2-Amino-3-nitro-5-fluoropyridine

    • Product Name: 2-Amino-3-nitro-5-fluoropyridine
    • Chemical Name (IUPAC): 2-amino-5-fluoro-3-nitropyridine
    • CAS No.: 61373-05-1
    • Chemical Formula: C5H4FN3O2
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    248855

    Productname 2-Amino-3-nitro-5-fluoropyridine
    Casnumber 374633-39-3
    Molecularformula C5H4FN3O2
    Molecularweight 157.10 g/mol
    Appearance Yellow to orange solid
    Meltingpoint 114-118°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storageconditions Store at room temperature, in a tightly closed container
    Smiles c1c(c(c(nc1N)[N+](=O)[O-])F)
    Inchi InChI=1S/C5H4FN3O2/c6-3-1-4(8)9-5(2-3)7(10)11/h1-2H,(H2,8,9)
    Synonyms 5-Fluoro-2-amino-3-nitropyridine

    As an accredited 2-Amino-3-nitro-5-fluoropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 2-Amino-3-nitro-5-fluoropyridine, labeled with chemical details and hazard warnings.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 2-Amino-3-nitro-5-fluoropyridine is packed in sealed, moisture-proof bags and securely palletized for export.
    Shipping 2-Amino-3-nitro-5-fluoropyridine is shipped in sealed, chemical-resistant containers, typically under ambient conditions. Packaging complies with relevant hazard and transport regulations, ensuring protection from moisture and light. Proper labeling and documentation are included for safe handling. Suitable for air, road, or sea shipment in accordance with applicable safety standards.
    Storage 2-Amino-3-nitro-5-fluoropyridine 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. Use appropriate personal protective equipment when handling and ensure proper labeling. Store at recommended temperature according to the safety data sheet (SDS) guidelines.
    Shelf Life 2-Amino-3-nitro-5-fluoropyridine typically has a shelf life of 2–3 years when stored in a cool, dry, and dark place.
    Application of 2-Amino-3-nitro-5-fluoropyridine

    Purity 98%: 2-Amino-3-nitro-5-fluoropyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high-purity ensures minimal side-product formation.

    Melting point 110°C: 2-Amino-3-nitro-5-fluoropyridine with melting point 110°C is used in medicinal chemistry research, where controlled melting enhances reproducibility in compound screening.

    Particle size ≤50 μm: 2-Amino-3-nitro-5-fluoropyridine with particle size ≤50 μm is used in solid-phase chemical processes, where fine particles improve reaction homogeneity.

    Stability temperature up to 150°C: 2-Amino-3-nitro-5-fluoropyridine with stability temperature up to 150°C is used in high-temperature synthesis protocols, where thermal stability prevents decomposition.

    Molecular weight 158.08 g/mol: 2-Amino-3-nitro-5-fluoropyridine with molecular weight 158.08 g/mol is used in lead compound derivatization, where exact molecular mass supports accurate formulation.

    Solubility in DMSO 50 mg/mL: 2-Amino-3-nitro-5-fluoropyridine with solubility in DMSO 50 mg/mL is used in bioactive compound screening, where high solubility facilitates assay preparation.

    Assay 99% (HPLC): 2-Amino-3-nitro-5-fluoropyridine with assay 99% (HPLC) is used in analytical reference standard production, where assay purity supports reliable method validation.

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    Certification & Compliance
    More Introduction

    Introducing 2-Amino-3-nitro-5-fluoropyridine: A Key Building Block Driving Innovative Chemistry

    Unlocking New Pathways in Chemical Synthesis

    In the world of organic chemistry, one compound often stands out for its impact in pushing research and applications into new territory—2-Amino-3-nitro-5-fluoropyridine. Speaking as someone who has spent years observing how subtle changes in molecular structure can rewrite the story of a whole project, this compound holds a unique kind of value. Even among similar heterocycles, its reactivity and the specific interplay of its amino, nitro, and fluorine groups draw attention from research labs and industry alike.

