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HS Code |
898710 |
| Iupac Name | 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Molecular Formula | C14H22BNO3 |
| Molecular Weight | 263.14 g/mol |
| Cas Number | 1347946-22-2 |
| Appearance | Pale yellow solid |
| Purity | Typically ≥95% |
| Solubility | Soluble in DMSO, DMF, dichloromethane |
| Storage Conditions | Store at 2-8°C, desiccated |
| Smiles | CC(C)OC1=NC=C(C2OC(C)(C)C(C)(C)O2)C=C1 |
| Inchi | InChI=1S/C14H22BNO3/c1-10(2)18-13-8-7-12(9-16-13)14-15-11(19-14,20-14)17-14/h7-10H,1-2H3 |
As an accredited 2-isopropoxy-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 of 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, sealed and labeled, with safety cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine: Secure, bulk packaging ensures safe, efficient international shipment. Temperature and hazard compliant handling. |
| Shipping | 2-Isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is typically shipped in tightly sealed containers under ambient conditions. Packaging ensures protection from moisture and air. It is labeled according to chemical safety standards and may be shipped as a non-hazardous material, unless otherwise specified by relevant regulatory guidelines. |
| Storage | 2-Isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, and protected from moisture and air. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition, strong acids, and oxidizing agents. Store at room temperature or as specified by the manufacturer. |
| Shelf Life | Shelf life: Stable for at least 2 years when stored in a cool, dry place, protected from air, moisture, and light. |
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Purity 98%: 2-isopropoxy-5-(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 minimal contamination. Melting Point 92°C: 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a melting point of 92°C is used in solid-phase synthesis, where it provides consistent handling and controlled processing conditions. Molecular Weight 289.19 g/mol: 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a molecular weight of 289.19 g/mol is used in medicinal chemistry intermediate production, where it facilitates precise stoichiometric calculations and formulation accuracy. Stability Temperature 25°C: 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with a stability temperature of 25°C is used in laboratory storage applications, where it maintains its chemical integrity over extended periods. Particle Size <50 μm: 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine with particle size less than 50 μm is used in fine chemical synthesis, where it offers improved dispersion in reaction mixtures for enhanced reactivity. |
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Through the years working at the heart of chemical manufacturing, we have seen a steady rise in the demand for highly pure, specialized reagents that push modern synthesis forward. 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine stands out as an example of how thoughtful chemical design opens new doors in synthetic chemistry. We dedicate time, resources, and daily attention on the shop floor to ensure that every batch meets consistency and purity standards that academic and industrial research require.
The full name might seem a mouthful, but every part matters. Our team knows its backbone—the pyridine ring—and the attached pinacol boronate for a reason. Over the last decade, boronic esters like this model have transformed cross-coupling chemistry. In our operations, technicians have optimized step-wise synthesis routes and purification steps to safeguard against side products that could jeopardize your downstream work.
Our laboratory technicians frequently see this intermediate move from bench scale to larger lots. Chemists often reach for this boronic ester in Suzuki-Miyaura reactions, aiming to forge new carbon-carbon bonds with higher selectivity. The isopropoxy group at the 2-position of the pyridine ring presents fewer electronic and steric interferences during reaction, which becomes clear in our pilot studies and client feedback from pharmaceutical partners.
Over the years, we have processed hundreds of kilograms in multi-step synthesis. This experience tells us that compared to simple arylboron reagents, the tetramethyl dioxaborolane ring protects the boron center against hydrolysis and oxidation. Our purification workers have handled many such boronic esters, but this one resists breakdown longer under ambient conditions, reducing batch losses and increasing shipment reliability for overseas partners.
Day-to-day lot testing brings a clear message: minor variations in impurity levels or physical properties can stop a downstream project in its tracks. Chemists give us feedback on yields, color, melting points, and how things handle in reactors. Our on-site analytical team checks every lot for purity using HPLC and NMR. Nobody wants an off-color, slightly impure intermediate after weeks of effort. The production crew, the quality department, and the R&D group keep records on every batch for traceability because we have seen how a single variable undermines a project’s reproducibility on a customer’s end.
We often receive calls from clients at research sites who struggle with batch-to-batch inconsistency from other sources. Years of fine-tuning our own process allow us to offer a material with tight purity ranges, consistent physical appearance, and reliable solubility profile. Our teams care about delivering a lot that dissolves properly and works reliably under standard Suzuki coupling conditions, saving you troubleshooting time in research and scale-up runs.
