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HS Code |
794177 |
| Name | 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Molecular Formula | C12H18BNO3 |
| Molecular Weight | 235.09 g/mol |
| Cas Number | 1420764-14-6 |
| Appearance | White to off-white solid |
| Smiles | B1OC(C)(C)OC1c2cc(COC)ccn2 |
| Inchi | InChI=1S/C12H18BNO3/c1-12(2)16-11(17-12)10-6-9(15-3)5-8-14-7-4-10/h5-8,11H,1-3H3 |
| Melting Point | 70-74°C |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Storage Conditions | Store at 2-8°C, protected from moisture and light |
As an accredited 2-methoxy-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 packaged in an amber glass bottle, 5 grams, with a tamper-evident seal and hazard labeling for laboratory use. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Typically holds 8–11 metric tons of 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, securely packed in drums or bags. |
| Shipping | This product, **2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine**, is shipped in a tightly sealed container under ambient conditions. It should be handled with care and stored in a cool, dry place. All compliance and safety regulations for chemical transport are strictly followed during shipping. |
| Storage | Store **2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine** in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from light. Store under inert atmosphere (e.g., nitrogen or argon) if recommended to prevent hydrolysis or degradation. Avoid exposure to air and humidity. |
| Shelf Life | Shelf life of 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is typically 2 years if stored cool, dry, and protected from light. |
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Purity 98%: 2-methoxy-4-(4,4,5,5-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 selectivity. Molecular weight 263.16 g/mol: 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine of molecular weight 263.16 g/mol is used in pharmaceutical intermediate synthesis, where it offers controlled stoichiometry in active compound development. Melting point 74°C: 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a melting point of 74°C is used in fine chemical applications, where it allows for efficient purification via recrystallization. Particle size < 10 µm: 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with particle size < 10 µm is used in homogeneous catalysis, where it enhances reaction rate and uniformity. Stability up to 120°C: 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine stable up to 120°C is used in high-temperature organic synthesis, where it maintains reagent integrity and minimizes decomposition. Water content < 0.5%: 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with water content < 0.5% is used in moisture-sensitive organoboron chemistry, where it prevents side reactions and ensures high reproducibility. Assay by HPLC ≥ 98%: 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with assay by HPLC ≥ 98% is used in medicinal chemistry research, where it enables accurate dosing and formulation consistency. Residual solvents < 500 ppm: 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with residual solvents < 500 ppm is used in API manufacturing, where it guarantees product safety for regulatory compliance. |
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Standing on our factory floor, we see plenty of reactions come and go, but few compounds earn a reputation as solid and reliable building blocks for modern synthesis as 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine. We manufacture this compound in batches that demonstrate consistent color and purity, suited for exacting research and production requirements. From weighing and charging the pyridine derivatives, to managing sensitive boronic ester conversion, our team tracks every step to guarantee top-end quality for demanding users.
Each lot rolling off our line passes strict checks, with analytical results that reflect industry standards and offer traceability. The chemical itself finds a stage in couplings, ligand attachments, and functional group manipulations essential to medicinal chemistry, materials science, and agrochemical discovery. This is no generalized intermediate. Its specific architecture—a pyridine ring ortho-substituted with a methoxy, para-substituted with a dioxaborolane group—delivers selectivity and reactivity that our clients in advanced organic synthesis have come to expect.
Work in a chemical plant exposes you to the daily tug of reliability versus innovation. Anyone pushing for new pharmaceutical candidates or functional materials depends on coupling chemistry that doesn’t let them down. Suzuki–Miyaura reactions have grown into a staple for forming biaryls and wider C–C bonds, so the choice and quality of boronic esters matter more with each passing year.
We have seen chemists convert this compound smoothly, using it with a wide spectrum of aryl or vinyl halides. It takes on transformations well, showing tolerance to many functional groups—a practical advantage for complex molecule construction. The methoxy substitution in the 2-position of the pyridine ring sets this derivative apart from simpler analogs, tuning its reactivity, and allowing for more selective coupling patterns. This isn’t only theoretical value; we hear directly from project teams who bring forward feedback about increased yields and cleaner profiles in their multistep syntheses.
