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HS Code |
735871 |
| Product Name | 2-Chloro-5-fluoropyridine-4-boronic acid |
| Cas Number | 330792-87-9 |
| Molecular Formula | C5H4BClFNO2 |
| Molecular Weight | 174.36 g/mol |
| Appearance | White to off-white solid |
| Melting Point | Approximately 169-174°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in DMSO and methanol |
| Smiles | B(C1=CC(=NC(=C1)Cl)F)(O)O |
| Inchi Key | CSJSAGRJHBWRCI-UHFFFAOYSA-N |
As an accredited 2-Chloro-5-fluoropyridine-4-boronic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in a 5g amber glass vial, tightly sealed with PTFE-lined cap, labeled with product details, hazard information, and CAS number. |
| Container Loading (20′ FCL) | 20′ FCL: Typically loaded in 25kg fiber drums, lined with plastic, total 8–10 metric tons safely per container. |
| Shipping | 2-Chloro-5-fluoropyridine-4-boronic acid is shipped in tightly sealed containers, protected from moisture and light. Standard shipping includes appropriate labeling for hazardous chemicals, ensuring compliance with regulatory requirements. Transport occurs via approved carriers, with documentation provided for safe handling and storage. Temperature control may be recommended to maintain product integrity during transit. |
| Storage | 2-Chloro-5-fluoropyridine-4-boronic acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated). Store away from incompatible substances such as strong oxidizers and acids. Proper labeling and safe handling procedures are essential to prevent contamination and degradation. |
| Shelf Life | 2-Chloro-5-fluoropyridine-4-boronic acid typically has a shelf life of 2 years when stored cool, dry, and protected from light. |
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Purity 98%: 2-Chloro-5-fluoropyridine-4-boronic acid with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures increased yield of target active compounds. Melting Point 180-184°C: 2-Chloro-5-fluoropyridine-4-boronic acid with a melting point of 180-184°C is used in Suzuki coupling reactions, where stable thermal properties enhance process reliability. Low Moisture Content <0.5%: 2-Chloro-5-fluoropyridine-4-boronic acid with low moisture content of less than 0.5% is used in electronic materials production, where minimized hydrolysis risk improves product stability. Particle Size D90 <50 µm: 2-Chloro-5-fluoropyridine-4-boronic acid with particle size D90 less than 50 µm is used in formulation of catalytic systems, where fine dispersion increases surface reactivity. Stability Temperature up to 120°C: 2-Chloro-5-fluoropyridine-4-boronic acid with stability temperature up to 120°C is used in high-throughput screening, where chemical integrity under process heat is maintained. Assay ≥99%: 2-Chloro-5-fluoropyridine-4-boronic acid with an assay of at least 99% is used in agrochemical compound development, where high analytical purity results in consistent formulation outcomes. |
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Our team has spent years perfecting the manufacturing of specialty pyridine derivatives, with 2-Chloro-5-fluoropyridine-4-boronic acid drawing more requests from chemists each year. Chemists and process engineers in both active pharmaceutical ingredient (API) research and advanced materials segments look closely at this compound due to the unique boronic acid moiety combined with the electron-withdrawing chloro and fluoro substituents on the pyridine ring. This combination makes it a strong asset in Suzuki-Miyaura cross-coupling, allowing for efficient creation of complex, highly functionalized molecules that would otherwise require lengthy multi-step synthetic routes.
In real-world plant operations, reliable access to this compound supports tight project timelines. Its structural features, especially the placement of the boro group at the 4-position and substituents at the 2 and 5 positions, help direct reactivity. The specific connectivity gives greater control over selectivity, which impacts downstream purity and yield—a concern nobody in process scale-up can ignore. By working hands-on with this molecule, our chemists notice how it reacts more predictably than close relatives missing one of the halogen atoms, reducing unwanted side reactions and helping to keep batch reproducibility within tighter margins.
Producing 2-Chloro-5-fluoropyridine-4-boronic acid requires a balance between stringent moisture controls and scrupulous purification steps. Consistent handling of the boronic acid functionality is especially important. Boronic acids sometimes show tendency toward hydrolysis or formation of cycles such as boroxines if ignored, leading to variable loading performance in automated synthesizers or reactors. Our methodology, refined by direct technical feedback from customers, leans on precise isolation—crucial for kilo-lab and pilot scale users looking to minimize variability at every transfer point.
