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1,3-Dibromotetrafluorobenzene

    • Product Name 1,3-Dibromotetrafluorobenzene
    • Alias 1,3-Dibromo-2,4,5,6-tetrafluorobenzene
    • Einecs 215-578-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    VTB
    Specifications

    HS Code

    629495

    Chemical Name 1,3-Dibromotetrafluorobenzene
    Cas Number 17318-08-0
    Molecular Formula C6Br2F4
    Molecular Weight 293.87 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 173-175 °C
    Density 2.19 g/cm³
    Refractive Index 1.480 (approx.)
    Solubility Insoluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Synonyms 1,3-Dibromo-2,4,5,6-tetrafluorobenzene
    Smiles C1=C(C(=C(C(=C1F)Br)F)Br)F
    Inchi InChI=1S/C6Br2F4/c7-2-1-3(8)6(12)5(11)4(2)9
    Ec Number 241-387-1

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 1,3-Dibromotetrafluorobenzene, tightly sealed with a screw cap and labeled with safety information.
    Shipping 1,3-Dibromotetrafluorobenzene should be shipped in tightly sealed containers, clearly labeled, and protected from physical damage. Transport must comply with local and international regulations for hazardous chemicals, including UN identification numbers. Store upright in a cool, dry, well-ventilated area, separate from incompatible materials, and avoid sources of ignition during shipping and handling.
    Storage 1,3-Dibromotetrafluorobenzene should be stored in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Keep the chemical in a tightly closed, labeled container made of compatible material. Protect from moisture and direct sunlight. Store at room temperature, avoiding excessive heat or open flames. Use secondary containment to prevent leaks or spills.
    Application of 1,3-Dibromotetrafluorobenzene

    Applications of 1,3-Dibromotetrafluorobenzene in Industrial Manufacturing

    1,3-Dibromotetrafluorobenzene serves as a critical aromatic intermediate in several specialized industrial sectors, providing unique substitution patterns for advanced molecule construction. Below, we detail established application areas where manufacturers rely on this compound for downstream integration, including regulatory compliance, exact dosing in formulations, operational process stages, and the types of functional products delivered to the market.

    1. Advanced Pharmaceutical Intermediate Synthesis

    Process chemists and pharmaceutical manufacturers select this benzene derivative for constructing fluorinated building blocks in targeted small-molecule APIs, particularly where ortho/para reactivity and halogenation are essential for further functionalization. The material enters pilot and commercial scales where integration with other protected aromatics guarantees traceability and consistent impurity profiles across batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP General Chapter <1078> Good Manufacturing Practices for Bulk Pharmaceutical Excipients
    • REACH Registration for intermediate status in the EU
    • 21 CFR Part 211 US FDA cGMP

    Typical usage ratio

    • Reaction input: 0.7–1.2 molar equivalents, adjusted for target molecule substitution requirements and anticipated downstream derivatization yields

    Downstream process integration

    • Introduced in the coupling or aromatic substitution stage, prior to heterocycle formation, halogen-metal exchange, or nucleophilic aromatic substitution steps

    Final product types

    • Pharmaceutical intermediates with multi-fluorinated aromatic rings
    • Active substance precursors for oncology and anti-inflammatory drugs

    2. Liquid Crystal Material Manufacturing

    Manufacturers of advanced electronic displays and specialty optical devices employ this compound to introduce multiple halogen and fluorine atoms into rigid-core mesogens. The molecule’s geometry and substituent configuration are essential for tailored phase behavior and electro-optical performance in downstream liquid crystal mixtures.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for hazardous substances in electrical and electronic equipment
    • IEC 60417 safety labeling for chemical supplier integration
    • ISO 9001:2015 for quality management in material production
    • REACH compliance for supplied intermediates

    Typical usage ratio

    • Component input: 0.5–2.5% by weight in precursor blends, varying by mesogenic target structure and blend formulation

    Downstream process integration

    • Added during the synthesis of fluoroaromatic cores, prior to terminal group attachment and purification of LC mixture ingredients

    Final product types

    • Intermediate monomers for nematic and smectic liquid crystal formulations
    • Finished mixtures for thin-film transistor (TFT) and advanced LCD panel production

    3. Agrochemical Active Ingredient Precursor

    Makers of novel crop protection chemicals utilize this molecular scaffold in early-stage synthesis, where its halogenation profile enables further transformations for high-selectivity pesticides or herbicides. Its use provides key reactivity for constructing stable, environmentally resistant aromatic units adhering to modern agrochemical requirements.

