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Fluoroacetonitrile

    • Product Name Fluoroacetonitrile
    • Alias 2-Fluoroacetonitrile
    • Einecs 206-982-9
    • 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
    VTB
    Specifications

    HS Code

    141444

    Chemicalname Fluoroacetonitrile
    Molecularformula C2H2FN
    Molarmass 57.05 g/mol
    Casnumber 353-90-2
    Appearance Colorless liquid
    Density 0.994 g/cm3
    Boilingpoint 82-83 °C
    Meltingpoint -69 °C
    Refractiveindex 1.333
    Flashpoint 15 °C
    Solubilityinwater Soluble
    Vaporpressure 31 mmHg (20 °C)
    Pubchemcid 11259

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

    Packing & Storage
    Packing Fluoroacetonitrile is supplied in a 250 mL amber glass bottle, tightly sealed, with hazard labels and detailed chemical information.
    Shipping **Fluoroacetonitrile** should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be handled as a highly toxic, volatile chemical, complying with hazardous materials regulations. Ship using appropriate labeling, UN identification (UN 3286), and documentation, and ensure transport by trained personnel, under cool, well-ventilated conditions.
    Storage Fluoroacetonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible materials such as strong acids or bases. The container must be tightly closed and clearly labeled, made of materials resistant to nitriles. Access should be restricted to trained personnel, and all relevant hazard precautions must be taken due to its toxicity and volatility.
    Application of Fluoroacetonitrile

    Applications of Fluoroacetonitrile in Industrial Manufacturing

    Fluoroacetonitrile serves as a specialized fluorinated building block for advanced chemical synthesis, driving innovation across multiple downstream manufacturing sectors. Below, we detail well-established industrial uses where fluoroacetonitrile demonstrates its unique value, along with compliance standards, formulation specifics, process integration routes, and final product formats in each sector.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ fluoroacetonitrile as a key fluorinated intermediate during the preparation of specialty active pharmaceutical ingredients (APIs), especially for introducing fluoroalkyl moieties that enhance metabolic stability, receptor affinity, and pharmacokinetics. The compound enters targeted synthesis routes including nucleophilic substitution and condensation reactions, supporting the creation of highly regulated API molecules such as fluoro-containing antivirals or central nervous system agents.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API Manufacturing
    • United States Pharmacopeia (USP) General Chapters
    • European Pharmacopoeia (Ph. Eur.) Raw Material Purity Guidelines

    Typical usage ratio

    • 0.2%–1.5% molar ratio based on the targeted fluorinated scaffold; precise quantity determined by API molecular structure and target yield.

    Downstream process integration

    • Directly incorporated into multi-step organic reactions at controlled addition rates during early- or mid-stage synthesis of API intermediates; often handled under inert atmosphere due to reactivity and to minimize impurity formation.

    Final product types

    • Fluorine-containing API intermediates
    • Pharmaceutical bulk APIs with improved bioavailability
    • Advanced starting materials for oncology and antiviral APIs

    2. Agrochemical Active Ingredient Manufacturing

    Fluoroacetonitrile acts as a fluorinated synthon in agrochemical synthesis, specifically for constructing active ingredient cores that demand fluorine incorporation for enhanced pest resistance and environmental persistence. Leading pesticide and herbicide manufacturers utilize this compound in tightly controlled batch reactions, enabling the efficient construction of pyridine and pyrazole derivatives for advanced crop protection products.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for Quality Management in Chemical Manufacture
    • REACH Regulation (EC) No 1907/2006
    • Chemical Facility Anti-Terrorism Standards (CFATS) for regulated intermediates

    Typical usage ratio

    • 0.5%–2% by weight relative to overall batch mass, adjusted per synthetic pathway yield and targeted fluorine substitution.

    Downstream process integration

    • Dosed during the nucleophilic substitution step of agrochemical active synthesis, often in combination with other halogenated reagents; monitored via in-process HPLC for precise consumption and conversion rates.

    Final product types

    • Fluorinated herbicide actives (e.g., triazolopyrimidine derivatives)
    • Novel insecticidal compounds
    • Pesticide intermediates for further derivatization

    3. Specialty Fluorinated Fine Chemicals Production

    Chemical companies specializing in high-performance building blocks employ fluoroacetonitrile as a precursor or reagent for the targeted synthesis of value-added fine chemicals, where the introduction of a fluoro-functional group is essential for unique physicochemical properties. These applications require tight control of reaction conditions and impurity profiles, often serving niche electronics, specialty surfactant, or advanced monomer markets.

