Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

    • Product Name: Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
    • Chemical Name (IUPAC): 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
    • CAS No.: 959239-97-7
    • Chemical Formula: C13H20BNO2
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    717278

    Chemical Name Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
    Cas Number 870778-35-5
    Molecular Formula C13H20BNO2
    Molecular Weight 229.12
    Appearance White to off-white solid
    Melting Point 78-82°C
    Solubility Soluble in common organic solvents (e.g., dichloromethane, THF)
    Purity Typically ≥ 97%
    Smiles CC1=NC=C(C(=C1)B2OC(C)(C)C(C)(C)O2)C
    Inchi InChI=1S/C13H20BNO2/c1-9-7-11(10(2)15-8-9)14-12-16-13(3,4)18-17-12/h7-8H,1-4H3
    Density 1.07 g/cm3 (estimated)
    Storage Conditions Store at 2-8°C, dry and under inert atmosphere
    Hazard Statements May cause eye and skin irritation

    As an accredited Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 5-gram amber glass bottle with a secure screw cap, labeled with hazard, chemical name, and CAS number.
    Container Loading (20′ FCL) 20′ FCL container typically holds 160 drums (200 kg each) or 8000 kg of Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-.
    Shipping **Shipping Description:** Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- should be shipped in tightly sealed containers under inert atmosphere, protected from moisture and light. Transport at ambient temperature, following applicable regulations for handling and shipping of organoboron and pyridine derivatives. Ensure proper labeling and documentation for chemical and safety compliance.
    Storage Store Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as oxidizers and acids. Keep the container tightly closed under an inert atmosphere, such as nitrogen or argon, and protect from moisture and direct sunlight. Handle in compliance with standard laboratory safety procedures.
    Shelf Life Shelf life: Store in a cool, dry place under inert atmosphere. Stable for 2 years if unopened and properly stored.
    Application of Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-

    Purity 98%: Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with a purity of 98% is used in Suzuki-Miyaura cross-coupling reactions, where it ensures high coupling efficiency and minimal side product formation.

    Melting Point 158°C: Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with a melting point of 158°C is used in pharmaceutical intermediate synthesis, where it provides thermal stability during high-temperature processing.

    Moisture Content <0.5%: Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with moisture content below 0.5% is used in organoboron reagent preparation, where it prevents hydrolytic degradation and maintains reagent reactivity.

    Stability Temperature up to 120°C: Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- stable up to 120°C is used in electronic material manufacturing, where it ensures consistent compound performance under elevated process temperatures.

    Particle Size <10 μm: Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with particle size less than 10 μm is used in catalyst formulation, where it improves dispersion and maximizes surface area interaction in heterogeneous catalysis applications.

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    Certification & Compliance
    More Introduction

    Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-: Experienced Manufacturer’s Perspective on Crafting for Modern Chemical Synthesis

    A Closer Look from the Plant Floor

    Authenticity means everything in chemical manufacturing. As a producer deeply involved in the creation of Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, the job calls for more than just technical compliance or chasing purity records. This molecule, with its fused boronic ester and strategically placed methyl groups, stands as a cornerstone for synthetic chemists who demand precision and reliability. The world behind the glassware moves quickly, and so the way we manufacture and handle every batch must match that energy. We do not talk much about “product lines” because for us, every lot reflects a legacy of trial, error, and refinement. Reliability always starts with the process itself.

    Why Pyridine Derivatives Matter to Today’s Synthetic Community

    Developments in pharmaceutics, agrochemical research, and material science keep pushing complexity higher, and the demand for reagents that don’t just tick boxes but actively enable difficult transformations grows each year. This compound carries remarkable utility for Suzuki-Miyaura cross-coupling and related organoboron chemistry. Chemists expect not only the correct structure but also batch-to-batch consistency. These expectations keep manufacturers honest.

    Many clients remark on the unique performance features displayed by reagents like ours. The 2,6-dimethyl backbone brings subtle changes to reactivity by blocking certain activation gates on the pyridine ring, while the boronate functionality transforms the entire molecule into a flexible building block. When handled with technical discipline, this also lends itself to interesting late-stage diversification, in pharmaceutical intermediates or tailored ligand synthesis. Years of experience have taught us that reproducibility in reactivity under various coupling conditions matters much more than headline assay numbers alone.

    Craftsmanship in Managing Impurities

    Manufacturing this pyridine boronate brings its own set of challenges. During synthesis, boronic esters show real sensitivity to moisture and oxygen. Ignoring trace water or using compromised glassware never pays off. Our technicians—some of whom have worked these benches for decades—know that even small changes in solvent purity, or unvetted raw materials, show up five steps later as suboptimal yields or low-level impurities. These lessons cannot be faked, borrowed, or replaced by theoretical knowledge alone. What shows on spec sheets only tells part of the story; behind those numbers stand hours of vigilance and hands-on troubleshooting.