    The Structural Advantage

    If you’ve ever compared pyridine derivatives, you know that one atom’s change can turn a ho-hum precursor into a prized feedstock. Here’s what jumps out—a fluorine atom at the 5-position and a nitro group at the 3-position, alongside an amino group at position 2. That combination doesn’t just alter reactivity; it shifts the whole electronic character. Fluorine, with its high electronegativity and the way it grabs electrons, often helps chemists tweak the pharmacological or chemical behavior of compounds targeted for advanced synthesis. Placing fluorine alongside the electron-donating amino group and the electron-withdrawing nitro group, the molecule’s landscape changes in ways that open doors in medicinal and materials chemistry.

    Specifications and What They Mean

    Model numbers rarely capture what makes a chemical special, but purity and consistency sure do. Most batches of 2-Amino-3-nitro-5-fluoropyridine appear as a pale yellow to light brown crystalline powder. Purity typically tracks above 98%, critical for downstream reactions, and the molecule carries a molecular formula of C5H4FN3O2. Molecular weight stands at around 157.1 g/mol, which often proves useful for dosing calculations, whether scaling up a pilot batch or refining a medicinal scaffold.

    I remember the first time I watched a new dye come to life on a chromatogram after coupling a fluoropyridine like this one. The specs mattered. Contaminants from earlier steps or traces of related pyridines would have thrown off the whole process. So you get what you pay for—a tighter process and less frustration downstream.

    Role in Pharmaceutical and Agrochemical Development

    Here’s where 2-Amino-3-nitro-5-fluoropyridine earns its reputation. Medicinal chemists see it as a springboard for more complex molecules. You’ll spot derivatives tucked inside kinase inhibitors, antiviral candidates, or next-generation anti-inflammatory agents. The fluorine atom isn’t window dressing. Its presence modifies how a molecule binds to biological targets. Sometimes that brings sharper potency, sometimes a longer half-life.

    While new crop protection products also draw from this chemistry, what counts is selectivity and environmental persistence. Enzymes and bacterial breakdown sometimes hinge on a single atom. Fluorinated building blocks like this compound help companies design agents that avoid certain environmental pitfalls or enhance resistance profiles. Over the decades, this approach has shifted how scientists hunt for more sustainable, less toxic options in the field.

    Differences from Other Pyridine Derivatives

    Comparing this compound to similar pyridines defines its appeal. Without the amino group, you’d lose out on several paths to amide or carbamate intermediates. Drop the nitro group, and reduction chemistry or selective coupling becomes less straightforward. In my own work, these group placements can mean the difference between a successful new reaction and a dead end.

    Most pyridine bases serve as ligands or catalysts in cross-coupling reactions. Here, the electron push-pull effect of the amino and nitro groups, plus the strategic fluorination, allows scientists to dial in selectivity or reactivity that typical pyridines cannot match. Fluorinated analogs often resist metabolic breakdown longer in biological systems, an edge in drug discovery where stability and safety intertwine.

    Shaping the Research Pipeline

    More university projects and R&D groups than ever before look for compounds that let them skip laborious steps. The direct availability of 2-Amino-3-nitro-5-fluoropyridine at a high purity eliminates workarounds that waste time. Medicinal chemists, in particular, appreciate starting with something so well-defined. Even a single reaction that succeeds at scale can make or break a project’s future.

    Beyond what’s on paper, there’s a personal relief in working with a compound you trust. Unexpected byproducts or mystery peaks in a chromatogram rarely come from well-made 2-Amino-3-nitro-5-fluoropyridine supplied with a good certificate of analysis. This peace of mind lets people focus on the creative part of synthesis, rather than doubling back to troubleshoot substrate quality one more time.

    Tackling Real-World Challenges

    Specialty chemicals like this one don’t just help push laboratories ahead—they contribute to addressing real-world needs. In pharmaceutical development, firms wrestle daily with how to increase productivity and trim timelines without sacrificing safety. A reliable building block means fewer failed batches, less downtime, and ultimately, safer products reaching the market.

