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HS Code |
158154 |
| Chemical Name | Phenethylboronic Acid |
| Molecular Formula | C8H11BO2 |
| Molecular Weight | 149.98 g/mol |
| Cas Number | 1739-84-0 |
| Appearance | White to off-white powder |
| Melting Point | 112-114°C |
| Boiling Point | 327.2°C at 760 mmHg |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protect from moisture and light |
As an accredited Phenethylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Phenethylboronic Acid, 25 grams, is packaged in a sealed amber glass bottle with a tamper-evident cap and chemical safety labeling. |
| Shipping | Phenethylboronic Acid is shipped in tightly sealed containers, protected from moisture and light. It is classified as a non-hazardous substance but should be handled with care. Packages are cushioned to prevent breakage and labeled according to applicable regulations. Standard shipping methods are used, with expedited delivery available upon request. |
| Storage | Phenethylboronic acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store it in a cool, dry, and well-ventilated area, preferably under an inert atmosphere (e.g., nitrogen) to prevent hydrolysis. Keep it separate from incompatible substances such as strong oxidizers and acids. Always follow appropriate chemical storage and safety guidelines. |
Applications of Phenethylboronic Acid in Industrial ManufacturingAs a direct manufacturer of Phenethylboronic Acid, we supply this key compound to a range of specialized industries. Below, we have detailed specific industrial segments where downstream customers rely on this intermediate, each with its own regulatory frameworks, formulation needs, process flows, and finished goods profiles. 1. Pharmaceutical API Synthesis (Suzuki Coupling Reactions)Pharmaceutical companies integrate Phenethylboronic Acid in multi-step syntheses for active pharmaceutical ingredients, relying on its boronic functionality for carbon-carbon bond formation via Suzuki-Miyaura coupling. This application supports the construction of complex drug molecules, particularly those containing phenethyl motifs, by providing reliable selectivity and high yields in their API development pipelines. Industry compliance standards
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2. Agrochemical Intermediate ProductionLeading crop protection manufacturers utilize Phenethylboronic Acid to synthesize building blocks and intermediates for advanced pesticide and herbicide molecules. Its ability to introduce phenylethyl substituents through precision C–C coupling supports the scalable production of agrochemical actives with defined functionalization, crucial for both patent and off-patent formulations. Industry compliance standards
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3. Fine Chemical & Liquid Crystal Material SynthesisProducers of high-purity fine chemicals and specialty liquid crystal components incorporate Phenethylboronic Acid to construct designer molecules with controlled structural features. Its selective reactivity enables synthesis of advanced phenylethyl-containing aromatic frameworks used in optical, electronic, and specialized high-performance material markets requiring reproducibility and material purity. Industry compliance standards
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4. Research Chemical Synthesis & Custom Compound ManufacturingCustom synthesis service providers and corporate R&D centers require Phenethylboronic Acid for the rapid construction of non-commercial aromatic systems. By enabling pivotal Suzuki couplings in both mg- and kg-scale, this material supports research into new chemical entities, functional monomers, and specialty intermediates, each under project-specific workflows and strict laboratory recordkeeping. Industry compliance standards
Typical usage ratio
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Years of hands-on production have shown us that every batch of phenethylboronic acid reveals something new about the process and the needs of our industrial partners. From the earliest stages of reaction to the final crystallization and purity assessments, working with organic boron compounds has demanded close attention to every parameter. We realize that for many production chemists or researchers, reliability and purity are not just words on a label but expectations that affect downstream chemistry and costs.
Phenethylboronic acid has seen growing use as both a building block and a functional intermediate in synthesis applications, particularly in the pharmaceutical and fine chemical sectors. The unique ability of boronic acids to participate in Suzuki–Miyaura coupling provides countless avenues for constructing carbon–carbon bonds even in challenging synthetic targets. Unlike simple boronic acids, phenethylboronic acid contains a phenethyl group, opening further options for molecular design where a two-carbon linker and aromatic system are needed together.
Factory-scale production has taught us the practical differences between this molecule and other boronic acids. Phenylboronic acid, a structurally similar compound, might suffice for certain applications but cannot deliver the same flexibility in linker length or ring spacing. Optimal results in chemical synthesis often depend on such subtleties; from optimizing yields in combinatorial chemistry to exploring more selective binding motifs in medicinal candidates, these structural features matter.
Every lot of phenethylboronic acid coming off the line passes through a suite of analytical tests. Purity checks—confirmed by HPLC and NMR—have become standard practice in-house because slight impurities can wreak havoc in downstream steps, particularly in medicinal chemistry. The practical melting point, color, and appearance tell a lot before any advanced equipment gets involved. If a visual inconsistency turns up, that signals an upstream issue. Early batches taught us that stability during storage deserves stricter attention than many assume. We use tightly sealed packaging and limit light and atmospheric exposure to slow down any degradation or polymerization.
