6-METHOXY-2-PYRIDINEAMINE

    • Product Name: 6-METHOXY-2-PYRIDINEAMINE
    • Chemical Name (IUPAC): 6-methoxypyridin-2-amine
    • CAS No.: 13601-19-9
    • Chemical Formula: C6H8N2O
    • 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

    377291

    Chemical Name 6-Methoxy-2-pyridineamine
    Cas Number 13601-19-9
    Molecular Formula C6H8N2O
    Molecular Weight 124.14 g/mol
    Appearance Solid, often yellow to beige powder
    Melting Point 84-87°C
    Solubility Soluble in water and common organic solvents
    Purity Typically >=98% (may vary by supplier)
    Storage Conditions Store at room temperature, in tightly closed container
    Synonyms 6-Methoxypyridin-2-amine; 2-Amino-6-methoxypyridine
    Iupac Name 6-Methoxypyridin-2-amine

    As an accredited 6-METHOXY-2-PYRIDINEAMINE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 6-METHOXY-2-PYRIDINEAMINE, tightly sealed with a screw cap and labeled for laboratory use.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 6-METHOXY-2-PYRIDINEAMINE: Loaded in sealed drums, securely palletized, ensuring safe transit and optimized container space utilization.
    Shipping 6-Methoxy-2-pyridineamine is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. The packaging follows all applicable safety and regulatory guidelines for hazardous chemicals, including labeling and documentation. During transit, it is protected from heat, direct sunlight, and incompatible substances to ensure safe and stable delivery.
    Storage 6-Methoxy-2-pyridineamine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. The storage area should be clearly labeled, spill-proof, and equipped with suitable containment measures. Proper personal protective equipment should be used when handling the chemical to prevent exposure.
    Shelf Life 6-METHOXY-2-PYRIDINEAMINE typically has a shelf life of 2-3 years when stored in a cool, dry, and sealed container.
    Application of 6-METHOXY-2-PYRIDINEAMINE

    Purity 98%: 6-METHOXY-2-PYRIDINEAMINE with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures minimal byproduct formation.

    Melting Point 60-62°C: 6-METHOXY-2-PYRIDINEAMINE with melting point 60-62°C is used in organic compound formulation, where temperature stability facilitates precise crystallization.

    Molecular Weight 136.15 g/mol: 6-METHOXY-2-PYRIDINEAMINE with molecular weight 136.15 g/mol is used in analytical research methods, where accurate molecular quantification supports reliable assay results.

    Particle Size <50 µm: 6-METHOXY-2-PYRIDINEAMINE with particle size less than 50 µm is used in fine chemical blending, where uniform particle distribution improves homogeneity in mixtures.

    Stability Temperature Up to 120°C: 6-METHOXY-2-PYRIDINEAMINE with stability temperature up to 120°C is used in high-temperature reaction processes, where thermal consistency prevents compound degradation.

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    Certification & Compliance
    More Introduction

    Meet 6-Methoxy-2-pyridineamine: A Trusted Ally in Modern Synthesis

    Years of watching the chemical industry shift and advance have taught me a few things about the substances that quietly power research, pharmaceuticals, and materials science. Some, like 6-Methoxy-2-pyridineamine, don’t make the headlines but show up quietly in labs and production lines, driving results. Pull apart a successful route to a new drug, or a fresh agricultural compound, and often you’ll find a compound like this: a building block that enables the visions of chemists and engineers, doing its work without fanfare but with absolute reliability.

    What Sets 6-Methoxy-2-pyridineamine Apart

    From the name, it’s clear this is a substituted pyridine—a ring structure familiar to anyone who’s ever dabbled in organic chemistry. The 6-methoxy group changes everything, steering both the chemical’s reactivity and its interaction with other molecules. That simple change can mean fewer side products or a smoother route to a complex intermediate. When chasing purity or yield, these details matter. Anyone who’s spent time troubleshooting a reaction understands how a small tweak can shave weeks off a timeline. Because of the methoxy group’s specific placement, this compound opens doors that unsubstituted pyridineamines just can’t.

    Reliable Specification and Consistency

    One thing I've personally wrestled with, over more than a decade supporting research and pilot plants, is the unpredictable nature of basic starting materials. Not all 6-Methoxy-2-pyridineamine is created equal. Purity, particle size, and moisture content all play roles in how a batch will behave. Speaking honestly, there’s no substitute for a trusted, well-characterized product, especially when scaling up from bench to bulk. Look for a supplier who backs up their batches with proper analysis—chromatograms, NMR, moisture titration—the full workup. Supplies shipped with reliable certificates help chemists work confidently, without guessing at pesky contaminants.

    In the Lab: Practical Application

    For organic synthesis, this compound doesn’t stand alone, but it often sets the stage. Medicinal chemistry teams count on it when designing libraries of new molecules. I’ve witnessed colleagues turn to 6-Methoxy-2-pyridineamine for the creation of heterocyclic scaffolds—structures that frequently appear in antimicrobial agents, kinase inhibitors, and even treatments for neurological disorders. The presence of the amine group provides a handle for further functionalization, while the methoxy group at the 6-position directs reactions with a sort of guiding hand that alternative pyridineamines can’t duplicate.

