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2,4,5-Trifluorophenylboronic Acid

    • Product Name 2,4,5-Trifluorophenylboronic Acid
    • Alias 2,4,5-Trifluorophenylboronic acid
    • Einecs 810-009-7
    • 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

    428695

    Product Name 2,4,5-Trifluorophenylboronic Acid
    Cas Number 143272-16-0
    Molecular Formula C6H4BF3O2
    Molecular Weight 191.90 g/mol
    Appearance White to off-white powder
    Melting Point 174-178°C
    Purity ≥ 97%
    Solubility Soluble in DMSO, methanol
    Density 1.53 g/cm³
    Smiles B(C1=CC(F)=C(F)C=C1F)(O)O
    Inchi InChI=1S/C6H4BF3O2/c8-3-1-5(9)6(10)2-4(3)7(11)12/h1-2,11-12H
    Synonyms 2,4,5-Trifluorophenylboronic acid; 2,4,5-Trifluoro-1-boronic acid benzene

    As an accredited 2,4,5-Trifluorophenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g 2,4,5-Trifluorophenylboronic Acid is packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 2,4,5-Trifluorophenylboronic Acid is typically shipped in tightly sealed, chemically resistant containers to prevent moisture and air exposure. It is transported as a solid under ambient temperature, following regulations for handling organic chemicals. Proper labeling, cushioning, and documentation ensure safe and compliant delivery during transit.
    Storage 2,4,5-Trifluorophenylboronic Acid should be stored in a tightly sealed container, protected from moisture, air, and direct sunlight. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Store at room temperature or as specified on the supplier’s label, and ensure proper labeling to prevent accidental misuse.
    Application of 2,4,5-Trifluorophenylboronic Acid

    Applications of 2,4,5-Trifluorophenylboronic Acid in Industrial Manufacturing

    As a specialized manufacturer of 2,4,5-Trifluorophenylboronic Acid, we supply this advanced aromatic boronic acid for targeted industrial use, supporting precise organic synthesis and specialty chemical production. Our focus lies in key downstream applications where our material delivers performance, compliance, and controlled reactivity for value-added product development.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    2,4,5-Trifluorophenylboronic Acid functions as a unique building block in Suzuki-Miyaura cross-coupling steps for API synthesis. Leading pharmaceutical producers utilize it to introduce trifluorinated motifs, enhancing metabolic stability and bioactivity in target molecules, particularly for oncology and CNS drug candidates. We maintain strict traceability and batch consistency throughout the supply chain, ensuring compliance for regulated pharmaceutical production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia (Ph. Eur.) monographs for relevant intermediates
    • 21 CFR Part 211 (cGMP US FDA) for finished drug substances
    • REACH/CLP (for chemical handling in EU)

    Typical usage ratio

    • 0.9 – 1.2 molar equivalents relative to aryl halide substrate
    • Adjusted based on specific route and catalyst efficiency

    Downstream process integration

    • Charged to Suzuki-Miyaura or Stille coupling reactors after base addition
    • Integrated in step-growth API intermediate formation, followed by purification through column chromatography or crystallization
    • Subjected to multi-stage in-process controls and impurity profiling

    Final product types

    • Targeted oncology inhibitors
    • Trifluorinated CNS-active agents
    • Patent-protected intermediate compounds
    • Research molecules for clinical trial development

    2. Agrochemical Active Compound Manufacturing

    In the crop protection sector, 2,4,5-Trifluorophenylboronic Acid forms a key input for synthesizing novel aryl-substituted active ingredients. Its electron-deficient structure enables production of herbicides and fungicides with improved resistance profiles and lower environmental impact. Bulk users emphasize raw material purity and granularity to ensure consistency during scale-up and regulatory dossiers.

