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1,3-Difluorobenzene

    • Product Name 1,3-Difluorobenzene
    • Alias m-Difluorobenzene
    • Einecs 205-573-0
    • 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

    902228

    CAS_Number 372-18-9
    Molecular_Formula C6H4F2
    Molecular_Weight 114.09 g/mol
    Appearance Colorless liquid
    Boiling_Point 88-90 °C
    Melting_Point -31 °C
    Density 1.172 g/cm3 at 20 °C
    Refractive_Index 1.447 at 20 °C
    Flash_Point 14 °C (closed cup)
    Solubility_in_Water Insoluble
    Synonyms m-Difluorobenzene, 1,3-DFB
    EC_Number 206-749-8

    As an accredited 1,3-Difluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,3-Difluorobenzene is supplied in a 500 mL amber glass bottle with a secure screw cap and tamper-evident seal.
    Shipping 1,3-Difluorobenzene is shipped in tightly sealed containers, typically glass or compatible plastic bottles, to prevent leakage and contamination. It should be transported as a hazardous liquid, following relevant regulations (such as DOT and IATA). Packages must be clearly labeled, protected from physical damage, and kept away from ignition sources during transit.
    Storage 1,3-Difluorobenzene should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it separate from incompatible substances such as strong oxidizing agents. Ensure proper labeling and restrict access to trained personnel only. Always follow local regulations and safety guidelines for storage of flammable liquids.
    Application of 1,3-Difluorobenzene

    Applications of 1,3-Difluorobenzene in Industrial Manufacturing

    As a direct producer of 1,3-difluorobenzene, we understand the critical roles this compound plays in multiple high-value chemical manufacturing sectors. Below we detail the principal downstream scenarios, with in-depth, scenario-specific guidance for compliance, formulation, workflow, and end use based on established industry practice and regulatory expectations.

    1. Agrochemical Intermediate Synthesis

    1,3-difluorobenzene serves as a core intermediate in synthesizing several important herbicidal and fungicidal active molecules. Fluorination of the aromatic ring is prized for increasing crop protection target selectivity, metabolic stability, and field persistence. Agrochemical producers integrate this raw material during the early condensation or nucleophilic aromatic substitution steps of their multi-stage synthesis lines, forming building blocks for patented actives registered across global agricultural markets.

    Industry compliance standards

    • REACH (EC/1907/2006) for registration and use in the EU
    • EPA FIFRA regulations for pesticide intermediates in the United States
    • China Pesticide Administration Regulation (PAR) for technical grade raw materials
    • Good Manufacturing Practice for Active Substances Used as Starting Materials (ICH Q7, as applicable)

    Typical usage ratio

    • Batch inputs: 10–25% by mole as a starting aromatic core, depending on the specific herbicide or fungicide structure
    • Formulation adjustments consider downstream functional group introductions and yield optimization

    Downstream process integration

    • Charged direct into high-temperature nucleophilic aromatic substitution reactors
    • Combined with tailored amines, haloalkyls, or sulfonyl groups in closed-system pressure vessels
    • Subjected to continuous distillation and purification workflows for downstream reactivity

    Final product types

    • Triazole-based fungicide actives
    • Difluorinated phenyl herbicides and intermediates
    • Precursor chemicals for patent-protected crop protection agents

    2. Pharmaceutical API Building Block

    This compound is frequently utilized by pharmaceutical manufacturers in the preparation of fluorinated aromatic cores found in the structure of several commercial APIs, including select anti-inflammatory, anti-infective, and CNS-active agents. The difluorinated phenyl moiety provides metabolic resistance and specific receptor-binding profiles required for today’s medicinal chemistry innovations. Process chemists introduce this ingredient during the earliest aromatic coupling stages, followed by stepwise functionalization and stringent purification.