    Industry compliance standards

    • FAO/WHO Guidelines for the Registration and Control of Pesticides
    • EPA 40 CFR Part 158 Data Requirements for Registration
    • OECD Principles of Good Laboratory Practice for synthesis and evaluation
    • ISO 9001 for consistent manufacture of technical intermediates

    Typical usage ratio

    • Precursor inclusion: 1.0–1.5 equivalents per target molecule, adjusted in scale-up based on pilot conversion rates and impurity clearances

    Downstream process integration

    • Incorporated at the aromatic core formation stage, enabling downstream custom halogen exchanges, cyclization, or ether formation reactions

    Final product types

    • Active ingredient intermediates for selective pesticides
    • Herbicidal core compounds designed for crop protection formulations

    4. Specialty Polymer Monomer Sourcing

    This compound functions as a structural unit in the synthesis of specialty high-performance polymers, specifically where its tetrafluoro and dibromo functional groups introduce rigidity, fire resistance, or enhanced dielectric properties. Polymerization chemists target controlled substitution to construct materials for demanding industrial electronic and aerospace applications.

    Industry compliance standards

    • UL 94 for flammability of plastic components
    • ISO 17025 for laboratory material testing
    • EN 45545-2 for railway applications—fire protection of rolling stock
    • ASTM D638 for tensile properties of plastics

    Typical usage ratio

    • Monomer additive: 2–8% by molar ratio depending on polymer backbone design and application-specific mechanical or electrical targets

    Downstream process integration

    • Fed into the aromatic monomer synthesis and pre-polymerization stage, often involving Suzuki or Ullmann coupling reactions to assemble extended aromatic chains or crosslinked networks

    Final product types

    • Fluorinated specialty resins for advanced electronic insulating parts
    • Fire-retardant components for cable and aerospace assemblies

    5. OLED and Photonic Material Precursor

    Electronic material producers use this compound in the intricate synthesis routes for donor–acceptor conjugated molecules engineered for organic light-emitting diode (OLED) displays and high-sensitivity photonic sensors. The specific halogen substitution pattern offers controlled absorption and emission properties after downstream arylation or cross-coupling transformations.

    Industry compliance standards

    • IEC 62471 for photobiological safety of lamps and lamp systems (device-level integration)
    • RoHS compliance for optical device raw materials
    • ISO 14001 Environmental Management during chemical material production
    • REACH registration as an R&D intermediate in photonic chemicals

    Typical usage ratio

    • Precursor level: 0.3–1.0 equivalents per fluorinated arene unit, carefully adjusted to maintain chromophore substitution uniformity and performance reproducibility

    Downstream process integration

    • Introduced prior to palladium-catalyzed cross-coupling in the formation of extended aromatic electronic building blocks

    Final product types

    • OLED emitting layer molecule intermediates
    • Photonic sensor dyes and light conversion agent components
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    Certification & Compliance
    More Introduction

    1,3-Dibromotetrafluorobenzene: A Manufacturer’s Perspective

    Introduction to Our Experience with 1,3-Dibromotetrafluorobenzene

    Manufacturing high-purity halogenated aromatics requires technical diligence and patience. Over years of operation, our facility has produced a range of fluorinated intermediates. Among the portfolio, 1,3-dibromotetrafluorobenzene stands out for both its distinctive reactivity and broad application in synthesis. The molecule’s structure, with bromines in positions 1 and 3 and four fluorines filling the remaining sites on the benzene ring, creates a unique balance of stability and reactivity not seen in less substituted aromatics. Fluorination resists oxidation, while the bromine atoms act as excellent leaving groups during substitution. These attributes have shaped our daily approach to batch refinement, reaction monitoring, and process control.

    Why 1,3-Dibromotetrafluorobenzene Matters in Chemical Synthesis

    Reliance on consistent quality remains a top priority. 1,3-dibromotetrafluorobenzene plays a supporting role in the assembly of advanced building blocks for pharmaceuticals, agrochemicals, and liquid crystal compounds. Researchers appreciate how bromines in these positions allow for selective coupling, giving chemists a reliable handle for further modification. For us, this value shows up in the demand for narrow purity specifications and strict control over isomer content. After years of scaling this compound, we’ve found two recurring expectations from customers: batch-to-batch reproducibility and the absence of less-substituted or over-substituted byproducts.

    In production, the choice of bromination conditions determines not just overall yield but also the ratio between ortho, meta, and para isomers. We routinely monitor the process by in-house chromatography. The meta isomer (1,3-) consistently provides the best compromise between accessibility and reactivity under modern catalytic cross-coupling methods. Our staff have seen that less selective batches lead downstream to wasted raw materials or laborious separations. Quality control, in this sense, means every kilogram supports customers’ needs for purity above 98%, tailored particle size, controlled moisture, and guaranteed absence of chlorinated and non-fluorinated congeners.

    Specifications Shaped by Real-World Demands

    Years of dealing with strict procurement departments and research chemists have taught us not to cut corners. Our production lines operate with attention to particle size and flow properties. The appearance of 1,3-dibromotetrafluorobenzene—white to off-white crystalline solid—signals to our technical staff that purification steps are working as intended. Any color shift or change in melting point means the process must be checked.

