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HS Code |
556076 |
| Chemical Name | Diethyl(3-Pyridyl)Borane |
| Cas Number | 149885-02-5 |
| Molecular Formula | C9H14BN |
| Molecular Weight | 147.03 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Smiles | CCB(CC)c1cccnc1 |
| Purity | Typically ≥98% |
| Storage Conditions | Store under inert atmosphere, cool and dry place |
| Solubility | Soluble in common organic solvents |
| Synonyms | 3-Pyridylboronic diethyl ester |
| Application | Used as a coupling reagent in organic synthesis |
As an accredited Diethyl(3-Pyridyl)Borane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, with tamper-evident cap and hazard labeling. Clearly marked: "Diethyl(3-Pyridyl)Borane, CAS#, handle under inert atmosphere." |
| Shipping | Diethyl(3-Pyridyl)Borane is shipped in tightly sealed containers under inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Packaging complies with all local and international regulations for hazardous materials. Temperature control and proper labeling ensure safe transport. Handle with appropriate precautions upon receipt. |
| Storage | Diethyl(3-Pyridyl)Borane should be stored under an inert atmosphere, such as nitrogen or argon, in a tightly sealed container. Keep it in a cool, dry place away from moisture, heat, and sources of ignition. Protect from light and incompatible materials like oxidizers and strong acids. Handle inside a well-ventilated fume hood, and use appropriate personal protective equipment. |
Applications of Diethyl(3-Pyridyl)Borane in Industrial ManufacturingAs a specialized producer of Diethyl(3-Pyridyl)Borane, we supply this advanced organoborane compound to global manufacturers across critical chemical synthesis sectors. Downstream partners apply this borane derivative primarily as a tailored intermediate and coupling agent where high selectivity and functional group compatibility are paramount. Please review the below industry-driven application scenarios, each illustrating how formulators and process engineers leverage our material according to regulatory and process-specific requirements. 1. Pharmaceutical API Synthesis – Heterocyclic Drug IntermediatesInnovators in pharmaceutical synthesis utilize Diethyl(3-Pyridyl)Borane to build complex heterocyclic scaffolds for small-molecule active pharmaceutical ingredients (APIs). This compound enables precise pyridine ring modifications during palladium-catalyzed cross-coupling reactions, especially in Suzuki-Miyaura processes, producing high-purity pharmaceutical intermediates used for chronic therapeutics and advanced clinical candidates. Industry compliance standards
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2. Electronic Materials – Functionalized Pyridine Ligand ManufacturingElectronic chemical producers rely on Diethyl(3-Pyridyl)Borane for constructing functionalized ligands that anchor metal centers in OLED emitters, organic photovoltaic device layers, and electronic sensor arrays. The compound’s stable borane group facilitates controlled transfer reactions, delivering high-purity pyridyl units into specialty ligand systems required for advanced materials with reproducible electronic properties. Industry compliance standards
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3. Agrochemical Intermediate Production – Pyridyl Building BlocksAgrochemical manufacturers incorporate our borane derivative in the formation of selective herbicide and fungicide intermediates, taking advantage of its tailored reactivity when constructing pyridyl-based agroactive compounds. Its inclusion ensures high yield in downstream transformations such as coupling and alkylation steps, enabling scalable production while meeting stringent industry requirements for process safety and traceability. Industry compliance standards
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4. Polymer Additive Synthesis – Specialty Cross-Linking AgentsProducers of high-performance polymers use Diethyl(3-Pyridyl)Borane as a functional cross-linking additive to introduce well-defined pyridyl units into engineering plastics and thermoset networks. The reactivity of the borane group allows precise incorporation within the polymer backbone or as pendant moieties, delivering property enhancement such as improved flame retardancy or chemical resistance for end-use in demanding industrial environments. Industry compliance standards
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5. Fine Chemical Synthesis – Advanced Research ReagentsManufacturers serving the fine chemicals sector select Diethyl(3-Pyridyl)Borane for constructing advanced research reagents and specialty coupling partners needed in medicinal chemistry, catalysis, and material science. Strict control of boron content and pyridyl substitution profile enables reproducibility in research-scale and pilot production batches, addressing the needs of specialty reagent catalogs and contract synthesis labs. Industry compliance standards
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At the manufacturing end of the chemical supply chain, Diethyl(3-Pyridyl)Borane stands as more than just a reagent name on a bottle. We create Diethyl(3-Pyridyl)Borane in controlled reactor systems where reproducibility, purity, and practical application guide our decision-making. No batch leaves our site without us knowing its real-world performance meets demanding standards from research chemists and process engineers.
