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4-Nitro-2-(Trifluoromethyl)Benzonitrile

    • Product Name 4-Nitro-2-(Trifluoromethyl)Benzonitrile
    • Alias 4-Nitro-2-(trifluoromethyl)benzonitrile
    • Einecs 619-516-2
    • 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
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    Specifications

    HS Code

    534703

    Chemical Name 4-Nitro-2-(Trifluoromethyl)Benzonitrile
    Cas Number 877-68-5
    Molecular Formula C8H3F3N2O2
    Molecular Weight 216.12
    Appearance Yellow crystalline solid
    Melting Point 91-94°C
    Density 1.53 g/cm3 (approximate)
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C=C1C#N)[N+](=O)[O-])C(F)(F)F
    Pubchem Cid 144284
    Inchi InChI=1S/C8H3F3N2O2/c9-8(10,11)6-2-1-5(4-12)7(3-6)13(14)15/h1-3H
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Nitro-2-(Trifluoromethyl)Benzonitrile, sealed with a red screw cap and labeled for laboratory use.
    Shipping 4-Nitro-2-(Trifluoromethyl)Benzonitrile is shipped in tightly sealed containers away from light, heat, and moisture. It must be handled as a hazardous chemical, with proper labeling and documentation according to regulations. Transport is usually via ground or air within secondary containment to prevent leaks or spills, following all safety guidelines.
    Storage 4-Nitro-2-(Trifluoromethyl)benzonitrile should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong reducing agents and bases. Protect from moisture and direct sunlight. Store at room temperature and keep away from heat and ignition sources. Use appropriate safety labeling and ensure access to safety equipment.
    Application of 4-Nitro-2-(Trifluoromethyl)Benzonitrile

    Applications of 4-Nitro-2-(Trifluoromethyl)Benzonitrile in Industrial Manufacturing

    As an established manufacturer, we supply 4-Nitro-2-(Trifluoromethyl)Benzonitrile to specialized segments of the chemical synthesis industry, supporting high-value applications with stringent technical and regulatory requirements. Below we detail practical industrial scenarios where this intermediate is essential, including quality standards, formulation practices, process roles, and finished products delivered by downstream producers.

    1. Pharmaceutical Intermediate Synthesis (Active Pharmaceutical Ingredients)

    Pharmaceutical process engineers employ this compound as a key intermediate during multi-step API syntheses, particularly in constructing substituted aromatic scaffolds and bridged benzamide derivatives. It fits advanced medicinal chemistry projects seeking electron-withdrawing groups to modulate molecular reactivity and physicochemical properties during route development and scale-up, with traceability under regulated environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <1062> Bulk Pharmaceutical Chemicals
    • European Pharmacopoeia (Ph. Eur.) monograph requirements for intermediates
    • FDA 21 CFR Part 210/211 for cGMP finished pharmaceuticals

    Typical usage ratio

    • Intermediate input between 1.2–1.7 molar equivalents per batch, adjusted relative to downstream core structure yield and impurity profile management

    Downstream process integration

    • Introduced during the aromatic nitrile coupling or nucleophilic substitution stages for constructing pharmaceutical core structures; often subjected to reduction or condensation transformations downstream

    Final product types

    • Kinase inhibitor precursors
    • Anti-inflammatory drug intermediates
    • Heteroaromatic synthetic building blocks
    • Lead compounds for oncology research

    2. Agrochemical Active Ingredient Manufacture

    This molecule is widely implemented as an advanced intermediate in the agrochemical sector, incorporated into diverse pesticide and fungicide precursor programs. Researchers and process chemists leverage its trifluoromethyl and nitro functional groups to engineer target compounds with improved persistence and biological activity profiles against specific pests and resistant pathogens.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management for Agrochemical Manufacturing
    • FAO/WHO Specification for Plant Protection Products
    • REACH (EC) No 1907/2006 registration for commercial use in Europe
    • BPR (Biocidal Products Regulation, EU 528/2012) for downstream formulations

