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3,5-Difluoronitrobenzene

    • Product Name 3,5-Difluoronitrobenzene
    • Alias 1,3-Difluoro-5-nitrobenzene
    • Einecs 221-716-6
    • 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
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    Specifications

    HS Code

    813750

    Iupac Name 3,5-Difluoro-1-nitrobenzene
    Molecular Formula C6H3F2NO2
    Molecular Weight 159.09 g/mol
    Cas Number 323-74-6
    Appearance Pale yellow liquid
    Melting Point −12 °C
    Boiling Point 204 °C
    Density 1.44 g/cm3
    Refractive Index 1.546
    Solubility In Water Slightly soluble
    Flash Point 84 °C
    Smiles C1=C(C=C(C=C1F)[N+](=O)[O-])F
    Pubchem Cid 211574

    As an accredited 3,5-Difluoronitrobenzene 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 3,5-Difluoronitrobenzene, labeled with hazard symbols, product details, and safety instructions.
    Shipping 3,5-Difluoronitrobenzene is shipped as a hazardous chemical, typically in tightly sealed, chemically resistant containers to avoid leaks. Labeling in compliance with international transport regulations (such as UN Number 1663) is required. It should be kept away from heat, sparks, and incompatible substances, with appropriate safety and handling documentation provided.
    Storage 3,5-Difluoronitrobenzene should be stored in a tightly sealed container, kept in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers or reducing agents. Protect the chemical from light and moisture. Ensure appropriate labeling and access only to trained personnel. Use secondary containment to prevent accidental release or environmental contamination.
    Application of 3,5-Difluoronitrobenzene

    Applications of 3,5-Difluoronitrobenzene in Industrial Manufacturing

    3,5-Difluoronitrobenzene serves as a precision fluorinated intermediate for synthesis-driven sectors where stringent performance and purity are vital. Its electrophilic aromatic profile enables targeted transformations supporting multiple global industries, notably in agrochemical actives, pharmaceutical building blocks, and advanced materials. Below are sector-specific applications, focusing on real downstream activities, technical integration, and the practical framework of our manufacturing partners.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical companies employ this intermediate to develop fluorinated herbicide and fungicide actives. Its specific di-fluoro, nitro-substitution promotes desired chemical reactivity for constructing triazole and phenoxy herbicide moieties. Manufacturers prioritizing retention of functional groups for later-stage coupling favor use at early synthesis stages to ensure precise molecular architecture, facilitating scalable and traceable ingredient registration under strict jurisdictional oversight.

    Industry compliance standards

    • ISO 9001:2015 quality management system
    • European Union Regulation (EC) No 1107/2009 for plant protection product active substances
    • Japanese Agricultural Standards (JAS) for agrochemical raw materials
    • US EPA Good Laboratory Practice Standards (40 CFR Part 160)

    Typical usage ratio

    • Intermediate charge: 0.8–1.3 molar equivalents relative to core synthesis flow; precise ratio tailored by downstream aromatic substitution requirements and conversion yields

    Downstream process integration

    • Introduced during initial or early intermediate condensation and halogen-exchange steps
    • Undergoes nucleophilic aromatic substitution then reduction/transformation before later-stage agro active assembly
    • Material traceability maintained across batch-to-batch scaling in reaction vessels 500 L and above

    Final product types

    • Triazole fungicide AI (e.g., difenoconazole derivatives)
    • Fluorinated phenoxy herbicides
    • Advanced pre-emergent weed control actives for global registrants

    2. Pharmaceutical Intermediate for API Synthesis

    Global pharmaceutical manufacturers rely on its highly controlled reactivity to install essential fluoroarene fragments into next-generation active pharmaceutical ingredient (API) APIs, especially within the cardiovascular and CNS (central nervous system) therapy pipelines. The intermediate supports patent-protected synthesis routes, often entering as an electrophilic construct for catalyst-driven cross-couplings, with every lot traceable under cGMP and pharmacopeia-driven QA.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210, 211 for pharmaceutical manufacturing
    • European Pharmacopoeia monographs (Ph. Eur.)
    • Chinese Pharmacopoeia (ChP) standards for raw API intermediates

