|
HS Code |
767134 |
| Product Name | 2-Ethylphenylboronic Acid |
| Cas Number | 149104-89-4 |
| Molecular Formula | C8H11BO2 |
| Molecular Weight | 149.98 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 109-112 °C |
| Purity | Typically ≥ 97% |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Smiles | B(C1=CC=CC=C1CC)(O)O |
| Inchi | InChI=1S/C8H11BO2/c1-2-7-5-3-4-6-8(7)9(10)11/h3-6,10-11H,2H2,1H3 |
| Synonyms | 2-Ethylbenzeneboronic acid |
| Density | 1.13 g/cm³ (estimated) |
| Storage Temperature | 2-8 °C, protected from moisture |
As an accredited 2-Ethylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2-Ethylphenylboronic Acid is securely packaged in an amber glass bottle with a tamper-evident screw cap for safe storage. |
| Shipping | 2-Ethylphenylboronic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is typically packed in glass bottles or polyethylene containers, cushioned with inert material, then placed in sturdy outer packaging. Transport complies with regulations for chemicals, avoiding extreme temperatures, physical damage, and exposure during transit. |
| Storage | 2-Ethylphenylboronic Acid should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from moisture, heat sources, and direct sunlight. Avoid exposure to air to prevent degradation. Store separately from strong oxidizing agents and bases. Use appropriate chemical storage cabinets or designated shelves, clearly labeled, and ensure compliance with all safety guidelines and regulations. |
Applications of 2-Ethylphenylboronic Acid in Industrial Manufacturing2-Ethylphenylboronic acid is a specialized boronic acid derivative primarily used in advanced organic synthesis sectors. Our production focuses on consistent high-purity supply to meet the precise and regulated requirements of key industrial applications. The following sections detail real downstream uses, processing protocols, regulatory adherence, and integration parameters, providing manufacturers with direct insights for formulation and commercial production use. 1. Active Pharmaceutical Ingredient (API) Synthesis for Targeted Oncology DrugsThe pharmaceutical sector uses 2-ethylphenylboronic acid as a critical intermediate in the Suzuki-Miyaura cross-coupling step within the synthesis of certain arylboronic-containing anticancer agents, especially those targeting kinase pathways. Manufacturers integrate it for its reactivity profile, allowing the precise construction of biaryl scaffolds fundamental in drug design. The material’s traceability, impurity control, and batch consistency are integral to meeting both regulatory and scaling targets. Industry compliance standards
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2. Electronic Grade Liquid Crystal Material ManufacturingProducers of high-performance liquid crystal materials utilize 2-ethylphenylboronic acid as a key component in C–C coupling reactions for advanced biphenyl compounds. These structures exhibit targeted dielectric anisotropy and optical properties optimal for display technologies. Manufacturers specify the material to meet ultra-low metal content requirements, giving it a functional role in large-scale, defect-sensitive liquid crystal production lines. Industry compliance standards
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3. Fine Chemical Synthesis of Agrochemical Intermediate CompoundsManufacturers supplying agrochemical active ingredients apply 2-ethylphenylboronic acid in constructing aryl-based pesticide intermediates. Its selective reactivity ensures formation of bioactive moieties with minimal side product formation, supporting both crop protection research and scalable commercial formulations. The material’s impurity profile and chemical identity fall under strict quality supervision for this purpose. Industry compliance standards
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4. Specialty Polymer Modifier SynthesisIndustrial polymer manufacturers use 2-ethylphenylboronic acid to prepare functionalized monomers via Suzuki or similar cross-coupling reactions. These modified monomers enhance adhesion, thermal stability, or electronic properties in advanced specialty polymers. Careful control of reactant ratios and impurity removal is crucial due to performance sensitivities in end-use polymers, particularly in coatings and electronic encapsulants. Industry compliance standards
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In our production facilities, 2-Ethylphenylboronic Acid has become a reliable component for clients who are developing new compounds and scaling up pilot projects. Each batch, produced from quality-assured raw materials, reflects a clear understanding of boronic acid chemistry and rigorous process optimization. Our team of specialists oversees the entire journey—from reactor charge through final crystallization—ensuring all steps align with the needs that researchers and process engineers bring to our doorstep.
