|
HS Code |
659480 |
| Product Name | 6-Isopropoxypyridine-3-boronic acid pinacol ester |
| Cas Number | 1229386-62-8 |
| Molecular Formula | C14H22BNO3 |
| Molecular Weight | 263.14 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically >97% |
| Smiles | CC(C)OC1=NC=C(C2C(C)(C)C(C)(C)O2)C=C1 |
| Inchi | InChI=1S/C14H22BNO3/c1-10(2)19-13-7-6-12(15(17)18-14(3,4)5)8-16-9-13/h6-10H,1-5H3 |
| Solubility | Soluble in organic solvents such as DMSO, dichloromethane |
| Storage Condition | Store in a cool, dry place, under inert atmosphere |
| Synonyms | 6-(Isopropoxy)pyridine-3-boronic acid pinacol ester |
| Chemical Class | Boronic acid ester |
As an accredited 6-Isopropoxypyridine-3-boronic acid pinacol ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in a 5g amber glass bottle with a tamper-evident seal, labeled with product name, CAS number, and safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Chemical packed in sealed drums, securely loaded onto 20′ full container, ensuring safe transport and compliance standards. |
| Shipping | **Shipping Description:** 6-Isopropoxypyridine-3-boronic acid pinacol ester is shipped in sealed, chemical-resistant containers, protected from moisture and air. The package complies with relevant safety regulations for organic boronic esters, with clear hazard labeling. Transport is typically at ambient temperature unless specified otherwise on the Safety Data Sheet (SDS). Handle with appropriate PPE upon receipt. |
| Storage | 6-Isopropoxypyridine-3-boronic acid pinacol ester should be stored in a tightly sealed container, under an inert gas such as nitrogen or argon. Keep it in a cool, dry, and well-ventilated area, away from moisture, air, and incompatible substances such as strong oxidizers. Store at room temperature or lower, and protect from direct sunlight and sources of ignition. |
| Shelf Life | Shelf life of 6-Isopropoxypyridine-3-boronic acid pinacol ester is typically 2 years if stored dry, cool, and protected from light. |
|
Purity 98%: 6-Isopropoxypyridine-3-boronic acid pinacol ester with purity 98% is used in pharmaceutical synthesis, where it ensures high yield and minimized by-product formation. Molecular Weight 263.14 g/mol: 6-Isopropoxypyridine-3-boronic acid pinacol ester with molecular weight 263.14 g/mol is used in Suzuki-Miyaura cross-coupling reactions, where it allows precise stoichiometric calculations for efficient catalyst loading. Melting Point 105-110°C: 6-Isopropoxypyridine-3-boronic acid pinacol ester with melting point 105-110°C is used in solid-phase organic synthesis, where it provides thermal stability during reaction processing. Particle Size < 50 µm: 6-Isopropoxypyridine-3-boronic acid pinacol ester with particle size less than 50 µm is used in automated chemical reactors, where it enables rapid dissolution and consistent reaction rates. Stability Temperature up to 80°C: 6-Isopropoxypyridine-3-boronic acid pinacol ester stable up to 80°C is used in high-temperature coupling reactions, where it maintains structural integrity and reactivity. |
Competitive 6-Isopropoxypyridine-3-boronic acid pinacol ester prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Every chemist in a production environment knows how much hinges on the fine details: starting with stable reagents, keeping impurities under strict control, and making sure each batch lands right on spec. At our manufacturing site, the synthesis of 6-Isopropoxypyridine-3-boronic acid pinacol ester (often referred to for shorthand as IPP3B-PE) has presented both challenges and opportunities to push the standard higher. We chose to invest in this molecule due to several of its unique handling properties and the growing demand coming from pharmaceutical researchers, agrochemical R&D, and companies scaling up heterocycle-based reactions.
The structure—anchored by a pyridine ring with isopropoxy and boronic acid pinacol ester groups—offers a mix of stability and reactivity. Genuine manufacturing stability means less batch-to-batch variation, which is a common pain point affecting downstream yields. Many customers have stories about generic boronic esters decomposing or forming sticky resinous byproducts, often coming down to poor synthesis control. At our facility, we stick to thoroughly dried glassware and inert atmospheres throughout synthetic and purification stages. Technicians route each step through proprietary in-line monitoring instead of relying solely on off-line sampling. With each kilogram, you can trace the process through a real audit trail.