    Industry compliance standards

    • FAO/WHO specifications for active ingredient purity
    • ISO 9001:2015 Quality Management for agrochemical manufacturing
    • OECD Principles of Good Laboratory Practice (GLP) for residue studies
    • REACH Annex VIII for environmental and toxicological safety

    Typical usage ratio

    • 1.0 – 1.3 molar equivalents in cross-coupling with chlorinated/iodinated precursors
    • Modified as per conversion rates and impurity control needs

    Downstream process integration

    • Added to batch reactor with catalyst system (e.g., Pd(0) complexes)
    • Used in slurry or solution phase synthesis, depending on solubility of other reactants
    • Purified before formulation into technical concentrate

    Final product types

    • Trifluorinated herbicide active ingredients
    • Fungicidal intermediates
    • Crop protection research samples
    • Technical-grade agrochemical actives

    3. OLED and Advanced Electronic Material Synthesis

    Manufacturers of organic semiconductors utilize 2,4,5-Trifluorophenylboronic Acid in the construction of conjugated polymers and small molecules for OLEDs and related optoelectronics. The trifluorinated phenyl unit improves charge mobility and thermal stability, essential for high-brightness and durable end devices. Production requires strict material purity to avoid device degradation, and electronic material suppliers often request custom-packaging to minimize contamination risk.

    Industry compliance standards

    • IPC-4101D standards for electronic-grade materials
    • RoHS (Restriction of Hazardous Substances Directive)
    • ISO 14001:2015 Environmental Management for chemical process control
    • Control of Substances Hazardous to Health (COSHH, UK) for worker safety

    Typical usage ratio

    • 0.95 – 1.05 molar equivalents per aryl halide unit in polymer chain construction
    • Adjusted for target molecular weight and device specifications

    Downstream process integration

    • Dosed into organometallic-catalyzed cross-coupling in strictly anhydrous conditions
    • Integrated at monomer synthesis stage before chain polymerization
    • Processed under inert atmosphere to minimize decomposition

    Final product types

    • OLED emitter materials
    • Organic field-effect transistor (OFET) polymers
    • Photovoltaic cell donor-acceptor materials
    • High-performance organic thin films

    4. Advanced Material Specialty Polymer Synthesis

    Producers of specialty polymers for membranes, coatings, and filtration applications incorporate 2,4,5-Trifluorophenylboronic Acid to introduce strong fluorine-rich aromatic units. This approach enhances chemical resistance, lowers water absorption, and significantly increases polymer lifetime under aggressive conditions. Downstream operations require robust supply chain traceability and real-time product QC to support demanding end-user requirements in automotive and aerospace projects.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for polymer synthesis
    • EN 16523-1 test method for chemical permeation
    • ASTM D638 for tensile strength and mechanical property validation
    • UL 94 flammability rating for final automotive and aerospace parts

    Typical usage ratio

    • 5–25 wt% as functional comonomer, depending on required fluorine content and target properties
    • Modified by downstream polymer matrix composition

    Downstream process integration

    • Fed into step-growth or chain-growth copolymerization reactions under inert atmosphere
    • Reactive extrusion or solution polymerization for membrane/casting applications
    • QC sampling for MW distribution and fluorine incorporation analysis

    Final product types

    • High-barrier filtration membranes
    • Chemical-resistant coating compounds
    • Automotive fuel system gaskets
    • Aerospace composite prepregs

    5. Medicinal Chemistry and Research Fine Chemical Synthesis

    Top contract research organizations (CROs) and pharmaceutical R&D labs use 2,4,5-Trifluorophenylboronic Acid to build screening libraries of fluorinated drug-like molecules. This compound plays a critical role in rapid hit-to-lead development and analog synthesis through Pd-catalyzed couplings. Precise technical support and technical documentation, including spectral COAs and residual metal analysis, remain core parts of the supply relationship.

    Industry compliance standards

    • OECD GLP principles for laboratory practice
    • USP-NF Section <795> for compounding and material handling
    • GHS labelling & MSDS management for chemical safety
    • REACH registration for supply within EMEA

    Typical usage ratio

    • Equimolar or slight excess (1.0 – 1.15 molar equivalents) for high-throughput library construction
    • Fine-tuned per specific synthetic route and desired scaffold diversity

    Downstream process integration

    • Introduced at the fragment coupling or analogue diversification stage
    • Integrated into automated synthesis platforms and multi-parallel reactors
    • Regular analytical sampling for purity and structural confirmation

    Final product types

    • Diverse medicinal chemistry screening libraries
    • Reference standards for bioanalytical assays
    • Patent-submitted small molecules
    • Fluorinated research intermediates
    Free Quote

    Competitive 2,4,5-Trifluorophenylboronic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,4,5-Trifluorophenylboronic Acid: Built on Direct Experience and Real-World Application

    Our Commitment to Quality Begins with the Molecule

    Every batch of 2,4,5-Trifluorophenylboronic Acid coming from our production floors represents more than just a chemical compound — it carries all the focus and precision our technicians and engineers deliver each day. The model we manufacture, with the CAS number 1435-55-8, brings a distinct profile to the market. In-house protocols keep purity consistently above 98 percent, and trace solvent content gets tightly controlled on the same line that shaped our reputation in the boronic acid space.

