Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid

    • Product Name 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid
    • Alias (2-Fluoro-5-(trifluoromethyl)phenyl)boronic acid
    • Einecs 410-020-2
    • 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

    958103

    Productname 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid
    Casnumber 871329-21-2
    Molecularformula C7H5BF4O2
    Molecularweight 208.92
    Appearance White to off-white solid
    Meltingpoint 110-114°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥ 97%
    Smiles B(C1=CC(C(F)(F)F)=CC=C1F)(O)O
    Inchi InChI=1S/C7H5BF4O2/c9-6-2-1-4(7(10,11)12)3-5(6)8(13)14/h1-3,13-14H
    Storageconditions Store in a cool, dry place; protect from moisture and light
    Synonyms 2-Fluoro-5-(trifluoromethyl)benzeneboronic acid

    As an accredited 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 1-gram amber glass vial with a secure screw cap; labeled with product name, quantity, and hazard warnings.
    Shipping **Shipping Description:** 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid is shipped in a tightly sealed container, protected from moisture and light. It is packed in compliance with relevant chemical transport regulations, labeled with appropriate hazard information, and typically shipped at ambient temperature unless otherwise specified by the manufacturer’s recommendations. Handle with suitable protective equipment upon receipt.
    Storage Store **2-Fluoro-5-(trifluoromethyl)phenylboronic acid** in a tightly sealed container under an inert atmosphere (such as nitrogen or argon) to prevent moisture uptake and decomposition. Keep it in a cool, dry place, away from direct light and incompatible materials such as strong oxidizing agents. Recommended storage temperature is 2–8°C (refrigerator). Avoid prolonged exposure to air and humidity.
    Application of 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid

    Applications of 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid in Industrial Manufacturing

    As a manufacturer specializing in 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid, we serve a global base of industrial partners across pharmaceutical intermediates, agrochemical synthesis, specialty chemicals, and advanced material production. Our technical team works closely with formulation scientists and plant engineers to ensure consistent material quality aligns with both strict regulatory requirements and unique end-use processing demands.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use our material primarily in Suzuki-Miyaura cross-coupling as a key building block for fluorinated drug molecules, particularly where high metabolic stability and receptor selectivity are essential. The precise modification of active pharmaceutical ingredient (API) backbones requires careful adjustment of boronic acid concentration to control side reactions and ensure regulatory purity benchmarks in multi-step small-molecule programs.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Parts 210/211 (US FDA cGMP)
    • EU GMP Part II (APIs)
    • USP/NF Monographs (where applicable to intermediates or final APIs)

    Typical usage ratio

    • 0.45–1.2 molar equivalents per aryl halide substrate, tailored based on target step yield and minimization of by-products

    Downstream process integration

    • Charged during the C–C bond-forming stage in batch or continuous stirred-tank reactors, following reactor charging and before catalyst introduction
    • Post reaction, crude mixtures require flash chromatography or crystallization for purification prior to downstream derivatization steps

    Final product types

    • Fluorinated drug candidates for oncology, anti-infective, and CNS indications
    • Advanced pharmaceutical intermediates for contract development and manufacturing organizations (CDMOs)

    2. Crop Protection Active Ingredient Development

    Leading agrochemical companies deploy this boronic acid in the synthesis of trifluoromethylated heterocyclic scaffolds, where the introduction of electron-withdrawing groups enhances both target pest specificity and field stability. Integration generally occurs in mid-stage flow-chemistry platforms or automated combinatorial reactors to develop pipeline herbicides and fungicides compliant with evolving global MRLs and ecotoxicology demands.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 (Quality Management Systems in Agrochemical Production)
    • Regulation (EC) No 1107/2009 (EU Market Authorization for Crop Protection Products)
    • OECD Guidelines for the Testing of Chemicals (Section 1 and 2: Physical-Chemical Properties, Effects on Biotic Systems)

    Typical usage ratio

    • 0.8–1.5 molar equivalents per coupling partner, dependent on core scaffold design and reactivity of leaving group substrates

    Downstream process integration

    • Mainly introduced post-halogenation in high-throughput modular flow reactors; process monitored with HPLC or GC-MS prior to downstream cyclization
    • Incorporated as late-stage fluorinated vector for structure-activity-relationship (SAR) libraries

