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HS Code |
234340 |
| Chemical Name | 4-Trifluoromethoxyphenylboronic acid |
| Cas Number | 5122-89-8 |
| Molecular Formula | C7H6BF3O3 |
| Molecular Weight | 205.93 |
| Appearance | White to off-white powder |
| Melting Point | 123-127°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents such as DMSO and methanol |
| Smiles | B(C1=CC=C(OC(F)(F)F)C=C1)(O)O |
| Inchi | InChI=1S/C7H6BF3O3/c9-7(10,11)14-6-3-1-5(2-4-6)8(12)13/h1-4,12-13H |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Synonyms | 4-(Trifluoromethoxy)phenylboronic acid |
As an accredited 4-Trifluoromethoxyphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is supplied in a 25-gram amber glass bottle, securely sealed, with a white screw cap and a detailed chemical label. |
| Shipping | 4-Trifluoromethoxyphenylboronic Acid is shipped in tightly sealed containers, protected from moisture and light. Packaging meets international safety regulations for chemical transport. The product is labeled with hazard information, and temperature control is applied if required. Shipping is typically via ground or air freight, depending on destination and urgency. |
| Storage | 4-Trifluoromethoxyphenylboronic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents and moisture. Protect the compound from light and avoid excessive heat. Recommended storage temperature is typically between 2–8°C (refrigerator). Ensure proper labeling and follow all relevant safety regulations for handling boronic acids. |
Applications of 4-Trifluoromethoxyphenylboronic Acid in Industrial ManufacturingAs a direct chemical manufacturer, we supply 4-Trifluoromethoxyphenylboronic Acid to specialized industrial clients across multiple sectors where high-purity boronic acids are required for precision synthesis. This material performs a vital function in the construction of advanced molecules, specifically where demanding regulatory, process, and formulation criteria exist. 1. Pharmaceutical API Synthesis (Suzuki Coupling Intermediate)Pharmaceutical manufacturers utilize our material as a boron coupling partner during Suzuki-Miyaura reactions, especially for constructing structures with trifluoromethoxyphenyl motifs. This step is common in the production of kinase inhibitors, CNS-active agents, and anti-cancer drug candidates. Strict impurity control and adherence to regulatory filing data are required due to its proximity to the final API. Industry compliance standards
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2. Agrochemical Actives SynthesisAgrochemical producers incorporate our boronic acid as a core building block in the synthesis of advanced organic molecules, facilitating aryl–aryl bond formation for herbicide and fungicide actives that demand fluorinated aromatic rings. Downstream QC must verify residual boron levels and conform to environmental legislation regarding process effluents. Industry compliance standards
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3. Specialty Electronic Chemicals (OLED and LCD Intermediates)Manufacturers in the electronic chemicals field exploit the electron-withdrawing nature of the trifluoromethoxy group for designing building blocks in OLED emitters, hole-transport materials, and liquid crystal compounds. Stringent material purity and trace metal analysis are essential to meeting device performance and reliability requirements. Industry compliance standards
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4. Advanced Material R&D (Fluorinated Polymer Modifiers)Industrial R&D centers and specialty material formulators employ this boronic acid for synthesis of custom fluorinated aryl monomers utilized in high-performance polymers. The integration enables tailored solubility, chemical resistance, and dielectric properties in coatings and engineered components. Downstream QC enforces trace impurity and batch reproducibility standards. Industry compliance standards
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5. Fine Chemical Synthesis for Analytical Reference StandardsAnalytical laboratories and accredited standards producers use this advanced boronic acid for trace synthesis of reference materials needed in method validation and proficiency testing, particularly for the pharmaceutical, environmental, and food quality sectors. Batch-to-batch consistency and traceability are mandatory under audit conditions. Industry compliance standards
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After years working with chemists at pharmaceutical, agrochemical, and specialty material companies, we've heard the same requests: reliability, purity, and clear differentiation from off-spec lots that slow down development. 4-Trifluoromethoxyphenylboronic acid, or MOCF3-PhB(OH)2, holds a solid place in modern synthetic chemistry labs. This compound enables the rapid assembly of complex molecular architectures. As the manufacturer, we pay close attention to the fundamentals—starting materials, reaction controls, and isolation protocols—because any shortcut can compromise downstream performance. Our approach combines robust quality control with feedback loops from customers conducting scale-ups and downstream transformations.