    Customers often ask about trace impurities, especially during pharmaceutical synthesis. Our specifications require HPLC and GC trace analyses to show related impurities remain below 0.2%. Water content stays below 0.1% by Karl Fischer titration, preventing unwanted side reactions in sensitive applications. After years of shipping, we have adopted tamper-evident packaging lined with high-density polyethylene to solve issues with deliquescence and cross-contamination, drawing directly on client feedback.

    Unlike monobromo or monofluoro analogues, this compound brings the desired blend of stability and chemical activation. The high fluorine content reduces aromatic nucleophilicity, letting the aryl bromide undergo selective cross-coupling or nucleophilic aromatic substitution with minimal side reactions. As manufacturers, we noticed that some users expect material that dissolves cleanly in common solvents without haze or residue. Our crystalline product, free from dust or persistent sticky residues from incomplete drying, answers this need.

    Production Realities: Managing Reagents, Waste, and Energy

    Behind every drum of 1,3-dibromotetrafluorobenzene, a training cycle of process optimization, waste minimization, and worker safety runs continuously. We source the starting tetrafluorobenzene from reliable upstream partners precisely because contaminated feed disrupts subsequent bromination. The bromination itself proceeds at modest temperature, with strict control over exothermicity. Years ago, uncontrolled reactions led to poor selectivity and challenging cleanups; those lessons now drive our investment in temperature probes and semi-batch feed systems.

    Disposal of spent bromine reagents and byproducts draws as much attention as production. Our team treats and neutralizes halogen-rich waste streams with a focus on regulatory compliance and environmental responsibility. In the past, overlooked halide byproducts increased downstream treatment costs. Now, dedicated abatement units recover bromide wherever possible, and our on-site monitoring ensures we respect tightening industrial discharge rules.

    Energy usage remains significant. We schedule batch processes to optimize heat recovery and avoid downtime. The need for cooling and purification, especially during crystallization, led us to invest in efficient jacketed vessels and upgraded solvent recovery systems. Realistically, these investments only pay off when demand stays steady, but the expertise we’ve gained helps us head off unplanned shutdowns and ensure delivery on schedule.

    Comparisons: Differences from Related Aromatic Compounds

    Clients sometimes ask how this product stacks up against other halogenated benzenes. From experience, handling difluorobromo or chlorotetrafluorobenzene brings different technical requirements. Chlorine analogues, though slightly less expensive, introduce complications in certain cross-coupling reactions due to slower oxidative addition. Products with fewer fluorine atoms often show higher nucleophilicity, limiting selectivity when chemists attempt to functionalize just one site. Our 1,3-dibromotetrafluorobenzene, by contrast, marries high fluorine density with accessible bromides, so lab teams access both stability and reactivity in one molecule.

    The ability to tune reactivity, by nature of substitution, often sets projects back months when the wrong isomeric mixture lands in the pilot plant. We have learned from clients that even small deviations in isomer ratio or impurity content can spoil scale-up or cause registration setbacks for pharmaceuticals. Our efforts focus on blocking these small mistakes at source. An overlooked difference between 1,3- and 1,4- isomers means hundreds of hours in additional analytical and formulation work for users—something we mitigate through targeted process and analytical controls.

    Applications: Putting the Product to Work

    Real contributions to research and production come from high-quality intermediates. This specific dibrominated, tetrafluorinated aromatic finds routine use whenever a developer must introduce two separate functional groups on a fluorine-rich aromatic ring. Medicinal chemists, for instance, use it to prepare advanced intermediates for kinase inhibitors and central nervous system agents. Our teams see the compound’s uptake in processes that require transition-metal-catalyzed coupling, such as Suzuki, Stille, and Buchwald-Hartwig reactions. These methods depend on consistent halogen activation and minimal side reactions—deliverables we target through hands-on quality assessments.

    The electronics industry, particularly in the field of liquid crystals, prizes fluorinated aromatics for their dielectric and alignment properties. We have seen requests for this compound matched with unusual purity requirements, sometimes extending to specifications on metal ion content and particle morphology. Meeting these needs took collaboration across our analytical, production, and logistics staff. The respect earned through solving repeated technical challenges with demanding users now underpins our confidence in the product and our willingness to invite audits or visits.

    Academic researchers call on this compound for studying substitution patterns and creating model systems for halogen flux experiments. Feedback from multiple institutions has driven us to maintain robust documentation and reference spectra, streamlining grant proposal work and regulatory filings on their end. Our recordkeeping, updated over multiple cycles of customer feedback and compliance reviews, now supports both day-to-day batch tracing and long-term product stewardship.