The current model for 6-Isopropoxypyridine-3-boronic acid pinacol ester that leaves our facility is typically produced at 98% minimum assay by HPLC. Every batch receives full spectral confirmation through NMR, and purity evaluations always include checks for pinacol and pyridine-related side-products by GC-MS. We run particle size and bulk density measurements not for the sake of adding technical specs, but because we realized that these small factors make a difference in how the compound handles during weighing and transfer in walk-in fume hoods or glove boxes. Powder flow and reconstitution affect speed in high-throughput screening and milling steps.
Placing emphasis on analytical transparency keeps us honest about what leaves the reactor. In the main production stream, we avoid the classic issue of residual starting boronic acids, which can alter downstream coupling reactions. Any trace moisture is kept to a minimum by vacuum drying and storage with fresh desiccant, since pyridine-based compounds readily absorb water if left unprotected. When shipments leave, the labeling references the actual measured content and packaging lot, not a theoretical average or generic label.
The reality is that this boronic ester goes beyond the academic world—it has become an important building block in pharmaceutical intermediate synthesis, Suzuki–Miyaura cross-coupling, and combinatorial library development. In the early stages of drug discovery projects, medicinal chemists look for heterocycles that combine physical stability with distinct vectors for modification. The isopropoxypyridine motif allows functionalization at the 3-position, while the boron ester stands up well to both standard and microwave-assisted cross-coupling protocols.
Traditional boronic acids or esters often run into issues with air or water instability and limited shelf life. Years ago, we saw teams struggling with pinacol boronate esters hydrolyzing in storage, with unpredictable reactivity in the glove box environment. By refining overhead controls—tightening inert atmosphere policies and vacuum sealing methods—we tackle potential hydrolysis concerns head-on. Our compound remains workable over longer periods without generating byproduct residues that would gunk up filtration and workup steps.
Agrochemical companies are another strong group of users. The search for new crop protection actives often requires high-diversity parallel synthesis. Rapid coupling and scale-up depend on high-purity boronic esters that transfer reproducibly and stay free-flowing—otherwise, bottle-to-bottle clumping slows the assembly process. In our experience, changes in particle size and purity drive process interruptions and lost cycles, so we’ve tightened controls on powder homogeneity and moisture sensitivity. Both small gram- and multikilogram-scale processes benefit from these details, avoiding unnecessary reprocessing.
From time to time, customers ask why our product seems to give more reliable results in multistep reactions compared to generic stock offered by trading houses or less specialized supply chains. It boils down to hands-on production knowledge, and not just a rigid adherence to old protocols. Every operator on our synthesis floor knows how easily cross-contamination and minor procedural missteps can tank an entire run. We apply pre-weighed reagents, regularly calibrate filtration rigs, and track temperature profiles in real time.
While the pinacol esterification is a textbook reaction, the moment you increase batch scale or introduce automation, you run into side-reactions that only appear under non-lab conditions. Our process development chemists didn’t just lift methods from journals—we recreated syntheses at both pilot and production volumes, monitoring for minor byproducts and degradation spots that can slip past basic TLC or single-point HPLC.
For each lot destined for export or local distribution, we pull and archive sub-samples that get long-term stability checks. More than once, re-testing three months post-manufacture uncovered subtle decomposition patterns—bottle darkening, emergence of faint acidic odors, or powder clumping—that we could address by adjusting purification dryness and storage. Learning from these signals, we now regularly fine-tune our storage atmospheres based on batch-to-batch real world feedback instead of resting on literature conditions.
Among boronic esters available for cross-coupling, pyridine derivatives commonly appear in various substitution patterns—chloro, alkoxy, or amido substituents being just a few. The isopropoxy group in our compound lends steric and electronic protection to the pyridine ring, reducing the likelihood of unwanted side reactions at the ortho or meta positions. Other pyridine boronic esters, particularly methyl- or free-hydroxy analogs, don’t always offer the same balance between stability and synthetic flexibility.
Some suppliers push out quick-batch pyridine boronic esters by shortcutting drying steps and using basic filtration without final recrystallization. Customers receiving these batches describe off-odors, pink or orange hues, and rapid breakdown on exposure to the air in sample hoods. We approach every synthesis knowing that even a small shift in process water content will change boronate activity at the bench scale—chemists notice ruined spots in TLC plates or unacceptably low yields in their first run. Over time, we adjust our drying and purification so the powder maintains the pure, faintly off-white color that signals stability.