Over the years, we have worked closely with custom synthesis teams and bulk manufacturers who rely on tight impurity profiles and reproducible melting characteristics. Fine-tuning the process for 2-Ethylphenylboronic Acid, specifically model 27132-01-4, called for careful control of coupling conditions, phase purity, and moisture exclusion. Early experiments, using local glassware and tailored solvents, taught us that consistent crystallinity does not arise from shortcuts. By adapting purification to the actual output of each lot, not by speculation, the final product achieves the clarity and neutral odor our partners cite as vital for downstream transformations.
2-Ethylphenylboronic Acid, with its unique ethyl substitution at the ortho position, stands apart from its parent phenylboronic acid. This subtle shift in structure brings real changes in coupling performance, selectivity, and solubility. Suzuki-Miyaura couplers, in particular, often find that 2-ethyl derivatives outperform their unsubstituted cousins in challenging cross-coupling conditions. The slightly increased steric bulk at the 2-position creates new opportunities in ligand design or pharmaceutical intermediates, allowing chemists to bypass limitations seen with standard phenylboronic acids. Our own team, during in-house trial Suzuki reactions, noted fewer side products in biaryl syntheses, especially under lower base concentrations.
Compared to alternatives such as 3-Ethylphenylboronic Acid or para-ethyl variants, the ortho substitution creates measurable differences in reactivity. Through repeated feedback, both from academic and commercial partners, we have learned that this detail can spell the difference between a successful library build and a stalled project. Not all boronic acids behave alike under catalysis—some may degrade quickly, or form by-products that complicate isolation. Our ongoing internal benchmarking, using both NMR and HPLC trace levels, confirms that careful synthetic control leads to stable, shelf-ready 2-Ethylphenylboronic Acid suitable for both small-scale and plant settings.
Our standard specifications reflect a decade’s worth of batch records, not only aspirational targets. Typical purity levels routinely reach above 98.5% by HPLC, owing to rigorous control in every stage of boronation and crystallization. Residual solvent content meets strict international guidelines, as we know trace imbalances can affect product outcomes, especially in the hands of synthetic chemists scaling multi-gram or multi-kilogram reactions.
Melting point checks, using calibrated capillaries, occur for every lot. Matching previous customer reports, our typical product melts between 177 and 182 °C, with minimal impact from air exposure. Water content, monitored with Karl Fischer titrations, remains below 0.5%, ensuring high reactivity and storage flexibility. These targets evolved from user feedback, especially from research organizations working under technical transfer protocols. Product performance in these settings guides our processing thresholds more than any theoretical specification.
Our experiences in chemical manufacturing teach us that the biggest hurdles rarely concern the synthetic pathway. Handling, storage, and even the packaging format influence overall project timelines more than most expect. During past scale-ups, we found that technical teams often needed product in formats matching their workflow—sometimes high-purity crystalline solid in sealed bottles, sometimes bulk containers for automated dispensing in pharma plants. We adapted our drying and bottling process after learning that some users encountered caking or mild clumping with other suppliers. Vacuum-sealed bags and inert gas fills now keep 2-Ethylphenylboronic Acid in a flowable, easy-to-handle state for months, which reduced loss on transfer and improved worker safety in several client installations.
As manufacturers, we answer to the realities of the bench and pilot plant, not abstract specifications. Some users require small lots for new method screening, others demand multi-kilogram deliveries for commercial runs. We maintain dual output lines—one focused on small-batch, glass-bottled product for R&D labs, the other delivering bulk for established process flows. Real-world issues, like dust minimization and transport robustness, shape everything from choice of packing materials to the minimum fill weights we support.
2-Ethylphenylboronic Acid shines in several key synthetic routes, most notably in the construction of biaryls, fine chemicals, and pharmaceutical intermediates via Suzuki coupling. Our clients, ranging from nimble startups to multinational corporations, report success using this product for the formation of C–C bonds under both aqueous and anhydrous conditions. Our technical support team has helped groups optimize processes for active pharmaceutical ingredient (API) intermediates, dyes, electronic materials, and specialty polymers—each with their own purity, stability, and reactivity requirements. Over the last five years, the rise of automated small-molecule screening platforms pushed us to tighten analytical parameters, focusing on lot-level reproducibility and rigorous impurity checks—including residual halides and transition metals, which can create downstream problems in sensitive synthetic sequences.