    Final product types

    • Selective herbicide actives (e.g., aryl-triazole and aryl-pyrimidine classes)
    • Fungicidal intermediates containing CF3-phenyl motifs

    3. Electronic and OLED Material Synthesis

    Developers of next-generation organic electronic materials employ this boronic acid to build high-purity, fluorinated aryl units in custom OLED emitters and charge-transport layers. Purity control is essential to prevent electrical defects during device fabrication. The fluorinated structure modifies both electron mobility and photostability, contributing to extended operational lifetimes in commercial display and lighting applications.

    Industry compliance standards

    • SEMATECH/International SEMI Standards for Organic Optoelectronic Materials
    • ISO 14001:2015 (Environmental Management in Electronic Specialty Chemicals)
    • IEC 62341 Family (OLED Device Performance and Reliability Testing)

    Typical usage ratio

    • 0.65–1.1 molar equivalents relative to complementary aryl halide, modulated for purity specification of >99.5% in semiconductor layers

    Downstream process integration

    • Integrated in solution-phase coupling reactors as part of multi-step syntheses for emitting or hole-transport layers
    • Final products purified using preparative column chromatography and vacuum sublimation to meet optoelectronic grade specifications

    Final product types

    • OLED display emitters (blue, green, and red pixel materials)
    • Fluorinated charge-transport intermediates for display backplanes

    4. Advanced Specialty Polymer Synthesis

    Specialty polymer manufacturers adopt this compound for the creation of high-performance, fluorinated polyarylenes and block copolymers used in membranes, coatings, and separation technologies. The boronic acid’s unique electronic profile enables the synthesis of materials with increased chemical resistance and reduced surface energy, important in applications such as battery separators and anti-fouling films for industrial filtration systems.

    Industry compliance standards

    • ASTM D882/D3983 (Film Tensile Properties and Thermal Endurance)
    • ISO 9001:2015 (Quality Management in Polymer Processing)
    • REACH Regulation (EC) No 1907/2006 (Polymer Chemical Registration)

    Typical usage ratio

    • 3–8% by weight (wt%) of total monomer mass in co-polymerization, adjusted based on backbone reactivity and targeted mechanical properties

    Downstream process integration

    • Added during the prepolymer feed stage of solution or suspension polymerization reactions, following catalyst charging
    • Ensures uniform incorporation into block copolymer chains; typically followed by precipitation and membrane formation under inert atmosphere

    Final product types

    • Battery separator films for advanced lithium-ion and sodium-ion batteries
    • Fluorinated membrane sheets for industrial ultrafiltration and pervaporation
    • Anti-fouling specialty coatings

    5. Fine Chemical Building Block for Research & Development

    Contract research organizations (CROs) and chemical discovery labs utilize this boronic acid to introduce both fluorine and trifluoromethyl substituents into benzenoid frameworks, supporting proprietary structure-activity screenings and analytical reference standard development. R&D settings require flexible charge quantities and documentation to trace chemical origin, purity, and lot-specific analytical validation.

    Industry compliance standards

    • ISO/IEC 17025:2017 (General Requirements for Testing and Calibration Laboratories)
    • GLP (Good Laboratory Practice) Compliance where applicable
    • GHS/CLP Labeling for laboratory chemical handling

    Typical usage ratio

    • 0.2–1.0 molar equivalents by project requirement; small-scale SAR and reference standard syntheses frequently adjust loadings for purity or analytical comparison

    Downstream process integration

    • Applied in microwave-assisted cross-coupling or parallel library syntheses in microreactor systems, often followed by LC-MS or NMR validation
    • Hand-dosed or automated liquid handling in miniaturized batch experiments

    Final product types

    • Custom reference standards for regulated pharmaceutical and agrochemical testing
    • Structure-activity research compounds for medicinal chemistry and agrochemical development pipelines
    Free Quote

    Competitive 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid: Practical Experience from a Chemical Manufacturer

    Introducing a Specialized Building Block for Modern Synthesis

    Working inside a chemical factory gives a clear perspective on how each raw material shapes the pace and possibilities of research and production. Take 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid as an example. Years spent in process optimization and batch production underline its importance for chemists who focus on pharmaceuticals, agrochemicals, and advanced materials. This compound isn't just another entry on a product list. Its structure, marked by a boronic acid group joined to a highly substituted fluorinated aromatic ring, supports demanding Suzuki–Miyaura couplings and other cross-coupling reactions where selectivity and stability make or break a project.

