2-pyridinecarbonitrile, 5-fluoro-

    • Product Name: 2-pyridinecarbonitrile, 5-fluoro-
    • Chemical Name (IUPAC): You have not provided the product name. Please provide the product for which you want the IUPAC name.
    • CAS No.: ''
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    190755

    Chemical Name 2-pyridinecarbonitrile, 5-fluoro-
    Molecular Formula C6H3FN2
    Molecular Weight 122.10 g/mol
    Cas Number 32349-58-7
    Appearance White to off-white solid
    Melting Point 57-59°C
    Smiles C1=CC(=NC=C1F)C#N
    Inchi InChI=1S/C6H3FN2/c7-5-1-2-6(3-8)9-4-5/h1-2,4H
    Solubility Slightly soluble in water
    Synonyms 5-Fluoropicolinonitrile

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

    Packing & Storage
    Packing 500g of 2-pyridinecarbonitrile, 5-fluoro-, supplied in an amber glass bottle with tamper-evident seal and hazard labeling.
    Container Loading (20′ FCL) 20′ FCL loaded with tightly sealed drums of 2-pyridinecarbonitrile, 5-fluoro-, compliant with safety and export regulations.
    Shipping 2-Pyridinecarbonitrile, 5-fluoro- is shipped in tightly sealed containers to prevent moisture or air exposure. It is classified as a hazardous chemical and requires appropriate hazard labeling. The shipment follows all relevant safety, handling, and documentation guidelines, including UN packaging standards, to ensure safe transport by air, sea, or ground.
    Storage **2-Pyridinecarbonitrile, 5-fluoro-** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature, away from direct sunlight and sources of ignition. Ensure proper labeling and secure the storage area to restrict unauthorized access.
    Shelf Life 2-Pyridinecarbonitrile, 5-fluoro- typically has a shelf life of 2-3 years when stored in cool, dry, and dark conditions.
    Application of 2-pyridinecarbonitrile, 5-fluoro-

    Purity 99%: 2-pyridinecarbonitrile, 5-fluoro- with purity 99% is used in pharmaceutical intermediate synthesis, where it enhances reaction yield and product consistency.

    Melting point 50°C: 2-pyridinecarbonitrile, 5-fluoro- with a melting point of 50°C is used in agrochemical formulation, where it ensures easy processing under controlled temperatures.

    Molecular weight 136.10 g/mol: 2-pyridinecarbonitrile, 5-fluoro- with a molecular weight of 136.10 g/mol is used in organic electronics research, where it provides precise molecular control for device fabrication.

    Particle size <50 µm: 2-pyridinecarbonitrile, 5-fluoro- with particle size less than 50 µm is used in catalytic applications, where it improves surface area and reaction efficiency.

    Stability temperature up to 120°C: 2-pyridinecarbonitrile, 5-fluoro- stable up to 120°C is used in high-temperature polymer synthesis, where it maintains chemical integrity during processing.

    Free Quote

    Competitive 2-pyridinecarbonitrile, 5-fluoro- prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@boxa-chem.com

    Get Free Quote of Nantong Acetic Acid Chemical Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Pyridinecarbonitrile, 5-Fluoro-: Reliable Support for Precision Chemical Work

    A Close Look at 2-Pyridinecarbonitrile, 5-Fluoro-

    2-pyridinecarbonitrile, 5-fluoro- stands out in a crowded world of organic intermediates. In chemical research, consistency matters a lot more than brochures ever admit. Some people think chemicals look the same from one bottle to the next, but in my own lab years I saw how even small batch variations could trip up a synthesis or ruin a months-long project. Products like this one—pure, reliable, traceable—save a lot of headaches by living up to their label.

    This compound features a nitrile group attached to a pyridine ring, with a fluorine substituent at the 5-position. That simple structure carries a lot of weight, especially for those building more complex molecules for use in pharmaceuticals, materials science, or agricultural research. The reason boils down to the tight tolerances needed during fine chemical synthesis. When a team is pushing to develop new drugs or crop protectants, purity and positional accuracy keep a project on track. I remember times spent dialing in a process, only to watch yields drop because a reagent brought in too many residuals from a sloppy source. One can’t afford that when every variable counts.

    Specifications and What Sets It Apart

    2-pyridinecarbonitrile, 5-fluoro- most often appears as a white crystalline solid. Purity generally runs above 98 percent by HPLC, a detail not usually bandied about outside research but mighty important to the chemists depending on it. A melting point typically falls in the 50s Celsius, which makes sample manipulation pretty straightforward. Density and solubility align well with other pyridine derivatives, which means you don’t get caught off guard during a tricky purification.

    Fluorinated pyridines like this one differ meaningfully from their non-fluorinated relatives. That fluorine atom doesn’t just change the molecule’s weight. It rewires electron density across the ring, driving changes in reactivity and biological activity. Think of it like swapping out a single chess piece and watching your whole endgame open up. Companies and universities regularly invest in halogenated building blocks because they offer reliable routes to fluorinated drugs and chemical probes. The careful positional selection—here, the 5-position—reflects deep planning, not guesswork, in molecular design.

