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2-Chloro-4-Trifluoromethylphenylboronic Acid

    • Product Name 2-Chloro-4-Trifluoromethylphenylboronic Acid
    • Alias (2-Chloro-4-(trifluoromethyl)phenyl)boronic acid
    • Einecs 817-743-6
    • 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
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    Specifications

    HS Code

    137253

    Product Name 2-Chloro-4-Trifluoromethylphenylboronic Acid
    Cas Number 872122-56-2
    Molecular Formula C7H5BClF3O2
    Molecular Weight 224.38 g/mol
    Appearance White to off-white powder
    Melting Point 92-98 °C
    Purity Typically ≥ 97%
    Solubility Soluble in DMSO, methanol
    Density 1.49 g/cm³ (estimated)
    Storage Temperature 2-8 °C (refrigerated)
    Synonyms 2-Chloro-4-(trifluoromethyl)phenylboronic acid
    Smiles B(C1=CC(=C(C=C1)Cl)C(F)(F)F)(O)O
    Inchi InChI=1S/C7H5BClF3O2/c9-6-2-1-5(7(10,11)12)3-4(6)8(13)14/h1-3,13-14H

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

    Packing & Storage
    Packing The 10g of 2-Chloro-4-Trifluoromethylphenylboronic Acid is packaged in a sealed amber glass bottle with a secure screw cap.
    Shipping 2-Chloro-4-Trifluoromethylphenylboronic Acid is shipped in tightly sealed containers to prevent moisture and contamination. The package is labeled according to chemical safety standards and transported as a non-hazardous item under normal conditions. Shipping is typically via ground or air, complying with local and international regulations for laboratory chemicals.
    Storage 2-Chloro-4-Trifluoromethylphenylboronic Acid should be stored in a tightly closed container, protected from moisture and air. Store in a cool, dry, and well-ventilated area away from incompatible substances like oxidizing agents. Preferably, keep at 2–8°C (refrigerated) to maintain stability. Avoid exposure to direct sunlight and sources of ignition. Handle under inert atmosphere if prolonged storage is required.
    Application of 2-Chloro-4-Trifluoromethylphenylboronic Acid

    Applications of 2-Chloro-4-Trifluoromethylphenylboronic Acid in Industrial Manufacturing

    2-Chloro-4-Trifluoromethylphenylboronic Acid functions as a key building block in multiple fine chemical sectors due to its strong electron-withdrawing substituents, enabling precise cross-coupling and custom molecular synthesis. Our plant delivers consistent quality tailored to facilitate downstream product consistency, purity, and process reliability. Below, we outline several high-value industrial application paths with specifications and process details suited for B2B manufacturing environments.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers use this boronic acid in Suzuki–Miyaura coupling reactions to construct advanced intermediates for modern kinase inhibitors and other heterocyclic compounds. The compound's stability in aqueous and polar organics supports high-yield, low-impurity profiles during medicinal chemistry upscaling and late-stage drug substance production.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for APIs
    • USP General Chapter <821> Chromatography
    • 21 CFR Part 211 (FDA cGMP for Finished Pharmaceuticals)
    • EMA Guideline on Specifications: Test Procedures and Acceptance Criteria for Pharmaceuticals

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to halogenated partner; developers optimize based on assay purity and coupling efficiency

    Downstream process integration

    • Dosing at the cross-coupling unit operation following substrate activation; followed by reaction workup, crystallization, and QC-released isolation

    Final product types

    • Small-molecule investigational drugs
    • Patented kinase inhibitors
    • NCE (New Chemical Entity) scaffolds
    • Advanced GMP API intermediates

    2. Agricultural Fungicides and Herbicides Intermediate

    Process chemists in agrochemical plants employ this raw material to introduce trifluoromethyl-aryl motifs into selective fungicidal and herbicidal active ingredients. Its structure enables unique binding properties and environmental persistence, serving as a coupling reagent in the construction of potent difenoconazole or related triazole derivatives under pilot-scale or commercial production conditions.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • ISO 17025 Laboratory Accreditation
    • REACH Registration (EC 1907/2006, Annex IX for intermediates)
    • OECD Good Laboratory Practice (GLP) for environmental exposure

