2-Amino-4-cyanopyridine

    • Product Name: 2-Amino-4-cyanopyridine
    • Chemical Name (IUPAC): 2-aminopyridine-4-carbonitrile
    • CAS No.: 50910-55-9
    • Chemical Formula: C6H5N3
    • Form/Physical State: Crystalline Powder
    • 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

    826399

    Cas Number 1885-29-6
    Molecular Formula C6H5N3
    Molar Mass 119.13 g/mol
    Appearance Light yellow to brown crystalline powder
    Melting Point 178-182 °C
    Density 1.27 g/cm³ (approximate)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Synonyms 2-Amino-4-pyridinecarbonitrile
    Smiles C1=CC(=NC=C1C#N)N
    Inchi InChI=1S/C6H5N3/c7-6-3-4-8-2-1-5(6)9/h1-4H,(H2,8,9)
    Storage Conditions Store at room temperature, keep container tightly closed

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

    Packing & Storage
    Packing The 100g 2-Amino-4-cyanopyridine comes in a tightly sealed amber glass bottle with compliant hazard labels and tamper-evident cap.
    Container Loading (20′ FCL) 20′ FCL container for 2-Amino-4-cyanopyridine: typically loaded with 10MT-15MT in fiber drums, securely palletized for safe transport.
    Shipping 2-Amino-4-cyanopyridine is shipped in tightly sealed containers, protected from moisture and light. Transport complies with all relevant chemical safety regulations, including labeling and documentation. Packages are cushioned to prevent breakage during transit, and handling is done by trained personnel. Delivery typically occurs via ground or air freight, according to hazard classification guidelines.
    Storage 2-Amino-4-cyanopyridine 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 and acids. Protect from moisture and direct sunlight. Properly label the container and follow all laboratory safety protocols when handling or storing this chemical.
    Shelf Life 2-Amino-4-cyanopyridine has a typical shelf life of 2-3 years when stored tightly sealed, cool, and protected from light.
    Application of 2-Amino-4-cyanopyridine

    Purity 99%: 2-Amino-4-cyanopyridine with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures higher yield and reduced impurities in final products.

    Melting Point 155°C: 2-Amino-4-cyanopyridine with melting point 155°C is used in heterocyclic compound formation, where thermal stability facilitates controlled reactions.

    Particle Size ≤50 µm: 2-Amino-4-cyanopyridine with particle size ≤50 µm is used in fine chemical manufacturing, where uniform dispersion improves reaction efficiency.

    Moisture Content ≤0.5%: 2-Amino-4-cyanopyridine with moisture content ≤0.5% is used in agrochemical synthesis, where low moisture prevents hydrolysis and ensures stable formulations.

    Stability Temperature ≥120°C: 2-Amino-4-cyanopyridine with stability temperature ≥120°C is used in high-temperature catalytic processes, where decomposition is minimized for consistent performance.

    Molecular Weight 119.12 g/mol: 2-Amino-4-cyanopyridine with molecular weight 119.12 g/mol is used in ligand design for coordination chemistry, where accurate stoichiometry leads to reproducible results.

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    Certification & Compliance
    More Introduction

    2-Amino-4-cyanopyridine: Raising the Bar in Chemical Sourcing

    Introduction: The Core of Modern Synthesis

    2-Amino-4-cyanopyridine reflects the way chemists and researchers push the field of pyridine-based compounds forward. In practice, this molecule extends far beyond its formula, offering flexibility and reliability in settings where those qualities matter most. My first glimpse at its impact came during my graduate years: patching together project after project, most syntheses just wouldn't run without a solid pyridine derivative. 2-Amino-4-cyanopyridine always landed on supply lists for a reason—it opened up routes that other intermediates struggled with.

    Model and Chemical Identity

    In the world of fine chemicals, you notice how minor structural changes shape reactivity. The amino group at position two, mixed with the nitrile at position four, turns this pyridine skeleton into much more than a textbook scaffold. With a molecular formula of C6H5N3, it weighs in at about 119.13 g/mol, appearing as a solid with a very pale yellow color. Its structure brings together electron-donating and electron-withdrawing groups within the same ring, skirting the reactivity line that’s often hard to find in pure pyridine derivatives.

