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HS Code |
435693 |
| Iupac Name | 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Molecular Formula | C13H20BNO2 |
| Molecular Weight | 233.12 g/mol |
| Cas Number | 1473772-18-7 |
| Smiles | CCc1ncc(C2OB(B(O2)(C)(C))C)(C)cc1 |
| Appearance | White to off-white solid |
| Storage Temperature | 2-8°C (Refrigerated) |
| Solubility | Soluble in organic solvents such as DMSO, dichloromethane |
| Purity | Typically ≥97% |
| Inchi | InChI=1S/C13H20BNO2/c1-5-11-8-10(6-7-15-11)12-14(13(2,3)16-12)17-12(4)9-11/h6-9H,5H2,1-4H3 |
| Usage | Suzuki-Miyaura cross-coupling reagent |
As an accredited 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 1-gram amber glass vial, tightly sealed with a PTFE-lined cap, labeled with identification and hazard details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 12 metric tons (MT) packed in 25 kg fiber drums, shipped on pallets, securely loaded for export. |
| Shipping | This chemical, **2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine**, should be shipped in tightly sealed containers, protected from moisture and light. It must comply with relevant chemical transport regulations. Typically shipped at ambient temperature unless otherwise specified, appropriate labeling and documentation for handling and safety are required according to international and local guidelines. |
| Storage | Store **2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine** in a tightly sealed container under an inert atmosphere, such as nitrogen or argon. Keep in a cool, dry, well-ventilated area, away from moisture, acids, and oxidizing agents. Protect from light and heat. Handle using proper personal protective equipment (PPE), including gloves and safety goggles, and follow institutional safety protocols. |
| Shelf Life | 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is stable for at least 2 years if stored dry and under inert atmosphere. |
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Purity 98%: 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with 98% purity is used in Suzuki-Miyaura cross-coupling reactions, where it delivers high reaction yield and selectivity. Melting Point 78-80°C: 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a melting point of 78-80°C is used in pharmaceutical intermediate synthesis, where it ensures batch consistency and process efficiency. Molecular Weight 261.20 g/mol: 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine at 261.20 g/mol is used in organic electronics manufacturing, where it facilitates optimal film-forming properties. Stability Temperature 150°C: 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine stable up to 150°C is used in catalyst precursor preparation, where it offers thermal stability during processing. Particle Size <50 μm: 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with particle size below 50 μm is used in fine chemical formulation, where it improves dispersion and reactivity. Water Content <0.5%: 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with water content less than 0.5% is used in moisture-sensitive syntheses, where it prevents hydrolysis and degradation. Assay ≥99% (HPLC): 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with assay ≥99% (HPLC) is used in high-purity compound development, where it ensures minimal impurity interference. Residual Solvents <0.1%: 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with residual solvents below 0.1% is used in API production, where it meets stringent pharmaceutical standards. |
Competitive 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine prices that fit your budget—flexible terms and customized quotes for every order.
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In the modern landscape of organic synthesis, chemists rely on precision and consistency. Our role as the manufacturer for 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine brings us into daily contact with the challenges and rewards of advanced boronic esters. Listening to end-users and working side by side with research teams, we shape the process with every kilogram that leaves our reactor. This isn't just another reagent from a catalog; this is the result of years refining operational protocols, setting purity benchmarks, and finding the right balance between robustness and flexibility.
Direct requests from both pharmaceutical and agrochemical labs shape the core of our philosophy. Every researcher needs reagents that meet both performance and documentation requirements, which keeps us focused on process transparency. With 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, we see demand from those developing heterocyclic scaffolds, especially for Suzuki-Miyaura cross-couplings. This molecular scaffold doesn’t settle for routine, bringing a C–B bond in a sterically protected dioxaborolane format. It combines the stability needed for storage and shipment with the reactivity required during the transformation stage.
We’ve stood beside our clients from the pilot stage through full-scale production. Feedback keeps surfacing around the need for purity above 98%. Lower grades slow research, generating side products during coupling reactions. Our experience manufacturing this boronic ester at scale has shown us that relying on robust purification and crystallization processes builds trust and reliability. We don’t cut corners – the real cost isn’t in raw materials but in safeguarding against batch-to-batch variability. The fine particulate that escapes filtration, the tiny impurity peaks hardly visible on HPLC, all teach us lessons. Customers have pointed out that slight differences in end product reactivity sometimes trace straight back to impurity levels. So, we keep batch records searchable and traceable, and don’t ship without rigorous internal QC. This means rare events like incomplete reactions are avoided and researchers don’t lose time troubleshooting reagent quality.
