|
HS Code |
261552 |
| Compound Name | 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Molecular Formula | C11H16BNO2 |
| Molecular Weight | 205.07 g/mol |
| Cas Number | 850568-18-8 |
| Appearance | white to off-white solid |
| Melting Point | 76-80 °C |
| Purity | ≥98% |
| Solubility | Soluble in organic solvents such as DMSO, DMF |
| Storage Conditions | Store at 2-8°C, protect from moisture and light |
As an accredited 3-(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 | A 5-gram amber glass bottle with a secure screw cap, labeled "3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, 98% purity." |
| Container Loading (20′ FCL) | 20′ FCL contains 10–12 metric tons of 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine in sealed drums or fiberboard packaging. |
| Shipping | **Shipping Description:** 3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is shipped in tightly sealed, chemically compatible containers under ambient conditions. The package is clearly labeled with appropriate hazard information, if required. Protect from moisture and extreme temperatures. Transportation complies with local and international chemical shipping regulations to ensure safe delivery and handling. |
| Storage | Store 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine in a tightly sealed container, under a dry, inert atmosphere such as nitrogen or argon to prevent moisture and air exposure. Keep it in a cool, well-ventilated area away from strong oxidizing agents and direct sunlight. Ensure proper labeling and store according to all relevant chemical safety regulations. |
| Shelf Life | Shelf life: Stable for at least 2 years when stored in a cool, dry place, tightly sealed, protected from moisture and light. |
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Purity 98%: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with purity 98% is used in Suzuki-Miyaura cross-coupling reactions, where it ensures high product yield and minimized byproduct formation. Molecular weight 218.09 g/mol: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with molecular weight 218.09 g/mol is used in pharmaceutical intermediate synthesis, where precise mass balance and reaction control are achieved. Melting point 64-67°C: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine at a melting point of 64-67°C is used in solid-phase organic synthesis, where reliable phase transition facilitates efficient processing. Stability temperature up to 120°C: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with stability up to 120°C is used in high-temperature catalysis, where chemical integrity is maintained during extended heating protocols. Particle size <50 µm: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with particle size below 50 µm is used in homogenous catalyst preparations, where rapid dissolution and reaction kinetics are optimized. Water content <0.5%: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with water content less than 0.5% is used in moisture-sensitive coupling reactions, where it prevents side reactions and improves product selectivity. Assay (HPLC) ≥98%: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with assay (HPLC) ≥98% is used in analytical chemistry applications, where precise quantification and reproducibility are necessary. Residual solvent (THF) <0.1%: 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with residual THF below 0.1% is used in fine chemical synthesis, where purity is critical for reliable downstream processing. |
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In our journey as a chemical manufacturer, synthetic chemists have kept turning to us for specialized boron-containing reagents. Creating molecules that bridge academic desire and real application requires patience, precision, and a willingness to innovate. Over the past decade, 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine emerged as an essential intermediate for research and production. This is not just another catalogue item; it’s a molecule that connects breakthroughs in pharmaceuticals, agrochemicals, and materials science to daily laboratory work.
The heart of this compound lies in the reliable versatility of its boronate ester structure. Chemists widely use the 1,3,2-dioxaborolane motif to form stable boronic esters, making this compound more than just a protected pyridine. The tetramethyl groups offer effective steric protection, granting improved shelf stability and lower susceptibility to hydrolysis compared to less hindered boronates. For us on the manufacturing floor, this translates into solid batches, consistent purity, and minimal reprocessing—a win for labs and factories alike.
Our production line frequently handles a range of pyridine derivatives, but introducing this dioxaborolane group was a game changer. It has become a staple in Suzuki-Miyaura coupling reactions, where mild conditions and broad substrate compatibility let chemists create complex biaryl motifs or functionalized heterocycles. From the first run, product quality and reactivity consistently gave customers a smooth experience from vial to reaction flask.
3-(Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine arrives as a crystalline solid that packs well and keeps a uniform texture. Its melting point provides a quick quality check, but what matters most is the assurance that water content stays controlled and active boron content is spot on. In our facility, every batch passes through strict HPLC and NMR checks. We learned early that trace metal contamination or moisture can throw a synthesis off course, so we maintain strict limits without compromise.
Many in the market offer boronic esters, but not all can guarantee the consistency with which our product handles and dissolves. Our quality team starts with ultradry solvents, keeps glassware spotless, and monitors every crystallization closely. The result: solid material that resists clumping, free-flowing in automated feeders and syringes or scoops. Reliable handling counts for high-throughput labs and traditional glassware chemists alike.
