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HS Code |
774941 |
| Product Name | pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- |
| Molecular Formula | C11H15BClNO2 |
| Molecular Weight | 239.51 g/mol |
| Cas Number | 869301-40-8 |
| Appearance | White to off-white solid |
| Solubility | Soluble in common organic solvents such as DMSO and DMF |
| Smiles | CC1(C)OB(B2=NC=CC(Cl)=C2)OC1(C)C |
| Inchi | InChI=1S/C11H15BClNO2/c1-10(2)15-12(16-11(3,4)5)9-7-6-8(13)14-9/h6-7,10-11H,1-5H3 |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Synonyms | 2-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine |
| Pubchem Cid | 11582995 |
| Purity | Typically >97% (varies by supplier) |
As an accredited pyridine, 2-chloro-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 | The 5-gram quantity of **2-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine** is packaged in a tightly sealed amber glass vial. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- maximizes capacity, ensures secure, regulated chemical transport. |
| Shipping | **Shipping Description:** Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- should be shipped in tightly sealed containers, protected from moisture and light. It must be transported as a hazardous material, compliant with local, national, and international regulations. Proper labeling and accompanying safety documentation, including SDS, are mandatory to ensure safe handling and transit. |
| Storage | **Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-** should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon. Keep in a cool, dry, and well-ventilated area away from moisture, heat, and incompatible substances such as oxidizers and acids. Protect from light and store in a designated flammable materials cabinet. |
| Shelf Life | Shelf life of 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is typically 2 years when stored cool, dry, and sealed. |
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Purity 98%: Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Molecular weight 271.60 g/mol: Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with molecular weight 271.60 g/mol is applied in Suzuki-Miyaura cross-coupling reactions, where it enables precise stoichiometric control. Melting point 72–75°C: Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with a melting point of 72–75°C is used in organic electronic material synthesis, where it offers good processability during purification steps. Particle size <50 µm: Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- with particle size under 50 µm is utilized in fine chemical production, where it provides enhanced dissolution rates and homogeneous reactions. Stability temperature up to 110°C: Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- stable up to 110°C is employed in catalyst development processes, where it maintains structural integrity during thermal processing. |
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Producing pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- requires a close eye on every detail from raw material sourcing through final quality assurance. In the lab, chemists know this compound by its unique boronate structure bound to a chlorinated pyridine ring. All too often, a synthetic project runs into a wall with poorly controlled boron intermediates or variations in halogen placement—but our plant works to a different standard of reliability and precision. We have invested years of experience into scaling up this compound, and every batch demonstrates reproducible purity and consistent performance.
As demand for advanced boronic esters grows, we notice how chemists working in pharmaceuticals and materials science rely on stable, high-purity building blocks. Our R&D and manufacturing teams frequently discuss the intricate relationship between structure and reactivity for these pyridine-boronate derivatives. Experience has shown us: a subtle shift in crystallization temperatures, or a different grade of solvent, can lead to measurable differences in reactivity downstream. We find it essential to maintain full control at each step, especially during the Suzuki-Miyaura coupling applications where reliability drives success.
Through hands-on production, we know that off-the-shelf stock doesn’t always meet the realities of research or scale-up. We refine the product to offer a standard white to off-white crystalline solid, carefully dried and double checked for minimal moisture—since trace water can sabotage cross-coupling yields. Typical deliveries measure a minimum purity of 98%, but years of troubleshooting synthetic bottlenecks reveal the added advantage of lower residual pyridine or boronic acid impurities. Chemists relying on precise molar balances value this detail, as unwanted side products in the reagent bottle turn up easily in LC-MS chromatograms and downstream product profiles.
Our plant lab tests every lot for melting point consistency, NMR fingerprint, and boron content. Unlike many alternatives found in catalogues, we control both the steric hindrance at the boron center and the electronic character arising from the pyridine ring. This careful attention ensures the molecule accommodates both electron-rich and electron-poor partners during cross-coupling reactions.
Many chemical manufacturers chase commodity benchmarks, but our motivation stems from working directly with scientists facing new synthetic challenges. The 2-chloro substituent on the pyridine ring offers a unique combination: it slows certain side reactions yet maintains compatibility with a wide variety of palladium catalysts. Our experts have seen time and again how this balance speeds up medicinal chemistry programs and produces cleaner reaction profiles than similar bromo- or iodo-pyridine boronates.