    Some products claim broad compatibility or versatility, but that’s just talk until put to the test. During my time working on heterocyclic ligand syntheses, I relied on derivatives like this to introduce both stability and electronic tuning. The presence of a nitrile group makes the compound reactive in just the right places without sending a cascade of side-products down unrelated pathways. This kind of control helps medicinal chemists build molecules that survive in living systems longer, sometimes leading to drugs with better half-lives or improved bioactivity. Plenty of medicinal chemistry patents highlight this detailed approach to scaffold decoration.

    Where 2-Pyridinecarbonitrile, 5-Fluoro- Goes to Work

    In practical use, 2-pyridinecarbonitrile, 5-fluoro- usually acts as an intermediate. Chemists reach for it when modifying nitrogen-containing scaffolds, targeting new pharmacophores, or laying out routes to agrochemicals. The pyridine backbone, well-known for its water solubility and ability to coordinate metals, makes this compound a favorite in catalytic systems as well. A good example comes from cross-coupling chemistry, where the nitrile and fluorine groups steer reactions toward desired products while helping avoid useless by-products.

    The fine chemicals world moves quickly these days, with shorter cycles between project kickoff and success or failure. Researchers who need tailored intermediates look to well-characterized compounds compiled with detailed analytical data: NMR, HRMS, chromatographs with clear retention times, not just a vague promise of “high purity.” Regulatory submissions and peer-reviewed papers increasingly expect this level of proof. Providing compounds like 2-pyridinecarbonitrile, 5-fluoro- with a detailed Certificate of Analysis has become a baseline practice for reputable suppliers.

    Many young chemists I know value the peace of mind from a well-documented synthetic history. They sleep easier knowing each link in the supply chain played by the same rules on purity and batch control. It’s not just about avoiding a bad experiment; it’s about the cumulative culture of trust that lets bigger projects succeed. No one wants to retrace three steps because a raw material failed a hidden test.

    The Organic Chemistry Behind This Molecule

    The unique reactivity of the nitrile and fluorine on this scaffold gives 2-pyridinecarbonitrile, 5-fluoro- genuine utility. During nucleophilic substitution or palladium-catalyzed couplings, electron-withdrawing groups pull reaction pathways in new directions. That widens the available menu for medicinal chemists and synthetic method developers. In my own postdoc work on transition metal catalysis, I noticed how fluoro-pyridines sluiced electron density toward the nitrogen, creating unique ligand behaviors for catalytically active centers.

    In the broader context, demand for such intermediates only grows as more research groups focus on the design of small molecules with specific shape and electronic profiles. Fluorine may seem a humble addition, but it radically alters lipophilicity, pKa, and membrane permeability. Drug hunters like to talk about “magic methyl effects”—the way a small change unlocks major pharmacological shifts. Fluorine brings that same kind of magic, tuning binding sites and clearance rates in subtle but invaluable ways.

    Synthetic approaches to this compound typically rely on careful halogenation, sometimes starting from readily available pyridine sources, then proceeding through selective cyanation. Seeded crystallization or controlled solvent removal keeps finished product within spec. The process optimization behind each batch, often carried out at the scale of a few grams to a few kilos, draws a line between high-value intermediates and run-of-the-mill chemicals. Each producer must balance waste, cost, and workplace safety—a real juggling act with the push for green chemistry.

    Comparing to Alternatives: What Actually Changes?

    Some might ask, “Why not just use a non-fluorinated pyridine nitrile?” The difference isn’t academic. Non-fluorinated analogs usually show higher basicity and distinct metabolic stability, which might work for early screening but falls short during late-stage optimization. Fluorine brings in powerful metabolic blocking, protecting molecules from stubborn enzymatic breakdown. This usually feeds directly into increased bioavailability or a longer action profile. Drug discovery journals regularly point out that many blockbuster treatments today rely on at least one fluorinated ring.

    Compared to larger or more complex halogen substitutions, the 5-fluoro group is easier to introduce during synthesis, causes less steric hindrance, and plays nicely in crowded reaction flasks. Fluorination at the 5-position supports more precise modulation of biological activity than, say, a 2-chloro substitution. Each shift in atom placement translates into a ripple of changes through receptor binding, solubility, or pH-dependent behavior. Medicinal chemists spend long nights charting SAR (structure-activity relationship) charts, and every subtle shift matters.

    Other suppliers sometimes market similar structures—5-chloro, 6-fluoro, or unsubstituted versions—but users come back to the 5-fluoro variant when working on CNS-active drugs, kinase inhibitors, or new agricultural protectants. Familiarity isn’t just inertia. Researchers share experimental successes with colleagues, building a kind of consensus around the tools that deliver real, repeatable gains in the lab and in the field. Quality, in this case, gets measured one successful experiment at a time.

