3,4-Difluorobenzonitrile

    • Product Name: 3,4-Difluorobenzonitrile
    • Chemical Name (IUPAC): 3,4-difluorobenzonitrile
    • CAS No.: 64248-64-6
    • Chemical Formula: C7H3F2N
    • Form/Physical State: Crystalline powder
    • Factroy Site: No. 36, Beisan East Road, Shihezi Development Zone, Xinjiang
    • Price Inquiry: sales2@boxa-chem.com
    • Manufacturer: Tianye Chemical
    • CONTACT NOW
    Specifications

    HS Code

    756433

    Productname 3,4-Difluorobenzonitrile
    Casnumber 64248-62-2
    Molecularformula C7H3F2N
    Molecularweight 139.10
    Appearance White to off-white solid
    Meltingpoint 49-52°C
    Boilingpoint 208-210°C
    Density 1.29 g/cm3
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Smiles C1=CC(=C(C=C1F)F)C#N
    Inchi InChI=1S/C7H3F2N/c8-6-2-1-5(4-10)3-7(6)9/h1-3H
    Refractiveindex 1.497 (predicted)
    Synonyms 3,4-Difluorocyanobenzene

    As an accredited 3,4-Difluorobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 100 grams of 3,4-Difluorobenzonitrile, tightly sealed with a screw cap, labeled with hazard symbols.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 13 metric tons of 3,4-Difluorobenzonitrile packed in 250 kg drums, securely palletized for export.
    Shipping 3,4-Difluorobenzonitrile is shipped in tightly sealed containers to prevent moisture ingress and contamination. The packaging complies with relevant hazardous material regulations, as the compound may be harmful if inhaled or ingested. Proper labeling, documentation, and handling precautions are observed during transit to ensure safety and regulatory compliance.
    Storage Store 3,4-Difluorobenzonitrile in a tightly closed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure proper labeling and keep away from ignition sources. Use appropriate personal protective equipment when handling, and store in accordance with local, state, and federal regulations.
    Shelf Life 3,4-Difluorobenzonitrile has a typical shelf life of 24 months when stored in a cool, dry, and well-sealed container.
    Free Quote

    Competitive 3,4-Difluorobenzonitrile prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615380400285 or mail to sales2@boxa-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615380400285

    Email: sales2@boxa-chem.com

    Get Free Quote ofTianye Chemical

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

    Certification & Compliance
    More Introduction

    3,4-Difluorobenzonitrile: A Closer Look From the Manufacturer’s Bench

    Understanding 3,4-Difluorobenzonitrile in Manufacturing

    Every chemical plant, regardless of size, runs into crossroads where careful material selection translates into better yield, safer environments, and smoother downstream processing. 3,4-Difluorobenzonitrile (DFBN) often enters the discussion at these moments—particularly in fields where fluorinated aromatics make a difference, like pharmaceutical and agrochemical production. We’ve spent over a decade running batch after batch, refining the synthesis and purification of this compound, and instead of abstract accolades, the focus remains rooted in reliability and traceability.

    Our 3,4-Difluorobenzonitrile is engineered for consistency. The formula, C7H3F2N, gives this compound a unique combination of two fluorine atoms positioned at the 3 and 4 sites on the aromatic ring, which sets it apart structurally from other mono- or di-fluorinated benzonitrile isomers. This position impacts not just reactivity but also physical behavior, which matters throughout storage, transportation, and use.

    Why the 3,4-Substitution Pattern Matters

    Location of substitution changes more than just a name on a label—it shapes downstream chemistry. The 3,4-di substitution enables a subtle electronic influence, lending an edge in coupling reactions and facilitating smoother transition to target products compared to 2,4- or 2,5- analogues. In our reactors, this pattern reduces unwanted byproducts in nucleophilic aromatic substitution, making reaction workups less cumbersome and boosting overall throughput.

    Chemists seeking active pharmaceutical ingredients opt for the 3,4-difluoro isomer for this reason; it tends to deliver cleaner profiles in the formation of intermediates, especially where stability under harsher conditions is necessary. The same goes for modern crop chemistry, where predictable behavior in subsequent halogenation, amination, or reduction steps streamlines development pipelines.

    Reliable Specifications Lead to Predictable Performance

    Every industry veteran has handled benzonitriles that throw off process controls: impurities that foam, unwanted isomers that bring in regulatory headaches, product that cakes or clumps on the line. We designed our purification and quality routines around these challenges, not just for compliance but to minimize surprises for the next chemist down the line.