    Industry compliance standards

    • ICH Q7 / GMP Part II for chemical intermediates
    • USP/NF or Ph. Eur. impurity control limits (where applicable at intermediate stage)
    • FDA 21 CFR 211 (for API manufacture in the U.S.)
    • EDQM CEP or DMF registration for use in regulated pharmaceutical supply chains

    Typical usage ratio

    • Starting material: 8–22% by weight of reaction mass, tailored by the synthetic route
    • Ratio can vary based on subsequent ring substitution or side-chain elaboration

    Downstream process integration

    • Introduced during Suzuki, Buchwald-Hartwig, or other palladium-catalyzed coupling processes
    • Subjected to reductive amination, etherification, or halogen exchange as required by structural targets
    • Followed by in-line HPLC or GC monitoring for residual fluorinated intermediates

    Final product types

    • Nonsteroidal anti-inflammatory drug (NSAID) precursors
    • Fluorinated benzylamine intermediates for CNS pharmaceutical candidates
    • Building blocks for anti-infective and oncology small molecules

    3. Liquid Crystal and Display Material Manufacturing

    Display and electronics material manufacturers use 1,3-difluorobenzene for producing high-purity liquid crystalline monomers integrated into advanced LC display panels. The fluorinated ring structure imparts specific dielectric and viscosity profiles essential for improving response speed, electro-optical properties, and environmental resistance of final display media. The compound enters anhydrous, monitored conditions to preserve purity and function in the subsequent step-growth polymerizations and further modification reactions.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (limiting hazardous substances)
    • IEC 61249-2-21 electronic material standards
    • Chinese GB/T 2423.1-2008 for environmental reliability
    • IECQ QC080000 for hazardous substance process management

    Typical usage ratio

    • Used at 3–7 mol% as a comonomer or modifying unit in LC masterbatches
    • Ratio adjusted based on target birefringence and phase transition temperatures

    Downstream process integration

    • Charged to inertized glass-lined vessels for stepwise condensation or Suzuki-type reactions
    • Immediately followed by purification under reduced pressure to remove trace impurities
    • Blending into proprietary LC mixtures under N2 or argon atmosphere

    Final product types

    • Twisted nematic (TN), in-plane switching (IPS), and vertical alignment (VA) liquid crystal mixtures
    • Organic LC panel monomers for TFT display fabrication
    • Polyfluorinated oligomers for specialty display films

    4. Advanced Polymer and Resin Production

    High-performance polymer and specialty resin manufacturers rely on this difluorinated aromatic for producing engineering plastics and thermoset resins with improved chemical barrier and dielectric properties. The introduction occurs at the initial monomer synthesis, participating in condensation or addition processes that demand low halide and water content for reliable molecular weight growth. Such resins are crucial components in demanding automotive, electronics, and aerospace assemblies.

    Industry compliance standards

    • ISO 9001:2015 for quality management across polymer batch production
    • UL 94 (flammability standard of plastic materials)
    • IEC 60243-1 for electrical strength of insulating materials
    • Automotive OEM specification compliance (e.g., VW TL, Renault 36-05-801/--)

    Typical usage ratio

    • Integrated at 2–10 mol% based on end-use dielectric strength or chemical stability requirements
    • Formulation balances achieved via iterative pilot-scale production with real-time viscosity and glass transition testing

    Downstream process integration

    • Feeds directly into ring-opening polymerization or condensation stages with co-monomers
    • Monitored via NMR and GPC for incorporation efficiency and chain integrity
    • Finished polymers extruded, molded, or compounded further depending on application

    Final product types

    • Fluorinated polyimide films for insulation and flexible electronics
    • Thermoset fluorinated resins for electronic encapsulants
    • Chemical-resistant automotive and industrial plastic components

    5. Fine Chemical and Specialty Intermediate Manufacturing

    Producers of fine chemicals exploit 1,3-difluorobenzene for accessing complex, multi-functionalized benzene derivatives valued in photographic chemicals, dyes, and metal complex ligand fields. These downstream users require consistently controlled impurity profiles and specific isotope patterns, integrating the raw material at precision-controlled alkylation, acylation, or halogen exchange stages within their synthesis chains.