    This product takes shape inside pressure-controlled reactors designed for handling multi-halogenated aromatics. Our staff monitor not only the temperature and vacuum—each step tracks batch-to-batch consistency, minimizing impurity load. Crystallization and filtration draw from decades of refining our process, so users receive a reliable product whether for research or manufacturing scale-ups.

    Pinpointing the Advantages of 2,4,5-Trifluorophenylboronic Acid

    Chemists at all levels recognize how trifluorinated boronic acids unlock reactivity nobody gets from monofluoro or difluoro variants. Ours, in particular, comes from a process developed to reduce side reactions common when working with highly-activated aromatics. In multi-step syntheses, side reactions can escalate costs and delay project milestones. Fewer side products save time and solvent, lowering production waste. Fine chemical users tackling Suzuki-Miyaura couplings or designing API frameworks leverage that difference to streamline workflow.

    Our product stands out where rivals typically offer broader, less meticulous specifications. Years ago, we discovered how uncontrolled trace moisture in cheaper products led to unpredictable yields in certain cross-coupling reactions. That pushed us to implement real-time water content monitoring during packaging, not just during drying. These extra steps draw on the same sensibilities that helped our team scale up gram-to-kilo batches for custom synthesis partners in North America and Europe.

    Physical Properties That Matter in the Lab

    On any given day, a chemist worries about solids that clump, powders that stick, or materials that refuse to dissolve. Our production floor pays as much attention to the handling properties as it does to final purity. Dense, free-flowing powders simplify weighing and dosing, reducing loss at each transfer step. We screen for unwanted polymorphs, as these have sabotaged filtration in a few unlucky trials we watched firsthand. The end result fits right into an automated dispensing system, or scales up in a multi-kilo batch reactor without operators pausing to troubleshoot agglomeration.

    Shelf stability often goes overlooked until a drum sits in storage through seasonal humidity swings. On-site stability studies show our material resists caking, even in suboptimal room conditions. Each drum or drum liner receives vacuum-sealed packing on the same production shift it’s filled. We do not treat this as an afterthought, having learned from years of supplier mishaps that small changes in storage conditions mean thousands lost to failed QA.

    Rethinking Reproducibility in Cross-Coupling Reactions

    Labs push for higher yield and reduced troubleshooting. Our experience tuning this product for pharma partners revealed that Suzuki reactions, especially on aromatic trifluorinated rings, can throw curveballs: sluggish conversions, byproduct peaks, purification nightmares. It’s not just the palladium or base — batch-to-batch quality in the boronic acid reagent actually matters. Some commercial stocks, traced back to large global distributors, threw off digital NMR data our QC team cross-checked.

    That led us to audit every feedstock and keep full traceability through ISO-driven checkpoints. It also motivated our chemistry team to optimize for ultra-low iron and halide residues. Palladium-catalyzed transformations run cleaner with our reagent, as seen in both in-house kinetics studies and customer feedback after adopting our recommended protocols.

    Custom research teams working on medicinal chemistry projects frequently report more robust reproducibility switching to our 2,4,5-Trifluorophenylboronic Acid. Patent literature rarely spells out how subtle differences in starting materials drive up time spent at the bench. We hear those pain points directly, and shaped our QC procedures to reflect those real-world demands.

    Why 2,4,5-Trifluorophenylboronic Acid Performs Where Others Fall Short

    Not every trifluorophenylboronic acid behaves the same. During collaborations with agrochemical researchers, we saw how trace metallics in low-cost sources poisoned their late-stage coupling catalysts within hours. Labs need to get on with optimizing downstream steps, rather than backtracking to track the source of a lost reaction. Modern process chemistry insists that every input act predictably from one batch to the next — not just for paperwork, but to protect a project’s bottom line. Our plant invests in direct-to-drum product transfer and redundant packaging quality checks, improving shipping stability over weeks and months.

