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HS Code |
767850 |
| Productname | 2,3,4-Trifluorophenylboronic Acid |
| Casnumber | 5122-88-1 |
| Molecularformula | C6H4BF3O2 |
| Molecularweight | 175.90 |
| Appearance | White to off-white solid |
| Meltingpoint | 80-84°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Density | 1.53 g/cm³ |
| Smiles | B(C1=CC(=C(C(=C1)F)F)F)(O)O |
| Inchi | InChI=1S/C6H4BF3O2/c8-3-1-2-4(9)6(10)5(3)7(11)12/h1-2,11-12H |
As an accredited 2,3,4-Trifluorophenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5g 2,3,4-Trifluorophenylboronic Acid comes in a clear, tightly sealed glass vial within a labeled, protective cardboard box. |
| Shipping | 2,3,4-Trifluorophenylboronic Acid is typically shipped in sealed containers to prevent moisture ingress, as the compound is sensitive to air and humidity. Packaging complies with relevant chemical safety regulations, and transport may require labeling as a specialty chemical, with appropriate documentation for safe handling and delivery per local and international guidelines. |
| Storage | 2,3,4-Trifluorophenylboronic Acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store at room temperature in a cool, dry, and well-ventilated area. Keep separate from incompatible substances such as strong oxidizers. Ensure the container is clearly labeled and avoid prolonged exposure to air to prevent degradation or contamination. |
Applications of 2,3,4-Trifluorophenylboronic Acid in Industrial Manufacturing2,3,4-Trifluorophenylboronic Acid plays an essential role in advanced organic synthesis and specialty manufacturing processes. Our material integrates directly into high-value production pipelines across several demanding industries, where reliability, traceability, and performance consistency are critical to end-use quality. 1. Pharmaceutical Intermediate SynthesisThis chemical is widely used in the pharmaceutical sector as a coupling reagent for the preparation of complex drug intermediates via Suzuki-Miyaura cross-coupling reactions. It serves as a key building block to introduce trifluorophenyl groups into heterocyclic and aromatic targets, including kinase inhibitors, anti-inflammatory agents, and oncology candidates. Process engineers control reactivity and purity to support downstream cGMP manufacturing. Our material meets critical impurity thresholds for regulatory compliance, and batch histories support audit requirements. Industry compliance standards
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2. Agrochemical SynthesisProducers of crop protection agents use this material in the production of fluorinated agrochemical intermediates, which improve metabolic stability and biological activity of herbicides and fungicides. The trifluorophenyl moiety enhances selectivity and field persistence. Our supply supports production protocols requiring stringent QC analysis and traceability, and enables scale-up from pilot to commercial quantities without compositional drift. Industry compliance standards
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3. Electronic Material ManufacturingThis compound supports specialty electronics material suppliers in synthesizing organic semiconductors, display materials, and fluorinated monomers for photoresists. The fluoroarene structure improves thermal stability and performance in OLEDs and other high-end applications. Our facility exercises strict analytical control to guarantee charge-transport properties and to reduce trace metals critical to material purity. Industry compliance standards
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4. Specialty Fine Chemical ProductionChemical manufacturers exploit the selective reactivity of this trifluorinated boronic acid to generate bespoke fine chemicals required for pigments, UV absorbers, and liquid crystals. Its controlled reactivity profile delivers batch-to-batch uniformity, while the unique substitution pattern supports process development for stable specialty chemicals. Downstream users require detailed QC documentation and full traceability regarding synthesis route and raw material origin. Industry compliance standards
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5. Active Ingredient for Advanced Polymer SynthesisPolymer manufacturers employ this material to create fluorinated blocks or sidechains for specialty polymers, imparting hydrophobicity and chemical resistance to coatings, membranes, and engineering plastics. The compound’s consistent purity minimizes side reactions and gel formation during polymerization, and all batches include full trace analytical data to meet downstream technical requirements. Industry compliance standards
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Competitive 2,3,4-Trifluorophenylboronic Acid prices that fit your budget—flexible terms and customized quotes for every order.
