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3,5-Difluorobenzonitrile

    • Product Name 3,5-Difluorobenzonitrile
    • Alias 3,5-DFBN
    • Einecs 238-641-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    211168

    Chemical Name 3,5-Difluorobenzonitrile
    Cas Number 64248-64-6
    Molecular Formula C7H3F2N
    Molecular Weight 139.10
    Appearance White to off-white solid
    Boiling Point 221-223°C
    Melting Point 38-42°C
    Density 1.30 g/cm3
    Solubility Slightly soluble in water
    Smiles C1=CC(=CC(=C1F)C#N)F
    Inchi InChI=1S/C7H3F2N/c8-6-1-5(4-10)2-7(9)3-6/h1-3H
    Refractive Index 1.517 (predicted)
    Flash Point 100°C

    As an accredited 3,5-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, tightly sealed with screw cap, labeled "3,5-Difluorobenzonitrile, 100g," featuring hazard symbols and safety data.
    Shipping 3,5-Difluorobenzonitrile is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material and should be handled according to regulatory guidelines. Ensure proper labeling, use appropriate personal protective equipment, and store in a cool, ventilated area during transportation to prevent accidental release or exposure.
    Storage 3,5-Difluorobenzonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from heat, sparks, and incompatible substances such as strong oxidizers. It should be kept away from moisture and direct sunlight. Use appropriate safety precautions, including chemical-resistant gloves and goggles, when handling or transferring the material. Store following local regulations for hazardous chemicals.
    Application of 3,5-Difluorobenzonitrile

    Applications of 3,5-Difluorobenzonitrile in Industrial Manufacturing

    As a primary manufacturer, we supply 3,5-Difluorobenzonitrile to downstream producers across several precise industrial sectors. This raw material serves specific roles in advanced synthesis and specialty chemical production. Below are focused application scenarios reflecting rigorous quality, integration requirements, and specific product outcomes.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    API manufacturers utilize 3,5-Difluorobenzonitrile as a fluorinated building block during the multi-step synthesis of select anticancer, antiviral, and central nervous system (CNS) drug entities. Its unique aromatic fluorine substitution enables direct introduction into core pharmaceutical scaffolds during Suzuki coupling, nucleophilic aromatic substitution, and carbonylation reactions for target molecule assembly.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia monographs where applicable
    • US FDA 21 CFR Part 211
    • ChP (Chinese Pharmacopoeia) for intermediate registration

    Typical usage ratio

    • 0.8–2.2 molar equivalents based on target compound and synthetic route
    • Formulation adjustment determined by downstream yield requirements
    • Higher ratios applied in literature for multi-step reactions involving high fluorine atom retention

    Downstream process integration

    • Introduced during initial aromatic ring construction stage
    • Used as starting substrate in Pd-catalyzed coupling reactions
    • Feeds into continuous flow or batch reactor lines under GMP conditions
    • Residuals tracked during API crystallization and purification

    Final product types

    • Anticancer APIs with fluorinated aromatic core
    • Antiviral therapeutic agents
    • CNS active pharmaceutical ingredients
    • Intermediate building blocks for further downstream Pharma synthesis

    2. Agrochemical Synthesis for Selective Herbicide Production

    Producers incorporate 3,5-Difluorobenzonitrile as a critical intermediate in the preparation of advanced herbicides. The double fluorine substitution pattern aids in boosting pesticide lipophilicity and metabolic stability, particularly in the synthesis of pyridinecarboxamide and benzoylurea derivatives, through nucleophilic aromatic substitution and hydrolysis protocols.

