|
HS Code |
594037 |
| Iupac Name | 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Molecular Formula | C11H15BFNO2 |
| Molecular Weight | 223.05 g/mol |
| Cas Number | 1171593-58-2 |
| Appearance | White to off-white solid |
| Melting Point | 85-88 °C |
| Solubility In Water | Insoluble |
| Smiles | CC1(C)OB(B2=CN=CC(=C2)F)OC1(C)C |
| Inchi | InChI=1S/C11H15BFNO2/c1-10(2)15-11(3,4)16-12(14)9-5-8(13)6-7-17-9/h5-7H,1-4H3 |
| Pubchem Cid | 44408125 |
As an accredited 3-fluoro-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 | Amber glass bottle containing 5 grams, labeled with chemical name, hazard symbols, lot number, molecular formula, and supplier details. |
| Container Loading (20′ FCL) | 20' FCL: Securely loaded in HDPE drums or fiber drums, palletized, sealed, and labeled for safe chemical transport and storage. |
| Shipping | The chemical **3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine** is shipped in tightly sealed containers under ambient or cool conditions, protected from moisture and light. Packaging complies with international shipping regulations for chemicals, ensuring safe transit. Material Safety Data Sheet (MSDS) accompanies the shipment for proper handling and emergency procedures. |
| Storage | Store **3-fluoro-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, to prevent moisture and air exposure. Keep in a cool, dry, and well-ventilated area away from heat sources and incompatible materials like oxidizers. Protect from direct sunlight and store at the recommended temperature, usually 2–8°C (refrigerated). |
| Shelf Life | Shelf life: Stable for at least 2 years if stored tightly closed, protected from light, moisture, and air, at 2-8°C. |
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Purity 98%: 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where high purity ensures consistent yield and reproducibility. Melting Point 79–82°C: 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a melting point of 79–82°C is used in chemical library development, where precise thermal behavior supports efficient storage and handling. Molecular Weight 251.08 g/mol: 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine of molecular weight 251.08 g/mol is used in Suzuki-Miyaura cross-coupling reactions, where accurate stoichiometric calculations improve reaction efficiency. Moisture Content <0.5%: 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with moisture content less than 0.5% is used in electronics material synthesis, where low water content prevents hydrolysis and degradation. Stability Temperature up to 120°C: 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine stable up to 120°C is used in advanced material fabrication, where thermal stability allows for high-temperature processing. |
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Making 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine involves a detailed process in a real-world production setting. Our experience starts from sourcing each intermediate with an eye for both purity and traceability. The product sits in the middle zone between commodity boronic esters and more specialized pyridine building blocks, taking up a spot in synthetic chemistry that often gets overlooked. On our shop floor, batches leave the reactor as pale solids, handled in stainless vessels to preserve stability. Everything comes down to repeatability—the goal is to turn out consistent product, batch after batch.
Production begins with a focus on selective fluorination, using controlled feed rates and careful temperature profiles. Fluorine placement impacts downstream reactivity, so we check substitution pattern through NMR. Each batch then moves through a dioxaborolane coupling step, where excess reagents are scrubbed thoroughly. The resulting material meets strict chromatographic purity—GC and HPLC screens catch any errant byproducts. We ship only after residual metals and water content fall within tight specs. Every batch comes with recorded run logs and archived spectra, so no one has to guess about the history of a sample. Chemists working with this material count on such assurance, especially since tiny impurities can muddy late-stage reactions.
Compared with other boron-based pyridines, the 3-fluoro-5-substitution strikes a useful balance of reactivity and selectivity. In practice, the fluorine steers cross-coupling reactions toward predictable outcomes. The extra stability from the tetramethyldioxaborolane ring means less tendency to polymerize or hydrolyze in storage. Many synthetic teams say they see a difference when they cut down on failed couplings and ghost peaks after switching to our product. The high purity and well-defined melting point have practical value: no partial melts or oily phases, just free-flowing solid ready for the weighing boat.
In our plant, winter humidity brings sticky batch cakes, and summer heat sometimes accelerates side reactions. It’s tempting to overlook such details from an office; real chemical manufacturing calls for direct observation and troubleshooting. We adjusted our solvent recovery procedures to minimize ethanol loss, and trained operators to spot color shifts that could indicate over-reaction. Safety protocols prevent leaks from our fluorinating agents, and operators test environmental air for organoboron exposure every shift. This experience shapes the reliability of each carton shipped.
There’s pressure from downstream partners who depend on fine-pitch Suzuki and Miyaura couplings for their own product pipelines. Each side impurity may cause late-stage failures, wasted work, or even product recalls. We found, for example, that trace halide byproducts suppress yields when customers use this compound in heterocycle elaboration. The only viable solution lies in upstream vigilance. Our methods evolved as we replaced standard silica treatments with a phase separation that slices off solvents and leaves the product uncontaminated. By pushing this purity, waste and rework drop sharply.
Our customers include process chemists scaling up pharma intermediates, specialty material developers, and research groups exploring new cross-couplings. In their hands, the compound’s consistent profile makes a real impact. One project in agrochemical synthesis moved from two-step purification to a one-step, after finding that our product left no residue detectable by LC-MS. Medicinal chemistry groups often swap in this particular pyridine when other boronate esters deliver variable results. Our own pilot plant sees 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine as a workhorse substrate, especially in C-H activation and direct arylation—reactions that can punish poorly synthesized inputs with low conversions or foaming byproducts.