    Industry compliance standards

    • ISO 9001:2015 for Specialty Chemical Manufacturing
    • Responsible Care® Initiative (American Chemistry Council)
    • REACH chemical safety assessment dossier submission
    • Japan Chemical Industry Association (JCIA) voluntary standards

    Typical usage ratio

    • 1%–5% by weight as the main fluorine donor, with adjustment depending on required chain length and degree of fluorination in the final molecule.

    Downstream process integration

    • Fed into batch or continuous flow reactors for synthesis of fluorinated amides, ethers, or heterocycles; introduced post-purification to ensure consistent reaction performance and minimal byproduct formation.

    Final product types

    • Specialty monomers for advanced polymer synthesis
    • Fluorinated surfactant intermediates
    • High-purity fluorinated additives for semiconductor processing

    4. Advanced Material and Polymer Intermediate Synthesis

    Producers of specialty fluoropolymer and advanced material grades leverage fluoroacetonitrile in the synthesis of unique polymer intermediates, targeting improved hydrophobicity, chemical resistance, and tailored dielectric properties. The raw material is incorporated during functional group transformation steps preceding polymerization, ensuring efficient fluorine incorporation and material integrity for demanding end-use environments.

    Industry compliance standards

    • ISO 14001 Environmental Management for Chemical Synthesis
    • RoHS Directive 2011/65/EU compliance for restricted substances
    • Chemical Control Law (CSCL, Japan) record and reporting
    • ASTM D5630 for fluorinated polymer quality analysis

    Typical usage ratio

    • 0.3%–2% by total monomer input, with variation according to target polymer structure, end-use durability requirements, and finished resin specifications.

    Downstream process integration

    • Supplied during pre-polymer functionalization reactions, typically as a nucleophile or electrophile, to develop fluorinated intermediates; integrated prior to polymer chain building or crosslinking stages.

    Final product types

    • High-durability fluoropolymer resins
    • Dielectric materials for electronics encapsulation
    • Chemically resistant industrial coatings

    5. Veterinary Pharmaceutical Synthesis

    Animal health manufacturers employ fluoroacetonitrile as a fluorine donor in veterinary API synthesis, particularly in the production of fluorinated antiparasitic and anti-inflammatory agents. This application emphasizes controlled batch-scale chemistry under GMP conditions to achieve target substitution patterns vital for veterinary medicine bioavailability and pharmacological profile.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practice for Veterinary Products
    • China Veterinary Pharmacopoeia (latest edition) chemical input regulations
    • EU Regulation (EC) No 726/2004 for veterinary medicinal products
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.1%–1% molar ratio (relative to route-specific intermediate), dependent on synthesis route efficiency and desired final molecule substitution.

    Downstream process integration

    • Added during the intermediate modification phase of veterinary API synthesis, monitored for reaction completion by HPLC or GC-MS, typically handled with multistep purification for regulatory compliance.

    Final product types

    • Fluorinated antiparasitic agents (e.g., novel anthelmintics)
    • Veterinary anti-inflammatory active ingredients
    • Intermediate precursors for veterinary injectable and oral dosage forms
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    Certification & Compliance
    More Introduction

    Fluoroacetonitrile: A Manufacturer’s Perspective on Its Value and Applications

    The Essence of Making Fluoroacetonitrile

    Years in chemical manufacturing rarely bring routine; some products, like fluoroacetonitrile, ask for dedication to both detail and safety. Handling fluoroacetonitrile goes beyond technical skill. Each batch we synthesize means evaluating not just purity numbers but the reliability of our supply chain, the resilience of our corrosion-resistant reactors, and the steadfast performance of skilled chemists. In the workshop, you sense how even small changes in pressure, starting materials, or cooling rates can affect yield and profile. Those subtle differences show up later, in customer feedback or downstream process efficiency. The product itself is much more than a bottle on a shelf; it’s the sum of these daily hands-on lessons.

