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2,4-Difluorophenylacetonitrile

    • Product Name 2,4-Difluorophenylacetonitrile
    • Alias 2,4-DFPAN
    • Einecs 252-014-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    674598

    Cas Number 455-02-3
    Molecular Formula C8H5F2N
    Molecular Weight 153.13
    Appearance White to off-white solid
    Melting Point 40-45°C
    Boiling Point 256-258°C
    Density 1.24 g/cm3
    Purity Typically ≥98%
    Solubility In Water Slightly soluble
    Flash Point 110°C
    Smiles C1=CC(=C(C=C1F)F)CC#N
    Inchi InChI=1S/C8H5F2N/c9-7-3-1-2-6(8(7)10)4-5-11/h1-3H,4H2
    Synonyms 2,4-Difluorobenzyl cyanide
    Refractive Index 1.506 (20°C)

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

    Packing & Storage
    Packing The 2,4-Difluorophenylacetonitrile is supplied in a 100g amber glass bottle with a secure, tamper-evident screw cap.
    Shipping 2,4-Difluorophenylacetonitrile is shipped in tightly sealed containers, protected from moisture and light. It is classified as a chemical substance, so transport must comply with relevant regulations (such as DOT, IATA, or IMDG). Appropriate hazard labeling is applied, and handling is limited to trained personnel using proper protective equipment.
    Storage Store 2,4-difluorophenylacetonitrile in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep away from heat and ignition sources. Use only in a chemical fume hood. Ensure containers are clearly labeled, and store at room temperature or as recommended by the supplier. Avoid moisture exposure.
    Application of 2,4-Difluorophenylacetonitrile

    Applications of 2,4-Difluorophenylacetonitrile in Industrial Manufacturing

    2,4-Difluorophenylacetonitrile serves as a key intermediate in advanced chemical synthesis pipelines. As a manufacturer, we support industrial partners with consistent, high-purity supply for targeted applications across pharmaceuticals, agrochemicals, specialty chemicals, and liquid crystal intermediates. Below, we detail practical downstream scenarios with their specific compliance, formulation, process integration, and end-use products.

    1. Pharmaceutical Intermediate for Antipsychotic Agents

    Pharmaceutical manufacturers use 2,4-difluorophenylacetonitrile in the synthesis of substituted benzyl derivatives, often as building blocks for atypical antipsychotic APIs, including aripiprazole analogs. The material enters the process during the nitrile alkylation or reduction step, directly impacting product purity and yield. Controlled handling ensures compliance with regulatory standards, particularly regarding residual solvents and impurity profiles.

    Industry compliance standards

    • ICH Q7 GMP Guideline for Active Pharmaceutical Ingredients
    • USP <1059> Residual Solvents
    • European Pharmacopoeia (Ph. Eur.) quality standards for intermediates
    • FDA 21 CFR Part 211 for finished drugs

    Typical usage ratio

    • 1.05 to 1.15 molar equivalents relative to the target benzene ring substrate, depending on conversion efficiency and scale-up purity control

    Downstream process integration

    • Charged after solvent selection and before catalytic hydrogenation or Grignard addition, under inert gas conditions to minimize oxidation

    Final product types

    • Aripiprazole and its analogues (bulk APIs)
    • Benzyl-substituted heterocycles for CNS therapeutics
    • Pharmaceutical raw intermediates for R&D and regulatory submission
    • Reference standards in analytical research

    2. Advanced Agrochemical Synthesis (Herbicide Precursors)

    Downstream agrochemical producers incorporate this intermediate for the preparation of difluorinated phenyl ring compounds, particularly in the design of new-generation herbicides targeting resistant weed species. The handling and dosing must follow environmental and safety guidelines because the final active ingredients often require registration and compliance review.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Intermediates
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 for quality management in chemical manufacturing
    • OECD Test Guidelines for Environmental Safety

    Typical usage ratio

    • 0.80 to 1.25 molar equivalents depending on the final herbicide structural requirements and yield optimization strategy

    Downstream process integration

    • Added during nucleophilic aromatic substitution or coupling with alkoxyamine groups, preceding cyclization or oxime derivatization

    Final product types

    • Difluorophenyl-triazole herbicides (e.g., for wheat fields)
    • Selective post-emergence weed control agents
    • Herbicidal screening samples for EU and US regulatory trials
    • Intermediates for fungicide development

    3. Synthesis of Liquid Crystal Intermediates

    Electronics and display panel manufacturers value this compound as an upstream intermediate for the production of fluorinated aromatics, which impart enhanced dielectric and optical anisotropy properties essential in modern liquid crystal materials. High-purity processing is crucial to achieve the strict control of isomer ratio and minimal metal impurity critical in LC applications.