Working in a chemical plant, we know that practical requirements must trump textbook promises. For this pyridine boronic ester, customers look for a solid product free of sticky residue. The color, texture, and melting profile must fall within a narrow range, since even slight irregularities from hydrolyzed boronic acid or pinacol impurities alter chromatographic behavior. Our typical lot achieves high purity with moisture content well below tolerances that would interfere with palladium-catalyzed cross-couplings. The compound’s stability during storage and transport is a direct result of process controls and container selections refined over many shipments.
We continue to run shelf-life studies and invest in packaging solutions to protect the boronic ester against air and moisture ingress. Container choice influences stability, so the warehouse staff downgrades any lot from last year’s inventory that shows color or form change. If issues arise, production batches are investigated and root-caused promptly. Every time we receive feedback about an outlier batch or a customer request for tighter specs, it triggers reviews for both incoming raw materials and our SOPs.
New chemists sometimes ask why—out of dozens of pyridine-based boronic esters—this one has found such steady demand. Years of collaboration with synthetic groups show the details make a difference. The isopropoxy group at the 2-position influences reactivity and selectivity in ways plain-pyridine models do not. Pinacol boronate esters generally handle better in air, but not all handle with equal stability depending on the added functionality. We have measured batch performance on exposure to ambient humidity and found this model holds up with lower tendency to form boronic acid, which can tie up catalyst and slow coupling reactions.
Some pyridine derivatives with other alkoxy substituents bring unwanted hydrophilicity or degrade under modestly basic coupling conditions. Our 2-isopropoxy model balances solubility in polar aprotic solvents and compatibility with a range of coupling partners. The steric bulk of the isopropoxy group prevents dimerization or polymerization during storage, saving customers headaches.
There are always alternatives, and after years spent evaluating them on the pilot scale, our technical team has seen that some boronic acids or less-protected esters hydrolyze too quickly, making them impractical for delivery to humid climates. Without adequate protection, boronic compounds can lose activity before even reaching the customer’s bench. Repeat business from pharmaceutical clients who use this model week after week suggests that reliability beats saving a few dollars on cheaper variants that introduce downstream headaches. We have learned to weigh cost against end-use reliability over many product cycles and under strict audit of project deadlines.
We listen closely to the chemists who count on us for this building block. The best feedback comes from those who scale up a method from milligram to kilogram without issues in solubility or reaction rate. Some models clump or degrade even under gentle handling; this one stays free-flowing, especially when stored dry and cool. Reports from long-term users indicate fewer work-up complications, lower rates of protodeboronation, and more predictable coupling yields, especially when reactions run under standard Suzuki, Buchwald, or Negishi conditions.
Synthetic groups in both R&D and manufacturing settings prefer a reagent that behaves predictably over many runs. Clients in pharmaceutical applications confirm that troubleshooting is reduced when using our boronic ester, due to fewer side reactions or batch-to-batch surprises. This feedback matches our own small and pilot scale-up experience, where side reactions often trace back to unstable or poorly characterized input materials. By prioritizing purity, stable packaging, and rapid delivery, we tackle these issues early and shield end users from preventable setbacks.
We constantly monitor and refine our process, using input from line operators, QC chemists, and pilot plant staff. Their experience guides every improvement. In manufacturing, a multi-step process like this creates opportunities for improvement in throughput, waste minimization, and safety. People handling the product daily notice the nuances: particle size affects solubility, trace metals from the synthesis can undermine key couplings, and improper storage introduces decomposition early.
Our facilities use closed systems and nitrogen blankets during synthesis and transfer. This keeps moisture out, protecting the boronic ester’s integrity. Over the course of each production run, experienced staff check for appearance, odor, and handling ease—not just by-the-book analytics. We have seen how tiny irregularities snowball in downstream processing, so every team member is empowered to reject or flag outlier material.
Compared to simpler arylboronic acids, this compound requires more care in synthesis and handling, but our process is set up to maintain this without adding cost at the customer’s end. Technicians have extensive training, from the reactor to the loading drum, and every repeat batch benefits from process notes and ongoing QA input gathered on the shop floor. Over the years, lessons from process hiccups and successful recoveries inform updated SOPs and improved safety measures.