    Typical usage ratio

    • Process integration at 0.9–1.2 molar equivalents per API synthesis batch; adjusted based on target molecule and yield optimization data from process development sites

    Downstream process integration

    • Fed into Suzuki-Miyaura, Buchwald-Hartwig, or nucleophilic aromatic substitution during early or mid-stage route design
    • Purified via column methods and in-line crystallization ahead of chiral or selective hydrogenation stages
    • Stringent in-process control (IPC) protocols ensure QP-release eligibility

    Final product types

    • Fluorinated CNS API intermediates (e.g., in selective serotonin reuptake inhibitors)
    • Cardiovascular API scaffolds
    • Custom pharmaceutical fine intermediates for contract API manufacturing organizations (CMOs)

    3. Electronic Materials and Photoresist Precursors

    Electronics chemical manufacturers use this compound as an aryl-fluorine donor to tailor dielectric properties and heat resistance in specialized electronic material resins and advanced photoresist systems. Its high-purity structure helps control contamination levels critical in submicron-lithography and FPC (flexible printed circuit) applications, with compliance and QC maintained per microelectronics standards and integrated production audit requirements.

    Industry compliance standards

    • SEMI S2/S8 Environmental, Health, and Safety Guidelines for Semiconductor Manufacturing
    • IEC 61249 series for base materials in printed circuit boards
    • RoHS Directive (2011/65/EU) for hazardous substance restriction
    • IATF 16949:2016 for automotive electronics materials

    Typical usage ratio

    • Feed concentration: 2–12% by weight in aryl-fluorine modified oligomer blends; adjusted according to target resist performance and dielectric requirements

    Downstream process integration

    • Reactive incorporation during synthesis of polyarylene ether resins or as a functional group introducer in resist polymerization reactors
    • Quality-controlled addition monitored by HPLC and GC-MS for low contaminants
    • Batch documentation meets device-level traceability and customer auditability policies

    Final product types

    • High-temperature photoresist precursors for semiconductor lithography
    • Specialty fluorinated binder resins for FPC substrates
    • PCB material intermediates for high-speed communications

    4. Fine Chemical Synthesis: Crop Protection Intermediates

    Companies in the fine chemicals sector introduce this fluorinated nitroarene into custom synthesis routes for high-value crop protection intermediates, focusing on selective transformations such as reduction, halogenation, or coupling to confer unique bioactivity features. Such production is regulated at every stage: from QA-lot tracking, raw material audits to GRAS-reporting, as applicable in non-food-use applications or industrial biocide manufacturing.

    Industry compliance standards

    • REACH (EC) No 1907/2006 for chemical registration in the European Union
    • ISO 14001 Environmental Management System
    • Chemical Facility Anti-Terrorism Standards (CFATS, US)
    • Third-party traceability audits by downstream agricultural supply chain partners

    Typical usage ratio

    • Used between 0.5–2.0 molar equivalents per synthesis campaign, based on downstream reactivity and desired selectivity for intermediate modifications

    Downstream process integration

    • Charged during nitro-group reduction, fluorine retention, or functional group exchanges in jacketed reactors (50 L to 1000 L scale)
    • Integration closely tracked by process analytical technology (PAT) for impurity control and yield maximization
    • Standard operating procedures logged for every synthesis step per contract manufacturing agreement

    Final product types

    • Pyridyl and phenyl-derived intermediates for custom crop protection agents
    • Building blocks for industrial biocides not regulated as pesticides
    • Halogenated intermediates for next-generation fungicidal blends

    5. Specialty Chemical Intermediates: Performance Polymer Precursors

    Producers of advanced performance polymers utilize this nitroarene in aromatic substitution or reduction steps to generate functionalized monomers, especially for polymers demanding defined fluorine content to impart low surface energy or chemical resistance. The integration process supports tailored resin synthesis with careful control of side reactions, and all activity is monitored in compliance with customer-dictated release specifications and relevant material safety verification.