    Industry compliance standards

    • IEC 61249-2-51:2017 for halogen-free material content
    • RoHS Directive 2011/65/EU for electronic-grade chemicals
    • Company-specific internal QC limits for residual fluorides, heavy metals, and isomer ratios
    • JEITA guidelines for essential substances in display materials

    Typical usage ratio

    • 0.95 to 1.10 molar equivalents for core fluorination, with ratio adjustments based on target birefringence and mixing compatibility

    Downstream process integration

    • Used in initial condensation stages, followed by chlorination or etherification steps, prior to final purification by repeated distillation

    Final product types

    • Mixed fluorinated biphenyl intermediates
    • Commercial nematic and smectic liquid crystal mixtures for AMOLED and LCD applications
    • Monomers for side-chain liquid crystalline polymers
    • Specialty fluids for temperature compensation films

    4. Specialty Fine Chemical Building Block (Organic Synthesis)

    Fine chemical makers integrate this difluorinated benzyl nitrile unit into synthetic routes for complex aromatic frameworks. The material’s electron-withdrawing profile and controlled reactivity make it suitable for use in multi-step syntheses including cross-coupling, selective reduction, and ring construction, supporting projects in advanced materials chemistry and custom synthesis.

    Industry compliance standards

    • ISO 9001:2015 for production and traceability
    • Internal process-specific SOPs for organic synthesis
    • EPA TSCA regulations for chemical handling and reporting
    • Good Laboratory Practice (GLP) Guidelines (for pilot/lab scale)

    Typical usage ratio

    • 1.0 molar equivalent in single-step synthesis; 0.7–1.3 equivalents for multi-step processes depending on conversion and purification demands

    Downstream process integration

    • Employed at nucleophilic addition or cyclization stages, often as an active methylene component or aromatic substituent

    Final product types

    • Customized fluorinated aromatic scaffolds
    • Building blocks for specialty dye and pigment manufacturers
    • Chiral intermediates for asymmetric catalysis research
    • Reference compounds for analytical chemistry
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    Certification & Compliance
    More Introduction

    Introducing 2,4-Difluorophenylacetonitrile: Practical Insights from the Production Floor

    Real-World Experience with 2,4-Difluorophenylacetonitrile

    Making chemicals for a living never really gets dull. Every reaction tells you a little more about how little details matter, especially with products like 2,4-Difluorophenylacetonitrile. Many people in the lab world know this compound by its CAS number 455-86-7, but for us, it’s just “DFP-acetonitrile”—a building block that keeps popping up in pharmaceutical projects and fine chemical synthesis. The production process calls for experience, patience, and steady hands. One misstep with the raw materials or temperature control, and the purity can suffer. From batch to batch, we wrestle with finicky yields, color concerns, and the fact that the difluoro substitution doesn’t always play nice with standard process steps. So, in a sense, producing this chemical isn’t formulaic—it’s craftsmanship, and the result supports research and development all over the world.

    Why 2,4-Difluorophenylacetonitrile Matters in Modern Chemistry

    We see research requests come through asking for a range of fluorinated intermediates. The 2,4-difluoro pattern stands out in medicinal chemistry. As manufacturers, we pay close attention to this because adding fluorine atoms to aromatic rings dramatically affects bioactivity, physicochemical properties, and metabolic stability. Growing demand for new active pharmaceutical ingredients (APIs) and agrochemicals means the call for high-quality aryl nitriles like this one keeps increasing.

    The pharmaceutical sector dives deep into customization, and 2,4-Difluorophenylacetonitrile hits a sweet spot. The difluorinated motif often shows up in kinase inhibitors, antiviral agents, and herbicides. Chemists reach for this intermediate as it allows them to access scaffolds that would be difficult or expensive to introduce using post-fluorination methods. With two of the ortho and para positions blocked, the electronic profile of the ring shifts, giving molecules different reactivity patterns compared to their mono-fluorinated or unsubstituted relatives. This seemingly small chemical difference matters a great deal across research and manufacturing.

    From Reaction Vessel to Finished Product

    In our plant, the process starts long before the customer receives a bottle. We draw on years of fine-tuned reaction conditions to maximize purity and minimize side product formation. Working with difluoro compounds isn’t as forgiving as dealing with their non-fluorinated analogues. Corrosive reagents, moisture sensitivity, and the distinct smell in the air tell us the synthesis is running as planned—or point to tiny leaks or contamination that might keep us up at night. Our team regularly runs thin layer chromatography and gas chromatography-mass spectrometry to check for trace impurities.