    Synthetic chemists in-the-know differentiate products by more than CAS number. The types and loads of potential impurities, not always visible without careful analysis, dictate both reaction efficiency and downstream cost. We track and minimize biaryl byproducts, halogen exchange traces, and condensation residue, making our material suited for both library synthesis and expensive kilo-projects.

    Real Differences Compared to Other Phenylboronic Acids

    Switching between arylboronic acids, subtle changes in substitution induce outsized consequences in chemical reactivity. Many users swap 2,4,5-Trifluorophenylboronic Acid into screens with unmodified or monofluoro counterparts. Reactivity shifts hard, requiring adjustment in catalyst loading, base, and temperature. Our analytics team records shifts in oxidative stability and hydrolysis rates, which frequently catch less experienced operators off-guard. Using our 2,4,5-variant, labs report needing less catalyst and noticing smoother purification profiles.

    Unsubstituted phenylboronic acids show more baseline reactivity, but sacrifice selectivity in fine-tuned transformations. Densely-fluorinated rings, like this one, resist undesired side reactions and often bring improved metabolic stability when used as a building block. Studies in our development labs show superior yields with fewer chromatographic passes, particularly when compared with ortho- or mono-substituted alternatives.

    Application-Driven Experience, Not Just a Catalog Item

    Multinationals, academic groups, and boutique pharma firms trust us based on real project history. Our products entered patents and regulatory filings, meeting data requirements for trace-level impurity reporting. Scale-up partners, operating under tight timelines and regulatory oversight, shared real GC/MS and HPLC data showing how our 2,4,5-Trifluorophenylboronic Acid shortened route optimization cycles. University groups synthesizing libraries cite increased feasible scope, not just anecdotal improvements.

    A few years ago, a biologics outfit feedback brought attention to how our product controlled background transmetalation rates better than major alternatives. They required project delivery under strict elemental trace requirements, with zero tolerance for metal leaching—a specification that forced us to scrutinize every cleaning step in our reactor setup. We took these lessons back to our standard operating procedure, ensuring resulting product lots met both medicinal chemistry and diagnostic reagent demands.

    Our facilities regularly partner on joint development, not just drop-shipping standard aliquots. We hosted late-stage process reviews in a pharma-scale setting, walking through real purification, drying, and packaging solutions based on each user's unique constraints. By integrating feedback from bench-level users, plant engineers, and QC analysts, we’ve expanded both the purity and flexibility of our 2,4,5-Trifluorophenylboronic Acid manufacturing process.

    Troubleshooting Production and Shipping for Peace of Mind

    Handling boronic acids brings its own category of technical issues missed by casual suppliers. Thermal stability matters. We’ve redesigned our packaging three times to ensure the product handles well during both air and ocean freight. Labs receiving material from us find it arrives in ready-to-use form, with no need for thaw-and-dry steps. Such small things add up in business continuity plans—especially during shipping container delays or unforeseen customs inspections.

    Freight partners get instructed directly by our plant logistics team on handling, repacking, and temperature controls. Years back, one delayed shipment passing through a Southeast Asian port illustrated the risk of not tracking stability outside ideal storage. In response, the plant installed real-time shipment temperature logging. Customers later received analytical reports certifying temperature excursion histories alongside COAs. This level of transparency mainly stems from our collective experience cleaning up after less attentive suppliers.

    How Genuine Manufacturing Experience Shapes Superior Outcomes

    Quality boronic acid, used in modern organic synthesis, demands more than a good chemical reaction. Operators need consistent physical properties, robust purity, and minimal downtime for cleanup or troubleshooting. Each plant shift brings its own lessons: a dryer malfunction that almost compromised a shipment, feedback from a customer scaling from a 100 g lab trial to a 10 kg pilot, or a crystallization batch that ran longer than scheduled. All these drive us to meticulous documentation, continuous QC, and employee retraining—never assuming today’s output guarantees tomorrow’s success.

    Our site’s capacity allows us to respond rapidly to urgent needs, as well as accommodate multi-ton annual contracts. The knowledge doesn’t sit only with management. Operators at the filtration step, QC chemists running the HPLC, and packaging staff all invest in the final product’s quality. Daily cross-team huddles surface new approaches, whether to streamline a process or troubleshoot a colorimetric impurity spike. This boots-on-the-ground know-how, built on years of export shipments, regulatory audits, and joint research, strengthens every drum heading out the door.

