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2,4-Difluoronitrobenzene

    • Product Name 2,4-Difluoronitrobenzene
    • Alias 1,3-Difluoro-2-nitrobenzene
    • Einecs 209-846-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    435643

    Chemicalname 2,4-Difluoronitrobenzene
    Casnumber 446-35-5
    Molecularformula C6H3F2NO2
    Molecularweight 159.09
    Appearance Pale yellow liquid
    Boilingpoint 177-179°C
    Density 1.405 g/cm3
    Refractiveindex 1.535
    Flashpoint 69°C
    Solubility Slightly soluble in water; soluble in organic solvents
    Synonyms 2,4-Difluoro-1-nitrobenzene
    Smiles c1c(cc(cc1F)F)[N+](=O)[O-]
    Pubchemcid 98343

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

    Packing & Storage
    Packing Brown glass bottle containing 100 grams of 2,4-Difluoronitrobenzene, tightly sealed, with hazard labels and product information affixed.
    Shipping 2,4-Difluoronitrobenzene is shipped in tightly sealed containers, typically glass or compatible plastic, clearly labeled with hazard information. It is transported as a hazardous material due to its toxic and potentially combustible nature. Proper cushioning and secondary containment are used to prevent leaks, in compliance with local and international chemical transport regulations.
    Storage 2,4-Difluoronitrobenzene should be stored in a tightly sealed container, placed in a cool, dry, and well-ventilated area away from direct sunlight, heat sources, and incompatible materials such as strong acids, bases, and reducing agents. Avoid moisture contact. Ensure proper labeling and keep away from oxidizers. Use appropriate precautions and PPE when handling or transferring the chemical.
    Application of 2,4-Difluoronitrobenzene

    Applications of 2,4-Difluoronitrobenzene in Industrial Manufacturing

    2,4-Difluoronitrobenzene is an essential intermediate used in the fine chemicals sector, supporting complex chemical syntheses across agrochemical, pharmaceutical, and specialty chemical industries. Our manufacturing expertise ensures consistent supply, stringent quality, and traceability for downstream integration into demanding industrial processes.

    1. Pharmaceutical Intermediate for Fluorinated Active Compounds

    Leading pharmaceutical manufacturers utilize this raw material as a key fluorinated building block in the synthesis of advanced APIs, particularly for second-generation fluoroquinolone antimicrobials and other specialty active pharmaceutical ingredients. The compound’s dual fluorine atoms and nitro functionality make it indispensable for introducing defined fluoro groups onto aromatic rings during complex, multi-step organic syntheses, particularly via nucleophilic aromatic substitution routes. Its integration requires close attention to quality standards and impurity profiles to satisfy regulatory submissions and downstream GMP manufacturing requirements.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, JP Monographs (as applicable for target APIs)
    • 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • REACH Registration for Supply Chain Traceability

    Typical usage ratio

    • Commonly 0.2–1.0 molar equivalents relative to the backbone aromatic substrate; exact proportion varies per synthesis and target molecule, adjusted based on required fluorination pattern and batch yield optimization.

    Downstream process integration

    • Introduced during the early or mid-stage aromatic substitution process (typically nucleophilic aromatic substitution or reduction steps), followed by hydrolysis, reduction, or further functionalization, under controlled reaction conditions to maintain product identity and impurity levels for subsequent API synthesis.

    Final product types

    • Second-generation fluoroquinolone antimicrobial agents (e.g., levofloxacin intermediates)
    • Specialty fluorinated heterocyclic drugs
    • Selected anti-cancer and anti-viral small molecule APIs

    2. Agrochemical Intermediate for Fluorinated Herbicide Manufacturing

    Major agrochemical producers employ this material for the preparation of advanced herbicidal actives, leveraging the difluoroaromatic structure to enhance metabolic stability and bioactivity in crop protection agents. Its precise handling ensures reliable production of high-purity intermediates required for large-scale synthesis of fluorinated phenoxy and pyridine-based herbicides, as demanded by current environmental and efficacy standards.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • ISO 9001:2015 Quality Management in Agrochemical Production
    • OECD Guidelines for the Testing of Chemicals
    • REACH and EPA TSCA Substance Compliance

    Typical usage ratio

    • Usually 0.5–1.5 molar equivalents per batch, relative to the primary aromatic precursor, fine-tuned based on the route toward target herbicide and scale of the manufacturing campaign.

