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4-(Trifluoromethylsulfonyl)Benzonitrile

    • Product Name 4-(Trifluoromethylsulfonyl)Benzonitrile
    • Alias 4-(Cyanophenylsulfonyl)trifluoromethane
    • Einecs 697-722-8
    • 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
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    Specifications

    HS Code

    669428

    Productname 4-(Trifluoromethylsulfonyl)Benzonitrile
    Casnumber 328-71-0
    Molecularformula C8H4F3NO2S
    Molecularweight 235.18
    Appearance White to off-white solid
    Meltingpoint 86-88 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles C1=CC(=CC=C1C#N)S(=O)(=O)CF3
    Inchikey UVZNLMYRPSCDDE-UHFFFAOYSA-N
    Storageconditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a tightly sealed cap, labeled "4-(Trifluoromethylsulfonyl)Benzonitrile, purity ≥98%, for laboratory use."
    Shipping 4-(Trifluoromethylsulfonyl)Benzonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight. The chemical is classified as non-hazardous for transport but should be handled with care. Standard shipping methods are used, complying with relevant regulations to ensure safe delivery. Temperature and impact controls are maintained during transit.
    Storage Store 4-(Trifluoromethylsulfonyl)benzonitrile in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizers. Protect it from moisture and light. Use appropriate chemical storage cabinets, and keep it clearly labeled. Follow standard laboratory safety procedures, and ensure access to spill containment materials and safety data sheets.
    Application of 4-(Trifluoromethylsulfonyl)Benzonitrile

    Applications of 4-(Trifluoromethylsulfonyl)Benzonitrile in Industrial Manufacturing

    As a specialized manufacturer of advanced nitrile functionalized aromatic compounds, we serve industrial users seeking high-performance intermediates for demanding chemical synthesis. Our expertise ensures consistent quality for downstream sectors requiring controlled reactivity and selectivity. Below, we outline genuine application scenarios where 4-(Trifluoromethylsulfonyl)Benzonitrile is actively integrated into commercial-scale production, with process, compliance, and use-level specifics for each sector.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical companies utilize this intermediate in the convergent synthesis of novel pyridine, triazine, and benzamide herbicides and fungicides. The trifluoromethylsulfonyl group enables late-stage modification, enhancing biological activity and soil persistence. Process engineers add the compound at the ring construction or functionalization step to achieve precise substitution patterns required for patented molecules, while maintaining compatibility with downstream formulation and registration requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • European Union REACH Regulation (EC 1907/2006) for intermediates
    • US EPA Registration for pesticide technical grade active ingredient manufacturing
    • FAO/WHO Specifications for Pesticide Active Ingredients

    Typical usage ratio

    • Typically 0.5–3.0 mol% relative to final active compound, with range adjusted by target crop application spectrum and molecule substitution complexity.

    Downstream process integration

    • Charged at the heterocycle formation stage via palladium-catalyzed cross-coupling or nucleophilic aromatic substitution; quality control relies on HPLC purity and controlled residual moisture content.

    Final product types

    • Technical grade herbicide actives
    • Triazine-based fungicide intermediates
    • Selective pre-emergent herbicides

    2. Pharmaceutical API Building Block

    Global pharmaceutical manufacturers select this benzonitrile derivative as a modular intermediate for synthesizing specialty kinase inhibitors and centrally acting nervous system agents. Its electron-withdrawing sulfonyl group promotes regioselective coupling and facilitates further amination or methoxylation without side reactions, supporting high-purity routes required for GMP API production pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • European Pharmacopoeia General Monograph for Starting Materials
    • CEP/EDQM certification for API supply

    Typical usage ratio

    • Generally 1.2–1.5 molar equivalents relative to core scaffold; ratio depends on substitution yield and reaction kinetics for specific API target.

    Downstream process integration

    • Integrated during late-stage intermediate condensation or Suzuki-Miyaura coupling, followed by continuous crystallization purification; monitored for trace residual solvent and genotoxic impurities as per current GMP guidelines.

