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3-Bromo-2-Fluorobenzotrifluoride

    • Product Name 3-Bromo-2-Fluorobenzotrifluoride
    • Alias 3-Bromo-2-fluoro-(trifluoromethyl)benzene
    • Einecs 813-655-7
    • 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

    882160

    Product Name 3-Bromo-2-Fluorobenzotrifluoride
    Cas Number 57381-58-7
    Molecular Formula C7H3BrF4
    Molecular Weight 243.00
    Appearance Colorless to pale yellow liquid
    Boiling Point 156-158°C
    Density 1.73 g/cm³
    Melting Point -12°C
    Refractive Index 1.460
    Purity ≥98%
    Flash Point 64°C
    Synonyms 1-Bromo-2-fluoro-3-(trifluoromethyl)benzene
    Solubility Insoluble in water; soluble in organic solvents
    Smiles FC1=CC(=CC(=C1)C(F)(F)F)Br
    Inchikey UMPODZWQKBOFNN-UHFFFAOYSA-N

    As an accredited 3-Bromo-2-Fluorobenzotrifluoride 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 100g of 3-Bromo-2-Fluorobenzotrifluoride, secured with a screw cap and labeled with hazard warnings.
    Shipping **Shipping Description for 3-Bromo-2-Fluorobenzotrifluoride:** Shipped in sealed, chemical-resistant containers, 3-Bromo-2-Fluorobenzotrifluoride is transported in compliance with relevant hazardous materials regulations. Packages are labeled according to safety guidelines and accompanied by a Safety Data Sheet (SDS). Protect from heat, moisture, and direct sunlight during transit. Handle with appropriate personal protective equipment.
    Storage 3-Bromo-2-Fluorobenzotrifluoride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from light, heat, and moisture. Ensure that storage areas are clearly labeled and that containers are kept upright to avoid leaks or spills. Handle using proper chemical safety precautions.
    Application of 3-Bromo-2-Fluorobenzotrifluoride

    Applications of 3-Bromo-2-Fluorobenzotrifluoride in Industrial Manufacturing

    Our advanced production facilities supply 3-Bromo-2-Fluorobenzotrifluoride primarily to specialized manufacturers in the pharmaceutical, agrochemical, electronic chemicals, and liquid crystal materials industries. The material’s performance and compatibility profile allows precise integration into multistep synthesis, contributing to key downstream products with strict regulatory and quality requirements.

    1. Pharmaceutical Intermediate Synthesis

    3-Bromo-2-Fluorobenzotrifluoride serves as a halogenated aromatic building block in the manufacture of advanced pharmaceutical intermediates, where its substitution pattern assists in designing molecules with targeted bioactivity and improved metabolic stability. Companies rely on this compound to introduce trifluoromethyl- and bromo-functionality into complex core structures during the late stages of active pharmaceutical ingredient (API) synthesis, especially for anti-infective and oncology candidates. Production lines use it for Suzuki-Miyaura, Buchwald-Hartwig, and N-arylation coupling reactions under GMP conditions, supporting scalable lot sizes with full traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) and European Pharmacopoeia (Ph. Eur.) guidelines on residual solvents and impurities
    • FDA 21 CFR 210/211 Current Good Manufacturing Practice (cGMP)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.2 to 1.0 molar equivalents per coupling reaction, varies according to target molecule substitution; scale adjusted for batchwise or continuous production

    Downstream process integration

    • Charged after initial ring construction, typically as a final-step reactant for halogenation or cross-coupling in reactor synthesis lines

    Final product types

    • Advanced pharmaceutical intermediates for small molecule APIs, especially kinase inhibitors and anti-viral agents
    • Registered drug substance intermediates for R&D and commercial production

