|
HS Code |
596464 |
| Cas Number | 1121-22-8 |
| Molecular Formula | C6H7NO |
| Molecular Weight | 109.13 g/mol |
| Iupac Name | 2-methyl-6-hydroxypyridine |
| Appearance | White to beige solid |
| Melting Point | 120-124 °C |
| Boiling Point | Unknown, decomposes |
| Solubility In Water | Slightly soluble |
| Pubchem Cid | 11809 |
| Smiles | CC1=NC(=CC=C1)O |
| Inchi | InChI=1S/C6H7NO/c1-5-3-2-4-6(8)7-5/h2-4,8H,1H3 |
| Synonyms | 6-Hydroxy-2-picoline |
As an accredited 2-Methyl-6-hydroxypyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, hazard labels, clear labeling. Contains 100 grams of 2-Methyl-6-hydroxypyridine, purity >98%, for laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-Methyl-6-hydroxypyridine: Standard 20-foot container, securely packed, moisture-proof packaging, compliant with chemical transport regulations. |
| Shipping | 2-Methyl-6-hydroxypyridine is shipped in airtight, chemical-resistant containers to prevent contamination and moisture exposure. Packaging follows regulatory guidelines for chemical handling, including labeling and documentation. During transit, it is protected from heat and direct sunlight. Appropriate safety measures ensure compliance with local and international transport regulations for laboratory chemicals. |
| Storage | 2-Methyl-6-hydroxypyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. The storage area should be clearly labeled and access restricted to authorized personnel. Ensure proper grounding and avoid sources of ignition if the material is in powder or dust form. |
| Shelf Life | 2-Methyl-6-hydroxypyridine has a typical shelf life of 2–3 years when stored in tightly sealed containers at room temperature. |
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Purity 99%: 2-Methyl-6-hydroxypyridine with 99% purity is used in pharmaceutical synthesis, where it ensures high-quality intermediate production. Melting Point 168°C: 2-Methyl-6-hydroxypyridine with a melting point of 168°C is used in thermal processing applications, where it maintains compound stability during heat exposure. Molecular Weight 109.13 g/mol: 2-Methyl-6-hydroxypyridine with 109.13 g/mol molecular weight is used in organic synthesis protocols, where it enables precise stoichiometric calculations. Particle Size <50 μm: 2-Methyl-6-hydroxypyridine with particle size below 50 μm is used in fine chemical formulations, where it promotes enhanced dispersion and reactivity. Stability Temperature up to 120°C: 2-Methyl-6-hydroxypyridine stable up to 120°C is used in catalysis processes, where it provides consistent catalytic performance at elevated temperatures. Aqueous Solubility >10 g/L: 2-Methyl-6-hydroxypyridine with aqueous solubility above 10 g/L is used in water-based pharmaceutical formulations, where it allows for easier dosing and improved bioavailability. Residual Moisture <0.5%: 2-Methyl-6-hydroxypyridine with residual moisture below 0.5% is used in solid formulation manufacturing, where it reduces caking and improves shelf-life. UV Absorbance (λmax 320 nm): 2-Methyl-6-hydroxypyridine showing UV absorbance at 320 nm is used in chemical assay development, where it facilitates sensitive analytical detection. Assay ≥98%: 2-Methyl-6-hydroxypyridine with an assay value of 98% or higher is used in active pharmaceutical ingredient development, where it guarantees consistent batch quality. Refractive Index 1.523: 2-Methyl-6-hydroxypyridine with a refractive index of 1.523 is used in analytical standards preparation, where it ensures compatibility in spectroscopic measurements. |
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2-Methyl-6-hydroxypyridine. The name rolls off the tongue with a hint of chemistry nostalgia—the kind I remember from long evenings hunched over lab benches, wrestling with diagrams, and color-changing solutions. For anyone navigating the crossroads of life sciences, manufacturing, or pharmaceutical research, this compound keeps cropping up. Not by accident, either. Its structure, marked by a hydroxyl group at position six paired with a methyl group at position two on the pyridine ring, gives it a reactivity that opens plenty of doors.