    Final product types

    • Small molecule kinase inhibitor APIs
    • Neuropharmaceuticals for CNS disorders
    • Patent-protected fine chemical intermediates

    3. Specialty Polymer Modification

    High-performance polymer producers employ this compound for functionalizing aromatic backbones or introducing pendant nitrile-sulfonyl groups into specialty copolymers. The resulting polymers demonstrate increased chemical resistance and controlled surface energy, suitable for membrane technology and electronics encapsulants where precise tuning of hydrophobicity and dielectric properties is critical at commercial scale.

    Industry compliance standards

    • ISO 9001:2015 for polymer chemicals
    • RoHS Directive 2011/65/EU for electronics materials
    • UL 94 for flammability rating of plastics
    • EN 60216 for thermal endurance properties

    Typical usage ratio

    • Used at 0.05–0.2 wt% based on total monomer feed, level adjusted for desired polymer end-group functionality and bulk property tuning.

    Downstream process integration

    • Co-dosed in bulk polymerization or melt-extrusion lines; batch processes adjusted for targeted molar incorporation, followed by in-line FTIR analysis and post-polymerization extraction to ensure batch consistency.

    Final product types

    • Ion-exchange membranes
    • Semiconductor encapsulants
    • Chemical-resistant engineering plastics

    4. Electronic Chemicals – Photoresist Intermediate

    Semiconductor fabrication supply chains demand high-purity aromatic sulfonyl nitriles for use in advanced photoactive compounds within positive- and negative-tone photoresists. The nitrile group enhances effective charge transfer and pattern resolution, while the sulfonyl substituent imparts excellent thermal and oxidative stability, critical in photolithography under aggressive manufacturing conditions.

    Industry compliance standards

    • SEMATECH F63 for photoresist raw material purity
    • JEITA ET-7304 for organic electronic materials
    • ISO 14644-1 Cleanroom standards for semiconductor processing
    • RoHS and REACH for global electronics compliance

    Typical usage ratio

    • Introduced at 0.1–0.8 molar ratio with respect to diazo or novolac resin main component, depending on feature size and energy dose parameters for photolithographic process.

    Downstream process integration

    • Added during synthesis of quinone diazide or sulfonate ester precursors, typically via solution-phase coupling with stringent control of trace ionic and metallic impurities; followed by micron-scale filtration and particle analysis for downstream lithography steps.

    Final product types

    • IC fabrication photoresists
    • Printed circuit board (PCB) pattern resists
    • LCD photolithography materials

    5. Advanced Dyestuff and Pigment Intermediates

    Producers of high-performance dyes and pigments for automotive coatings and printing inks utilize this functional benzonitrile to introduce trifluoromethylsulfonyl electron-withdrawing effects into anthraquinone or azo pigment structures. Such structural modification results in improved lightfastness and solvent resistance, supporting stringent end-use requirements in automotive finishes and specialty inkjet formulations.

    Industry compliance standards

    • DIN EN ISO 9001 for pigment manufacturing
    • Automotive OEM paint standards (e.g. Ford WSS-M99P9999)
    • European Printing Ink Association (EuPIA) Exclusion Policy
    • REACH Annex XVII for pigment substances

    Typical usage ratio

    • Applied at 0.2–1.0 molar ratio versus primary chromophore-forming reactant, modulated to achieve target chroma and permanence.

    Downstream process integration

    • Charged during coupling or sulfonation reaction stages in pigment paste manufacturing; subsequent filtration and high-shear grinding remove aggregation before dispersant addition and quality tint assessment.

    Final product types

    • Automotive grade pigments
    • Inkjet and specialty printing dyes
    • Anti-corrosive industrial coatings
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    Certification & Compliance
    More Introduction

    Introducing 4-(Trifluoromethylsulfonyl)Benzonitrile: A Practical Perspective

    Our Experience in Crafting 4-(Trifluoromethylsulfonyl)Benzonitrile

    At our site, the journey of making 4-(Trifluoromethylsulfonyl)benzonitrile runs deeper than catalog numbers and paperwork. We see this compound every day — the white powder on a glass tray, the faint tang during the final purification steps, the pride mixed with tension as each batch is tested for traces of moisture or colored impurities. We don’t broker shipments; we take raw, sometimes volatile chemicals and bring them together under real-world conditions, taking the responsibility for every step. Each drum that leaves our floor reflects hundreds of tiny decisions and decades of shared know-how.