Bulk purchasers often want fine, free-flowing powders for automated weighing and dosing, but these preferences put pressure on us to continually optimize both crystallization and drying steps. Moisture content, particle size distribution, and resistance to caking affect not only the bulk handling but also the accuracy of scale-up syntheses. Our technical staff spends as much time monitoring post-production handling as running reactors, because consistent downstream performance depends on reproducibility at every stage. Packing phenethylboronic acid the right way means less waste and faster uptake in deployment.
Chemists working on complex organic syntheses choose phenethylboronic acid because it brings flexibility into molecular construction. While methyl and phenyl analogues have their place, only the phenethyl group strikes a balance between hydrophobicity and steric bulk, which some catalyst systems demand. Its utility in cross-coupling reactions is not just theoretical. The coupling to halide-containing starting materials yields biaryl and diarylalkane motifs needed in active pharmaceutical ingredients.
We hear often from clients working in early-stage drug discovery that the two-carbon ethyl spacer in phenethylboronic acid breaks new ground in receptor binding or metabolic stability studies. By contrast, shorter chain analogues cannot offer the same reach or flexibility in a molecule. Formulators in agrochemical or material science segments have told us directly that core modifications using our product improved performance and even patent positioning. Field feedback from synthetic chemists influences how we fine-tune our processes, impacting the consistency and practical reactivity of the final product.
Early on, requests for phenethylboronic acid started from researchers frustrated by the limited options with shorter-chain boronic acids. Phenylboronic acid and benzylboronic acid set the benchmarks in this field, but laboratory comparisons show that neither matches phenethylboronic acid for certain electronic and steric properties. From our manufacturing experience, the two-carbon chain between the ring and boron atom changes solubility and reactivity. The extra flexible linker affects not only the molecule’s fit in cross-coupling reactions, but also solubility in popular organic solvents.
Subtle structural differences also drive differences in shelf stability and moisture sensitivity. Phenethylboronic acid, though robust, absorbs water differently compared to its methyl or benzyl counterparts. The result: packaging and desiccant selection pays off in preventing hydrolysis. It becomes especially important in environments with variable humidity. Our own shipping trials taught us the value of anti-caking liners and reduced headspace in the container.
From a practical perspective, reactions using phenethylboronic acid can proceed under milder conditions compared to more sterically hindered analogues. This sometimes leads to improved functional group compatibility and fewer side products, which increases reaction yields and reduces purification steps. We've also noticed in field work that its reactivity in transition-metal catalyzed coupling feeds directly into process scalability, a fact attested by several industrial clients scaling reactions from gram to kilogram scale.
The main motivation for many companies to seek phenethylboronic acid lies in the increased demand for advanced intermediates—particularly those used in medicinal chemistry. Suzuki–Miyaura cross-coupling remains a principal application, but the product's influence has grown in the construction of bioactive scaffolds in pharmaceuticals and complex fine polymers. Our production teams interact regularly with process chemists during technical transfer to confirm that our product integrates seamlessly with their protocols.
Custom API synthesis brings its own challenges. Some clients have transitioned from phenylboronic acid or other competitors’ analogues, reporting higher compatibility with sensitive functional groups, especially in heteroaromatic systems. For companies developing libraries of potential drug candidates or agrichemicals, having a more modular boronic acid boosts efficiency in iterative design-loop cycles. Early success stories from such applications shape our ongoing process improvements. Before phenethylboronic acid entered the market in scale, labs either extended syntheses with additional protection–deprotection steps or settled for shorter chain analogues that delivered less effective biological activity.
Feedback from materials researchers using phenethylboronic acid in advanced polymer synthesis has pushed us to further refine our drying and filtration procedures. Some polymerization reactions demand ultra-low residual water and homogenous particle size. Technical teams devote substantial time to monitoring each step and sharing best practices between departments. Equipment upgrades to filtration and drying have followed directly from feedback.
Scaling up production from laboratory to multi-ton scale brings out differences that do not appear in glassware. Temperature profiles, agitation, and addition rates need optimization in every new vessel size. Boronic acid chemistry requires attention to trace metal content, reaction pH, and organic solvent purity. Over the years, our teams have had to troubleshoot clogging, variable crystallization rates, and off-odors, all of which trace back to fine adjustments in time, order of addition, or post-processing. Close attention to waste handling and emission controls keeps our process efficient and sustainable.
Handling the isolated product safely and efficiently for packing often sets the upper limit on manufacturing rates. Slower drying at controlled temperature preserves product consistency, but lowering moisture must not impact the acid's chemical integrity. Full drying in a vacuum oven and anti-static packaging help maintain flow and reduce batch-to-batch variability. A tightly managed materials handling sequence ensures that every drum, pail, or bag meets expectations. Regular investment in plant equipment pays off with fewer product holds and lower out-of-spec incidents.
