|
HS Code |
258019 |
| Product Name | 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Cas Number | 852337-28-1 |
| Molecular Formula | C11H14BCl2NO2 |
| Molecular Weight | 290.96 |
| Appearance | White to off-white solid |
| Melting Point | 63-68°C |
| Purity | >97% |
| Smiles | CC1(C)OB(B2=CC(Cl)=NC(Cl)=C2)OC1(C)C |
| Inchikey | JDOXKPZXRUUHKZ-UHFFFAOYSA-N |
| Solubility | Soluble in organic solvents such as DMSO, DMF, and dichloromethane |
| Storage Temperature | 2-8°C (refrigerated) |
| Application | Suzuki-Miyaura cross-coupling reactions |
As an accredited 2,6-Dichloro-4-(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 5-gram amber glass vial with a tamper-evident screw cap and detailed labeling for safety. |
| Container Loading (20′ FCL) | 20′ FCL: Standard loading is 8–10 metric tons in 25kg fiber drums or bags, safely palletized for moisture-sensitive chemical transport. |
| Shipping | The chemical **2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine** is shipped in tightly sealed containers under cool, dry conditions. Packaging meets regulatory standards for safe transport of laboratory chemicals. Ensure it is kept away from moisture, direct sunlight, and incompatible substances during transit to maintain stability and prevent degradation. |
| Storage | `2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine` should be stored in a tightly sealed container, protected from moisture and air, in a cool, dry, and well-ventilated area. Keep it away from sources of ignition, direct sunlight, and incompatible substances such as strong oxidizers. Store under an inert atmosphere (e.g., nitrogen or argon) if recommended to prevent degradation. |
| Shelf Life | Shelf life: Stable for at least 2 years when stored in a cool, dry place, tightly sealed, and protected from moisture. |
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Purity 98%: 2,6-Dichloro-4-(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 enables high coupling efficiency and product yields. Melting point 112–115°C: 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a melting point of 112–115°C is used in organic synthesis workflows, where it ensures controlled melting and ease of integration into reaction protocols. Particle size <20μm: 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with particle size below 20μm is used in catalyst preparation, where it promotes uniform dispersion and reactivity. Moisture content <0.5%: 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with moisture content below 0.5% is used in pharmaceutical intermediate synthesis, where it reduces the risk of hydrolysis and degradation. Stability temperature up to 80°C: 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with stability up to 80°C is used in heated batch reactions, where it maintains structural integrity under process conditions. |
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Years spent in industrial synthesis have turned technical names into everyday conversation. 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, or often shortened in discussion as the “dioxaborolane-pyridine,” has become one of those names mentioned when a project calls for solid reliability and versatility. As direct producers, we see this compound from the earliest runs in our reactors to the final packed drums. Each batch tells its own story, shaped by the demands of those using it for cross-coupling and related reactions, but the purpose remains clear: this compound bridges technical requirements and scalable reality.
The molecule brings together a pyridine ring, chlorinated at the 2 and 6 positions, joined to a boron substrate protected by a dioxaborolane group. This design, achieved through careful chlorination and borylation, offers direct benefits for medicinal, agrochemical, and advanced materials research. For every researcher looking to introduce a boronate ester group through a Suzuki-Miyaura or analogous palladium-catalyzed reaction, this compound provides a deliberate balance between reactivity and controlled handling, which growers, bench chemists, and formulators recognize as much in practice as theory.
Few structures allow such reliable downstream transformation. The boronate unit, safeguarded by its tetramethyl dioxaborolane cage, resists ambient moisture while maintaining consistent transfer in cross-coupling. The dual chlorines anchor selectivity and block unwanted pathways. In-house, we notice that purification, shelf life, and batch reproducibility hinge on this molecular arrangement. Our reactor runs consistently provide the crystalline product needed for high-stakes process chemistry.
Clients come to us with a range of goals. Some work in preclinical drug discovery; others optimize production for crop protection candidates or electronic materials. Across these areas, what unites their approach is the need for boron-containing synthons that hold up under physical and regulatory scrutiny. We tailor each run for strict purity, often tracking residual solvents, halide balance, and boron content closely. Larger manufacturers especially appreciate knowing every container holds what the specification promises without deviation—boron content matches precisely, and the material resists caking and breakdown through storage cycles.
The molecule’s size seems modest. At the core, though, lies adaptation—the ability to withstand extensive work-up, isolation, and multi-step processing without degradation. In our experience, repeat handling stands as a meaningful test. After months on the shelf, our product still produces the correct output by NMR and HPLC, and dusting or grit never confuses the purification plant. Several long-term partners source truckloads for pilot runs, trusting the same consistency we verify at every stage. These aren’t small claims; high-throughput screening and large-scale pharmaceutical runs both bring consequences for impurities and off-spec batches. Regular feedback pours in, often with a nod to the ease of weighing, transfer, and dissolution, reflecting choices we made years ago on crystallization process and drying rates.