The 4,4,5,5-tetramethyl-1,3,2-dioxaborolane group stabilizes the boron center without sacrificing reactivity. Some boronic acids come with baggage—instability, sensitivity to moisture, or polymerization during purification. In practice, our dioxaborolane-protected pyridines show strong shelf-life, remain free-flowing, and resist degradation under standard storage conditions. Chemists don’t face surprises with sticky residues or variable reactivity, so plans and costings run smoother. For folks on tight timelines or with limited raw material, these differences become real advantages.
Running a chemical plant means tracking every parameter. Composition, appearance, and analytical data flow into our process records. Each kilogram of 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine gets checked for purity, commonly using HPLC and NMR, so we meet or exceed the 97% benchmark most research customers request. Impurity profiles, residual solvents, and moisture content receive scrutiny, since even a percent or two of byproduct can present headaches downstream for scale-up or regulatory filings.
We rarely see issues with the core batch chemistry, but in rare cases where humidity creeps into a storage area, we have implemented container rotation and desiccant replenishment routines to head off degradation. Clean packaging, liners with low extractables, and clear labeling mean scientists can pull material straight from the drum and trust their results match ours.
Spec sheets don’t tell the whole story. Sometimes, even compounds with identical assay numbers react differently if the impurity spectrum varies. Our plant team catches batch-to-batch differences with ongoing NMR analysis to track possible changes in chemical environment. Having stepped in to resolve customer complaints from inappropriate materials supplied by less meticulous vendors, we felt the need to build a more robust QC framework. This is not about ticking regulatory boxes, but supporting users who depend on error-free reactions at every turn.
Chemists who have tried bulk boronic acids often mention two common frustrations: poor solubility and rapid hydrolysis. Traditional 4-boronated pyridines bring higher sensitivity and lower yields in cross-coupling. Even some commercial dioxaborolane esters lag on purity, or mix in unknown isomers. These flaws aren’t academic—they show up in wasted time and unsatisfying yields.
Our 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine consistently dissolves across a range of solvents, standing up during inert-atmosphere handling. The material doesn’t clump or cake when stored as directed, and heat-testing confirms thermal stability above most laboratory requirements. Some boronic acids release pungent odors on exposure to air, but this dioxaborolane remains mild, reducing lab incidents and keeping operators comfortable. Handling convenience ranks high on our watchlist, thanks to direct experience training new lab workers and observing their challenges.
Looking wider, other pyridyl boronic derivatives often feature less robust protection or suffer from side-reactions under cross-coupling. The 2-methoxy group has more value than meets the eye—it directs reactivity, blocks unwanted pathways, and pairs well with electron-withdrawing partners. This makes it particularly handy for late-stage diversification or introductions of a functionalized pyridine into fragment libraries. Unlike simple para-substituted isomers or acid versions, this compound stands up in challenging synthetic routes.
Over the years, research and development users share real-world stories from the bench. Pharmaceutical chemists tap the 2-methoxy-4-borylated pyridine route to build complex heteroaryls for kinase inhibitor scaffolds, and some agrochemical clients use it to create tailored pyridine structures for structure-activity relationship (SAR) studies. Polymer researchers sometimes include this unit in ladder or conjugated polymer systems, spinning up new optoelectronic materials.
Feedback often centers on how our compound launches cleanly into Suzuki and similar transformations. Cross-coupling with aryl bromides, iodides, and pseudo-halides proceeds under mild conditions, allowing retention of delicate motifs elsewhere in the molecule. One group in Europe described moving from a less stable boron reagent, with repeated chromatographic purification, to our dioxaborolane derivative, finding reliable isolation and less regulatory hassle over residual impurities. Academic labs, pressed for time, now skip laborious pre-filtration and just charge the solid into the flask. Technical details matter, but so do simplicity and repeatability.
The market features cheaper boronic acids and more exotic masked boronates, yet in workflow after workflow, our clients keep returning to this product. From late-stage diversification to the first build-out steps of a new medicinal core, the value lies in consistent, straightforward handling and a track record of direct compatibility with popular catalytic systems. No product offers universal solutions, but by holding close to feedback from active users, we focus our manufacturing on those features that support versatility, safety, and low material loss.
Anyone running a chemical plant faces the push to reduce process waste and improve operator safety. Boronic esters stand at a crossroad—stable enough for shipping yet reactive enough for coupling. We track boron source quality, control air exposure, and improve crystallization to minimize mother liquor residue. Early on, some production runs showed trace oxidative byproducts. Iterative process tweaking, including controlling light exposure and scavenging for dissolved oxygen in the feedstock, brought down these incidents. We learn directly from each campaign, constantly driving towards better consistency.
