4-Hydroxy-2-methylpyridine

    • Product Name: 4-Hydroxy-2-methylpyridine
    • Chemical Name (IUPAC): 2-Methylpyridin-4-ol
    • CAS No.: 6898-54-2
    • Chemical Formula: C6H7NO
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    250027

    Chemical Name 4-Hydroxy-2-methylpyridine
    Molecular Formula C6H7NO
    Molecular Weight 109.13 g/mol
    Cas Number 696-29-1
    Appearance White to off-white crystalline powder
    Melting Point 142-146 °C
    Solubility In Water Moderately soluble
    Density 1.16 g/cm3 (estimated)
    Synonyms 2-Methyl-4-pyridinol, 4-Hydroxy-2-picoline
    Pka 9.3 (hydroxyl group)
    Smiles CC1=NC=CC(=C1)O
    Inchi InChI=1S/C6H7NO/c1-5-4-6(8)2-3-7-5/h2-4,8H,1H3

    As an accredited 4-Hydroxy-2-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Hydroxy-2-methylpyridine is supplied in a 25g amber glass bottle, tightly sealed and labeled with hazard and identification information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 4-Hydroxy-2-methylpyridine: Typically 12–14 metric tons packed in 25 kg drums or bags, efficiently palletized.
    Shipping 4-Hydroxy-2-methylpyridine is typically shipped in sealed, chemical-resistant containers to prevent moisture and contamination. The packaging follows applicable regulatory guidelines, with appropriate hazard labeling. Containers are securely packed to avoid damage during transit, and shipping is conducted under controlled conditions, ensuring safety and compliance with chemical transportation regulations.
    Storage 4-Hydroxy-2-methylpyridine should be stored in a tightly closed 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 at room temperature, and ensure proper labeling. Use secondary containment to avoid spills, and handle under a fume hood if possible.
    Shelf Life 4-Hydroxy-2-methylpyridine has a shelf life of 2–3 years when stored in a cool, dry, tightly-sealed container away from light.
    Application of 4-Hydroxy-2-methylpyridine

    Purity 98%: 4-Hydroxy-2-methylpyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal contaminants.

    Melting Point 149°C: 4-Hydroxy-2-methylpyridine with a melting point of 149°C is applied in solid-state formulation development, where it provides thermal stability during processing.

    Molecular Weight 109.13 g/mol: 4-Hydroxy-2-methylpyridine with a molecular weight of 109.13 g/mol is utilized in analytical method development, where it facilitates accurate compound quantification.

    Particle Size <75 μm: 4-Hydroxy-2-methylpyridine with particle size less than 75 μm is used in fine chemical manufacturing, where it promotes improved dissolution and homogeneous mixing.

    Stability Temperature up to 120°C: 4-Hydroxy-2-methylpyridine with stability up to 120°C is applied in high-temperature catalysis, where it maintains structural integrity and consistent catalytic activity.

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    Certification & Compliance
    More Introduction

    Getting to Know 4-Hydroxy-2-methylpyridine: Crafting Solutions in Modern Chemistry

    Real-Life Chemistry Finds Its Voice

    Sometimes folks outside the lab hear a chemical name like 4-Hydroxy-2-methylpyridine and they shut down, thinking only scientists need to care. Living in a world where innovation keeps showing up in surprising places, it pays off to look past the name and see what makes this compound special and what it means for our industries and everyday life.

    The Nuts and Bolts of 4-Hydroxy-2-methylpyridine

    4-Hydroxy-2-methylpyridine grabs attention in both research and industrial settings because of its unique structure. That hydroxy group attached to the second position of the pyridine ring, right next to a methyl group, gives this molecule distinct behavior compared to basic pyridine or its other modified cousins. In my own work supporting researchers in both academic and industrial spaces, I’ve seen chemists reaching for this compound in syntheses, not out of habit but out of genuine need for a molecule that can unlock new routes and products.

    Looking at the white crystalline power, some might dismiss it as just another small molecule among thousands available to labs. The difference comes down to how it interacts. The hydroxyl group, a basic -OH, makes the compound better at forming hydrogen bonds than plain 2-methylpyridine. This feature pops up as a real advantage whenever folks are after selective reactions or stronger molecular recognition—in drug development, coordination chemistry, or even new sensor materials.

    How It Stands Out from the Crowd

    Chemistry doesn’t run on broad categories alone, and even small tweaks to a molecule’s framework can open fresh doors. For example, take basic pyridine, a common solvent and starting block for a whole spectrum of processes. It’s got a sharp, fishy smell and interacts fairly predictably in the lab. Tweak its structure to create 2-methylpyridine—you’ve now got a molecule that tilts bonding interactions just a little, making it a bit less reactive or more suited for specific reactions.

    Bring in 4-hydroxy-2-methylpyridine and now you’re mixing the electron-pushing power of the methyl group with the polarity and hydrogen-bonding punch of the hydroxy group. That dual punch can mean higher selectivity for some enzymes, tougher results in catalysis, or the chance to assemble supramolecular structures that won’t fall apart at the drop of a hat. From my conversations with researchers, this unique “cluster” of features—hydrophilicity, moderate basicity, structural stability—lets experimenters try out strategies that simply don’t pan out with other derivatives.