    Typical usage ratio

    • Generally 2.5–4.5% by weight in the precursor synthesis charge, based on desired yield and reaction stoichiometry of the targeted agrochemical

    Downstream process integration

    • Feeds into chloro-substitution reactions, coupling, or further nitration/hydrolysis, serving as a core building block in development pipelines for new-generation pesticides or fungicides

    Final product types

    • Herbicide intermediates
    • Seed treatment active ingredients
    • Fungicide backbone precursors
    • Crop protection compounds with enhanced degradation resistance

    3. Advanced Dye and Pigment Intermediate Supply

    Industrial pigment and dye manufacturers value this material for synthesizing highly specialized colorant intermediates, especially where stability under aggressive photochemical and chemical conditions is needed. Its electron-withdrawing groups help achieve precise chromatic effects and performance in high-temperature or solvent-intensive textile, electronic, and automotive coating applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals, when applicable
    • ISO 9001:2015 for pigment and dyestuff production
    • EU Regulation (EC) No 1907/2006 REACH compliance for industrial dyestuffs
    • DIN EN 71-3 Safety requirements for toys pigments (when relevant)

    Typical usage ratio

    • 1.0–3.2% incorporated in the key coupling or diazotization stage, with adjustment based on shade strength, dispersibility, and required resistance to light or chemicals

    Downstream process integration

    • Enters during azo or anthraquinone dye core formation, forming substituted aromatic rings that drive final pigment properties; also used in condensation reactions for high-performance pigment backbones

    Final product types

    • High-fastness textile dyes
    • Technical colorants for electronics
    • Solvent-resistant automotive pigments
    • Specialty inkjet and digital printing dyes

    4. Chemical Material for Specialty Polymers

    The intermediate serves as a functional monomer precursor in the high-performance polymer sector, where manufacturers require tailored electronic properties and environmental stability. Its inclusion in monomer synthesis steps allows formulation of specialty fluorinated polymers and functional materials for demanding electrical and optoelectronic applications.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) on hazardous substance restrictions
    • IEC 61249-2-21 standards for halogen-free base materials
    • ISO 9001:2015 for specialty polymer manufacturing
    • UL 94 Flame Classification (for downstream electrical uses)

    Typical usage ratio

    • Utilized at 0.7–1.8% of total polymerizable mass, varied based on desired dielectric properties and process compatibility requirements in polymer backbones

    Downstream process integration

    • Integrated in copolymerization or functionalization stages, linking into polymer chains to impart trifluoromethyl group benefits such as enhanced durability and modified surface energy

    Final product types

    • Fluorinated specialty resins
    • Electronic encapsulation materials
    • High-performance wire and cable coatings
    • Optical film base layers

    5. Intermediate for Liquid Crystal Material Synthesis

    R&D and scale-up teams in the advanced material sector incorporate this compound to synthesize functional intermediates for liquid crystal material development. Its aromatic core and electron-withdrawing substitutions are crucial when building core structures for LC mixtures with precise dispersion and electro-optical requirements.

    Industry compliance standards

    • IEC 61747 Thin-film transistor liquid crystal display standards
    • ISO 14001 Environmental Management System for production lines
    • RoHS and REACH chemical safety compliance for display subcomponents
    • JPCA-ES-01 standards for electronic display materials

    Typical usage ratio

    • Generally 0.5–1.6 molar equivalents in precursor reaction steps, calibrated to achieve target optical thresholds and mixture viscosity profiles

    Downstream process integration

    • Feeds aromatic ring-forming reactions or is used in the synthesis of fluorinated and nitrile-functionalized mesogenic intermediates, essential for proprietary LC formulations

    Final product types

    • Mixing bases for LCDs and OLED displays
    • Electro-optical switching media
    • Phase compensator materials
    • Flexible display pixel enhancers
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    Certification & Compliance
    More Introduction

    4-Nitro-2-(Trifluoromethyl)Benzonitrile: Practical Insights from the Manufacturer’s Line

    Producing for Progress: Why We Choose 4-Nitro-2-(Trifluoromethyl)Benzonitrile

    Every day in our factory, beakers bubble and columns hum with new batches of 4-Nitro-2-(Trifluoromethyl)Benzonitrile. From raw feedstock delivery to packaging the final product, we see not just chemicals, but the backbone of new ideas in pharmaceuticals and agrochemicals. This compound, known in-house as the 9145F batch, stands out because of its steady demand among R&D teams and process engineers looking to streamline synthetic routes.

