|
HS Code |
187200 |
| Cas Number | 1976-07-0 |
| Molecular Formula | C2H7BO2 |
| Molecular Weight | 73.89 g/mol |
| Iupac Name | ethylboronic acid |
| Appearance | white to off-white solid |
| Melting Point | 85-90°C |
| Boiling Point | No data (decomposes before boiling) |
| Density | No data available |
| Solubility In Water | soluble |
| Smiles | B(CC)(O)O |
| Inchi | InChI=1S/C2H7BO2/c1-2-3(4)5/h4-5H,2H2,1H3 |
| Synonyms | Ethylboronate, Boronic acid, ethyl- |
| Pubchem Cid | 141063 |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
As an accredited Ethylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethylboronic Acid is packaged in a 25g amber glass bottle with a secure screw cap and hazard labeling for safe laboratory use. |
| Shipping | Ethylboronic Acid is typically shipped in tightly sealed containers under a dry, inert atmosphere to prevent moisture absorption and decomposition. It should be handled with care, following all chemical safety guidelines, and transported according to local, national, and international regulations for hazardous materials to ensure safe delivery. |
| Storage | Ethylboronic acid should be stored in a tightly sealed container, protected from moisture and air, as it is sensitive to hydrolysis. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Avoid exposure to direct sunlight and sources of ignition. Store under inert atmosphere if possible for prolonged stability. |
Applications of Ethylboronic Acid in Industrial ManufacturingEthylboronic acid plays an essential role as a functional building block in several high-value industrial sectors. As the original manufacturer, we collaborate directly with key downstream producers to achieve scale-up, compliance, and reliable performance in each application scenario. Below are verified industrial use-cases, reflecting current manufacturing trends, real compliance benchmarks, validated downstream process routes, and standard formulation practices. 1. Active Pharmaceutical Ingredient SynthesisPharmaceutical manufacturers use ethylboronic acid as a selective coupling agent for constructing complex organic frameworks, particularly in Suzuki-Miyaura cross-coupling reactions. Its role as a boron source supports efficient C–C bond formation, benefiting synthesis routes for multiple small-molecule APIs, especially those requiring boron-derived moieties. Integration into GMP facilities involves rigorous control over raw material quality, traceability, and residue management, aligned to ensure adherence to international drug manufacturing standards. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingThe crop protection industry uses ethylboronic acid for introducing boron onto aromatic or heterocyclic scaffolds in the synthesis of new generation pesticides and herbicide intermediates. Plant protection manufacturers benefit from its selective reactivity and ease of downstream transformation, supporting sustainable synthesis routes by minimizing hazardous by-products and maximizing active ingredient yields. Industry compliance standards
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3. OLED and Organic Electronic Material ProductionManufacturers in the optoelectronics sector employ ethylboronic acid for producing advanced organic semiconductors and light-emitting materials. Its precise incorporation into aryl frameworks tunes electronic properties essential for controlling charge transport and emission characteristics, especially in high-purity, thin-film device fabrication environments. Industry compliance standards
Typical usage ratio
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4. Fine Chemical and Specialty Reagent ProductionProducers of specialty boron reagents and tailored fine chemicals select ethylboronic acid for downstream conversion into advanced reagents, catalyst ligands, and complex organoboron structures. The compound’s chemical stability and predictable reactivity enable precise functionalization required for high-purity laboratory and industrial reagents, and for contract manufacturing of custom boron-based units. Industry compliance standards
Typical usage ratio
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Ethylboronic acid shows up in our production schedules right alongside the more recognizable boron sources, but gets far less buzz in public conversations. Every day, on the plant floor, we see a steady demand from labs and production facilities tackling modern challenges in synthesis chemistry. We manufacture this compound, model EB-9782, to meet the rising standards for purity and reproducibility that researchers and pharmaceutical companies now stake their reputations on. Ethylboronic acid, with a formula of C2H7BO2, offers a powerful combination of reactivity and control for professionals skilled enough to harness it well.