    Our typical product runs as a fine, white to off-white crystalline solid with minimal variance in melting range, holding steady at 62 to 65°C. This tight window signals a strong handle on both raw materials and process setup—core to repeatable reactivity and safe handling. Water content and residual solvents are tracked closely; GC and NMR analyses confirm isomeric purity above 99 percent, and we never leave by-products like trifluorotoluenes or unreacted acid lurking in finished lots.

    We ship in lined drums or FIBCs to protect from ambient moisture, which keeps caking in check and supports longer storage. We avoid unlined metal packaging for this nitrile—the risk of trace hydrolysis or corrosion is real, and learning that lesson early helped shape our current standards.

    Differences Between 3,4-Difluorobenzonitrile and Other Isomers

    Benzonitriles with different fluorine placements might look similar on paper, but we see clear splits during purification and in our customers’ campaigns. The 2,4- and 2,5-difluoro variants require retooling of reaction conditions when substituted into a known synthetic route: pH optimization, catalyst swapping, more aggressive purification regimes. These are real costs—both in resources and lost time when scaled up.

    3,4-Difluorobenzonitrile in particular responds well under palladium catalysis, often providing higher coupling yields than the 3,5- isomer. Differences in solubility and crystallization tendencies also impact handling. We have handled 3,5-difluorobenzonitrile that required multiple recrystallizations, whereas the 3,4- isomer routinely crystallizes with fewer steps, saving time and solvent. On an industrial floor, these traits influence batch size, tank cleaning schedules, and shipping logistics—details that only surface once real-world scale is considered.

    Applications Shaped by Practice

    The core customer base uses 3,4-difluorobenzonitrile as a building block, but actual transformation steps stretch beyond textbook Suzuki or Buchwald reactions. In our facility, most of the output heads towards pharmaceutical intermediate synthesis, where speed to final API counts. The difluoro group offers balance between lipophilicity and metabolic stability, so medicinal chemists gravitate to this substrate when constructing lead compounds with fluorinated motifs.

    The pattern holds strong in crop protection. Modern fungicides and insecticides often start as a difluorinated benzonitrile. Here, the location and number of fluorines shape both synthetic feasibility and biological performance. Agrochemical partners report improved selectivity from the 3,4- isomer during their screening, likely due to the unique electronics introduced by the pattern.

    We have also supplied loads to specialty chemical makers who pursue dyes and advanced materials, seeking not just novelty but upgrades in thermal and UV stability that only come from certain fluorinated cores. Each of these users shares the same pain point: raw material regularity. They rely on predictable melting, defined particle size after milling, and zero cross-contamination.

    No Substitute for Batch Consistency

    It’s one thing to offer high purity, but batch repeatability matters just as much. We stopped using mixed acid fluorination routes when we noticed run-to-run swings in isomer ratios and impurity profiles. Current production draws on a Sandmeyer modification, optimizing copper(I) catalyst levels and precisely controlling reaction time and temperature. These steps reduced both tar formation and formation of side-halogenated byproducts.

    Routine in-process testing reveals upsets early, which means less scrap, tighter margins, and fewer headaches downstream. We use dedicated lines for each isomer to prevent cross-contact—one tank mishap taught us how easily cross-contamination can sabotage both analytics and final product use. Health, safety, and trace residue questions—those are non-negotiable, not marketing slogans.

    After filtration and drying, our product typically holds less than 500 ppm of volatiles. That figure might not look dramatic until someone needs 500 kilos for a sensitive reduction and ends up with part of the batch fuming or losing mass in vacuum—details that make a real dent in conversion rates and downstream drying ops.

    Handling Lessons From the Shop Floor

    3,4-Difluorobenzonitrile carries some sting if treated lightly. Solid material is easier to handle in modern plants, but the nitrile group means odors and toxicity need real management plans. Operators wear half-face respirators, nitrile gloves, and splash shields even during routine mill cleaning. Dust controls are simple but critical. Our process rooms have negative pressure and HEPA filtration, as even light airborne dust can trigger complaints or, worse, regulatory intervention.

    The product flows well when kept dry. Any ambient moisture transforms the product into brittle lumps or causes bench scale clogs that escalate into unloading delays when the job goes to FIBCs. We strictly nitrogen blanket packaging lines for this reason; even with desiccant, open bins only breed trouble.

