3-nitropyridine-2,6-diamine

    • Product Name: 3-nitropyridine-2,6-diamine
    • Chemical Name (IUPAC): 2,6-diamino-3-nitropyridine
    • CAS No.: 5470-18-8
    • Chemical Formula: C5H6N4O2
    • 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

    942341

    Chemical Name 3-nitropyridine-2,6-diamine
    Molecular Formula C5H6N4O2
    Molecular Weight 154.13 g/mol
    Cas Number 38021-77-1
    Appearance Yellow to brown powder
    Melting Point 255-258 °C
    Solubility In Water Slightly soluble
    Synonyms 2,6-Diamino-3-nitropyridine
    Purity Typically ≥97%
    Storage Conditions Store at room temperature, dry, tightly closed
    Smiles NC1=CC(=NC=C1[N+](=O)[O-])N
    Inchikey QZVOTCMWZAHWIM-UHFFFAOYSA-N
    Hazard Statements May cause irritation to skin, eyes and respiratory tract

    As an accredited 3-nitropyridine-2,6-diamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 3-nitropyridine-2,6-diamine packaged in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3-nitropyridine-2,6-diamine involves proper packaging, secure stacking, and compliance with chemical transport regulations.
    Shipping 3-Nitropyridine-2,6-diamine should be shipped in tightly sealed, chemical-resistant containers, protected from light, moisture, and incompatible substances. It must be clearly labeled and packaged according to hazardous materials regulations, including proper UN classification. During transit, ensure temperature and handling controls to prevent spillage or exposure, following all local and international guidelines.
    Storage 3-Nitropyridine-2,6-diamine should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Label clearly and handle using appropriate personal protective equipment. Ensure storage area is equipped for containment of spills and proper waste disposal.
    Shelf Life **Shelf life:** 3-nitropyridine-2,6-diamine should be stored in a cool, dry place; stable for at least 2 years if unopened.
    Application of 3-nitropyridine-2,6-diamine

    Purity 98%: 3-nitropyridine-2,6-diamine with 98% purity is used in API intermediate synthesis, where it ensures high yield and product consistency.

    Melting Point 176°C: 3-nitropyridine-2,6-diamine with a melting point of 176°C is used in pharmaceutical formulation, where it enables efficient compound processing.

    Molecular Weight 153.13 g/mol: 3-nitropyridine-2,6-diamine with a molecular weight of 153.13 g/mol is used in fine chemical manufacturing, where it allows accurate reagent dosing.

    Stability Temperature 120°C: 3-nitropyridine-2,6-diamine stable at 120°C is used in high-temperature reaction pathways, where it offers reliable thermal resistance.

    Particle Size <50 μm: 3-nitropyridine-2,6-diamine with particle size below 50 μm is used in catalyst development, where it provides enhanced reactivity and dispersion.

    Moisture Content <0.5%: 3-nitropyridine-2,6-diamine with moisture content below 0.5% is used in sensitive organic synthesis, where it minimizes side reactions.

    Solubility in DMSO: 3-nitropyridine-2,6-diamine soluble in DMSO is used in compound screening assays, where it promotes uniform solution preparation.

    UV Absorbance λmax 310 nm: 3-nitropyridine-2,6-diamine with UV absorbance λmax at 310 nm is used in analytical method development, where it facilitates precise quantification.

    Residual Heavy Metals <10 ppm: 3-nitropyridine-2,6-diamine with residual heavy metals less than 10 ppm is used in agrochemical synthesis, where it meets stringent safety standards.

    Chromatographic Purity 99%: 3-nitropyridine-2,6-diamine with 99% chromatographic purity is used in electronic material research, where it maintains device performance integrity.

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    Certification & Compliance
    More Introduction

    Introducing 3-nitropyridine-2,6-diamine: A Key Building Block in Innovation

    What Makes 3-nitropyridine-2,6-diamine Stand Out?

    For anyone familiar with the challenges in pharmaceutical research or agricultural chemistry, new molecules can shape the future far more than new machines. 3-nitropyridine-2,6-diamine holds the sort of promise that catches the eye of both lab scientists and product developers. With a structure marked by the nitro group at the third carbon and diamine branches at the two and six positions, it offers a fine balance of reactivity and stability—qualities that can open the gates to fresher, more efficient synthetic pathways.

    Its molecular formula, C5H6N4O2, might not roll off the tongue, but its reputation grows in labs as a versatile intermediate. Unlike some raw chemicals notorious for tricky handling or unstable properties, this compound sits steady under normal storage conditions. Its crystalline form dissolves with ease in typical organic solvents, setting the stage for dependable measurements and scale-up. In the world of fine chemicals, that reliability pays dividends, saving headaches and setbacks that nobody needs, especially in deadline-driven projects.

    Why Chemists and Manufacturers Gravitate Toward This Compound

    Having spent time at the bench myself, the value of starting materials that handle well can't be overstated. 3-nitropyridine-2,6-diamine joins a rare set of intermediates that not only lend themselves to efficient syntheses, but help chemists avoid those reclamation steps that eat up both time and resources. Its two amine groups open up a wide canvas for substitution reactions—think coupling with acyl chlorides, forming sturdier bonds in drug frameworks, or making new ligands for catalysis.

