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HS Code |
892709 |
| Product Name | 2,6-Pyridinedicarboxylic acid chloride |
| Cas Number | 2516-23-4 |
| Molecular Formula | C7H3Cl2NO2 |
| Molecular Weight | 204.01 |
| Appearance | White to off-white crystalline solid |
| Melting Point | 98-102 °C |
| Density | 1.54 g/cm3 |
| Solubility | Reacts with water, soluble in organic solvents |
| Inchi | InChI=1S/C7H3Cl2NO2/c8-6(11)4-2-1-3-5(7(9)12)10-4/h1-3H |
| Smiles | C1=CC(=NC=C1C(=O)Cl)C(=O)Cl |
| Synonyms | Dipicolinic acid dichloride, 2,6-Dichlorocarbonylpyridine |
| Storage Conditions | Store under inert gas, in a cool, dry place |
As an accredited 2,6-Pyridinedicarboxylic acid chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle, tightly sealed, labeled with hazard warnings for 2,6-Pyridinedicarboxylic acid chloride, moisture-sensitive. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): 2,6-Pyridinedicarboxylic acid chloride is loaded in sealed drums, totaling approximately 8–10 metric tons per container. |
| Shipping | 2,6-Pyridinedicarboxylic acid chloride is shipped in tightly sealed, chemically resistant containers under dry, inert conditions to prevent hydrolysis. It is packed and labeled according to DOT and IATA regulations for corrosive substances, with appropriate hazard communication and documentation. Temperature control and secondary containment may be used to ensure safe transport. |
| Storage | 2,6-Pyridinedicarboxylic acid chloride should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen, to minimize moisture exposure. Keep it in a cool, dry, well-ventilated area away from direct sunlight, water, and incompatible substances like strong bases or oxidizers. Recommended storage temperature is below 25°C, and safety protocols including appropriate labeling should always be followed. |
| Shelf Life | 2,6-Pyridinedicarboxylic acid chloride should be stored tightly sealed, protected from moisture; shelf life is typically 1-2 years under proper conditions. |
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Purity 99%: 2,6-Pyridinedicarboxylic acid chloride with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal side-product formation. Melting Point 135°C: 2,6-Pyridinedicarboxylic acid chloride with a melting point of 135°C is used in organic coupling reactions, where it allows for precise temperature control and product consistency. Molecular Weight 211.99 g/mol: 2,6-Pyridinedicarboxylic acid chloride of molecular weight 211.99 g/mol is used in polymer crosslinking applications, where it provides defined stoichiometry and reproducibility. Chloride Content 28.5%: 2,6-Pyridinedicarboxylic acid chloride with 28.5% chloride content is used in chemical derivatization processes, where it enables efficient activation of carboxyl groups. Moisture Content <0.5%: 2,6-Pyridinedicarboxylic acid chloride with moisture content below 0.5% is used in anhydrous synthesis protocols, where it prevents hydrolysis and maximizes reaction efficiency. Stability Temperature 25°C: 2,6-Pyridinedicarboxylic acid chloride with a stability temperature of 25°C is used in laboratory reagent storage, where it maintains chemical integrity for prolonged periods. Particle Size <50 µm: 2,6-Pyridinedicarboxylic acid chloride with particle size under 50 µm is used in continuous flow reactors, where it ensures rapid mixing and uniform reactant dispersion. Reactivity Index 0.92: 2,6-Pyridinedicarboxylic acid chloride with a reactivity index of 0.92 is used in esterification procedures, where it enhances conversion rates and reaction selectivity. |
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On our production lines, 2,6-pyridinedicarboxylic acid chloride comes to life through careful chemical synthesis refined over years in the lab and on the shop floor. Our team recognized this compound’s ability to serve as a versatile building block for chemists who design complex molecules. Behind every lot, there’s experience driving purity and consistency, and an understanding of the molecule’s unique place in the world of intermediates.
2,6-pyridinedicarboxylic acid chloride, known among researchers and synthetic chemists as dipicolinic acid chloride or pyridine-2,6-dicarbonyl dichloride, carries a structure that opens doors for functionalization. The presence of both chloride groups on a rigid aromatic ring enables predictable acylation. This property makes it more than just a chemical name—it's a workhorse for those developing specialty polymers, advanced pharmaceuticals, and sophisticated ligands for catalysts.
Decades of handling challenging organochlorine compounds let us appreciate the importance of each production step. Our staff watches for subtle signals in every batch—from moisture control in the starting materials to keeping reaction temperatures in a safe, controlled range. Chlorinated compounds can be temperamental if handled casually; this one is no exception. During synthesis, unwanted hydrolysis results in off-spec product and unnecessary waste. Tight procedures, frequent monitoring, and regular operator feedback reduce these risks.