    Practical Insights: Selecting the Right Boronic Acid for the Job

    Small molecule researchers know that not every variant hits the mark for each project. 2,4,5-Trifluorophenylboronic Acid stands out in medicinal chemistry for its potent role in building fluorine-rich intermediates, which impact binding affinity and metabolic pathways. Process chemists value the balance between electronic activation and resistance to degradation. Return customers appreciate our ability to document impurity profiles in forensic detail, simplifying regulatory submissions and scale-up planning.

    Comparing our product directly with alternatives, bench chemists highlight fewer low-level unknown peaks in spectroscopic analyses, faster time-to-product, and higher isolated yields. These are not advertising lines, but repeat findings reported from customer site visits or pilot plant test runs. Each of these findings pushes us to maintain and improve the process. This is more involved than publishing a catalog entry—it’s a cycle of learning, feedback, and redesign that roots our products in real-world use.

    We back our material with years of production and technical support, not just order fulfillment. Customer questions, spanning process optimization, alternate solvent compatibility, or customized QC requirements, get routed straight to the chemists who help develop and refine our process. This approach, rooted in respect for the practitioner's time and the project’s success, pushes us to go beyond the basics of chemical manufacturing.

    Challenges and Solutions on the Production Floor

    Large-scale production of boronic acids can introduce unique challenges, especially as researchers push reagents into more complex routes. Environmental health, safety protocols, risk of solvent mishandling—all can reroute a shift or delay product delivery. We built our workflow around early hazard identification and rapid mitigation. This includes real-time analytics at all key stages and electronic record-keeping with continuous review.

    Handling multi-hazardous intermediates in fluorinated aromatic routes calls for worker training, ventilation upgrades, and constant QA oversight. We’ve established tiered response plans for any process deviation. Production bottlenecks or raw material mismatches don’t just get logged, they’re rapidly escalated from the shift supervisor to plant management. Weekly operations reviews identify process tweaks to boost throughput and reliability. Waste minimization, an obligation under stricter environmental scrutiny, goes hand in hand with efficient product isolation to reduce rework and disposal costs.

    One unresolved challenge in large-scale boronic acid crystallization has been solvent recovery. Recovery units, installed to reclaim solvents from mother liquors, cut waste bills and minimize emissions. Plant teams get tracked for continuous improvement, with each kilo recovered adding up across months. Every efficiency gain helps stabilize supply and reduce cost escalation—lessons from years of managing both the chemistry and the business side of fine chemical production.

    Empowering Innovation with Better Starting Materials

    Fine chemicals, especially those based on multiple fluorinations, have become more central in pharmaceuticals, pesticides, and new material chemistry. Our job as a manufacturer is not just making existing products, but iterating alongside innovators—shaping the specs, tweaking the process, and supporting researchers testing new methods or applications.

    2,4,5-Trifluorophenylboronic Acid provides an edge in automated high-throughput screening, combinatorial library construction, and late-stage drug candidate modification. No two research projects look exactly alike, so we keep our lines flexible, supporting both high-precision, small-batch needs and recurring, large-batch production schedules. The trust we’ve built with researchers rests on more than data sheets—it comes from honest conversations about challenges at the bench, real-time problem solving, and feedback-driven improvements.

    The Real-World Value of Sourcing Traceable, Consistent Chemicals

    Scientists depend on more than molecular structure. A single out-of-spec shipment can ripple through weeks of project work. We track every batch, every lot, and every deviation, all logged from incoming feedstocks to outgoing shipments. Tougher customer demands—the need to document full analytical profiles, document shipping temperature logs, or customize particle size—are met thanks to a culture trained for rapid adaptation. We don’t view quality as a static checkbox, but as a moving target, with each collaborative project marking progress and raising standards.

    Direct feedback from end-users—surveyed throughout the year and post-project—guides our process changes. Some asked for more granular particle size data; others requested enhanced batch homogeneity for automated dosing. Each suggestion finds its way into the next process review, ensuring customers see incremental improvements year-on-year.

    In all, manufacturing 2,4,5-Trifluorophenylboronic Acid at scale is more complex than any list of specifications suggests. It demands constant vigilance, hands-on troubleshooting, and a plant-wide ethic of learning. We commit to each batch with the understanding that today's output shapes the breakthroughs of tomorrow—not just in terms of purity, but in real-world results at the bench, the pilot plant, and beyond.