2-fluoro-4-methylpyridine-3-carbonitrile

    • Product Name: 2-fluoro-4-methylpyridine-3-carbonitrile
    • Chemical Name (IUPAC): 2-fluoro-4-methylpyridine-3-carbonitrile
    • CAS No.: 86393-34-2
    • Chemical Formula: C7H5FN2
    • Form/Physical State: Solid
    • 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

    974309

    Name 2-fluoro-4-methylpyridine-3-carbonitrile
    Molecular Formula C7H5FN2
    Molecular Weight 136.13 g/mol
    Cas Number 141848-65-7
    Appearance White to off-white solid
    Boiling Point 252.3 °C at 760 mmHg (estimated)
    Density 1.22 g/cm3 (estimated)
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC1=CC(=N(C(=C1)F)C#N)
    Inchi InChI=1S/C7H5FN2/c1-5-2-6(4-9)7(8)10-3-5/h2-3H,1H3
    Storage Conditions Store in a cool, dry place and keep container tightly closed

    As an accredited 2-fluoro-4-methylpyridine-3-carbonitrile 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, labeled "2-fluoro-4-methylpyridine-3-carbonitrile, 5 grams," with hazard symbols and lot number.
    Container Loading (20′ FCL) Container Loading (20′ FCL): Securely packed 2-fluoro-4-methylpyridine-3-carbonitrile in drums or bags, maximizing FCL space, ensuring safe transit.
    Shipping 2-Fluoro-4-methylpyridine-3-carbonitrile is shipped in tightly sealed, chemically resistant containers. It should be handled as a hazardous material, complying with relevant regulations for transport. The chemical must be kept dry, away from heat and incompatible substances, and clearly labeled during shipment to ensure safety and compliance with international shipping standards.
    Storage 2-Fluoro-4-methylpyridine-3-carbonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep it away from sources of ignition. Store at room temperature and avoid excessive heat or moisture to maintain chemical stability and prevent decomposition.
    Shelf Life 2-Fluoro-4-methylpyridine-3-carbonitrile is stable under recommended storage conditions, typically exhibiting a shelf life of at least two years.
    Application of 2-fluoro-4-methylpyridine-3-carbonitrile

    Purity 99%: 2-fluoro-4-methylpyridine-3-carbonitrile with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation.

    Melting Point 73°C: 2-fluoro-4-methylpyridine-3-carbonitrile with a melting point of 73°C is used in solid-phase organic synthesis, where stable temperature control improves reaction selectivity.

    Molecular Weight 136.13 g/mol: 2-fluoro-4-methylpyridine-3-carbonitrile with a molecular weight of 136.13 g/mol is used in agrochemical active ingredient development, where precise dosing supports accurate formulation.

    Stability at 40°C: 2-fluoro-4-methylpyridine-3-carbonitrile with stability at 40°C is used in storage and transportation of chemical reagents, where it prevents degradation during logistics.

    Particle Size <20 μm: 2-fluoro-4-methylpyridine-3-carbonitrile with particle size below 20 μm is used in catalyst support preparation, where increased surface area enhances catalytic efficiency.

    GC Assay >98%: 2-fluoro-4-methylpyridine-3-carbonitrile with GC assay above 98% is used in medicinal chemistry research, where analytical consistency improves reproducibility of experimental results.

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    Certification & Compliance
    More Introduction

    2-Fluoro-4-methylpyridine-3-carbonitrile: Bringing Precision to Fine Chemical Synthesis

    Our Journey with 2-Fluoro-4-methylpyridine-3-carbonitrile

    Working in the chemical manufacturing business, we constantly navigate shifts in demand across pharmaceuticals, agrochemicals, and specialty materials. Among compounds that stand out in our production portfolio, 2-fluoro-4-methylpyridine-3-carbonitrile earns special attention. This isn’t a textbook curiosity—it’s a practical, hard–working intermediate that enters dozens of value-added syntheses where precision and reliability matter. We’ve been making this material at production scale for years, and every kilo tells a story about evolving chemistry and industry needs.

