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2,3,4-Trifluorobromobenzene

    • Product Name 2,3,4-Trifluorobromobenzene
    • Alias 1-Bromo-2,3,4-trifluorobenzene
    • Einecs 701-203-8
    • 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
    VTB
    Specifications

    HS Code

    327701

    Cas Number 1435-51-6
    Molecular Formula C6H2BrF3
    Molecular Weight 210.98 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 142-144 °C
    Melting Point -22 °C
    Density 1.679 g/cm³ at 25 °C
    Refractive Index 1.493
    Flash Point 46 °C
    Purity ≥98%
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 1-Bromo-2,3,4-trifluorobenzene
    Smiles C1=C(C(=C(C=C1F)F)Br)F
    Ec Number 216-990-4
    Un Number 2810

    As an accredited 2,3,4-Trifluorobromobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, sealed with a red cap, labeled clearly; contains 25 grams of 2,3,4-Trifluorobromobenzene, for laboratory use.
    Shipping 2,3,4-Trifluorobromobenzene is shipped in tightly sealed containers, typically made of glass or high-density polyethylene. It should be stored and transported in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling, adherence to relevant safety regulations, and documentation of hazardous material status are required during shipping.
    Storage 2,3,4-Trifluorobromobenzene should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition. Protect from direct sunlight, moisture, and incompatible materials such as strong oxidizers. Store at room temperature and ensure that the storage area is equipped to contain any accidental spills or leaks.
    Application of 2,3,4-Trifluorobromobenzene

    Applications of 2,3,4-Trifluorobromobenzene in Industrial Manufacturing

    2,3,4-Trifluorobromobenzene functions as a specialized building block in various industrial downstream sectors. Our manufacturing expertise ensures reliable supply for critical segments, emphasizing precise integration within multi-step syntheses and regulated processes. Reviewed below are key professional use cases, detailing compliance, usage ratios, process integration, and typical end products.

    1. Pharmaceutical Intermediate Synthesis

    Several active pharmaceutical ingredient (API) manufacturers employ 2,3,4-Trifluorobromobenzene as a core halogenated aromatic intermediate in the assembly of small-molecule drugs, particularly for oncology and CNS agents. This compound's trifluorinated structure enables selective cross-coupling reactions, such as Suzuki and Buchwald–Hartwig protocols, for late-stage diversification. Its consistent high-purity meeting ICH Q7 and cGMP expectations is essential for downstream registration files. Use typically begins at the kiloliter scale in pilot plants, scaling via flow or batch under controlled conditions.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 for drug manufacturing
    • EDQM CEP requirements
    • EU GMP for chemical intermediates

    Typical usage ratio

    • Batch formulation: generally 0.5–1.8 molar equivalents relative to target core scaffold, adjusted by synthetic pathway and required yield

    Downstream process integration

    • Introduced at aromatic halogenation or cross-coupling step in multi-step small-molecule API syntheses

    Final product types

    • Active pharmaceutical ingredients (oncology, neurology, antivirals, rare disease treatments)
    • Regulatory starting materials

    2. Agrochemical Active Ingredient Manufacturing

    Producers of crop protection chemicals utilize this compound to construct fluorinated phenyl motifs in pesticide and herbicide actives. The electron-withdrawing trifluoromethyl substitution pattern enhances bioactivity against resistant weeds and crop pests. 2,3,4-Trifluorobromobenzene enables reliable aryl bromide insertions, typically integrated into alkylation or amination reactions to yield next-generation actives with improved environmental degradation profiles. Strict recordkeeping and traceability support full regulatory dossiers.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for test chemical synthesis
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • FAO/WHO JMPR quality requirements
    • ISO 9001:2015 quality assurance in chemical production

    Typical usage ratio

    • Concentration between 1.1–2.0 equivalents, modulated per structure–activity targets and downstream functionalization step

    Downstream process integration

    • Feeds in at initial aryl halide stage of active ingredient synthesis, typically via Grignard, reductive amination, or transition-metal-catalyzed coupling processes

    Final product types

    • Selective herbicides (e.g., for cereals, soybeans, orchards)
    • Insecticides and fungicides incorporating trifluorophenyl moieties

    3. Electronic Materials and Liquid Crystal Intermediate Production

    Specialty electronics manufacturers source this compound for constructing advanced liquid crystal monomers and organic semiconductor structures. The defined substitution impacts dielectric performance and thermal stability critical to display backplane and flexible electronics. Manufacturers control purity and impurity profile to meet REACH and electronics-specific QC protocols, ensuring compatibility with downstream lithography and device assembly. Trace residue management during post-coupling purification is tightly monitored.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for SVHC and registration
    • RoHS Directive (EU) 2011/65/EU for hazardous substances
    • IEC 61249-2-21 PCB material requirements
    • JIS standards for optical and electronic chemical materials

