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HS Code |
962848 |
| Chemical Name | 2-Methylpyridine-3-boronic acid HCl salt |
| Molecular Formula | C6H9BClNO2 |
| Molecular Weight | 173.41 g/mol |
| Cas Number | 1436548-13-6 |
| Appearance | White to off-white powder |
| Purity | Typically ≥98% |
| Solubility | Soluble in water and polar organic solvents |
| Storage Temperature | 2-8°C (Refrigerated) |
| Synonyms | 2-Methyl-3-pyridineboronic acid hydrochloride |
| Mdl Number | MFCD28343681 |
| Inchi Key | CYKPVVJLBGNSCN-UHFFFAOYSA-N |
| Smiles | B(C1=CN=CC=C1C)(O)O.Cl |
As an accredited 2-Methylpyridine-3-boronic acid HCl salt 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-Methylpyridine-3-boronic acid HCl salt is sealed in a labeled amber glass bottle with tamper-evident cap. |
| Container Loading (20′ FCL) | Container loading (20′ FCL): Securely packs 2-Methylpyridine-3-boronic acid HCl salt, using moisture-proof, sealed drums or bags, maximizing container space. |
| Shipping | 2-Methylpyridine-3-boronic acid HCl salt is shipped in tightly sealed, chemically resistant containers. It is transported under cool, dry conditions and clearly labeled as a research chemical. Proper documentation accompanies the shipment, and all handling follows relevant safety, regulatory, and hazardous material guidelines to ensure safe delivery. |
| Storage | Store 2-Methylpyridine-3-boronic acid HCl salt in a tightly sealed container, protected from moisture and light, ideally in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong bases and oxidizers. Ensure appropriate labeling and follow standard safety protocols for handling and storage of chemical reagents. Avoid prolonged exposure to air to prevent degradation. |
| Shelf Life | **Shelf Life:** Store 2-Methylpyridine-3-boronic acid HCl salt in a cool, dry place; stable for at least 2 years if unopened. |
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Purity 98%: 2-Methylpyridine-3-boronic acid HCl salt with 98% purity is used in Suzuki-Miyaura cross-coupling reactions, where it ensures high reaction yield and product selectivity. Molecular Weight 172.44 g/mol: 2-Methylpyridine-3-boronic acid HCl salt with a molecular weight of 172.44 g/mol is used in pharmaceutical intermediate synthesis, where it facilitates accurate stoichiometric calculations for scalable reactions. Melting Point 228°C: 2-Methylpyridine-3-boronic acid HCl salt with a melting point of 228°C is used in high-temperature organic synthesis, where it maintains structural integrity and consistent reactivity. Particle Size <50 microns: 2-Methylpyridine-3-boronic acid HCl salt with particle size less than 50 microns is used in automated solid-phase synthesis, where it allows for uniform dispersion and optimal mixing efficiency. Stability Temperature up to 150°C: 2-Methylpyridine-3-boronic acid HCl salt stable up to 150°C is used in thermal processing applications, where it resists decomposition and supports process reproducibility. Water Solubility 10 mg/mL: 2-Methylpyridine-3-boronic acid HCl salt with a water solubility of 10 mg/mL is used in aqueous-phase bioconjugation, where it enhances reagent accessibility and reaction kinetics. UV Absorbance (λmax 260 nm): 2-Methylpyridine-3-boronic acid HCl salt exhibiting UV absorbance at λmax 260 nm is used in purity verification via HPLC, where it enables precise detection and quantification. |
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In the world of pyridine derivatives, 2-Methylpyridine-3-boronic acid HCl salt stands out for its clean conversion and utility in synthesis. In the plant, our workers see demand from companies looking to build complex molecules, especially when exploring cross-coupling reactions. The model we bring to the market has been developed through years of incremental improvements, driven by real feedback from research laboratories and process chemists. With each batch, consistency and low moisture content top the list of what matters for people buying this material.
Every shipment of 2-Methylpyridine-3-boronic acid HCl salt needs careful attention—not just in what comes out of the reactor, but in the choice of raw materials, handling of exothermic steps, and time spent controlling crystal formation. Operators here know that the hydrochloride salt form handles better than the free acid. In the ordinary lab environment, the HCl salt pours with less caking, dissolves more predictably, and shelves get less sticky over time. The choice of hydrochloride, over other counterions or the neutral compound, reflects more than just tradition; it comes from years of chemists demanding less variability in solubility and stability.
People often ask about the specifications beyond the pure chemical formula. For us, it’s about bringing total organic purity well into the high ninety-percent levels—typical batches pass 98% through HPLC with tight controls on trace metal content. We control for water content using Karl Fischer titration, and as a manufacturer, the data actually matters. High water content makes scale-up unpredictable and storage unfavorable, so each step in drying happens under vacuum lines designed specifically for products of this family.