    Challenges Along the Way

    Manufacturing specialty chemicals brings a specific rhythm of stop-start. During periods of raw material price instability or global logistics disruptions, supply security rises to the top of the worry list. We manage this by holding safety stock, maintaining multiple qualified suppliers, and keeping a clear calendar for plant maintenance. Mishandling purification waste or underestimating utility needs in hot weather both teach lessons not forgotten. In our drive to reduce batch failures, we set aside extra time for pilot-scale runs to validate starting materials and catalysts.

    Batch variation can’t be eliminated by paper systems or spot checks. Years ago, fluctuating moisture during wet months forced us to revise drying schedules and experiment with desiccant storage. Just as often, changes in regulatory or import rules meant adapting documentation and training on short notice. Our approach relies on regular operator briefings and clear records. From the warehouse to the QC lab, everyone understands the knock-on effect that a single contaminated bag or leaky drum can have across dozens of partners.

    Each export shipment brings a risk of customs delays, sudden regulatory reviews, or new customer declarations. We recertify batches after any disruption and track each drum for traceability, anticipating the questions that come from government agencies or customer QA teams. The upshot, from where we stand, is a culture built around flexibility, transparency, and learning from each challenge.

    Technical Support: Direct Line from Plant to User

    Over the years, requests for technical support have shaped the information we provide and the speed with which we respond. Synthesis questions often cover the compatibility of Pak-213 with various catalyst systems or the effect of trace water in downstream reactions. Our technical team often assists by supplying detailed NMR, GC-MS, and HPLC data. Each time a partner faces yield drops or unexpected byproducts, they turn to us for troubleshooting—sometimes after only a single unscheduled phone call.

    We recommend process adjustments based on how the product reacts to changes in solvent exposure, stirring speed, or catalyst lot. Documentation, updated with each run, supports user QA and regulatory filings for both small-scale research and commercial production. The most valuable partnerships grow from quick feedback cycles—confirmation of compatibility or resilience under slightly off-nominal conditions, rather than delayed and incomplete problem solving.

    Repeat customers have built trust in our willingness to go beyond paperwork, sharing best practices or contributing input on project scale-up. Issues such as trace solvate formation, evaporation loss, or shipping delays all find swift attention. Our staff, familiar with the product at every stage, rarely encounter problems that remain unsolved after a few focused exchanges with our client’s technical leads.

    Handling and Storage: Practical Observations

    Sensitive aromatic halides often draw risk management scrutiny. We have learned to respect the material’s stability under dry, well-sealed conditions. Evaporation risk exists at higher temperatures; we only recommend room-temperature storage with desiccant and a tightly closed seal. Chemical compatibility with steel, aluminum, and HDPE allows versatile packaging options, but direct contact with acids or strong alkalis remains off-limits.

    On the shop floor, operators need to avoid prolonged direct skin contact and inhalation of dust; we provide nitrile gloves and fitted dust masks for all staff working near the material. Spills, while not frequent, require prompt sweeping and careful waste handling—fluorinated organics sometimes persist in soil or water if left unmanaged. Our training program covers both spill prevention and rapid response, keeping every shift prepared to handle the unexpected.

    Continuous Improvement: Refining the Product and Process

    Modifying production processes, even for a familiar item like 1,3-dibromotetrafluorobenzene, brings cascading effects across the business. New reactor coatings cut down on trace metal contamination but require calibration of batch times and product transfer protocols. The decision to add more rigorous analytical checks, based on both internal audits and customer suggestions, lengthens each batch cycle but pays off through fewer complaints and wider acceptance of our documentation overseas.

    Sometimes, incremental process upgrades lead to insights we pass along to customers. For example, shifting final drying to lower-pressure distillation reduced persistent solvent traces and shortened downstream purification steps for a major pharma partner. Process engineers embrace tight feedback loops with research chemists and purchasing managers, trading insights on cost, scale, and technical fit.

    No manufacturing route remains static. We constantly appraise the environmental impact of selected reagents, update our energy management plans, and work with local regulators on improving emissions abatement. Transparency begins at process review meetings and grows stronger each time a customer brings us a new challenge.

    Final Thoughts from the Manufacturing Floor

    From source material sourcing to drum shipment, every step in the creation of 1,3-dibromotetrafluorobenzene involves real people—operators aligning pumps, chemists poring over chromatograms, and logistics coordinators tracking shipments across borders. Nothing beats hands-on process knowledge and the will to adapt, whether fine-tuning a thermal profile or adapting a drying cycle for a fresh humidity spike. Real-world manufacturing always surprises, but the ongoing appeal of this versatile intermediate ensures it remains a core part of our daily business.

    We have grown confident in our ability to deliver reliable, high-purity material that supports customer projects ranging from basic academic research to high-value commercial synthesis. Decades of feedback, trial, and technical inquiry have led us to shape our product and service in directions that value practical improvements over empty promises. Each kilo that leaves our site represents times tested learning and a genuine commitment to moving advanced science forward.