3-Amino-6-fluoropyridine

    • Product Name: 3-Amino-6-fluoropyridine
    • Chemical Name (IUPAC): 3-amino-6-fluoropyridine
    • CAS No.: 399-59-5
    • Chemical Formula: C5H5FN2
    • 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

    764736

    Chemicalname 3-Amino-6-fluoropyridine
    Casnumber 399-60-2
    Molecularformula C5H5FN2
    Molecularweight 112.11 g/mol
    Appearance Off-white to yellow solid
    Meltingpoint 60-64°C
    Boilingpoint 247°C
    Purity Typically >98%
    Solubility Soluble in organic solvents (e.g., DMSO, ethanol)
    Density 1.3 g/cm3 (approximate)
    Smiles c1cc(N)nc(F)c1
    Inchi InChI=1S/C5H5FN2/c6-4-2-1-3(7)5(8)9-4/h1-2H,7H2,(H,8,9)
    Synonyms 6-Fluoro-3-pyridinamine
    Storagetemperature Store at room temperature, in a dry place
    Hazardclass Irritant

    As an accredited 3-Amino-6-fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 3-Amino-6-fluoropyridine (25g) features a sealed amber glass bottle with a clear hazard label and product information.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3-Amino-6-fluoropyridine ensures secure, compliant bulk packaging for efficient international chemical transport.
    Shipping 3-Amino-6-fluoropyridine is shipped in tightly sealed containers, protected from light and moisture. It is packed according to regulations for hazardous chemicals, typically under ambient or cool conditions. Appropriate labeling and documentation, including safety data, are provided to ensure secure transport and compliance with international shipping standards.
    Storage Store **3-Amino-6-fluoropyridine** in a tightly sealed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. The storage area should be equipped with proper spill containment and suitable labeling. Use secondary containment and keep the chemical away from sources of ignition and direct sunlight.
    Shelf Life 3-Amino-6-fluoropyridine typically has a shelf life of 2 years when stored properly, in a cool, dry, and tightly sealed container.
    Application of 3-Amino-6-fluoropyridine

    Purity 99%: 3-Amino-6-fluoropyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side product formation.

    Melting Point 140°C: 3-Amino-6-fluoropyridine with a melting point of 140°C is used in solid-state organic reactions, where it provides precise thermal stability during processing.

    Particle Size ≤10 µm: 3-Amino-6-fluoropyridine with particle size ≤10 µm is used in fine chemical formulations, where it allows for improved reaction kinetics and uniform blending.

    Molecular Weight 112.10 g/mol: 3-Amino-6-fluoropyridine with molecular weight 112.10 g/mol is used in heterocyclic compound design, where it enables accurate stoichiometric calculations for scalable synthesis.

    Stability Temperature up to 80°C: 3-Amino-6-fluoropyridine with stability temperature up to 80°C is used in temperature-sensitive catalytic processes, where it maintains chemical integrity and performance.

    Water Content ≤0.5%: 3-Amino-6-fluoropyridine with water content ≤0.5% is used in moisture-sensitive pharmaceutical applications, where it minimizes hydrolytic degradation and enhances shelf life.

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    More Introduction

    3-Amino-6-fluoropyridine: A Look at a Key Pyridine Derivative

    Getting to Know 3-Amino-6-fluoropyridine

    Chemistry stands on the shoulders of peculiar molecules. Some substances don’t attract attention at the grocery store, but within the walls of research labs, they act as workhorses. 3-Amino-6-fluoropyridine is one of those quietly influential compounds. Seasoned chemists recognize its significance in pharmaceutical synthesis and agrochemical research. With a pyridine backbone, this compound links two powerful functional groups — an amino and a fluorine — neatly placed at the three and six positions, respectively. Its molecular formula, C5H5FN2, gives you an idea of its weight and complexity in a single glance.