    Repeated filtration and washing steps follow. Getting the last traces of less desired positional isomers out takes more than one wash. Solvents run through thick beds of adsorbents. Every kilogram of finished DFP-acetonitrile tells a story about teamwork: operators, QC techs, and engineers share what worked and what didn’t. Problems get solved by people who’ve faced clogged lines, unusual odors, or color changes before. Delivering on the most stringent purity specifications is about understanding these day-to-day headaches and fixing them before the drum gets sealed.

    Understanding Specifications and Meeting Customer Standards

    Lab requests look simple on paper: “We need 99% or higher purity, and the rest under the detection limit.” On our side, that means running comprehensive spectra for every lot, not shying away from repeating analysis if the profile looks off. Customers in pharmaceutical development tolerate no ambiguities. Unidentified peaks cloud the confidence of research teams, so we adopt an aggressive stance on analytical transparency. Proton and fluorine NMR show us what’s happening at the atomic level, and high-performance liquid chromatography confirms the absence of co-eluting impurities.

    Moisture levels go under the microscope, quite literally; Karl Fischer titration tells us if more drying is necessary. To us, a high-quality 2,4-Difluorophenylacetonitrile isn’t just about a GC trace that clears a passing bar. It means knowing how to answer questions in detail: Are there traces of residual halides? Are any metal catalysts lurking below the parts-per-million range? Did the batch ever come into contact with materials that could introduce extractables or leachables? We document every run, every cleaning, and every inspection so that both our customers and our own team remain confident batch by batch.

    Model, Quantity, and Handling: Balancing Scale with Quality

    We ship DFP-acetonitrile in glass bottles or fluoropolymer-lined containers, depending on size and customer preference. Handling bulk shipments brings its own challenges, since fluorinated aromatics sometimes behave differently in drums than in small-scale vials. We cycle materials through a dedicated packaging room. Cross-contamination from other aromatic nitriles or fluorinated compounds is a risk we address head-on by rigorous training and time spent cleaning down lines. We don’t cut corners on solvent rinses; repeated acetone and methanol cycles cost time and money, but that’s part of sustaining a reputation for reliability.

    From gram-scale to several hundred kilograms per month, we adjust our production vessel sizes and cooling profiles to match the order. People tend to assume chemical manufacturing is a ‘scale up and forget it’ job—our experience says otherwise. Exotherms and foaming risks shift as the batch size increases. The heat transfer profile across a vessel changes and the mixing pattern never matches up linearly. To maintain the same batch quality, we adjust agitation rates, monitor in-line temperature probes, and stay ready to abort and rerun if data goes sideways. This obsessiveness is more necessity than habit; it’s the kind of hard-earned knowledge no spec sheet covers.

    Separating 2,4-Difluorophenylacetonitrile from Similar Building Blocks

    Why not just use 4-fluorophenylacetonitrile, or its 3,4-difluorinated cousin? Purity and substitution patterns mean everything in downstream chemistry. The location of both fluorine atoms in the 2,4-positions matters for binding to proteins, for resonance effects, and for how the ring interacts with other groups during coupling reactions. Our R&D team spends a good portion of their time running competitive synthetic routes just to verify the separation efficiency against close analogues. Tiny amounts of off-target isomers frequently show up in less disciplined manufacturing environments. By learning to pick apart these subtle differences over many years, we keep our 2,4-difluoro product from bleeding into neighboring compound profiles.

    We’ve seen customers try substitutions, thinking an available mono-fluorinated intermediate will function the same way. The feedback loop from failed couplings or reduced yield guides their return to the original 2,4-difluoro variant. So, as much as every molecule of product shipped must be chemically precise, the relationship is about more than just numbers on a report. Customers trust that they get exactly what they paid for; our job is to meet that expectation through both process discipline and close attention to the subtleties of aromatic substitution chemistry.

    Applications: Unlocking Complexity in R&D and Commercial Products

    In pharma synthesis, the role for difluorinated intermediates keeps expanding. Smaller firms and major developers use our DFP-acetonitrile to build drug candidates that hinge on the unique electronic characteristics fluorine donor groups provide. Several research teams report that these motifs, when introduced at the start of a synthetic sequence, let them skip lengthy and expensive halogen exchange or selective fluorination later. Early introduction can mean increased molecular stability, better metabolic scrambling resistance in biological systems, and sometimes patentable structural differences from prior art.

    Agrochemical developers are not far behind. The 2,4-difluoro group carries over into pesticide and herbicide scaffolds, lending these compounds the environmental persistence and targeted activity critical for modern crop protection. In our feedback from global formulators, we hear how purity affects not just initial screening but regulatory acceptance, as non-compliant isomeric impurities can trigger re-testing or outright delays. We build traceability into shipment records for this reason; knowing exactly which batch, from which reactor, on which week, went into a registration file matters for years down the line.