    Typical usage ratio

    • 0.9–1.3 molar equivalents, depending on the desired conversion rate and co-reactant reactivity in batch or continuous manufacturing

    Downstream process integration

    • Catalytic reaction input post-alkylation of precursor; subsequent reaction streams pass to isolation, purity analysis, and formulation lines

    Final product types

    • Triazole fungicide intermediates
    • Herbicidal technical concentrates
    • Specialty agrochemical building blocks
    • Crop protection active substance precursors

    3. OLED and Advanced Material Synthesis

    Producers of organic electronic materials and specialty polymers use the boronic acid for targeted installation of fluoroaryl segments in small-molecule emitters and charge-transport materials for OLEDs and displays. Its high purity and defined reactivity support strict batch-to-batch consistency essential in high-value thin-film deposition and device fabrication workflows.

    Industry compliance standards

    • IEC 61249-2-21 (halogenated content in electronic materials)
    • RoHS Directive 2011/65/EU and its amendments
    • ISO 9001:2015 Quality Management Systems
    • QC benchmarks for optoelectronic-grade raw materials

    Typical usage ratio

    • 0.95–1.1 equivalents relative to organohalide partner in cross-coupling; ratio adjusted by emission tuning requirements for final material

    Downstream process integration

    • Input at organic synthesis reactor prior to spin-coating or vapor deposition preparation; in-line monitoring for residual boronic acid content

    Final product types

    • OLED small-molecule emitters
    • Electron/hole transport materials
    • Optoelectronic conductive polymers
    • Functionalized display intermediates

    4. Custom Synthesis of Specialty Chemicals

    Custom synthesis CDMOs and fine chemical producers leverage this raw material in precision aromatic coupling to yield specialty monomers, advanced ligands for catalysts, and regulated labeling substances. Its chemical profile meets strict regulatory demands for specialty grades and downstream clients seeking custom-tailored molecules for R&D or pilot production.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 Integrated Systems
    • REACH (for downstream intermediate applications)
    • Responsible Care (global chemical safety initiative)
    • Specific client validation and analytical release specifications

    Typical usage ratio

    • 0.8–1.5 equivalents, adjustable depending on downstream molecular complexity, stoichiometric need, and byproduct minimization

    Downstream process integration

    • Early-stage or late-stage coupling within multi-step syntheses; integrated into either bulk production or kilo-lab precision workflows

    Final product types

    • Specialty monomers
    • Chiral catalyst intermediates
    • Analytical reference substances
    • Labeling-enhanced compounds for regulated sectors
    Free Quote

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    Certification & Compliance
    More Introduction

    Experience Drives Excellence in the Manufacture of 2-Chloro-4-Trifluoromethylphenylboronic Acid

    Every day, chemistry challenges us to balance purity, precision, and consistency. Our experience in manufacturing 2-Chloro-4-Trifluoromethylphenylboronic Acid stretches over a decade, and during that time, we have worked closely with scientists and scale-up teams in pharmaceuticals, crop protection, and materials chemistry. This compound, also known as 2-Chloro-4-(trifluoromethyl)phenylboronic acid, brings unique value to users who know that not all boronic acids are the same.

    We produce this material under the visual eye of experienced chemists. Its batch quality results from hard-earned understanding of air sensitivity, water content, and trace metal impurity control. Some manufacturers allow small process drifts; we take a hands-on approach, frequently testing and watching the tiniest changes that can affect downstream Suzuki couplings and other cross-coupling reactions. The model we offer keeps a carbon-based melting point in the 128–131°C range. Our batches are characterized by an ultra-low moisture level, and we will only release product after it passes NMR, HPLC, and elemental checks. Years of direct conversation with synthetic chemists taught us that even minor impurities can cause headaches during catalyst loading, so we’re relentless in limiting trace halides, isomeric by-products, or homocoupling side-products.

    You will find it as a white to off-white crystalline solid. It’s sold in a standard purity over 98%, measured by assays we’ve refined using calibration against ICH traceable standards. Chemists looking to move beyond lab scale can contact us for 10- or 100-kilo lots. We understand scale-up issues: boronic acids, and especially those with electron-withdrawing substituents like chlorine and trifluoromethyl groups, can change their behavior based on batch size, packaging, and even slight atmospheric shifts. We store and ship under nitrogen as a rule, based not on theoretical risk, but on seeing firsthand how moisture uptake can degrade product over the course of international transport.

