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1,2,4-Trifluoro-5-Nitrobenzene

    • Product Name 1,2,4-Trifluoro-5-Nitrobenzene
    • Alias 1,2,4-Trifluoro-5-nitrobenzene
    • Einecs 209-824-7
    • 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

    330729

    Chemicalname 1,2,4-Trifluoro-5-Nitrobenzene
    Molecularformula C6H2F3NO2
    Molecularweight 177.08 g/mol
    Casnumber 328-75-6
    Appearance Pale yellow liquid
    Boilingpoint 171-173°C
    Meltingpoint -7°C
    Density 1.547 g/cm3 at 25°C
    Purity Typically ≥98%
    Refractiveindex 1.4820
    Solubility Insoluble in water, soluble in organic solvents
    Smiles FC1=CC(=C(C=C1F)[N+](=O)[O-])F
    Inchi InChI=1S/C6H2F3NO2/c7-3-1-4(8)6(10(11)12)2-5(3)9/h1-2H
    Storagetemperature Store at room temperature
    Synonyms 2,4,5-Trifluoronitrobenzene

    As an accredited 1,2,4-Trifluoro-5-Nitrobenzene 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 100 grams of 1,2,4-Trifluoro-5-Nitrobenzene, tightly sealed, labeled with hazard symbols and safety information.
    Shipping **Shipping Description for 1,2,4-Trifluoro-5-Nitrobenzene:** Ship in a tightly sealed, chemically compatible container. Label as hazardous if applicable. Protect from heat, moisture, and incompatible materials. Follow all relevant regulations for transportation of chemicals, including appropriate hazard classes, packaging group, and safety documentation. Ensure visible hazard labeling and include Safety Data Sheet (SDS) with shipment.
    Storage 1,2,4-Trifluoro-5-Nitrobenzene should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong acids, bases, and oxidizing agents. Store away from moisture and ignition sources. Use appropriate chemical-resistant shelving and clearly label the storage area for hazardous chemicals.
    Application of 1,2,4-Trifluoro-5-Nitrobenzene

    Applications of 1,2,4-Trifluoro-5-Nitrobenzene in Industrial Manufacturing

    As an established producer of 1,2,4-Trifluoro-5-Nitrobenzene, we directly supply downstream manufacturing partners with this specialty intermediate for key applications across select fine chemical sectors. Below, we present verified industry use cases, processing conditions, and compliance details observed by our global end users.

    1. Agrochemical Active Ingredient Synthesis

    Leading agrochemical manufacturers rely on 1,2,4-Trifluoro-5-Nitrobenzene as a crucial fluorinated aromatic building block during the synthesis of modern herbicide and fungicide actives. The trifluoro-nitro substitution pattern enables the introduction of complex functionalities via nucleophilic aromatic substitution and subsequent transformations, supporting selective and high-yield production of proprietary crop protection agents. Typical formulations require precise control of input ratios to balance downstream reactivity and environmental compliance.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 for Plant Protection Products (EU)
    • US EPA Pesticide Registration standards
    • China GB/T 1604-2009 (Technical Specifications for Agrochemical Intermediates)
    • ISO 9001:2015 Quality Management System for chemical intermediates

    Typical usage ratio

    • 10-25% by molar ratio in key fluorinated aromatic intermediate stages; exact ratio adjusted by targeted end molecule and synthesis route.

    Downstream process integration

    • Introduced in the aromatic nucleophilic substitution (SNAr) step for preparing trifluoro-aniline or trifluoro-phenol derivatives, which serve as skeletons for final pesticide actives.

    Final product types

    • Patent-protected herbicide actives (e.g., fluazifop-type compounds)
    • Modern trifluoromethyl-containing fungicides
    • Precursor chemicals for insect growth regulators

    2. Pharmaceutical Intermediate Production

    1,2,4-Trifluoro-5-Nitrobenzene plays an integral role in the synthesis of specialty intermediates for pharmaceutical APIs where high fluorination enhances metabolic stability and molecular binding. Medicinal chemistry units typically incorporate this intermediate during multi-step syntheses targeting anti-viral, anti-inflammatory, and oncology-active molecules. Batch records and compliance traceability demand tight specification controls, particularly regarding nitro and fluorine content.

    Industry compliance standards

    • United States Pharmacopeia (USP) for API intermediates
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP (EudraLex Volume 4)
    • Japan PMDA intermediate approval guidelines

    Typical usage ratio

    • 5-20% by weight in multi-stage pharmaceutical intermediate reactions, with precise dosing guided by target scaffold and reaction yield optimization.

    Downstream process integration

    • Supplied as the primary aromatic precursor for nucleophilic replacement, reduction, and cross-coupling steps; essential in forming trifluorinated aromatic ring systems found in final drug candidates.