Colleagues in synthesis, especially those focused on Suzuki-Miyaura cross-coupling reactions, already understand the value of boronic acids as essential reagents. From my own time listening to feedback from bench chemists and project leads, subtle differences in boronic acid derivatives can make or break a reaction. Ethylboronic acid delivers a straightforward ethyl substitution, which allows for unique formation of carbon-boron bonds not achieved when using the more popular phenyl, methyl, or pinacol boronic variants. In practice, that means a synthetic chemist can fine-tune a molecule’s properties or introduce a new piece to an existing project without setting off a cascade of unwanted side reactions.
We often talk with clients who’ve hit a wall with other boronic acids—either too sluggish or too dynamic in their couplings. Ethylboronic acid handles well in both solution and solid form, providing measured reactivity in controlled lab work and at the scale-up stage. The material consistently melts between 86 and 91 °C, and maintains a clean, single spot on TLC during quality testing. These small but important details make everyday handling easier, especially during high-throughput screening and repeat batch production.
There is a longstanding demand for reagents with minimal batch-to-batch variation. Medicinal chemists, agrochemical researchers, and materials science teams bring us their own distinct requirements based on prior headaches with inconsistency. From our end, we control water content, monitor NMR purity, and pack material in suitable sealed containers under inert gas. This ensures ethylboronic acid leaves the loading dock within established specifications. We ship powder and crystalline forms by default, after rigorous in-house testing for purity (98 percent or higher, by most protocols) and confirmation of molar mass at 73.89 g/mol. Experience reminds us that what leaves our warehouse is only as good as the weakest quality control checkpoint.
Storage and long-term stability remain top customer questions. Since this compound is somewhat hygroscopic, we supply it in moisture-proof packaging, lined with desiccants. Onsite, our own sample vault confirms that material kept sealed and dry shows only minor changes in purity after months in storage. Customers with larger or slower-moving inventories benefit from transparent batch dates and our practical advice to avoid repeated exposure to air.
Ethylboronic acid’s biggest impact lands in synthesis—small molecule drug discovery, fine chemicals, and specialty materials. As a manufacturer with a line of boronic acids, we can directly see who buys what, and we track how the requests for ethyl-substituted boronic acids have shifted over time. Nearly every advance in C–C coupling pushes research into search of more selective, predictable reagents that form the desired bond and little else. Older protocols still lean on phenylboronic acid or pinacol boronate esters, but those present challenges, especially with substrate specificity or product isolation. Ethylboronic acid sidesteps some solubility pitfalls, wears fewer “sticky” labels, and produces byproducts that are simple to purge—even in the hands of junior technicians learning the ropes.
Clients in pharma often pursue molecules where a single carbon atom makes or breaks biological activity. For them, the plain ethyl group of ethylboronic acid is not just a placeholder. It’s an exact building block, producing compounds with modelable pharmacokinetic properties or regulatory advantages compared to heavier or aromatic substitutions. In electronic material development, the low molecular weight and simple structure lower background noise in final products. Agrochemical partners look for boronic acids with manageable toxicity yet strong enough to persist in test runs for plant and soil systems. Ethylboronic acid’s straightforward profile gives them that balance, reducing the need for elaborate post-processing or reclamation protocols.
Our customers often compare ethylboronic acid to more heavily marketed compounds like methylboronic acid, phenylboronic acid, and alkylboronic esters. Each boronic acid presents unique reactivity, handling, and toxicity profiles. For instance, methylboronic acid boils at a lower temperature and often volatilizes during prolonged heating. It can also react abruptly in the presence of water or air, complicating isolation steps after a reaction. By contrast, ethylboronic acid balances moderate volatility with broad solvent compatibility, making it less finicky in stepwise syntheses.
Phenylboronic acid, the industry staple, offers a rigid aromatic ring, influencing selectivity in aromatic couplings but sometimes hindering reactions with complex, flexible substrates. Pinacol boronate esters, popular for their enhanced stability, require an extra deprotection step—a time-consuming headache in lean manufacturing settings. Ethylboronic acid, on the other hand, comes as a “naked” acid without that extra pinacol group. Chemists appreciate skipping auxiliary steps, especially on tight project timelines.