Our Diethyl(3-Pyridyl)Borane finds its place in the toolkit of those pushing the field of functionalized heterocycles, the heart of many pharmaceutical and fine chemical syntheses. Our reactors consistently feed the borane into downstream processes where 3-pyridyl groups matter, often forming intermediates that drive the next invention or advancement in molecular medicine, crop science, or advanced materials.
Every drum and flask of our product carries our internal model code—one that signals not only specification but a set of craftsmanship marks. From the start, we engineered the borane reaction with a focus on minimizing side reactions. Close control of temperature and exclusion of moisture stops unwanted hydrolysis or oxidation, two pitfalls that turn promising boranes into costly waste if ignored. Our technicians monitor batch purity by NMR and chromatography, but our job doesn't stop at laboratory analytics. We also run pilot-scale tests to ensure that scale-up doesn't sneak in new impurities, so our Diethyl(3-Pyridyl)Borane maintains consistency whether shipped in gram vials or industrial barrels.
Water content matters deeply with organoboron compounds. Each completed batch is sampled for Karl Fischer titration because even low ppm moisture can change the way this borane behaves in coupling chemistry. End-users regularly tell us that our product cuts down on reaction troubleshooting, allowing the coupling step to proceed without post-purification headaches. Residual solvents are kept far lower than the threshold that would cause problems in sensitive transformations.
Our Diethyl(3-Pyridyl)Borane typically moves in glass-liner containers or specialized fluoropolymer drums; we avoid contact with metals that catalyze decomposition or with plastics that may leach impurities at trace levels. Over the years, our selection of closure systems and liners evolved in response to feedback from end-users who run air-sensitive or moisture-sensitive coupling chemistry.
Chemical manufacturers live in the nuts-and-bolts world of reactivity, not just catalog listings. Our Diethyl(3-Pyridyl)Borane finds use mainly in Suzuki-Miyaura and related cross-coupling reactions. Many research groups, including those working under tight regulatory compliance, build 3-pyridyl-substituted scaffolds for kinase inhibitors, CNS agents, and agricultural actives. Traditional pyridylboronic acids often decompose under storage, especially under minor pH variation or upon exposure to open air. The diethylborane version resists hydrolysis better, surviving long storage and repeated opening.
We sometimes field calls from R&D chemists working on scale-up projects who ran into trouble with the instability of other pyridylboronates during workup. Even if they could get the coupling to proceed on a small scale, product purity dropped after exposure to traces of water or atmospheric oxygen. By using our stabilized Diethyl(3-Pyridyl)Borane, they see higher yields and less byproduct formation, which means less time spent on purification and less raw material lost to waste streams.
A real-world example comes from a customer process route toward a novel anti-infective drug substance. Their process replaced the previously used 3-pyridylboronic acid with our diethylborane variant. On the plant scale, they saw not just increased product yield but also shorter crystallization time and improved API purity. Downstream, the waste handling operation found fewer boron-containing residues, helping them meet local environmental discharge rules without a costly redesign.
Material handling safety is not just a checkbox. Unlike some pyridylboronic acids that can cake or deliquesce in open containers, our diethylborane’s handled in standard drybox or Schlenk lines without the unpredictable clumping or acid-base reactivity that can surprise an experienced process chemist. Over time, this advantage adds up to fewer batch failures and less time spent grubbing around with polymerized gunk in transfer lines.