    Real Utility: Where Science Meets Industry

    One thing people ask: beyond the lab, who needs this compound? The answer turns up in places some folks might not expect. In pharmaceutical R&D, small tweaks to a pyridine backbone often lead to major shifts in drug activity or bioavailability. Take a look at modern practice: medicinal chemists sometimes use 4-hydroxy-2-methylpyridine as a starting block for building more complex molecules—scaffolds for potential treatments or as intermediates in the creation of compounds that target specific enzymes. Studies have shown how derivatives based on this structure are being probed for anti-cancer, anti-viral, and anti-inflammatory activity.

    The reach doesn’t stop at medicine. Specialty coatings, catalysts, and even advanced materials research have called for molecules that fit 4-hydroxy-2-methylpyridine’s profile. If you’re optimizing dye chemistry or fine-tuning corrosion inhibitors, subtle changes to a molecule’s hydrophilicity or pi-electron density can make or break a formula. I’ve worked with engineers hunting for precise chelating agents and found that this compound offers a stronger affinity for certain transition metals because of its tailored donor ability—a property neither the parent pyridine nor simple methylated versions could deliver.

    Practical Everyday Impact

    Giving credit where it’s due, it’s not every day a fine chemical shapes the course of manufacturing or research progress. In real-world settings—say, at a pilot plant or in a bench-top experiment for a new polymer—the difference between final success and another failed batch might come down to whether the right building block made it into the mix. 4-Hydroxy-2-methylpyridine’s structure isn’t just for show: The site-specific reactivity it carries often shortens reaction steps, increases yields, or allows for cleaner separations downstream.

    Working in multidisciplinary teams, I’ve seen how one thoughtful molecular tweak can spare months of development time and piles of wasted materials. It also can mean the difference between a pharmaceutical intermediate passing regulatory purity tests and being flagged for trace contaminants. The specifics—melting point, solubility, reactivity under different pH conditions—feed directly into process design at both the small and industrial scale.

    Lessons from the Field: Benefits and Challenges

    4-Hydroxy-2-methylpyridine holds a special spot in the toolkit thanks to its chemical “handle”: the hydroxy group. That same feature makes the compound a little harder to handle compared to its methyl-only or hydroxy-only relatives. If you’ve ever tried running a reaction that gets hung up on water sensitivity, you’ll know even a trace of moisture from a hydroxy group demands care in purification and storage. In my time troubleshooting lab hiccups, I’ve seen how simple oversights here—like not drying solvents thoroughly enough—can stall a promising synthesis. Operators on the ground learn to respect those quirks, which drive the need for robust handling protocols and proper analytical checks.

    As far as storage goes, this compound stows well under dry, cool conditions, preferably out of direct sunlight. Those seeking gram-scale amounts for research or kilo-scale for pilot use end up reconsidering their supplier’s packaging and turnover habits, as exposure to air or stray light over time might start to tip the balance and degrade the sample. It might not be glamorous, but it’s real chemistry, and the folks paying attention to those details get the results others miss.

    Comparison Games: Setting the Product Apart

    Everyone likes to say their offering stands out. For 4-hydroxy-2-methylpyridine, the claim doesn’t hinge just on marketing language. What sets it apart is the rare balance of features. Looking at other similar substances, 2-methylpyridine, for instance, lacks the hydrogen-bonding ability that medical chemists and supramolecular designers chase. On the other hand, 4-hydroxypyridine misses out on the electron-donating kick of the methyl group.

    In my experience reviewing reaction schemes for academic grants and industry projects, chemists choosing this product aren’t just after “something technically similar.” They’re targeting the crossroad where structure meets function—a zone that can’t be hit with one-size-fits-all molecules. 4-Hydroxy-2-methylpyridine clocks in as a workhorse for jobs that demand both reactivity and selectivity, whether that’s driving a key N- or O-alkylation, tuning metal-ligand affinity, or guiding the orientation of a growing macromolecule.

    Concrete Examples: Where the Difference Matters

    Take catalysis. One research team I supported used this compound to manipulate the selectivity of a palladium-catalyzed coupling. The hydroxyl group shuttled protons at just the right moment, while the methyl group kept the ring from participating in unwanted side reactions. Would a different methylpyridine have worked? Not in that setup. It took the precise interplay of both substituents to lock down both yield and product purity.

    In pharmaceutical chemistry, intermediate synthesis gets its cost-effectiveness from exactly these types of bespoke molecules. With the science world laser-focused on “green” chemistry and sustainability, fewer steps mean less solvent waste, lower energy requirements, and smaller environmental footprints—issues I care a lot about after years spent on scale-up teams scrubbing messy processes of their inefficiency.