Another significant difference comes from packaging and transport. Many third-party and low-volume traders simply repack larger containers into smaller bottles, missing critical exposure control steps in the process. We use only freshly sealed, inert-gas-flushed containers at batch split-off, and every secondary container includes vacuum-sealed desiccant to absorb trace moisture. Instead of risking powder breakdown in warehouses, we control logistics end-to-end, integrating QA checkpoints on both temperature and humidity.
Handling sensitive materials in real-world production isn’t just about chemical performance—it’s also about operator safety and workflow reliability. Boronic esters pose risks when handled without proper ventilation and PPE, so our manufacturing protocols include regular air monitoring and worker training. Every year, we upgrade containment and fume extraction hardware based on operator input and tracked exposure events. We found that by keeping product granularity within a certain range, airborne dust is reduced, minimizing inhalation risks and lowering cleanup headaches.
Pure boronic esters sometimes emit faint, characteristic odors that signal purity—or, in the case of degradation, potential hazards. Getting to know that subtle difference requires hands-on familiarity; our shift supervisors regularly walk the lines, checking not only equipment calibration but also simple sensory cues like bottle feel or powder texture. We encourage chemists who receive our product to give feedback if they notice uncharacteristic powder characteristics on arrival, and we take that input seriously in quality meetings.
In our production site, past incidents with off-spec batches, or shipments delayed by customs or seasonal weather variations, shape every SOP revision. We transitioned to only a handful of trusted raw material vendors, run on-call support for troubleshooting, and regularly audit supply chain partners for packaging and transport reliability. The experience taught us that smooth production isn’t just a laboratory goal—it enables downstream chemists to cut troubleshooting, lower hazardous byproduct generation, and meet their own timelines.
Among the major production hurdles faced over the years, moisture sensitivity rates high. Despite textbook protocols emphasizing rapid workup and careful filtration, we found early on that air humidity creeps in during weighing, filtration, or packaging. The result: micro-impurities, visible clumping, or worse—hidden hydrolysis that produces unwanted acid or alcohol byproducts. Siting our facilities with specialized climate control, regularly checking ambient humidity, and inserting sealed glovebox stations between main synthesis and packaging areas got us ahead of this persistent problem.
Another challenge—a subtle one—comes from batch scale. Small research runs give excellent HPLC purity, yet ramping output for kilogram or tens-of-kilogram demand exposes temperature and mixing inconsistencies that classic flask reports gloss over. Engineers and production chemists wrangled for weeks with jacketed reactors and agitation adjustment, learning how solvent choice and order of reagent addition swing yields by several percentage points. Iterative small-pilot runs guided the establishment of breakpoints for optimal boronate formation, leading to a reliable, clean crystallization profile that scales predictably.
Waste management for organoboron compounds raises another practical question that both production teams and sustainability officers must deal with. The waste stream may contain non-trivial levels of organic boron, requiring carefully monitored collection and destruction. Our in-house protocol neutralizes boron residues in a multi-step process, separating organic and aqueous phases and sending boron-rich residues to certified disposal contractors. As a manufacturer with local and global compliance requirements, these steps are not optional—they protect our people, the environment, and our downstream partners who must audit their own traceability and disposal.
Another focus is analytics. Vendors downstream rely on accurate data to accurately dose, scale, and order. Rather than resting on catalog values, we run triplicate analyses with every product batch, archive chromatograms, and provide actual purity readings to clients. In the rare case of a spec deviation, we trace back every batch ingredient, run re-tests, and pull QA hold on affected packages until we’re satisfied with the remediation.
Industry feedback is direct and unambiguous. Missed delivery windows, unexpected powder behavior in coupling reactions, or questioned purity specs prompt immediate reconsideration of both process and logistics. We don’t see manufacturing as a static skill, but as a craft honed batch by batch, working alongside those who depend on reliable access to high-quality building blocks. Every synthesis run feeds back into our files; even small customer complaints on powder clumping, batch color, or shipment delays drive process tweaks. The view from the lab—catching those telltale shifts in powder feel or handling behavior—inform the decisions during scale-up and distribution.
Our approach isn’t just about turning out lots of product. It’s about delivering consistently high-quality 6-Isopropoxypyridine-3-boronic acid pinacol ester, learning from setbacks, and sharing the real-world impacts of process improvements. Over time, the biggest gains come from listening, observing, and revising—so that researchers, formulations scientists, and process chemists working at their benches spend less time troubleshooting and more time advancing their projects.
With every batch, we take pride not just in the molecule itself, but in the stories of efficiency, reliability, and creative chemistry it supports.