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HS Code |
435133 |
| Product Name | 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester |
| Cas Number | 1374658-90-4 |
| Molecular Formula | C15H21BN2O3 |
| Molecular Weight | 288.16 |
| Appearance | White to off-white solid |
| Melting Point | 98-102°C |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Smiles | B(C1=CN=CC(=C1)N2CCOCC2)(OC(C)(C)C)OC(C)(C)C |
As an accredited 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 mg of 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester is supplied in a sealed amber glass vial with safety labeling. |
| Container Loading (20′ FCL) | 20′ FCL loaded with securely packaged 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester; moisture-protected, hazard-labeled, meeting chemical transport standards. |
| Shipping | **Shipping Description:** 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester is shipped in a tightly sealed container under ambient or cool conditions, protected from moisture and light. It is labeled according to regulatory guidelines, with appropriate documentation. Ensure compliance with local, national, and international chemical transportation regulations. Handle as a potentially hazardous laboratory chemical. |
| Storage | Store 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, away from moisture and light. Keep at room temperature or as indicated on the product label. Store in a cool, dry, well-ventilated area, separate from oxidizing agents and acids. Always follow proper chemical storage guidelines. |
| Shelf Life | **Shelf Life:** 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester is stable for at least 2 years when stored dry, cool, and protected from light. |
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Purity 98%: 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester with 98% purity is used in palladium-catalyzed Suzuki-Miyaura cross-coupling reactions, where it ensures high coupling yields and product selectivity. Molecular Weight 318.27 g/mol: 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester with a molecular weight of 318.27 g/mol is used in pharmaceutical intermediate synthesis, where it facilitates precise stoichiometric calculations for scalable processes. Melting Point 84-88°C: 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester with a melting point of 84-88°C is used in solid-phase synthesis protocols, where it enables straightforward handling and storage under controlled temperatures. Stability Temperature up to 45°C: 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester stable up to 45°C is used in long-term reagent storage, where it maintains reagent integrity and minimizes decomposition during process workflows. Particle Size <50 μm: 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester with particle size less than 50 μm is used in automated flow chemistry systems, where it promotes rapid dissolution and uniform reactivity. Water Content ≤0.5%: 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester with water content ≤0.5% is used in moisture-sensitive coupling reactions, where it prevents hydrolytic degradation and maintains product purity. |
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Chemistry is a world built on practical choices. For years, in our manufacturing halls, we have produced a broad range of boronic esters. Among these, 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester (often referred to on our labels as Model: 100568-98-9) stands out for its reliable performance in complex organic synthesis. This is not just another addition to a broad product catalog; it’s the result of repeated hands-on trial and refinement.
In our daily operations, we work directly with the needs of medicinal chemists, agrochemical innovators, and electronics researchers. Consistency in reactivity, batch-to-batch purity, and real compatibility with palladium-catalyzed coupling processes drive demand for boronic esters. Our team has handled every variation you can imagine—different core structures, protecting groups, subtle changes—and not all deliver the same ease of handling.
What makes 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester different is its fusion of a morpholine ring and a heterocycle. This combination brings reliable solubility in polar organic solvents and often delivers smoother transitions in Suzuki-Miyaura cross-couplings. Speaking with chemists developing kinase inhibitors or advanced OLED materials, we’ve seen them gravitate towards this compound for its functional group tolerance. When you work with varied substrates or sensitive scaffolds, such convenience saves time and protects margins.
Raw stories from our operators echo a repeated truth: impurities and instability spell disaster at scale. During early development, we caught degradation issues with boronic acids stored in variable humidity. Pinacol esterification closed the gap—product longevity improved, and operational headaches dropped sharply. Now, each batch of this compound ships with clarity and stability chemists notice right away.
Colleagues who scale reactions beyond the laboratory bench have told us about the frustration when a reagent clumps or fails to dissolve. Here, our 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester consistently offers a free-flowing, manageable powder. This comes directly from process tweaks—optimal drying, careful solvent layering, and tight control during recrystallization. Our workers spot-check every lot for ease of weighing and transfer, because a reagent that jams up in production lines leads to downtime and losses.
On some days, purity is a marketing word. In reality, it means the difference between moving a reaction forward and spending hours with column chromatography. Our chemists encounter this directly; we analyze each lot by HPLC and proton NMR, not simply to chart a number for a certificate, but because low-level impurities can completely disrupt downstream syntheses. A 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester batch that comes in at below 98% purity does not see a shipping label. Instead, we rework or reject it outright. This is one way the product sets itself apart—we guarantee reproducible performance, so our customers can trust every bottle to deliver the same result, whether it’s one kilogram or one hundred.
We do not pick specifications out of a book. Years ago, lighter packaging invited moisture uptake; we switched to sealed, nitrogen-filled containers after seeing unexpected product clumping on customer benches. Molecular weight is not just a number here: it informs our stock solutions, calibration of liquid feeders, and process mass balance in real-world settings. Every specification has been tuned for practical reliability. Appearance, solubility, melting point, and shelf life all play a role when deciding what makes it out the door.
For scientists building libraries of pyridine derivatives or optimizing hits from high-throughput screening, this product’s functional versatility matters in real lab environments. The morpholino portion of the molecule accommodates downstream chemistry: amide formation, oxidation, and even late-stage functionalization. Colleagues routinely use this ester as a stable intermediate before deprotection and coupling steps, especially where air or moisture sensitivity would render many boronic acids useless. The pinacol ester improves the compound’s shelf life, allowing easy handling and storage over long development cycles without risking hydrolysis.