    Fluoroacetonitrile Basics from a Manufacturer’s Bench

    Our team produces fluoroacetonitrile to a standard shaped by decades of hands-on tweaks and feedback from demanding application chemists. The core formula centers on C2H2FN, but purity metrics can shift the whole picture. High assay content—consistently above 99%—matters in many synthesis pathways, not solely for regulatory checkboxing, but because impurities in this compound introduce unpredictable side reactions. These cost time, raw materials, and sometimes create downstream purification headaches.

    Synthetic routes typically begin with reaction of fluoroacetate and a dehydrating agent, with moisture control dictating how much hydrolysis you have to scrub out later. For us, the genuine test is holding volume production steady without swapping purity for output. It’s tempting to push runs harder; quality always takes precedence, so production rates never outpace what we can test and guarantee.

    What Sets Fluoroacetonitrile Apart in Practice

    Fluoroacetonitrile is not just another simple nitrile. Fluorination changes everything—volatility, toxicity, storage requirements, and, most importantly, reactivity. Projects that succeed with acetonitrile or chloroacetonitrile can fail if you try to swap in fluoroacetonitrile without changing the protocol. Demand for this particular molecule usually comes from fine chemical manufacture, advanced pharmaceutical R&D, and agrochemical labs. In most cases, customers need the fluorine specifically: introducing the fluorine atom into a molecule can change both biological activity and metabolic stability in dramatic ways.

    We see its role especially in the synthesis of fluoro-substituted heterocycles or when building blocks need to survive metabolic enzymes longer. Sometimes, only fluoroacetonitrile can deliver the desired electron-withdrawing effects or enable subsequent transformations at a nitrogen, which you won’t get from methyl or chloro analogues. Chemists aiming for unique fluorinated scaffolds, for instance, find that our product brings reliable conversion rates during nucleophilic substitutions—much higher than what standard acetonitrile could ever give.

    Beyond the Bottle: Reliability and Consistency Take Center Stage

    Making fluoroacetonitrile is only half the job. Each outgoing shipment represents a reputation. Beyond the technicalities, the storage and logistics of this compound require carcinogen-proof containers, air-tight seals, and unwavering documentation. Right from our plant floor, strict temperature control and shelf-life tracking cut down on quality degradation risks. Over the years, customers have come back to us not only for the certificate of analysis, but for the certainty that next month’s batch will work exactly like the one they received last quarter.

    No chemical is immune to supply-chain wrinkles. We’ve weathered freight delays, upstream disruptions in fluoroacetate intermediates, and evolving international regulations. Being the manufacturer, not a trader, we confront shortages and rising feedstock costs directly. Instead of passing on problems, we try to communicate potential fluctuations as early as possible—this practice reflects our commitment to transparency, which our partners value as much as technical strength.

    Handling: Practical Considerations from Daily Operations

    Every operator in our plant treats fluoroacetonitrile with respect. The material’s irritant properties require gloves, tight venting, and double-checks on leakproof lines. Exposure incidents lead to immediate medical review and retooling of the affected procedures. Over time, we have implemented incremental changes—improved local exhaust, redundancy on pressure checks, better goggles—not just because of regulations, but because every handler’s safety directly reflects in product quality and shop morale.

    Even routine filling of containers brings lessons. The compound’s volatility leads to rapid vapor loss if open transfer lines develop even minor leaks. Repeated small losses not only pose hazards, but hurt cost structures and affect reported inventory. We built a double-verification system involving both digital pressure gauges and manual nose checks. Anything that even hints at a malfunction stops the fill; no pushback from production targets can excuse a safety gap.

    User Feedback: The Real-World Test Lab

    Our understanding often grows outside the manufacturing floor. Feedback from pharmaceutical synthesis teams has been the single greatest teacher. For instance, one large agrochemical group shared how a minimal impurity spike in one lot stalled their pilot plant. Swift resolution needed more than a lab writeup—we adapted the filtration protocol for that batch, increasing check points before shipment. Other customers pointed out that custom packaging—smaller glass ampoules versus standard drums—saved them both material wastage and improved shelf stability.

    Customers seeking to introduce novel fluoro motifs into small-molecule drugs have described increased yield stability and cleaner downstream fractionations from our material, especially compared to generic-grade shipments acquired elsewhere. Often, they need more assurances around trace metallic content—something upstream processes can overlook. To address this, we overhauled our in-process alloys and started using closed steel transfer lines lined with fluoropolymer. That cut down on both iron and nickel trace findings in final bottles.