    Understanding the Road 3-Amino-6-fluoropyridine Travels

    The impact of a chemical like this comes from its chemical identity and the role it plays in downstream applications. In labs around the world, researchers pursue safer medicines, pest controls, and analytical reagents. They reach for 3-Amino-6-fluoropyridine 98% because it opens doors to a range of heterocyclic compounds not possible with simpler starting materials. The amino group can act as a nucleophile in a range of transformations, helping chemists craft new bonds and structures. A fluorine atom, strategically placed, offers greater metabolic stability and can significantly change the bioactivity profile of the resulting molecules.

    Specification and Real-World Expectations

    Molecules don’t always look the same in practice as they do on paper. The best 3-Amino-6-fluoropyridine comes as a solid, usually powder, and tends toward a light color. Its melting point sets it apart from many similar compounds, giving laboratories a sense of purity without fancy instrumentation. At 98% purity, this product enters the scene without many surprises. Skilled chemists appreciate the importance of a clean product. Impurities introduce headaches, waste time, and drive up the cost of synthesis. With traces of related pyridines or other by-products kept below strict thresholds, this material supports high-precision work.

    Why the Amino and Fluorine Combo Matters

    Chemists spent decades optimizing fine-tuned molecules for human health and environmental safety. A pyridine ring alone can serve as a building block, but tuning it with substituents makes all the difference. The amino group on the third carbon gives the molecule a site for further derivatization. The fluorine atom on the sixth carbon can influence electronic properties, making the ring more resistant to metabolic breakdown and helping delivered drugs escape rapid clearance. In practical terms, this structure offers a compact and versatile starting point for research teams working on new antibiotics, antivirals, and crop protectants.

    Labs and Industries Put This Molecule to Work

    Synthetic and medicinal chemists have their favorite reagents, and 3-Amino-6-fluoropyridine earns its spot for several reasons. Medicinal chemistry groups use it to reach analogues that push beyond the reach of more basic pyridine derivatives. The molecule lends itself to Suzuki or Buchwald cross-coupling, nucleophilic aromatic substitution, and other staple transformations. Each reaction, well-trodden by generations of chemists, brings incremental gains — and sometimes big surprises. Agricultural labs seek new leads for weed and pest control. The right molecular tweak, such as introducing a fluorine, can shift a candidate from marginal to effective.

    Practical Challenges and Best Practices in Handling

    Working with nitrogen- and fluorine-containing heterocycles takes attention to detail. In my own experience, dust control and solvent choices can make or break a project. The powder will disperse if left open in a breezy lab, and its slightly hygroscopic nature means moisture in the air could become a problem during storage. It pays to keep containers tightly sealed and work in a fume hood. Many chemists have wasted days tracking down impurities that creep in during hasty transfers. High-quality grades, as represented by 98% purity, narrow the lane for these mistakes. For labs operating under strict traceability standards, a well-documented supply chain helps keep rejections and delays off the project schedule.

    Comparing to Other Building Blocks

    Pyridine derivatives stretch across organic chemistry. Some bring nothing but the base ring, others stack on halogens, methyl groups, or more exotic substituents. 3-Amino-6-fluoropyridine finds itself in a sweet spot. The partnership of an amino with a fluorine, rather than a chlorine or bromine, supports specific electronic effects. Fluorinated building blocks, while often pricier, bring the promise of better biological activity through increased stability and modulated polarity. Many alternative pyridines either lack fluorine or position their amines elsewhere on the ring. Changing these positions shifts reactivity, which can send a project into uncharted territory. For certain routes, starting from this precise substitution pattern is what gets molecules to market at all.

    Impacts on Synthesis and Route Design

    It’s not just what’s in the bottle, but how it makes life easier for scientists. Countless times, a reliable supply of a well-characterized intermediate kept projects on track in my own graduate research. Introducing an amino group to a heteroaromatic ring on a multi-kilo scale isn’t trivial — unexpected oxidation, over-reaction, or contamination can balloon costs and timelines. With a ready-made 3-Amino-6-fluoropyridine, teams gain days or weeks of workflow, giving them more time to iterate and less to troubleshoot. This saves more than just dollars and hours; it extends to safety, waste management, and compliance.