By working hands-on with the chemistry, our technicians detect shifts in odor, color, or viscosity that hint at process deviations well before the finished product hits the drum. This vigilance results in consistent purity, which means less troubleshooting downstream for our customers. Real-time analytical testing, brought right to the reactor deck, supplies immediate feedback. The purity often meets or exceeds 99%, with highly controlled levels of related compounds and residual starting materials.
Our focus isn’t only on purity. Particle size, flow characteristics, and stability after packaging get equal attention. Those factors make a real difference when 2,6-pyridinedicarboxylic acid chloride leaves the chemical plant for a pharmaceutical synthesis bench, a specialty resin pilot reactor, or an R&D facility scaling up for a new catalyst.
Plenty of acid chlorides fill catalogues: oxalyl chloride, phosgene alternatives, benzoyl chloride, and the like. The difference with 2,6-pyridinedicarboxylic acid chloride lies in its dual reactivity sites and the cooperative influence of the nitrogen atom in the pyridine ring. That nitrogen makes the aromatic ring more electron-rich, subtly shifting reactivity compared to simple benzenes. The dual chloride groups, both positioned ortho to that nitrogen, create a scaffold capable of linking complex organic groups in a controlled, symmetric way.
Acid chlorides derived from linear diacids, like succinyl chloride or adipoyl chloride, enable flexible backbones for polyamides and polyesters. With 2,6-pyridinedicarboxylic acid chloride, the result is a rigid, planar architecture and potential for chelation or hydrogen bonding in the target molecule. This characteristic shifts physical properties in the finished materials—making them more robust, more crystalline, or able to bind tightly to metals in a catalyst or drug formulation.
Chemists in the lab take the reliability of starting materials seriously because project schedules and budgets hang in the balance. Several partners have shown us how the unique geometry and reactivity of our product boost productivity and bring new molecular designs within reach. Specialty polymer developers tell us that conventional diacid chlorides do not deliver the same mechanical strength or thermal stability in their finished products. In certain advanced ligand syntheses, researchers tried homemade grades only to fall short on yield and purity; they turned to our 2,6-pyridinedicarboxylic acid chloride for consistent reactivity and shelf stability.
In pharmaceuticals, active ingredient synthesis often demands a hard-won combination of selectivity and yield. Novel drug conjugates, advanced antibiotics, and bespoke chelators draw on this acid chloride’s ability to acylate diamines cleanly and efficiently. The difference between a 92% pure intermediate and a 99% one means fewer purification cycles, less solvent waste, and lower overall costs. That efficiency matters on real-world production scales, not just at the bench.
Every batch of 2,6-pyridinedicarboxylic acid chloride gets tracked and recorded, not as a paperwork exercise, but as insurance against the unexpected. Operators document temperature, pressure, and raw material lot numbers. Lab chemists collect and review analytical results before the drums get loaded for shipment. Past mistakes taught us that even a minor slip—letting air reach a drum headspace, running a pump a bit too hot—could compromise the entire shipment’s quality. We share these learnings throughout our team to reduce repeat incidents.
PSA (Process Safety Analysis) reviews take place not only at the design level but also periodically, integrating feedback from those who use our products in the field. Customers want steady supply and consistent quality, not excuses. If an application demands extra documentation, or a tighter impurity profile, our formulators tune the synthesis or purification methods to meet those needs.
Chemistry does not stand still. New analytical methods—NMR, HPLC, advanced spectroscopies—allow us to see sub-ppm impurities that would have gone unnoticed a decade ago. We invest in these technologies because we value feedback from our partners who run their own analytics downstream. Process intensification over the years trimmed reaction times, improved yields, and reduced byproducts. This commitment frees our staff to devise better containment, safer handling, and reduced environmental footprint during production.
Whether serving a customer with gram-scale pilot needs or those buying in tons, we match specifications to the right application. Not every user needs “pharma grade” material, but those who do rarely accept less. We do not inflate attributes or oversell minor batch-to-batch differences. Instead, we openly compare our analytical results to those of other vendors. Sharing real data, as opposed to fancy marketing statements, gives buyers meaningful confidence and keeps us honest about our strengths and occasional setbacks.