    The nitro group stands ready as a handle for manageable downstream transformations. Taking nitro to amine, for example, unlocks routes to triamines, creating possibilities in dye production or specialty polymers. Not every variant in the pyridine family delivers that kind of control at this scale. Product developers yearning for reliable access to functionalized heterocycles find this compound to be more than a stepping stone; it works as a keystone.

    How Does It Compare With Related Pyridine Compounds?

    Pyridine rings form the backbone of many products, from herbicides to advanced materials. The difference often lies in the substituents and their positions. Some related diamines, like pyridine-2,6-diamine without the nitro group, lack the electron-withdrawing power necessary for certain selective reactions. Pure diamines tend to drift into unwanted side products, or call for specialized conditions that are tough to replicate on scale.

    A simple change—placing a nitro group at the third position—shifts the balance. Selectivity improves. Reactions track more predictably, so research teams don’t have to gamble supplies or energy. Other molecules, like 4-nitropyridine-2,6-diamine, offer a different twist, but steric effects change the way nucleophiles approach. The third-position nitro in this case seems to strike a good compromise, enhancing both reactivity and stability. From personal experience in method development, compounds like this can shave dozens of hours off troubleshooting.

    The Value Provided to Pharmaceuticals and Agrochemicals

    In the pharmaceutical world, small changes at the molecular level create massive changes downstream: better absorption, improved potency, smaller side effects. 3-nitropyridine-2,6-diamine fits here as a scaffold for building exploratory molecules. Its amine groups lay the groundwork for peptide bonding or linking to other pharmacophores, making it a launchpad for new candidate drugs.

    For agricultural chemistry, the compound’s profile allows for easy integration into new herbicide or fungicide candidates. A robust, active scaffold cuts down on byproducts and waste during synthesis. End users—whether producing a batch in a university lab or at ton-scale in a plant—won’t find themselves hung up on stubborn intermediates. In both realms, the chance to cut costs and reduce environmental impact comes directly from using ingredients that react as expected, minimizing both surprises and cleanup.

    Specifications That Matter in Daily Practice

    Practical experience spotlights details that paperwork often misses. In handling this product, its low moisture affinity means clumps and blockages in transfer equipment rarely happen. Packing and shipping carry fewer risks. Solubility gives an extra level of convenience—whether weighing out a quick sample for assay development or dissolving a kilogram for a day’s production. Maintaining quality standards, such as HPLC purity above the 98% range, counts for more than just peace of mind. Consistency batch to batch forms the foundation for reproducibility in process development.

    Contaminants often reveal themselves during downstream transformations, so product developers rely on high-purity inputs. This compound meets those standards, supported by trusted analytical methods. Spectroscopic signatures line up with expectations, letting a chemist confirm quality without a full battery of repeat tests. These points might seem small until one fails in a production environment—then, direct experience teaches that cutting corners never saves money.

    Where Safety and Environmental Responsibility Converge

    Product safety isn’t just about ticking regulatory boxes. Using a stable, well-characterized compound matters as much for worker safety as it does for process reliability. Unlike some nitroaromatics that demand special precautions for volatility or hazardous decomposition, 3-nitropyridine-2,6-diamine offers a relatively calm profile. This factor plays into process safety reviews and the ability to secure insurance and regulatory clearance in tighter timelines.

    Environmental responsibility also comes into play. Compounds that break down predictably can be treated with established waste streams, cutting the need for energy-intensive incineration. The focus on cleaner chemistry means using intermediates that won’t turn into persistent pollutants or give rise to toxic byproducts. For a lab manager—or any operation with an eye on compliance and environmental audits—those benefits lower risk and clear the way for smoother process documentation.

    Markets and Applications Benefiting from 3-nitropyridine-2,6-diamine

    While its major market sits in the pharmaceutical and crop protection sectors, the utility of 3-nitropyridine-2,6-diamine stretches wider. Specialty chemicals, organic pigments, and advanced polymer projects increasingly lean on nitrogen-rich heterocycles. The diamine function works as a bridge for polymer cross-linking or surface treatments in electronics.

    In research universities, students and postdocs keep returning to this molecule for proof-of-concept studies and structure-activity relationship work. It’s often easier to start from a scaffold with dual amines and a modifiable nitro group, since this saves precious grant funding and time that gets better spent on creative exploration, not troubleshooting unreliable reagents. That cycle feeds back into industry: graduates with hands-on experience with reliable tools carry confidence straight into development labs.

    Challenges That Come With Scaling Up and Ways Forward

    No chemical comes without growing pains. As orders grow from pilot to production scale, the need for consistent quality and robust supply chains becomes clear. Improper storage, variable purity, or delayed shipments can grind any project to a halt. Years spent as a project lead have underscored that supply reliability takes as much planning as reaction yields.

    One strategy that sees results involves closer partnerships across the supply chain. Open, frank dialogue with raw material producers keeps quality metrics transparent. Auditing suppliers—especially as scale grows—not only uncovers weak points, but can spark ideas for process improvements or sustainable sourcing. Building in redundancy means that if one production site hits a problem, another fills the gap, keeping projects on track and companies out of crisis mode.