    Early in our experience with this class of molecules, we learned that the methylation pattern on the pyridine ring tends to complicate chromatographic separation after borylation. That forced us to refine purification, often beyond what reference methods suggest. True to the hands-on ethos of chemical manufacture, our team went through cycles of learning: iterative solvent selection, temperature tuning, and patient washing. The effort paid off with improved crystal formation and tighter mass balance. The final outcome—a product whose HPLC and NMR profiles align with demanding standards—is what adds value for research scientists aiming to scale novel reactions.

    Everyday Realities and Lessons Learned

    What matters most to chemists is not just purity, but confidence in every gram delivered. Even the most advanced catalysis protocols will flounder if the input ingredients falter. A batch that reads above 99% purity might still disappoint if residual solvents or unidentified isomers disrupt reactivity or create ghost peaks in analytic runs. It turns out a consistent protocol for trace impurity control, built from direct experience, shields end-users from unreliable results.

    Regular dialogue with laboratory users reveals the pain points: products from some sources lack solubility, show inconsistent melting points, or fail to couple cleanly under standard Suzuki-Miyaura conditions. That lights a fire under our operations. Each new customer, each follow-up call about performance, feeds back into our own practices. Soon after we began manufacturing pyridine boronic esters, we shifted to using rigorously dried, pre-cooled glassware and implemented batch-specific drying protocols for key intermediates. These tweaks sound like minor details from afar, but in practice, they close the gap between research reliability and real-world scale-up.

    The Real Differences: Structure, Reactivity, Experience

    This molecule’s structure, with the 2,6-dimethyl substitution on the pyridine ring, creates a unique blend of electronic and steric effects. Compared to its mono-methylated or unsubstituted cousins, this pattern enhances both selectivity and stability. These benefits do not appear overnight. They stem from our team tuning reagent ratios, modifying protection and deprotection schedules, and revalidating every new synthetic run. Academic papers and patent filings regularly cite the importance of methylation pattern—yet only hands-on production of hundreds of kilograms truly reveals how the practical differences manifest.

    Commercially, the market is flooded with “generic” boronic esters and industrial-grade pyridines. Most lack the nuanced benefits needed for pharmaceutical lead development or late-stage functionalization. Our experience tells us that off-the-shelf supply does not guarantee transformations free of unknown byproducts or drifting yields. The most innovative labs run their reactions with an eye on subtle side-processes, and we support them by backing up every delivered batch with detailed analytic histories. No batch moves forward until those numbers are right.

    Why We Compete on More Than Price

    It’s easy to fixate on market price, but those who work the flask know that price alone hardly pays for downtime, failed reactions, or mystery contaminants. Our customers learn that a fair cost, coupled with true reliability and speedy technical support, beats the headaches caused by bargain-bin chemicals. The ripple effects of a failed batch are real—lost days, lost experiments, grant money spent to solve avoidable problems. Years of riding this cycle have convinced us to put direct communication at the core. With every lot, we offer not only supporting documentation, but also access to technical personnel ready to work through unexpected issues—no chatbots, no deflection, just a call or an email away.

    The temptation always exists to cut costs by lowering production controls. We say no. Not because of static “corporate commitment” language, but because shortcuts show up in performance soon enough. We have witnessed the difficulties that arise from sourcing lower-grade material—a single lot with undetected dioxaborolane hydrolysis, or traces of residual mineral acid, ruins months of work downstream. This stubborn refusal to compromise comes directly from experience and respect for our customers’ work.

    Understanding Our Customers at the Reaction Bench

    From startups working on new therapeutic targets to industrial teams designing specialty electronic materials, our production mindset grows out of listening to chemists. A postdoc rushing to optimize a reaction cares about solubility profiles and fast delivery as much as certificate printouts. A process engineer building for launch wants to know the lot history, current manufacturing status, and what backup inventory exists if demand scales unexpectedly.

    To keep projects on track, we run lot-specific analytic checks that go beyond standard COA thresholds—cross-checking HPLC retention times, confirming absence of hard-to-remove boroxine impurities, and running water content checks by both K.F. and NMR. These touchpoints reveal what end users actually value: transparency, support, and proven performance. Any feedback, whether praise or complaint, makes its way into operational reviews. Upstream from finished goods, every step—raw material selection, temperature and humidity controls, waste management—gets regular scrutiny.

    Addressing Stability: Shipping and Storage Realities

    Boronic esters live in the gray zone between easy handling and troublesome degradation. We build our process around that reality. Years ago, we switched to specialty packaging with moisture barriers, desiccant pouches, and tamper-evident seals. Customers seeking bulk material benefit from secondary containment options or cold-chain shipping on request. All of this flows directly from first-hand experience: emergency calls and panicked emails from researchers whose shipments sat too long in customs or on a sunny dock. By sharing handling advice and updating customers about storage risks, we give them tools to protect their investment in every container.