    Typical usage ratio

    • Usually applied at 0.9–1.2 equivalents in monomer formation; ratio varies with target mesogenic core and functional group conversion

    Downstream process integration

    • Utilized as a key aryl halide precursor in coupling or alkylation steps during monomer and oligomer design for display matrix manufacturing

    Final product types

    • Liquid crystal monomers for TFT-LCD and OLED panels
    • Organic semiconductors for flexible electronics and sensors

    4. Specialty Polymer Modifier Synthesis

    Advanced polymer producers incorporate this compound to introduce trifluorophenyl units into specialty resins. Such modification typically enhances thermal, chemical, or UV stability. These applications serve demanding environments in aerospace, automotive, or chemical processing sectors, with formulation adjusted for target glass transition temperature or flammability compliance. The compound is dosed in controlled polymerization or grafting reactions, requiring documentation for downstream traceability.

    Industry compliance standards

    • ISO 9001/14001 for quality and environmental management
    • EN 45545-2: Fire protection for railway rolling stock polymers
    • ASTM D4066 for fluoropolymer resin grades
    • REACH Annex XVII (restricted substances)

    Typical usage ratio

    • Modifier addition at 0.8–3.0% by polymer precursor weight; adjusted based on desired end-use property enhancement

    Downstream process integration

    • Introduced during solution polymerization, polycondensation, or melt blending to achieve functional side-chain grafting or backbone integration

    Final product types

    • High-performance fluorinated engineering plastics
    • UV- and chemical-resistant specialty coatings
    • Wire and cable insulation with flame retardancy
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    Certification & Compliance
    More Introduction

    2,3,4-Trifluorobromobenzene: A Manufacturer's Perspective

    Getting to Know 2,3,4-Trifluorobromobenzene

    From decades of chemical manufacturing, product selection always comes down to raw material handling, production flexibility, and the bottlenecks faced in process development. Among a growing catalog of fluorinated building blocks, 2,3,4-Trifluorobromobenzene has become an option that engineers and chemists choose when they need predictable reactivity and stability. Many specialty chemical manufacturers have found value in sourcing this compound directly from a plant where the quality control and batch documentation can be traced back to the original reactor charge.

    Why Precision Matters with Trifluorinated Bromobenzenes

    2,3,4-Trifluorobromobenzene stands out for its substitution pattern. The trifluoro groups at the 2, 3, and 4 positions deliver electronic effects difficult to replicate with mono- or difluorinated rings. These substitutions influence both the rate of downstream reactions and product selectivity, helping deliver intermediates that perform reliably in pharmaceutical and agrochemical pipelines. Manufacturers have learned that the location of each halogen on the benzene ring cannot simply be swapped for convenience: similar-sounding isomers produce strikingly different results, both in reactivity and in the behavior of the compound under scale-up conditions.

    For any company handling kilogram to ton-scale quantities, consistent quality can make or break a campaign. Variability in trace byproducts, residual solvents, or halide content can show up downstream as headaches for reaction control and purification. By controlling source materials, drying conditions, and packaging, chemical plants specializing in halogenated aromatics have worked through these challenges batch after batch. This is key for research teams and production departments scaling up pilot runs into full production.

    Applications in Modern Chemistry

    Product decisions ripple through supply chains. 2,3,4-Trifluorobromobenzene finds its value in providing reliable starting material along a chain of transformations. Its most common application involves nucleophilic aromatic substitution and cross-coupling reactions, especially Suzuki, Buchwald-Hartwig, and Ullmann-type couplings. The bromine atom is a handle for these reactions; the ring’s particular fluorine substitution can drive either selectivity or help achieve a challenging transformation that would otherwise require multiple synthetic steps. For instance, medicinal chemists often use this intermediate to construct novel aromatic scaffolds bearing combinations of fluoro and functional groups, which are highly sought in drug screening for their metabolic stability.

    Agrochemical developers have also pushed for highly electron-withdrawing fluoroarene motifs. In this setting, 2,3,4-Trifluorobromobenzene serves not only as a substructure but as a flexible module for tuning herbicidal and pesticidal molecules. Reactions on the aromatic core permit late-stage functionalization, which increases efficiency and reduces total waste. On the manufacturing floor, the advantages are clearer: the compound's boiling point, manageable vapor pressure, and crystalline nature allow for fewer ventilation concerns during drum filling or vessel charging.

    Academic groups and process chemists report that using 2,3,4-Trifluorobromobenzene saves time versus starting from less fluorinated precursors. By inserting the trifluoro motifs early, synthetic routes can omit hazardous fluorination steps that risk exotherms or require specialized HF handling. Moreover, the product dissolves easily in widely used organic solvents, which helps during all steps from reaction to work-up and crystallization.