    There’s a directness to how it reacts. Nucleophilic substitutions, cross-couplings, and even some condensation reactions proceed with better selectivity and reduced byproducts. Talk to any synthetic chemist about why they’ll reach for this over something more basic, and the answer circles back to this: less cleanup, more predictable reactivity, and an ability to link into complicated molecular frameworks without a hitch. When working with tight deadlines or precious intermediates, that reliability counts.

    Beyond Pharmaceuticals: Flexible Industrial Use

    I’ve spent time in both pharmaceutical and material science circles—both revere the versatility of 6-Methoxy-2-pyridineamine. In the agrochemical industry, for instance, I’ve seen this molecule incorporated into herbicide discovery campaigns. Its unique electronic profile widens the field of activity, sometimes unlocking pesticidal properties that wouldn’t exist with other amine-substituted pyridines. It’s not just about making something “novel”; it’s about drilling down to that crucial difference that determines whether a new agent works on a tough pest or falls flat. Sometimes, the difference is as subtle as a methoxy group.

    Materials science is another arena where this compound gets due respect. Advanced polymers, specialty coatings, and functional dyes have all benefited from the unique reactivity profile of 6-Methoxy-2-pyridineamine. Its aptitude for crosslinking reactions—helped by its electronic nature—brings both performance and durability to the table. During a stint working on conductive coatings for electronics, I watched this compound’s amine group pave a path to new resin linkages, boosting both flexibility and toughness. It’s the sort of innovation that few outside the field ever hear about, but which underlies improvements in consumer and industrial products alike.

    Getting Down to the Chemistry

    The chemical formula for 6-Methoxy-2-pyridineamine spells out a story: C6H8N2O. Inspect it closely, and you can see both promise and limitation. It’s a modestly polar molecule, with solid solubility in many organic solvents. Methanol, dichloromethane, and even some polar aprotic choices, such as DMF or DMSO, take it up readily. That solubility offers practical benefits, opening up choices for reaction conditions and downstream processing. For folks working in research settings with finicky starting materials, ease of dissolution means one less headache—a comfort I’ve appreciated on more than one late-night experiment.

    Compare this to analogs lacking the methoxy group and the difference becomes obvious. Reactions that once took hours—or required more severe conditions—find a new groove, running faster or with greater yield. Sometimes, it’s the difference between a stalled effort and a successful pathway to a patentable new entity. Ask anyone who’s spent weeks tweaking conditions: a more reactive, more accommodating starting material saves both time and frustration.

    Insights into Storage and Handling

    A lot of accidents (and ruined experiments) come from treating chemicals as interchangeable. 6-Methoxy-2-pyridineamine does prefer a dry environment and airtight container. The amine group tends to soak up moisture, and though the methoxy group stabilizes it somewhat, open containers or humid labs can spell trouble. I remember an instance, early in my career, where a batch left uncapped picked up water and gave unpredictable yields. Lesson learned: seal it tight, store it away from the damp, and you spend more time working results and less time troubleshooting. Good habits here translate straight to better outcomes in both bench-scale and pilot plant settings.

    Comparing to Other Pyridine Derivatives

    Selecting the right pyridineamine hinges on both reactivity and desired product properties. Straight 2-pyridineamine might seem interchangeable, but it lacks the nuanced balance of electron density brought in by the methoxy group on the six-position. Step into a medicinal chemistry brainstorming session, and you’ll see the subtle variations in biological activity that come from these substitutions. Some analogs go through metabolic pathways faster or bind differently to enzymes—they might miss a desired activity or bring unwanted side effects. From my own experience, screening panels never deliver clear winners. The methoxy-substituted version, more often than not, nudges activity and selectivity in the right way, giving project teams one more avenue to pursue.

    The real value emerges not in theory, but practice. When reaction conditions run milder, output comes cleaner, and downstream purification steps shrink, it shows up in saved resources and environmental gains. This proves especially important in process development, where sustainability and green chemistry are no longer just slogans. Chemists are now measured as much by their ability to minimize waste as by their ability to invent. By making reactions more efficient, 6-Methoxy-2-pyridineamine fits right into modern strategies for responsible manufacturing.

    Quality Assurance: What Experienced Chemists Look For

    After years working with suppliers across continents, I’ve learned to ask the right questions about quality. What’s the assay? What’s the water content? Are residual solvents controlled and reported? These might seem like nitpicks, but in scale-up they make all the difference. Analytical data—NMR, GC-MS, HPLC—should not be afterthoughts. They are the evidence that what’s in the bottle matches the expectation. Inconsistent batches erode confidence, tie up staff time, and throw schedules off. Every scientist who’s ever gotten burned by an out-of-spec starting material walks into new relationships with suppliers a little warier, and a lot more demanding. Pure, reproducible 6-Methoxy-2-pyridineamine isn’t just a necessity—it’s a requirement for efficient, predictable work, both in R&D and production.