    Industry compliance standards

    • ISO 9001 and ISO 14001 for quality and environment
    • UL 94 for polymer flammability classification
    • ASTM D2863 for oxygen index of polymers
    • Customer-specific technical approval cycles per application segment, e.g., electrical or medical devices

    Typical usage ratio

    • Charged at 1–4% by monomer mass, tuned for targeted functional group density and final polymer specifications

    Downstream process integration

    • Enters aromatic nucleophilic substitution (ArSN) or reduction stages in specialty monomer preparation
    • Closely monitored via NMR and IR to verify complete transformation prior to resin polymerization
    • Production lots aligned to batch release and customer validation protocols

    Final product types

    • Fluorinated specialty polymers for wire coating and sealing materials
    • Chemical-resistant adhesives and joint fillers
    • Block copolymer intermediates for medical and laboratory device applications
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    Certification & Compliance
    More Introduction

    3,5-Difluoronitrobenzene: Purpose-Built for Exacting Chemical Synthesis

    Introduction to a Distinctive Intermediate

    At our manufacturing facility, 3,5-Difluoronitrobenzene stands out among our aromatic nitro compounds. Years spent fine-tuning the process have ensured it offers the high purity and consistency that downstream syntheses demand. Each batch is produced with careful attention to reagent choice, solvent control, and raw material qualification, which has become ever more important as customer specifications tighten year after year.

    This compound, known simply as 3,5-DFNB among our team, shifts the discussion beyond standard nitrobenzenes such as monofluoronitrobenzenes and their common isomers. Chemical manufacturing, at its core, involves picking the right tool for the right job; in the toolbox of fluorinated aromatics, 3,5-DFNB fills gaps that single-fluorine derivatives or non-fluorinated nitrobenzenes leave open.

    Crafting High-Quality 3,5-Difluoronitrobenzene

    Our experienced operators observe the process as if it were second nature, monitoring color and reaction temperature, aware that slight deviations from the ideal can translate into unwanted byproducts or tricky purification problems. We select starting fluoronitrobenzenes with a focus on trace impurity levels since even minor contaminants can complicate hydrogenation steps in later syntheses. Once the reaction winds down, we employ fractional distillation and analytical verification, relying on gas chromatography results to ensure that what we deliver conforms to specification.

    Raw material fluctuations, operational downtimes, and logistical distractions regularly test the system. Strong relationships with suppliers of fluorinating agents and nitro precursors help neutralize these challenges. Staff expertise—gained from managing hundreds of batches for agrochemical and pharmaceutical clients—keeps our quality bar high, from kilogram pilot runs to multi-ton shipments.

    Specifications Forged by Industry Demands

    We do not regard specifications as arbitrary paperwork or obstacles to overcome. The industry mindset recognizes how trace water or color impurities, even those undetectable to the eye, alter downstream chemistry. Reactivity profiles for selective reduction, nucleophilic aromatic substitution, and cross-coupling each depend on fine-tuned aromatic substitution patterns. Fluorine atom placement at the 3 and 5 positions, for example, is critical—synthesizing 3,4- or 2,5-difluoronitrobenzene would never support the same target molecules.

    In all steps leading to the final product, we track purity (GC area percent frequently at or above 99.5%), moisture (Karl Fischer titration to well below the half-percent range), and color (APHA or Hazen scale). Consistency matters most for repeat customers who integrate our product into well-established process routes. Their operations do not pause for procedural abstraction—they require clear, reliable consistency.

    Where This Compound Matters

    3,5-DFNB does not serve every chemical process. Its best-known roles appear in the synthesis of specialty agrochemicals and pharmaceutical intermediates, especially targets that demand electron-withdrawing, ortho-para directing effects in further aromatic substitutions. In contrast to mono-fluorinated nitrobenzenes, dual fluorine occupancy at the 3 and 5 positions changes reactivity—offering both increased selectivity and altered solubility for certain transformations.