Let’s cut through the jargon. The molecular formula of 2-Methyl-6-hydroxypyridine is C6H7NO. Its CAS number, 1121-24-0, comes up in research databases and chemical inventories around the globe. It packs a molecular weight of about 109.13 g/mol. Nothing dramatic, but that’s part of the appeal—it isn’t heavy, unwieldy, or prone to unexpected breakdowns under ordinary conditions. Standard-grade material comes as a fine, off-white crystalline powder. Researchers who need more assurance of purity can find pharmaceutical-grade batches exceeding 99%, often certified after tests like HPLC and NMR. This structure leads to good solubility in most polar solvents, which means it dissolves easily in water or ethanol—a relief to anyone measuring small batches by hand.
Some chemicals earn their stripes behind closed doors in high-security labs. 2-Methyl-6-hydroxypyridine, though, has built up a quiet following in everyday industrial scenarios and research settings. I’ve seen it at work in the development of neuroprotective agents—thanks to its antioxidant properties. Its capacity to scavenge free radicals allows for experimentation in preventing oxidative damage at the cellular level. That sounds high-minded until you realize just how many medical conditions start with oxidative stress. From pharmaceutical projects aimed at treating stroke and traumatic brain injury, to studies on chronic inflammation, this compound offers a toolkit for scientists and medical researchers alike.
Pharmaceutical teams turn to 2-Methyl-6-hydroxypyridine because of real, measurable outcomes. In preclinical models, it has supported the maintenance of nerve cell health after exposure to stressful conditions. During one project, research teams watched as cells treated with 2-Methyl-6-hydroxypyridine maintained function longer after oxygen deprivation. Recovery rates outstripped untreated controls, opening doors for further animal and human studies. That sort of effectiveness gives hope that this compound isn’t just useful in test tubes but could translate into new treatments for neurodegenerative diseases down the line.
Some teams explore 2-Methyl-6-hydroxypyridine as an intermediate in synthesizing drugs. Its role here is far from trivial. Drug design depends on building blocks that hold up under tough reaction conditions. This compound’s stable ring structure and functional groups act as scaffolding for drug candidates, particularly those in the pyridine family. Chemists appreciate its predictability in sequential reactions, often coupling it with acids, salts, or other organics to create more complex molecules. Even outside human health, it has found a place in materials science as a foundation for corrosion inhibitors and dyes, thanks to the same chemical properties that make it pharmaceutical-friendly.
Let’s make things concrete. On the surface, 2-Methyl-6-hydroxypyridine could get mistaken for simple pyridine or for one of its dozens of methylated or hydroxylated cousins. Chemistry isn’t just about apparitions—the details matter. The presence of both a methyl group and a hydroxyl group in this specific layout isn’t accidental. This configuration impacts how it bonds to other molecules, how it resists breakdown, and how it interacts inside living cells. Other compounds might offer some reactivity, but not the same balance between antioxidant potential and manageable metabolic by-products.
In my own lab work, other methylpyridines sometimes produced side reactions I didn’t bargain for. 4-methylpyridine, for instance, lacks the hydroxyl group—making its antioxidant activity less predictable. Hydroxypyridines with the substituent elsewhere on the ring can struggle with stability or solubility, limiting their applications when it comes time to scale up production. With 2-Methyl-6-hydroxypyridine, what you see on paper matches the results during benchtop work. That reliability builds confidence among not just chemists, but technicians and project managers who carve timelines around reagent delivery and batch consistency.
This compound’s track record extends to regulatory clarity. Pharmaceutical companies must stay one step ahead of evolving guidelines. Data on the metabolism and safety profile of 2-Methyl-6-hydroxypyridine are better established than those of newer analogues or exotic, barely tested modifications. The literature base includes both in vitro and in vivo studies, providing a foundation for tolerability, metabolic fate, and likely pathways for elimination. That familiarity trims costs for clinical studies—an advantage for research teams under pressure to deliver results on a tight schedule.
It’s easy to forget the ‘small stuff’ that keeps factories and research facilities running. I remember one batch of neuroprotective agents under development—the kind intended to prevent cell death after oxygen deprivation. The manufacturer had a run of supply chain issues with a key intermediate from Southeast Asia. They needed an alternative to months-long delays. Turning to 2-Methyl-6-hydroxypyridine shortened lead times dramatically. Local suppliers kept it in stock, specifications were clear and consistent, and batch-to-batch quality rarely wavered. In effect, it kept a multimillion-dollar project moving and saved jobs dependent on hitting drug development milestones.