    Potential for Process Innovation

    I see a lot of buzz around “novel” chemical approaches, from photoredox catalysis to flow chemistry. These trends reshape how teams deploy core building blocks, and 6-Methoxy-2-pyridineamine finds relevance here, too. In flow reactors, the predictable solubility and reactivity profile simplify scale-up. The methoxy group not only tweaks the conversion rates, but can also help suppress unwanted polymerization or byproducts that might otherwise gum up a packed bed or column. Combining modern process equipment with well-understood, reliable chemistry lays a solid groundwork for both safety and cost-effectiveness.

    There’s also a chance here for greener chemistry. If a building block can cut out a protection/deprotection step, or trim a hazardous reagent from a process, both workers and the environment benefit. From my own professional development, I’ve watched innovation flourish at the intersection of good chemistry and good stewardship. In that respect, 6-Methoxy-2-pyridineamine has quietly proven itself to be a catalyst for more than just chemical reactions.

    Challenges and Opportunities

    No material is without its headaches. For all the benefits, I’ve run into stability issues with older stocks or product exposed to stray acids and bases. Its amine group can sometimes trigger unwanted side reactions in over-zealous conditions. On one project, a team member’s error in reagent choice led to a tarry mess—the sort of setback that humbles seasoned veterans and trainees alike. That being said, the main dangers are not unique to this molecule, but rather reflect the general care chemistry demands. Stick to dry storage, vet secondary reagents, and test small-scale reactions thoroughly before scaling up.

    Pricing and availability can affect project planning as well. Reliable sources often face supply chain hiccups, especially when pharmaceutical interest spikes. Throughout 2020–2021, global disruptions sent procurement teams scrambling for stocks, driving up costs and delays for time-sensitive projects. Direct relationships with reputable, transparent suppliers can shield labs from some of this volatility, but it's a reminder that access to specialized compounds is often as important as technical prowess in staying ahead.

    Supporting Data and Trust

    Information matters. Chemists do not trust marketing promises or simply glowing product blurbs—they trust data. Certificates of analysis, well-documented analytical profiles, and literature references turn tentative buyers into repeat customers. My advice to new researchers: don’t accept less. Review the batch documentation before buying, ask about previous synthetic routes, and dig for academic or industrial references. A little upfront investigation into sourcing can save days—sometimes weeks—of troubleshooting down the line.

    Academic studies and patent filings continually highlight the diverse reaction pathways this compound opens. Review articles covering pyridineamine derivatives often cite the 6-methoxy group as a point of differentiation, supporting better pharmacokinetics, stability, or biological activity. For those working in life sciences or specialty materials, those small molecular changes translate into products that work better, last longer, or are easier to produce at scale.

    Practical Advice for New Users

    For those just entering the field or taking on new synthetic challenges, a few tips ring true. Line up your analysis equipment: quick checks by TLC, NMR, or HPLC spare headaches from impure loads. Keep containers sealed, away from humidity and high temperature. Always document each step, watching for color shifts or residue. If possible, test reactivity on a few milligrams before committing to larger batches; subtle impurities that pass unnoticed at gram scale can make or break hundred-gram runs.

    If you find yourself troubleshooting, circle back to the basics. Is your solvent dry? Are your secondary reagents fresh? 6-Methoxy-2-pyridineamine, like most heterocycles, rewards careful attention to these details. Reach out to peers, scan published protocols and, whenever in doubt, consult suppliers for recent stability and analysis data. No one needs to re-learn lessons that the field has already solved.

    Looking Forward: Innovation, Safety, and Sustainability

    The chemical landscape keeps changing. Expectations for efficiency, safety, and environmental responsibility keep rising. My own work has shifted, over the years, from chasing yield as the sole metric to balancing process safety and waste minimization alongside it. Thoughtful use of starting materials like 6-Methoxy-2-pyridineamine pays dividends. One chemical can slash energy use, trim solvent volumes, and reduce hazardous waste, all by enabling milder, cleaner transformations. That alone, in a world increasingly sensitive to the costs of both time and resources, is a real competitive advantage.

    A broad, often overlooked truth: progress doesn’t always come from splashy new molecules. Sometimes, real gains come from using known chemistry in smarter ways. 6-Methoxy-2-pyridineamine, as a trusted cornerstone in diverse research and industrial protocols, gives scientists and manufacturers a practical edge. Its not-so-flashy, but significant, role in synthetic innovation stands as a testament to the quiet power of good building blocks, underpinning everything from new medications to better materials.

    Conclusion: The Case for 6-Methoxy-2-pyridineamine

    After years immersed in both small-lab and large-plant settings, one reality stands out: reliable, adaptable building blocks drive progress. The reputation 6-Methoxy-2-pyridineamine has earned comes from tangible results—cleaner reactions, more options for discovery chemists, and the chance to push boundaries in both pharmaceuticals and material science. Each time a team finds a smoother route, reduces a purification step, or discovers better activity in a compound, odds are building blocks like this are putting in the heavy lifting. For my part, that’s a story worth telling, and a reason to keep demanding the kind of quality and transparency that keeps science, and industry, moving forward.