Through our own trials, we’ve watched this material hold up over time when stored in tightly sealed containers, free of direct humidity. Dehydration and batch-to-batch differences can cause headaches (for example, if a lot partially converts to a boroxine form), so we adopt incremental drying rather than blast heating, which risks altering the final crystalline form. By measuring and adjusting moisture down to the percentage point, we’ve pushed our product’s reliability even on long projects that open drums repeatedly for weighing and sub-sampling.
For scientists and engineers mapping out a route for a new small molecule, reproducibility and purity demand equal attention. Our current process version for 2-Chloro-5-fluoropyridine-4-boronic acid targets a purity level of at least 98 percent by HPLC, but even more stringent grades are available for certain pharmaceutical or electronic applications that cannot tolerate trace organics or metal residues. We track both the boronic acid content and potential halide impurities after each synthesis run. Downstream transformations, particularly palladium-catalyzed couplings, become much less troublesome when the starting acids carry no more than 0.1 percent unknown impurities, a target rooted in direct experience on the plant floor.
As the original producer, we keep a closed eye on aspects often missed by third-party resellers: not only on regulated contaminants, but also seed crystal size, dryness, and flowability through automated feeders. Factories moving into scale-up have strict deadlines and fine-tuned processes, so even minor shifts in material properties can delay entire production campaigns and cost many days in lost productivity. Carefully managing granule size helps avoid clogs in feeding lines, a critical but understated factor if you’ve ever stood next to a stuck feeder at 2 a.m. and watched a project’s timeline slip away. Our direct feedback loop from production to R&D speeds up identification of tiny, batch-dependent anomalies and lets us rapidly solve them at the plant level before product ships.
Pyridine boronic acids come in many variations, but few offer the balanced reactivity found with both chloro and fluoro substituents. The presence of fluorine at the 5-position and chlorine at the 2-position makes a fundamental difference in both electronic and steric environment at the reactive 4-boronic acid site. In practice, we see that the dual halogen arrangement deters overreaction and side-processes better than mono-halogenated counterparts. For chemists seeking to maintain selectivity under challenging conditions—like those in high-throughput medicinal chemistry or late-stage functionalization—this translates into crisper, higher yielding transitions.
Other pyridine boronic acids, such as 2-chloro-4-pyridineboronic acid or 5-fluoro-pyridine-4-boronic acid, typically bring increased reactivity on one face of the ring or increased sensitivity to hydrolysis. Run side-by-side in traditional Suzuki reactions, our compound provides more controlled conversion, fewer unidentified by-products, and noticeably easier work-up. This has been observed repeatedly in pharmaceutical screens and OLED precursor routines, where time and isolation efficiency add up fast.
Across many years and thousands of kilograms of this material shipped, we have seen research teams wrestle with synthetic bottlenecks, especially in high-stakes environments like drug discovery and specialty pigment development. 2-Chloro-5-fluoropyridine-4-boronic acid finds most application as a coupling partner for attaching heteroaromatic groups under mild conditions. Interest from R&D labs and larger volume plants continues rising as regulatory agencies push for cleaner, more step-efficient processes with reduced waste profiles. Each gram of material that couples cleanly can shave days off a project timeline and lessen the environmental impact of purification.
Electronic materials manufacturers lean toward this boronic acid because its purity, consistent melting range, and defined morphology influence the optoelectronic performance and stability of finished devices. Slight differences in lot-to-lot profiles—variation in trace halogen content, micro-trace metals, or even crystal habit—may alter product reliability after assembly. Through our plant’s close coordination with QC specialists, we limit these factors at the root, not just in selective downstream purifications. We offer custom packaging and conditioning for particularly sensitive customers, all based on practical insights from seeing what works well at bench and at multi-tonne scale.
Some molecules walk a narrow line between reactivity and stability; this compound keeps a tight balance, letting chemists scale up or down without the surprise losses or sluggish reactions that plague more capricious reagents. Production teams in pharma outsourcing, agrochemical R&D, and materials science prefer materials that store well on the shelf, handle without fuss, and react consistently—even after multiple transfers in a busy lab.