    Years ago, the market leaned heavily on older nitrile intermediates with simpler substitutions. The industry needed something that combined the electron-withdrawing punch of a trifluoromethyl group and the synthetic utility of a nitro group, locked into the benzene ring. The result brought more reaction handles into play, paving the way for steps like nucleophilic substitution, reduction, or cross-coupling. Watching our partners design more efficient synthetic routes around this molecule’s features has been a reminder that chemistry never stands still.

    The Chemical Model: Trusted Performance and Clear Advantages

    4-Nitro-2-(Trifluoromethyl)Benzonitrile (CAS No. 793-76-6) showcases a balanced profile chemists appreciate: high purity, consistent batch-to-batch quality, solid shelf stability, and a manageable, crystalline solid form. We analyze each production run with HPLC and NMR spectroscopy—nothing leaves the plant under 99.5% assay. Color, melting point range, and moisture level all line up with what seasoned synthetic chemists expect on their bench.

    The molecular structure includes both the nitro and trifluoromethyl groups positioned ortho to the nitrile. This substitution pattern delivers more than a name—it influences reactivity in palladium-catalyzed formations and reduction steps. Over the years, the compound has made itself at home in our reactors, holding up under heat and pressure when alternative benzonitriles wouldn’t make the cut.

    Applications in the Real World: Where the Chemistry Lands

    We see most of our output move toward companies crafting active pharmaceutical ingredients and specialty agrochemical molecules. Our feedback comes direct from process development teams. For example, one customer shared how our 4-Nitro-2-(Trifluoromethyl)Benzonitrile trimmed a two-step preparation down to a single pot. Another group fed it straight into a Suzuki coupling to access trifluoromethyl benzoic acid derivatives, saving them hours of tricky purifications and boosting overall yield.

    Production doesn’t just stop at grams in an R&D flask. We scale into drums and totes for kilo production, making sure particle size, dust formation, and bulk density hold uniformity from start to finish. Every day we handle requests from buyers searching for scalable intermediates. They want molecules that behave under real plant conditions—the sort that keep the project on the rails from pilot batch to ton-scale output.

    Over time, the compound has become a staple entry point for more than one blockbuster drug. Its unique profile—nitrile for further derivatization, nitro for reductions, and trifluoromethyl for tuning lipophilicity—helps process chemists shortcut synthesis without sacrificing downstream versatility. In the pesticide sector, it serves as a precursor that brings robust activity, helping developers get closer to next-generation crop protection agents.

    From Factory Floor to Fine Details: Practical Insights on Handling and Stability

    Handling and storage play a role as critical as molecular design. Our teams learned early on that well-sealed containers and a dry atmosphere extend shelf life well past one year, without clumping or discoloration showing up in storage. Thanks to its crystalline nature, the product keeps dust levels manageable, cutting down on airborne contamination when transferring bulk quantities.

    The melting point hits consistently in the expected range, making bulk transfer and dissolution reliable in both small and large-scale reactors. Our QC team checks every drum for off-white appearance, proper crystalline form, and lack of visible impurities. This relentless checking means our downstream partners see fewer headaches with repeat reactions or QC failures.

    Waste processing and environmental stewardship factor into our production run. Each batch leaves behind only modest levels of organic waste, and we send scrubber residues through on-site treatment before disposal. The synthesis balances robust yields with manageable byproducts, adhering to our commitment to cleaner operations. Plant managers appreciate intermediates that don’t complicate environmental permitting or push up treatment costs.