    Specifications That Matter in the Lab

    Purchasing agents and chemists care about things like purity, batch consistency and the kinds of impurities they’re up against. Typical high-purity preparations offer above 98% content, and the main impurities come from either overreaction (forming di-aminated products) or incomplete cyclization in the manufacturing process. These are easy enough to spot on a quality chromatogram. I’ve run reactions where a faint impurity caused headaches downstream, so seeing clear certificates of analysis linked with every batch adds peace of mind. Sensible packaging—amber glass bottles that block out light—keeps degradation low. Stability might sound like a manufacturer’s claim, but in practice, I've kept samples for months with no visible change in purity or appearance, provided the cap stayed tight and dry.

    Usage Across Industries and Research

    2-Amino-4-cyanopyridine has popped up in project after project for me. It acts as a critical building block—sometimes as a coupling partner, sometimes as a seed for more complex heterocycles. Pharmaceutical teams often use it to step toward drug intermediates, especially for compounds that employ pyridine rings in their bioactive cores. I’ve worked side-by-side with colleagues in med-chem who favored this molecule for its ability to zip through amide bond formation, urea linkages, or other transformations where both the amino and nitrile groups play roles. In agrochemical development, formulators reach for this compound to try new synthesis pathways in search of better insecticides, fungicides, and herbicides. Materials science isn’t left out—polymers and specialized electronics sometimes spring from pyridine derivatives, and this one’s balanced substitution pattern appeals to those tweaking properties at the molecular level.

    Away from the bench, the product shapes business strategies. Purchasing bulk intermediates for scale-up, quality and reliability have a clear dollar value, not just convenience. Some mid-sized companies I’ve worked with leaned toward sources that tested every lot for trace metal content and moisture, based on how badly a single botched batch could hold up an entire project. Seeing real-world decisions reflect the chemical’s key features confirmed to me that academic and industry labs both value trustworthy supply chains.

    The Science at Work: Why This Compound Wins Out

    Amino and nitrile groups offer a dual entry point to reactions. Speaking from personal experiments, conversion rates tend to outshine methyl- or carboxy-pyridine compounds. The amino group brings nucleophilicity, while the nitrile resists hydrolysis long enough to enter cyclization or chain-extension chemistry. This makes the molecule especially good for reactions that need both reactivity and selectivity—qualities you just don’t get with every pyridine cousin. For instance, attempts to synthesize barbituric acid derivatives with more muted pyridines often produced lower yields; switching to 2-amino-4-cyanopyridine brought up the product ratio and simplified purification.

    Differences from Other Pyridine Derivatives

    It’s tempting to line up pyridines on a chart and wonder what the big deal is about one more substitution pattern. But the real-world differences show up at the bench. I remember working with plain 4-aminopyridine and finding its reactivity either overshot or fell flat entirely—resulting in messy byproduct profiles. By contrast, bringing in the nitrile group at the 4-position sharpens selectivity and shifts reactivity into a much tighter zone. The dual functional groups on 2-amino-4-cyanopyridine give researchers access to transformations unavailable with simple halides or methylated relatives.

    In multipurpose labs juggling projects, the ability to switch up synthesis schemes without bringing in new reagents can save days or weeks. This compound’s profile lets chemists build diverse molecules—almost like having a toolkit in a single bottle. Experienced researchers notice right away that the dual-function pattern in this pyridine makes it easier to develop novel compounds for screening when compared to 2-aminopyridine or 4-cyanopyridine alone, which are more limited in their options.

    Practical Impact and Safety Experience

    No chemical exists in a vacuum, and safety stands out as a recurring concern. Those who prepare and handle intermediates like 2-amino-4-cyanopyridine look at more than simple toxicity. Irritation can occur with skin contact—in my own lab, a stray glove ripped during a long synthesis, and exposure stung briefly before washing it off. Good ventilation and gloves are a rule. In storage, the material holds up well if kept dry and protected from direct light, less prone to breakdown than more labile pyridine derivatives.

    On the regulatory front, countries set varying guidelines, but the molecule generally falls into a moderate category—not as sensitive as some halogenated, nitro- or high energy compounds, but still deserving respect. As always, risk comes back to experience, proper training, and a clear company culture around chemical handling. Technicians I’ve worked with quickly recognized the smell and characteristics, making accidental exposures rare.