    Specifications and Handling in Manufacturing

    The purity of 2,3,4-Trifluorobromobenzene is more than a number on a datasheet; it directly shapes the ease of downstream separations and the reliability of analytical data. As a group, manufacturers have standardized on specifications above 99 percent, limiting water, acid bromide content, and other halogenated impurities. Traditional methods, such as gas chromatography and NMR, combine with more recent real-time analytical tools for lot release. The addition of online sample tracking and robust documentation processes ensures full traceability from raw material intake through finished goods shipments.

    Tolerances for discoloration, melting point, and solvent residue are set based on actual user feedback. Production facilities implementing closed transfer lines and jacketed vessels have found that airborne contamination or humidity pick-up can undermine even the best purification regime, especially during periods of high throughput. By investing in better containment and real-time moisture monitoring, manufacturers have reduced product rejection and recall rates over tenfold.

    The needs of large users often require deviations from standard drum quantities, so bulk supply and packaging have become routine. Intermediate-sized containers and lined ISO tanks protect material during long-haul shipments or extended storage. Storage best practices recommend a cool, dry environment — experience has shown that direct sunlight, even short-term, accelerates degradation and impacts both the handling characteristics and chemical integrity of the material.

    Practical Differences from Other Halogenated Aromatics

    Chemists comparing 2,3,4-Trifluorobromobenzene to other halogenated benzenes notice differences starting with its melting and boiling points. Unlike lighter mono- or difluorinated bromobenzenes, the trifluoro pattern tunes the product’s volatility, which impacts how engineers handle distillation and solvent recovery. Attempts to swap with either 2,4,5- or 3,4,5-trifluorinated versions almost never replicate the same chemical behavior, since the electronic properties depend on both the type and position of halogens. These effects show up during coupling reactions where catalyst loading, base compatibility, or solvent selection can shift dramatically as the substitution around the ring changes.

    For those who have handled 2,3,4-Trifluorobromobenzene in production, color and physical state consistency provide clues about impurity profiles. Some similar bromofluoro compounds suffer darkening or form oils with storage, complicating dosing and charging. This product, when made under strict conditions, holds a nearly colorless, crystalline character for months under the right conditions. Managing isomeric purity requires careful process control and targeted purification steps, since side products or over-bromination can compromise reproducibility in later synthetic stages.

    Challenges and Solutions in Manufacturing and Usage

    No process exists without hurdles. Fluorination steps demand careful selection of reagents and process controls. Historically, manufacturers struggled to control side reactions during bromination of fluorinated rings, especially under harsh conditions or scale-up, where yield or selectivity could collapse. This challenge pushed process innovation, leading factories to adopt continuous-flow systems and improved reactor designs that deliver halogenation with fewer hot spots and more even mixing.

    After bromination, the product requires purification steps to strip byproducts such as dibromo- or polyfluorinated impurities. Early on, distillation and recrystallization created yield loss and safety risks from over-heating. Modern installations now integrate low-temperature crystallization, using solvent systems tuned to maximize recovery while safeguarding worker safety. Process analytics track not only target content, but residual water, halide balance, and color to ensure every batch moves through packaging without performance drift.

    Disposal and recycling emerge as pain points—halogenated residues and spent solvents often face stringent controls. Full-lifecycle planning on the plant floor makes recovery and recycling essential. Engineers have redirected these waste streams through incineration units with off-gas scrubbing, or by designing closed systems that return recovered solvents directly to upstream steps.

    Supply reliability becomes a second challenge, particularly for customers locking in longer-term campaigns that cannot tolerate finished-goods shortages. As a response, manufacturers have invested in dual-source fluorine supply lines, local bromine storage tanks, and IT-driven raw material monitoring. These investments limit downtime from upstream logistics snags, and during periods of global price spikes, these reserves buffer production and help keep customer lines running.

    Worker Safety and Environmental Commitment

    The direct handling of organofluorine compounds always brings unique risk. Over the years, chemical plants have invested heavily in local exhaust, vapor monitoring, and operator training while working with 2,3,4-Trifluorobromobenzene. Experience taught that even modest accidental releases can cause persistent odors or impact plant hygiene. To counter this, most manufacturers established perimeter vapor detectors and scheduled routine PPE and process safety audits. Closed charging of reactors and double-sealed transfer hoses minimize releases and keep both products and workers safe.