    Industry compliance standards

    • Kosher/Halal as required for specialty organic chemical exports
    • ISO 14001 for environmental management during chemical handling
    • Local regulations on discharge and emissions (e.g., BAT/BREF notes in Europe)
    • Custom in-house analytical release specifications set by major customers

    Typical usage ratio

    • Input rates between 5–18% by mole depending on substitution pattern and scale
    • Adjusted based on multi-step route yields and endpoint product purity

    Downstream process integration

    • Used in Friedel–Crafts, Grignard, or Ullmann coupling reactors with precise temperature and pressure control
    • Feeds monitored with in-process GC-MS to guarantee conversion and limit byproducts
    • Purified products advanced to crystallization or further organometallic derivatization

    Final product types

    • Fluorinated dyes and pigments for specialty coatings
    • Photographic imaging agents and developers
    • Bipyridine and terpyridine ligands for metal catalysts
    Free Quote

    Competitive 1,3-Difluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1,3-Difluorobenzene: A Core Building Block for Advanced Synthesis

    Practical Insights from Direct Manufacturing Experience

    Producing 1,3-difluorobenzene (m-difluorobenzene, CAS 372-18-9) forms part of our core chemistry practice. This compound stands out because it pairs the stability of the benzene ring with uniquely positioned fluorine atoms, opening a route to a broad range of downstream chemicals. Our plant operators and technical staff have worked with this material for years, so we’ve seen firsthand the precise parameters needed to deliver a product that meets demanding specifications, supports large-scale syntheses, and maintains reliability batch after batch.

    How We Prepare and Verify Quality

    Every drum, iso-tank, or container of 1,3-difluorobenzene we ship has passed through careful production steps. We rely on established synthesis routes—most often halogen exchange or dehydrofluorination reactions—tuned for high selectivity at the 1,3-positions. Our quality group runs gas chromatography and NMR checks for purity, typically aiming for >99% content, minimizing mono- or tri-fluorinated isomers and a suite of potential aromatic contaminants. Technical support routinely discusses detection limits on supply calls, since trace impurities can impact downstream reactions, especially in pharmaceutical or agrochemical syntheses. We’ve tailored our purification setups over the years so our product’s color, odor, and water content stay well inside spec even on extended shipments.

    Model Grades and Packing Details

    Standard 1,3-difluorobenzene leaves our plant as a clear, low-viscosity liquid, packaged for chemical industry requirements. We offer drum-size or bulk-pack solutions compatible with both solvent-handling and production environments. Our experience with temperature-controlled logistics ensures the material’s low volatility and stability are preserved. Customers producing larger volumes of specialty chemicals value the options to scale cost-effectively, since transition from pilot to commercial production usually means hundreds or thousands of kilograms.

    The Realities of End Use: Putting 1,3-Difluorobenzene to Work

    Chemists come to us with a range of projects using 1,3-difluorobenzene: fluorinated pharmaceuticals, liquid crystals, OLED intermediates, fluorinated polymers, and agricultural actives. In our own use, this compound often acts as a foundation for more complex construction—especially where meta-substitution brings out electronic or steric effects that single fluorine or other difluorobenzene isomers don’t provide. We’ve worked with research groups scaling up heterocycle syntheses, directed lithiation, or cross-coupling using our material as the starting block. Some production lines need extra attention to residual metals, so our sales and tech support teams keep detailed logs on customer feedback and process adjustments.

    Comparison to Other Aromatic Fluorocarbons

    Many chemical companies offer mono-fluorobenzenes and different isomers of difluorobenzene; each has a distinct profile relevant to pharmaceutical, materials, or electronics work. By direct operator experience, we’ve noticed that ortho (1,2-) and para (1,4-) difluorobenzenes demand different reaction setups, sometimes leading to variations in regioselectivity or product purity. Process chemists in fine chemicals or electronics often need the meta (1,3-) isomer to achieve specific physical and electronic effects in polymers, bioactive compounds, or intermediates. Customers have run into solubility or reactivity challenges using other isomers, prompting many conversations over how our 1,3-difluorobenzene improves their bottom-line yield or reduces downstream purification burdens.