    Industry compliance standards

    • ISO 9001:2015 for pesticide intermediate production
    • FAO/WHO Guidelines for Quality Control of Pesticide Products
    • REACH registration for EU chemical supply
    • Local Ministry of Agriculture & Rural Affairs (China) pesticide registration requirements

    Typical usage ratio

    • 1–1.8 equivalents relative to synthesis endpoint based on targeted compound
    • Ratio fine-tuned by desired fluorine content in final herbicides
    • Process scale: 15–50 kg per production batch for commercial runs

    Downstream process integration

    • Reactant in key introduction step for fluorinated aromatic ring
    • Processed in stirred-tank or flow-bed reactors with catalyst control
    • Intermediates isolated before coupling to active herbicide moieties
    • QC labs monitor unreacted raw material during purification

    Final product types

    • Fluorinated pyridinecarboxamide herbicides
    • Benzoylurea derivatives for selective weed control
    • Novel pre-emergent and post-emergent herbicidal compounds
    • Registered crop protection agents with improved degradation profile

    3. Liquid Crystal Material Precursor for Advanced Display Technologies

    Specialty chemical producers synthesize high-performance liquid crystal compounds using 3,5-Difluorobenzonitrile as a substituted aromatic unit. The precision placement of fluorine atoms improves dielectric anisotropy, contributes to the thermal stability, and fine-tunes birefringence properties in new LC mixtures for high-end TFT-LCD panels and OLED substrates.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management for electronic raw chemicals)
    • RoHS Directive (2011/65/EU) for hazardous substances
    • REACH SVHC compliance for liquid crystal substances
    • IEC 61249-2-21 for halogen-free materials (where applied)

    Typical usage ratio

    • 0.3–1.5 molar equivalents per liquid crystal core molecule
    • Proportion adjusted to meet end-user birefringence and viscosity specifications
    • Batch scale: typically 2–10 kg per run depending on display size requirements

    Downstream process integration

    • Feeds into aromatic etherification or cyanation step in LC intermediate synthesis
    • Mixed with biphenyls or terphenyls in blend formation
    • Purified via rectification and flash chromatography before blending
    • QC includes FTIR and HPLC analysis of inclusion and residuals

    Final product types

    • Twisted Nematic (TN) and In-Plane Switching (IPS) liquid crystal mixtures
    • High-purity LC materials for LCD manufacturing
    • OLED display intermediates (aromatic nitrile-containing)
    • Specialty LC mixtures for automotive and industrial displays

    4. Fine Chemical Intermediate for Specialty Dye and Pigment Manufacture

    Colorant manufacturers employ 3,5-Difluorobenzonitrile as a halogenated aromatic component to construct dye intermediates with tailored hue and solubility profiles. It participates in nucleophilic aromatic substitution and diazotization processes, enabling synthesis of fluorinated azo and anthraquinone dyes, which deliver both enhanced weather resistance and targeted color range for automotive, textile, and plastic applications.

    Industry compliance standards

    • EN 71-3 (Migration of certain elements in colorants for toys)
    • OEKO-TEX Standard 100 (applicable for textile dye end-uses)
    • REACH Annex XVII restrictions for aromatic amines
    • ISO 12040 for fine chemical pigment quality

    Typical usage ratio

    • 0.5–1.0 molar ratio in the aromatic substitution or coupling step
    • Batch scale: 3–20 kg depending on pigment class and order volume
    • Adjusted for desired color strength and lightfastness of the dye

    Downstream process integration

    • Used during ring functionalization or as starting substrate in azo coupling
    • Diazotized and condensed with aromatic amines
    • Transferred to pigment lakes via salt formation or sulfonation
    • Residuals monitored to below specified ppm thresholds

    Final product types

    • Fluorinated azo dyes for textile printing
    • Anthraquinone pigments for plastic coloring
    • Specialty auto-refinish and architectural pigments
    • High-durability industrial colorants for coatings and inks
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    Certification & Compliance
    More Introduction

    3,5-Difluorobenzonitrile: A Closer Look at a Key Fluorinated Intermediate

    Understanding the Role of 3,5-Difluorobenzonitrile in Specialty Chemistry

    In our daily routines inside the plant, we see shifting demands of the chemical industry reflected in the steady calls for 3,5-difluorobenzonitrile. This compound, with its difluoro substitution pattern, does much more than serve as another checkmark on a production schedule. Laboratories and manufacturers depend on this molecule for its performance in pharma synthesis, advanced materials, and crop protection innovation. Our experience making this product has given us a close perspective on its practical strengths and what sets it apart from less specialized fluorinated aromatics.