    Structure, Purity, and Real-World Handling

    This molecule offers a unique combination: a phenyl ring substituted with both a fluorine atom and a bulky trifluoromethyl group. That means chemists gain access to fluorinated motifs with minimal post-reaction modification. The purity of the product isn't something left to regulatory documentation—in daily plant practice, consistently reaching LC-MS purities above 98% means fewer failed reactions downstream. Our team handles both bulk drums and small-batch orders, and we track each lot’s melting points and water content because it directly impacts solubility and reactivity on the bench.

    Why Consistency Matters: Lessons from the Plant Floor

    Anyone who has monitored a reaction where moisture crept in knows the headaches that follow. 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid will hydrolyze if left exposed, so controlling residual moisture during packaging avoids disaster mid-synthesis. After dozens of campaign runs, we know exact moisture levels and contamination risks. Even minor deviations in boronic acid purity or trace metal content can derail a Suzuki-coupling, so in-house quality checks extend beyond COA paperwork. Long experience shows clients appreciate batches that behave the same way every time, and it also reduces debugging time for scale-up chemists.

    Supporting Research and Production at Every Scale

    Research teams in both pharma and materials science struggle with stubborn aryl halides that resist coupling. The electron-withdrawing CF3 and F on this boronic acid don’t just alter reactivity—they open up access to target molecules that plain phenylboronic acid never could. Scale-ups from grams to multi-kilogram campaigns put strain on stock management, so a steady supply has to back every shipment. Our own plant allocation team works closely with R&D to anticipate changing annual demand: drug discovery surges, downstream synthesis spikes, and even regulatory-driven process modifications. This keeps real-world innovation moving rather than stalling for missing intermediates.

    Differences from Standard Phenylboronic Acids: A Practical Comparison

    Standard boronic acids serve routine Suzuki reactions, but once a project calls for site-selective substitutions or enhanced electronic effects, gaps open between generic reagents and this molecule. The fluorine atom and CF3 group don’t just alter polarity—they shut down unwanted side-reactions and improve yields for electron-poor targets. These effects show up starkly during late-stage functionalization, especially in heterocycle construction or arylation work. From our technical support desk, most troubleshooting calls come from teams who only realize these differences after mixed results in the lab. Over years supplying both the standard and fluorinated boronic acids, we track more repeat orders, fewer production hiccups, and significantly higher isolated yields from projects using this product. That feedback explains its growing market share year after year.

    Handling and Storage: Minimizing Losses and Maximizing Shelf-Life

    A lot of customers ask about storage. Our internal storage rooms keep 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid under N2 or dry air, sealed in amber bottles to protect it from light-induced decomposition. Forgetting this can mean moisture-induced oligomerization, which shows up as clumping or unexpected losses in reactivity. Packing staff monitor every batch—not as an afterthought, but because the cost of failed syntheses downstream often dwarfs any cost-saving shortcuts on the storage end. Labs with busy schedules depend on predictable performance, and our storage protocols reflect that through years of troubleshooting. Winter and summer temperature swings make a difference, especially in regions with humid climates.

    Environmental and Worker Health Considerations

    Process chemists spend as much time thinking about safe handling as about the chemistry itself. Boronic acids aren’t the most hazardous class out there, but strong ventilation, gloves, and direct skin protection remain standard precautions in our plant. The aromatic substitution pattern makes this molecule more volatile than some boronic acids, so exhaust systems are checked regularly and spill kits stand at workbench level. Each bulk shipment comes with its own containment plan, routed through environmental management teams. Site audits over the years emphasize that even low-frequency exposure to certain boronic acids can cause irritation, and our operators notice that strong chemical odors disappear when protocols stay tight.