    A less discussed but no less important route is advanced plastics and fine materials where dense fluorination creates polymers that stand up to harsh environments. The acetonitrile group provides a handle for further chain extension or crosslinking—DFP-acetonitrile’s structure offers greater control than unsubstituted or 3-fluoro alternatives.

    Challenges We Overcome: Practical Solutions from Manufacturing

    Scaling up synthesis of aryl acetonitriles runs into bottlenecks. With DFP-acetonitrile, some issues show up more acutely: strong acids and bases necessary for synthesis cause increased wear on metallic reactors. Safety rushes to the forefront, with engineers inspecting joints and gaskets after every run. To prevent moisture ingress—critical for both safety and quality—we use nitrogen overlays and monitor dew points in storage tanks as a matter of routine. Leaky valves get replaced quickly; experience with similar materials tells us repairs done next week can cost several ten-thousand dollars in lost time and scrapped batches.

    Disposal of fluoroaromatic residues takes seriousness. We neutralize acidic residues with specialized neutralizers rather than dumping into a generic waste stream, keeping both employees and downstream waste handlers safe. Our region’s environmental permitting requires documentation down to the kilogram for anything leaving the plant tagged as hazardous. We built entire waste tracking systems around this reality and share learnings with peer manufacturers as regulations tighten. That collaborative approach reduces compliance headaches—and builds a more resilient safety practice across the sector.

    Sometimes technical issues are less about plant mechanics and more about knowledge. Newer team members face a steep learning curve on handling aryl nitriles—skin, mucous membrane, and eye protection form part of our standard uniform, and we train everyone on emergency procedures before they step on the floor. Having a culture that talks openly about near-misses does more to keep our teams safe than rules posted on a wall ever will.

    Quality, Trust, and the Manufacturer’s Mindset

    Formulating a plan that balances cost, timelines, and batch quality rarely feels simple. We adapt to shifts in solvent pricing, respond to changes in purity specifications, and stay in touch with regulatory agencies that update guidance with a few months’ notice. Through it all, one constant remains: the people on our floors who bring experience and pride into every stage of manufacturing. More than once, a supervisor or QC lead has noticed something odd in a spectrum or drum weight and stopped a shipment—ultimately saving our customer from major headaches and preserving our reputation in a competitive field.

    A compound like 2,4-Difluorophenylacetonitrile is as much about depth of industry knowledge as it is about chemical composition. We rarely say a batch is “finished” just because it looks good on paper; we investigate odd behaviors, maintain transparency with every buyer, and keep communication lines open for troubleshooting. Questions from scientists or procurement teams get answered by people who’ve spent years working with the raw material and finished product, not just by sales scripts.

    Looking Forward: Building on a Strong Foundation

    The pathway from lab bench to production scale has shaped how we view customer needs. Orders for fluorinated intermediates may come from a start-up biotech, a major crop protection conglomerate, or a university pilot project. Each sees a different role for 2,4-Difluorophenylacetonitrile, but all value immediate answers, consistent results, and traceable supply. For us, staying a step ahead means investing in analytical equipment, refining synthetic routes, and keeping our own team looped into industry advances and regulatory updates. We seek feedback to drive incremental improvements, and we don’t shy away from discussing mistakes or near-misses that shaped how we operate today.

    The role of a manufacturer goes beyond filling bottles. The relationship extends well past the purchase; troubleshooting unexpected reactions, fielding technical questions, or recertifying old lots is just part of how we define doing the job right. Whether for a one-time order or ongoing supply, our approach to 2,4-Difluorophenylacetonitrile remains the same—precision, openness, and a respect for both the molecule and the people depending on it. Years spent improving our processes, training staff, and learning from setbacks have built up a bank of real practical knowledge that gets passed on with every batch delivered. As demand for fluorinated building blocks continues to grow, we welcome every chance to prove why experience at the source matters.

    Collaborative Science, Reliable Supply

    Practicing chemistry at the manufacturing level brings its own set of demands, often missed by those who only read catalogs and certificates. Each order for 2,4-Difluorophenylacetonitrile represents months—sometimes years—of development and relationship building. Our customers rely on unbroken chains of supply, rapid answers to changing project specs, and forthright news when conditions shift. That transparency and reliability get built into our workplace values and show up in every pound or gram shipped.

    Whether you’re a major pharmaceutical developer, a research lab, or a chemical innovator, our experience manufacturing 2,4-Difluorophenylacetonitrile means more than formulae and structure charts. We see our job as a partnership—helping you bring new products to market, sharpen your research edge, and breathe easier knowing your supply chain stands on a strong foundation of know-how and care. Sharing that expertise, learning together, and pushing for the next level of product reliability form the backbone of what we do every day.