One aspect that up-and-coming chemists appreciate is the stability offered by our 4,4,5,5-tetramethyl-1,3,2-dioxaborolane group. It resists hydrolysis in open air for extended handling on the bench, yet cleaves cleanly under the chosen reaction conditions. Each molecule, produced at our site, reflects hard experience in mitigating hydrolytic loss during drying and bottling. For process chemists who deal with larger volumes, that margin of stability saves on reprocessing and ensures consistent yield.
We have learned how scale matters for this product. Small flask chemistry in drug discovery—where each milligram counts—requires a highly pure and dry solid, since any undetected impurity or trace water can disrupt expensive catalyst cycles. During process optimization or tech transfer to pilot scale, the focus shifts towards ease of weighing, rapid dissolution, and minimized by-product formation. Over the years, our plant has gathered direct feedback from industrial partners showing that these subtle properties affect not just the final yield, but also the isolation and purification steps of target compounds.
Clients often compare our 2-chloro-3-boryl pyridine with other functionalized pyridine derivatives. The tetramethyl-dioxaborolane provides greater shelf life and less batch-to-batch variability than the pinacol boronate variants, which sometimes show variable solubility or instability on storage. We control crystal form and minimize surface moisture, avoiding the problematic caking or clumping that slows down big-batch dispensing. Unlike vendors who package product in unsuitable jars or with broad mesh particle sizes, we maintain logistics built on real-world lab usage.
Research chemists running parallel syntheses benefit from each bottle matching the last, regardless of order size or weather outside our plant. We have seen how even a small drift in NMR or IR spectrum over several months can confound method validation and force unnecessary troubleshooting. Pharmaceutical firms trust us because we put every batch through a final round of analytics, comparing against historical reference spectra and chromatograms logged in our plant’s quality archive. As a result, shipments to labs and pilot lines arrive ready for immediate use, no extra drying or purification required.
End-users frequently comment that our batches dissolve quickly and transfer easily, with no clumps stuck to spatulas. In one major customer’s automated weighing system, our product poured smoothly without causing loss of material due to bridging or static. Small details like this often make the difference between a completed synthesis and a wasted shift on the plant floor.
Medicine developers favor this building block for introducing boronic acid derivatives onto drug-like cores, particularly via Suzuki-Miyaura coupling with aromatic and heteroaromatic chlorides. Our direct customers, both academic and industrial, highlight its role in enabling SAR (structure–activity relationship) studies where robust cross-coupling is necessary for high-throughput analogue synthesis. The pyridine structure plays well in libraries aiming at kinase inhibitors, CNS drugs, and agrochemical candidates.
Beyond medicinal chemistry, we watch this molecule unlock access to advanced materials. Electronic and polymer researchers incorporate the boronate group in constructing complex frames, as the dioxaborolane handles humidity better than open boronic acids. Where previous generations of pyridine-based materials suffered from instability during device fabrication, our product’s tight manufacturing control reduces those headaches for our customer base. The ruggedness of our boronate protection strategy earns praise from groups making light-emitting materials, sensors, and photoactive layers.
Traceability remains a big concern in regulated industries. We document every batch from raw input onward, storing full synthesis, drying, and purification records. Our plant’s operators sign off all in-process steps and deviations, with sample retainment to allow independent verification months—even years—later. This level of transparency differs sharply from generic supply houses, where production often shifts between sites or is subcontracted. Consistent documentation enables our downstream clients to speed up regulatory submissions by including full traceability and quality attribution from the actual manufacturing source.
We ship each lot with full analytical data—NMR, HPLC, melting point, and impurity profile. Our standard operating procedures minimize unknowns; any deviation gets documented and, if needed, flagged for customer review before product leaves our facility. Feedback loops between our technical support staff and end-users drive continuous improvement: we have made formulation adjustments for customers needing higher bulk density for automated powder handling, or tighter control on trace halogens to avoid interference in sensitive downstream synthesis.
Scaling up 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-pyridine changes everything. Early in development, most small-batch makers could get away with hand-crystallizing product, but process chemists find reliability matters far more during multi-kilogram manufacturing. We long ago transitioned from lab glassware to jacketed steel reactors with closed-loop temperature control, freeing product from variable moisture uptake and ambient contamination. Using nitrogen-blanketed systems for every stage, from alkylation to quenching, preserves purity and stability.