    Supporting Regulatory Submission and Traceability Needs

    Research-driven companies, especially those in pharma, increasingly look for full traceability of every chemical reagent. This boronic acid, supplied by our plant from raw aromatic fluorination through to isolation and drying, supports these traceability demands with batch history and source-verifiable certificates. Over the past five years, regulatory audits have paid close attention to the chain of custody between raw material intake and final shipment. Our shift foremen and logistics teams learned to adapt: every kilo can be traced back through drying logs, purification records, even details as granular as the grade of drying agent used. Modern buyers recognize the critical link between documented traceability and successful submissions for drug or material approvals.

    Batch Variation, Process Optimization, and Customer Feedback

    Some compounds are more forgiving than others, but subtle variation in synthesis—whether it’s solvent ratios, catalyst loading, or temperature swings—shows up clearly in this class of boronic acids. We run side-by-side scale-up batches on identical starting material to minimize such variability, and we document all deviations before any shipment. When pilot customers reported inconsistent melting points two years ago, we reworked the crystallization process, shaving the standard deviation on assays by 40%. The result: smoother performance for downstream customers and fewer phone calls to technical support. On this product, small details at the plant relate directly to fewer lost workdays for our clients, and real cost savings.

    Application Stories: Successes and Setbacks from the Field

    Our technical team stays close with innovators who depend on this molecule, sharing stories both of breakthroughs and setbacks. In one case, a pharmaceutical research group switched from a generic phenylboronic acid to 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid, unlocking a new route for a kinase inhibitor study. Their previous attempts stalled at arylation, but the fluorinated variant pushed the reaction forward and increased isolated yield by twenty percent. In another case, a material science start-up struggled with batch-to-batch differences that boiled down to hidden impurities in their boronic acid supplier’s lots. By switching to our material and implementing side-by-side purity testing, their process reliability increased and they pushed past development hurdles that had set them back quarters. These stories echo what we hear in roundtables and customer support forums: a good batch makes all the difference.

    Supplying for R&D and Manufacturing: Flexibility in Fulfillment

    We notice that the lead time for a high-purity, specialty boronic acid can make or break a development schedule, especially when sudden shifts in project timelines happen. From kilo-scale drum orders down to gram samples for method development, our team builds extra stock around anticipated spikes. In rush cases, in-plant team leads coordinate packaging and release runs even on weekends. Over the past year, increased demand from Asia’s agrochemical sectors brought extra pressure on delivery windows, so plant teams trained in expedited order picking and shipping. People developing pilot processes value fast, reliable refills so experiments keep pace with the data they need. That attention to fulfillment turns into longer-term partnerships.

    Supporting Sustainable Manufacturing: Practical Steps over Theory

    The chemical industry faces real pressure to reduce waste and hazardous footprint, even for specialty reagents. For this boronic acid, we audit our waste streams every quarter, and new workstations focus on solvent reclamation and closed-system processing. Operators found that even minor tweaks in drying reduced both emissions and batch losses. In production, switching to more efficient crystallization solvents cut our energy consumption per kilo by twelve percent across three years. Fewer off-spec lots mean less raw material scrapped. As the plant pushes in this direction, every operator—from reaction kettle to QA—contributes feedback on process improvements. Our focus is on steps that work in practice, not just on paper.

    Trust and Know-How in Every Shipment

    Customers expect more than just a drum with a label; it’s the experience baked into every batch that keeps our relationships strong. By linking up with end users at each step, from order review to after-sales support, we catch challenges early and solve them with the technical detail that only comes from in-house manufacturing. Years of direct feedback build a knowledge base about what researchers actually see at the bench, not just what is supposed to happen from textbook reactions. These lessons feed back into plant SOPs, driving constant improvement in the way we synthesize, package, and support each order of 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid.

    Meeting the Challenge of Scale

    Often, a synthetic route or custom process proves itself in the lab, only to choke at scale. We pour thousands of hours into batch reproducibility, vigilance at every transfer, and feedback loops with quality control. Scale-up isn’t a simple matter of doubling volumes. The reactivity profile of the trifluoromethyl and fluorine-substituted ring system brings unique flow and heat transfer considerations, so our engineers constantly adapt plant infrastructure—whether it means updating glass reactor linings, improving agitation speeds, or installing more responsive temperature sensors. These hands-on improvements mean downstream chemists and formulators see less batch drift and more confidence in repeatable performance.