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Manufacturing boronic acids isn’t just a process; it's a commitment forged through years spent at our reactors, adjusting parameters, learning directly from each batch. Our team invests in understanding the nuances of each molecule—tweaking conditions, expanding research, and pushing the boundaries on purity and consistency. This approach has guided the development and production of our 2,3,4-Trifluorophenylboronic Acid, CAS number 128306-55-8, a specialty intermediate whose synthesis draws on both deep technical knowledge and practical factory know-how.
Every sample you encounter reflects iterations run through our own equipment. Rather than copying textbook routes, we’ve refined our method to ensure reproducibility whether you order grams for research or kilos for pilot campaigns. Whether researchers or process engineers visit our site, most walk away recognizing the hands-on engagement woven into every lot. Our process engineers don’t stop at theoretical yields. They solve bottlenecks right on the factory floor, observing reactions until crystal clarity materializes batch after batch.
2,3,4-Trifluorophenylboronic Acid emerges as a white to pale yellow crystalline powder, handled by our technicians under local exhaust and climate-controlled conditions to discourage moisture uptake. The typical melting range sits between 133°C and 137°C, a detail confirmed in each QA cycle with muffle-furnace checks and DSC analysis. Purity hits 98% or above (HPLC), as our customers demand sensitive, reliable reagents whether for Suzuki couplings, sensor applications, or new material platforms.
Our packing routines reflect lessons learned during countless rainy and humid seasons. Industrial-grade liners lock out water vapor, while bottles and drums use chemically resistant HDPE, double-sealed. Even shipping is part of our responsibility. We train our warehouse team to prepare batches capable of enduring weeks at sea or road, remaining free-flowing and uncontaminated. Every batch ships with our own COA, traced back to individual operators running the production and inspection lines. The accountability is tangible, monitored by real people, not just serial numbers.
Among the phenylboronic acids, 2,3,4-trifluoro substitution stands out. Fluorination at these specific ortho and para positions alters both electron density and steric profile in a way felt directly at the lab bench. From our experience supplying bench chemists and bulk synthesis teams, this configuration offers distinctly different reactivity. The electron-withdrawing trifluoro pattern tunes the boronate’s reactivity towards oxidative addition and transmetalation steps central to Suzuki-Miyaura reactions.
Many customers compare this product with either mono- or di-fluorinated analogues. Mono-fluoro compounds display certain selectivities, and di-fluoro variants nudge electronic properties in specific directions. Yet, the 2,3,4 arrangement delivers a unique balance: increased stability during storage, lower susceptibility to protodeboronation, and an improved profile for certain cross-couplings that demand more robust electron withdrawal. The difference translates into higher yields, even with trickier substrates or less-forgiving process variables. Over time, we’ve seen teams cut down on repeat runs simply by switching to our 2,3,4 variant, saving both materials and hours of operation.
Chemists harness 2,3,4-Trifluorophenylboronic Acid for cross-coupling work, bioconjugation, and sensor platform development. From our vantage, the Suzuki-Miyaura reaction dominates usage, especially in pharmaceutical intermediate synthesis. We’ve worked side-by-side with API manufacturers who encounter challenges like low yields, competing side reactions, and problematic product isolation. Our batch consistency means that process teams spend less time troubleshooting unexpected impurity profiles.
On several occasions, customers in the fine chemicals sector report dramatic improvements—not just in the purity of downstream products, but also in operational uptime thanks to the crystalline, stable nature of our compound. Such feedback aligns with our own process monitoring: fewer shutdowns for equipment washing, less issue with caked feed hoppers, and reduced staff time spent manually reworking clumpy, moist powders.
Analytical chemists and R&D specialists gravitate toward the compound because it allows for more predictable behavior amid broader arrays of functional groups. The unique electronic properties of the trifluorinated aromatic ring mean researchers can maintain orthogonality in protecting group manipulations, even when scaling up. Our staff answers questions daily—not from procedure sheets, but from time spent in unpredictable production conditions. We share tips on solubilization, filtration, and recovery, because those details make the difference between successful trial runs and costly delays.
