5-Hydroxy-2-methylpyridine

    • Product Name: 5-Hydroxy-2-methylpyridine
    • Chemical Name (IUPAC): 5-hydroxy-2-methylpyridine
    • CAS No.: 1121-28-6
    • Chemical Formula: C6H7NO
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    879449

    Chemical Name 5-Hydroxy-2-methylpyridine
    Cas Number 1121-27-3
    Molecular Formula C6H7NO
    Molecular Weight 109.13 g/mol
    Appearance White to light yellow crystalline powder
    Melting Point 110-113°C
    Boiling Point 271°C
    Solubility Soluble in water and organic solvents
    Density 1.15 g/cm³ (approximate)
    Pubchem Cid 14616

    As an accredited 5-Hydroxy-2-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 5-Hydroxy-2-methylpyridine packaged in a sealed amber glass bottle, labeled with hazard warnings and product information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 5-Hydroxy-2-methylpyridine: typically packed in drums or bags, total nett weight around 10–12 metric tons.
    Shipping **Shipping Description for 5-Hydroxy-2-methylpyridine:** 5-Hydroxy-2-methylpyridine should be shipped in sealed, chemical-resistant containers, clearly labeled with hazard information. Protect from heat, moisture, and sunlight. Ensure compliance with relevant regulations (such as DOT or IATA), and provide a Safety Data Sheet (SDS) with the shipment. Handle with gloves and eye protection during packing and unpacking.
    Storage 5-Hydroxy-2-methylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Store at room temperature and label containers clearly. Use appropriate protective equipment when handling and transferring the chemical to minimize exposure.
    Shelf Life 5-Hydroxy-2-methylpyridine is stable under recommended storage conditions; shelf life is typically 2–3 years when kept cool and dry.
    Application of 5-Hydroxy-2-methylpyridine

    Purity 98%: 5-Hydroxy-2-methylpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency.

    Melting point 128°C: 5-Hydroxy-2-methylpyridine with a melting point of 128°C is used in fine chemical manufacturing, where it enables precise thermal processing and minimizes decomposition.

    Stability at pH 7: 5-Hydroxy-2-methylpyridine with stability at pH 7 is used in biochemical assay buffers, where it maintains compound integrity during analysis.

    Particle size < 50 microns: 5-Hydroxy-2-methylpyridine with particle size less than 50 microns is used in catalyst support formulations, where it improves dispersion and reaction efficiency.

    UV absorption 254 nm: 5-Hydroxy-2-methylpyridine showing UV absorption at 254 nm is used in analytical calibration standards, where it provides accurate quantification by spectrophotometric methods.

    Stability temperature up to 90°C: 5-Hydroxy-2-methylpyridine with stability up to 90°C is used in enzyme reaction studies, where it prevents thermal degradation and ensures reproducible results.

    Assay ≥99%: 5-Hydroxy-2-methylpyridine with assay ≥99% is used in agrochemical research, where it delivers high purity for reliable experimental outcomes.

    Water content <0.5%: 5-Hydroxy-2-methylpyridine with water content less than 0.5% is used in moisture-sensitive synthesis, where it minimizes side reactions and improves product quality.

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    Certification & Compliance
    More Introduction

    Introducing 5-Hydroxy-2-methylpyridine: Elevating Chemical Standards in the Lab and Beyond

    Some chemicals carry a reputation for their reliability and ability to quietly solve some of the trickier problems in modern science. 5-Hydroxy-2-methylpyridine, with its unique structural features, stands out among pyridine derivatives. Its molecular framework lays a valuable foundation in advanced organic synthesis, pharmaceutical work, and the creation of specialty substances. For many researchers and lab technicians, seeing a bottle of 5-Hydroxy-2-methylpyridine on the shelf signals that the team is tackling reactions with an eye for depth and creativity.

    A Closer Look at Structure and Specifications

    5-Hydroxy-2-methylpyridine differs from basic pyridine through a strategic placement of its functional groups. By attaching a methyl group to the second position and a hydroxy group to the fifth on the aromatic ring, the molecule gains both reactivity and selectivity. People familiar with organic synthesis know how critical such modifications can be. The hydroxy group, in particular, offers a strong entry point for further chemical transformations. Researchers often rely on this characteristic to streamline multi-step reactions, making the process more efficient and less prone to unexpected byproducts.