    4-(Trifluoromethylsulfonyl)benzonitrile, known to chemists as TFMS-BN, begins its story on our production lines through a series of critical steps. Our teams handle the trifluoromethanesulfonyl chloride with care, managing its high reactivity with strict process controls in jacketed vessels. The benzonitrile ring starts as a clean, high-purity substrate. Each reaction demands close temperature management to steer clear of side products. Any deviation can throw an entire run off course. The hard-won expertise that guides our operators comes from years spent in the plant, not in a sales meeting.

    Appearance, Purity, and What Sets Our TFMS-BN Apart

    Our process delivers TFMS-BN as a white to off-white crystalline solid. Operators judge every batch not just with numbers, but also with their eyes and hands. Standard purity for this product lands above 98% measured by HPLC, but real-world performance hinges on more than those figures. We check residual water content by Karl Fischer titration, since moisture dramatically impacts its shelf stability and reactivity downstream. During shipment preparation, a slight pinkish tint in the crystals can signal incomplete reaction or decomposition, and the batch won’t leave our plant without those issues resolved. These everyday checks matter as much as the final assay certificate.

    The sulfonyl group on the molecule introduces a high level of electron withdrawal. Chemists in the lab count on this effect during cross-coupling or nucleophilic aromatic substitution reactions, where the TFMS group activates the arene ring in a way that standard benzonitriles — including plain 4-cyanobenzene — simply do not match. From a synthetic chemistry standpoint, the difference is quite tangible: reactions that sputter along for days with less activated rings can often finish in hours, or may be possible at all only through the use of TFMS-BN as a building block. Our technical team often works directly with customers’ R&D chemists to troubleshoot these transformations, since the devil tends to lie in the slight differences batch to batch.

    We keep our internal process documentation open across our teams so that small changes in input materials — a shift in the water content of the incoming trifluoromethanesulfonyl chloride, a different supplier of solvent — get flagged right away. This tight feedback loop brings the kind of batch-to-batch consistency that process chemists in scale-up or validation depend on, especially when they face regulatory scrutiny for pharmaceutical or specialty chemical production. The engineers who review the data have walked the lines, not just the laboratories.

    Reliable Handling and Packaging

    We use moisture-proof drums or lined foil bags depending on customer request and intended use. Almost every batch is capped under a stream of dry nitrogen, since we’ve seen firsthand how even brief exposure to air during summer humidity can cause clumping or hydrolysis. The inside of a poorly sealed container after sitting for a week in the plant, especially during a heatwave, leaves a lasting impression. Package selection isn’t left to chance, since the impact on downstream purity shows up in both customer feedback and our own reanalysis.

    Our packaging teams inspect every seal and lining before shipping, trained to recognize the telltale signs of improper closure — a few grains clinging to the lip of a drum, or the sharp chemical scent that means something’s not quite right. Feedback from partners handling scale-up campaigns often points out that this attention to detail helped them avoid complications during recharging and sampling, where dust and unwanted exposure can waste precious material.

    Primary Applications from a Manufacturer’s Viewpoint

    4-(Trifluoromethylsulfonyl)benzonitrile moves through our facilities mainly bound for companies developing advanced intermediates in pharmaceuticals, agrochemicals, and materials science. Those on the receiving end count on its intense electron-withdrawing capacity. TFMS-BN sits at a sweet spot for chemists engineering molecules where high reactivity is required, but the arene backbone needs to stay robust.

    Medicinal chemists value the trifluoromethylsulfonyl group for more than its activating properties. The CF3SO2 moiety resists metabolic breakdown, often increasing a compound’s stability in vivo. Colleagues working up new kinase inhibitors and anti-tumor scaffolds share stories with us about combining TFMS-BN with amines and thiols to generate libraries of potential drug candidates. Compared to standard benzonitriles substituted with methoxy or simple halo groups, these structures resist rapid metabolic clearance — a quality that sometimes makes the difference in bioactivity screens.

    Crop science research teams often seek out our TFMS-BN as well. The electron-poor arene delivers agrochemical molecules more resistant to degradation from environmental stress, especially in formulations meant for use in challenging climates. Our support staff occasionally helps troubleshoot process problems in larger reactors, sending out fresh samples for pilot campaigns, since unforeseen variations in formulation — gumminess during granulation, foaming in reactors — often come down to trace residuals in the starting TFMS-BN. Our plant operators’ experience with large-scale blending and drying often guides subtle tweaks to customer formulations.