    Traditionally, our customers searched for more versatile pyridine derivatives, molecules that offer reactivity for targeted transformations but not at the cost of side reactions. The synthesis and consistent supply of 2-fluoro-4-methylpyridine-3-carbonitrile answered this call. As direct manufacturers, the bar is set high not just in terms of purity—the batch-to-batch uniformity and scalability of the process bring a peace of mind that trading companies simply can’t guarantee. Working at source allows us to build in robust quality control from each raw material received right through every purification step.

    Getting Specific: Identity, Structure and Why it Matters

    The compound—also known by its structural cues as a fluoro-methyl nitrile substituted pyridine—packs a lot into a compact molecule. The fluorine atom at the 2-position boosts electron deficiency compared to typical methylpyridines. This has real-world impact: downstream chemists routinely report sharper selectivity in their functionalization steps when starting with this framework. The methyl group at the 4-position grants a balance, steering the reactivity profile in a way that unlocks new synthetic doors not available to unsubstituted analogs. Throw in the nitrile at position 3, and you have a latent functionality primed for further derivatization, whether it’s for coupling, amide formation, or heterocycle construction.

    We’ve worked closely with medicinal chemistry clients who use it to introduce pyridine rings into drug candidates. The substitution pattern helps modulate metabolic stability and binding properties—key elements in small-molecule discovery. In our hands, developing the process for this compound revealed that slight variations in temperature or reagent quality could drive impurity formation. By taking full ownership over every reaction and downstream workup, we gained tight reins on purity, delivering materials with minimal fluoropyridine byproducts and clear FTIR and HPLC signatures product after product.

    Model and Specifications: A Practiced Standard, Not Just a Number

    Our batch code or “model” for 2-fluoro-4-methylpyridine-3-carbonitrile reflects process innovations over several years. Consistent melting point, moisture, and color indices matter to chemists taking product into process scale. We’ve calibrated drying and storage to keep water content low, critical for those using organometallic reagents down the line. Typical material leaves our site as a crystalline solid, pale in color—an indicator of low tarring and minimal oxidative side products. Each drum is filled through validated procedures; we log every in-process check from solvents to final packing.

    What comes in as raw fluoropyridine is transformed through custom reactors fitted out for precise temperature mapping and controlled addition of key intermediates. Our teams can spot telltale signs of incomplete conversion well before a sample ever makes it to QA. In practice, this vigilance means our nitrile content stays above 98 percent, with residual solvent and water levels kept below 0.5 percent by weight. We’ve found that this level of control eliminates most of the troubleshooting later, saving both our customers and our technical service teams from avoidable headaches.

    Usage: From Lab Scale to Plant Scale

    Demand for 2-fluoro-4-methylpyridine-3-carbonitrile comes mainly from pharmaceutical researchers and process chemists who value unambiguous NMR and LC-MS signals. The compound serves as a linker, scaffold, or building block for more complex molecules. Its combination of ring substitution and functional groups fits seamlessly into Suzuki couplings, Grignard additions, and transition-metal catalysis. As manufacturers, we take pride in how our material enables vital steps: for example, during the late-phase introduction of a nitrile into a lead structure, which often becomes a bottleneck due to ambiguous reactivity with less pure intermediates.

    On the agrochemical side, this molecule’s substitution pattern gives rise to active ingredients with better soil retention and altered bioavailability. We’ve been on the receiving end of requests for customized packaging, extra drying, or tailored particle sizing: all aimed at ensuring the compound integrates efficiently into each end user’s process. We keep feedback loops tight; a formulation scientist can call in, flag a process quirk, and we’ll review the batch records and suggest next steps. This level of dialog is only possible when you own the process—and its constraints.

    Pilot plant teams and kilo-lab operators value shipment consistency, not only by technical test results but also in practical aspects—flowability, pour rate, and response to humidity. By controlling every variable, we make sure those working at different scales get the same material as the R&D lab, with no surprises as they scale into production.