Customers sometimes ask for modifications—improved recovery for pilot-scale reactors, larger volumes, or custom packaging that fits with automation. Our production model is flexible enough to cater to both multi-gram research and multi-kilogram industrial clients. Changing a drum size or using anti-static liners might sound minor, but contributes significantly to minimizing spills and exposure during handling. Stability under transit conditions remains a priority; we have reinforced shipping containers and implement impact indicators for sensitive cargos.
Most important to us is safe, responsible manufacturing. Regulatory landscapes shift, and scrutiny of boron-containing compounds has increased worldwide. We stay informed about registration and notification developments, adjusting paperwork and documentation as appropriate. Every new revision to safe handling guidance gets rapid translation into our internal protocols, reflected in employee training refreshers and updates to our partners. Community and employee safety mean more than photo-ready certifications—they present an everyday responsibility.
Our longstanding relationships with customers run beyond order sheets and purchase orders. Direct conversations with research leads and process chemists yield insights into where our material fits or falls short. We often hear requests for tighter particle size distribution, lower limits on trace metals, or validation in new reaction classes. Instead of treating such requests as annoyances, we incorporate them into process improvement cycles, investing in new filters, dryers, or detection technologies as needed.
Feedback cycles shape batch scale, packaging, and documentation. We see demand shifting towards green chemistry and minimal-waste protocols. Our own facility has made moves to recover and reuse solvents from purification, and switched to less hazardous cleaning agents. No single building block offsets larger process impacts, but continual improvement ripples through the supply chain. Every time we make a batch of 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine that exceeds customer expectations, we set a new internal benchmark for what high-quality means and how service should feel on the other end.
Our experience sits squarely in the world of technical details and operational realities. Each order draws on what we have learned about packaging, stability, and user experience, and each batch carries the intention to cut complication and raise productivity. Pharmaceutical innovators, fine chemical developers, and advanced materials researchers all share similar goals—consistent quality, honest specification, and a partner who values results over spin.
In the real world, compounds don’t exist as isolated catalog entries. From initial charging of raw materials to the final drum seal, we interact with chemical reality at every step, making ongoing choices about safety, stability, and true buyer value. When clients need documentation, technical support, or troubleshooting, we respond from direct process knowledge—the same perspective that shapes our standards in plant and in shipment.
That’s why so many teams choose to stick with our 2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, project after project. The trust we earn comes from real conversations, resolved problems, and material that performs cleanly, batch after batch. Our drive comes from that feedback, and from the technical progress that comes when a reliable building block supports new discoveries.
Mass spectrometry labs in global biotech hubs and university groups breaking new ground in heterocycle synthesis share much in common with our own operators. Everyone values certainty—knowing that each drum or bottle received will propel a project forwards with minimal fuss and maximum efficiency. We invest in process transparency, meaningful analytical data, and careful batch release because we understand the costs down the line when a single impurity or inconsistency creeps into a synthetic sequence.
As graduated licensing, changing environmental norms, and broader adoption of automation spread across our customer base, we work to stay one step ahead. Lab automation systems appreciate reproducible, well-documented input materials. Young researchers stepping into the field expect error-free protocols and honest technical support. We keep those expectations at the front as we adapt our manufacturing, distribution, and customer support systems.
2-Methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine stands as more than a chemical name or a formula on paper. It represents years of incremental learning about production nuance and end-user expectation. Our team brings a hands-on approach, whether prepping the next distillation column or troubleshooting tricky chromatographic steps, and we root product information in lived experience rather than process charts copied from generic catalogs.
This compound earned its popularity among researchers and industrial chemists for solid reasons—ease of use, high purity, batch consistency, and a willingness on our part to tweak the production cycle when improvement makes sense. We see the benefit most clearly through customer success stories, where a clean batch carries a project over the finish line or trims days from a synthetic route.
Manufacturing this pyridine derivative ties together technical discipline with open communication. Our efforts do not stop at hitting minimal standards; our process grows from every new question or suggestion that comes at us from the lab bench or process suite. Every batch shipped out the door owes something to this cycle of honest feedback and continuous improvement. Hand in hand with our partners in research and industry, we look ahead to ever-higher expectations and sharper demands, ready to make sure every kilogram stands up to the promises we make.