The trifluoromethoxy group brings unique electronic effects and high metabolic stability, a trait that often improves drug and agrochemical candidates. Many alternatives, such as the non-fluorinated phenylboronic acids or simple trifluoromethyl analogs, can't deliver the same balance between reactivity and stability. Those pursuing fluorinated building blocks recognize that the trifluoromethoxy moiety extends the design space for discovery chemistry, influencing both lipophilicity and interaction with biological targets. By producing this material ourselves—sourcing high-purity precursors and guiding every synthesis step—we ensure controls that can’t be matched by brokers or secondary suppliers.
The standard we manufacture meets or exceeds 98% purity by HPLC with less than 0.5% total impurities. We introduced additional purification stages after troubleshooting early issues with inconsistent melting points and color variance. Routine batch sampling analyzed by GC-MS, NMR, and Karl Fischer titration shows water content routinely under 0.3%. Over time, our batches show sharp, repeatable melting points and freedom from degradation byproducts. Consistency stems from controlling hydration levels and carefully monitored crystallization steps, honed through years of direct customer feedback and real-world process data.
The debate between boronic acids and other arylation agents never lacks for complexity. Our customers in medicinal chemistry, catalysis, and material science value the particular features of 4-trifluoromethoxyphenylboronic acid. Compared to boronate esters, the free acid supports broader cross-coupling conditions, and our batches show reliable reactivity in established Suzuki-Miyaura protocols. Lower solubility can sometimes challenge early-stage reactions, but steady crystal habits and controlled particle size in our batches ease handling challenges. Grignard-based methods struggle with the same trifluoromethoxy functionality, often producing hydrolytic side-products or deviating from stoichiometry.
We have supplied pilot and commercial quantities to groups facing late-stage diversification, radiolabeling, and chiral C–C bond formation. Several routes to complex biphenyls and polyaromatic scaffolds use our compound for efficient installation of a strongly electron-withdrawing substituent. Our own R&D team has adjusted synthetic procedures, improving crystallization and filtration workflow based on firsthand lab troubleshooting. Because we walk the same benches as our customers, every lot tells the story of incremental process improvement rather than off-the-shelf distribution.
We purchase fluorinated raw materials from vetted upstream sources, fragmenting supply lines to minimize risk from shortages and impurity spikes. Each step involves real-time analytics—infrared, chromatography, and NMR—rather than relying on post-process spot checks. Years ago, a spike in unknown low-level impurity forced us to overhaul our quench and workup conditions, leading to a new standard operating procedure that eliminated recurring color and solubility issues. These lessons stick, and every improvement feeds back into our quality program.
During isolation, we filter out particulate and collect crystals with controlled solvent gradients. Vacuum drying finishes the workflow, protecting the acid from moisture uptake that would otherwise dissolve into trace water. Storing product in moisture-resistant drums and using nitrogen purging reduces caking and hydrolytic shifts—details that make a daily difference at bench and pilot scales.
The places this molecule turns up vary: late-stage intermediates for kinase inhibitors, crop protection candidates looking to improve metabolic stability, advanced ligands for electronic materials. Usually, researchers report consistent coupling yields and low background reactivity when MOCF3 sits on the aryl ring. Those working on radiolabeling for tracers find the electronic profile of this substituent enables more efficient incorporation routes, saving time compared to less robust analogues that risk hydrolysis or rearrangement.
One standout example comes from a pharmaceutical customer scaling a library of potential enzyme inhibitors. Standard phenylboronic acids failed due to metabolic instability, while trifluoromethyl derivatives introduced solubility hurdles. Formulations incorporating our product let them reach required metabolite profiles and achieve higher plasma half-lives. In-house tests confirm that product lots support batch-to-batch reproducibility—critical in regulatory submissions and transfer to commercial-scale plants.
Safety in production and downstream use deserves direct attention. The trifluoromethoxy group, while chemically persistent, doesn’t bring high acute toxicity but may raise persistence questions. All our production lots trace to specific raw material batches, minimizing the chance of contamination with regulated fluorinated byproducts. Facility engineers designed waste capture streams for spent solvents and residual arylboronic species, using carbon capture beds and high-temperature neutralization—decisions shaped by growing regulatory pressure on all fluorinated organics.