    Clients in the crop protection sector ask for 3,5-difluoronitrobenzene for specific active ingredient cores, often because single-fluorine isomers generate too many side products. A practical example involves the preparation of 3,5-difluoroaniline by catalytic hydrogenation: the dual fluorine arrangement influences reduction rates and product profiles, giving process advantages not achievable with other isomers or single-fluorine compounds.

    Medicinal chemistry teams regularly lean on this compound to build structures where electron-deficient aromatic rings are key for biological activity or for modulating metabolic stability. A common challenge pharmaceutical chemists face: introducing diversity late in the sequence. Here, 3,5-DFNB acts as a versatile starting block, the nitro group offering a reliable handle for further transformation.

    Experience from Decades of Supply

    Unlike commodity chemical traders, we see the reality of the manufacturing floor every day. From time to time, pressure variations alter reaction exotherms or solvent recovery throws up issues when purification columns start clogging. Our technical teams document each deviation, sharing these learnings across our network. Last winter, a solvent supply interruption forced us to trial an alternative. The output temporarily dipped, but process improvements halved our previous batch-cycle time by spring.

    Our customers value direct access to the chemists running the reactors and the analysts confirming product quality. We often guide clients through tailored reactivity or isolation steps, drawing on our hands-on understanding. We learn from customers, too—their feedback alters in-plant procedures, sometimes even tuning our process to match downstream hydrogenation catalyst requirements or to minimize halogenated impurity carryover.

    Changes in regulation or end-use application influence our handling and shipping protocols. Stricter environmental requirements have pushed us to modify solvent recovery and waste treatment, reducing both the environmental footprint and operating costs.

    Comparing to Alternative Products

    The chemical marketplace offers a host of fluorinated aromatics and nitro arenes—no single compound can fit every purpose. For basic aromatic substitution, single-position nitrofluorobenzenes may suffice, providing lower cost but less selectivity in certain reactions. As process chemists ourselves, we've seen many formulations where the difference between a single and double fluorine atom dictates overall process economics and product purity.

    Other difluoronitrobenzenes, such as the 2,4- or 2,5-isomers, may be less expensive but do not share the unique reactivity profile needed for selective halogen displacement or controlled reduction. One customer who switched from 2,5- to 3,5-DFNB nearly doubled their para-selectivity in a downstream nucleophilic aromatic substitution, reducing byproduct removal steps and overall waste. Success in such cases does not come from luck, but from molecular insight and the ability to adapt manufacturing operations for more precise control.

    Some may look to non-fluorinated nitrobenzenes or even partially reduced compounds to economize. Yet in real-world production, these substitutions rarely work out. The downstream impact—lower isolated yields, complicated chromatography, or the need for more aggressive reaction conditions—often cancels out the anticipated savings. In comparison, the design of 3,5-difluoronitrobenzene, crafted through robust, reproducible methods, consistently serves teams with high-precision demands.

    Strategy for Problem-Solving in Supply and Application

    Manufacturing is a discipline where troubleshooting never really ends. Should a client struggle with solubility or isolation problems during product development, our technical crew steps in to suggest alternative crystallization solvents or purification aids based on first-hand experience. When minor supply chain setbacks occur, our logistics teams reroute production or, if necessary, adjust packing sizes for easier customs processing.

    Some geographic regions raise concerns about fluorinated intermediates due to local handling regulations. By investing in documentation and building relationships with logistics partners, we help anticipate regulatory shifts, ensuring the uninterrupted flow of 3,5-difluoronitrobenzene to our customers’ plants.

    On the application side, feedback matters. Sometimes we hear unexpected results: yields that stray from literature values, unexpected spots in chromatography, or small shifts in melting range. Direct communication between our formulation chemists and the client’s technical experts often reveals practical workarounds—adjusting pH, refining reaction times, or introducing an in-situ base. All parties gain long-term advantages from sharing these field-level technical details.