    Why Usage Context Matters: Specialist Applicators Build Value

    Most requests for fluoroacetonitrile stem from synthetic organic projects aiming for very specific knowledge gains. One common route is the production of fluorinated amino acids or heterocycles for medicinal chemistry. Here, every analytic difference counts. We routinely analyze not just global purity but also look out for specific byproducts, especially those that could catalyze unexpected degradation or color changes in pharmaceutical compounds. By aligning our QC data with real-world user requirements, we reduce surprises downstream.

    A common misconception is that purity specs serve only marketing or regulatory purposes. Through countless technical discussions with advanced users, we know otherwise. The smallest trace of hydrolysable debris can derail a route that counts on nucleophilic substitution at the carbon next to the nitrile. Our methods now include both NMR fingerprinting as well as mass spectral matching to known byproducts—steps that smaller outfits or trade-focused sellers often skip to reduce costs.

    Distinct Chemical Behavior: Fluoroacetonitrile Versus Common Nitriles

    Other nitriles such as acetonitrile and chloroacetonitrile surface in our product portfolio. Differences between those and fluoroacetonitrile go beyond small tweaks in toxicity or boiling point. Fluoroacetonitrile’s fluorine atom transforms its electron density and reactivity in synthesis. For example, in nucleophilic addition reactions, the electron-withdrawing effect of the fluorine atom renders the nitrile carbon more susceptible to attack—a boon when constructing nitrogen-containing intermediates in pharmaceutical exploration.

    On toxicology: while acetonitrile remains classified as an irritant, fluoroacetonitrile carries significantly more acute risks. This has real consequences; early-career lab workers, fresh out of school, often come expecting acetonitrile-like handling. We make sure to reinforce the stricter hazard requirements—with direct, ongoing training and in practice through our incident review board—because our operators’ safety cements the company’s long-term reliability.

    From a reactivity standpoint, our experience confirms that chlorinated analogues, although reactive, cannot offer the same precision in constructing fluoroalkyl groups critical for modern drug design. Downstream, molecular pharmacologists increasingly request fully characterized, single-fluorine functional compounds. The unique electronic signature of fluoroacetonitrile fits their screening requirements, advancing the search for novel synthetic or metabolic pathways.

    Purification, Packaging, and Shelf Life: Insights from the Factory Floor

    Getting fluoroacetonitrile pure, packed, and shelf-stable feels like a test of both engineering and persistence. We’ve refined intermediate washing steps to keep metallic contamination below pharma-grade thresholds—sometimes requiring several cycles of liquid-liquid extraction and then final distillation under inert atmosphere to prevent rapid degradation. Crystal-clear color isn’t always a guarantee of success; we run full spectral checks looking for hidden peaks that betray trace organic byproducts.

    Long-term stability remains a persistent challenge, even for seasoned crews. Over the years, we’ve learned that certain glass vials, if not vapor-tight, allow slow hydrolysis, especially when stored above recommended temperatures or if exposed to micro-punctures in cap liners. Tight QA standards mean that containers pass multiple checks—not just for gross physical integrity but also for microleaks evidenced by analytical weight-loss tracking over weeks. Every container runs through a pre-shipment review, where both fill weight and purity must confirm to historical benchmarks.

    While glass ampoules offer the best stability, some buyers require high-output drums for plant-scale experiments. In these cases, we custom-produce fluoropolymer-lined metal containers, then purge filled space with dry nitrogen. This extra step cuts down oxygen and moisture ingress, ensuring that large-scale users see the same consistent reactivity and purity as boutique research groups.

    Supporting Innovative Chemistry: Responding to Evolving Needs

    Our production and technical support teams watch the research landscape closely. Growth in fluorinated pharmaceuticals and new agrochemicals keeps changing demand for specialty building blocks like fluoroacetonitrile. Collaborations with academic researchers revealed early on that generic or low-end offerings—often sourced through traders or brokerages—left too many questions unanswered. Directly manufacturing allows our chemists to speak from firsthand knowledge, advising on best storage, pre-reaction conditioning, or specific analytical concerns.