    Thermal stability holds up through short excursions, but persistent overheating during storage or transport produces off-odors and, in rare cases, resinous films inside drums. The underlying chemistry does not forgive sloppy temperature management. We offer clear guidance, built from documented incidents, on what range maintains quality: 15–30°C with short-term room temperature deviation, entirely feasible in standard warehousing with a bit of oversight.

    Supply Chain Reliability—Built From the Source

    In the past, buyers faced erratic lead times, inconsistency in product tone or smell, and a waiting game around shipment delays from overseas traders. Manufacturing in dedicated lines allows us to keep surprises out of schedule. Direct ties with fluorine and acetonitrile suppliers mean we check input specs, audit deliveries, and wake up calls are few.

    We source main raw materials within a tight radius of the plant, controlling both cost and traceability. If a supplier batch skews on purity, automated alerts trigger a hold before production starts—no point letting off-grade solvent feed into a multi-ton run. This hands-on oversight reduces waste and translates to real value: hardly a drum comes back for retesting, and process documentation covers each step.

    Customers who experienced bulk supplier rotation or inconsistent isomer mix-ups in the market now trust direct-from-plant shipments, largely because of the documented lineage at each stage. Sophisticated buyers can access historical batch records, quality certificates, and analytic confirmations. Those details give peace of mind before major campaigns, not just a post-delivery sales pitch.

    Continuous Improvement Driven by Field Knowledge

    Mistakes teach more than textbooks. Early batches sometimes showed faint yellowing due to oxidation in storage, a problem tracked back to long warehouse stays and non-optimal venting designs in drums. We adopted lined, UV-resistant packaging and improved stock rotation. Production teams got hands-on with end-user feedback, adapting batch monitoring to flag markers before shipment, not just after customer complaint.

    It’s not the certificate of analysis that drives most partners to stay; it’s clear communication and the willingness to change based on equipment trials or a missed spec. In one case, a large pharma user flagged pressure buildup in reactors—a result of trace acids in our product, exposed only through large-scale hydrogenation. By tweaking quench routines and adding extra in-process filtration, the problem disappeared.

    Improvements keep rolling. Switches to greener solvents, closed-loop vent scrubbing for clean air, and recycling spent reagent streams become not just environmental policy but practical process measures. Every upgrade folds back into safer, steadier 3,4-difluorobenzonitrile production.

    Regulatory Tails and Analytical Realities

    While rules change across countries, expectations around trace impurities rarely relax. Fluorinated organics mean sharp regulatory eyes, and global clients require compliance to ICH, REACH, or EPA thresholds. Internally, we maintain tight records on heavy metals, class 1–3 solvents, and even trace halogenated aromatic contaminants—even if not strictly required by local code.

    Routine third-party audits do not rattle us. Labs can reproduce purity metrics, solvent content, and impurity spectra without issue. In a field where memories stick when things go wrong, each batch leaving our facility tracks a clear analytic path—NMR, GC-MS, and HPLC reports go out with every shipment, based on data, not assumptions or best guesses.

    Working in lockstep with global customers taught us that compliance is not just a tick box. For users in Japan or the EU, even a faint trace of chlorinated or brominated byproducts can undermine efforts to commercialize a new active. By having dedicated lines and routine cleaning verification, we eliminate cross-substitution or ghost peaks that throw off customer QC.

    On-the-Ground Impact and Future Perspective

    It is easy to look at fine chemical products like 3,4-difluorobenzonitrile as mere commodities, but true value appears on the manufacturing floor and in the lab. Each drum succeeds or fails based on reliability, not just purity stats. We’ve seen raw material tweaks that saved weeks on a project or minimized hazardous waste runs, turning a reliable supply chain into a competitive advantage.

    As demand intensifies for targeted, fluorinated intermediates across pharma, agro, and performance material fields, the margin for error narrows. Those who have weathered the learning curve know that detailed, consistent manufacturing delivers real-world benefits for both operational teams and end users. Lower variability cuts rework, missed QC, or out-of-spec rejection risk. Trust builds batch by batch—not through glossy brochures but through steady supply, open responsiveness, and adaptation to real-world processing feedback.

    Ready access to pure, well-defined 3,4-difluorobenzonitrile drives project momentum. Ongoing efforts in greener synthesis, stricter impurity control, and direct customer collaboration mark the path forward. Day-to-day, plant operators, lab managers, and R&D teams reap the benefit of quality. For every kilo supplied, a story of process demands, field solutions, and persistent tweaks shapes the solid product that lands on your loading dock.