    Tackling Concerns in Supply and Sustainability

    The worldwide demand for finely tuned building blocks like this compound highlights underlying challenges. Not every supplier delivers consistent quality batch after batch. I’ve known scientists who have nearly lost months to overlooked differences between lots — color variances, subtle odors, or trace metals that don’t show up on a routine COA. Sustainable production matters, too. As with every chemical, the synthesis route matters. Some older approaches to preparing pyridine derivatives relied on harsh reagents or made large quantities of waste. Efforts to update methods now focus on reducing hazardous solvents and improving atom economy. Every academic and industrial group that demands cleaner, greener production sends market signals back to the supply chain.

    Shaping the Future: Research and Application Frontlines

    Innovation runs on the fuel of high-quality intermediates. Pharmaceutical teams might use trifluoromethyl or other halogenated analogues, but a reliable 3-Amino-6-fluoropyridine still plays a unique part in constructing potential drugs against cancer, neurological disorders, or infectious diseases. Agrochemical discovery relies on similar logic. The right substituents can weaken pests without toxic residues. Even in dye chemistry and material science, subtle changes to a ring system can open new vistas.

    Addressing Risk: Safety Culture and Transparency

    Handling fluorinated amines inside a busy lab underlines the value of strong safety culture. Years in industry taught me that overconfidence around “routine” chemicals leads to more mistakes than the toughest compounds. Even relatively benign substances pose risk through allergic responses, irritation, or, in rare cases, system toxicity. Good training, easy-to-follow documentation, and ready access to PPE shore up the best intentions. Reliable analytical support, including NMR, LC-MS, or IR, zest up the confidence that scientists work with exactly what they intend. Investing in proper tools, maintaining accurate records, and partnering with transparent supply networks help businesses and academic groups cut wasted effort and rework.

    Solving for the Next Decade: Approaches to Long-Term Reliability

    As research needs evolve faster than many supply models, working chemists need to think about scale, availability, and regulatory support. Bulk chemical makers have spent the past few years rethinking storage, transit, and documentation, prompted in part by disruption and renewed focus on risk management. Partnerships with proven logistics providers help mitigate mishaps. Smart labeling, temperature controls, and robust barcoding further shield projects from setbacks. Once a bottleneck, rapid analytical protocols and automated batch testing now help confirm the contents before researchers ever open a vessel. This extra effort pays off far downstream.

    Sourcing and the Global Laboratory Network

    Every bench chemist and research director eventually faces the costs of balancing homegrown synthesis with trusted commercial supply. For most academic groups, running a custom preparation of a compound like 3-Amino-6-fluoropyridine from basic precursors rarely pays. Scale, overhead, and compliance demands tilt the calculus toward specialty suppliers — those who can offer certificates backed by clear HPLC, NMR, and melting point data. Some research organizations lock in supply contracts with preferred vendors, betting on longer-term collaborations that keep their shelves stocked and administrative headaches at bay. These arrangements, built on transparency and shared problem-solving, have helped research environments weather systemic shocks, such as global supply crunches or sudden surges in demand.

    Lifting the Lid on Quality: Avoiding Pitfalls

    Chemistry rewards curiosity and preparation. Poorly sourced intermediates kill efficiency, but more than that, they can shape the reputation of whole programs. In some memorable cases, late-stage failures traced back to irregularities in early building blocks. Ambitious development programs can dry up, budgets can shrink, and teams lose momentum. The simple assurance of tight lot control, dated analysis, and clear communication between labs, sales teams, and logistics staff can stave off these disappointments. The days of trusting in a bag with an old label are over. Now, investors, research managers, and regulators all demand traceability and clear handling instructions, underlining the growing role of professional stewardship in scientific supply.