Operators receive regular training and risk assessments, especially during scale-up and drum filling procedures. The material’s dusting tendency and sensitivity to moisture require careful control of workplace humidity and careful drum selection. Transport packaging follows guidelines set for organoboron compounds with added barriers for persistent fluorinated organics. We do not compromise on these points even if increased costs require budget allocation—resource commitments reflect lived experience managing process safety for specialty chemicals.
Variability in boronic acid supplies comes mostly from hidden process changes or unchecked impurity creep in raw materials. Comparing with alternatives, we found imported products regularly showed higher %H2O and inconsistent melting points. We tackled these with multi-step purification, repeated solvent exchanges, and investing in trace analytics equipment. No shortcut substitutes for in-house synthesis route validation or real-world user feedback—chemical manufacturers see too many failed scale-ups from boxed products that go untested outside a catalog.
For customers running high-throughput synthesis or seeking gram to kilogram lots, main concerns often relate to batch availability, solubility, and analytical confirmation. Our logistics team updates forecasts weekly, rather than monthly, reducing lead times and allowing customers to plan production runs accurately. We ship in high-barrier drums or custom glass packaging for research-grade requests, and always maintain chain-of-custody through production to delivery.
Where boronic acids fail—either from hydrolysis, oxidation, or incompatibility—the fix lies in balancing shelf stability, purity, and freedom from colored degradation products. By controlling upstream storage and investing in batch traceability, we offer a more trustworthy standard than resellers mixing lots or cutting cost on key precursors. Direct conversations with formulation chemists guide our improvements and set priorities for next year’s process redesigns.
Inside the manufacturing plant, every staffer—from synthesis chemists to drum-fill operators—sees the difference that process discipline and honest conversation make. Laboratory notebooks don’t sit idle; they feed real improvements in production train design, solvent recycling, and purification protocol. Customers who visit leave with an understanding of our traceability and see how batch data cross-reference with in-process monitoring. That transparency brings customers back and builds the trust missing from faceless commodity sales.
Compared to generic offerings, our product’s distinguishing features—purity, batch traceability, authentic documentation, and sustained inventory—come from process oversight, not marketing spin. On-the-fly adjustments, dual-sourcing of key precursors, and contingency planning happen weekly. Analytical teams keep one eye on current performance and another on regulatory risks, especially as the world’s fluorochemical regulations tighten.
Chemists turning to a supplier for answers, not just shipments, shape the way we run the support team. If a coupling fails on a Thursday night or an impurity ticks up, the lab tech responsible for that batch may pick up the phone or join the call. There’s no script—just matter-of-fact troubleshooting grounded in real analytical data and upstream process knowledge. Fielding technical questions drives new improvements, whether that means adding a drying stage, adjusting particle size targets, or helping a customer rerun a key reaction at a different scale.
Direct sourcing brings a feedback cycle no importer or catalog re-labler can offer. Failures, adjustments, unexpected customer requests—each feeds the process. We update supporting analytical reports and reaction notes based on those dialogues. Over time, this approach outpaces the generic matching of spec sheets to catalog entries.
Beyond daily shipping and laboratory troubleshooting, we track industry trends. Higher demand for fluorinated building blocks in pharmaceuticals, tighter environmental controls on fluorine emissions, and increasing calls for analytical transparency drive our investments. The push into green chemistry motivates us to investigate alternative fluorinating agents, greener solvents, and closed-loop recycling for spent reaction media. Our participation in industry consortia and direct feedback from regulatory specialists ensures we stay ahead of emerging standards for purity, traceability, and environmental compliance.
We see a trajectory where customers ask not just for product, but for data—impurity profiles, source transparency, supply chain verification, digital batch release files for submission to regulatory authorities. These requirements direct our future upgrades, from expanded analytics to automated inventory flagging and integrated customer track-and-trace portals. Close attention to these shifts builds stronger partnerships and minimizes stockouts or surprises at scale-up.
Reliable boronic acid supply transforms laboratory planning and accelerates the development timeline for both academic projects and commercial manufacturing. Years of hands-on problem-solving, process improvement, and transparent communication define how we deliver 4-trifluoromethoxyphenylboronic acid. Customers count on critical features: high purity, reproducibility, and trusted analytical support, because those are exactly the points we address each production cycle. By manufacturing this compound ourselves, bringing real-world experience to every lot shipped, our team ensures long-term confidence for research and production alike.