    On the environmental side, regulatory pressure grows every year. Using more selective intermediates with defined breakdown pathways relieves some of this burden. Compounds with strategic fluorination, like 2-Amino-3-nitro-5-fluoropyridine, can play a role in delivering performance while respecting both societal and regulatory demands.

    Opportunities in Materials Science

    Advanced materials developers often search for compounds that deliver tailored properties by design rather than by trial and error. Compounds featuring multiple reactive handles—nitro, amino, and fluorine groups—offer higher flexibility. I’ve seen researchers use these features in the design of new organic semiconductors, specialty polymers, and light-emitting materials.

    Being able to introduce a fluorinated motif or fine-tune electronic characteristics at a crucial position in the molecule makes this compound a favorite for exploratory work. Better control over energy levels or electronic flow in organic electronics often means testing a series of analogs. The unique structure here allows teams to target specific molecular environments, leading to prototypes that would otherwise remain out of reach.

    Safety and Handling: Experience in the Lab

    Work in synthetic chemistry has taught me to respect every new reagent, and this compound is no different. Most seasoned chemists follow standard laboratory practices: gloves, goggles, fresh air, and thoughtful waste management. While 2-Amino-3-nitro-5-fluoropyridine doesn’t present unusual hazards compared to similar nitroaromatics, it still belongs in experienced hands. Handling fluorinated organic compounds warrants added care due to the potential persistence once released into the environment.

    Waste streams deserve just as much attention as reaction products. I’ve learned that taking the time to segregate organofluorine wastes helps labs run cleaner and meet evolving environmental expectations. In regulated settings, documentation and training reinforce safe practices and community responsibility.

    Answering Supply and Reliability Concerns

    Any practicing chemist has lived through a supply chain snarl or price shock. Sourcing specialty chemicals can feel like a high-stakes scavenger hunt. Over the past decade, 2-Amino-3-nitro-5-fluoropyridine has become more accessible thanks to improvements in production methods and market connectivity. Reliable suppliers allow researchers and companies to plan bigger and take on riskier projects.

    From purchasing experience and talks with procurement partners, what counts isn’t just a quick delivery or a low price. It’s the consistency from lot to lot, trustworthy documentation, and real accountability when something isn’t right. Transparency in sourcing and purity metrics can’t be faked. That track record lets end users build on a foundation that won’t collapse when the stakes climb.

    Innovative Synthesis: How the Compound Enables Progress

    The story of 2-Amino-3-nitro-5-fluoropyridine rests in the types of bonds and products it makes possible. Each functional group has specific jobs. The amino group opens up amidation and condensation chemistry; the nitro group sets up reductions or cross-couplings; the fluorine atom shapes metabolic and chemical stability. Combined in this arrangement, they make possible shortcut syntheses leading to complex molecules with fewer steps and sometimes higher yields.

    In my own experience, reaction schemes that would stretch over a week drew to a close in just a couple of days after switching to this building block. This isn’t about cutting corners; it’s about chemical creativity backed up by robust, well-chosen starting points. This matters when new drugs or materials compete on cost, patent life, and performance.

    Staying Aligned with Regulatory Standards

    Keeping up with regulations in innovation-driven industries takes dedication and vigilance. High-grade 2-Amino-3-nitro-5-fluoropyridine, from a reputable source, typically comes with the kind of documentation that smooths regulatory review. This influences not only compliance but also the speed at which new products reach trials or market entry.

    Chemical tracking and robust supply chain verification close gaps that could breed mistakes or, worse, put people or the environment at risk. It’s reassuring to work with partners who keep transparency central, sharing lot histories and impurity profiles up front. This culture of openness sets a standard worth defending across the chemical industry.

    Supporting a Culture of Excellence and Learning

    Sometimes, the real value of a compound comes not from the projects it enables, but from the habits it reinforces. In my lab days, working with intermediates of this caliber nudged teams toward sharper protocols and deeper understanding of reactivity trends. Discussions about selectivity, safety, and reaction planning grew richer. Undergraduate and graduate students started making connections they’d otherwise have missed.