As a manufacturer, we cannot ignore the environmental impact of our products. Boron compounds pose challenges if not managed correctly. Our plant manages solvents and by-products with scheduled solvent recovery and responsible waste processing. Customer requests for information about downstream waste confirm the importance of designing processes for easier recycling and fewer emissions. The tetramethyl dioxaborolane ring is more resistant to hydrolysis than some alternatives, making for easier containment and treatment at end-of-life, whether in-lab or as part of bulk synthesis campaigns.
We regularly audit waste streams to minimize environmental burden and report results to regulators and customers upon request. Process improvements over the last five years have lowered our solvent usage and reduced the footprint per batch. This aligns us with broader green chemistry initiatives and gives users confidence that their suppliers actively pursue sustainability—not just for compliance but out of long-term necessity.
Lessons from years shipping across climates and time zones influence our logistics. We demand sturdy, moisture-tight packaging and work closely with logistics teams to avoid unnecessary delays. Many graduates from our plant have moved to customer labs worldwide, only to report that even a single cracked drum cap or poorly sealed liner can ruin half a batch before arrival. We rigidly test packaging under simulated transit conditions; every year brings additional scrutiny and ongoing fine-tuning.
Shipping boronic esters remains sensitive work. In humid or hot climates, the risk of breakdown rises fast, so we prefer smaller units and triple-layer packaging to preserve quality. Air shipment, where needed, occurs with extra insulation and tracked temperature monitors. Many clients now ask for shipment history, which our staff documents from cleanroom loadout through every checkpoint. For urgent orders, we prioritize fresh lots and never hesitate to rerun stability tests mid-warehouse season.
Our experience shows that listening beats any technical specification in the long run. We engage regularly with researchers who push boundaries in medicinal chemistry, agrochemicals, materials, and academic research. Adjustments in drying times, blending times, or storage conditions emerge directly from conversations with those who use our product in the most demanding experiments or production runs.
In pilot programs, we invite client chemists to tour our facilities, review batch records, and inspect process run sheets. Their insights spot improvement opportunities—whether optimizing filtration procedures or switching to a new vacuum-drying step that shaves a day off lead time. In every improvement, experience guides us: protecting the sensitive boronic center during synthesis, refining isolation, and tightening in-process controls makes a measurable difference in real-world lab or plant outcomes.
Responsible chemical manufacturing is more than shipping a specification-compliant lot. Our technical team publishes updated process data for each calendar year, including anonymized performance results and side-product trends. Clients comparing our material with competitor batches have shared detailed head-to-head results, supporting a broader body of evidence for performance and reliability in various synthetic routes.
We share data on trace metals, residual solvents, and impurity levels by request, supporting open science and reproducible chemistry. Requests for new documentation or regulatory filings—ranging from REACH dossiers to internal risk assessments—help benchmark our material against the highest industry standards. The result is a product trusted in both small-molecule discovery and large-scale process chemistry, anchored in decades of practical manufacturing commitment.
We have watched trends in organic synthesis shift. Some years, simple boronic acids see more use; in others, stability and selectivity needs make protected models like 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine a preferred building block. The tetramethyl dioxaborolane ring ensures longer shelf life, and the isopropoxy group influences coupling site selectivity. Our clients consistently report higher yields, fewer purification steps, and less troubleshooting compared to less robust analogs.
We pay tribute to the chemists who solved the first cross-couplings with fragile boronic acids. Our production floor now celebrates regular shipments of a model compound that extends their legacy: robust, reliable, and ready for modern applications. Through daily commitment to quality and open collaboration with researchers, we keep this building block at the forefront of innovation.
The demands of chemical synthesis grow more complex each year. Outsourced research programs, international collaborations, and next-generation manufacturing all sharpen expectations for quality, compliance, and seamless supply. 2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine sits at the intersection of these demands, shaped by and for real-world experience.
Reliability emerges not from marketing but from daily efforts on reactors, in labs, on logistics docks, and through customer feedback. The difference between a successful campaign and a delayed launch can hinge on the smallest detail—stability under storage, trace impurities, or ease of handling—yet each improvement owes much to the lived knowledge of manufacturing staff as well as researchers. We encourage all our partners to keep sharing results, asking questions, and challenging us to refine this and future offerings. Only then can today’s trusted tool become tomorrow’s essential reagent, built on the foundation of genuine experience and open exchange.