Many customers ask about the true difference between our Diethyl(3-Pyridyl)Borane and more common boronic acids, pinacol esters, or MIDA boronates. The answer comes back to chemical stability, reactivity under neutral and mildly basic conditions, and survival in long-term storage.
Boronic acids can oxidize. Pinacol boronates, though more stable than many boronic acids, sometimes struggle with slow hydrolysis in water-rich or alcoholic solvents. MIDA boronates, favored for extended bench stability, sometimes run into activation problems in metal-catalyzed cross-couplings where rapid deprotection or easy transmetalation is required.
From the manufacturing side, we see the differences clearly: Diethyl(3-Pyridyl)Borane stands out by holding its molecular integrity over time, even in the hands of users who must transport and open containers frequently. We've analyzed shelf-life in accelerated aging conditions, cycling samples between cold storage and ambient exposure. Among available pyridylboronates, the diethylborane core keeps moisture uptake and byproduct formation lowest within a practical range for most modern synthetic operations. Our clients in medicinal chemistry see fewer “unknowns” in their LC-MS profiles when using this reagent—typically a sign that the starting material survived long enough to reach the transition state, not dying in the bottle.
In ligand and materials screening, trace impurities can confound assay data or poison sensitive catalysts. From the producer’s perspective, we’ve seen that diethylboranes tend to pass QC with fewer boron-related minor contaminants compared to their acid or more heavily protected cousins. This comes from the tight conditions under which we react and isolate the borane, then immediately seal the product under inert gas.
Every year we benchmark reactivity in standard Suzuki couplings side-by-side using our own borane, a freshly made 3-pyridylboronic acid, and pinacol or MIDA analogues. Parallel batches reveal that, in typical aqueous-organic solvent blends, our product accesses coupling conditions as mild as 40 °C at low palladium loadings. Pinacol esters need longer deprotection; boronic acids crash out impurities more frequently. None of this comes from marketing—it’s a response to observations at our own workbenches and feedback from clients chasing new compound libraries.
Our QC process borrows not just from textbook analytics but also the chemical instincts acquired from many years of handling reactive intermediates. We retain batch samples long enough to catch degradation that doesn’t show up on week-one tests. Even with best-in-class synthesis, it’s easy to overlook slow boronate hydrolysis or formation of unobserved side products if storage conditions vary, or if a drum sits in customs for a week on a hot tarmac.
Some competitors treat boronic acids or esters as “commodity” items to be churned out in bulk. Our approach comes from the fact that many users—especially those at scale or in regulatory-heavy environments—cannot risk unexplained peaks in HPLC or IR spectra. We check not just finished product purity, but also precursor and decomposed fragments. Packing under argon, in containers chosen for both chemical inertness and leakproof sealing, is standard here, not an afterthought. Even label adhesives are chosen for solvent resistance, as a reaction accident or spillage near a drum shouldn’t mean ruined handling instructions.
Because we keep records tied to production, not just batch number, process interruptions, raw material lot changes, and minor process tweaks are all logged and reviewed before each release. If a batch doesn’t measure up, or we suspect future instability, we rerun, not rebrand. This attitude costs us inventory space, but it marks the difference between a boutique R&D supplier and a production-scale manufacturer who protects both their reputation and their downstream clients’ timelines.
Feedback loops with key end-users give ongoing intelligence about real-world issues—from the impact of trace contaminants on API crystallization, to the need for containers that fit both glovebox and standard benchtop dispensers without risk. If we find a packaging change helps one customer save time during scale-up, it becomes the default for all orders.