    Materials scientists use 4-(trifluoromethylsulfonyl)benzonitrile for specialty polymers designed to withstand heat, oxidative stress, and prolonged use in electronics or membranes. Some of our largest-volume batches head directly to manufacturers of these high-performance materials. Each order brings an extra set of purity requirements, since downstream processing can amplify small differences in starting compound quality. Failed runs due to minor impurities lead to costly downtime; that’s a reality not lost on the technicians in our QC lab, where a late-night phone call may mean bringing in a supervisor for an unscheduled chromatogram check before approving shipment.

    What’s Different about 4-(Trifluoromethylsulfonyl)Benzonitrile?

    Our team often gets asked what sets TFMS-BN apart in practical terms. Compared to common benzonitrile derivatives — like 4-cyanobenzene, 4-fluorobenzonitrile or even 4-(trifluoromethyl)benzonitrile — the addition of the trifluoromethylsulfonyl group delivers a marked boost in both chemical stability and activation of the aromatic system. The electron-withdrawing strength overshadows that of fluoro or trifluoromethyl groups by a wide margin.

    Many chemists recognize this right away when checking pKa values or running test reactions. While a fluoro group on the para position pushes the arene toward higher reactivity, the trifluoromethylsulfonyl moiety multiplies that effect. This has practical upstream implications; slow or sluggish substitution reactions on standard benzonitriles may proceed far more easily using TFMS-BN. In our facility, we see these effects during downstream synthesis of sulfonamides, biaryls, and heterocycles. Reactions requiring milder base, lower temperatures, or taking less time reflect cost and safety savings, which process operators appreciate far more than any data sheet summary.

    Handling and storage provide another key difference. The trifluoromethylsulfonyl group imparts a bit more bulk and changes how the molecule packs in solid form. Some competitors report batch caking or poor flow in silo applications, but with careful dehydration and proper anti-caking agents, our bulk lots remain consistently free-flowing. Teams monitoring warehouse conditions run humidity checks more often than any guideline suggests, since a single night of high relative humidity can undo days of careful drying. That kind of vigilance has been shaped by direct production floor experience.

    From Chemical Plant to Customer Bench: Realities Along the Supply Chain

    As the manufacturer, our job doesn’t end with final packaging. Our technical support group often fields calls from researchers and plant managers running into snags during pilot-scale or commercial reactions. Some feedback touches on reactivity differences between TFMS-BN and other para-substituted benzonitriles; unexpected color changes, exotherms, or incomplete conversion can trace directly to the stronger electron-withdrawing effects or higher purity pulling reactions toward side-products. Our in-house chemists regularly run parallel syntheses, offering guidance on reaction conditions — temperature, solvent selection, and base choice — that reflect lessons learned scaling TFMS-BN from a bench curiosity to a production mainstay.

    Other challenges along the supply chain include stability and transit resilience. TFMS-BN’s crystalline form handles pressure well but can become electrostatically charged during bulk dispensing. More than a few operators have been surprised by powder clinging stubbornly to their gloves or dispensing equipment, slowing batching on otherwise busy process lines. We address these issues with static-dissipative liners and select drum construction, informed by repeated walkthroughs of our own shipping operations and customer receiving rooms.

    Once, a large customer’s logistics team reported unusual clumping in several 25-kg drums delivered during peak summer. Investigation traced the problem to a failure in the shipment’s climate control rather than production or formulation. Our logistics manager, a veteran with decades on the docks, quickly put controls in place for pre-shipment temperature and humidity tracking. That learning reshaped our shipping protocols and reduced shipping-related deviation incidents across all our products.

    Quality, Safety, and Consistency from the Production Floor

    Every drum of 4-(trifluoromethylsulfonyl)benzonitrile carries the accountability of our plant crew. Batch records stay tied to the original production run, open for inspection and traceability all the way back to raw materials delivery. Our operators know that even a minor deviation — an overlong wash, a substituted solvent, a fluctuation in reaction temperature during the coupling step — can surface months later as a performance issue at a customer site. That knowledge pushes our focus beyond certificates of analysis toward true batch consistency.