    Differentiation: Comparing with Other Pyridine Compounds

    Pyridine chemistry brings options. Some buyers look at 2-fluoropyridine, 4-methylpyridine, or unfunctionalized pyridines, weighing function and price. Our experience bridges these debates. Unsubstituted pyridines offer a blank canvas but demand extra synthetic steps for downstream transformation. Introducing a fluorine atom unlocks reactivity; it also deters certain metabolic pathways if the end-use is a pharmaceutical. The methyl at the 4-position raises solubility in common solvents—not a trivial matter for those working with dense, viscous reaction mixtures.

    We’ve fielded requests to compare our product against 2-fluoropyridine-3-carbonitrile or 2-chloro-4-methylpyridine. The difference lies not just in the atom swap, but in how the presence or absence of fluorine influences handling properties and reactivity profiles. The nitrile group, in particular, separates our material from simple methylpyridines, granting an anchor for further chemical modifications. Those involved in pairing pyridines with catalytic partners find that selectivity increases sharply when the fluorine and methyl are both present; fewer side products show up in the subsequent analyses. This proves useful during scale-up, where even small efficiency gains translate to material savings and less downstream purification.

    Another practical difference: our production route for the 2-fluoro-4-methylpyridine-3-carbonitrile delivers lower halide residue and a more neutral odor profile, outcomes valued by operators who may spend hours a day working with these substances. Occupational exposure limits for similar halogenated pyridines tend to be strict. By cutting impurities at the source, we help downstream users reduce their own air monitoring and cleaning burdens. This is a benefit that doesn’t show up on a COA, but anyone with process experience can appreciate it.

    Support Through Process Knowledge: Beyond the Product

    Manufacturing chemicals at scale isn’t just about running a reaction and bottling the result. It demands a view of the whole process: sourcing, reaction conditions, waste minimization, and traceability. Each year, we reinvest in our process, updating reactor designs or retrofitting filtration lines to reduce carryover and streamline cleanout. This benefits every user—less batch-to-batch variance means scientists can draw more confident conclusions from their data. Alongside materials, we share application notes and case histories with chemists trialing new reactions with our product.

    We’ve also responded to upticks in global compliance requirements by tightening our trace metals analysis and ensuring no residual catalysts carry through into the product. This matters for regulated industries: if a pharmaceutical customer faces an inquiry about elemental impurities, our full records can trace every batch constituent right to its source. The commitment runs deeper than ticking a box on an audit—it’s about demonstrating traceability and authentic production oversight.

    Environmental Practice and Worker Safety

    The drive for greener chemistry doesn’t skip specialty intermediates. We keep an eye on solvent choice and energy loads through all steps. For this product, process optimization allowed us to lower solvent waste by 25 percent compared to our first-generation route. Reducing solvent residue not only satisfies customer demand for purer material but also means a safer, cleaner workspace for everyone on our lines. This forms a virtuous cycle—safer manufacturing lowers turnover and attracts higher caliber process operators, who bring their own insights to refining throughput and minimizing “off spec” events.

    Worker safety extends beyond process tweaks. Our teams undergo hands-on hazard drills for handling pyridines and nitriles, including managing spills, inhalation hazards, and storage contingencies. Equipment is interlocked; venting is engineered for worst-case scenarios. These measures pay off over time—our recordable incident rate sits well below industry average, and many of our operators choose to stay with us for years, bringing valuable continuity to our production culture.

    Feedback Loops and Problem Solving in Real Time

    Feedback from the bench or plant floor makes us a better producer. A pharmaceutical team once reported variations in product flowability during humid months. Instead of pushing responsibility back on the user, we ran root-cause analyses, retrofitted our drying stage, and shared updated handling guidelines. These kinds of operational adjustments matter more when the same team oversees all steps, rather than farming out production to third parties. Fine chemical users rely on predictable quality to keep their syntheses and processes running smoothly. Our openness to input allows us to make concrete changes quickly—sometimes sending a revised batch within days, not weeks.