    2. Agrochemical Active Ingredient Synthesis

    Leading crop protection manufacturers use this specialty halogenated aromatic as a building block in patent-protected fungicide and herbicide molecule construction. It features in Grignard, direct arylation, or nucleophilic aromatic substitution reactions, supporting the selective introduction of fluoro and trifluoromethyl moieties that can enhance environmental stability and optimize field performance. Process teams work with multi-ton batches and require narrow impurity profiles to meet increasingly strict regulatory residue limits, ensuring consistent downstream performance in field applications.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals (Section 1: Physical-Chemical Properties & Section 5: Pesticides)
    • EPA 40 CFR Part 158 (Data Requirements for Pesticide Registration)
    • ISO 17025 Laboratory Testing for Residues

    Typical usage ratio

    • Typically 0.5 to 1.5 equivalents per reaction step, calculated according to the stoichiometry of the targeted active structure; optimization based on reaction yield and impurity management

    Downstream process integration

    • Introduced after substrate activation or as an electrophilic component in halogen exchange reactions during the penultimate or final synthesis stages

    Final product types

    • Key intermediates for fluorinated herbicides and triazole fungicides
    • Custom agrochemical building blocks for development of new pesticide molecules

    3. Electronic Chemicals: Liquid Crystal Intermediates

    Display component manufacturers rely on the purity and reproducibility of this aromatic compound for synthesizing liquid crystal precursors, where specific fluorinated and trifluoromethyl groups are required to achieve precise dielectric constants and temperature-dependent viscosity in end-use panels. Customers integrate the compound via directed ortho-metalation or lithium–halogen exchange processes to tailor unique biphenyl or phenylbenzoate structures for thin-film transistor (TFT) and high-resolution LCD display units, where batch-to-batch quality directly impacts downstream color performance and switching speed.

    Industry compliance standards

    • IEC 61249-2-41 (Materials for printed boards—Sectional specification for base materials for use in electronic equipment)
    • RoHS Directive 2011/65/EU for restriction of hazardous substances
    • IPC-4101E: Specification for Base Materials for Rigid and Multilayer Printed Boards
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Typically 0.3–1.2 equivalents depending on the ring substitution density required per downstream precursor synthesis; optimized according to dielectric property targets

    Downstream process integration

    • Fed into microreactor or flow chemistry units to synthesize biphenyl derivatives for subsequent esterification and fluorination steps, supporting continuous production lines

    Final product types

    • Liquid crystal mixtures for use in TFT-LCD panels, measurement devices, and optical shutters
    • Specialty fluorinated intermediates for organic light-emitting diode (OLED) host materials

    4. Advanced Material Coatings: High-Performance Polymer Modifier

    Producers of specialty fluorinated polymers and weather-resistant coatings integrate this compound as a monomer initiator or chain modifier, harnessing its trifluoromethyl functionality to impart chemical inertness and reduce surface energy in the end polymer. It enters production during copolymerization or grafting reactions, modifying backbone properties to improve solvent resistance and long-term environmental durability of engineered coatings for electronics and industrial components. Strict process controls and documentation are observed to meet quality consistency requirements for critical protection layers.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for Registration, Evaluation, Authorisation and Restriction of Chemicals
    • ASTM D5201 for chemical resistance testing of coatings
    • ISO 14001:2015 Environmental Management Systems
    • RoHS Directive 2011/65/EU

    Typical usage ratio

    • Used at 0.5–2.5% weight ratio in polymer feedstock; adjusted based on target coating thickness and performance property requirements

    Downstream process integration

    • Blended with base monomers and polymerization catalysts during initial feed preparation; functionalized through radical or anionic copolymerization steps

    Final product types

    • Fluorinated polymer coatings for electronic circuit protection, high-voltage insulators, and chemical process piping
    • Engineered weatherproof coatings for automotive and aerospace applications
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    Certification & Compliance
    More Introduction

    3-Bromo-2-Fluorobenzotrifluoride (Model: 71772-81-5) – A Manufacturer's Perspective

    Understanding the Chemistry and Its Place in Synthesis

    In the fine and specialty chemicals business, each compound plays its own set of roles, and 3-Bromo-2-Fluorobenzotrifluoride stands out as a versatile intermediate that helps drive innovation in pharmaceuticals, agrochemicals, and advanced materials. From our manufacturing floor, the path from raw materials to this trifluoromethylated aromatic compound reflects both technical precision and industry knowledge built over years. Made through a controlled process involving electrophilic aromatic substitution and halogen exchange, this product reaches the required purity above 99% by GC, crucial in downstream applications. Lot after lot, our production ensures a free-flowing, white to light pale powder with a melting point range checked for consistency, not because specification sheets demand it, but because an off-spec batch can ripple through a customer’s own process line. The faint, characteristic odor signals the underlying aromatic ring structure, never a stray note in the entire batch if our conditions stay accurate.