Some producers prioritize volume; our focus stays on performance. Specifications—purity, melting point, residual content—find relevance through the real demands of scale-ups and critical synthetic steps. Our experience shows even minor deviations in purity or water content can disrupt multi-step syntheses. So, we run parallel process validations: storing retained reference samples, running HPLC and NMR ourselves, not simply outsourcing for a certificate.
Most commercial boronic acids remain sensitive to moisture, and many competitors’ stocks solidify or degrade with extended storage. Our staff developed modified protocols to reduce hydrolysis and stabilize boronic acid under both inert and ambient supply chain conditions. Now, customers working in humid regions or with intermittent usage avoid product losses that previously cut into budgets.
Industrial partners point out the importance of residual solvents and trace metals. Our routine includes ICP-MS and Karl Fischer tests because overlooked levels—even in ppm range—can poison catalyst systems or distort analytic assays. We tune cleaning and crystallization steps to minimize these carryovers before bulk packing, not as an afterthought.
If you’ve worked with standard phenylboronic acids or more common ortho/meta/para substituted analogues, the unique character of the 2,3,4 trifluorinated compound becomes immediately apparent. Some synthetic chemists prefer more basic aryl boronic acids for their low cost and high reactivity with simple aryl halides. We talk with process developers who require more specific functional group compatibility. For example, mono-fluoro boronic acids rarely provide the stability and cross-coupling yield necessary for complex pharmaceutical intermediates.
The trifluorinated variant sits in a different reactivity space: less prone to protodeboronation, less vulnerable to deactivation in the presence of base, and showing improved recovery from workups involving water or protic solvents. Practical reports come back to us about fewer issues with lingering impurities—both organic and inorganic. Our operators routinely exchange findings from purification runs directly with research partners, so process improvements at the factory feed back into more robust user performance.
The upshot is not only better outcomes in the lab, but also more reliable project timelines. Our partners in custom manufacturing highlight that switching to our 2,3,4-trifluoro product can shave weeks off development by eliminating reruns. This streamlines everything from analytical verification to scaling feasibility checks, because quality and reactivity prove consistent every time.
Engineering 2,3,4-Trifluorophenylboronic Acid isn’t a “one and done” job. We meet demands for further customization—adjusting particle size, shifting crystallization solvents, and offering alternative packaging for automated dispensing systems. These are tweaks made in response to direct customer feedback, often through co-development programs that pull together both process engineers and synthetic chemists into joint problem-solving sessions.
One pharmaceutical team struggled for months to manage reaction foaming during scale-up. A change in the morphology of our product, achieved by tuning agitation rates and control of seeding during crystallization, reduced foaming and increased final yield by nearly 12%. These outcomes wouldn’t have been possible if we had not maintained a direct operating relationship, inviting feedback and rolling those observations back into plant operations.
Sometimes, the need for advanced customization means rapid deployment of new QC methods or special filling runs tailored for pilot plants. We commit to these projects when the chemistry and partnership warrant. This level of engagement yields new ideas for process improvement, which then translate back into our normal production schedule, raising quality for all users.
Many chemical producers encounter growing regulatory and societal pressure for cleaner, safer processes. We see these obligations as part of our manufacturing responsibility, not simply external requirements. Starting from years past, we invested in closed-cycle solvent recovery, energy management, and recycling of aqueous waste streams. Our 2,3,4-Trifluorophenylboronic Acid production harnesses these systems—recovering solvents that once would have gone straight to combustion, purifying water effluents so they meet discharge standards without compromising batch integrity.
Worker safety sits high among our values. Every process improvement incorporates risk assessments considering the staff operating the lines, not just the end product or regulatory compliance. Our in-house safety team regularly updates protocols and delivers hands-on training, ensuring that those closest to the chemistry remain well-protected. This reduces downtime from accidents and invests directly back into the community of workers powering the chemical industry.