    Handling and Safety Through the Production Chain

    1,3-Difluorobenzene has a distinct, sweetish odor and evaporates readily, so both plant and warehouse teams work with closed systems and vapor abatement. In daily operations, we lab-test each batch for water content down to a few ppm, since the presence of water can trigger side reactions or negatively impact many fluorination or metallation steps. Experience has shown us that traditional aromatic material handling doesn’t always suffice for fluorinated aromatics; lines, gaskets, and storage tanks must use compatible materials such as PTFE or specific stainless grades. We regularly update our protocols in collaboration with customer EHS teams, especially large buyers from pharmaceuticals and agrochemicals who factor regulatory reviews into their own hazard assessments.

    Environmental Control and Sustainability Commitment

    Decades of production have taught us chemical manufacturing will always have material and environmental impacts. Our internal teams have focused on solvent recovery and waste gas abatement, especially HF and aromatic byproducts, to minimize plant emissions and wastewater load. We also support customers switching from less sustainable halogenated raw materials by supplying 1,3-difluorobenzene at consistently high quality, so their greener routes work in real manufacturing—without upending established production times or approvals. Every tank that leaves our gate represents input from R&D, production, and compliance teams who have been through regulatory process changes, so we can back up our product quality with documentation for environmental and global compliance checks, including REACH and relevant inventories.

    Feedback from Downstream Users

    It’s easy to overlook how small impurities impact big processes until you run into a stalled reaction or a residue on high-sensitivity applications. We’ve seen customers in OLED or colorant synthesis operations switch to our 1,3-difluorobenzene after facing low-quality imports, mostly due to tighter purification, better stability on storage, or more responsive technical support. Distributors sometimes bring us questions about supply interruptions, shelf-life, or re-certification needs; we draw on our operations data to provide realistic answers about production lead times, real-world stability, and supply chain conditions—especially since demand patterns have shifted rapidly through past years. By sharing practical experiences on product handling, blending, and process bottlenecks, we give users confidence that our manufacturing standards support their highest value applications, rather than only minimum thresholds.

    Distinctives in Industrial and Lab-Scale Application

    Lab researchers and plant engineers have overlapping but distinct needs. At lab scale, flexibility in sample volume and package type matters most; so supply teams prepare small-volume, high-purity lots for pilot programs, delivered with full certificates and analytical support. In contrast, full production lines care most about bulk supply, ease of unloading, and secure documentation to back up regulatory submission. We login field questions from both groups and log real difficulties: line fouling, impurity carry-over, tank residue, or losses to evaporation during transfer. Because our product feeds dozens of chemical syntheses in both segments, our support group stocks reference data, troubleshooting notes, and hands-on feedback to cut out avoidable downtime or material waste on the customer side.

    What Sets 1,3-Difluorobenzene Apart

    Having worked hands-on with aromatic fluorocarbons, we know the position of fluorine on the benzene ring doesn’t just drive reactivity; it helps define physical properties, safety profiles, and end-product performance. The 1,3-isomer combines electron-withdrawing power with spatial separation, which can throttle reaction rates or direct the chemoselectivity of downstream transformations. This impacts everything from chemical intermediate fidelity to solvent compatibility in coatings and films. Our process lines maintain strict batch traceability for all 1,3-difluorobenzene output, and this has helped specialty pharma and durable goods companies standardize formulations that depend on our raw material matching their specification every time.

    Challenges in Market Supply and Demand

    We’ve seen interest in 1,3-difluorobenzene increase as new materials libraries and drug projects kick off around the globe. While supply bottlenecks occasionally crop up due to raw material tightness or shipping blockages, our just-in-time inventory system and established production partners help keep disruption brief. Demand for higher volumes and more frequent deliveries means our logistics team often works with customers to project future usage, reducing the risk of line stoppages or expensive downtime. More than once, awareness of global freight risks prompted us to switch shipping or packaging format with a client’s needs in mind, so their overall process flow stays intact. Production planners value this contingency support, especially on longer supply contracts.