    Putting the Molecule to Work – Real Uses and Insights

    3-Bromo-2-Fluorobenzotrifluoride draws attention because of the combination of bromine, fluorine, and the trifluoromethyl group on a single benzene backbone. Each functional group opens a new window for synthetic possibilities. Customers in pharma research often choose this molecular scaffold to build candidate molecules, especially where electron-withdrawing effects from CF3 and F tune the biological activity. The ortho-bromo substituent offers a direct handle for Suzuki, Stille, or Buchwald-Hartwig coupling—cross-couplings we know almost every specialty lab runs at one point or another. The fluorine atom, orthogonal to the bromo, can provide unique SAR (structure-activity relationship) options without introducing metabolic liability that other substituents might cause. Agrochemical clients rely on the inherent stability the trifluoromethyl group delivers. That ring holds up well against oxidative enzymes out in the field, resisting photolytic breakdown, which translates to longer effectiveness in herbicides or fungicides.

    Beyond these primary fields, material scientists and electronics researchers know that halogenated trifluoromethyl aromatics become important in creating high-performance polymers, liquid crystals, and specific coatings. Real manufacturing environments don’t tolerate lag. If a batch goes out the door with less than 99% GC, downstream crystallizations might fail, wastes increase, and timelines slip. Our hands-on monitoring reduces these headaches before the compound leaves our floor.

    The Manufacturing View – Purity, Handling, and Scale

    Every batch of 3-Bromo-2-Fluorobenzotrifluoride we make starts from certified suppliers whose own audit and testing align with our standards. From there, we use a halogenation step under controlled low temperature to avoid polysubstitution, followed by careful crystallization. Our operators use jacketed reactors with digital feedback—a setup that seems like overkill sometimes, but subtle impurities like dibromo derivatives can hide in traditional equipment. These aren’t textbook problems; they’re real issues that cost both time and trust. We wash, filter, and dry the product under reduced pressure, packaging it in sealed drums or carboys with nitrogen atmosphere to keep its quality stable through shipment. Customers who’ve experienced delays due to off-odors, caking, or discoloration know why tight environmental controls during synthesis and storage matter.

    We run particle size checks after drying because downstream milling wastes both solvent and time. You can feel the difference unloading free-flowing powder compared to a compacted lump. Static discharge and dust formation can crop up; with fluorinated aromatics, these aren’t theoretical hazards. Exhaust ventilation and double-gloving practices are standard; long years in this field make shortcuts unthinkable.

    What Sets 3-Bromo-2-Fluorobenzotrifluoride Apart

    Chemists often ask us, why choose this molecule over other brominated or fluorinated aromatics, like 2-Bromo-4-Fluorobenzotrifluoride or straightforward bromobenzotrifluoride? Three main differences stand out. The position of the substituents here lends itself far better to cross-coupling and nucleophilic substitution than more symmetrical analogs. The fluorine at the ortho-position tunes both reactivity at the bromo-site and electronic contribution to the overall ring, allowing more selective transformations. Trifluoromethylated rings frequently show enhanced stability and lipophilicity, important for drug design and bioavailability. By having both bromine and fluorine in these positions, researchers can optimize without swapping the core scaffold for each new lead.

    No two synthetic projects look alike. We’ve watched customers switch from other trifluoromethyl aromatics to this specific compound after control reactions show tighter selectivity or improved yields using this scaffold. The differences aren’t always dramatic on paper, but in multi-step campaigns, shaving two points off a purification step makes all the difference by the end.