    Production line safety remains a top priority. TFMS-BN can irritate the skin and upper airways. Anyone working the reactors or packing stations wears chemical-resistant gloves, goggles, and respiratory protection, since accidental splashing or airborne powder is a real-world hazard in our environment. We’ve learned through long experience that reminders alone don’t prevent accidents — plant safety walks, peer observations, and management presence on the floor have the most impact. No batch is rushed at the cost of personal safety.

    Investments in Sustainability

    Routine production of TFMS-BN requires careful waste management. Solvents and wash waters contain traces of the compound and the sulfur-containing byproducts. Our plant treats these streams through multiple-stage scrubbers and chemical neutralization before discharge; on days when process upsets occur, operators know to slow production to prevent out-of-spec effluent. Regular environmental monitoring gives us confidence that the waste we generate does not exceed regulatory limits — and we share these records during customer audits.

    Our focus on greener chemistry extends to solvent selection and recycling. On average, we recycle over half the organic solvents used in TFMS-BN synthesis, re-distilling them on-site to minimize external waste. These steps cut costs but reflect a broader company commitment to sustainable production, which matters to the global brands purchasing our material for pharmaceuticals and advanced materials. We’ve adopted energy-efficient separation equipment and have pursued outside certifications in responsible chemical manufacturing, although the day-to-day motivation comes from seeing the difference in waste reduction every week.

    Technical Advice for TFMS-BN Users

    We work directly with chemists and process engineers who use our product in synthesis or formulation. For those optimizing reactions, the electron-withdrawing power of the trifluoromethylsulfonyl group allows for faster reactions under milder conditions. We’ve seen this unlock stubborn cross-couplings and nucleophilic aromatic substitutions that stalled using less activated substrates. The purity and dryness of each batch make a significant impact: trace metals or excess water can suppress yields or trigger unwanted side-reactions.

    Users can expect a reliable melting range between 70 and 75°C with proper storage. Our technical department advises storing sealed containers in low-humidity, temperature-controlled rooms to prevent hydrolysis. Many of our largest clients pull samples on receipt, and we offer support interpreting NMR and HPLC data if incoming results deviate from specification.

    In scale-up campaigns, those switching from pilot-scale glassware to plant reactors may notice changes in stirring, powder handling, or dosing. In bulk transfer, proper precautions against static build-up and humidity exposure make a difference in preventing caked material and loss of throughput. Our process engineers often consult with customers setting up their equipment, recommending specific drum lift devices or nitrogen blanketing steps that have worked in our environment.

    Continuous Improvement and the Human Factor

    Many quality issues with specialty chemicals surface not at the end of the lab scale but during scale-up or first commercial production. Our open line of communication lets us catch issues before they turn costly for either side. Operators filing shift reports include observations about equipment drift, unusual crystal morphology, or subtle process upsets, all baked into our improvement cycles. We conduct quarterly reviews linking lab incidents to production, with everyone — from entry-level techs to senior management — sharing lessons and jointly proposing process tweaks.

    Customers often share their formulation fails with us during follow-up, and our technical team treats these as vital feedback. A pharmaceutical customer once reported that a minor batch-to-batch difference in flow properties complicated dosing on their tablet press. After reviewing production logs, a small tweak in the drying phase restored the expected behavior, saving time and downstream waste. Experience has taught us to respect the small details in handling and formulation, which impacts process reliability long after the initial delivery.

    Summing Up What We Deliver

    As one of the few manufacturers who follow TFMS-BN from reaction kettle through packing to shipment, we see firsthand what it takes to turn a challenging synthetic intermediate into a real-world tool for industry. Our roots in the production plant, not behind a sales desk, keep us focused on practical utility: sharply defined purity, batch consistency, attention to storage and handling, and clear communication across departments.

    Working with customers in pharmaceuticals, agrochemicals, and advanced materials shows that needs keep evolving. The push toward green chemistry, sustainable operation, and regulatory transparency sits alongside the everyday demand for reliability and speed. Our biggest investment continues to be both the people and hard infrastructure behind each drum of 4-(trifluoromethylsulfonyl)benzonitrile. Decades of trial and error, shared knowledge, and open customer engagement have shaped a product that not only meets specifications but performs under real-world conditions. That’s the real test, and one our entire team takes pride in meeting batch after batch.