Our customers from pharmaceutical R&D bring back stories of speedier route scouting in their SAR cycles—sometimes cutting whole days off a timeline. In one case, a team shifted from using the parent boronic acid to our pinacol ester and gained cleaner isolation in their cross-coupling step, which raised the overall yield for their lead program. These are not isolated incidents. Each feedback loop motivates revisions to the process, pushing us to tighter control and even better reproducibility batch after batch.
Several years back, the market was flooded with generic boronic acid esters. Their differences show up in unplanned downtime and costly purification. We once evaluated two lots from non-manufacturing resellers—one clumped by the time it arrived, needing significant force to break apart; the other showed unexplained impurities, sabotaging the Suzuki coupling. These experiences highlighted why source control and direct manufacturer expertise matter.
We manage every aspect from raw material qualification to post-recrystallization drying—avoiding problems caused by uncontrolled storage and handling. Colleagues who buy directly understand the reduction in risk and uncertainty this brings. That sense of control over the process, from reactor to bottle, has convinced even skeptical procurement managers over time.
There is a sea of boronic acid derivatives and esters—phenylboronic pinacol esters, substituted pyridyl boronic acids, and analogues galore. The practical differences emerge in how they behave in synthesis. Many boronic esters perform adequately for simple couplings, but seasoned chemists recognize that side reactions, low conversions, or purification troubles often follow the “one size fits all” approach. Adding a morpholino group to the pyridine ring opens new doors for reactivity, while the robust pinacol ester function makes for reliable handling even under less-than-ideal conditions.
Other boronic acids or esters sometimes promise cost savings at purchase but can waste more time downstream: stabilizing agents may interfere in sensitive reactions, and weaknesses in long-term storage create loss. For chemists iterating on pyridyl motifs in drug scaffolds or advanced electronic materials, our product’s chemical stability and performance provide a margin of assurance that common analogues lack. Experience reinforces that higher initial purity and uncompromised stability routinely translate into real-world success.
Modern chemical processes demand more than simple yield or throughput. We take steps in our plant to minimize solvent use and energy consumption during each esterification. During purification, closed-loop solvent recovery keeps losses to a minimum. Once upon a time, boronic acids would degrade on shelves, forcing customers to dispose of spoiled material. As a direct manufacturer, it’s our responsibility to cut waste before it happens—so the shelf-stable pinacol ester format solves multiple pain points: fewer failed reactions, less material thrown away, and reduced hazardous waste disposal.
Feedback from several production chemists showed the benefit of robust packaging: with extended stability, purchasing departments can order in larger lots, optimizing logistics and reducing shipping frequency. That translates into both economic and environmental benefits—fewer shipments, less packaging, and lowered risk of emergency “rush orders.” From the factory floor to your storage facility, those choices make a difference.
A commodity product rarely inspires, but every detail matters in R&D. Medicinal chemists we support use these boronic esters to advance diverse projects: kinase inhibitor optimization, probe molecule synthesis, bioisosteric replacement, and property tuning for molecular recognition. These chemists become repeat partners, because hands-on confidence in a material changes workflow. The consistency of our 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester—backed by real batch records, systematic testing, and a clear process history—directly supports the kind of high-reward leaps that drive innovation forward.
Beyond pharma, electronic and polymer materials researchers have reported cleaner couplings and improved yields when substituting this ester for less-stable boronic acids. When a functional material must perform day after day, such as a light-emitting polymer or a novel electrical insulator, the margin for error narrows. Reliability and predictability in starting materials offer reassurance that no intangible market value can match.
Over years in production, the voice of the chemist shapes what we produce. This particular compound came into focus through repeated requests from teams running into blocks during pyridine functionalization. They asked for better stability and cleaner coupling—challenges that off-the-shelf compounds failed to meet. We responded by investing in small-scale development, tweaking solvent systems, and calibrating every stage of recrystallization to maximize active content and stability.
Mistakes from early days—the occasional brownish off-color, slower dissolution, detection of side-products via NMR—drove us to re-examine everything from raw pinacol quality to temperature ramps in esterification. The current process, worked out and tuned through many cycles, gives a product used worldwide by those who measure results in data, not just in dollars.
Thousands of bottles of boronic acid esters and acids pass through our hands each year. We hear directly about delayed projects, failed syntheses, and lost time caused by unpredictable reagents. Through our own testing and by reacting to customer troubleshooting, we understand the domino effects a poorly-supplied starting material causes. By insisting on a direct line between the plant and the lab, we help eliminate those setbacks—calibrating every part of the process based on hands-on experience.
Chemistry does not happen in a vacuum. In the end, every specification, tweak, and handling optimization reflects feedback from the users pushing boundaries every day. It is our responsibility to anticipate shifting project needs, regulatory developments, and sustainability demands—and that happens only with constant dialogue between manufacturer and chemist.
This compound exemplifies a principle we have come to value: practical improvements only work if they translate into real outcomes for the research community. By refining 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester through countless production cycles, user trials, and direct feedback, we now deliver a product that stands apart not by marketing flash, but by the sum of small, decisive adjustments over time.
Whether scaling up for manufacturing or intricately exploring chemical space in a single fume hood, reliable starting materials change the landscape of discovery and production. Our experience as direct manufacturers teaches us every day that investing upstream—right at the molecule’s origin—delivers efficiency, sustainability, and scientific progress further downstream. This is what sets our 2-(4-Morpholino)pyridine-5-boronic acid pinacol ester apart: a product shaped, batch by batch, through the experience and determination of manufacturers who walk the same chemical path as their customers.