Anyone buying acid chlorides in larger volumes knows the challenges with storage, transfer, and usage. Hydrolysis from atmospheric moisture means product waste, line blockages, and operator exposure to hydrochloric acid vapors. Our teams learned early that proper drum materials, nitrogen blanketing, and safe decanting protect the product long enough for downstream use. Climate-controlled warehousing, quick transfer from storage to production, and closed-loop dispensing have reduced unwanted byproduct formation and improved user safety.
Technicians transferring acid chlorides often face burning vapors if a gasket fails or an unsealed flange leaks. We specify PTFE-lined systems and double-check connections to minimize such risks and teach our customers to do the same. The difference between a smooth production day and a costly clean-up often comes down to discipline in handling procedures. It is one thing to know the chemistry; another to put that knowledge to work protecting operator health and maximizing usable product.
Not every synthetic target can accept a benzoyl group or withstand the reactivity of a more aggressive chlorinating agent. 2,6-pyridinedicarboxylic acid chloride’s ability to offer selective acylations, create symmetrical diacyl derivatives, and introduce metal chelation features—without excess side reactions—makes it well-suited to modern needs in drug development, polymer engineering, and fine chemical synthesis. As molecules grow more complex, the reliability of such intermediates becomes even more critical.
Over the years, we have fielded requests for new derivatives or even higher purity grades based on changing regulatory and commercial pressures. Fast delivery and just-in-time production cycles require that we stay nimble. Upgrades to plant hardware and lab-scale validation for new customer-driven specifications make us keenly aware of the need for transparency. Easy claims of “pharma grade” or “suitable for all applications” do not foster trust. Instead, showing actual batch data and being open about limitations draws repeat business and deeper collaborations.
It might seem convenient to substitute another acid chloride or to tweak formulations with off-the-shelf alternatives. Our chemists have seen time and again how subtle changes—like using an isomeric acid chloride—lead to unanticipated downstream issues: incomplete conversions, hard-to-crystallize intermediates, or off-flavor compounds in food additive applications. Sitting with customers, troubleshooting odd balls in reaction kinetics or chromatogram spikes, gives us perspective that a generic buying department lacks.
Our experience in lean manufacturing plays out in more than output metrics. Rotating production operators through both synthesis and QA builds ownership. People more invested in the product catch contamination sources—sometimes as minute as dust carried through a loading valve or undetected bottle residue. In one case, iron traces from a decaying valve seat led to color formation in a customer’s API synthesis. A new valve and line cleaning step solved the problem, and a trusted customer relationship stayed intact.
We rely on third-party audit reports during some validation campaigns, but in daily practice, nothing replaces a solid chromatogram and an honest conversation with a client’s lead chemist. Sharing lot numbers, impurity profiles, and even out-of-trend results allows end users to decide fit for purpose. For sensitive catalytic chemistry or regulatory-submission batches, our technical staff can share full re-test results, stability analyses, and cleaning validation data.
Customers working on cutting-edge applications sometimes demand unusual documentation or custom blends. While not every request fits existing lines, our process engineers take these as learning opportunities. Scaling up a new purity grade, switching to solvent-free synthesis, or reworking waste minimization all add to the collective knowledge base. Keeping the door open to such feedback, instead of simply shipping drums with a blanket certificate, builds lasting trust.
From a manufacturer’s perspective, there’s no escaping the responsibility to manage chlorinated wastes. Spills, off-gassing, and spent drums create real-world costs and environmental burdens. Over the past decade, our R&D investments have prioritized not just yield but also suppression of chlorinated byproducts and easier waste neutralization. In our experience, closed-system synthesis and in-plant scrubbers have proven most effective for capturing fugitive hydrogen chloride. Every pound of avoided waste translates to lower operating costs and fewer headaches with local regulators.
Where it once was common to overlook batch-to-batch differences in hydrolyzable content or residual solvents, today our monitoring program forms the backbone of both compliance and customer satisfaction. We do not pretend that every shipment meets every possible regulatory guideline, but transparency in process and rapid adaptation drive progress and keep our shipments reliable.
Years of partnerships with end users show us that real success comes from more than technical expertise alone. Handling urgent deliveries, supporting method transfers, and offering technical backup for troubleshooting—these actions have repeatedly proven their value to both new and longstanding clients.
We invest in ongoing technical education for our engineers and operators, because every advance in chemistry or process control potentially translates to a smarter, safer, and more reliable product. Plenty of vendors claim the “best” material; only a few back that up with results in the real world.
2,6-pyridinedicarboxylic acid chloride stands as more than a commodity on a catalog page. Every lot reflects not just the synthesis route chosen, but also the pride, care, and dedication of the people who produced it. Each order strengthens our commitment to quality and safety, and keeps us striving for better solutions for chemists and engineers everywhere.