    Environmental watchdogs pay close attention to halogenated aromatic production, particularly for wastewater and vent gases. Modern manufacturers now operate zero-liquid discharge or closed-loop water systems for these production lines. Neutralization tanks, carbon beds, and catalytic incinerators remove any emissions before they leave the site. Compliance with international chemical control regimes gets built in from process development, avoiding retrofit headaches and smoothing the transfer of material across borders.

    Supporting Innovation in Downstream Applications

    Research and development teams often provide the first glimpse at where new demand for trifluorinated aromatics will come from. The stories returning from the lab range from pharmaceutical screening hits to new agrochemical leads requiring scalable, reproducible intermediates. Here, 2,3,4-Trifluorobromobenzene has enabled chemists to design reactions with higher yields or improved selectivity, compared with previous generations of intermediates. The consistency of supply and documented manufacturing controls let research shift quickly from gram-scale discovery to pilot and production batches.

    Long-term partners in pharmaceutical and agrochemical development have pushed manufacturers to offer more than just product. Collaboration on custom packaging, delivery forms, and on-site storage solutions have all grown straight out of experience managing specialized projects and new regulatory requirements. This level of transparency has led to better documentation, more accessible compliance support, and a feedback loop that improves product every year. The needs of end users in regulated industries focus the plant on ways to add certainty and minimize surprises.

    Trends in Market Demand and Supply Chain Resilience

    External markets change with geopolitical shifts and more demanding regulatory oversight. Fluctuations in the fluorspar and bromine markets can create uncertainty in production planning. Several major chemical manufacturers have responded by qualifying additional raw-material providers, investing in inventory buffers, and sharing risk data more openly with customers. As demand for specialty trifluorinated aromatics has grown, especially with the rise in fluoroarene-based pharmaceuticals, the entire supply chain needed to become more seamless.

    Experience managing product launches and rapid ramp-up schedules demonstrates that those on the ground—operators, quality managers, logistics teams—determine whether thousands of kilos can roll safely out the door without delay. This deep expertise, built through years of troubleshooting and continuous improvement, adds resilience when demand spikes or when a new application emerges from a research pipeline. In collaboration with users, manufacturers have developed customer forecasts, built-in redundancy, and improved digital tracking for both inbound and outbound shipments.

    In the broader discussion around strategic stockpiling and international movement of raw materials, chemical plants producing 2,3,4-Trifluorobromobenzene have seen pressure to uphold not only reliability but also transparency. End-to-end tracking, from incoming fluorine and bromine shipments through final lot release, provides peace of mind to both regulatory agencies and business partners. By adopting more advanced analytics and supply chain software, manufacturers have gained insight into potential jams before they develop into full-scale outages.

    The Realities of Production: No Substitute for Process Experience

    Those managing production schedules understand that chemical synthesis never boils down to a single reactor or reaction. Equipment selection, from agitator geometry to condenser duty, directly impacts throughput and impurity control during the bromination and purification of 2,3,4-Trifluorobromobenzene. Tight collaboration between process development, operations, and quality teams lets feedback cycle quickly, flagging even minor shifts in process variables that could affect the final product.

    Over the years, plant operators and process engineers have accumulated a library of solvent blends, quench protocols, and stabilization steps that prevent product drift or packaging failures. For products headed into high-purity applications, any overlooked change in process water or vessel passivation will reveal itself in downstream yields or residue profiles. This practical knowledge cannot be outsourced—only learned batch by batch and validated through years of consistent shipment.

    During audits or customer visits, the ability to back up every lot with process documentation and transparent analytical records gives partners the confidence to make long-term commitments. Working side by side with downstream users, manufacturers have even been able to anticipate changes in demand or application trends. This kind of responsive partnership strengthens knowledge on both ends, building a level of trust that rigid specifications and spreadsheets cannot deliver.

    Reflecting on What Sets Quality Apart

    Quality in 2,3,4-Trifluorobromobenzene emerges from more than just technical descriptors. The path from raw material through finished product weaves together thorough process design, robust analytical controls, and a workforce that takes pride in every step. Years spent troubleshooting yields, climbing inside reactors for inspection, and walking end users through technical adoption have shaped today's standards.

    Each kilogram that leaves a facility represents not only the performance of a single reaction, but the sum of all lessons learned: the temperature ramp profiles that best defend against side reactions, the blend of solvents that keeps the product crystalline, and the batch-to-batch adjustments that keep impurity profiles controlled even as input streams fluctuate. As customers push towards more efficient, more sustainable production, ongoing investment in plant upgrades, supply chain resilience, and digital inventory tracking will define long-term value.

    The market for halogenated intermediates like 2,3,4-Trifluorobromobenzene will continue to evolve. Chemical manufacturers who combine practical experience, investment in safety and stewardship, and a willingness to adapt production for new challenges deliver not just a compound—but a partnership that supports innovation where it matters most.