Our relationship with laboratory scientists runs deep. Researchers often approach us with feedback or specific challenges, from batch scale-up snags to fine-tuning catalyst loading for cross-couplings. This boron-containing pyridine plays a critical part in building molecular libraries, especially in projects demanding selective functionalization at the 3-position of the pyridine ring. Its predictable reactivity and manageable isolation steps keep it in the running, project after project.
A typical week might see this compound supporting the synthesis of kinase inhibitors, fluorescent tags, or even polymer-bound ligands. Its robust nature means it stays inert under a range of lab conditions until the boron group is needed for its signature cross-coupling chemistry. Unlike less stable boronate counterparts that suffer from decomposition or problematic purification, our material withstands extended storage without forming off-odors or degradation products. Teams using parallel synthesis racks, sealed reactors, or even open-flask assembly lines all report ease of use. The consistent crystalline quality means each scoop provides the correct boron content—no recalculating or mid-run corrections needed.
Years of hands-on feedback tell a simple truth: not every boronic ester makes the grade when labs scale from milligrams to multi-kilogram runs. Our 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine stands apart in several ways. Its higher melting point offers thermal stability that aids purification. The tetramethyl-1,3,2-dioxaborolane ring encases the boron atom, buffering it against humidity and routine handling. In contrast, simple boronic acids often struggle with variable hydration or irreversible oxidation, creating uncertainty at the bench and lower yields through the process.
Feedback from pilot plant chemists points to another advantage: processability. Our material’s regular particle size eases weighing and transfer through process equipment—critical for continuous manufacturing lines. In comparison, lower-grade material from secondary sources often arrives as sticky powders or lumpy aggregates. Tech transfer teams appreciate being able to plug our product into established process setups with minimal troubleshooting. This all comes back to a laser focus on every synthetic and purification step in our workflow.
Meeting strict regulatory and quality standards is not only about paperwork; it’s a philosophy that shapes every kilo we ship. Early on, we learned that diligent process development pays dividends not only for our clients but for the wider scientific community. Robust process controls—starting from pyridine ring chlorination, careful borylating agent addition, and pressure-controlled crystallization—translate to reliable products. Working hands-on through hundreds of batches, we’ve fine-tuned every detail, down to inert gas headspaces and tailored solvent drying protocols.
Unpredictable impurity profiles often trip up scale-up or downstream use. Through direct feedback and real-world troubleshooting, we developed in-line monitoring and batch-level traceability. Our technical support has fielded queries on scaling the product into continuous flow chemistry as well as in situ generation of related boronic acids for telescoped syntheses. We answer each with practical insights and openly share tips from our own trials—like solvent selection, storage practices, and reaction quenching steps—to help projects stay on track.
Our customers range from large pharmaceutical process teams to startup biotech labs. Each demands materials that meet tight purity, moisture, and trace metal standards. We saw firsthand how a robust boronate reagent can take the headache out of high-throughput screening or process validation. The broad applicability of this compound opens doors in modern C–C and C–N bond-forming chemistry, as well as elaboration of functionalized heterocycles and even the next generation of energetic or bioactive materials. It's rewarding to spot published breakthroughs and know our work supplied a key intermediate along the way.
Customers often ask about the relative merits of our product over traditional boronic acids and less substituted boronate esters. Having synthesized and purified thousands of batches across several analogues, we see differences that go beyond the datasheet. Simple boronic acids can show unpredictable solubility and instability. Lower substituted boronate esters may offer quick access but face issues with long-term shelf life and moisture resistance. Our 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, with its steric protection and crystalline bulk, manages to address both benchscale and industrial needs.
Developing a reliable route for 3-position pyridine functionalization is not easy. With many nitrogen-containing heterocycles, selectivity troubles can drain time and resources. The strong, consistent performance of this reagent in cross-couplings grew out of relentless process improvement and feedback cycles with users across the globe. Chemistry teams trust it for its straightforward filtration, reproducible yields, and broad compatibility with a variety of catalytic systems—ranging from classic palladium catalysts to newer ligand architectures.
Producing a high-performance intermediate at scale isn’t only about capital equipment or expensive starting materials—it’s about deep chemical understanding, embedded in every step. Years on the production floor showed us that boron reagents need consistent drying, gas blanketing, and full traceability from raw material to finished product. Every drum receives a unique batch record; every analytical result feeds into our continuous improvement pipeline. We spot patterns, identify bottlenecks, and share those insights openly with our customers.