    How 3,5-Difluorobenzonitrile Stands Out

    Compared with monofluorobenzonitriles or regular benzonitrile, the difluoro structure at the 3 and 5 positions introduces unique electronic effects. This makes it highly attractive for medicinal chemists who want to tune biological activity or metabolic stability. While we synthesize a range of aromatic nitriles, the double fluorine on the ring leads to different reactivity outcomes and offers selectivity in making pharmacologically active compounds. Colleagues working on the synthesis side tell us that the product performs consistently in Suzuki and other coupling reactions, opening doors for a wide spectrum of building blocks.

    The 3,5-difluoro substitution does more than just add cost. It introduces a certain level of electron withdrawal, steering the chemistry toward desired outcomes in amide formation, hydrolysis, or nucleophilic aromatic substitution. Where a traditional benzonitrile would react across the entire ring, the difluorinated version helps chemists steer the final molecule with greater precision. Our feedback loop with users has shown that yields can improve when the right intermediate is used, cutting down on both time and purification costs.

    Manufacturing Perspective: Consistency, Purity, and Process Know-How

    We approach the job of synthesizing 3,5-difluorobenzonitrile with the same detail-oriented attitude we'd bring to any critical ingredient. Each batch runs through a sequence of quality checks shaped by years of experience and the lessons we've learned tweaking our processes. In our early days, contamination from incomplete fluorination or side-reactions could creep in if temperature control slipped. These headaches taught our team that maintaining stability at every step is non-negotiable. Today, our process achieves a high standard for chemical purity—often above 99%—and moisture content can make or break later synthesis stages, so careful drying under nitrogen is a standard step.

    Our people keep an eye on trace impurities because customers building complex molecules do not want to troubleshoot product failure from an uncharacterized contaminant. We avoid cross-contamination from other halogenated intermediates by keeping dedicated lines and cleanouts in place. Regular monitoring by NMR and GC-MS is standard operating procedure, not a marketing line for spec sheets.

    We've also found that what comes out of the reactor is only part of the story. Crystallization and proper filtration can lead to greater batch-to-batch uniformity. We invested time in refining our washing steps, which reduced residual solvents and led to praise from downstream users whose reactions ran cleaner than before. Small improvements in process translate to smoother scale-up, less downtime, and fewer gripes from the people doing real chemistry with our material.

    Applications: More Than a Puzzle Piece for Pharma

    Pharmaceutical synthesis sits right at the top of the reasons for using 3,5-difluorobenzonitrile, but it does not stop there. Agrochemical research programs also rely on this intermediate for new-generation crop protection agents. Our feedback from these sectors always highlights the need for high reproducibility and clear specifications, which guides how we invest in analytical technology and traceability across all batches. Some customers bolt this product into ligands or engineered polymers designed for advanced electronics. The stable aromatic ring, toughened further by those strategic fluorines, survives demanding process conditions when other molecules might decompose.

    Medicinal chemists regularly remind us that small tweaks to a core structure—adding two fluorines, for instance—can radically change the biological profile of their lead candidates. This is not a theoretical curiosity to them; it is central to their process. 3,5-difluorobenzonitrile delivers the platform for making anti-infectives, cancer therapies, and CNS agents that might not be possible with unsubstituted or mono-fluorinated analogs. An agricultural chemist once told us that their project needed the electron-poor ring provided by this specific substitution pattern to achieve selectivity for certain metabolic pathways in plants. The difference is tangible in their test plots.

    Outside research, some specialty polymer manufacturers reach out to us for this product when designing high-performance materials requiring thermal stability. Although not the highest volume market sector, this small crowd values supply reliability and purity over price alone, because a little off-spec material can ruin a batch of expensive functional monomer.