Direct experience tells a different story than promotional flyers. Every time a batch leaves our plant, real-world outcomes shape our next move. Subtle differences in melting point or appearance cost companies time and credibility, and even a minor solvent discrepancy can spoil a catalyst screen downstream. We take pride in minimizing these variations. After optimizing quenching and solvent swap steps, we saw a dramatic drop in trace impurities, and not a week passes without some user commenting on the clean, clear profile of the product. Often, academic groups perform direct comparisons, writing back with spectral overlays and chromatograms, highlighting fewer unknown peaks versus samples produced elsewhere. Across dozens of lots, our figures show less than one percent deviation in boron loading, and moisture content remains low from first drum to last scoop.
Other boron reagents offer their own strengths, but the backbone of the dioxaborolane group, as attached to a doubly-chlorinated pyridine, strikes a careful compromise. Some borylated species arrive as sticky, viscous oils, tough to purify and harder to weigh accurately on busy lines. In contrast, our product remains easy to handle, pours evenly from drums, and resists unwanted side-reactions in complex synthetic environments. The twin chlorine atoms lock down parts of the pyridine, discouraging stray reactivity during metal-catalyzed transformations and driving higher product selectivity down the line. Alternative pyridine boronate esters may offer a single halogen or a different protective group, but lose out in market settings where both yield and robust logistics matter.
Where moisture control becomes key—especially in humid regions or during summer storage—the shielding effect of the dioxaborolane group staves off decomposition. Mashed product or glassy chunks simply do not arise under usual shipping conditions. Trusted third-party labs confirm each batch release, but for us, the hands-on experience counts for even more; we see the same fast transferability into glovebox, automated reactor, and open-vessel settings.
As the chemical landscape grows more competitive, fast cycles for patent portfolios and process patents demand reagents that don’t complicate scale-up. Innovation sometimes falters not from poor discovery but because of unreliable or unpredictable building blocks. Behind each kilogram stands a string of investments in cleaning, drying, packaging, and rigorous analytical checks aimed at reducing the risks others too often accept. Researchers, managers, and production teams with time constraints do not want to troubleshoot off-color batches or rewrite process documentation to fit one-off impurities.
We have watched dozens of discovery projects move from gram-scale proof-of-concept into pilot and commercial supply. Each time, the same lessons return: finely tuned intermediates affect not just yield but entire project timelines. Our experience shows that the dual-chlorinated pyridine boronate won’t gum up analytical equipment, and it keeps downstream issues at bay, even in demanding Suzuki and Buchwald-Hartwig coupling conditions. High-purity product shaves hours from characterization and method development, freeing R&D staff to focus on more valuable tasks. Improvements in catalyst efficiency and process throughput, routinely reported by customers, support this framework from startup labs to multinational supply runs.
Pharmaceutical and agrochemical pipeline managers often raise questions about regulatory standards and documentation. Solid traceability and in-plant audits have demonstrated, over many years, what sound documentation means for patient and environmental safety. Without inflated purity claims or hidden excipients, our product delivers on promises from the origin batch right through to final user application. From shipping manifests to certificates of analysis, transparency forms the backbone of our relationship with users. Numerous process validations in multiple jurisdictions reaffirm that the product holds up under scrutiny, supporting global regulations for quality, safety, and environmental compliance.
Every production run shares a focus on safety and predictability. Years in the plant have taught us that shortcuts in handling, washing, or drying bring headaches during multi-tonne campaigns. By dialing in precise reactor charging and carefully monitored crystallization, we prevent carryover and batch heterogeneity. These efforts mean trouble-free charging of reactors both at benchtop and in flow systems—a lesson learned after early users flagged challenges faced with less robust alternatives filled with dust, fines, or solvent residues.
Comparing this product to single-chlorinated analogues reveals genuine differences in both physical and chemical behavior. Monochlorinated pyridine boronates open channels for unwanted overreaction or metal-catalyzed side pathways. Adding both 2- and 6-chlorine atoms delivers steric protection and predictable electronic effects, shrinking risk in electrophilic reactions. Incorporating two chlorines into the ring, in our hands, cuts the number of impurities that appear during late-stage reaction by a third compared to mono-chlorinated versions—better selectivity, cleaner separations, less frustration on production lines.