    Differences That Impact Real Work: Choosing the Right Benzonitrile

    Comparing 4-Nitro-2-(Trifluoromethyl)Benzonitrile to other benzonitriles showcases why experienced buyers return for this specific compound. Simpler benzonitriles—such as the plain para- or ortho-substituted versions—often lack the combination of functional group tolerance and reactivity enhancement. Trifluoromethyl adds a level of metabolic stability and electron-withdrawing force not seen in methyl or chloro analogues; the nitro functionality, once slated for reduction or further elaboration, gives chemists more flexibility in manipulating the molecule’s fate.

    Our in-house trials and client feedback highlight how competing products—say, 2-chloro-4-nitrobenzonitrile or 4-cyano-3-trifluoromethyl nitrobenzenes—fall short in palladium-catalyzed couplings or fail during reduction steps. Some analogues lead to problems with isomer separation or create stubborn impurities at critical downstream stages. Meanwhile, the ortho arrangement of nitro and trifluoromethyl groups in our benchmark molecule has solved several column fouling nightmares, and allowed end users to fine-tune lipophilicity without adding extra synthetic steps.

    It's not only about individual projects. In our facility, we see how robust, well-defined intermediates can help process teams reduce cycle times and batch rejections, two performance metrics that shift the bottom line. Sourcing a compound that delivers predictable behavior under pressure and heat means fewer late-stage surprises and less unplanned downtime.

    The consistency of our finished batches—reflected in potent purity and reliable physical form—stands out when compared to generic imports or mixtures with variable particle size. End users get a product that weighs, pours, dissolves, and reacts in the way their process expects, batch after batch. These details add up, especially during scale-up for regulatory submissions or during process validations that allow no deviation in impurity profile.

    Building on Experience: Our Commitment to Real-World Chemistry

    Our facility didn’t start out perfect. Through years of batch processing, operator training, and honest feedback from customers, we adjusted and refined our methods for making and delivering 4-Nitro-2-(Trifluoromethyl)Benzonitrile. Trials with different drying techniques, improved packing processes, and batch traceability audits have helped us meet the ever-tighter requirements leading the industry.

    Close communication with R&D teams from global and local firms helps us adapt. Sometimes a client reports an issue downstream—a reduction step that runs too slow, a residue that throws off a column. Instead of laying blame, we set up side-by-side reactivity trials, reaching for real data so there’s no guesswork on what’s causing a bottleneck. Over time, these case studies add to our institutional memory, teaching us what to tweak for next month’s lot.

    Supply reliability comes from hands-on oversight. We witnessed firsthand what disruption feels like—just-in-time orders delayed by weather or transport snagging at customs. Keeping stocks on hand, running extra QC, and staying on top of logistics—these lessons stick because every hour shaved off delays helps keep a project’s critical path clear.

    Honing the Future: Listening to the Demands of the Industry

    Chemistry doesn’t reward shortcuts, and every batch of 4-Nitro-2-(Trifluoromethyl)Benzonitrile reminds us that detail drives progress. Listening to both large buyers and smaller pilot plants gives us the full picture. Scale brings its own friction—different stirring, pumping, and storage requirements. Each time a technical team asks about moisture tolerance or dusting, it’s a cue for us to revisit procedures and push for better control.

    A growing number of our partners push us toward lower residual solvents, tighter impurity specs, and more detailed documentation. It means moving beyond basic COAs toward full traceability, chromatography fingerprints, and supply chain visibility. Not simply box-checking, but understanding that every shift closer to transparency adds assurance for regulatory filings, batch release, and the safety of final-use substances.

    We’ve run stability checks beyond standard conditions, ensuring the product doesn’t drift outside specifications even after months at ambient storage. Regular in-process sampling lets us adjust on the fly and address trends before they turn into issues. Engaging with auditing teams—even signing up for voluntary inspections—pushes us toward higher standards, adding confidence for the next round of innovation.