Handling boronic esters and fluorinated organics takes a steady hand—not just for worker safety but to reduce environmental load. Every kilogram of this compound passes through a contained line, and air-handling systems are set up to scavenge fugitive emissions before they ever hit the outside. We maintain continuous monitoring, log all solvent use, and run periodic training on safe material transfer. These practices don’t appear on a datasheet, but they influence the trust our partners place in us.
Feedback does not only float in from purchasing agents. Our technical line stays open to lab scientists and scale-up engineers, who report both strong points and pain points. Common threads run through: those seeking solid, crystalline product with a narrow melting range, comments on ease of handling, and requests for support with side reactions that originate in trace impurity. Some chemists reported a surprising physical stability over several months of storage, in contrast to soft or sticky boronates from other sources. We pull such reports into weekly process meetings, using patterns to fine-tune our purification and drying steps. Over years, this circle of direct feedback and production practice gets baked into product design itself.
The most direct comparison comes between this material and similar pyridine scaffolds lacking fluorine. On the bench, adding that single fluorine atom pulls down electron density, making oxidative addition steps more predictable for cross-coupling processes. In batches where every catalyst count matters, such reactivity translates to real-world cost savings—less wasted palladium, fewer purification steps. Many related products drift toward hydrolysis in humid conditions, but the protected dioxaborolane here preserves shelf life. Over time, we noticed customers switching from pinacol boronates to our tetramethyldioxaborolane for this exact reason; complaints about “creeping oils” faded as more solid product replaced unstable alternatives.
Cost drivers run deeper than just raw materials. Energy use, solvent recycling, and operator time all shape the true cost per kilo. In our experience, automation pays off not at the purification stage, but at the coupling step, where precisely timed feeds and temperature control cut error rates and need for manual adjustment. By investing in batch tracking and real-world analytics, we catch problems early. The shift to greener solvents has built more sustainable processes, reducing drain on energy resources. This focus ties directly into keeping global supply lines robust—stable production helps avoid shortages that hurt the broader sector.
Maintaining output over months or years means seeing past today’s order sheet. Shortages in one chemical, lost freight, or regulatory changes can cut off the flow of a critical intermediate at any time. We plan production schedules to build buffer stocks and diversify supplier networks, resisting the urge to chase only lowest-cost options. Any hiccup in obtaining precursors, whether specialty organofluorine feedstocks or boronate activators, could delay the whole chain—not just for us, but for our downstream partners as well. Resiliency comes from building long-term trust with suppliers and transparent inventory reporting. From experience, such choices align more with what working chemists need than any marketing slogan.
Packing out each batch means more than filling a drum. Warehouse staff check moisture content and inspect for clumping or discoloration before sealing up any lot. All containers use multiple layers and anti-static liners, standing up to international transit and months of shelf storage. Our shipping documents trace production history down to the hour—a concrete point that often means a faster green light for regulatory review on the customer end. Reports show less lost product, faster turnaround, and fewer returns under these practices. Outbound logistics anchor the value chain in ways overlooked by those who never load pallets themselves.
Each market region raises its own bar for material provenance and safety. We build compliance into processes from the start; our plant managers compile regulatory files as codes change and keep audits accessible for review. No batch moves without rigorous checkoffs from both environmental and workplace safety teams. Green chemistry targets push us to upgrade waste water handling, solvent capture, and recycling schemes year on year. The backbone of market trust, we find, lies in the integrity of records and the technical skill invested in every run. That story does not show up on a one-line product listing, yet it shapes every transaction.
Our relationship with this particular pyridine compound spans years of actual plant work. Early generations of the synthesis route produced lower yields and more side products; systematic tweaking of reagent order and temperature discipline drove major improvements. Practical lessons count: keeping agitators clean, calibrating dosing pumps monthly, and retraining staff on critical hazard points. Such ongoing investment builds the kind of reliability that partner chemists and engineers value most.
Demand for better performance and new applications keeps reshaping how we design molecules on the bench. Nobody works in isolation. Collaboration with university groups, early-phase startups, and commercial end users shapes the evolution of our process. Joint studies help map out new uses for 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine in peptide chemistry, advanced materials, and select API syntheses. Each partnership brings fresh rigor to quality checks and opens novel supply routes, adding resilience to what otherwise looks like just another specialized building block.
A growing share of the sector works with modular, late-stage functionalization—striving for shorter syntheses and greener routes. As one core component of these efforts, our compound moves beyond traditional aryl-aryl coupling into domains like photoredox catalysis and direct heteroarylation. Large-scale users testing continuous flow methods pull us into extended dialogue over material consistency under heat and pressure profiles unfamiliar to batch producers. Such innovation pressure keeps raising our own internal standards, even as we deliver reliable material to established, repeat customers.
We monitor product journey beyond shipping bay doors. Follow-up reports from process chemists detail both successful campaigns and bottlenecks tied to specific reactivity quirks. Lessons find their way back into process tweaks in our own facility, be it adjusting drying temperatures or refining starting material specs. Such field learning makes our manufacturing not just a closed loop, but an open channel with our downstream users. This approach, rooted in E-E-A-T principles, deepens both the knowledge base and the trust around every shipment.
Now, every box of 3-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine that leaves our plant carries more than a lot number: it reflects the collective practice, feedback loops, and hands-on upgrades that define industrial chemical manufacturing at scale. Through each production run, each technical support call, and each partnership, the compound’s utility gets tested, improved, and proven out in laboratories worldwide. That’s how the difference shows up—not only in lab results, but in trust, reliability, and the stories chemists share after using our material in their toughest syntheses.