Sourcing raw materials from audited suppliers adds to consistent output. Many procurement teams struggle with batch differences in cheaper alternatives. We analyze every incoming chloropyridine and boronic precursor, holding vendors to our own specification thresholds, and reject lots that could introduce unknown variance into the process. Our on-site team samples, tests, and records outcomes—catching issues early so clients never have to question the source or quality of what they receive.
Synthetic chemists with years of experience recognize the importance of reliable reagents in accelerating project timelines. We regularly consult with our customers to address specific concerns—whether about solubility in mixed solvent systems, tolerance of sensitive substituents, or compatibility with emerging catalyst platforms.
Feedback from users of our pyridine boronate has led us to tailor drying temperatures and adopt multi-stage vacuum purging. This reduces trace acetonitrile and toluene, common nuisances for analytical chemists working under tight impurity mandates. For large projects, we sometimes contract direct analytical support, running customized chromatography to document process-related contaminants, then working backward to minimize their formation.
In forming these bonds, our specialists know success relies not just on chemical structure, but also on unseen details from packaging to storage conditions. Research partners return for repeat shipments because they see no slow degradation or caking, even after long storage under fluctuating ambient conditions. Consistent particle size and moisture profile matter more once a synthesis moves from bench to pilot scale, and we build these lessons into our quality framework.
Long-term experience has taught us not to rely solely on published methods or standard data sheets. Each plant and each batch brings its own learning curve. We have experimented with rotary versus static drying, slow cooling crystallization for better shape retention, and different wash solvents to optimize for both purity and practical handling. Our on-site analytics run fingerprint spectra for every lot. Over the years, we have seen that even a small change in storage drum lining or filter paper can affect the final organoleptic and analytical results.
Direct reports from our pharma and materials partners show time saved troubleshooting side-product formation and post-reaction workup when using our pyridine boronate. One research group’s process improved overall yield by 5% when switching to our tightly specified dioxaborolane derivative. They reduced time lost tracking down ghost peaks in their HPLC runs, confirming that contaminant minimization at source saves both labor and precious material.
Expanding output of this advanced boronate means watching environmental controls closely. Our process uses closed systems to limit vapors and dust, and we direct spent solvents into on-site recovery rather than bulk waste. Years ago, a minor solvent leak in our pilot plant led to upgrades in vapor recovery and active monitoring of exhaust airflow. Safety culture grows out of near-misses like that; operators now run each step with continuous oversight and prompt secondary containment setups.
The boron content and functionalization profile of our molecules undergo regular assessment for ecological impact. We invest in green chemistry improvements when feasible—whether integrating more solvent recovery cycles or earmarking streams for catalyst recycling. By maintaining a tight handle on reaction exotherms and choosing less hazardous auxiliaries, our plant avoids common incidents seen in unregulated settings abroad.
We contribute to technical forums and maintain direct dialogues with academic labs pushing the boundaries of pyridine chemistry. Feedback from those breakthrough projects guides our tweaks to process control; for example, a minor adjustment in crystallization rate helped one collaborator boost their catalyst throughput and reduce post-coupling residue. Real-world problem solving shapes future product generations better than isolated R&D ever could.
In the expanding world of molecular design, reliable, well-characterized boronate intermediates remain essential for anyone bridging lab discovery and scalable chemical production. Our history of iterating manufacturing parameters in real time—based on exactly what the end user needs—stands in contrast to anonymous catalogue supplies. From a bench chemist filling a single flask to a process manager overseeing ton-scale product lines, our commitment to exactly what works in application shapes every jar and drum that leaves our facility.
With decades spent tuning process controls, catching problems before shipment, and refining tanker-to-flask logistics, our teams understand that subtle changes in product profile ripple through every customer operation. A single review of batch variability can save a pharma developer weeks of investigation. Our constant diagnostic testing, packaging audits, and regular communication with users lead to an unbroken feedback loop—every conversation a chance to improve, every lot benefitting from the last round of experience.
The field keeps evolving. Chemistry develops new methodologies, and materials projects ask for tighter, faster, and cleaner transformations. Pyridine, 2-chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- remains a key enabler not because of its name, but due to the years of practical experience and direct problem-solving behind each manufactured lot. Our boots-on-the-ground approach ensures every bottle fits the realities of modern research and development, supporting progress across the chemical sciences, one reliable shipment at a time.