4-Amino-2-nitropyridine97%

    • Product Name: 4-Amino-2-nitropyridine97%
    • Chemical Name (IUPAC): 4-amino-2-nitropyridine
    • CAS No.: 119016-28-1
    • Chemical Formula: C5H5N3O2
    • Form/Physical State: Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    355717

    Product Name 4-Amino-2-nitropyridine
    Purity 97%
    Cas Number 1195-93-5
    Molecular Formula C5H5N3O2
    Molecular Weight 139.11 g/mol
    Appearance Yellow solid
    Melting Point 169-172°C
    Solubility Slightly soluble in water
    Smiles c1cc(nc(c1)[N+](=O)[O-])N
    Inchi InChI=1S/C5H5N3O2/c6-4-1-2-7-5(3-4)8(9)10/h1-3H,(H2,6,7)
    Storage Conditions Store at room temperature

    As an accredited 4-Amino-2-nitropyridine97% factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Amino-2-nitropyridine 97% is packaged in a sealed 25-gram amber glass bottle with a secure screw-cap for safety.
    Container Loading (20′ FCL) 20′ FCL: Securely packed 4-Amino-2-nitropyridine 97% in drums, palletized, moisture-protected, suitable for bulk chemical export.
    Shipping 4-Amino-2-nitropyridine, 97%, should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It is typically transported as a hazardous material, following all applicable regulations for chemical safety. The package requires clear labeling and handling by trained personnel to ensure safety during transit and delivery.
    Storage 4-Amino-2-nitropyridine (97%) 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 the chemical from light and moisture. Ensure proper labeling, and follow all regulatory and safety guidelines for storage of hazardous chemicals.
    Shelf Life Shelf life of 4-Amino-2-nitropyridine (97%) is typically 2 years when stored in a cool, dry, and sealed container.
    Application of 4-Amino-2-nitropyridine97%

    Purity 97%: 4-Amino-2-nitropyridine97% with high purity 97% is used in pharmaceutical intermediate synthesis, where it enables the production of high-yield active pharmaceutical ingredients.

    Melting Point 168°C: 4-Amino-2-nitropyridine97% with a melting point of 168°C is used in organic synthesis applications, where it ensures thermal stability during complex reaction steps.

    Molecular Weight 125.09 g/mol: 4-Amino-2-nitropyridine97% at a molecular weight of 125.09 g/mol is used in fine chemical production, where accurate stoichiometric control is required for reaction precision.

    Particle Size ≤ 150 µm: 4-Amino-2-nitropyridine97% with particle size ≤ 150 µm is used in high-performance material compounding, where rapid and uniform dispersion is achieved.

    Storage Stability 12 months: 4-Amino-2-nitropyridine97% with storage stability of 12 months is used in laboratory research settings, where long shelf life supports consistent reproducibility of experimental results.

    Water Content ≤ 0.5%: 4-Amino-2-nitropyridine97% with water content ≤ 0.5% is used in moisture-sensitive synthesis processes, where it minimizes side reactions and improves overall product yield.

    Chemical Stability at 25°C: 4-Amino-2-nitropyridine97% exhibiting chemical stability at 25°C is used in analytical reference standards, where prolonged sample integrity is critical.

    Low Impurity Level < 1%: 4-Amino-2-nitropyridine97% with impurity level below 1% is used in the development of optoelectronic materials, where purity ensures optimal electronic properties.

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    Certification & Compliance
    More Introduction

    4-Amino-2-nitropyridine 97%: A Specialist’s Ally in Chemical Synthesis

    Experience in Chemistry Sparks Creative Solutions

    In the daily world of synthesis labs, folks often look for compounds that stand out both in reliability and performance. Among a lineup of thousands, 4-Amino-2-nitropyridine 97% makes its presence felt for a few clear reasons. The molecule is no heavy lifter by sheer size, but its mix of amino and nitro groups opens doors for advanced chemical design. That placement on the pyridine ring—an amino at position 4 and a nitro at position 2—brings a kind of versatility that chemists, whether in academia or industry, always seem to chase down.