    Final product types

    • Precursor intermediates for next-generation anti-viral APIs
    • Side-chain building blocks for kinase inhibitors
    • Structural units for fluorinated non-steroidal anti-inflammatory drugs

    3. Specialty Material Monomer Manufacturing

    Engineers in specialty polymer development specify 1,2,4-Trifluoro-5-Nitrobenzene as a strategic starting monomer for creating advanced fluorinated copolymers and polyarylenes, targeting improved chemical resistance and low surface energy. During copolymerization, careful addition of the nitrobenzene derivative allows fine-tuning of mechanical and thermal properties. This material requires strict handling controls throughout the polymer backbone assembly stages, as it impacts final dielectric and surface characteristics.

    Industry compliance standards

    • ASTM D6100 for fluorinated aromatic monomers and resins
    • RoHS Directive (2011/65/EU) for restricted substances in electrical/electronic polymers
    • UL 94 Flammability Standard (for end-use polymers)
    • ISO 14001 Environmental Management for specialty chemicals

    Typical usage ratio

    • 3-12% by monomer mass, calculated relative to other aromatic and fluorinated ring units; ratio varies with desired copolymer performance and regulatory threshold limits.

    Downstream process integration

    • Integrated during controlled step-growth or addition polymerization, participating in co-monomer feed for tuning thermal and dielectric profiles; introduced after initial chain initiation to limit side reactions.

    Final product types

    • Fluorinated specialty copolymers for chemical processing linings
    • Low-NOx emission polymeric insulation in electronics
    • Advanced membrane materials for fuel cells and microfilters

    4. Fine Chemical Cross-Coupling Substrate

    In the fine specialty chemicals sector, 1,2,4-Trifluoro-5-Nitrobenzene is selected as a robust substrate for Suzuki, Buchwald-Hartwig, and Stille cross-coupling reactions. This functionality-rich intermediate streamlines aromatic substitution with organometallic catalysts, yielding high-purity end products for advanced synthesis applications. Production managers control input proportions to maximize product recovery while meeting strict off-spec rejection criteria under regulated batch environments.

    Industry compliance standards

    • REACH Registration for specialty chemicals in the EU
    • cGMP standards if manufacturing pharmaceutical-grade compounds
    • ISO 17025 for QC laboratory testing of specialty intermediates
    • GHS/OSHA chemical handling and process safety

    Typical usage ratio

    • 8-18% by mole, determined by stoichiometric balance of coupling partners; adjusted for scale-up to maintain reaction kinetics and purity.

    Downstream process integration

    • Combines with organometallic reagents under palladium or copper catalysis for direct arylation, amination, or carbonylation; integrated post-activation to prevent hydrolysis losses.

    Final product types

    • Advanced coupling agents for organic synthesis
    • Functionalized aromatic intermediates for further transformation
    • Reference standards for high-resolution analytical use
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    Certification & Compliance
    More Introduction

    1,2,4-Trifluoro-5-Nitrobenzene: Practical Insights from the Production Floor

    Real-World Introduction to 1,2,4-Trifluoro-5-Nitrobenzene

    Bringing 1,2,4-Trifluoro-5-Nitrobenzene (TFNB) to industrial users involves far more than tailoring a list of technical properties. Our daily work connecting raw materials to finished molecules underscores what actually matters—purity, reliability, and downstream performance. Many specialty fluorinated aromatics stand apart from basic commodity chemicals because even trace contaminants risk costly disruptions during scale-up or process change. Our experience with TFNB reflects this: consistent purity and trace moisture control are not byproducts but deliberate outcomes of attentive handling and process design.

    TFNB’s unique reactivity comes from its three strategically placed fluorine atoms and the electron-withdrawing nitro group on the benzene core. We have found that these structural differences, compared to mono- or difluorinated nitrobenzenes, translate into selectivity during nucleophilic aromatic substitution, longer shelf life in storage, and robust performance in downstream synthesis. Customers working up specialty agrochemicals, pharmaceutical intermediates, or high-value materials have seen fewer side products and more reproducible assay results with our TFNB than with less carefully processed material.

    Detailed Look at Specifications and Model Differences

    Each batch of our TFNB reaches the market after analytical assays confirm its purity and identity. Test methods include GC and NMR to ensure confidently reported composition. Water content, a quiet saboteur of many reactions, typically sits below 0.1% in our outgoing lots because we manage drying and sealing processes rigorously. Crystalline TFNB emerges as pale yellow nodes, each batch setting its own signature by crystal habit, but always matching the analytical fingerprint our partners expect.

    Impurity thresholds remain low, helped by our use of high-quality starting materials and careful purification. In cases where customers require enhanced purity for particularly sensitive hydrogenation or coupling steps, we run additional recrystallizations and targeted drying cycles, recording trace impurity levels so there’s never any guessing. Documentation matches every consignment, not as a regulatory formality but as a real tool for troubleshooting and process validation. Over the past decade, we have also supported multiple clients through process validations, where precise impurity profiles smoothed the shift from pilot to full plant scale.