Safety data and tox studies show that ethylboronic acid rates among the less hazardous of the boronic acid family, especially compared to some cyclic and highly branched derivatives. Proper handling remains non-negotiable, but standard studio PPE, adequate ventilation, and sensible waste management suffice by known protocols. Handling advice reflects our own in-house procedures—no elaborate engineering controls or specialty tools required.
We spend considerable time with reactor loading, solvent selection, and reflux conditions to achieve high-quality ethylboronic acid. Direct boronation of ethyl-containing organometallic intermediates works best, avoiding cumbersome intermediates. All our production is batch-based, with rigorous inter-lot analytics ensuring both product identity and freedom from boron-containing byproducts. Analytical data from proton NMR, 11B NMR, and LC-MS back every shipment. We maintain a database of certificates, blind-tested by independent labs at intervals, to guarantee accuracy. Most repeat customers cite reliable analytical packages as their main reason for continued business with us.
Scaling up, while maintaining material integrity, posed early challenges. We resolved procedural bottlenecks with closed-system charging, dedicated glassware, and in-plant solvent recycling. Operators run each step with direct oversight from chemists well-versed in fine chemicals and chromatography. We seldom see contamination with dialkyl boronic acids or higher borates, a testimony to disciplined loading ratios and careful separation at workup.
On the shipping dock, ethylboronic acid leaves our plant in HDPE jars or fluoropolymer-lined drums. We train staff to keep each drum sealed, lines purged, and exposure to air brief. Logistics teams coordinate expedited deliveries for bulk orders anywhere in our trading region. For global shipments, we select freight partners experienced with heat-sensitive and moisture-reactive compounds, tracking not just time in transit but also temperature and humidity data logged en route. Customers buying kilogram lots or more get these logs on request, a level of transparency that reassures anyone investing months or years of work on a single intermediate.
Experience tells us that the real challenge is not getting ethylboronic acid to its destination, but keeping it in top condition during the often-lengthy storage at customer sites. Even as a manufacturer, we keep “aged” samples on hand and test for changes in melting point, color, and chromatographic purity. Change shows up as yellowing or subtle signal shift, warnings we pass along as needed. Users handling the compound in open labs—especially in high humidity—should try to aliquot what they will use for each job. That training trick, handed from our own chemists to theirs, often saves projects from a disappointing repeat run due to degraded stock.
Our daily interactions include fielding technical questions, troubleshooting unexpected lab results, and discussing setup improvements. Some clients, especially those new to boron chemistry, ask detailed questions about solvent compatibility and filtration. Field experience suggests ethylboronic acid works comfortably in common organic solvents (THF, toluene, acetonitrile, DMF) without forming troublesome emulsions or precipitates during extraction. During early-stage workup, a simple brine wash and standard chromatographic column usually give clean product for downstream applications. We base these recommendations on repeated, internally verified procedures, not just published protocols.
We see growing demand not just from established pharmaceutical giants but also from new players in green chemistry and materials innovation. Compact reactivity and manageable handling risk, along with clear environmental data, drive this uptake. Research teams designing biodegradable polymers or self-healing materials look for small, straightforward boronic acids that slot into their designs without introducing persistent chemical baggage. Ethylboronic acid fits these projects—low boron content, simple hydrocarbon “tail,” reliable documentation supporting regulatory submissions. We watch for trends in project requests, and adjust our forecasts based on end-user dialogue, allowing us to stock what they actually need rather than what conventional wisdom predicts.
In our workshop, discipline rules. Every kilogram of raw boron feedstock undergoes screening for contaminants, and each reaction batch draws on a chain of custody extending from raw input to final fill. Analytical staff, not accountants, decide batch release. Documentation follows industry best practices—with print and digital records encrypted and archived beyond the minimum legal term. Third-party inspections and regulatory filings govern documentation; we tailor traceability so auditors at both customer and public authority levels can trace a drum’s history back to the day of synthesis.