Sourcing directly from our manufacturing facility shortens the chain of custody and reduces risk of adulteration or mislabeling, a concern that has surfaced among some past users of repackaged or resold boronic acids. Routinely, our analytical labs re-confirm purity on spot samples from the production line to deliver trustworthy numbers. We use both internal and third-party accredited laboratories for selected batches, so users have confidence in quality control claims they read on our documentation.
Long-term users—especially those in regulated manufacturing sectors—know that reliable supply only comes from close attention to process control measures. From monitoring raw material supply chains to regularly training operators, our facility’s procedures lock in best practices at each stage. Internal audits and certification schemes corroborate our commitment to finished product quality.
Anecdotal feedback from long-term users points towards fewer failed reactions and less downtime from out-of-spec reactivity compared to cheaper alternatives. Clients who switched to our phenethylboronic acid have highlighted cost savings from reduced labor, fewer purification steps, and greater overall throughput. Real-world reliability depends on details—like the precise water content, bulk density, and color consistency every time.
Safe production and use of boronic acids benefit from a robust understanding of their hazards, and our experience leads us to maintain open dialogue with downstream users on safe handling practices. Although phenethylboronic acid poses low inhalation risk when handled as a solid, standard engineering controls—dust containment, proper PPE, and airflow—minimize any exposure. Through regular safety training, we reinforce best handling procedures, both in our plant and by sharing information with downstream partners.
Our teams remain mindful of the waste implications during both manufacturing and users’ processes. Efforts to minimize solvent usage, recycle process streams, and safely capture all vented off-gas have become routine. Sustainable operation means engineering out cross-contamination risks or fugitive emissions. Our facility’s track record reflects this focus, with continuous improvement targets set each quarter.
The byproducts from coupling reactions—often halide salts and base residues—call for sound waste management practices in customers’ operations as well. Our technical support staff frequently consults with buyers on best practices to manage, neutralize, or recover valuable metals from catalyst residues—a service only someone with deep process familiarity can offer.
Scientific progress doesn’t stand still. Neither does production chemistry. Collaborating directly with end users allows us to catch improvement opportunities early. For example, customers working at high-throughput screening scales have requested tighter particle size distributions and faster dissolution profiles for automated synthesis modules. In response, we modified both grinding and sieving setups and fine-tuned crystallization conditions, achieving greater consistency.
Open lines of communication with research, development, and manufacturing customers provide a feedback loop that shapes our operational choices. Some feedback has led us to rework drum liners, reduce shipping delays, and invest in higher-precision batch labeling. Our sales and technical representatives spend as much time gathering process feedback as they do talking about product features.
Annual customer surveys, joint troubleshooting calls, and collaborative process optimization projects help us set priorities that impact both product quality and user experience. We see every customized request for documentation, packaging size, or special delivery conditions as an opportunity to refine our operation, not a burden.
There’s a big difference in outcomes between high-purity and lower-purity phenethylboronic acid. Even the smallest change in residual water, residual solvents, or by-product content can ruin a coupling step or delay an entire project. Internal protocols extend beyond minimal purity—HPLC, NMR, IR, and heavy metal testing set our acceptance criteria. Every operator on the line knows what to check for, and why it matters. We publish facts, not just numbers, because every number stands behind real equipment and people in our plant.
End users in the field know that poorly characterized boronic acids leave their own fingerprints: blackened reaction mixtures, unexplainable by-products, or substandard intermediate yields. With constant improvements to both reaction chemistry and downstream handling, we respond directly when a scientist flags an anomaly, chasing down root causes until they’re solved.
Market demand and research advances push our operation forward. Scientists are investigating ever more complex molecular scaffolds, and their tolerance for supply or quality issues continues to decline. We’re seeing more requests for tailored production runs, specialty pack sizes, and ultra-pure grades—particularly for export markets with tighter regulatory controls. Our investment in process analytics and feedback-driven plant upgrades keeps us ahead of these requirements.
Advances in coupling chemistry may soon stretch the capabilities of bulk boronic acid intermediates even further. Sustainable sourcing, energy minimization, and reduction of process hazards are active projects with real investment from our technical teams. We know that environmental and regulatory pressures on all chemical makers—including ourselves—require sustained innovation, not just compliance.
With decades invested in the technology and close collaboration with leading users, we build on every batch, every shipment, and every challenge. Phenethylboronic acid continues to find new applications in pharmaceutical, agricultural, and material laboratories—each pushing for new levels of reliability and performance. Our commitment stays pointed directly toward enabling faster, safer, and more efficient chemistry for all partners.
Phenethylboronic acid has changed how chemists think about modular carbon–carbon bond formation. As a manufacturer, witnessing its effect on synthesis, workflow, and business outcomes confirms the value of specialization and close process control. We remain dedicated to constant refinement, listening closely to those using our product on the front lines of research and production, and responding with practical, informed solutions shaped by experience.