    Downstream process integration

    • Fed into the nucleophilic aromatic substitution or reduction stage to introduce difluoro substitution, typically followed by etherification or amination steps during technical-grade herbicide synthesis, prior to formulation into finished crop protection products.

    Final product types

    • Fluorinated phenoxy herbicides and growth regulators
    • Pyridine-based selective herbicides
    • Intermediates for broadleaf weed control actives

    3. Specialty Chemical Precursor in Liquid Crystal Material Synthesis

    The electronics and display materials sector consumes this compound as a high-value precursor in the creation of advanced aromatic liquid crystal (LC) monomers. The unique substitution pattern provides critical thermal and dielectric properties needed for next-generation LCD and OLED display formulations, where molecular purity and consistent difluorination directly influence end-user device performance and lifespan.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for Substances in Electronic Components
    • IEC 62474 Material Declaration for Electrical/Electronic Industry
    • ISO 9001:2015 Certified QC for Display Material Manufacturers
    • JIS Standards for LC Material Purity (Japan Electronics Information Technology Industries Association)

    Typical usage ratio

    • Ranging from 5-15% w/w in liquid crystal monomer precursor synthesis, depending on the targeted mesogen’s structural rigidity and fluorine substitution requirements; precise formulation determined by LC temperature ranges and viscosity targets.

    Downstream process integration

    • Reacted with phenolic or biphenyl reagents through nucleophilic aromatic substitution to introduce the difluorinated motif, carried forward in subsequent esterification or etherification steps before final LC compounding and purification for display use.

    Final product types

    • High-performance LCD and OLED liquid crystal materials
    • Specialty mesogenic monomers and oligomers
    • Advanced dielectric films for flexible substrates

    4. Intermediate for Synthesis of Fluorinated Polymeric Coatings

    Producers of advanced polymer coatings use this aromatic to tailor-make fluorinated building blocks capable of imparting water, oil, and solvent repellency to surface finishes. The introduction of multiple fluorines through controlled aromatic substitution leads to end polymers with superior durability and resistance profiles required for automotive, electronic, and aerospace coatings, meeting demanding end-user and environmental specifications.

    Industry compliance standards

    • ISO 12944-6:2018 (Performance Requirements for Protective Paint Systems)
    • ASTM D5201: Chemical Resistance of Film Coatings
    • REACH Compliance for Industrial Polymers
    • Automotive OEM Approved Coatings Specifications (e.g., GM, Ford, Daimler standards)

    Typical usage ratio

    • Generally 1–5% w/w of resin precursor composition, adjusted according to targeted fluorination level, viscosity, and application method (spray, dip, flow coat).

    Downstream process integration

    • Incorporated via aromatic substitution or reduction steps in polymer precursor synthesis, followed by co-polymerization or crosslinking with aliphatic or heteroaromatic monomers, then compounded into masterbatches for subsequent coating application.

    Final product types

    • Water- and oil-repellent industrial coatings
    • Anti-corrosive layers for electronic casings
    • Automotive and aerospace exterior paint systems
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    Certification & Compliance
    More Introduction

    2,4-Difluoronitrobenzene: Careful Chemistry, Lasting Assurance

    An Honest Introduction from Our Factory Floor

    Each bottle and batch of 2,4-difluoronitrobenzene leaving our workshop carries more than chemical bonds—it carries trust, experience, and hard-earned consistency. Standing over the reactor, we watch two fluorines change a whole line of chemistry with just the right temperature and pressure. We pay attention to purity not through guesswork but through practiced eyes and rigorous testing. To us, the product isn’t simply a label or inventory sheet—it’s a direct extension of our years spent handling aggressive reagents and troubleshooting every stubborn impurity.

    The journey of 2,4-difluoronitrobenzene starts with precise raw material selection. We don’t simply source what’s available—our fluoroaromatics demand disciplined logistics. Every batch brings slight changes in moisture, particle size, or impurity profile, and we work through each communication step to secure reliability. There’s no shortcut around feedstock verification, and even a tiny fluctuation in physical properties shows up in the next step of synthesis. This vigilance matters because trace contaminants can halt a downstream reaction, trigger unexpected color changes, or throw off a separation entirely.

    Specifications That Matter in Daily Production

    We listen to technical teams and labs who actually use these intermediates to build pharmaceuticals, crop-protection chemicals, and specialty materials. For most end uses, it’s not just concentration or appearance, but the full impurity fingerprint that decides a process route’s yield and safety. So we sharpen our methods to achieve the lowest possible organic and inorganic by-product content, monitor halide levels, and track residual acidity with careful GC and NMR analysis. The boiling point, usually around 225 degrees Celsius under ambient pressure, emerges as a direct reflection of this purity—and we watch for any drift, knowing it signals an upstream issue.