    Tighter partnerships also allow us to trace usage quirks—like reaction inhibition tied to hidden impurities—and redesign purification steps to remove troublesome trace organics. Several times, we provided technical data to support control strategies for clients filing regulatory dossiers. Instead of room-temperature mass production, certain orders receive extra-low temperature storage and special packaging to keep them at optimum performance for key transformations.

    Challenges and What Lies Ahead

    Manufacturing pyridine-based intermediates brings its share of challenges. Sourcing high-purity starting materials places a premium on reliable supplier networks. Unexpected volatility in upstream precursor prices can stress production schedules. We address these disruptions through long-term supplier contracts and real-time inventory checks—a level of vigilance that comes from years of experience navigating the inevitable ups and downs of global chemical supply.

    Waste management remains a continuous improvement area. Latest process updates have targeted lower halogen and metal waste, aligning with both regulatory shifts and customer expectations. More downstream users are seeking declarations for Green Chemistry principles compliance or support for process validation, especially in drug application workflows. Our production methods leave out unnecessary additives or stabilizers, reducing user obligations when it comes time for their own regulatory filings.

    Automation and digitization present new avenues for quality assurance. We continue investing in automated reaction monitoring and digital batch records, reducing the risk of transcription errors and giving us cleaner trending data. This delivers knock-on benefits to clients: batch histories are accessible on demand, and anomalies can be spotted fast before they ripple into delivery schedules.

    Why Direct Manufacturing Makes a Difference

    Direct manufacturing means taking on the responsibility and opportunity of end-to-end control. We see first-hand how small gains in yield or purity at early steps create smoother experiences and returns for end users. There’s a craftsmanship to handling specialty intermediates that doesn’t surface in tidy spreadsheet comparisons. Every reaction, every dryroom check, every QA sign-off carries with it lessons from batches past and user feedback.

    There’s also a commitment to openness as regulations tighten and markets evolve. We can show a prospective partner not just a certificate of analysis, but also the real steps taken to deliver a reliable, high-specification product batch after batch. This embodies more than just a business model—it’s a point of pride for everyone on our team, from the shift leader in charge of the reactors to the chemists troubleshooting outliers before final drum filling.

    Continuous Innovation: Listening and Responding

    Customer needs keep changing as research directions shift or new product lines open up. As a manufacturer, we’re tuned in to these changes. Requests for finer particle size, different solvents, or tighter purity specs push us to innovate, not just copy what competitors offer. Each request tells us how our product fits into the real work of industrial chemistry or pharmaceutical development. Over time, this ongoing conversation guides us—batch records, test analytics, and user feedback form the roadmap we follow when we adjust process steps or invest in new reactor hardware.

    We document each innovation, so improvements aren’t lost with staff changes or as projects evolve. Each run of 2-fluoro-4-methylpyridine-3-carbonitrile builds on the last, with every specification change captured, assessed, and carried forward. This loop of production, delivery, feedback, and process tuning delivers ongoing benefits to our partners: predictability, responsiveness, and real technical support.

    The Value of Knowing Your Source

    In a marketplace crowded with resellers and repackagers, buying direct from a manufacturer provides clarity and confidence no spreadsheet or sales pitch can substitute. We’ve seen new users switch from distributor-supplied pyridine intermediates to our product, reporting back on reduced troubleshooting, easier regulatory documentation, and improved performance in their key chemical transformations. Every call or email from a user reinforces that the path from raw material to end-user product must be supported by technical experience, not just commerce.

    The real value of our 2-fluoro-4-methylpyridine-3-carbonitrile comes from process consistency, quality control at source, and the deep technical knowledge embedded in every batch. For those tackling complex chemical syntheses or scale-up challenges, this means fewer interruptions, steadier results, and a collaborative partner who stands behind each ton shipped out the door.