    Applications and Industry Feedback

    Our product moves most often to R&D labs at pharmaceutical companies designing kinase inhibitors, central nervous system therapies, and crop protection developers screening for novel action modes. Unlike pan-reactive halogenated aromatics, 3-Bromo-2-Fluorobenzotrifluoride offers both selective reactivity and consistent behavior under a variety of chemistries, including palladium catalysis, nucleophilic substitutions, and aromatic substitution.

    Agricultural chemists report fewer degradation byproducts in field trials using this molecule as a building block compared to single-halogen analogs. A few material science groups requested larger volumes for process scale-up, especially those tweaking dielectric constants in specialty films—the molecule’s high thermal and chemical resistance lines up with their property requirements. Throughout these sectors, the most common feedback is about batch consistency, reproducibility in reactions, and the ability to receive the product when production ramps up. Repeat customers come back asking for adjusted drum size or improved packaging more often than for changes in the chemical structure.

    Why Quality and Consistency Define Value

    Decades in chemical synthesis have taught us the hard way that it takes more than following a published route to deliver a product like 3-Bromo-2-Fluorobenzotrifluoride that researchers and process chemists can trust. Upstream impurities can quietly poison a cross-coupling reaction without obvious clues at first glance. Tiny changes in product color, melting point, or odor often signal that a catalyst or workup step needs tightening. Our team doesn’t wait for a customer complaint—routine checks, NMR scans, and impurity profiling look for red flags before product lands on a truck, because it saves everyone time and repeated troubleshooting.

    We do more than ship bottles. Our experts routinely field calls from process chemists about scaling up—solvent swaps, reaction exotherms, or whether a batch needs to be re-crystallized on their end to meet their own specs. Our technical QC team can trace back a particular lot to every step, including solvent batches and drying parameters. We maintain these records, not because regulators insist, but because clients with a rushed deadline need fast, practical answers, not templated SOP responses.

    Reducing Environmental Footprint – The Manufacturing Angle

    Environmental pressure on halogenated organics is rising, especially as regulatory bodies tighten rules about waste, emissions, and downstream safety. Our operations rely on closed-loop systems that recover both solvent and reaction byproducts. The focus isn’t just sustainability marketing—solvent recovery and proper waste handling lower costs and avoid buildup of halogen residuals in site effluent. Over the last three years, stricter air and water testing helped us rework our scrubbing and dehalogenation steps, ensuring both local compliance and peace of mind for our workforce.

    We also streamline logistics by scheduling runs for similar products in campaign mode, limiting changeovers that generate more waste. Now, instead of ramping up incinerator use, we integrate waste bromide into other processes down the line. Shippers now prefer drum types we pioneered to reduce in-transit risk and leakage, beneficial for both safety and regulatory paperwork.

    Safety, Handling, and Long-Term Storage

    Operators learn quickly—getting a nose-full of strong organic halide proves why proper fume hoods and extraction fans can’t be skipped. Though 3-Bromo-2-Fluorobenzotrifluoride isn’t acutely toxic, regular glove and goggle use remains SOP for a reason. We offer drum packaging that minimizes vapor escape, and batch certifications accompany every shipment, recording analytical results by HPLC, NMR, and GC. Customers tell us even small packaging changes—double-seal liners or nitrogen padding—make a visible difference in their own benchtop practice and longer-term storage.

    Statistical process control graphs in our facility aren’t there for show. Trending small changes in impurity profiles or handling issues enable us to improve ventilation design and valve selection year after year. If powders show signs of caking or if color shifts outside the norm, we act fast. Sometimes that means holding back a shipment; sometimes, it requires a redesign of a drying basket or a packaging closure. These are stories that don’t make marketing copy, but risk-averse chemists in our customer network appreciate the up-front honesty that comes from direct manufacturing oversight.

    Comparing with Other Aromatic Halides and Trifluoromethylated Compounds

    Chemists often debate which trifluoromethylated aryl bromide to use, especially for iterative synthesis. Some see potential in 4-bromo derivatives—reactions run faster, but the 2-bromo, 2-fluoro arrangement unlocks more specific substitution patterns in target molecules. Coupling yields stay higher on account of less deactivation by neighboring fluorine, and for several classes of agrochemical actives, metabolic pathways follow different routes depending on placement of bromo and fluoro groups.