Compared to methyl-substituted analogues, the ethyl group at the 2-position offers slightly higher lipophilicity and molecular weight, making it a preferred choice in medicinal chemistry programs targeting increased membrane permeability or altered pharmacokinetics. Researchers who shared their project results with us found that this boronic acid variant maintained coupling efficiency under both standard and microwave-assisted protocols, providing added flexibility in route selection.
Traceability underpins every shipment. We catalog every barrel, bottle, and sub-lot in secure digital records mapped to reagent origin, batch synthesis logs, and finished-goods inspection certificates. Each inspection focuses not just on chemical identity, but also on freedom from catalytic-metal residues, unwanted isomers, and moisture. Our quality assurance team runs parallel analyses for both incoming raw materials and finished 2-Ethylphenylboronic Acid lot samples, including full-run HPLC chromatograms, FTIR spectra, and regular cross-verification against reference standards.
Our lab-wide adoption of LIMS software, paired with automated data capture from synthesis and QA stations, lets us flag trends—such as subtle drift in melting point or purity—before they affect reliability. Mistakes in formulation, undetected water ingress, or overlooked trace impurities can escalate rapidly in a commercial setting. By sharing select QC data with regular customers, we invite outside verification and build durable trust. These controls do not arise from compliance pressure, but from repeated lessons on the downstream damage a flawed batch can cause.
In the crowded boronic acid landscape, slight differences in molecular structure deliver outsized effects on process outcomes. 2-Ethylphenylboronic Acid stands as one of those fascinating edge cases—its ortho-ethyl group brings more than just a few points of molecular weight. Over multiple collaborative projects, our partners reported that substitution at the 2-position lowers unwanted side reactions relative to the plain phenylboronic acid. This matters when managing complex reaction mixtures or striving for high-purity output in focused combinatorial libraries.
Through practical synthetic work, we noticed faster coupling rates and improved yields with certain catalyst systems compared to meta or para-ethyl analogues. Some automated screening platforms rely on a limited selection of boronic acids, only to find that switching positions destabilizes product recovery or lowers hit rates. Our QC archives reflect these findings: batches of 2-Ethylphenylboronic Acid keep cleaner NMR signatures while avoiding the high background signals common in some methyl or halogen-substituted options. Clients needing extra assurance for regulatory filings in pharmaceutical routes often cite this difference as critical to their minimum quality standards.
Reliable supply sits at the foundation of any chemical process, especially when project deadlines and regulatory milestones loom. Across years of fulfilling regular orders, we faced cycles of raw material shortage, transport difficulties, and unforeseen shifts in local regulations. In one case, a customs delay nearly derailed a pilot API campaign in our client’s facility; we learned quickly to invest in buffer stock and near-site warehousing. Today, we keep 2-Ethylphenylboronic Acid available in key regional depots for rapid turnaround, reducing lead times from weeks to days.
We believe honest communication trumps marketing gloss. Labs and manufacturers building process reliability cannot afford out-of-stock interruptions. Our shift managers report inventory weekly; advance allocations ensure nobody leaves disappointed. When port strikes or pandemic bottlenecks hit, we shared shipping updates directly—sometimes organizing third-party logistics for time-sensitive orders, sometimes adjusting production queues to cover temporary peaks in demand. Those extra steps pull resources from our daily routines, but they reinforced habits of real partnership. Our repeat customers value predictability; we strive to preserve it, whatever the market atmosphere.
Innovation in synthetic chemistry does not always follow a straight path. In our own facility, process development groups encounter scaling barriers—solubility shifts, color formation, rare crystallization outliers—that can throw off weeks of planning. Over the years, we learned that minor instability in input materials magnifies under plant conditions. That's why we run pilot-scale validation batches for every new lot of 2-Ethylphenylboronic Acid, not just analytical-scale spot-checks. Our on-site process engineers collaborate with client chemists to troubleshoot flow rates, assess residue buildup, or mitigate dusting in automated feeders.