Comparing this compound to similar pyridine boronic esters (like 2-ethyl-5-boronopyridine or those with different ester moieties), one clear distinction stands out in our hands-on experience. The tetramethyl-dioxaborolane group contributes superior shelf stability, especially in regions where ambient humidity swings widely between seasons. Some boronic acids hydrolyze, even before reaching the customer. We have found this dioxaborolane-protected form maintains its integrity months after packaging, showing minimal decomposition or polymeric byproducts. Several R&D groups have switched to this format after testing alternatives, telling us the reduced prep time for their handling protocols saves them several hours per batch.
The demand from medium and large-scale medicinal chemistry researchers tells its own story. Chemists working with aryl halides report consistent, high-yielding couplings without excessive side reactions. This compound’s steric and electronic properties mean you can build up diverse libraries by attaching heterocyclic blocks onto aromatic scaffolds, all while keeping side reactions at bay. Our manufacturing process prioritizes water content control and low base-sensitive decomposition, creating a more “forgiving” reagent for chemists who push the boundaries of catalyst loading and temperature ramps.
Our colleagues use high-throughput screening systems and appreciate reagents that perform identically over repeated runs. Every batch we send out supports these workflows by being homogeneous in particle size distribution and dissolving predictably in both THF and dioxane. We have regular customers who work in fields like pesticide lead optimization and share their observations: the precursor’s solid-state format simplifies their handling logistics, reducing variability by minimizing clumping or caking.
Developers working with next-generation OLED materials and certain organometallic complexes reach out for this compound because their target molecules need structural flexibility with precisely defined electronic properties. Slight alterations in boronic ester chemistry can sometimes introduce unwanted electron-donating or withdrawing effects, but the 2-ethyl group and pyridine ring combine with this ester to give a predictable outcome.
We stick to purity benchmarks that favor real-world research – levels above 98% (HPLC), verified via NMR and supported with GC-MS when needed. Chemists need traces of water kept low, since hydrolysis invites variable reactivity, transformations that stall, or competitive side reactions. Our solvent removal processes rely on vacuum and low temperature distillation. We never skimp on steps, since even a short-circuited dry down can let atmospheric moisture latch onto the product. By producing and sampling every larger-scale lot ourselves, we catch micro-contamination before customers do. Shelf lives stretch comfortably over 12 months, making long-term storage less of a worry for those stocking up ahead of campaigns.
Working directly with those scaling from milligrams to kilos, we see solvents and storage strategies varying. This compound ships well in usual amber glass with moisture-resistant seals, an operational must for those in tropical climates. Unlike free boronic acids, which show up in clumps or even start decomposing in transit, the dioxaborolane form we supply keeps its free-flowing, pale solid appearance. Warehouse managers have told us that reduced “off” odors and discoloration make inventory checks less of a hassle.
Plenty of generic boronic acids line up on order forms, but in practice, they often let down the teams counting on streamlined workflows. We’ve seen the extra time needed to re-purify those, frustration over variable quantities of active ingredient, and delays waiting for replacements. The robust design of this boronic ester—anchored by a tetramethyl dioxaborolane—eliminates most of these headaches. By manufacturing on demand and controlling the full supply chain, we’ve shortened delivery times and minimized bottlenecks between production and research milestones.
Direct feedback suggests that process chemists value this format for its stability in both ambient and cold-chain logistics. They can streamline project plans, secure in the knowledge that their boronic ester won’t degrade ahead of schedule. For researchers testing dozens of reactions per week, time is everything. One clinical trial team pivoted to this compound following batch failures traced to excessive boronic acid hydrolysis – a subtle but impactful change.
Unlike boronic acids or smaller alkyl boronate esters, our dioxaborolane-protected pyridine derivative minimizes the two main issues we see: hydrolytic instability and batch-to-batch inconsistency. It handles routine shipment, humid warehouses, and repeated sub-sampling in glove boxes with minimal signs of clumping or off-odor. Once in the lab, it keeps side reactions at bay, lets researchers dial in optimal bases and palladium sources, and accommodates a wider range of protocols.
No two routes to an active complex or pharmaceutical intermediate look exactly the same. Scale-up teams using flow chemistry platforms have pointed out how easy this product feeds into automated dosing systems, thanks to its solid-state uniformity. We hear from bioconjugation teams as well, who use mild conditions and find that this compound dissolves fast in their chosen solvents, facilitating rapid assembly of larger, modular structures.