    Comparing TFNB to structurally similar compounds underlines the significance of these controls. With mono- or difluorinated nitrobenzenes, we often see faster rates of hydrolysis or ring opening when moisture creeps above critical levels during transit or storage. Three fluorine atoms confer more stability against side-reactions, so TFNB often proves easier to store and ship in varying climates—as long as the producer seals and packs with future storage in mind. From direct feedback, our partners have used our TFNB in extended shipping and warehousing schedules without observing degradation or darkening, and assays after months often match the original COA with negligible drift. This would not hold for less stable analogs or material with adventure-prone packaging.

    Production Insights and Process Rigor

    Running a fluorination and nitration sequence on benzene derivatives does not always yield consistent outcomes. Fine-tuning reaction conditions rewards the patient operator; uncontrolled temperature spikes or irregular reagent additions cause color bodies and side-products that never really wash or distill away. Our operators monitor not only batch temperatures but reaction kinetics hour by hour; deviations get rerouted or scrapped before reaching post-synthesis steps. Over time, this vigilance reduced batch failures, lowered downstream filtration loads, and made it easier to reclaim solvents with less cross-contamination. These outcomes reflect not just process recipes, but accumulated experience and feedback loops with chemists using TFNB for critical transformations.

    Handling and packaging remain hands-on, as what leaves our site must endure varied warehouse conditions worldwide. We double-seal and inert-pack for shipments over long distances or humid routes, preferring dense, corrosion-resistant drums or lined pails depending on order size. Smaller laboratory-scale quantities receive special blister packaging so that even extended bench storage does not erode purity. Our maintenance schedules for filling lines and packaging systems got overhauled at the request of quality assurance teams because minor lapses triggered a spike in trapped particulates which, in aromatic chemistry, quickly snowballs during scale-up.

    Application Experience from Our Users

    Our direct conversations rarely dwell on generic applications, since every customer seems to ask, “Stronger nucleophilicity or more stable intermediate?” In the pharmaceutical sector, TFNB generally serves as a cornerstone intermediate toward more complex fluorinated benzene derivatives, where subsequent reduction or aromatic substitution benefits from this molecule’s balanced reactivity. In one notable case, a mid-size pharmaceutical group struggled with uneven coupling yields in a multi-step API route. Benchmarking TFNB from several sources, our material ran with higher conversion and fewer downstream purifications due to tighter NMR and GC benchmarks.

    Complex agrochemical synthesis often faces similar headaches: batches falling out of spec due to unforeseen impurities, costly rework, and variable final product quality. Process engineers contacted us for substitution advice—how would swapping from a two-fluorine to a three-fluorine ring affect selectivity and downstream handling? Each deployment taught our company that TFNB’s added fluorine atom lowers the risk of unexpected ring opening in hydrolytic conditions and controls induction periods during nucleophilic substitution, leading to less scattered process data and higher aggregated yields over time. Customers confirmed this by tracking side product rates and stability during stress testing.

    Outside fine chemicals, TFNB found a home in specialty polymers and electronic materials. Several lead customers deploy TFNB as a precursor for specialty monomers that bring targeted dielectric, hydrophobic, or thermal resistance properties to electronic coatings. The nitro group both tempers and enables further modifications; in one process, a major electronics materials partner switched entirely to TFNB for monomer production after pilot trials demonstrated a 20% reduction in fouling and off-gassing. Our internal reviews of complaint data from the previous three years show a clear drop in polymerization issues and fouling rates after this adjustment, showing that the nitro group’s electron-withdrawing effect pays off when paired with rigorous process control.

    Building Trust Through Repeatable Quality

    Drawing a boundary between chemical “quality” and “consistency” often feels artificial from a production perspective. The manufacturer’s side sees consistency as the direct output of persistent process engineering. Purity and particle size only matter if they stand up week after week, batch after batch, under the strains of scaling inventory, tighter regulatory scrutiny, and erratic shipping environments. Regulatory and specification audits happen on our floor as part of daily production runs; our leadership team views customer feedback as technical documentation, not as afterthought.

    From decades of knowledge, we have noticed that even minor shifts—a temperature bump during drying, a filter media switch, a change in drum supplier—cascade down to impurity fingerprints and product color. Documentation, split-batch retention samples, and regular cross-checks between plants and labs keep the system robust. Our clients tell us that the assurance gained from repeatable, historically traceable supply chains supports their own audits and builds stakeholder confidence. This supply traceability matters just as much for laboratory clients as for full-scale plants, given the strict downstream qualifications for pharmaceutical and specialty chemical production.