    Our 2,4-difluoronitrobenzene typically falls within a purity range exceeding 99 percent, according to GC area normalization—though for client-specific syntheses, tighter controls may apply. Water content rarely exceeds a tenth of a percent, since excess moisture can sabotage subsequent substitution or coupling reactions. Even seemingly minor batch-to-batch inconsistencies in color or odor prompt a full investigation, as these often hint at side products that, in quantity, can actually threaten plant operators or equipment over time. This is how quality stops being theoretical and starts being lived reality.

    Real-World Uses: Successes and Constant Challenges

    For over a decade, our main users of 2,4-difluoronitrobenzene have been research and development labs across pharmaceutical and agrochemical sectors. The molecule’s electron-deficient aromatic ring, with nitro at the para position relative to a fluorine, brings unusual reactivity to nucleophilic aromatic substitution (SNAr). That means our product frequently starts life as a building block for fluorinated arenes, aryl amines, or condensed ring systems. Even minor contamination—especially from unreacted starting material or isomeric fluoronitrobenzenes—causes havoc in multi-step syntheses.

    One innovation we’ve witnessed up close is using 2,4-difluoronitrobenzene in late-stage fluorination of medicinal scaffolds. Because the electronic effects of two fluorines and a nitro group let chemists perform precise substitutions, it opens up access to advanced molecules that would be impossible with many other arene templates. We often talk to scientists grappling with delicate catalysts or bio-relevant functional group installations. Here, they insist on a product that behaves predictably across larger batches. This is not about reputation or marketing copy—it’s about real material costs and the risk of project failure if a single shipment behaves inconsistently.

    Environmental and handling aspects matter too. 2,4-difluoronitrobenzene is volatile enough that minor leaks turn into occupational exposure incidents quicker than with heavier intermediates. We invest in sealed, lined drums and repeated leak testing not for regulatory box-ticking but because we have seen—directly—how quickly a minor spill can disrupt an entire shift. The explosion hazard lies not only in production but in careless decanting in poorly ventilated rooms. That’s why our packaging line doubles as a safety check, not just a logistical step.

    Standing Apart from Other Nitrobenzenes and Isomers

    Many newcomers assume fluoronitrobenzene products all behave alike, that one is simply a stronger version of another. In fact, 2,4-difluoronitrobenzene responds differently than the 2,6- or 3,4- isomers even under identical conditions. We have learned—often by troubleshooting customer complaints—that substitution patterns direct reactivity, influence environmental persistence, and change physical handling requirements.

    Take the common 4-fluoronitrobenzene. It substitutes much more sluggishly at positions other than the para, meaning that nucleophilic aromatic substitution proceeds unpredictably on larger scales. You may find a single degree of difference in reactivity makes or breaks an entire reaction scheme. Or compare to 2,6-difluoronitrobenzene: the ortho arrangement means steric hindrance climbs, and some substituents simply refuse to displace at room temperature—costing hours in added heating and increased risk of off-gassing.

    The practical impact extends beyond chemistry. 2,4-difluoronitrobenzene tolerates longer storage when water vapor is excluded, while some closely related compounds pick up color or break down within weeks if not kept under strict temperature and humidity control. We have replaced other isomers in a customer’s line only after lab trials confirmed that our 2,4- product solved chronic yield reduction and filtration headaches. These are not theoretical distinctions—they show up in utility bills, maintenance reports, rejected lots, and ultimately in the life of the scientist up at midnight, rerunning a reaction.

    Quality Is Not an Accident, Sustainability Isn’t a Slogan

    We earned our confidence through years spent tweaking each process variable, sometimes for weeks, just to wring out an extra fraction of a percent in purity or switch a hazardous step for a greener option. Our nitration stage relies on precision-controlled acid ratios to limit dinitro by-products, and we push continuous-flow systems where possible to cut batch instability. Workers train on every possible malfunction—fluctuations in agitation or raw material sourcing lead to batches getting flagged for reprocessing, no matter the added cost. Our approach relies not on chasing certifications, but on responding directly to what practicing chemists tell us the product must accomplish.