By listening directly to partners who tested our batches under different temperature, humidity, and inert gas conditions, we have fine-tuned the product’s particle size and water content to a level where even automated dispensing systems in large synthesis suites run smoothly. Customers sometimes share feedback on point-of-use clumping or changes in apparent color, and our development team makes real process adjustments in response. The benefit of handling not only manufacturing but also the troubleshooting phase means we get to the cause of any challenge right away.
Transitioning from research batch sizes to commercial scale puts upward pressure on consistency and reliability. Early experiments with gram quantities rarely show all the stress points that emerge during kilo or tonne-scale campaigns. As manufacturers, we don’t just ship from a spec sheet—we run our own validation reactions, testing each batch’s performance in Suzuki coupling and monitoring for by-product formation and conversion rates. These in-house runs demonstrate that even a half-percent shift in impurity level affects final yield and purification effort. We keep analytical charts on conversion profiles so project chemists or scale-up teams have direct, actionable data, not just certificates.
Many researchers also look for flexibility in the form of the product—some prefer fine crystalline powder for rapid dissolution, others a more granular material for easier handling in glove boxes or automated loading. We supply both, noting feedback from client labs and pilot suites using different types of glassware, screw-top vials, or high-throughput reactors. Having the manufacturer ready to customize—rather than relying on bulk, undifferentiated stocks—reduces the risk of downstream integration issues.
Making reliable 2-Chloro-5-fluoropyridine-4-boronic acid takes more than technical steps. As global regulations on hazardous substances and sustainable manufacturing grow stricter, the way substances like this are produced and documented comes under scrutiny. Regulatory inspectors have grown more familiar with boronic acids, especially in pharmaceutical and electronic supply chains. They dig into lot traceability, environmental fate, and even documentation around supplier control.
We have steadily refined our closed manufacturing processes to minimize organic solvent use, adopt more benign work-up agents, and ensure full traceability from starting materials to packaging. We keep comprehensive, real-time batch records and provide impurity profiles verified by independent labs. By acting as both manufacturer and quality steward, we take responsibility at each step, improving transparency for all downstream users.
It isn’t just about meeting minimum standards, either. Partnering with sustainable upstream suppliers—those using responsible fluorine and chlorinated building blocks—lets us offer customers better information to report in their own environmental, social, and governance (ESG) statements. Material that runs clean on paper must also deliver in the real world—our QC team runs stability assays to map shelf life under actual storage, then updates technical data accordingly.
Any manufacturer handling pyridine boronic acids will encounter the same core challenge: prevent trace decomposition and moisture uptake, maintain structural integrity across each shipping and storage event, and hit a moving target of customer requirements for form, purity, and packaging. In our experience, success comes from running material through full simulation cycles—from plant reactor to lab bench to supply chain warehouse—and continually learning from surprises big and small.
Over the years, we developed handling protocols not because regulations demanded it, but from hard lessons with pilot plant off-spec events or warehouse shelf failures. The quickest way to lose a customer’s trust is repeated batch-to-batch drift. Each problem—be it content degradation, container contamination, or unpredictable batch flow—leads our operations and R&D to adopt new quality gates. Even with years of practice, change remains part of the routine; chemists scale up processes, run new couplings, or move to automated dispensing, and every new request sparks further process optimization.
Demand for advanced synthetic intermediates continues to rise, especially where innovation in pharma, agriculture, and electronics requires ever finer control over structural complexity. As a chemical manufacturer, we do more than replicate last year’s processes: we invest steadily in analytic upgrades, more refined batch tracking, and logistics coordination. Key to this progress are regular technical exchanges with downstream users, who often share direct reaction data, isolating hard-to-spot impurities or reporting subtle batch features visible only in scaled protocols.
Moving forward, our goal stays focused on marrying reliable, high-purity product with solutions to real-life handling and application challenges—from the shipping dock through to the scientist running final couplings in the lab. Every time a batch of 2-Chloro-5-fluoropyridine-4-boronic acid ships, it represents more than a chemical lot—it stands as evidence of persistent adaptation, knowledge gained by practical observation, and the drive to make each customer’s project more successful, smooth, and ultimately productive.