    Troubleshooting Common Obstacles

    Boronic acids, including this one, can suffer from oxygen or water sensitivity during storage or handling, which reduces available content for crucial cross-coupling reactions. After more than a decade of plant operation, we found that even small modifications to atmospheric controls, vacuum drying, and anti-static measures cut down batch spoilage rates. Lab staff keep routine checks for clumping and discoloration---signs of exposure or slow degradation. Fast identification and careful handling minimize surprises for clients at the bench. Our routine also includes sending quick technical notes with every shipment, so in-house teams know what to expect if conditions or reactivity seem odd.

    Growth and Innovation: Partnering Beyond Procurement

    The past few years brought more interaction with research partners who don’t just buy chemicals—they collaborate on custom process tweaks and new applications. The unique electronic properties of 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid led collaborative teams to develop novel ligands and explore cross-coupling in previously intractable systems. Bringing plant engineers into direct conversation with research scientists uncovered ways to speed up purification, cut solvent use, and refine crystallization. This isn’t just about moving metric tons; it’s about meeting new synthesis challenges head-on, delivering a quality-controlled product that supports cutting-edge research and stays ahead as demands change.

    Why Reliability in Sourcing Matters

    Supply interruptions threaten every stage of research and pilot manufacturing. From power outages to global supply chain shocks, chemical plants bear the brunt and learn to diversify sourcing and backup logistics. Because this boronic acid often plays a role late in a synthetic sequence, a missed delivery can risk entire project timelines. Our logistics team invests in multi-modal distribution, regionally staged inventory, and regular notification channels with customers. Real experience through years of disruptive events taught us: communication and operational flexibility outdo theoretical contingency plans every time. Customers planning clinical or production milestones sleep better knowing their critical reagents arrive as scheduled, batch after batch.

    Looking Ahead: Continuous Improvement on Every Front

    Just as synthetic chemistry keeps evolving, the standards for intermediate production do too. At our plant, team meetings focus as much on incremental process upgrades and cleaner operations as they do on laboratory metrics. The next generation of 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid will reflect customer demands for even better stability and tighter batch specs. That means reinvesting plant profits in new drying technology, advanced packaging, and ongoing operator training. Every improvement in handling and synthesis feeds directly back to users — higher purity, better shelf life, and more predictable chemistry, batch after batch.

    Direct Channel for Questions and Technical Support

    Researchers and formulators come to manufacturers with real-world problems, not simple order numbers. Calls range from “Why is my reaction stalling?” to “Can you provide documentation for regulatory?” and “Is there a safer packaging option for hot climates?” Every answer comes out of a combination of technical reference and direct hands-on work in our facility. Years of supporting end users built know-how into our customer support, so queries don’t bottleneck in a generic helpdesk. The most valuable solutions emerge from blending process experience with up-to-date literature, practical plant data, and customer feedback.

    Summary of Essential Differences from Other Boronic Acids in Practice

    Comparing 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid to other boronic acids, our own manufacturing line shows tangible distinctions beyond the structure diagram. Material performance, reactivity, and end-result yields all vary. The electron-withdrawing CF3 and F groups open up activation patterns that make the difference in drug lead synthesis, specialty monomer construction, and late-stage arylations. Plant engineering finds this molecule more sensitive to water and heat than simpler boronic acids, so storage protocols differ and operator training includes specialty handling steps. Production runs confirm it offers more consistent selectivity, supporting a wider scope of challenging synthetic targets. These operational realities drive decisions from procurement through to bench chemistry.

    Final Thoughts: The Value of Direct Manufacturing Experience

    Building and supplying 2-Fluoro-5-(Trifluoromethyl)Phenylboronic Acid over years exposes us to every challenge, from upstream sourcing to operator safety and end-user troubleshooting. What matters most is keeping communication lines open with those who use our reagents daily. Field experience, operator feedback, and ongoing customer conversations turn every batch into a better tool for chemical innovation. It’s a cycle of hands-on learning that defines our approach to specialty chemical manufacturing, supporting research and production across industries demanding reliability and real-world technical support.