Technology adoption remains a steady process. Rather than jumping to expensive and untested equipment, we evaluate pilot trials for both process scalability and environmental footprint. Any upgrade, from automated filtration to solvent distillation columns, finds its origins in solving very real bottlenecks experienced during production runs. All waste and exotherms undergo detailed monitoring, reflecting years of cumulative factory know-how.
Research partners approach us for more than just supply; they want collaborative troubleshooting. Our technical staff bring firsthand insight into how aroma, particle size, hydration, or even packing method impacts lab-scale and kilo-scale needs. We work with formulation chemists, bio-conjugation specialists, and material researchers on everything from analytical best practices to packaging ergonomics.
The world of boronic acids keeps changing rapidly. New uses in biosensors, polymer chemistry, and electronic material synthesis push beyond the predictable boundaries of cross-coupling. Being the manufacturer means we stay close to the latest literature, running our own validation studies—not just reading journals, but putting fresh ideas through bench trials and pilot batches. Our people take pride in sharing tricks learned the hard way: how a subtle temperature shift can cut filtration time, or why switching drying room cycles produces a better flowability profile.
These solutions aren’t academic. They come from practical problem-solving, embedded inside the factory walls. Each lot of 2,3,4-Trifluorophenylboronic Acid reflects hundreds of hours of behind-the-scenes iteration, adaptation, and correspondence with real users in the field.
Most stories of chemical production focus on theoretical yields and stock list comparisons. The ground truth is much messier. Real operators contend with pipeline blockages, humidity swings, and raw material variation. Our factory team confronts these hurdles daily. Over years of feedback cycles with thousands of users, we’ve tuned both how we synthesize and how we deliver our product.
Yield improvement, purity, storage resilience—all stem from a cycle of incremental upgrades, not from “set-and-forget” factory planning. Each challenge—be it international shipping, rapid scale-up, or fresh compliance standards—feeds back into our hard-won process documentation. The result is a supply partner who has walked the same ground as your team, bringing chemistry knowledge together with in-depth experience running full-scale units and laboratory reactors alike. We stand behind every shipment, not because a standard says so, but because real people measure, test, and vouch for the work each day.
Relationships built in chemical manufacturing matter as much as technical data sheets. Researchers and production engineers return year after year, not out of habit, but from confidence built through every successful campaign. Our 2,3,4-Trifluorophenylboronic Acid reflects the depth of that trust—a product shaped as much by dialogue and problem-solving as by the raw ingredients we source each season.
We’ve learned the importance of transparency in every transaction. Our records track not only the chain of custody, but also feedback from every complaint, every improvement, and every new regulatory hurdle. These lessons feed directly into tighter controls, safer batches, and products that deliver what laboratories and plants genuinely require.
While advisory bodies issue new regulations, and supply chains face more headwinds, we face each shift with a hands-on approach—building from small-batch pilot campaigns up to consistent, commercial-scale operations. This responsiveness—the ability to pivot and solve problems with both agility and experience—ensures our customers receive a 2,3,4-Trifluorophenylboronic Acid that keeps pace with every new breakthrough and challenge.
No chemical journey ever rests with a single product. Each improvement in our plant, each late-night troubleshooting meeting, reminds us why careful, honest work matters so much to customers and staff. 2,3,4-Trifluorophenylboronic Acid offers more than the sum of its specifications—it stands as a statement on what cumulative, lived knowledge can create in the specialty chemicals sector.
We look forward to ongoing advancements. Chemical manufacturing never stands still, and each batch defines new opportunities to raise standards higher. Whether you work in synthesis, formulation, or R&D, the reliability and breadth of feedback behind our 2,3,4-Trifluorophenylboronic Acid aims to support your progress at every stage. From initial development, through scale-up, to routine commercial production, our team brings hard-earned insight and commitment to each filled drum and bottle.