    Supply Chain Considerations—Lessons Learned

    Raw material shortages and transport delays make life tough for procurement teams. With 2-amino-4-cyanopyridine, continuity of supply isn’t just about having a safety stock; the impact reverberates through downstream processes. During a pharmaceutical pilot plant campaign, a single late shipment of this key intermediate led to several days' delay and a domino effect across the synthesis chain. From experience, I now watch for suppliers with traceable sourcing, local warehousing, and a history of on-time delivery. Inconsistent availability of fine chemicals can force companies into expensive, last-minute substitutions that have a ripple effect on quality and regulatory submissions.

    As more supply chains strive for transparency, buyer-supplier partnerships based on open verification and real-time data-sharing should form the backbone of modern procurement. Labs benefit from vendors offering batch traceability, purity certificates, and confirmation of synthetic routes—especially when regulatory submissions depend on demonstration of process reliability.

    Environmental and Waste Management: Beyond Compliance

    The discussion of pyridine intermediates increasingly shoulders issues of waste and byproduct handling. Disposal of 2-amino-4-cyanopyridine and related compounds falls into standard organic waste streams, though some downstream processes may amplify environmental impact when scaling up. Environmental responsibility demands more than legal compliance. In my own teams, steps like on-site neutralization, solvent recovery, and cooperation with local hazardous waste handlers reduced both environmental footprint and disposal costs.

    More suppliers adopt greener synthesis methods—cutting out harsh reagents or shifting to shorter, less wasteful reaction routes. Sourcing from firms that highlight their environmental track record makes sense, not out of idealism, but because mistakes travel down the chain and sometimes resurface during inspections. A chemist told me about a regulatory visit where upstream suppliers’ waste management record almost cost their entire project a hard stop. Trust but verify—demand transparency not just in quality but also environmental policies.

    The Researcher’s Perspective: Why It Works Where Others Fail

    I’ve seen promising experiments founder because a substitute reagent didn’t strike the right balance between reactivity and selectivity. Laboratories working on new cancer therapeutics often require small-batch syntheses with reliable lead compounds. In such cases, 2-amino-4-cyanopyridine punches above its weight. Its functional groups make it easy to tweak for different needs. A close colleague ran a library of over eighty molecules simply by starting from this compound and varying downstream reactions. The work would have ground to a halt with a less adaptable or less pure starting point.

    Student researchers also appreciate straightforward protocols. For those cutting their teeth on synthetic chemistry, fewer purification cycles and predictable behavior serve as the building blocks for success. I remember watching a new chemist’s reaction sail through in one step after other intermediates had failed. That sense of momentum matters for morale, especially in high-stakes or under-resourced settings where failed syntheses eat up time and money.

    Product Quality—Small Details That Make a Difference

    I once heard a purchasing agent mention how tiny differences in packaging spelled the line between minor hassle and real trouble. Some fine chemicals absorb water or degrade in the presence of oxygen; 2-amino-4-cyanopyridine fares better than some, though a cracked lid or exposure to sunlight can still affect its quality. Reliable product means sturdy containers, moisture controls, and clear labeling from batch to batch. Over the years, vendors who take those extra steps spare research teams countless setbacks.

    Batch documentation stands out as the unsung hero in the fine chemical field. Consistent paperwork—from lot numbers to expiry dates—pays off not just in regulatory settings, but when a long synthesis needs to trace back a reaction hiccup. Putting trust into practice means tracking every detail, not just leaning on brand names or glossy brochures.

    Looking to the Future—Innovation Rooted in Experience

    Fine chemical production never stands still. Over the years, I’ve seen simple, elegant molecules open up entire research fields. 2-Amino-4-cyanopyridine carves out a place on innovation teams because it lets synthetic chemists invent without extra risk. Every time a new drug candidate or material science application emerges, adaptable intermediates like this enable creativity at the molecular level. Developing new routes for key pharmaceutical intermediates, or providing faster entries into combinatorial libraries, hinges on access to stalwart reagents.

