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HS Code |
858162 |
| Chemical Name | 2,6-Pyridinedicarbonyl dichloride |
| Molecular Formula | C7H3Cl2NO2 |
| Molecular Weight | 204.01 g/mol |
| Cas Number | 6615-38-1 |
| Appearance | White to pale yellow crystalline solid |
| Melting Point | 124-127 °C |
| Boiling Point | 344.1 °C at 760 mmHg |
| Density | 1.427 g/cm3 |
| Solubility | Hydrolyzes in water; soluble in organic solvents such as dichloromethane |
| Refractive Index | 1.603 |
| Synonyms | 2,6-Pyridinedicarbonyl chloride; Dipicolinoyl chloride |
| Smiles | C1=CC(=NC(=C1)C(=O)Cl)C(=O)Cl |
As an accredited 2,6-Pyridinedicarbonyl dichloride 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 "2,6-Pyridinedicarbonyl dichloride," with hazard symbols and safety instructions. |
| Container Loading (20′ FCL) | 20′ FCL: 12 metric tons, packed in 25 kg fiber drums, loaded on pallets to maximize stability and minimize spillage. |
| Shipping | **2,6-Pyridinedicarbonyl dichloride** should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transportation must comply with regulations for hazardous chemicals, using appropriate labeling and documentation. It should be handled by trained personnel, ensuring temperature control and minimizing exposure to water, acids, and bases during transit. |
| Storage | 2,6-Pyridinedicarbonyl dichloride should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, to prevent hydrolysis. Keep it in a cool, well-ventilated area away from moisture, heat sources, and incompatible materials such as strong bases or oxidizers. Store it in a designated corrosive chemical cabinet and clearly label the container. |
| Shelf Life | 2,6-Pyridinedicarbonyl dichloride typically has a shelf life of 2 years when stored tightly sealed in a cool, dry place. |
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Purity 98%: 2,6-Pyridinedicarbonyl dichloride with purity 98% is used in pharmaceutical intermediate synthesis, where it enables high yield of target heterocyclic compounds. Molecular Weight 204.97 g/mol: 2,6-Pyridinedicarbonyl dichloride with molecular weight 204.97 g/mol is used in agrochemical research, where it ensures precise stoichiometry for consistent reaction outcomes. Melting Point 71-73°C: 2,6-Pyridinedicarbonyl dichloride with melting point 71-73°C is used in organic synthesis, where controlled melting is crucial for efficient solid-phase reactions. Particle Size <40 µm: 2,6-Pyridinedicarbonyl dichloride with particle size less than 40 µm is used in advanced material fabrication, where enhanced surface area accelerates reaction kinetics. Stability Temperature Up To 120°C: 2,6-Pyridinedicarbonyl dichloride stable up to 120°C is used in polymer manufacturing, where elevated temperature resistance maintains product integrity during processing. Hydrolytic Sensitivity: 2,6-Pyridinedicarbonyl dichloride with high hydrolytic sensitivity is used in acylation reactions, where rapid reactivity increases overall synthesis efficiency. Reactivity with Amines: 2,6-Pyridinedicarbonyl dichloride with demonstrated reactivity towards amines is used in peptide coupling, where efficient amide bond formation is required for sequence accuracy. Colorless Crystalline Form: 2,6-Pyridinedicarbonyl dichloride in colorless crystalline form is used in analytical chemistry applications, where high purity and visibility support reliable quantification and quality control. |
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In the world of fine chemicals, choosing the right reagents makes all the difference. 2,6-Pyridinedicarbonyl dichloride, also recognized in labs and factories as 2,6-Pyridine dicarboxylic acid dichloride, has become a familiar sight in my own production schedule and across the shop floors of many chemical plants. The compound’s CAS number, 4023-34-1, appears often on packing slips bound for both domestic and export customers. Here, I want to share a ground-level perspective, drawn from hands-on manufacturing experience, about why this chlorinating agent keeps finding more work and more fans with each passing year.