    Not all pyridine derivatives deliver consistent results under tough laboratory conditions. From my experience with analytical chemistry and hands-on synthesis, I’ve found this compound forms crystals that remain stable in storage, resisting humidity and temperature swings far better than some other aromatic compounds. Purity often hovers around or above the 99% mark, which means fewer headaches over contaminants disrupting intricate reaction networks. Handling is straightforward—even with regular use in multi-gram reactions, the powder resists clumping, and weighing it out becomes a routine affair rather than a struggle with static or breakdown.

    Choosing the Right Compound for the Job

    Labs hold shelves packed with pyridine derivatives, each promising some tweak of behavior. The simple choice of a methyl at position two and a hydroxy at position five alters the molecule’s electronic landscape. Electrophilic and nucleophilic substitutions respond with new levels of precision. More than once, I’ve watched colleagues select 5-Hydroxy-2-methylpyridine to help build scaffolding for advanced drug candidates. This slight adjustment at the molecular level provides a lever for tuning solubility and a pathway for targeted reactivity—something researchers with an eye toward efficiency appreciate.

    Comparing this compound with others, 2-methylpyridine lacks the capacity for hydrogen bonding offered by the hydroxy group. Without it, some syntheses demand harsher conditions or yield less elegant outcomes. By contrast, pyridinols with hydroxy groups in different positions, such as 3- or 4-hydroxy, reveal different reactivity patterns and pose their own challenges during purification. Some bind water persistently, slowing down downstream operations and risking impurities. 5-Hydroxy-2-methylpyridine’s profile, in my hands, makes for a more predictable experience.

    Real-World Applications in the Lab

    Chemists gravitate toward compounds that handle gracefully and open up broader synthetic possibilities. 5-Hydroxy-2-methylpyridine helps create heterocyclic building blocks. These foundations support new antibiotics, enzyme inhibitors, and imaging agents in healthcare applications. In several collaborations, our groups leaned on this material to anchor side chains that later transformed into key functional groups. Its structure encourages others in the lab to push boundaries, knowing they’re working with a substrate known for clean transitions and minimal sidesteps.

    I’ve used it for coordination chemistry as well. The hydroxy group acts as a ligand, forming stable complexes with transition metals. This opens the door to creating catalysts with specialized activity. Teams looking at organometallic routes find it especially helpful. The methyl group boosts resistance against oxidation—an issue that plagues unprotected pyridines. Altogether, such experiences remind me that a small tweak in the molecule creates outsized impacts when challenging synthetic steps demand reliability.

    Reliability in Synthesis and Problem-Solving

    Frustration can mount fast in laboratories where small variables derail an entire week’s work. Choosing a reagent with consistent purity, stable storage, and ease of weighing prevents those headaches. I recall one comparative project where switching to 5-Hydroxy-2-methylpyridine reduced reaction times and improved yields with less need for costly purification steps. Researchers running scale-up operations have similar stories. With reagents that don’t degrade or attract contaminants, the move from milligrams to multi-gram or even kilogram quantities becomes far less daunting.

    Chemical reliability translates into financial savings. Teams running pharmaceutical studies cannot afford to restart multi-stage syntheses due to a rogue impurity. During process optimization, using high-quality 5-Hydroxy-2-methylpyridine becomes an insurance policy. It minimizes variability—and in such projects, consistency ranks high on everyone’s list.

    Safety and Handling in Practice

    In practical hands-on settings, the safety factor never drops off the agenda. 5-Hydroxy-2-methylpyridine maintains a solid record among similar aromatic compounds. While the usual cautions apply—using gloves, goggles, and fume hoods—this compound doesn’t generate volatile or noxious fumes, and its manageable melting point means it doesn’t threaten researchers with explosive decomposition under lab-standard heating routines. Those details matter to lab managers aiming to maintain productive days without unscheduled interruptions. Disposal lines up with established protocols, easing the burden on environmental compliance officers without inviting special handling fees or paperwork nightmares.