    Value Grows Where Transparency Meets Know-How

    The days of working in the shadows of larger-than-life chemists have given way to an era where collaboration and accountability matter as much as technical prowess. Practitioners share feedback with suppliers, pushing for lower trace metals, reduced moisture, and smarter packaging. This openness drives continuous improvement. Case in point: the increasing expectation for batch-level chromatograms and spectral data gives buyers the confidence to proceed. It takes energy to vet suppliers, but teams who do reap long-term benefits. High-quality 3-Amino-6-fluoropyridine, labeled honestly and delivered safely, can unlock months of productivity.

    New Demands, New Approaches

    Research never stands still. A compound with a storied record in drug discovery might find itself filling an unexpected gap in material science or diagnostics. Every year, a new class of therapeutic targets or organic frameworks tests the limits of what existing intermediates can support. The role of 3-Amino-6-fluoropyridine as a respected workhorse will likely change. Sustainability, regulatory oversight, and digital integration all matter more now than in the past. Progressive suppliers rethink energy use, upgrade equipment, explore greener alternatives, and partner more deeply with the scientific community. This open dialogue ensures that researchers get more than just a bottle — they get value that endures beyond a single experiment.

    Pyridine’s Place in Discovery

    Reflecting on several years in both academic and industry labs, certain molecules tend to pop up across projects. Pyridine rings, like the one in 3-Amino-6-fluoropyridine, serve as cornerstones. Each project draws on the hard-won knowledge of earlier failures and successes. Students learn to respect the utility and quirks of different derivatives. The right starting material cuts days from multi-step syntheses, improves yields, and clears regulatory hurdles before they loom large. Academic settings put a premium on flexible, accessible intermediates. Industrial programs, with tight deadlines and costly pipelines, bet on consistent, high-grade inputs to stave off disaster.

    Lessons from the Lab: What Works, What Doesn’t

    Working with 3-Amino-6-fluoropyridine, some pitfalls crop up again and again. Moisture control proves critical. Even minor lapses quickly turn productive days into detective work, tracing unanticipated species in HPLC or NMR. Getting lazy with transfer or storage rarely pays — dry boxes, clean spatulas, and careful labeling are all worth the effort. My own group, over several projects, learned patience in sourcing and verifying new lots. The effort to periodically recheck identity, rather than just trusting paperwork, saved significant time and expense. It takes discipline to keep up with best practices, but teams that do consistently outperform those that cut corners.

    Comparing Paths: Alternatives Aren’t Always Substitutes

    In theory, many pyridine derivatives can serve similar functions. Fluorinated, methylated, or nitro-analogues all have their place. Yet, certain synthetic targets demand a specific substitution pattern. Some projects tried jumping to less expensive or more easily sourced alternatives, hoping to shortcut supply chain hurdles. Most eventually returned to this key building block for its unique balance of reactivity and selectivity. The switch to alternatives most often resulted in headaches — lowered yields, purification troubles, or off-target biological activity. Knowledgeable chemists understand that the small cost savings of a substitute often pale compared to the downstream gains of correctly matched intermediates.

    Final Thoughts: Where Quality Meets Discovery

    3-Amino-6-fluoropyridine stands as a square peg for a square hole. For years, it has underpinned pharmaceutical investigations, agrochemical pipelines, and countless basic research projects. Despite market churn, regulatory changes, and new technologies, the humble building block continues to earn its keep. Those who work closest with molecules like this one — synthetic chemists, analysts, and project coordinators — know that unmatched purity and transparency aren’t just checkboxes. They represent the foundation on which safe and effective discoveries rest.

    Building Forward: An Ongoing Conversation

    Every year brings new challenges and possibilities for those on the frontlines of chemical research. As global supply grows more interconnected and demanding, the value of a well-made 3-Amino-6-fluoropyridine keeps rising. Investments in quality, transparency, and sustainability offer returns well beyond today’s experiments. Suppliers and users who embrace a spirit of continuous improvement — vetting, verifying, and sharing lessons — will shape the next wave of breakthroughs. For now, this workhorse molecule continues to power new stories in laboratories around the world, bridging the gap between dream and discovery.