    Why Process Reliability Matters at Scale

    For many research outfits, small-scale batches mask inconsistencies that only scale up with industrial production. Impurities below 1% often escape notice during benchtop work, yet in a metric-ton shipment, a fraction of a percent can translate into kilograms of intractable side product. Our plant teams understand this risk, which is why tracking each step—charging, mixing, cooling, purification—remains a daily habit.

    Batch documentation, in-line analytics, and continuous skill upgrading allow us to match new market specifications without costly revalidation. Several years ago, a change in local regulations gave us an abrupt deadline to alter solvent recovery practices for this product. By accelerating investment in off-gas scrubbing and automated process monitoring, we reduced turnaround time and achieved higher recovery without increasing contamination risk—efficiencies that keep our costs competitive and benefit the downstream users.

    Perspectives from the Manufacturing Floor

    Operators and chemists who walk the line every day see firsthand how small details determine success or failure. The daily rhythm includes checking reflux rates, logging GC results, and catching the off-odor that signals a potential leak or impurity. In summer, cooling loads may fluctuate, calling for a creative approach to solvent recycling or heat exchange. Each operator knows that what might be trivial in research, such as a 5% reduction in reagent excess, means a substantial saving and fewer environmental headaches at plant scale.

    Not every manufacturing challenge stems from chemistry: mechanical integrity, batch record-keeping, and regular training play their roles. The stability of 3,5-difluoronitrobenzene during storage under different climates, for instance, depends as much on packaging as process consistency. As direct manufacturers, we set aside part of each batch to test for changes in purity, color, or reactivity after prolonged storage, feeding back results that guide long-term process improvements.

    Traceability and Customer Collaboration

    No matter how confident we are about in-plant procedures, product recalls and root-cause analyses sometimes enter the picture. From batch barcode tracking to supply chain audits, traceability stays high on our priority list. Technical data packages go out not just as legal compliance but as shared knowledge customers depend on during scale-up or regulatory filing.

    Collaboration does not end after delivery. Teams reach out for troubleshooting, suggestions on solvents, or input on new reactions. Those companies who share even their “failed” projects often end up innovating their next-generation routes, sometimes uncovering new uses for 3,5-difluoronitrobenzene itself. We regard every customer inquiry as a route to incremental advance in both their manufacturing and ours.

    Sustaining Performance for Critical Applications

    Demand for specialty fluorinated aromatics like 3,5-DFNB keeps trending up across pharmaceuticals, crop protection, and electronics. Each of these sectors needs reliable supply chains, clear documentation, and fast turnaround for analytical results. The continuum between bench, pilot, and commercial production rewards those who master both flexibility and the repeatable protocols that real-world scale-up requires.

    Our operators and chemists see the trade-offs: adding a filtration step lengthens processing time but removes a problematic impurity; extending analytical verification costs more in labor but catches compositional drifts early. The importance of this compound grows as regulations tighten, especially regarding waste minimization and end-of-life product tracking for fluorinated compounds. We invest not in speculative “plant of the future” ideas but in real-world upgrades: solvent loop refinement, in-line purity sensors, and partnership with disposal vendors who close the cycle responsibly.

    Customers measure value not only in product cost but in minimized deviation, predictable performance, and responsiveness to unforeseen issues. Our philosophy has always rested on knowledge transfer—within our own production teams and outward to those who depend on our materials for their most challenging projects.

    Conclusion: A Product Forged by Experience

    3,5-Difluoronitrobenzene may look, on paper, like just another nitroarene, yet its production and application reveal layers of technical challenge and opportunity. Our legacy—as direct manufacturers—results from a pragmatic approach to process control and customer partnership. We respond to shifts in demand, technology, and regulation not by abstract theorizing but by daily engagement on the plant floor and unscripted problem-solving with each client.

    Among aromatic building blocks, 3,5-difluoronitrobenzene claims its place by meeting process reliability standards, supporting demanding syntheses, and delivering value born out of experience. In every metric, from purity control to practical support, we commit to delivering results that extend from our shop floor to yours.