    This Compound’s Place in the Industry Today

    Modern industries expect chemical suppliers to rise above generic expectations. Environmental, ethical, and quality concerns shape today’s sourcing decisions in ways my mentors didn’t always imagine. For 2-pyridinecarbonitrile, 5-fluoro-, this means rigorous QC, traceability from raw materials through finished product, and transparent reporting on process waste and resource use. It’s never just about providing a reagent; the supplier’s role continues after the shipment arrives.

    Having served as a buyer in both academic and industry settings, I’ve watched supply chain confidence evolve. Projects get greenlit or held back based on the ability to source key intermediates within weeks, not quarters. Delays caused by unknowns in the synthetic route, especially for custom intermediates, slow the pace of innovation. Stocks of critical compounds like this one show up in university and CRO inventories because the end users trust both the supply chain and the chemical itself to hold up under pressure.

    In safety-critical sectors, trace impurities or poorly understood by-products ruin entire campaigns. For those working under GMP constraints or preparing regulated filings, minor differences in fluorinated intermediate profiles mean real compliance risk. Consistency in lot analysis—beyond the basics of melting point and NMR—is part of the unwritten handshake between producer and researcher. Routine performance audits, including chiral or residual solvent tests, keep upgrades ongoing. Long-term partners value this transparency over any one catalog price.

    Improving the Chemistry of Tomorrow

    Discussions about sustainability and process intensification drift through every industry conference I attend. While some may see intermediates like 2-pyridinecarbonitrile, 5-fluoro- as commodities, more forward-thinking organizations try to close the loop on waste and reduce energy consumption in synthesis. Fluorine’s environmental story remains complicated; responsible labs seek out documentation showing minimized emissions, solvent recovery, and assessed worker exposure risks. A handful of green chemistry ventures now report on lifecycle data for starting materials, but mainstream adoption takes time.

    One potential way forward involves developing more direct catalytic routes to install the nitrile and fluorine groups in a single step. In my own reading, a few papers sketch out clever late-stage cyanation or C-F bond formation processes, but these often rely on rare metal catalysts or costly activating agents. The market rewards the fastest, least wasteful method—yet won’t tolerate data gaps or safety shortcuts. Collaborations between academic synthetic chemists and industry process teams could help bridge these challenges. Continuous flow technologies or enzyme-catalyzed steps might lower the environmental cost, and suppliers willing to invest in greener documentation will likely gain ground with procurement managers.

    A related challenge concerns analytical improvements. As regulation grows tighter, more customers demand full impurity profiling—down to the trace ppm. Equipment like high-res ultrafast LC-MS, which I first encountered just a decade ago, now sets the expectation for thorough, actionable CoAs. In the drive to reduce rework or batch recalls, this trend shows no sign of slowing. Smart suppliers aim to deliver not just a bottle of white powder, but a full paperwork trail, giving research teams more confidence in their results and regulatory standing.

    Looking Ahead: Opportunity and Responsibility

    Every advance in chemical supply brings new opportunity—and responsibility—for those who make and use complex building blocks. 2-pyridinecarbonitrile, 5-fluoro- illustrates both sides of this balancing act. At the benchtop, it helps speed synthesis and underpins dozens of potential innovations in medicine and agriculture. In process development, it tests the bounds of green chemistry and supply chain transparency. Today’s researchers bear the burden of careful sourcing, while suppliers build reputations on traceability, reliability, and continuous improvement.

    I see a widening divide between legacy vendors and agile producers willing to bring new production methods and fuller disclosure. Users reward those who offer value beyond the molecule—robust logistics, clear batch data, and serious engagement with modern regulatory expectations. Nimble startups sometimes outpace the old guard by offering the specialty products most needed for today’s breakthroughs. At the same time, larger suppliers invest in deeper compliance, auditing, and supply security, competing on both cost and confidence.

    Real progress requires honest collaboration. Chemists in the lab need to keep giving feedback on reagents that underperform or offer unexpected results. Suppliers who make a habit of listening—building in more robust impurity screens, reducing bottlenecks, or supporting greener syntheses—stand to lead. I’ve encountered plenty of situations where open lines of communication between the bench and the plant floor unlocked new efficiencies that spreadsheet-driven purchasing can’t see. There’s still no substitute for hands-on know-how.

    Wrapping Up Key Insights

    2-pyridinecarbonitrile, 5-fluoro- may look like one specialty chemical among thousands, but working chemists know the difference when a reagent truly delivers. Daily lab routines depend on it: the clear labeling, the matched batch reports, the confidence that if a reaction falters, the source won’t be in doubt. Its role in new drug development, agricultural R&D, and fine chemicals production speaks to the value of tight process control and strict analytical standards. Each subtle structural variation influences experimental outcomes in ways outsiders rarely see—and yet, it is in these nitty-gritty details that real scientific advances get built.

    My own experience taught me to appreciate this behind-the-scenes value. Experienced chemists seek partners, not just suppliers, in a market where speed, data, and sustainability matter more each year. This is how innovations reach market faster, with greater safety, and the confidence that progress won’t come at the expense of responsibility. For all its understated presence, 2-pyridinecarbonitrile, 5-fluoro- keeps earning its place in the toolkit of those shaping the future of chemical research and manufacturing.