on paper, chemists learn that shifting a methyl group from the three position to the six can create entirely different reaction outcomes. This can mean the difference between a clean synthetic route and a scramble to purify a stubborn byproduct.
For example, substituents at the three position may meddle with the nucleophilicity of the ring or block key reaction sites. Conversely, the six position’s methyl group keeps out of the way in many palladium-catalyzed couplings but still modulates electronic effects, tuning reactivity just so. The methanol group, anchored to the same ring but away from that methyl, further increases the compound’s potential, providing an easy handle for further transformation. From my own hands-on experience in route scouting, starting with the right pyridine isomer can cut down more than reaction steps—it sidesteps unforeseen complications that lead nowhere.
Digging into practical applications, 6-Methylpyridine-3-methanol finds itself indispensable in laboratories looking for both performance and adaptability. I still remember the day a colleague, deep in fragment-based drug design, needed a reactive but manageable starting point. His route failed repeatedly with related pyridines; the answer only emerged after switching to the six-methyl, three-methanol framework. The compound’s reliable physical properties—solubility in common organic solvents, controlled volatility—meant an easier time during workup and purification. Those details matter when deadlines close in and project budgets strain at the seams.
In newer fields like materials science, researchers rely on the unique mix of aromatic stability with modifiable sites for constructing new polymers and electronic materials. That dual nature is the calling card for 6-Methylpyridine-3-methanol. Its structure encourages innovation and reduces the friction that comes from using less accommodating analogues. For synthesis teams tasked with creating complex ligands or molecular sensors, that flexibility opens up routes which might otherwise stay theoretical.
In the chemical supply world, purity tells more than just a number—it reveals a supplier’s commitment and can shape research outcomes months down the line. Recollections of working through contamination incidents have made one thing very clear to me: the extra dollar spent on a well-vetted product is cheap insurance against mishaps. High-purity 6-Methylpyridine-3-methanol lasers in on that promise. Analytical teams lean on HPLC and NMR data not to dot bureaucratic i’s, but to keep projects on track and protect future reproducibility.
Many who have run scale-ups from milligrams to kilograms recognize how small issues during the research phase can snowball. If you’ve ever run a gram-scale reaction only to be blindsided by impurity spikes at the kilo level, you already know that bad starting material is more than a minor inconvenience. Reliable chemical specifications set a foundation for everything upstream and downstream—from reaction design to regulatory filings in pharmaceutical development.
Individuals in today’s research landscape feel the weight of both progress and responsibility. 6-Methylpyridine-3-methanol, like many of its peers, underscores this with its manageable safety profile. Safe handling guides rest not just on paperwork, but on real experiences: correct storage conditions, protective equipment, and spill protocols. While not the harshest chemical one can find in a lab, it commands respect like any concentrated organic substance.
Chemists aiming for greener synthesis appreciate compounds that can be readily incorporated into efficient, high-yield routes. Waste minimization starts with choosing starting materials and intermediates wisely. By anchoring synthetic steps to reliable, clean compounds, downstream processing stays simpler and emissions fall. Even beyond compliance, that culture of responsibility benefits everyone—from the research student learning best practices to the communities living near manufacturing plants.
No laboratory or factory wants to repeat work through inefficiency or unforeseen delays. Material choices have major downstream impacts. Selecting a compound like 6-Methylpyridine-3-methanol often leads to fewer purification cycles, less wasted effort, and quicker delivery on promised timelines. Over long projects, that efficiency compounds itself, turning small decisions into significant returns.
Project managers who measure every cost understand instinctively that reliable inputs safeguard investments. Impurities found late in the development cycle can lead to expensive investigations and, in the worst case, regulatory setbacks. 6-Methylpyridine-3-methanol proves itself by reducing such risks while supporting process intensification initiatives that many modern pharmaceutical and specialty chemical operations aim for.
Complex chemistry always carries some degree of unpredictability. Some laboratories express concerns about the availability and long-term stability of certain intermediates, especially specialty compounds with a limited number of manufacturers. I’ve seen projects pause, not due to a failed experiment, but because a critical reagent fell out of stock or purity dropped unexpectedly.