    For applications, many of our clients incorporate 2-Chloro-4-Trifluoromethylphenylboronic Acid into their programs for optimizing biaryl linkages. These linkages set the backbone of advanced pharmaceutical intermediates, active ingredients for next-generation agrochemicals, and materials like OLED or liquid crystal precursors. This compound’s boronic acid function stands out for compatibility with modern palladium catalysts, delivering high yields even under mild reaction conditions. Some may ask why to pick the 2-chloro-4-trifluoromethyl substitution pattern. The answer comes straight from conversations we’ve had with medicinal chemists: the electronic effects modify regioselectivity and reactivity to favor certain coupling patterns, reduce unwanted side reactions, and improve the stability of intermediates against decomposition. In many crop science projects, this structure improves performance too, as the balance of electron-withdrawing and steric groups can improve bioavailability targets.

    In terms of specifications, a question often comes our way: how does this product compare with simpler phenylboronic acids or those bearing only a single substituent? Direct experience tells us the duo of chloro and trifluoromethyl groups create a much more hydrophobic and metabolically robust structure. During coupling reactions, especially when working at process scale, the solubility differences mean you often see cleaner conversions and fewer purification steps post-reaction. From a manufacturer’s perspective, this not only supports efficiency on the chemist’s bench but reduces downstream solvent use and related disposal needs—a substantial factor in modern Green Chemistry considerations.

    We have watched the global landscape for boronic acids shift as regulatory and supply chain issues have forced shortcuts elsewhere. Our practice is to only source boron reagents from the most reliable origins and to validate every incoming raw material in-house. The trifluoromethyl group—difficult, sometimes costly to introduce—requires careful handling and thorough pre-testing for stability. Our facility is outfitted with scrubbing systems to prevent fluorinated byproducts from escaping, and every operator has specific training on handling volatile and corrosive reagents. We have seen cases where outsourced or “grey market” 2-Chloro-4-Trifluoromethylphenylboronic Acid contains measurable levels of side-products or even simple boric acid. For us, these are not acceptable. Our process integrates small-batch crystallization, repeated filtration, and direct instrumental QC. This means our final product meets a higher bar and is better suited to those looking for consistent batch-to-batch performance.

    Some users ask if our material is suitable for automated reactors or microfluidic systems. The answer, based on the feedback we’ve received, is yes. Our powder is fine and free-flowing, without static charge issues or caking. For research groups working on library synthesis or scale-out programs, speed and feeding reliability matter just as much as the chemical profile. Years ago, we saw that poorly made boronic acids could slow down high-throughput set-ups—so we regularly test particle size distribution and invest in packaging solutions that maintain product stability even after repeat openings. We advise storing under dry nitrogen and recommend amber bottles for users sensitive to photodegradation, though our batches have demonstrated strong shelf stability under standard cold storage.

    The conversation doesn’t end at the warehouse door. Teams often reach out to ask about handling tips and compatibility. Having run boronic acid chemistry at kilo scale ourselves, we share practical advice. Always measure and minimize the headspace oxygen; avoid prolonged exposure to high-temperature drying ovens. If moisture content creeps up, our testing shows minor losses in reactivity can accumulate, so we offer simple guidance on testing protocols with Karl Fischer titration. We invite researchers to share feedback, since even small improvements in process flow can translate to real cost savings and reduce waste.

    Our story is rooted in human connection. We’ve had our material loaded into reactors in Basel biotech labs, Chinese pilot plants, and leading agro labs in the American Midwest. Across every continent, we’ve heard consistent stories: after switching to high-quality 2-Chloro-4-Trifluoromethylphenylboronic Acid, researchers report shorter workup times, higher isolated yields, and smoother process validation. No compound is a magic bullet, but experience shows that small chemical differences—like swapping a methyl for a trifluoromethyl, or moving a chloro group from the para to the ortho position—can shift the entire outcome of a synthesis.