    Waste management challenges never remain simply waste management—treatment or recycling fluids and solvents runs up against the reality of evolving regulations. There’s a push—rightly so—for lower cumulative exposure and less cumulative waste per kilogram of product. The pushback from a factory comes when a so-called improvement changes the way our molecules behave, affects shelf life, or raises barriers for handling and transport. Every change—be it in raw material partner, process solvent, or finishing equipment—takes weeks of validation runs, not days, to verify that user tolerance stays protected. We advocate data, not guesswork, in making these calls.

    Real-World Complications and Everyday Solutions

    We have watched price spikes on fluoroaromatic precursors ripple through the entire specialty chemicals sector, especially after major plant shutdowns in Asia. The wave does not stop at the trader’s desk—it moves through receipts, inventories, and ultimately impacts who receives product when. Our direct relationships with fluorochemical suppliers let us smooth out many of these bumps, but crisis periods always test contingency planning. Once, during a winter power shortage, we had to adjust schedules and operate through scheduled blackouts, protecting both quality and delivery promises at no small expense.

    Shipping hazardous, high-purity nitrobenzene derivatives isn’t paperwork alone. Many times we have fielded urgent requests to adjust packing types, drum linings, or label languages, because shipments cross borders, climates, and government audits. These aren’t minor logistics—they’re relationship-defining interactions. Occasionally, customs will hold drums pending further analysis, and in those times, rapid back-and-forth between our QA lab and official inspectors keeps everyone on track. From the plant perspective, cooperation means prompt troubleshooting, not finger-pointing or delay.

    Plant engineers and chemists often seek our support troubleshooting their own bottlenecks—off-color product, incomplete conversions, or trace carry-over from previous product lines. Whenever a customer returns a sample with a hint of decomposition or unexplained residue, we not only supply replacement but examine that off-spec material in-house. Sometimes these reports reveal gaps in our own storage and shipment procedures. More commonly though, they push us to provide practical guidance: protective atmosphere storage, temperature cutoffs for scale-up, or time limits for exposure to light. This feedback loop saves real losses and keeps projects moving.

    Looking Forward—Meeting the Needs of Tomorrow’s Chemistry

    Demand for high-quality fluorinated nitrobenzenes continues to grow, especially from innovators in new material sciences and active pharmaceutical ingredients. New reaction platforms, such as photoredox catalysis or selective C–F activation, require both ultra-pure feedstocks and absolute consistency from drum to drum. We don’t see 2,4-difluoronitrobenzene as a commodity—it’s a core enabler for next-generation molecules where structure–activity relationships cannot compromise. Research teams working on bioactive scaffolds or advanced agrochemicals increasingly look to us not just for standard supply, but for collaborative problem-solving—helping bridge small-lab discovery to pilot lines and beyond.

    We have responded by investing in expanded analytical capabilities, so we trace minute levels of side products and guarantee tighter impurity specs. Equipment upgrades aren’t made for show—they mean more reliable temperature control, sharper separations, and faster cycle times. These investments grew from frank factory-floor discussions about where things go wrong in real-world use. As demand grows and regulations tighten, we continue to close the loop with actual users, whether that’s fine-tuning moisture limits, adapting containers for bulk scale, or integrating green chemistry steps.

    One persistent challenge: as sustainable chemistry goals advance, we keep pressure on ourselves to innovate greener solvent systems and reduce process waste, while holding batch reproducibility steady. Replacing legacy solvents or introducing energy-efficient distillations only counts if it delivers safer, cleaner, more reliable product to the people relying on it down the chain. So our research teams share findings with partnership labs, inviting independent scrutiny. When a supply chain glitch, emergent impurity, or new regulatory hurdle appears, we commit early and openly to finding solutions that benefit everyone—end-user, regulator, and factory alike.

    Why Our Approach Delivers Confidence

    At every step, our philosophy centers on responsibility—a willingness to learn from daily challenges, not just celebrate successes. We see how each small improvement in 2,4-difluoronitrobenzene quality pays off in fewer reworked lots, lower waste, and greater confidence for all hands on the line. The compound itself is not an end, but a vital stage in complex syntheses, where failure often means costly delays, scrapped runs, or exposures that put people at risk.

    We treat each shipment as if it could trigger a high-value pharma launch or a new diagnostic advance, not simply as an invoice. Our support stretches from synthesis advice to rapid troubleshooting—a dialogue built on mutual respect between our plant chemists and the research community worldwide. Through honest feedback, constant evaluation, and a dedication to both environmental and operational responsibility, we keep improving what we send out. By standing in continual dialogue with customers and partners, we ensure every drum of 2,4-difluoronitrobenzene reinforces trust in every new application it touches.