    My first run-in with this compound came during a hunt for a solid intermediate in heterocyclic synthesis. Other pyridine derivatives lined the shelf—some with halogen tweaks, some bulked up with extra methyls or ethers—but this one offered an effective bridge between aromaticity and easy functionalization. Its chemical identity shaped the choices in stepwise syntheses, especially when exploring medicinal candidates or exploring coordination chemistry. This isn’t just a building block; it’s a quiet but vital gear in the larger machine of innovation.

    Usage in Drug Research, Pigments, and More

    Researchers choose 4-Amino-2-nitropyridine 97% to start building new molecules that can drive discovery in pharmaceutical and pigment chemistry. The amino group adds nucleophilicity—a fancy way to say it reacts in many classic ways, such as coupling reactions for more complex heterocycles. On the other side, the nitro group can be reduced or further transformed, making this compound fit various synthetic ladders. I remember a colleague using this product to assemble precursors for kinase inhibitors. Compared to alternatives like simple aminopyridines, the added nitro group gives more leverage for tuning the final molecule. That gives real control in designing molecules for enzyme targets, colorants, or metal-binding ligands.

    Other materials, such as plain 2-aminopyridines or 4-nitropyridines, don’t hand out the same reactivity pattern. The dual substitution boosts both chemical reactivity and the range of downstream options. Modern organic synthesis leans on this property—one group can be protected, reduced, or exchanged, while the other remains, waiting its turn for late-stage functionalization. This grants researchers a kind of “choose-your-own-adventure” path through multi-step syntheses, rather than boxing them in early.

    There’s an added bonus in materials development, where pyridine rings lend rigidity and polarizability. Substituting both the 2- and 4- positions with donor and acceptor groups creates push-pull effects. That plays out in dye chemistry, where color fastness, shade, and even charge mobility come into play. These qualities would not shine in simpler, mono-substituted relatives. Someone working on OLED applications or advanced sensors can see the advantage here: the electronic structure and substituent pattern tune optical and conductive responses better.

    Comparing 4-Amino-2-nitropyridine to Similar Tools

    Walking along the shelves of any organic lab shows how many pyridine-based compounds are at hand. Still, most are tailored with a single functional group or modified for a very specific end. I once relied on 2-nitropyridine for a catalytic cycle, but it missed some bite for later-stage modifications. Turning to 4-amino-2-nitropyridine, the workflow picked up—yields improved, and the pathway allowed more stops for further derivatization. The product set my project apart by making functional tests more reliable.

    There are cheaper compounds, and there are bulkier ones. Many of them offer some degree of reactivity, but they lose this fine balance. Simply using 4-nitropyridine means missing out on late-stage amination, while a plain 4-aminopyridine lacks sites for oxidative chemistry or reductions. No one likes hitting a synthetic dead end, especially when stakes like patent timelines and grant deliverables are in play. 4-Amino-2-nitropyridine 97% stands out: it does not just follow the rules—it lets chemists break them with confidence.

    Quality counts for a lot here. With a purity of 97%, the compound gives reproducible results and helps those tricky purification steps. Impurity-ridden stock can throw off yields and alter analytical results—no one wants to repeat a thirty-hour purification because of a poor base material. With this product, reactions take less time, work-ups spin down faster, and analytical checks land right where they should.

    Applications on the Cutting Edge

    What really sets 4-Amino-2-nitropyridine apart surfaces when new research takes off. In pharmaceutical development, researchers keep returning to such dual-substituted pyridines to chase drug-like properties. Hydrogen-bonding from the amino, combined with electron-withdrawing nitro, enables selective binding and metabolic stability. A few kinase inhibitor patents hint at this approach, leveraging this exact structure to skirt resistance mechanisms and raise the bar on selectivity.

    In dye and pigment chemistry, this compound shapes up as a core scaffold. Its electronic attributes make it ideal in charge-transfer dyes, where push-pull frameworks produce sharper, more intense colors with better light stability. In sensor labs, it pops up in experiments measuring fluorescence shifts or signal enhancement, since dual substituents improve detection limits.

    People also look to this compound for advanced materials. For example, coordination chemistry with transition metals opens up when both donating and withdrawing groups are on offer. Ligand frameworks crafted from 4-amino-2-nitropyridine have found their way into organic electronics and catalytic cycles. Materials chemists who dig into literature on perovskites, OLEDs, or polymer treatments spot the same trend. Structures derived from this backbone often appear in schemes seeking novel conductivity, responsiveness, or durability.