Solutions to these issues are within reach. Partnerships between researchers and chemical suppliers strengthen supply chains and improve forecasting accuracy. Open dialogue around projected usage patterns equips suppliers to scale production responsibly. On the laboratory end, stockpiling chemicals with long shelf lives and clearly monitoring expiry dates ensures that research continues even as outside variables shift. For those with experience negotiating these landscapes, clear communication and advance planning are the tools that keep projects on stable footing.
Trust rarely comes from claims alone. Those of us who have managed large teams or training programs in chemical sciences know that reputation builds project by project, not by word of mouth or a glossy brochure. Suppliers that provide complete documentation—including detailed analytical reports, safety data, and transparent sourcing—make life smoother on the receiving end. Pharmaceutical auditors and grant reviewers will ask for evidence, and rightly so.
Within the research community, people tend to share feedback, both positive and negative. Products like 6-Methylpyridine-3-methanol earn their standing not through marketing, but from dependable performance in diverse, demanding settings. As an example, chemists logging notes on successful scale-ups or challenging transformations become informal references—the kind of verification regulators and collaborators look for.
Fields such as medicinal chemistry don’t stay static. Each year brings new disease targets, new therapeutic hypotheses, and, with them, new demands for building blocks that accommodate creative designs. The flexibility and precise reactivity profile of 6-Methylpyridine-3-methanol enables the exploration of fresh synthetic territory. Teams developing next-generation antibiotics, antivirals, or enzyme inhibitors will naturally gravitate toward intermediates with a proven track record and established handling profiles. While the compound supports today’s innovations, its structure remains open to tomorrow’s new uses.
Collaborations with academic and industrial researchers often yield the most productive pathways for applying molecules like 6-Methylpyridine-3-methanol. Shared data on reaction outcomes, process improvements, and analytical challenges accelerates collective learning. In my professional journey, having access to published application notes or post-market surveillance has turned difficult projects around, saving both time and doubt.
Pharmaceutical and specialty chemicals face an ever-rising bar for regulatory scrutiny. Regulatory agencies worldwide expect documentation not just of final products, but of every key intermediate touching the manufacturing pipeline. 6-Methylpyridine-3-methanol, with its consistently reported analytical profiles, fits neatly within this landscape. Well-prepared documentation satisfies both auditors and development scientists who later need that information to justify changes or respond to inquiries.
Experiences handling regulatory submissions have shown me how even a single ambiguous data point on a vital intermediate can stall an otherwise promising drug candidate. Rigorous traceability in the supply chain, thorough batch-wise analytics, and clear labeling practices help everyone avoid unpleasant surprises. The time saved by having validated data on hand cannot be overstated.
As more sectors adopt green chemistry principles, the spotlight will only intensify on those intermediates that promise lower energy consumption, higher atom economy, and safer profiles. For those actively shifting their synthetic strategies toward sustainability, compounds like 6-Methylpyridine-3-methanol reward those choices with routes that create less waste and consume fewer resources. In some projects, simply switching to a purer, more suitable intermediate eliminated multiple steps devoted to remediation and cleanup.
Looking ahead, the chemical industry’s shared responsibility will hinge on transparent partnerships with end-users, focusing not just on product availability but on responsible stewardship. The legacy of 6-Methylpyridine-3-methanol, as with other specialty reagents, will be measured as much by its contributions to streamlined, environmentally conscious science as to its technical achievements.
Bringing new scientists into the fold means more than teaching protocol—it carries the duty of highlighting why certain choices matter. Walking students through real-life reaction design featuring 6-Methylpyridine-3-methanol gives them practical experience navigating challenges and recognizing value in thoughtful material selection. For many first learning the ropes, abstract molecular diagrams only carry so far; seeing how careful intermediate choice unlocks smoother downstream chemistry leaves a lasting impression.
Mentoring younger peers in the lab has underscored that the best technical education happens through project work and discussion. Encouraging questions about why a compound with a methyl group on one part of the ring behaves so differently than its near-twin broadens perspectives. In the long run, developing this scientific intuition ensures that tomorrow’s discoveries rest on solid, well-informed foundations.
6-Methylpyridine-3-methanol reflects more than molecular finesse. It represents thoughtful design, consistent performance, and trust earned through countless experiments and industrial applications. The context in which it thrives—innovation, safety, sustainability—will continue to raise the bar for chemical intermediates. Future breakthroughs will rest on the trust nurtured in today’s supply chain and the wisdom shared by the scientists working at the bench. In the world of specialty chemicals, reliability remains the real catalyst for progress.