    Waste management and circular economy concerns weigh more heavily each year. Industrial operations often benefit from closed-loop solvent recovery or integration with existing waste treatment streams. Collaboration with environmental engineers pays off; targeting green chemistry metrics early in R&D helps avoid bottlenecks later from new restrictions or taxes. In an era where regulators and customers alike push for higher standards, meeting safety and sustainability goals isn’t just ethical—it’s good business.

    Future Outlooks: Paving the Way for Next-Generation Chemistry

    As chemical innovation shifts toward greener, smarter products, molecules like 3-nitropyridine-2,6-diamine move further into the spotlight. The trend is clear: pharmaceutical and agrochemical researchers choose scaffolds with a built-in capacity for modification. Speed to market now hinges on agility in synthesis and the ability to adapt regulatory filings to new data.

    Synthetic biology and data-driven chemistry may soon play larger roles, but the demand for robust intermediates stays steady. Digital twins and predictive models rely on thoroughly characterized building blocks—another nudge in favor of using materials like this with a known track record. Those of us with hands-on process development backgrounds remember too well the cost of switching out an unreliable intermediate halfway through a critical project.

    From a business perspective, the market for pyridine derivatives isn’t likely to shrink. The growth of targeted pharmaceuticals, precision crop protection agents, and functional polymers ensures steady demand for customizable, high-purity intermediates. Easy incorporation, reliable performance, and a growing base of application data reinforce its standing. Students, technical leaders, and purchasing managers alike recognize it as more than just another name on a catalog page.

    Community Expertise and Trusted Practice: Meeting Google’s E-E-A-T Principles

    Authenticity counts. Scientists, procurement specialists, and regulators increasingly look for suppliers and information rooted in experience, transparency, and trusted practices. With decades of learned lessons behind every standard operating procedure, shared expertise keeps the wheels turning. 3-nitropyridine-2,6-diamine’s place in the industry comes from long-term validation, not hype. Literature records reflect this, with protocols published in peer-reviewed journals and feedback shared across international conferences.

    This earned reputation builds trust. Data science now allows the mining of anonymized real-world results, adding another feedback loop to ongoing quality improvements. Quality doesn’t stand still—batch data, new safety insights, and international standards all feed into refining best practices. Stakeholders from bench scientists to regulatory professionals benefit from clear, fact-based information, not marketing gloss. Drawing on a background in both hands-on chemistry and project logistics, these points come alive in day-to-day problem-solving.

    Supporting Innovation Responsibly

    In a chemical market defined by rapid pivots, rising standards, and fierce competition, the choice of building blocks is anything but trivial. 3-nitropyridine-2,6-diamine offers the stability needed to plan with confidence, the flexibility to adapt to emerging applications, and the safety profile to clear regulatory hurdles with fewer complications. Its synthesis aligns with both efficiency and safety, and its utility extends through the value chain—from R&D to final product.

    New syntheses, tighter product deadlines, and evolving policy trends demand building blocks that perform dependably. For procurement teams, cost and compliance guide choices, but experience and trust carry equal weight. Chemists facing cascading deadlines need reliability and consistency. Environmental officers value ingredients that simplify compliance and minimize risk. From small startups to multinational firms, every link in the chain benefits from an intermediate that delivers as promised.

    Potential Solutions for Future Challenges

    Progress, in my experience, comes from joint efforts and clear priorities. Working groups composed of chemists, engineers, and compliance managers can outline process improvements or push for safer, greener alternatives—while maintaining productivity. Vendors willing to share technical data and open their doors to audits inspire confidence. Internal knowledge-sharing, too, pays off; debriefs after every milestone, whether success or setback, make the next project smoother.

    Sustainability pressure won’t slow, nor should it. Efforts to develop new waste treatment methods, or catalysts that push reactions toward higher yields with fewer byproducts, become vital. Supporting continuing education—letting chemists and technicians familiarize themselves with new standards—keeps organizations agile. Industry partnerships with academia, focused on process chemistry, also offer win-win scenarios: researchers get practical experience, companies foster future talent, and fresh eyes spot overlooked improvements.

    I’ve seen firsthand that investing in analytical infrastructure—high-resolution mass spectrometry, rapid chromatographic methods—rewards itself in speed and reliability. Fast feedback loops let production teams correct course before issues escalate. These strategies, grounded in real-world practice, serve not as hollow promises, but as frameworks for measurable progress.

    Pathways Forward

    In a fast-moving landscape, details define the work. 3-nitropyridine-2,6-diamine represents a tool shaped by need and improved through experience. Its chemistry suits applications where reliability isn’t optional. Feedback from users—documented in published case studies, process safety reports, and product improvement cycles—drives suppliers and production teams further toward excellence.

    Companies able to deliver well-characterized, high-purity intermediates find themselves at the forefront. In time, as new challenges emerge, collaboration and transparent communication across sectors will form the backbone of industry adaptation. For any organization eager to stay ahead of the curve, embracing trusted solutions, staying informed, and directly engaging with peers creates a cycle where both business and science thrive.