    Barriers and Ways Forward

    While the compound shines in lab development, there’s room for more open access and sustainability in its use. The production routes, often using nitration and selective reduction, should reduce byproducts and environmental impact. Green chemistry principles push for solvent reuse and milder conditions, which the chemical industry is only just starting to bring into everyday practice. Pushback comes from old habits or scale-up costs, but we’ve seen plenty of progress thanks to teamwork between industry and academia. As these changes take root, 4-Amino-2-nitropyridine could come with a lighter footprint, especially if more producers take up newer synthetic tricks.

    On the safety front, handling compounds like this means paying attention to storage, moisture, and stability. The nitro group can be sensitive, though at this substitution pattern, it’s a lot safer than bigger nitroaromatics. Industry users increase safety margins through better packaging and clear documentation. Labs that stick with known suppliers tend to see fewer headaches; real-world experience shows that buying from unknown sources often spells trouble for both consistency and compliance.

    Cost remains part of the discussion, as with most chemicals that sit just outside the commodity market. Volume discounts, long-term relationships with suppliers, and open dialogue with manufacturers all help keep expenses within reach for academic and commercial labs alike. Crowdsourcing data and collaborative procurement, something I’ve watched grow over the last ten years, put real power into the hands of smaller buyers. Collective bargaining can nudge down prices and raise quality, which means more teams—including students—can tap into these valuable intermediates.

    Personal Notes from the Lab Bench

    Chemists carry a love-hate relationship with intermediates. A solid intermediate like 4-Amino-2-nitropyridine can lift the spirits of a whole team. Nothing stalls progress more than discovering a product behaves weirdly, or that work-ups leave mysterious smears on TLC plates. Each time I pulled a fresh bottle of this compound from storage, a small relief came over the group. Reactions ran smoother, purification columns cleared faster, and the headaches caused by less consistent stock faded away.

    In training younger chemists, I saw the value of a reliable product firsthand. Entry-level researchers, just learning the ins and outs of practical chemistry, often run through valuable time and resources trying to diagnose a failed step. Usually it’s not the student’s hands or the instructor’s plan—it’s the inconsistency in starting materials. Watching new students succeed in multi-step reactions, thanks in part to solid base stock, almost always led to stronger morale and better learning outcomes.

    Having spent a good chunk of my career in both academic and industrial settings, I can say that 4-Amino-2-nitropyridine lands right in a sweet spot for synthetic work. Flexibility, reliability, and the chance for further tailoring matter more than simple catalog metrics. This compound delivers, especially when compared to alternatives that gate progress or leave chemists boxed in. Cutting-edge research doesn’t happen with mediocre materials.

    Bridging Research Fields: Interdisciplinary Synergy

    The mixture of use in pharmaceuticals, dyes, and materials shows me that chemistry’s best advances always come at the intersection of fields. I’ve sat on research boards that fund work stretching from medicinal chemistry to device engineering, where the most celebrated teams speak a language built on practical building blocks. 4-Amino-2-nitropyridine stands out as a shared word in this conversation. Organic chemists trust its reactivity, medicinal chemists value its scaffold, and physical chemists put its electronics to use.

    A classic example appeared a few years ago, when a team working on photodynamic therapy borrowed know-how from pigment chemistry to fine-tune a drug precursor. They made use of the compound’s dual substituents to modulate both light absorption and bioavailability—something that would have taken far longer if not for easy access to reliable base materials like this one. It’s moments like this, when a simple intermediate connects far-flung research corners, that remind me why such products are so valuable.

    Industry players, whether in pharma, inks, or advanced tech, crave this flow of knowledge. Having a common, reliable substrate means ideas pass more smoothly between teams, and that means fewer barriers and better, faster discovery. In my own shop, projects often cross over between drug design and functional material synthesis, and the same intermediate can make both lines possible. That flexibility shortens timelines and stretches grant dollars further.

    Supporting Innovative Education and Skill Growth

    Reliability in materials gives educators another tool for nurturing tomorrow’s leaders in science and engineering. In many undergraduate labs, running a stepwise series of transformations on a challenging molecule can mean the difference between inspiration and discouragement. A well-controlled intermediate like 4-Amino-2-nitropyridine makes it feasible to give students hands-on access to real research techniques. That means more skilled chemists entering graduate programs, better able to hit the ground running and tackle world problems.