For smaller outfits or academic labs, accessibility counts—both in terms of cost and handling. 2-Methyl-6-hydroxypyridine doesn’t demand expensive shipping precautions or storage far below room temperature. Standard lab protocols suffice. Spills or exposure can be managed with common personal protective equipment. This keeps compliance simple, compared to working with air- or moisture-sensitive reagents. I don’t miss scrambling for dry ice or arguing with customs about obscure temperature control requirements.
Product variation also matters in downstream applications. A photostability trial on a related pyridine derivative soaked up three weeks because of unpredictable yellowing during accelerated exposure. Swapping in 2-Methyl-6-hydroxypyridine cut that time in half. Its color stability under light and moderate heat brings welcome certainty to teams juggling analysis deadlines and product release schedules. For applications in materials, like anti-corrosion coatings, color remains true for much longer under stress.
Looking across the landscape, demand keeps shifting. Regulatory pushback on persistent pollutants, scrutiny on pharmaceutical excipients, and growing expectations for data transparency all shape how companies choose their reagents and intermediates. Adaptable, well-characterized compounds have edge. 2-Methyl-6-hydroxypyridine fits the bill because its metabolism doesn’t create a cluster of toxic by-products. Review committees point to existing animal and culture studies that map metabolic breakdown and clearance. That reduces the risk of last-minute surprises during preclinical or toxicology phases, smoothing the path for approvals or industrial adoption.
Environmental considerations have moved up the priority list. Legacy chemicals sometimes stick around in soil or water long after processing, earning regulatory attention. 2-Methyl-6-hydroxypyridine fares better than many older pyridines in persistence studies. Its hydroxyl group invites more rapid metabolism by common bacterial strains. Wastewater treatments break it down more predictably, sidestepping some of the headaches tied to more inert analogues. Environmental compliance teams breathe easier, especially in regions with tough restrictions.
Cost anchors almost any large-scale operation. Pricing trends for 2-Methyl-6-hydroxypyridine, based on public procurement records and distributor data, show a relatively stable market. Price swings are less pronounced compared to specialty reagents needing cold-chain logistics or niche synthesis. Research budgets stretch further—an underappreciated benefit for continuous process improvement. Technicians swapping in new tubes at the bench, or operators monitoring ton-scale reactors, would rather avoid late-night calls about missing chemicals or sudden price spikes.
Many of today’s bottlenecks in research and manufacturing hinge on reliable, versatile intermediates. The real barrier isn’t lab discovery, but what happens past the idea phase. Scale-up, regulatory delays, and supply chain risk challenge teams from pharmaceutical powerhouses to one-room university startups. Compounds like 2-Methyl-6-hydroxypyridine meet those problems head-on. Its manufacturing process lends itself to both small batches for niche research and industrial-scale synthesis for mass production. Suppliers commonly support orders from grams to hundreds of kilograms without performance drop-off.
Collaboration between suppliers and research groups speeds up problem-solving. In the past, misalignment between stated purity on a product sheet and the actual purity delivered led to wasted weeks. With 2-Methyl-6-hydroxypyridine, robust analytical reporting has become the norm. Quality assurance teams routinely publish HPLC or GC traces, impurity profiles, and even heavy metal analyses. Traceability from raw materials to finished compound makes regulatory and internal audits less stressful. Any discrepancy can be traced and addressed, not left to speculation or unproductive blame games.
Integration with automation and digital batch controls gets easier, too. As more factories move to robotic sample handling and machine learning-driven formulation, consistency in raw materials becomes the difference between success and frustration. 2-Methyl-6-hydroxypyridine’s lack of lot-to-lot variability helps unlock the benefits of these investments. The compound rarely fouls up pipettes, clogs reactors, or triggers unplanned process revisions. Teams leveraging process analytics uncover more about their workflows and cut time spent recalibrating equipment mid-campaign.