    Model and Specifications: Drawing from In-Plant Experience

    Our team runs 3,5-difluorobenzonitrile production to meet a handful of options. The most-requested model from our pipeline arrives as a white to pale yellow crystalline solid, easily handled and suited to most synthetic protocols. We've learned that trace moisture—often ignored by non-specialists—can cause issues downstream, especially in sensitive cross-coupling reactions. So we’ve committed to delivering material with low water content, typically less than 0.2%.

    Particle size can affect ease of handling. Some customers with automated dosing or small-scale screening setups want fine-grained material that flows smoothly, while others working in kilo quantities prefer larger crystals to minimize dust and exposure. We fine-tune the drying and sieving process depending on what the customer requests. This comes from years of listening to the shop floor rather than sending out a one-size-fits-all product.

    Our internal specification for the most popular grade includes an assay by HPLC above 99%, low halide contamination, and thorough testing for residual solvents using both gas chromatography and NMR. In practice, meeting or exceeding these specs is always the target. If something feels inconsistent from batch-to-batch, our QC team raises the flag and tracks down the source before shipping anything out. A costly return might sting the bottom line, but the trust of our long-term partners matters more.

    What Sets Us Apart from Distributors and Repackagers

    Making something from scratch gives a deeper sense of the nuances and the technical hurdles. Our engineers live the pulse of synthesis, not just the numbers in a procurement system. When we see a run go off the rails because a reaction profile drifted, we are the ones who troubleshoot and adjust the solution. This boots-on-the-ground approach filters through to the customer in the form of predictability, quick feedback on questions, and a willingness to tweak properties based on user feedback.

    Customers who have switched over from traders tell us that they value this direct dialogue. Distributors might shuffle material from storage tanks to drums, but knowledge about a batch’s backstory often gets lost. Our team sees the whole picture, from raw fluorobenzene to the finished nitrile, and we field technical questions by drawing on actual production and failure logs rather than browsing a data sheet. A customer with a unique reactivity issue can talk to the people who crafted the molecule, not just a sales channel without direct chemistry experience.

    Challenges and Solutions in Production

    Each fluorinated intermediate comes with its own headaches, and 3,5-difluorobenzonitrile is no exception. The supply chain for source materials can fluctuate—fluorinated aromatics are not simple to get in some regions, especially when geopolitical events squeeze upstream producers. We hedge risk through diverse sourcing and by maintaining more inventory than a spreadsheet would suggest. Planning this way means we’ve been able to keep delivering even during tight markets, though sometimes at the cost of margin.

    Environmental and safety aspects draw continual attention, both from regulators and within our plant. We have long experience handling the hazards of cyanide chemistry and halogenation steps, so our safety culture prioritizes routine drills, equipment maintenance, and real-time monitoring. We’ve upgraded fume extraction and process containment systems, not waiting for regulations to catch up, but responding to real-world exposures and incident reports. Our compliance record did not come from ticking boxes but from learning by doing—sometimes the hard way—over many years.

    Disposal of waste streams with complex halide content also challenges us. We manage this by investing in advanced incineration, off-gas scrubbing, and in some cases, separating streams for recycling when feasible. Our site engineers worked with research chemists to install real-time monitoring of emissions and solvent recovery. These investments do not always win applause from accountants, but those in production know how a small leak can become a big issue fast. This attention to waste and emissions takes some pressure off customers down the supply chain, especially in sensitive end-use sectors like pharmaceuticals.

    Supporting End Users Beyond the Drum or Bag

    We have seen more technical requests come in from process development labs, many of which are under pressure to reduce waste, cut energy use, or switch from traditional solvent systems. Our technical support team consists of production veterans and analytical chemists who bring plant reality into the conversation. Sharing our own optimization strategies, such as ideal solvent pairings or post-reaction workup tips, sometimes helps a partner troubleshoot a stubborn bottleneck without reinventing the wheel.