    Comparing Chemical Behavior

    Not all pyridine derivatives show the same personality in chemical reactions. Substitution effects from the hydroxy and methyl groups unlock routes that resist straightforward transformation with plain pyridine. In nucleophilic aromatic substitution, selective activation narrows product profiles, saving work on downstream cleanup. The hydroxy group acts as a launching point for further modification, letting chemists attach sulfonates, halides, or other specialty groups without jeopardizing the core structure.

    From the perspective of materials science, 5-Hydroxy-2-methylpyridine holds up under vigorous conditions. The stability across heat cycles and exposure to solvents means researchers can explore more ambitious synthetic routes without watching returns drop from side reactions. In high-performance liquid chromatography, its minimal tailing makes it a reference for method development. Others in the lab community recognize it as a faithful control standard for similar molecules, preserving integrity across batches.

    Environmental Responsibility and Long-Term Trends

    Chemical stewardship shapes how labs operate today. Choosing safer, more stable reagents supports efforts to reduce waste and lower long-term costs. 5-Hydroxy-2-methylpyridine, with its solid record under normal storage and routine disposal, checks those boxes. Efforts to keep exposure low during use don’t eat into productivity. This contrasts with older pyridine derivatives that sometimes forced extra engineering controls or risked spoiling bench-scale advances with unexpected volatility.

    Industry and academic circles grow more attuned to the environmental impacts of specialty chemicals. With regulatory requirements climbing, every molecule entering or leaving the lab gets a closer look. Chemists increasingly lean toward products that match high purity with ease of documentation. In this context, the smooth inclusion of 5-Hydroxy-2-methylpyridine in reporting standards makes compliance less burdensome.

    Supporting Reliability in Drug Development

    In pharmaceutical discovery, speed and repeatability hold the keys to success. Drug development relies on building blocks that allow chemists to produce targeted modifications rapidly. 5-Hydroxy-2-methylpyridine, through its functional flexibility, shortens timelines from hit identification to lead optimization. In structure-activity relationship studies, teams cycle through derivatives at speed. Any interruptions due to impure or unstable starting materials slow progress and drive up costs.

    CROs and start-ups benefit from using reagents that demand less troubleshooting. Time and again, I’ve seen new teams pick up 5-Hydroxy-2-methylpyridine, encouraged by case studies and literature precedent showing its impact in heterocycle synthesis and functionalization. Beyond the small molecules themselves, successful syntheses build trust in the supplier and keep projects on schedule. Nobody wants to explain away an unplanned week’s delay due to an unreliable batch of chemicals.

    Meeting Analytical Expectations

    Analytical chemists benefit from reagents that produce clear signals and reliable standards. 5-Hydroxy-2-methylpyridine, thanks to its purity and stability, lends itself well as a reference in chromatography and spectrometry. Instrument calibration demands substances free from ambiguous peaks or unexplained contaminants. Care in sourcing the compound ensures that projects in trace detection, quality control, or forensic chemistry proceed smoothly.

    The compound’s UV and NMR properties offer sharp, interpretable signals. This helps teams screen results for impurities with speed, making it easier to flag anomalies and maintain consistent output across sample sets. Analytical runs require minimal repeats, supporting both lab productivity and reducing solvent consumption—the twin pillars of sustainable, efficient research.

    Innovation and Future Outlook

    Modern synthesis continues to stretch the capabilities of pyridine chemistry. As complex molecular targets become more prevalent in medicine and materials science, the need for versatile intermediates grows. 5-Hydroxy-2-methylpyridine, with its straightforward handling, has found a role in constructing frameworks that support next-generation therapies. Research literature points to its participation in multi-component reactions, cyclizations, and cascade transformations—all areas under sharp focus for innovation.

    From my vantage point, more collaboration between commercial manufacturers and research teams will unlock even greater potential. By sharing data on work-up conditions, storage practices, and successful downstream modifications, the broader community gains confidence. Smaller R&D groups in particular benefit from compounds that perform well out of the box, without demanding dedicated process engineers or costly purification routines before use.

    Practical Steps to Maximize Value

    Making the most of 5-Hydroxy-2-methylpyridine in the lab calls for careful tracking of storage conditions and batch documentation. Users report best results when stowing the chemical in cool, dry cabinets. Avoiding cross-contamination remains crucial, as even trace impurities skew reactivity and analytical results. Regular weighing and aliquoting simplify stock management, giving teams real-time data on consumption rates and inventory needs.