The chemical might appear as a white or off-white crystalline solid in its packaged form, but the real value comes in how it performs during synthesis. Stable under ordinary storage, the material travels well and stands up to typical seasonal swings in warehouse environments without turning lumpy or off-color. Each monthly batch is checked for purity by in-house HPLC and titration, since even a slight deviation can throw downstream reactions off course. In practice, we supply a purity north of 99% and pack in tight-sealing HDPE drums sized for practical use in development labs or for larger-scale operation.
Across my career, I have rarely seen a more versatile diacid chloride for the synthesis of organics, particularly as an intermediate for specialty polymers, agrochemicals, and bespoke pharmaceutical structures. The two acyl chloride groups attached to the nitrogen-bearing pyridine ring open the door for an entire world of selective reactivity. Peptide coupling, acylation, and the modification of heterocyclic frameworks seem to reliably succeed where simpler or more volatile reagents would threaten a runaway reaction or unwanted byproducts. Our technical support teams frequently field questions about side product formation, but with this reagent, we see a very clean transformation under standard lab procedures.
Early on, small batches dominated the orders, especially from R&D wings of pharmaceutical players testing new routes to proprietary molecules. Over time, we began investing in batch reactors designed with robust corrosion-resistant linings to accommodate the dichloride’s modest but distinct reactivity with water and atmospheric moisture. Reliable yields became the rule, not the exception. Because our process delivers tight particle-size control, the feeding rate into reactors has stayed predictable, with minimal dusting or clogging in auger or screw feeders. This not only helps environmental safety in the plant, but also reduces cleanup time after each production run.
Each impurity in a chemical intermediate pulls added time and resources away from the end goals of partnering companies, especially those running combinatorial optimization for new pharma candidates or next-generation materials. Over the last decade, we tuned our distillation and crystallization setups to chase out high-boiling pyridine and related tars that can sneak through on poorly watched production lines. Rather than racing for volume at the expense of quality, we found downstream customers would circle back to suppliers providing batches without standing odor, colored residues, or other signals of incomplete reaction. That reputation took time to build but has led to preferred-supplier status again and again.
Comparing this compound to run-of-the-mill chloroformates or aromatic acid chlorides, the differences are clear both in the yields observed and in product selectivity. Typical benzene ring chlorides might offer similar reactivity, yet they often require extra protective groups or coaxing conditions, especially with sensitive amines or alcohols. The electron-deficient nature of the pyridine core leads to much greater compatibility with nucleophilic partners, and modification patterns allow more predictable downstream tailoring. Whether a customer wants to build imides, modify biopolymers, or introduce spacers in rigid frameworks, the dichloride almost always leaves a cleaner, more isolated product—cutting down on rework and filtration cycles.
Chemists far removed from the actual production process sometimes overlook how handling properties shape reagent choice. As the manufacturer, we see every phase, from wet chemistry to packaging and logistics. In our own plant, I’ve seen more than a few overfilled bags rupture because some acid chlorides wreak havoc on standard plastics. 2,6-Pyridinedicarbonyl dichloride behaves far more predictably—proper HDPE or stainless-steel containers, dry atmosphere, and modest desiccant additions keep the material ready for accurate weighing and transfer into glass-lined or PTFE-coated reaction vessels, even on humid days. The material’s low volatility relative to more aggressive acid chlorides means less risk to operators if handled with established protocols, though gloves and light respiratory protection always stay within arm’s reach.
Emission controls always demand vigilance. While the dichloride does release some HCl gas on hydrolysis, especially if spilled or left open to air, running local scrubbers and directing effluent streams through basic traps has contained incident rates well below typical industry figures. Our waste management team tracks each barrel from emptying to final disposal, ensuring compliance without hidden corners. Regrettably, not every facility takes environmental risk seriously. We have invested heavily in real-time monitoring—halogen acid sensors, ventilation with quadruple-stage filtration, and detailed exposure logs. These steps didn’t happen overnight but reflect a steady build-out in response to local and global regulatory tightening.