    Looking across the field, some chemists debate the need for routine boronic acid purification or argue over the benefits of pinacol esters versus free acids. Direct experience gives us perspective. Our manufacturing approach favors the free acid for maximum versatility—the acid survives typical coupling preps but can be easily converted if required for specialty applications. Batch control allows us to offer custom lots with alternative particle sizes, or alternative counterions on request, though most research groups find our “house” recipe meets their needs. We’ve learned not to cut corners: purification may eat into throughput, but we would rather deliver a product that builds trust and long-term collaboration.

    What differentiates our 2-Chloro-4-Trifluoromethylphenylboronic Acid from similar entrants in the global market? It’s not just specification sheets. Our operation uses process feedback from real users, and this has led to tangible changes in our workflow. Scale-up chemists in pharma and fine chemicals know what it feels like to run with an unreliable source: time-wasting re-purifications, missed deadlines, failed scale-up runs. By controlling every step in our process—from boronic ester hydrolysis to final drying and packaging—we own the quality, and every lot leaves with a profile we can stand behind. We also maintain a traceable batch history, so clients can request documentation and know exactly how their lot performed in our hands before it left our plant.

    We’ve invested in equipment, but people make the difference. From raw material sourcing to shipment preparations, our team holds closely to the lessons learned from the shop floor and the lab bench. This goes beyond passing inspections; it’s a matter of pride. For example, packaging design changes came after discussions with logistics teams who watch finished product move through long, sometimes hot journeys. Our nitrogen-flushed, tamper-resistant containers shield against both moisture and accidental cross-contamination—a lesson learned after seeing how unpredictable customs inspections could lead to ruined shipments of less well-protected boronic acids in previous years.

    Some chemists ask us why to bother with such focus on detail, given the race to lower costs worldwide. From years spent reviewing root causes of batch failures, we know that a faulty boronic acid can cost much more in lost time and product than any minor savings on price per kilo. Minimizing process variability means your catalyst spends time productively driving your main coupling, not scavenging unintended by-products. When we talk to process engineers, we hear the same priority: chemical uniformity is important, but reliability in supply and performance over time shapes the projects that move from idea to scalable reality.

    Research doesn’t stop, and neither does our drive to improve this and other specialized building blocks. Our technical team regularly reviews emerging literature and case studies. We speak directly with reaction engineers and analytical specialists about trends in Suzuki–Miyaura couplings, new ligand developments, or sustainability improvements. Being up front in sharing insights—good and bad—means we support users facing new synthetic challenges and provide a sounding board when they troubleshoot their first runs with new ligands or bases. We respect IP boundaries, yet believe in real-world experience sharing, because good chemistry happens in the open as well as the confidential.

    As regulations evolve and the world tightens its grip on hazardous raw materials, we work transparently with our partners. Regulatory audits, documentation for compliance, and environmental responsibility are not afterthoughts—they’re part of how we work. As a chemical manufacturer, we face up to growing responsibilities: tracking and minimizing residues, making sure safety data is accurate, and training every member of our staff to spot risks. We attend conferences, monitor peer-reviewed work, and host workshops where customers share both success stories and frustrations. Every exchange pushes us to refine our process, remove blind spots, and keep reliability at the center of our work.

    We remain proud of our track record but always look for improvement. Our process equipment gets regular upgrades, and our QC department maintains a “zero defect” ambition—children of many nights spent troubleshooting imperfect runs and investigating every out-of-trend result. Batch failures have taught us humility, persistence, and an obsession with root causes. Customers come to us for both the product and the knowledge that stands behind it. By offering a high-purity, rigorously evaluated 2-Chloro-4-Trifluoromethylphenylboronic Acid, we contribute actively to the progress of fields reliant on exacting standards and innovation.

    Taking a product all the way from concept through scale-up to reliable supply is more than a technical challenge. It’s a promise kept by everyone who takes ownership along the journey. In this sense, each unit shipped reflects the hands and minds involved in keeping quality ahead of compromise. As we continue to supply this important boronic acid, we know we’re not just sending out a chemical, but providing support that ends up inside the next generation of medicines, advanced materials, and discoveries. Experience—earned through trial, refinement, and open conversation—remains our surest guide.