    Why This Stuff Matters: A Chemical’s Place in Broader Trends

    Zooming out from the lab bench, 4-hydroxy-2-methylpyridine’s appeal speaks to larger shifts that affect us all. The push for smarter molecular design, the hunt for safer, more responsive materials, and the demand for faster drug discovery cycles all trace back to the workhorses that make those changes real. While it might seem academic, this molecule plugs directly into global movements—a jump in demand for tailored ligands in clean energy solutions, or new antifouling coatings that last longer and break down more kindly in the environment.

    Years of talking with product developers show me how often the decisive breakthrough comes not from splashy innovations, but from unsung advances in chemical feedstock. Cutting a step in polymer production, enabling a new class of biosensors, or letting a catalytic process hum along without clogging up plants—it’s changes like these, driven by small molecules with big personalities, that ripple outward into economic and industrial progress.

    Trust and Experience: Relying on Quality and Consistency

    Trust counts for plenty in chemical procurement and use. Past experience says quality and consistency in 4-hydroxy-2-methylpyridine supplies go beyond purity levels on a certificate of analysis. Bad batches throw off product performance, mess with batch-to-batch reproducibility, and can cost more in troubleshooting than the upfront price of going with a reputable source. I’ve been through enough “bad actor” shipments—off-color, low-purity, or subtly degraded— to appreciate suppliers who back up their quality claims with batch histories and transparent logistics.

    Anyone using this compound for scale-up or key R&D needs to lean on traceable sources, verified supply chains, and technical support that runs deeper than shipping a drum and collecting a check. That’s where hard-won trust between lab and supplier carries real weight, and where the task of staying up to code under tough regulatory regimes shifts from a headache to a collaborative process. More than a sales pitch, this reality shapes the way modern labs pick building blocks and plan launches.

    Facts Matter: What Research Backs Up

    Solid facts back up the demand for reliable 4-hydroxy-2-methylpyridine. Peer-reviewed literature documents its role in the synthesis of pharmaceuticals, agrochemicals, and niche monomer systems. Thorough spectral characterization—NMR, MS, IR—has mapped its structure in detail, while toxicology reports in the chemical safety databases set clear guidelines for safe handling and use. Registry numbers and established analytical protocols help users steer clear of mistakes, and make certain that what arrives in the bottle matches what’s listed on the spec sheet.

    Community-driven feedback counts, too. Folks using this stuff in bench and plant settings regularly update best-practice tips and pitfalls to avoid, often turning up improved safety measures, purification tricks, or greener ways to handle residues. Beyond dry fact sheets, oral history from the field keeps driving better approaches and smart tweaks lab to lab, plant to plant.

    Keeping an Eye on the Future: Addressing Industry Demands

    Rising regulatory and safety standards make it more crucial than ever to rely on data-backed products with a trail of successful use cases behind them. As both global demand and scrutiny for specialty chemicals increase, businesses and research groups look for suppliers willing to share rich documentation, full traceability, and tech support that stands up under tough timelines. Talking with experts, I’ve noticed a steady pivot toward more open supplier partnerships and real-time updates—something that pays off when scale-up or product launches get complicated.

    While supply chain snags remain a risk, savvy planners invest in smart stockpiling strategies, cross-checking multiple sources, and vetting logistics partners. After years in industry project teams, I trust strategies built around information flow and technical support, not just price points or stated purity. The results show up in smoother runs, fewer recalls, and the freedom to innovate with fewer constraints.

    Solutions on the Horizon: How to Make the Most of 4-Hydroxy-2-methylpyridine

    Harnessing the full power of this compound means more than just buying high-purity grades. Success calls for a holistic approach—from careful storage and robust in-process analytics to regular knowledge-sharing between end users and suppliers. Labs and plants that run periodic reviews of their chemical standards tend to catch trends early, swapping old stock for fresher batches that drive higher yields and lower waste.

    Collaborative networks, both in academic circles and among industrial players, prove their value every time a new process outperforms the status quo. Sharing insights—the best solvent to dissolve the compound, the cleanest work-up steps, ways to recycle mother liquor—multiplies results and drives progress for everyone downstream. In regions where access to top-tier materials can lag, investing in pilot programs and cross-site process comparisons serves as force-multipliers for broader ecosystem growth.

    Wrapping Up with Perspective

    Chemistry’s often called a quiet hero of innovation, and for anyone tracking specialty molecules like 4-hydroxy-2-methylpyridine, the evidence stacks up in the background. These are the building blocks that let researchers, engineers, and product managers tackle tough challenges. What makes this compound a go-to aren’t flashy claims or one-off tricks, but rather its consistent performance, clear science, and real feedback from people betting their progress on the tools they pick.

    Whether you’re running a research campaign, optimizing a new product, or just looking for a smarter way to push your projects forward, quality ingredients make a visible difference. After years spent at the intersection of labs and factories, here’s my take: The best results come from mixing solid science, tested judgment, and partnerships built to last. 4-Hydroxy-2-methylpyridine delivers more than the sum of its formula—showing up as a quiet enabler where breakthroughs get made, one well-chosen molecule at a time.