    Environmental and Regulatory Challenges: Inside the Gate

    Managing production of specialty pyridine boronic esters creates waste streams that require careful attention. We spent years fine-tuning recovery systems, selecting compatible solvents, and running bench trials to reduce hazardous outputs. Supporting our customers’ sustainability goals means more than posting compliance badges. In our operation, solvents undergo recovery and recycling cycles. Non-reclaimable residues follow coded waste paths before safe disposal. No single improvement solves every issue, but the value accumulates over repeated runs; less waste, more return per kilogram, fewer headaches for everyone downstream.

    Staying current with regulations also requires direct interaction with product users, especially those in regulated fields such as pharmaceutical or crop protection research. Early notice of upcoming rule changes, documentation updates, and import/export restrictions benefits both us and our customers. Periodic internal audits and mock product recalls keep everyone practiced in real-world action, not just theoretical compliance. In our cumulative experience, the hidden value of such discipline gets noticed only after the supply chain is stress tested—by customs, paperwork delays, or new tariff codes. Customers who run pilot programs with our support see these efforts as more than bureaucratic checklist; they see them as insurance against worst-case scenarios.

    Collaborative Problem Solving: Sharing Lessons Across the Industry

    Down on the production floor or at the service desk, real-time feedback from the laboratory often sparks direct improvement. Once, a customer’s late-stage coupling process flagged an increase in side-product formation. Conventional wisdom pointed to in-lab error, but iterative follow-ups led us to tweak the protective group deprotection schedule and adjust the aging window ahead of shipment. This guided intervention curbed the rogue pathway, but more importantly, reminded everyone that strong supplier–chemist relationships drive breakthroughs.

    For those developing new protocols, transparency about possible byproducts or solvent incompatibilities builds trust. We publish data on thermal stability, hydrolytic breakdown points, and batch-to-batch impurity signatures from typical runs. By publishing these lessons, labs can plan for contingency—selecting quench points, setting chromatographic conditions, or adjusting autoclave cycles before problems occur. Mutual support—built from hard-earned, practical knowledge—ensures project continuity and more predictable research outcomes.

    Handling Scale: Transitioning from Bench to Commercial Needs

    Scaling synthesis of Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- often separates experienced manufacturers from casual producers. Each step up in batch volume reveals flaws invisible at milligram scale. Thermal management, mixing efficiency, impurity carryover, and safety considerations all require new solutions at scale. Not long ago, we encountered heat buildup and foaming during the borylation stage when moving from bench-top to pilot-plant runs. Only by supplementing standard operating procedures with operator observations did we eliminate runaway reactions and improve phase separation—critical for high-yield performance on kilo runs.

    The shift from laboratory to plant means changes in crystallization, longer residence times, and more challenging solvent recovery. Customers who want to take their own synthesis up in scale benefit from our operational experience. Direct consultation, on-site support, and real-time troubleshooting cover more territory than mere paperwork. We view every scale-up as a partnership—mistakes or shortcuts at any stage show up in the downstream product, so honesty in reporting, root cause identification, and preventive improvements make economic and technical sense.

    Protecting Innovation: Intellectual Property, Confidentiality, and Data Security

    Pharmaceutical and advanced material clients rightly fret about risk to their proprietary research. Our team recognizes the sensitivity associated with both method details and new target molecules. Many years of handling non-disclosure agreements, controlled access to batch histories, and off-site recordkeeping taught us how easily small leaks become large issues in close-knit R&D communities. We commit training resources to staff at every level so that confidentiality gets baked into routine practice rather than just laminated onto the wall.

    Supporting innovation extends to intellectual property management. Clients trust us not just to supply high-purity chemical but to respect the investments, time, and breakthroughs they represent. Our own in-house research and process optimization respect the difference between shared progress and protected proprietary steps. Updates on supply challenges, insight into potential patent issues, and collaborative troubleshooting always occur within agreed bounds—built from earned trust.

    Looking Outward: What the Future Demands

    The world of specialty chemicals keeps growing. As research teams pursue ever more complex target molecules, the building blocks behind those efforts must keep pace. Subtle evolution—such as a new isomer reported in the literature, or a process tweak that boosts yields by a few points—can ripple across an entire sector. Practical, experience-based product improvements will outlast trendy marketing stories. Our crew’s accumulated wisdom—much of it learned the hard way—yields products that function not just on paper, but in real reaction jars and pilot plants, supporting the ongoing march of modern science.

    From this vantage, Pyridine, 2,6-dimethyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- completes a full circuit: tailored for demanding synthetic work while drawing every ounce of value from collaborative exchange, operational discipline, and shared commitment to science. Our journey with this molecule means more than just successful manufacture. It means giving fellow chemists an edge in every reaction, every time.