    One example: more than one pharma company approached us about problems with scale-up from gram to multi-kilogram reactions. The answer often lies not just in the chemistry, but in how to deliver the material in exactly the right form—particle size, purity, and packaging all play a part. Sometimes we run small-scale pilots to make sure what comes off our line fits the real-world workflow, not just theoretical processes from academic literature.

    Certificates of analysis are not just paperwork for us. Every document reflects real batch data taken from hands-on analysis. With stricter demands in regulated markets, especially when supporting clinical or pre-clinical drug candidates, customers lean on our documentation transparency. We also field regulatory inquiries about traceability, and our site records make auditing or due diligence much smoother than patchwork documentation from repackaged supply.

    Responding to Industry Trends and Customer Needs

    The pharmaceutical and agrochemical sectors continue to shift toward greater use of fluorinated building blocks. Demand for 3,5-difluorobenzonitrile grows as a direct result. That means we keep a finger on trends coming out of patent filings, new patents, and the changing focus in target molecules. Our technical team scans the horizon for new process routes—whether that means upgrading reactors for better containment, improving product isolation, or integrating greener solvents.

    Conversations with our partners highlight not just a need for product, but for solutions to recurring pain points: unpredictable lead times, slow tech support, or unresponsive problem resolution. In practice, we try to keep lines of communication open, offer pre-shipment samples, and share lessons learned from our own failures and successes with this compound.

    Comparing to Other Fluorinated Benzonitriles

    We have synthesized and supplied a spread of benzonitriles with varying fluorine substitution. Staff with years on the production lines make one thing clear: double-fluorinated models like 3,5-difluorobenzonitrile show more challenging chemistry but offer greater value for advanced synthesis. The molecular symmetry and substitution pattern impact not only the cost, but reaction pathways and biological performance. Users switching from mono- or tri-fluoro versions report changes in selectivity and metabolic resistance, especially in pharma.

    We see the same pattern on the process side. The more complicated the substitution, the more demanding the process controls. For example, purification of 4-fluorobenzonitrile can be relatively straightforward, but each extra fluoro atom imposes tougher requirements for separation and equipment cleaning. There are times we’ve paused production lines just to clear out traces from similar products, knowing that a little cross-over could become a big downstream problem. Our commitment to precise manufacturing lies in these details, earned by solving problems directly on the plant floor.

    Looking Ahead: Sustainable Approaches and Advanced Manufacturing

    We track progress in green chemistry and push to step away from legacy solvents or reagents that generate hard-to-treat waste. Research is ongoing into using flow chemistry in fluorination steps, aimed at both reducing risk and improving isolated yield. Our R&D group runs pilot projects toward catalyst reuse, alternative fluorine sources from more benign precursors, and smarter in-line monitoring. Experience shows that these steps sometimes take years to pay off, but once implemented, they deliver long-term process reliability.

    Through industry collaborations, we stay current with regulatory shifts, both local and international, shaping what can and cannot be used in final routes to active ingredients. Process adaptability reduces lock-in to a single regulatory regime. This gives customers more freedom when pursuing filings in different jurisdictions.

    Cost pressure remains a fact of life in specialty chemicals. While some large makers cut corners on equipment maintenance or source subpar fluorinated feedstocks, our practice holds to higher-grade materials and committed maintenance. Many of our buyers operate in tightly regulated environments, and they count on the absence of surprise contaminants or variable impurity profiles.

    Final Thought: The Value of Direct Production Know-How

    What matters most in 3,5-difluorobenzonitrile supply circles back to predictability and an earned reputation for chemical craftsmanship. With so many moving parts in the specialty chemical value chain, our focus has not shifted from quality at scale and technical dialogue that helps our partners win. Delivering on this requires investment, hands-on knowledge, and humility to learn from each run. Any new project involving this product brings fresh challenges, but with our hard-earned know-how, we continue supporting innovation across industries.