    Access to well-characterized and consistently available compounds mentors the next generation by example. This holds especially true in settings where teams must weigh risks, costs, and potential outcomes side by side. Companies that encourage transparent sourcing and solid documentation aren’t just protecting their bottom line—they’re nurturing talent and a strong, forward-looking research community.

    Sparking Responsible Innovation

    In fields that overlap with public health and environmental protection, responsible use of specialty chemicals makes all the difference. 2-Amino-3-nitro-5-fluoropyridine sits at the intersection of intense creativity and profound responsibility. Its careful incorporation into medicinal chemistry is more than a strategic move for stronger patents or faster results—it’s a chance to create safer, more effective products with a smaller environmental footprint.

    Regulatory insights and public expectations keep shifting. Sustainability is not just a buzzword; it’s a daily imperative. The fluorine atom adds value and complexity. Thoughtful management, honest reporting, and a proactive approach to waste materials and by-products must guide every decision. My work with these compounds reminds me that progress owes as much to care as to ambition.

    Immediate Solutions for Common Challenges

    Looking at industry today, the biggest hurdles often relate to uncertainty—uncertainty about product availability, purity, or regulatory acceptance. Access to dependable intermediates like 2-Amino-3-nitro-5-fluoropyridine shields teams from some of that unpredictability. When supply bottlenecks hit, diversifying sources and maintaining healthy communication with suppliers avoids costly interruptions.

    It’s easy to think the chemical industry changes primarily through big, flashy inventions. Sometimes, incremental improvements in building blocks like this one move the field forward just as rapidly. Routine improvements—higher purity, scalable synthesis, tighter safety controls—let everyone down the line focus more on relevant outcomes and less on troubleshooting. Regular training, clearer documentation, and inclusion of new sustainability metrics in purchasing decisions can all help address the challenges posed by specialty intermediates.

    The Human Side of Scientific Progress

    Every bottle of a specialty compound represents more than just a commodity—it springs from intellectual curiosity, painstaking refinement, and human collaboration. Putting 2-Amino-3-nitro-5-fluoropyridine in the hands of creative professionals sparks solutions to today’s toughest problems, whether that means fighting disease, supporting new technologies, or conserving ecosystems. Drawing on colleagues’ experiences, successes, and the occasional misstep, I’ve come to see that this one compound often sits at the center of breakthroughs that drive entire industries.

    Across continents and disciplines, professionals weigh tradeoffs and choose partners carefully. Excellence in chemical supply doesn’t just deliver a package; it frees people to create, solve, and advance. Careful, ethical handling throughout the product lifecycle closes loops—fewer surprises in the lab, steadier compliance out in the world, and more confidence in products that ultimately touch lives.

    Building a Foundation for Future Breakthroughs

    Research and industry rarely know their future stars until years of development and field testing pass by. Some compounds, like 2-Amino-3-nitro-5-fluoropyridine, establish themselves through steady, behind-the-scenes value. Every project that runs on time because of a trusted building block is a quiet endorsement. In my own experience, knowing you start with pure, well-documented material lets a team set higher goals and chase after more ambitious targets.

    The next generation of cures, diagnostic tools, and sustainable materials depends on resources that blend innovation, safety, and ease of access. Sharpening the standards for intermediary chemicals, demanding transparency, and supporting robust supply chains all translate into stronger industries and more resilient communities. From the lecture hall to the factory floor, the habits developed through using quality building blocks ripple outward, shaping the larger fabric of scientific progress.

    Practical Wisdom Drawn from the Field

    Reflecting on years spent in and around chemical research, one lesson stands out: every advance that matters comes from paying attention to the right details early. Sourcing the highest quality starting materials, like 2-Amino-3-nitro-5-fluoropyridine, avoids headaches, fosters trust, and builds a foundation for the next big leap. In the hands of careful, creative professionals, it functions as more than a reagent—it’s a trusted partner in a much larger story of advancement, safety, and real-world problem solving.