    Some labs test 2,6-dibromo analogs, but steric hindrance leads to incomplete couplings and higher metal content in finished APIs. We see fewer problems in workups with our 3-Bromo-2-Fluorobenzotrifluoride because its planar geometry and weaker steric crowding allow more straightforward purification. For scientists scaling up, this difference in downstream cleanup has real impact—a day saved on chromatography frees up resources and keeps projects on budget. It’s this practical knowledge, picked up batch after batch, that matters far more than catalog data or theoretical reactivity maps.

    Supply Chain, Bulk Delivery, and Customization

    Most customers working in kilo quantities don’t want fixed-quantity jars or variable purity blends. Custom drum sizing and real-time logistic tracking improve both planning and flexibility on the user’s end. We ship from bulk reactors directly to conditioned storage, and seasonal demand spikes taught us to keep larger volumes ready to avoid supply disruptions. Experienced buyers appreciate these background steps—no one wants an R&D milestone missed because a supplier couldn’t deliver, and process chemists need continuity in every delivery cycle.

    Special requests for handling recommendations in particular reactions are common, especially among new process teams who haven’t run halogenated trifluoromethyl aromatics at scale before. Advice around stirring speed, loading protocols, or in-line sampling came from years of seeing what works and what leads to costly rework. Those bits of wisdom often matter as much as the product’s formal certificate.

    Reliability and Long-Term Relationships – A Manufacturer’s Perspective

    Every kilo of 3-Bromo-2-Fluorobenzotrifluoride goes out with a record behind it—a record built by the operators, QC analysts, and tech managers who put their name to that lot. We’ve watched research chemists return for more material after early hits in their screens, and process developers scale from bench to pilot. Consistency and real-world advice drive these relationships, not just price per kilo. Sometimes the questions are simple—like ideal storage temperature or compatibility with a new solvent system. Other times, customers call about one-off crystal forms, trace metal content, or residual solvent problems in their own campaigns. Flexibility and quick troubleshooting separate direct manufacturers from resellers—sourcing directly from us means answers rooted in actual production, not just catalog claims.

    We face increasing scrutiny about product traceability and safety, both from customers and regulatory bodies. Batch printouts, in-process analysis, and chain-of-custody logs have moved from good practice to daily requirement. Years ago, small deviations might have slipped through; today’s standards require a tighter discipline. Sharing this information with clients directly, and offering supporting data instead of boilerplate statements, sets the groundwork for trust and repeat business.

    Looking Ahead – Adaptation and Smart Manufacturing

    3-Bromo-2-Fluorobenzotrifluoride remains a key intermediate for many customers whose own fields evolve quickly. As new synthetic routes emerge and next-generation drugs or advanced materials reach development, demand patterns and required specifications shift. We have invested in modular scale-up equipment, digital material tracking, and in-house analytical capacity that allows us to handle both kilo-scale pilot lots and multi-ton manufacturing. Commitment to direct feedback, technical support, and process transparency ties every department in our plant—not just R&D—to the needs of our customers. Over years, the best improvements and process interventions have come not from boardroom ideas but from hard-earned experience on the manufacturing floor and in customer labs.

    Summary of Key Differences and Practical Knowledge

    3-Bromo-2-Fluorobenzotrifluoride offers a balance of reactivity, stability, and synthetic utility unmatched by close analogs. Its specific arrangement of bromo, fluoro, and trifluoromethyl groups on the benzene ring unlocks application options for pharma, agro, and material science. Direct manufacturing brings insights into handleability, shipping, and scale-up—details often missing from generic datasheets. Real differences live not just in GC or NMR numbers, but in how easily a lot gets dissolved, filtered, stored, or loaded onto a reactor. Working with those details every day gives us a firm understanding of both molecule and market, shaping every batch of product before it lands in your hands.