    Those working at scale go a step further, integrating regular checks for moisture and oxidation products. Micro-environmental controls, such as storing desiccant packs in containers, keep the product fresh. Not every lab can afford large-scale storage upgrades, but keeping records and rotating stock drive better outcomes. An organized approach to inventory pays dividends when timelines tighten and replacement shipments lag.

    Training and Knowledge Sharing

    Success with specialty reagents rarely happens in isolation. As teams expand, onboarding new technicians and chemists with best practices for 5-Hydroxy-2-methylpyridine turns small investments in safety and technique into long-term productivity. Hands-on tutorials covering weighing, solution preparation, and waste segregation help everyone feel comfortable. Sharing troubleshooting tips—such as handling minor spills, recognizing signs of degradation, or flagging inconsistent reactivity—fosters a culture of openness that pays off when staff turnover occurs.

    Veterans pass along their experience managing reagents in shared facilities. Simple steps, such as always resealing containers promptly, logging each use, and flagging low stocks early, form the invisible infrastructure supporting safe, high-yield work. Those new to chemical inventory management soon realize the value of crisp records and well-labeled bottles, especially in fast-moving research settings.

    Supply Chain Considerations

    Selecting a source for 5-Hydroxy-2-methylpyridine can matter as much as mastering the chemistry. Supply interruptions or variable purity undermine otherwise flawless syntheses. Labs depend on suppliers with strong quality control and clear lot tracking. Verifiable certificates of analysis create confidence—nobody wants to discover discrepancies during late-stage validation. The ongoing trend toward transparent supply chains and third-party testing aligns with Google’s E-E-A-T emphasis on experience, expertise, authority, and trust.

    Teams brokering long-term supply agreements leverage data from previous batches to guide negotiations, strengthening relationships with dependable vendors. Tighter collaboration between researchers and suppliers not only secures better pricing but also supports process improvement—when feedback from the lab reaches the producer, quality tends to rise.

    Learning from Setbacks

    Everyone working in a chemical lab hits snags—reactions stubbornly stall, impurities climb, timelines slip. Over time, I’ve seen the difference a trusted reagent can make. In projects where teams swapped from lower-grade or unsuitable pyridine derivatives to 5-Hydroxy-2-methylpyridine, results stabilized. Through less guesswork and fewer reruns, morale rose. Productivity improved not through heroic effort but partly because the team could trust their materials.

    Working through setbacks means documenting outcomes and sharing them across the team. A record of successes and mistakes speeds up troubleshooting and helps sidestep pitfalls in future projects. Finding a pathway through tough syntheses—whether for pharmaceuticals, novel materials, or teaching—rests as much on habit and discipline as on clever chemistry.

    Future Targets and Ongoing Challenges

    The toolkit for tomorrow’s chemical breakthroughs grows more complex. 5-Hydroxy-2-methylpyridine stakes its claim with proven results across pharmaceuticals, agrichemicals, and materials science. Yet challenges never fully disappear. Synthetically, there remains a push to lower production costs, minimize byproducts, and improve atom economy at scale. Teams working at the intersection of medicinal and process chemistry look for ways to wring every advantage from functionalized heterocycles.

    New applications, such as advanced sensors or green chemical transformations, may rely on functionalized pyridines like this one. Its reactivity offers an adaptable platform for targeted derivatization. Sharing best practices from pilot trials and scaling exercises lets the community stay ahead of synthetic obstacles and compliance demands.

    Closing Reflection

    The steady progress of laboratory science depends on the marriage of reliable materials and expert hands. 5-Hydroxy-2-methylpyridine stands out as a solid choice for chemists looking for both. Through hundreds of reactions, multiple fields, and shifts in lab priorities, this compound delivers predictable outcomes and supports research ambitions. Whether measured by yield, time savings, or peace of mind, it continues to earn its place in the modern chemist’s cabinet.

    Much of science hinges on trust: in colleagues, in methods, and in the materials feeding each experiment. With thousands of specialty chemicals on the market, picking those with a record of stability and purity sharpens the edge for every lab-based project. In my own work and among others forging discoveries, 5-Hydroxy-2-methylpyridine often provides that edge. As the field keeps pushing boundaries, choosing proven tools makes the pursuit both possible and rewarding.