Supporting documentation remains critical for our clients facing regulatory oversight and stringent documentation standards. For every batch, we archive multiple chromatography profiles, trace solvent lots, and maintain a full synthetic record. Having complete transparency over the process helps project teams cut through red tape and build internal confidence regarding quality and repeatability.
One area we’ve focused on is staying in tune with the specialized demands of medical chemistry researchers. A common concern revolves around late-stage functionalization — tacking on building blocks when the molecular scaffold is already crowded. Our boronic ester’s steric features, combined with predictable reactivity, allow attachment of aromatic rings in the final steps, limiting the need for structural modification earlier in the sequence.
From our vantage point, understanding the full risk profile matters as much as the chemistry itself. Safe handling instructions and up-to-date SDS accompany each package, with transparent labeling and precise origin tracking. We’ve trained our logistics partners to understand special precautions around packing and shipping, reducing mishandling risks. It’s more than just compliance; it’s about protecting both end-users and our team on the floor.
Staying ahead of regulatory shifts requires close relationships with both domestic and overseas customers. Every time there’s an update to globally recognized standards (such as REACH for EU shipments or US TSCA notifications), we adjust labeling and documentation accordingly. We also make sure to archive these compliance reports so research teams don't face delays during audits. Raw material transparency stays front-of-mind — we never blend with unidentified intermediates or off-label sources — so what you see on the invoice reflects our best-practice sourcing and manufacturing controls.
Producing this boronic ester at scale isn’t plug-and-play. Every new lot teaches us something about crystal morphology, solvent removal efficiency, or filtration techniques. We believe in granular process monitoring, right down to the last purification wash. Rising global demand sometimes strains key supply chains, especially for high-purity precursors like dioxaborolane and pyridine derivatives. Investing in multiple upstream vendors and holding safety stocks has kept our delivery times stable, even when global logistics waver.
A big lesson came during the recent raw material scarcity. Instead of chasing quick fixes or diluting operational standards, our team expanded in-house QC protocols. Chemists from partnering universities came on site to validate instrument readings and methodology, keeping our standards high under pressure. The result: zero rejected batches shipped, minimal returns, and durable partnerships built on trust. This cycle of feedback and adjustment continues to sharpen both our product and our team.
Our day-to-day isn’t theory — it’s getting cleaner coupling partners into researchers' hands, helping them build the next pharmaceutical, catalyst, or specialty material. As research shifts to more complex and environmentally aware protocols, the need for boronic esters with proven consistency only rises. Academic groups moving toward automated and data-driven synthesis strategies rely on our lot-to-lot uniformity for reproducibility in large screening libraries.
A big development in this field involves C–H activation methodologies, where boronic esters move beyond Suzuki reactions to enable new cross-coupling strategies. Leading labs have pointed out the need for boronate protection strategies that resist hydrolysis and can be easily deprotected or manipulated. We’re investing R&D resources into next-generation boronate esters, leveraging what we’ve learned to bring new variants to market that meet advanced functionalization needs.
Sustainability weighs more on the minds of purchasing managers and end-users alike. Chemists choosing our product often ask about byproduct minimization, waste-handling strategies, or potential introduction of greener solvents to production. Over the past year, we’ve swapped some legacy solvent systems for those with a lighter footprint, passing the benefits down the line in both compliance reporting and real chemical savings. Our work continues to balance throughput with environmental goals, motivated by feedback from scientists and sustainability officers.
One production chemist who works with us on patent-protected intermediates shared a rewarding outcome: moving to this specific boronic ester cut their synthesis steps by more than 10%, since they could avoid extra protection and deprotection cycles. In another customer’s process, batch failures due to unstable boronic acids dropped to zero once our more robust dioxaborolane format replaced legacy options. These stories play out across research, pilot, and commercial teams, giving us daily insight into the cascading impact of small changes in reagent quality.
We believe the real difference for our customers—whether biotechnologists, process chemists, or academic investigators—stems from our active role in refining each production step. The result is a boronic ester that fits naturally into workflows, facilitates efficient purification, and reduces headaches for both buyers and bench chemists.
For us, 2-ethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine reflects best practices, driven by direct input from those who rely on consistency, reactivity, and transparency in chemical manufacturing. Our approach stays rooted in what happens on the ground: working closely with end-users, adjusting for every hiccup, and responding to new research challenges. The value in this boronic ester comes not just from molecular structure but from an unbroken chain of efforts, insights, and real-world validation that stretches from our reactors to your lab bench.
New applications will continue to emerge in chemocatalytic routes, advanced drug discovery strategies, and specialized manufacturing verticals. Together with clients, our future work will keep evolving, always with an eye on the details that matter in daily research and production practice.