Batch-to-batch reproducibility matters more than simple purity—whether a customer is making grams for a small structure-activity-relationship study, or running multi-kilo campaigns for a pharmaceutical candidate, they notice when the solid flows differently, absorbs air, or dissolves unevenly. Product intended for Suzuki cross-coupling needs careful control of residual solvents, so the analytical team checks for traces of DMF, THF, and lower-aliphatic alcohols.
2-Methylpyridine-3-boronic acid HCl salt’s main appeal comes from its role in C–C bond formation, particularly in Suzuki-Miyaura reactions. In practice, it allows the attachment of the methylpyridyl unit onto aryl and heteroaryl groups with low byproduct formation. Customers who know their chemistry value fast dissolving and robust yields, without investing extra time optimizing the step for different salt forms.
We have seen small biotech companies and large pharmaceutical firms use it as a building block in kinase inhibitor research, where methylpyridine motifs tune pharmacokinetic properties. Academic groups show up with requests tied to new ligand or catalyst development, since the boronic acid functionality matches well with emerging cross-coupling strategies using different transition metals. Recently, materials science groups showed us new uses in interface chemistry and functional polymer development. In those labs, yield is not the only concern—repeatability and shelf stability share equal importance.
Technical teams used to spend time comparing the free acid and salt forms of many boronic acids. The hydrochloride salt form of 2-Methylpyridine-3-boronic acid delivers tangible workflow improvements: less hygroscopic behavior, smoother solubilization, and more predictable boron availability. These features reduce guesswork in both parallel synthesis and continuous flow processes, translating into fewer failed reactions and more reliable transfer to pilot scale.
The choice of HCl brings logistical benefits. In the warehouse, packs stay free from clumping and open easily, reducing losses to partial containers gone bad. In the reactor bay, time savings add up as operators measure true mass without accounting for chemical water gains or caked portions. People rarely talk about these practical headaches, even though they add real cost to project timelines.
During synthesis, impurities like homoboronic esters and starting halides need careful removal through crystallization and liquid-liquid extraction steps. These challenges stretch far beyond analytical specification sheets. We took lessons from output variability to upgrade our crystallizers and reengineer solvent systems that keep product out of troublesome polymorphic forms. Part of our daily work involves sample testing from different lines and geographies, making sure a customer in North America and another in East Asia receive identically behaving product, regardless of seasonal climate shifts or upstream supply issues from pyridine sources.
Inside the production building, 2-Methylpyridine-3-boronic acid HCl salt is kept in tightly sealed, inert-lined drums. Frequent checks ensure that temperature does not exceed the narrow bands where boronic acids begin to change. Every technician knows that once water sees the salt form, it can trigger partial decomposition over extended periods, so we stress quick re-packaging and controlled humidity.
Our operations staff use blinding powder handling protocols because of the product’s potential dusting. Site management couples this with up-to-date documentation and batch tracking, so each lot carries a full record from boronic acid formation through acidification, drying, QC, and dispatch.
Companies working with free boronic acids or ester derivatives have told us about issues with reaction reliability and shelf life. Boronic esters may have easier handling but cost extra steps to convert and carry added risk of hydrolysis during workup. The HCl salt strikes a balance—ready reactivity, easier storage, and predictable mass transfer. The product avoids the need to pre-activate or add extra bases, because hydrochloride leaves no basic counterions behind to complicate downstream chemistry.
Technical buyers often compare our material against both ester- and acid-forms from competitors. Many note a drop in side-reactions or off-spec material with our salt, which simplifies process troubleshooting. Others point out lower air and moisture sensitivity, making the product a good fit for high-throughput screening campaigns where dozens or hundreds of parallel reactions might otherwise suffer batch-to-batch deviation with less stable alternatives.
Process validation teams, especially in pharma, want clarity on raw material provenance and control. We equipped our operations with barcoded lots, full COA tracking, and real-time environmental monitoring at storage sites. Customers now expect to see full traceability right back to base pyridine vendors. Sometimes we work under confidentiality with new synthetic routes, but the core message remains—we built these protocols because one failed audit years ago led to days of lost production.
Regulators also call for limits on impurities such as arsenic, lead, and residual organics below thresholds. We invest in new screening tools for elemental impurities, and operate GC-MS analysis on each batch. These steps mean every drum carries clear data, supporting pharmaceutical filings globally. The team here cross-trains on current regulatory guidelines for emerging markets so nothing goes missed in shipments headed for clinical, commercial, or animal health applications.