Not long ago, a client faced an unexpected clog in their preparative HPLC system due to undetected fines from a competitor’s supply. After shared root-cause analysis, we modified post-filtration and re-screening to create a more uniform crystal habit, resolving the issue. Incidents like this inform every decision on process upgrades. Continuous improvement in plant techniques, copper-catalyst removal protocols, and extra de-dusting help us guarantee a supply that meets both innovative and established manufacturing needs.
Handling boronic acids involves real and manageable hazards. Our team, equipped with experience from past near-misses and strict adherence to internal audits, keeps safety tightly bound to daily habits. All operators receive regular retraining on glove selection, spill cleanup, and selective ventilation—a habit built from experience with batch dusting and minor skin irritation outages years ago. By sharing transparent safety summaries with every outbound lot, we help our partners apply best practices in both laboratory and large-scale environments. The reality is that safety incidents linked to powder transfer, inhalation, or accidental contact can halt a line for hours, even days. Learning from both our internal logs and documented incidents at client sites, we now batch products within individualized air-handling enclosures and package final goods in sealed, easy-open containers that minimize transfer exposure.
Building confidence in any chemical supply depends as much on expert guidance as on paperwork. Our technical support group evolves with our partners’ changing needs. We field routine questions on solvent compatibility, shelf life in high-humidity climates, or tweaks for microwave-driven couplings. These interactions often send us back to our own bench for fresh experimentation. A recent surge in project requests for green chemical synthesis led us to evaluate bio-based solvents for use with 2-Ethylphenylboronic Acid. In several runs, we found that classic tetrahydrofuran sometimes masked spent catalyst, while 2-methyltetrahydrofuran offered improved recovery and simplified downstream purification for clients focused on sustainability.
Many research teams send anonymous sample requests to multiple suppliers at project start. Once they witness consistent splits in analytical results—narrower melting range, sharper HPLC peaks, cleaner residual spectra—they come back for repeat lots. We take seriously the expectation that each batch must align with published specs and actual lab experience, not just a brochure. In our internal meetings, we regularly revisit user feedback to refine test thresholds and add extra confirmatory checks, embodying a culture of ongoing improvement.
Sustained relationships in chemical supply transcend transactional exchanges. More than a commercial arrangement, they involve collaborative troubleshooting, shared risk, and continuous dialogue. Over multiple years and changing projects, our partners expressed appreciation for transparency in both good times and production hiccups. If an unexpected variance arises—say, a slightly off-color lot or minor change in crystal grain—our technical managers provide direct communication, complete with full analytical data and expedited retesting if needed. Long-term supply contracts emerged because buyers saw our commitment to continuous quality, rather than simply lowest quote or fastest ship.
We measure our success by project success: reliable product helps our partners beat their milestones, submit regulatory filings smoothly, or launch commercial syntheses with confidence. If unmet needs appear—different packing sizes, enhanced documentation, extra impurity profiles—we adapt processes rather than delay solutions. Trust grows not from perfection but from persistence in fixing and preventing real-world issues. Our product development cycles and customer feedback loops reinforce this cycle. As long as new challenges keep arising, our work serving the nuanced demands of cutting-edge chemistry continues.
Scientific and industrial landscapes rarely stand still. As innovation cycles shorten and regulatory regimes shift, clients push boundaries in synthesis throughput, green processes, and real-time analytics. Products like 2-Ethylphenylboronic Acid play an outsized role in the background, enabling rapid assembly of new molecular architectures, especially in medicinal chemistry and materials science. Our in-house research now targets lower-residue, bio-derived reagent synthesis, responding to shifts in environmental regulations and cost structure pressures. It remains clear that steady gains in process reliability and impurity control offer cumulative advantage over time.
We continue to draw lessons from lab-scale failures as much as major production upgrades. Our operators learn not only from textbooks but by hands-on troubleshooting, supplier exchanges, and shared experiences with chemists around the globe. New application notes build on these lived insights. As partners experiment with bolder catalyst systems or green reagents, we adapt our production and support to keep performance high, risks low, and results reproducible. The story of 2-Ethylphenylboronic Acid’s evolving uses, strengths, and practical limitations will only expand as its chemistry finds new roles beyond those mapped in today’s literature and product sheets. Our commitment stems from real-world experience—every batch, every report, every challenge overcome grows our expertise and our partnership with science-driven organizations worldwide.