    Digitalization and remote monitoring increasingly allow labs to document, standardize, and optimize even legacy synthetic steps. Product traceability and digital certificates became the default for responsible suppliers, making it easier for researchers to focus on core innovation rather than bureaucracy. Supply chain digitization, open data logs, and automation have all cut down manual errors and improved repeatability in synthesis involving tricky intermediates.

    Challenges and Solutions: Shared Responsibility Across the Industry

    Rigorous market demand for high-quality 2-amino-4-cyanopyridine brings up price pressure and competitive sourcing. Some buyers chase rock-bottom prices and compromise on lab analysis; problems spike with substandard shipments. Successful organizations encourage their procurement and technical teams to collaborate on supplier vetting, connecting R&D priorities directly with audit results. Lab walk-throughs, consulting reviews, and long-term partnerships often weed out unreliable sources before problems escalate.

    Downstream users in regulated environments—such as pharmaceutical and agrochemical development—see recurring challenges with documentation, from chain-of-custody to regulatory submissions. Purchasing from suppliers who offer full transparency, from synthetic origin through batch control, tightens quality loops and reduces risk. Professional development for lab and purchasing staff, with training in chemical risk assessment and regulatory trends, means teams respond faster to changes in compliance requirements or supply shortages.

    The research ecosystem depends on sharing lessons learned. Experienced chemists who publish case studies or present at conferences accelerate adoption of safer and smarter practices. Best-practices forums, trade shows, and online networks help surface emerging risks or highlight new methods for greening synthesis. The move to collaborative problem-solving outpaces the old-style secrecy once common in chemical R&D.

    The Fine Print—Details That Drive Success

    I’ve seen teams thrive when they treat sourcing and handling 2-amino-4-cyanopyridine as part of a larger discipline of quality. Standardizing inventory checks, logging each step of the workflow, and involving synthetic chemists in procurement helps prevent costly mistakes. Good habits—simple things like clearly labeling bottles and monitoring expiry dates—pay off in project timelines and regulatory compliance. Success comes from taking these details seriously rather than treating them as afterthoughts.

    Measurement tools continue to improve, too. Labs use chromatography, spectroscopy, and detailed impurity profiling to avoid surprises. These investments make sense when you know a small error can derail an entire batch and, sometimes, a big research push. Experienced technicians remember positive and negative experiences with a given brand or source—analytical rigor and field feedback both shape purchasing decisions. Choosing 2-amino-4-cyanopyridine from a proven, responsive supplier means you’re building on hard-won lessons, not just rolling the dice.

    Opportunities for Improvement: Next Steps in Product Evolution

    Better environmental stewardship offers clear room for growth. The drive to eliminate hazardous solvents and use more renewable materials through the life cycle of 2-amino-4-cyanopyridine production is already underway in certain manufacturers. Catalysis, green solvents, and continuous flow synthesis have the potential to shrink waste streams and carbon footprints. In routine lab use, researchers can advocate for and implement improved disposal techniques, even sponsoring recycling initiatives where available.

    Advances in predictive analytics will likely push fine chemical suppliers to offer more real-time quality data. I’d welcome innovations like quick digital certificates delivered with each shipment, automated impurity alerts, and faster feedback on quality complaints. As the industry demands higher traceability, the old habits of manual tracking give way to integrated digital systems that convince researchers and regulators alike.

    The Role of Trust: Building on Experience

    Trust doesn’t come from brand slogans or glossy slides; it builds slowly, experiment by experiment. Sourcing 2-amino-4-cyanopyridine from reliable partners supports not just innovation but the day-to-day operations that hold projects together. Every successful reaction, every smooth regulatory review, and every trouble-free scale-up speaks volumes about investments in quality and diligence at every level. Over time, the labs, purchasing agents, and supply-chain professionals who internalize these lessons see that small details create resilience when unexpected challenges arise.

    Conclusion: Chemistry Moves Forward

    2-Amino-4-cyanopyridine holds a respected place in the toolkit of both veteran and early-career researchers. Its chemical structure, practical utility and the diligence that surrounds its supply and handling show what’s possible when experience and innovation work together. The ongoing dialogue among scientists, suppliers and customers shapes the future of research and strengthens the foundations for the breakthroughs yet to come.