Handling boron reagents means respecting their sensitivity—especially in bulk production. On the manufacturing floor, every drum we fill grows out of insights learned from earlier incidents and close tracking of global regulatory trends. Our safety program insists on pre-checks for oxygen and moisture sensors, trace metal contamination monitoring, and regular audits of valve materials. The move to automated dispensing cut accidental exposure and occupational exposures. Any vented gas or wash solvent with boron loading is flagged for waste management separately from “ordinary” organic byproduct. We send samples for independent environmental analysis, not just to clear regulatory hurdles but to close any data gaps in boron fate downstream.
Process safety teams handle periodic training refreshers for the nuances of borane chemistry, not just standard spill-cleanup routines. Staff must demonstrate proficiency with inert gas gloveboxes and film-wrapped containment before they work on the Diethyl(3-Pyridyl)Borane line. We remind every new operator that a pinhole leak or a jar left cracked on a bench can cost more in lost product and hazard control than any day’s worth of overtime.
On the environmental end, our wastewater treatment receives separate trucks of boron-containing water. No “gray zone” blending occurs, and concentrations are reported openly to local agencies. Routine checks on soil and surface water near effluent locations back up our claims that we control chemical emissions. We invest in primary and secondary containment for liquid storage—large-scale manufacture always carries risk, and prevention beats clean-up every time.
Getting real chemical feedback from end-users matters. If one batch, despite passing purity checks, leads to lower yield in a pharma client's coupling step, we ask for their full reaction sequence and analyze possible trace impurity interactions—not just shipping a refund. One case involved nitrosamine background contamination in an unrelated synthetic cluster. We built extra quality screens for our own process, eventually ruling out our product as the root cause, but finding a decomposition pathway in a related commodity solvent. True partnership with chemists means scrutiny at every level.
It’s common to get requests from labs requiring extended traceability for regulatory filings. In those situations, we share not just a certificate of analysis but also stability profiles, transportation logs, and—where permitted—data on comparative reactivity. This level of transparency builds trust, but also sharpens our own process discipline. Every batch leaving our site must be ready for regulatory audit, analytical scrutiny, and tough field use by people we often know by name from years in the trenches.
We stand behind the full production journey. Raw materials are sourced only from longstanding partners who match our own standards for impurity controls and documentation. Incoming lots are sampled and held for dual analysis, and supply chain logs are kept on file for every drum—no batch enters production without full clearance, because we've seen the mess a “just good enough” raw material introduction can cause in long-chain processes.
The chemical landscape doesn’t stand still, and neither does our approach to Diethyl(3-Pyridyl)Borane production. Increased automation is being phased in, aiming to tighten reproducibility and narrow the window for human error during critical steps like borane transfer and final reagent isolation. Expansion plans include investment in inline moisture and oxygen analysis—catching process drifts before they lead to off-specification batches.
We continually tune production parameters in response to both internal pilot data and field reports. Two years ago we lowered maximum allowed alkali metal contaminants after a surge in reports of unexpected catalytic side reactions in advanced coupling steps. Last year, after hearing about sporadic waxy deposits in large drums, we changed our dryer and flask filtration protocol. Each loop of feedback means fewer surprises for our partners down the line.
As customers require not just product but also technical backup, we maintain a team with firsthand field and scale-up experience, encouraging feedback on both performance and bottlenecks encountered during protocol optimization. This way, even as barcodes and batch records evolve, the core offering—reliable, high-purity Diethyl(3-Pyridyl)Borane—remains informed by practical laboratory and plant experience, not just checklists.
People don’t buy chemicals like Diethyl(3-Pyridyl)Borane just for shelf inventory. Every bottle means a step forward: a new route, a cleaner product, or a reliable supply chain update. Our role as producer is to own both the chemistry and the responsibility that comes with seeing it through, from raw materials to the last residue after coupling. Better technical support and process transparency help every user speed their route to meaningful results.
The outcome? End-users see stronger process reliability and more robust discovery campaigns. We, in turn, keep raising the bar on what a real manufacturing partner delivers in today’s demanding chemical landscape.