Over the last decade, we saw requests increase from CROs and CDMOs who want fast turnaround and supply flexibility. Some companies only need small research packs, while others request kilogram or larger quantities on short notice. Our operations team designed packaging that works for both—vacuum sealed, with optional argon sparging, and lots divided for easy split-batch analysis. This work meets more than a logistical hurdle; it helps research teams keep costs down by not overordering or wasting on stale product.
As newer reaction technologies like microreactors or continuous flow platforms become common, customers rely on materials with guaranteed solubility and flow properties. Our technical group, who have real carpet-time in both small and large plants, gives feedback to the production floor about slight tweaks in bulk density and particle size distribution, based on process demands from peptide synthesis to agrochemical pilot lines.
Our R&D lab keeps tabs on new literature reports using 2-Methylpyridine-3-boronic acid derivatives in energy materials, catalysts, diagnostics, and ligands for asymmetric synthesis. Many researchers mention that off-the-shelf availability of the HCl salt speeds up early-stage development because it removes long delays caused by custom synthesis of rare building blocks. For many experimental trials, chemists need enough reproducibility to run three or four parallel routes—having a known product lets them focus attention on process variables instead of patching inconsistent raw materials.
We also make technical support available to teams scaling from bench to kilogram quantities. Many customers write in with feedback about reaction optimization, and we pass that information upstream to adjust handling guides, or labelling on container usage so that field teams aren’t surprised by stability limitations or sudden clumping in humid environments.
Industry disruptions ripple fast—whether from upstream supply chain volatility in basics like pyridine or global transport slowdowns. Local reserves of 2-Methylpyridine-3-boronic acid HCl salt buffer against these shocks, but true continuity rests on deep supplier partnerships and redundant manufacturing lines. Our experience through past disruptions led us to invest in flexible plant infrastructure, building inventory management closer to customers’ needs rather than relying on “just-in-time” deliveries prone to failure in a crisis.
We also work with alternate suppliers for critical reagents after witnessing price spikes and outages. Quality benchmarking and real-life process simulation on each raw material confirms that switching doesn’t affect the analytical signature or downstream use of the final product.
Regular conversations with customers gave us insights beyond technical data. One major issue people face comes from materials that age poorly—reactivity degradation, batch separation, or impurity growth happens over months if storage is not right. After collaborating directly with clients, we modified our containers and added silica-pouch moisture guards to every drum. We now encourage users to break up larger shipments into smaller operational packs if their site suffers frequent temperature swings.
People also report process blockages from micro-impurities that never appear on a generic certificate but impact catalyst cycles or biological assays. In response, our QA incorporates higher-resolution LC-MS and GC analysis on outgoing lots, capturing these details years ahead of some industry norms.
Despite best efforts, unanticipated challenges surface in client workflows. Some labs find local water contamination, affecting reproducibility. Our team supports those clients by reviewing sampling techniques and even sending out technical advisors to set up environmental monitoring for their storage areas. In cases where solubility surprises arise, we adjust batch physicals to keep dissolution curves within process norms.
Transport damage and customs delays remain tough. To address this, we now vacuum-pack shipments and stack them with dampening inserts inside drums, extending useable shelf life even when external shipping times jump unexpectedly.
From our vantage point at the interface of chemical engineering and end-use application, product improvement remains an everyday pursuit. Advancements in crystallization technique, tighter moisture controls in warehouse practice, and constant feedback from live process campaigns shape quality gains. Each new synthesis route informed by literature, each piece of feedback on handling quirks, is tested in our full-scale plant environment before batch scale-up.
We encourage customers to challenge our specs—it’s those tough questions that led us to accelerate impurity analysis protocols and branch into alternative packaging designs. In this field, where a failed reaction or shipment bottleneck can set back developments for months, transparency and solution-driven adaptation bring the most value—not just incremental changes in a datasheet, but meaningful enhancements in how chemists access and use core building blocks like 2-Methylpyridine-3-boronic acid HCl salt.
We see companies testing boronic esters and other salt forms for similar transformations. Boronic esters often bring easier handling at the expense of additional deprotection steps and inconsistent solubility, especially under certain reaction conditions. Some specialized salts show promise in niche reactions, but lack broad applicability or proven track records for scale-up concerning storage and handling.
Many of our customers confirm that alternative forms often underperform when throughput or reactivity under widely varying conditions stands as the priority. No single intermediate suits every need, and choosing the most robust building block requires feedback loops between manufacturer and end-user—a dialogue we foster through active technical support and routine process audits.
Ultimately, it’s not just the analytic profile, but the consistency, shelf life, and ease-of-use that builds confidence batch after batch. 2-Methylpyridine-3-boronic acid HCl salt, as manufactured with our practices, delivers these qualities daily to R&D and manufacturing scientists pushing boundaries in pharmaceuticals, materials, and advanced applications.