    Supporting Innovation with Reliability and Clarity

    Every year brings requests for new pack sizes—small bottles for pilot plant R&D, bulk sacks for full-order synthesis, and custom blends for unique downstream applications. Meeting these needs isn’t about stacking more offerings onto a list. It’s about recognizing that process development never follows a blueprint, and each project can hit a snag if the intermediate doesn’t behave as expected. We put time into training our operators, tuning milling equipment, and testing new liners and seals, all so each kilogram moving out the door fits its intended use. This kind of attention comes from working hand-in-hand with chemists who value every hour shaved off their project timeline.

    Projects move fast, research pivots quickly, and formulas never stop evolving. What doesn’t change is the need for intermediates delivering on every promise—pure enough for tough reactions, stable enough for scale-up, and consistent enough to cut rework. The stories we hear at conferences and over email underscore the pressure every buyer faces to prove their product works, batch after batch. We take these stories seriously, engineering our workflow to support them.

    Quality and Value: Beyond the Basics of Supply

    Our job doesn’t end at filling an order. Real partnership with downstream users means standing ready for troubleshooting, process optimization advice, and post-delivery queries. We’ve answered questions at midnight about possible alternative drying methods, helped customers sort out batch records needed for agency filings, and provided impurity spectra for regulatory review. This isn’t just extra service—it's the product of experience rooted in manufacturing, not just selling.

    Margins in chemical manufacturing are thin, but the cost of a failed batch or unexpected downtime dwarfs the price of premium intermediates. The most experienced buyers know—sourcing the right benzonitrile isn’t just about getting the best deal today, but about locking in supply, reliability, and support for every step that follows.

    We keep close tabs on every stage of production, recognizing that one missed detail can spiral into delays or regulatory headaches. This attention protects our clients, who trust that our 4-Nitro-2-(Trifluoromethyl)Benzonitrile won’t introduce unexpected complications downstream. Every innovation in quality control—inline monitoring, rapid testing methods, real-time data tracking—translates into value that goes beyond the product’s price tag.

    Facing Supply and Safety Challenges with Transparency

    Making and shipping fine chemicals brings its share of challenges. International logistics grow more complex with shifting regulations, container backlogs, and rising documentation needs. We invest time and resources upfront to anticipate, and where possible, mitigate these roadblocks. Clients ask for assurance that each drum holds what the label claims, and we back our product with batch history, certificates, and open lines of communication to address questions before, during, and after delivery.

    On the safety front, we’ve learned that nothing trumps clear labeling, sealed packaging, and reliable product literature. Process safety starts with purity, carries through to manageable particle size, and gets reinforced with a support network that answers questions fast. We field technical calls from users setting up new syntheses, walking through reactivity or handling questions based on firsthand plant experience.

    Investing in Progress: Continuous Improvement and Industry Collaboration

    It’s clear that chemistry built on experience doesn’t just serve today’s projects—it prepares labs and plants for the next wave of development. By keeping lines open to teams pushing for faster reactions, greener synthesis, or more robust regulatory packages, we gain insight that drives ongoing improvement. We regularly send samples for customer evaluation, adapt packaging based on user feedback, and upgrade process controls to lock in every gain.

    Industry events, technical gatherings, and direct site visits bring more than just business—they foster understanding. Every shared challenge, from crystallization hiccups to solvent system tweaks, sharpens our own approach. Sticking with the market’s best practices in plant safety, environmental management, and data integrity keeps us ready for whatever regulatory or technical demand emerges.

    Final Thoughts from the Production Floor

    We make 4-Nitro-2-(Trifluoromethyl)Benzonitrile because experience tells us it works where others fall short. The compound’s unique substitution opens doors for creative synthesis, lean process design, and efficient downstream elaboration in pharmaceuticals and agriculture. Bringing together solid purity, physical reliability, and customer-driven continuous improvement, we meet the daily challenges facing chemists around the globe. Every drum and bottle that leaves our plant reflects real-world expertise, a commitment to detail, and a promise to support the people pushing chemistry forward. For us, that mix makes all the difference.