We also monitor feedback about competing boronate esters. Some report frustration with triphenyl or pinacol boronate systems, especially in high-throughput reactor settings, where unwanted pinacol rearrangement or sticky residues stall progress. By contrast, our dioxaborolane system boasts outstanding resistance to rearrangement and hydrolysis; we verify by forced decomposition testing and hold product samples under multiple conditions over months. The find: no significant drop in reactivity or presence of breakdown products even after storage through temperature swings and transit delays.
Those outside manufacturing often overlook the subtle differences between a product working in a test tube and one delivering full reliability at kilo-scale. Over the years, we have opened tech support lines to research sites worldwide, listening closely to every story of a reaction that suddenly clicks into place or, on a bad day, stalls out. Patterns emerge quickly. Users in academic groups notice fast crystallization during isolation, saving days in their synthetic calendars. Production chemists at multinational pharma report that handling losses drop close to zero, a rare claim in finely powdered intermediates.
Bench feedback tells us the material flows dry, packs easily, and leaves behind minimal residue on glassware—a direct function of the crystallization and purification choices we made. As one senior chemist in electronic materials remarked, “We no longer see unexpected baseline drift in HPLC, and the lot number traceability means we can chase down any issue, knowing the source is fixed.” In the plant, no one needs to retool dissolution steps or add extra drying cycles; the material comes ready for immediate use.
Even more telling, pharmaceutical process teams direct fewer inquiries about compliance checks, pointing to our clean records of validated testing and real-world scenario runs. In one case, direct use in a route to an oncology API brought forward a timeline by nearly two weeks after switching to our product—less downtime for troubleshooting, fewer out-of-spec results, and more focus on process improvement.
Supply chain turbulence across continents makes consistency a daily concern. To keep pace, we maintain real-time logs on production, prioritize rapid QC turnaround, and support flexible batch sizes. Downsizing or upscaling happens without loss of quality: pilot batch or full production, the output stays within spec. Quality teams document every step, tying analytical numbers back to each drum. Lab partners count on this, especially where regulatory filings or market launches hinge on continuity.
Since global volatility often disrupts timelines, we keep both inventory and rapid shipping capacity ready. Whether end-users require a hundred grams for a research kickoff or several metric tonnes for new molecule validation, we adapt to changing forecasts. Unlike commodity traders, our factory knowledge closes the loop, feeding back every complaint, suggestion, and incremental win into better runs. Over the years, we have rebuilt loading bays, added temperature-monitored storage, and streamlined packing lines—practical, sometimes costly steps that pay off in customer trust.
In the harshest conditions, like high humidity or extreme temperature shipments, the product resists caking and hydrolysis, thanks to both its chemical structure and how we handle drying, packaging, and transport. Quality control teams check every consignment for moisture content, particle size, and appearance, often with spot assessments at the point of dispatch. Much of this work goes unseen by end-users, but these details matter—a lesson learned from past years where even small changes at the plant shaped big outcomes at customer sites.
Markets never stand still. Regulatory frameworks tighten, reactions change, and alternative coupling agents gain ground. We believe in keeping open channels with every lab and facility using our product. Listening to those on the R&D line, we have incrementally adjusted grind sizes, improved packaging seals, and issued real-time supply chain notices. The transparency pays off; direct feedback solved a critical clogging issue in automated feeders after we switched drying protocols ahead of a major launch.
Environmental standards evolve just as commercial pressures do. In anticipation, our in-house teams regularly review new guidelines, update internal processes, and invest in cleaner solvents and greener production pathways. Regular audits confirm both compliance and product safety, but even more, we test every suggestion that promises reduced carbon footprints or waste at scale. In this way, our dioxaborolane-pyridine stands at a junction of performance and sustainability, holding steady as new requirements emerge across the pharmaceutical and advanced chemical sectors.
In the public and patent literature, this molecule pops up frequently as a preferred intermediate for selective coupling. As manufacturers, we see the effect first-hand—researchers adopt it for the flexibility it brings to late-stage diversification and for the predictability in analytical profiles. Fewer side products, predictable coupling outturns, and robust handling make it a staple reagent.
Every success story from customers feeds into future production upgrades. We continue to refine each parameter, from the milling process to the moment the container leaves our site. Active sampling and customer debriefs offer clues on how small changes (like anti-static lining or denser packing) can make a chemist’s life easier. Supply consistency, data transparency, and a constant ear to the market sharpen our sense of purpose.
Our direct experience as the manufacturer gives us an edge no brochure can capture. From raw material selection to the last seal on a dispatch drum, we stand by the choices made for 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine. Each lot reflects years of iteration, not just a chemical formula. By answering the phone late at night to solve a shipping issue, or guiding a customer through tricky scale-up, we deliver more than an intermediate. Every kilogram carries our name and stands as proof to the value of making chemistry work, under real-world conditions, for those who depend on every single reaction going right.