Teams working on next-generation synthesis require not only purity certificates, but answers that come from experience. We do not hesitate to share our perspective on reaction troubleshooting, handling methods, or storage logistics. Our investments in process analytics—like in-line moisture detection and HPLC method updates—help keep downstream processes flowing. This continuous feedback loop ultimately guarantees that every lot of 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine performs to the same high bar as the last, regardless of scale or application.
Scaling chemistry from a single flask to a multi-hundred kilo vessel is a unique challenge. Chemists in R&D sometimes overlook handling considerations that become pivotal during batch manufacture—issues like caking, static charge buildup, or trace peroxide formation under storage. Years of operating across these scales taught us to implement procedures that mitigate risk and maintain clean, predictable product every time.
Our team keeps in close contact with production chemists to discuss metrics like bulk density, flow properties, and reactivity in larger reactors. This ongoing exchange led to improvements in our own process—whether optimizing filtration steps, tweaking crystallization solvents, or refining particle size profiles. Our goal is simple: deliver a product that transfers easily, dissolves consistently, and reacts cleanly—no surprises for scale-up teams or researchers starting a new project.
Chemical safety isn’t about checking boxes; it’s a culture shaped by daily practice. Production workers, quality inspectors, and logistics staff each play a crucial role in delivering the purest product safely. Years of direct handling shape the way our material is packed, labeled, and stored. Moisture ingress and oxygen exposure at any point can compromise sensitive boron compounds, so we use airtight, inert-lined drums and small, factory-sealed vials for lab quantities.
Teams receive full handling guides, based on our own best practices—it’s information we refine after every customer interaction. We encourage storage under nitrogen, in cool, dry conditions, and we periodically measure long-term stability and packaging integrity. Real hazards—dust, static, solvent contamination—are addressed through simple, practical steps. We never hand off safety as someone else’s problem; it’s everyone’s responsibility from bench to bulk delivery.
Our interactions with scientists rarely end when a batch leaves the loading dock. Regular conversations with chemists reveal new uses, unexpected challenges, and creative process hacks. These exchanges seeded many of the improvements we rolled into later batches—better particle size control, tighter color specifications, or adjustments to our drying cycles to improve flow in automated loading stations. We actively solicit feedback and treat every technical question as an opportunity to refine our practice.
It’s not unusual to see our team collaborating with research groups on new reaction protocols, or supporting process optimization for a client’s internal supply chain. Building this molecule’s reputation has as much to do with reliability and responsiveness as with the underlying chemistry. Every new requirement, each emerging analytical trend, shapes how we approach the next production run and helps us anticipate where the science is headed next.
Having our compound at the bench or in a process plant supports advances in drug discovery, crop protection, and functional materials. Many research projects—ranging from borylation catalyst screenings to iterative heterocycle modifications—rely on the performance and reliability of 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine. Working closely with contract research organizations, global pharma, and academic centers, we've seen how a dependable reagent unlocks new synthetic possibilities while avoiding troubleshooting delays.
The compound’s utility in Suzuki-Miyaura coupling isn’t limited to carbon-carbon bond formation. Customization with electron-rich or electron-poor partners gives chemists a foothold for designing next-generation scaffolds. Whether in batch or continuous flow, its clean conversion profile and easy purification keep it in the running for route scouting, library building, and even specialty polymer production. Manufactured with care, stored under the right conditions, and used in accordance with practical guidance, this material pulls more than its weight in any laboratory or pilot plant.
In manufacturing, reliability is won through every repeated batch, not with bold promises. Our experience with 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine—across syntheses, purification, storage, and shipment—gave us insight into what really matters: reproducibility, safety, and technical support grounded in actual production challenges. Recommending a product we’ve spent years perfecting, tested in-house and in the hands of hundreds of researchers, gives us confidence in every shipment, every time.
We continue to learn from each new customer challenge. Whether adapting to a shift in regulatory standards, supporting a rush synthesis, or helping troubleshoot a tough cross-coupling, we don’t just sell a reagent—we back it up with the lessons, data, and hands-on know-how of a mature chemical manufacturer. Our commitment to full traceability, responsive documentation, and continual refinement makes all the difference.
With growing demand for reliable, high-purity boron intermediates, we stay focused on process improvement and technical depth, not shortcuts. Each kilogram of our 3-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine tells a story written by chemists, for chemists—a story composed of careful planning, technical fortitude, pride in craftsmanship, and respect for the science. As new fields emerge, from complex drug molecule construction to innovative material development, we’ll keep advancing the chemistry and supporting the people behind tomorrow’s discoveries.