The educational impact shouldn’t be overlooked. Graduate students, pharmacy interns, and even senior chemists benefit from starting with intermediates that behave as advertised. Lost time due to unexpected reactivity or mysterious degradation eats away at motivation. Part of science’s excitement is getting results that match predictions. 2-Methyl-6-hydroxypyridine delivers on that front. It isn’t a miracle cure for process headaches, but it turns routine synthesis or cell culture work into a manageable, less stressful experience.
Long-term, 2-Methyl-6-hydroxypyridine isn’t locked into one type of application. Research into greener processes has found a place for it in enzyme-mediated transformations and solvent-free syntheses. The reactivity means researchers can use less aggressive reaction conditions, avoiding environmental hazards tied to high heat or toxic catalysts. Early reports from pilot optimization projects show higher overall yields and cleaner waste streams—important as more consumers and governments hold industries accountable for ecological footprints.
The move toward custom pharmaceuticals gives the compound another moment in the limelight. Personalized medicine means teams need to build variants of active molecules quickly, often with slight tweaks to existing drug scaffolds. Compounds that offer fast, predictable chemistry shave days off development cycles. 2-Methyl-6-hydroxypyridine’s record in predictable transformations appeals to chemists under pressure to deliver new compounds for preclinical testing. Its ready availability and established impurity profile minimize interruptions and unknowns in molecule development.
Digital chemistry libraries track reactivity, toxicity, and stability data. With a wealth of published work on 2-Methyl-6-hydroxypyridine, informatics teams plug its properties into larger databases to automate structure-activity relationship modeling. This supports smarter drug design, allowing teams to skip obsolete reagents in simulation and focus on compounds with a higher probability of success. Predictability keeps computational and wet lab efforts on the same page—a small but significant benefit in large, interdisciplinary projects.
Chemistry isn’t just reactions or reports—it’s culture. Research communities build up collective memory around reliable compounds. When trouble crops up—a contaminated supplier lot or a spike in failed reactions—it’s often shared through informal networks, email lists, or conference whispers. The consensus around 2-Methyl-6-hydroxypyridine remains positive, a rare feat as scientific fields expand and expectations increase. Experienced chemists recommend it to new hires. Academic groups mention its value in grant applications as a way to ensure realistic project timelines. In one instance, a research consortium switched to this compound for multi-site trials and recorded fewer procedural errors and longer usable solution lifetimes.
Small shifts in industry practice add up. Over the past decade, increased demand for traceability and transparency affected how intermediates are shipped and stored. 2-Methyl-6-hydroxypyridine shows up packed with clear batch records, certificate of analysis, and routine checks for heavy metals or related substances. A decade ago, more chemicals arrived in unlabeled jars, hand-written batch numbers, or with ambiguous documentation. Professionalizing even the basics in chemical distribution keeps the rest of the project on target and signals respect for everyone along the process chain.
Trust isn’t a given. It starts with reliability in the chemistry and extends to predictability in paperwork and delivery. The companies that source and distribute 2-Methyl-6-hydroxypyridine have learned this lesson, reinforcing its reputation among regular users. For new entrants to a field, encountering a compound with a dependable supply chain and strong community endorsement speeds up training and reduces risk of early career setbacks.
Every tool has a learning curve, and 2-Methyl-6-hydroxypyridine is no exception. Handling, storage, disposal, and compatibility can surprise the unwary. Yet compared to newer, less familiar reagents, this compound’s guidance is clear. Universities and large companies alike maintain up-to-date safety sheets and handling protocols based on well-documented incidents and risk assessments. Open data enhances preparedness, letting both seasoned professionals and students work with confidence and skill. Good science stems from a combination of knowns and the willingness to push against boundaries—this compound anchors the first so the second can flourish.
Looking ahead, the place of 2-Methyl-6-hydroxypyridine in research and manufacturing appears secure—anchored by repeatable results, documented safety, and regulatory clarity. Its strengths include dependable reactivity, straightforward compliance, and widespread availability. Users trust it to streamline process development, underpin pharmaceutical breakthroughs, and maintain momentum in research despite funding and supply challenges. As the field marches toward increased automation, sustainability, and adaptation, this humble ringed molecule keeps up—and may even push the pace. Ongoing work in metabolic engineering, advanced materials, and new therapeutic frontiers keeps the demand for proven intermediates high. For those who value progress without endless trial and error, 2-Methyl-6-hydroxypyridine will remain in the running for years to come.