    Science education relies on more than information in textbooks. It depends on what’s found and used in the actual working lab. Every positive student experience, built on reliable materials and clear-cut procedures, strengthens the entire field. More than a few of my students picked up core concepts in electrophilic aromatic substitution or nucleophilic attack thanks in large part to the distinct behavior of this intermediate. That practical learning shaped their future success, far beyond any quiz or exam.

    Lab safety, often overlooked in favor of rushing results, connects closely to material quality. With a reputable source for intermediates, safety notes are more accurate, hazards lower, and results come easier. Older chemists pass down these lessons—they lived through times when sourcing was hit-or-miss, and every junior chemist had war stories of failed reactions from contaminated, out-of-spec starting materials. Today, tighter standards let those stories become rarer, thanks in part to reliable products that do what they promise.

    Paving a Smoother Path from Bench to Market

    Chemistry’s journey from bench to finished product depends on steps that work every time. 4-Amino-2-nitropyridine 97% helps close the gap between exploratory research and scalable process. Every researcher I’ve known who prepared a patent application felt the tension of needing consistent yields and clear analytical signatures, not only for the invention itself but for the pathway taken to get there. This product scores points on both counts.

    With repeatable reactivity, tight analytical profiles, and amenability to classic work-ups, this compound pushes progress along. In regulatory review or method scale-ups, a consistent intermediate means documentation checks out faster and scale-up engineers face fewer surprises. Commercial teams appreciate that, since time literally means money when setting up pilot plants or tuning final steps for clinical-grade manufacturing.

    Technicians know too well how bad raw material cascades through every downstream process—side-products, waste streams, analytical headaches, and sometimes outright project delays. Feedback from people managing kilo lab batches backs up the importance of a trusted product here. The more predictable and pure an intermediate, the fewer cycles an entire research program spends untangling process knots. That momentum matters, whether launching a new drug or rolling out a smart material.

    Factoring Ethics and Responsibility into Science

    Modern chemistry must carry ethical standards that reflect both human and environmental health. Having spent time on review panels and in compliance audits, I’ve seen that strong supply chains in specialty chemicals shape the field’s reputation as much as its technical achievements. Good vendors for 4-Amino-2-nitropyridine support documentation on sourcing, handling, and even post-use disposal without dodging tough questions. That transparency helps everyone up and down the chain—from a bench scientist all the way to the public, who want to know products meet high standards for safety and stewardship.

    Calls for greener chemistry keep getting louder. Whole sectors have built certification and oversight processes to reduce the toll of specialty intermediates. As global regulations tighten, suppliers committed to cleaner, smarter, and safer products will draw more trust and drive broader adoption. For users on the ground, that means a safer lab today and a healthier environment for the years ahead.

    Researchers take comfort in materials that arrive as expected, perform without surprises, and tick the boxes on ethics and sustainability. This compound has shaped many successful chapters in modern science, and its continued use can help more discoveries find their way from idea to impact.

    Looking Ahead: Future Possibilities

    Innovation never stays still, and neither should chemical tools. 4-Amino-2-nitropyridine 97% still has untapped potential in next-generation fields—areas like AI-driven molecular design, advanced photonics, and regenerative medicine. As digital tools map reaction pathways or search for new candidate drugs, having reliable intermediates will speed up both virtual and real-world cycles of discovery.

    Collaborative research between different scientific fields continues to shine light on unexpected uses. Drawing from my own consulting experience across startup biotech and materials science labs, every year brings new twists: peptides coupled to pyridine frameworks, novel diagnostic probes, and smart coatings. None would have reached the proof-of-concept stage without reliable access to advanced intermediates, and 4-Amino-2-nitropyridine sits high on that roster for many teams. The more broadly it gets used, the more likely new scientific surprises will turn up.

    Future generations will tackle more complex challenges—in health, technology, and the environment. Tools like this compound, trusted across research fields, can unlock answers nobody has thought of yet. That marks the true legacy of a specialty intermediate: not only powering the ideas of today, but fueling tomorrow’s breakthroughs too.