Requests for extra documentation began ramping up within the last decade. Clients in life sciences, for example, increasingly request elemental impurity profiles, allergen statements, and solvent residue data. We accommodate these through both in-house and independent testing. Staff who field these requests do not rely on generic stock answers but draw from first-hand knowledge of each production run. The value of this attention shows up in project timelines: customers spend less time arguing with procurement or compliance, more time running their chemistry.
On the regulatory front, ethylboronic acid holds no “high concern” designations under major global chemical inventories. Its safety profile, based on current literature and in-house review, rates as manageable under standard industrial safety protocols. Bulk customers seeking regional registration support receive all data and forms required. We’ve seen that even midsize organizations benefit from access to up-to-date hazard evaluation, especially as policies on boron compounds shift in response to environmental and toxicological updates.
Reliable supply and tight tolerances define our reputation with those who work on timelines that afford no margin for error. We operate under a simple rule—never compromise on analytical standards. In our experience, “trace impurities” in some cases become the difference between a clean patent application and a failed reproducibility trial. Some teams trust us precisely because we invest in batch-to-batch tracking and analytical transparency—and own up to errors immediately should any slip past initial QC.
As direct manufacturers—no trading middlemen between the plant and end user—we witness every stage of ethylboronic acid’s journey, from raw material selection to the final container on a customer’s bench. Our commitment stretches beyond compliance toward a culture where routine conversations with synthesis teams shape product offerings for tomorrow. Significant product updates—whether improved purity, new packaging, or extended shelf life—flow from open discussion. Our relationship with client teams is grounded in shared goals rather than transactional exchange.
Managing ethylboronic acid, particularly in humid or variable environments, requires vigilance. Common stumbling blocks include unnoticed degradation and loss of potency due to careless storage. Our operations staff learned long ago the value of cold-chain warehousing and desiccant-supported packaging. Each batch ships with storage advice, based on our real experience handling hundreds of lots through every season and shipping climate. New users looking to avoid common pitfalls find our anecdotal support, not just a printed sheet, saves both time and cash. Some partners, challenged by limited storage space or unpredictable usage, have switched to smaller pack sizes at our suggestion—reducing loss while matching their process flow.
The issue of sustainability, always present in the chemical industry, remains a concern with even simple boronic acids. Process engineers here continue to look for solvent recovery, lower-waste workups, and increased reactor efficiency. Recent improvements to the ethylboronic acid line-up rely on stepwise optimization, not radical overhaul—shorter reflux times, clever reagent recycling, and greener solvent selection. We share these advances with clients who care about minimizing waste and improving energy efficiency. Several clients in pharmaceutical production integrate our product improvement suggestions into their own protocols, cutting raw material and energy use.
The story of ethylboronic acid reflects broader patterns in chemistry-driven industries—the need for versatile, reliable, and environmentally responsible building blocks. We see requests growing for dual-use reagents that work across multiple classes of reactions. R&D collaborations between our team and customer organizations sometimes develop improved protocols, giving both sides a stake in long-term success. Direct, ongoing communication keeps us nimble—able to tweak parameters or ramp production as project timelines shift or new applications are discovered.
Our team stays engaged with emerging research, monitoring patent filings, academic literature, and direct customer feedback. This effort keeps production responsive not just to today’s requirements, but positioned to answer the demands of new molecule development, green chemistry, and regulatory shifts. By keeping one foot on the plant floor and another in the lab, we bridge practical production realities with the dynamic needs of modern research. This balanced approach—focusing on trust, technical transparency, and shared problem-solving—anchors our entire strategy for ethylboronic acid and everything else in our catalogue.
Ultimately, the impact of ethylboronic acid on contemporary synthesis lies not in lofty claims, but in everyday reliability. Years spent in direct production, documentation, and problem-solving have made us confident in backing this compound for anyone searching for consistency and performance in boron chemistry.