    As emerging startups chase new chemical matter with improved bioavailability or metabolic stability, the specificity of each project means our product must integrate not just as a reagent, but as a partner in achieving those aims. Problem-solving sometimes means modifying packaging, ramping small-batch scheduling, or supporting rigorous third-party analytical verification prior to shipment. For us, value lies not in bulk, but in listening and adapting. Every kilo that ships out reflects both today’s standards and the lessons learned from yesterday’s challenges.

    Environmental Responsibility During Production and Downstream Handling

    Fluorinated organics draw scrutiny for their environmental profile. Dealing with fluoroacetonitrile means keeping our waste protocols more robust than mainstream solvent management allows. Purge and vent lines integrate activated carbon scrubbing; wastewaters route through on-site neutralization before any external shipment for hazardous waste treatment. Our site-specific policy focuses on preventing both unintentional air releases and downstream contamination, aiming for net zero accidental emissions each quarter.

    Downstream users, especially in regulated markets, have asked us to supply tracking information and robust disposal instructions that fit local compliance frameworks. Rather than generic sheets, our technical and compliance teams equip customers with waste-handling best practices from their earliest R&D stages. Since environmental stewardship counts toward long-term partnership, we push to improve both process yields (creating less waste per product kilo) and accountability for every step of the journey from synthesis to application.

    Trust Built Through Direct Manufacturing

    Traceability means more than a paper trail. Because we make fluoroacetonitrile in-house, every liter carries our internal batch records, operator signoffs, instrument logs, and outbound purity reports. Third-party sellers or distributers do not always offer such transparency. From repair logs on synthesis reactors to logs from our QA chromatographs, the heartbeat of every product is visible on demand. Security for buyers and our own risk management improves when there’s no ambiguity about origin or process.

    Mistakes can happen in any process; how they’re addressed reveals the manufacturer’s commitment. We’ve experienced mislabeling events—caught through final inspection—and resolved not only by correcting the paperwork but by stopping every related batch, retraining staff, and reviewing root process causes. This cycle-mature approach builds the foundation for reliability and word-of-mouth reputation among experienced chemists.

    Future Directions: Rising Standards and Production Challenges

    Expectations for purity and environmental responsibility only increase. Our ongoing investments focus on more automated purity detection, improved sealed system engineering, and faster in-line analysis. As regulatory bodies worldwide become stricter with both transport and use of hazardous organics, we engage with both our local authorities and international standards setters to stay ahead of mandatory changes. This involvement helps us anticipate paperwork and develop safer, more sustainable packaging.

    Resource efficiency plays into our daily operations as energy and precursor costs shift on the world stage. By developing longer-life catalysts and reusing certain solvent streams in upstream processing, we aim to keep cost and environmental impact as low as technically possible without cutting corners on quality. All of our continuous improvement efforts reflect a wider recognition: success comes from minimizing both invisible environmental “footprints” and visible quality deviations. Every batch is built on that promise.

    Practical Tips for Labs and Scale-Up Users

    The best outcomes come when downstream users treat fluoroacetonitrile not only as a reagent but as a critical step requiring thoughtful planning. Use in a fume hood; store under dry, dark conditions; always wear the appropriate gloves and face protection. Onsite training pays dividends—these lessons have been earned not by theory, but through decades of small incidents, each prompting a re-evaluation and subsequent update of our best practices.

    With each inquiry, our priority is to listen. Sometimes, the answer lies not in tweaking the product’s specs but in helping a buyer adapt their process or troubleshoot unexpected challenges. Open dialogue—far more than any brochure or specification list—keeps quality and trust at the forefront of every transaction. That relationship isn’t brokered through platitudes, but earned through repeated delivery, technical honesty, and respect for both people and the products they use.

    Conclusion: The Ongoing Story of Making and Supplying Fluoroacetonitrile

    Fluoroacetonitrile means more than just a line item in a specialty chemical product list. For us, manufacturing this compound ties together technical mastery, regulatory diligence, environmental mindfulness, and a relationship-driven approach with every end user. Earning trust, ensuring purity, and meeting both familiar and evolving needs—these take daily attention and experience, not merely automation or paperwork. That’s what sets our product, and our team, apart in a world where quality and reliability cannot be left to chance.