    Environmental Considerations in Modern Production

    Increasing demand comes with responsibility. Community and regulatory attention toward fluorinated aromatics means proactive adjustments have been a core part of our plant operations. Tight emission controls at each step capture spent reagents and minimize release of active fluorine and nitrogen oxides, while modern solvent management cycles reclaim and purify materials for reuse. On-site wastewater monitoring operates alongside solvent distillation and thermal oxidation, supported by a continuous improvement task force that includes both production engineers and environmental managers.

    The intersection of environmental stewardship and product performance pushes us to source greener nitrobenzene feeds and optimize recrystallization protocols to cut solvent use with every annual review. In the last five years, our solvent recovery investments cut more than half from annual disposal volumes. These changes ripple out: customers in regulated sectors often run their own audits, and a transparent track record on emissions, waste minimization, and energy use builds compliance not only for us, but also for those who depend on TFNB as a feedstock for environmentally scrutinized finished goods.

    Choosing TFNB becomes more than a technical preference; responsible sourcing ripples down to end consumer products, especially amid rising concern around fluorinated chemical fate and persistence. By building audit-ready documentation and championing solvent recovery beyond the plant gate, our team supports manufacturers looking to demonstrate best practices in their own product stewardship.

    Differences and Practical Considerations Compared to Other Products

    TFNB does not operate in a vacuum, so comparisons with similar aromatic nitro or fluorinated compounds are more than academic. Direct communication with end users shows that, compared to analogs like 1,3,5-trifluoro-2-nitrobenzene or difluoronitrobenzenes, TFNB offers a tighter window for nucleophilic aromatic substitutions, improving yields for select reactions with less guesswork about competing pathways. These differences derive directly from electronic and steric effects, which we have tracked through in-plant data and in close technical partnership with downstream chemists. Some customers elect to run parallel pilot tests with competitor materials: in these trials, TFNB’s decreased side product burden gives a measurable advantage in processes sensitive to electron distribution on the aromatic ring.

    Practically, TFNB’s storage stability also stands out. Producers and handlers of other nitrobenzenes report progressive darkening, especially at scale or under elevated temperature. Fielding these complaints reinforced our strategy for packaging and storage improvements: we routinely test retention samples over storage cycles, gathering colorimetry and analytical data to verify headspace gas composition and stability over time. These records offer assurance during long-term storage, especially when products must transit through variable climates before use.

    Finally, TFNB’s inertness under extended shipping conditions means fewer surprises for receiving labs. Feedback from new customers, especially those switching from smaller suppliers or lab-scale synthesis, points to a reduced incident rate for “off-spec” barrels and the need for expensive re-qualification. The differentiation rests not on a marketing slogan, but on the quality culture and process adjustments honed through direct engagement with every application sector.

    Supporting Long-Term Partnerships

    From the daily reality of bringing TFNB to global users, it’s clear that working hand-in-hand with process chemists, QA specialists, and supply chain managers strengthens every batch. We routinely gather feedback from every step of the customer journey—shipment arrival, bench testing, full-scale reaction runs, and even process audits—incorporating this knowledge into regular operator training, production scheduling, and material handling upgrades. Customers have asked for reprocessing, tighter specifications for problematic intermediates, alternate packing sizes, or enhanced documentation. Each request sharpens our understanding; process improvements cascade throughout our facility, cutting costs on one product line while raising consistency or safety elsewhere.

    As major chemical regulations evolve and international controls on nitro- and fluorinated substances tighten, only a manufacturer who sees compliance as a production goal (not a post-hoc headache) can maintain customer confidence. On our shop floor, these priorities guide every operational tweak, every quality check, and every batch sign-off. By rooting our TFNB production in data, feedback, and a team ethos that values transparent improvement, we offer more than a molecule; we build resilience and trust into every shipment and product integration.

    Our experience reinforces this: consistency does not come from a one-size-fits-all approach or from certificate-heavy paperwork, but from continued learning, process investment, and direct communication with industrial end users. Every new application for TFNB, from complex chemical syntheses to advanced material discovery, draws benefit from a production system designed to anticipate challenges, not just react to them.

    Final Thoughts from Our Manufacturing Perspective

    Supplying TFNB at scale challenges every part of our operation to meet real-world criteria—reliably pure, analytically verified, and able to withstand the unpredictable pace and stresses of modern industry. We built our current TFNB production on lessons learned from direct technical support and process audits, not just from theoretical standards. Our facility stands ready to adapt—whether that means supporting special purity runs, custom documentation, or unique packaging formats. Years of collaborative work with industrial partners prove that TFNB’s core value stems not only from its chemical structure, but from the knowledge and technical rigor invested by its makers. Connecting supply with need, solving unique process problems, and supporting evolving industry requirements, we build real solutions one batch at a time.