    Technical Factors That Matter Most to End Users

    Process engineers in charge of continuous synthesis lines highlight product purity, especially low levels of non-target isomers or residual halogenated byproducts. Small differences in boiling point, vapor pressure, or flash point between 1,3-difluorobenzene and near analogs can translate to avoidable handling hazards or product losses during storage. We monitor these technical details as both a safety practice and a guarantee that every drum meets or exceeds the physical properties expected by R&D chemists or QA labs. Technical bulletins, practical support, and on-call support are part of our supply, since real plant operations occasionally run into transfer line blockages, off-odors, or discrepancies on delivered certificate values. Experience shows that preemptive troubleshooting with suppliers means fewer firefighting surprises for our users.

    Lessons from the Field

    Over years of production and shipment, we’ve compiled a library of best practices drawn from lab and plant user feedback. In some cases, chemists working with high-spin catalysts or solid-state syntheses reported improved performance when switching to our grade of 1,3-difluorobenzene, owing to lower amounts of paramagnetic or colored impurities. Electronic materials specialists pointed out how tiny trace levels of metallics or residual acids affected dielectric properties or film formation, so batch-to-batch trace reporting and enhanced filtration became standard practice. All of these operational upgrades trace back to end-use realities, not just abstract quality metrics.

    Global Trends Shaping Production

    Rising attention to sustainable chemistry and halogen management in fine chemical production continues to inform how we approach raw material selection and waste abatement. For 1,3-difluorobenzene, this translates into practical choices around raw material sourcing, solvent selection, and downstream process compatibility. Many customers in Europe, North America, and Asia Pacific now opt for raw materials that shorten their own regulatory review cycles and reduce compliance costs. We work alongside their teams to ensure our documentation, sample tracking, and supporting evidence stands up to the scrutiny of internal and external auditors. This commitment supports our position as a preferred long-term partner, not just a one-time supplier.

    Real-World Examples from Manufacturing

    Pharmaceutical synthesis teams have used our 1,3-difluorobenzene to produce intermediates for both clinical candidates and commercial APIs, because tight control on fluoride substitution and trace organics can make the difference between success and failure of a purification campaign. For the electronic materials sector, OLED and fluoropolymer researchers rely on the meta-fluoro orientation to fine-tune thermal or electrical properties beyond what 1,2- or 1,4-isomers allow. Some plant-scale colorant producers switched to our grade after running process comparison trials, reporting better product stability and less costly rework downstream. Every report from the field is logged to update our production procedures and provide actionable process advice for new buyers facing similar decision points.

    Innovation, Partnership, and Consistent Quality

    No supply contract, no matter how large or small, can replace the value of a strong working partnership built on shared technical experience. We know the importance of consistent quality—experiments succeed or fail based on small differences that trace back to raw material reliability. Our in-house chemists and plant operators remain available to discuss real problems, whether predicting the reactivity of 1,3-difluorobenzene with a new ligand or troubleshooting an unexpected byproduct in a finished batch. We stay current on advances in synthetic methodology, regulatory requirements, and scale-up protocols, so our recommendations come anchored in factory-floor experience and data, not just abstract promise.

    Future Pathways and Industry Direction

    The demand for finely tuned aromatics with precise substitution patterns will keep growing, especially as specialty pharma, renewable chemicals, and next-generation electronics expand. Growth in green chemistry and regulatory oversight pushes our industry to minimize residual halogens and optimize production against both output quality and environmental impact. Customers rely on our experience, process controls, and technical openness to bridge the gap between research concept and reliable large-scale supply. We remain committed to this role and continually improve our production, analytical, and logistic capability to meet the evolving needs of chemistry, manufacturing, and sustainable practice through the dependable supply of 1,3-difluorobenzene.