Over the years, customers have reported excellent results when building polyamides, polyimides, and a variety of specialty acrylics where the dichloride group selectively engages primary and secondary amines. Certain manufacturers of advanced electronics components, working on insulation layers and dielectric films, have shared photos of smooth, bubble-free coatings traceable to the consistency of our batches. In high-end pigment and dye work, precise substitution patterns enabled by the pyridine core translate to colorfast, light-resistant final products. Even outside the lab, in coatings for specialty fabrics and membranes, formulators value this dichloride for the resilience and reproducibility it brings to their process.
Regular acid chlorides—from acetyl chloride to benzoyl chloride—have been on the scene for decades. Each offers something, but many bring headaches: excess volatility, broad-spectrum reactivity, or persistent side-chain contamination. Our experience with 2,6-pyridinedicarbonyl dichloride shows a consistent edge in reactions requiring site-specific activation. The aromatic, nitrogen-based backbone pushes the reagent’s reactivity into a sweet spot: it’s neither too sluggish for fast coupling, nor so energetic that it chews through delicate functional groups. During a series of contract synthesis runs for a global agrochemicals group, our chemists recorded far less unwanted cross-linking and, in some cases, higher molecular weights in final polymers compared to runs with terephthaloyl chloride or isophthaloyl chloride.
Nothing stays static in industrial chemistry. Early on, a few inconsistencies led to detective work inside the plant. Some years ago, we found that switching from bulk crystalline starting material to a finer granular feed reduced batch time by almost 12%, with a corresponding decrease in trace color contaminants. Since then, all drums leaving our facility are checked not just for nominal chlorination but for color index, pourability, and residual solvent—all factors that impact daily work for customers at any scale. Updates in analytical equipment, especially walk-away NMR and FTIR, slashed turnaround times on the shop floor and freed up chemists to run parallel trials.
Packaging and transit laws for chlorinated intermediates are constantly evolving. We have taken direct part in local chemical safety committees, supporting updated training for logistics staff and reworking MSDS documents to reflect real-world transport issues. Palletizing strategies have shifted from simple shrink-wrap to reinforced, labelled modules, after one unfortunate incident in mid-summer resulted in package warping and minor spillage. Documentation for customs and inspection moves faster due to our complete chain-of-custody reporting, and repeat buyers now routinely pass on positive feedback to new procurement teams. Staying on top of transport standards reduces headaches for end users, especially when tight lead times or international shipping cycles are in play.
Few manufacturers dedicate resources to two-way feedback from chemists using their products daily. Over the last decade, we formalized a feedback program, where scientists working with 2,6-pyridinedicarbonyl dichloride provided suggestions that shaped real change. For example, one repeated concern about static electricity buildup during winter prompted us to line key transfer hoppers with conductive, nonreactive materials. These tweaks cost little but paid off both in process safety and batch consistency. We field regular questions on solvent compatibility, optimal charging regimes, and the best vessel liners for maximizing yield. That information returns not just to our teams but also gets compiled and shared with our network of customers facing similar synthetic puzzles.
It’s easy for third parties to treat this compound as just another entry in a spreadsheet of chlorinated reagents. For the folks mixing, pouring, and sampling day-in, day-out, traceability makes all the difference. Our “from kettle to carton” approach, with every lot number linked to reactor logs and in-process analytics, cuts down time chasing issues and shortens lead time for repeat orders. In one case, a pharmaceutical pilot line reported a subtle yield drop, which our trace logs pinpointed to a barely out-of-spec purity shift—allowing us to backtrack, test, and remedy the issue on a future batch long before it became a lost opportunity.
Synchronous with rising global expectations, our facility has invested in more sustainable upstream supply chains for pyridine sources and new acid chlorination technologies that reduce byproduct salts. Solvent recycling has become standard not only because it’s required by regulation but because it recirculates high-purity materials back into the process, lowering costs and reducing municipal burden. Collaborations with university research laboratories have produced pilot catalytic methods that, while not yet commercial scale, hint at further environmental and cost savings. Transparency and open reporting of our process inputs and outputs have allowed customers and certification auditors to confirm fair environmental performance year over year.
High-volume chemical plants live or die by the competence of their staff. Regular onboarding and continuing education about the specifics of handling pyridine-based dichlorides have kept incident rates low and quality metrics high. Our technical leads not only walk plant operators through procedures but also keep chemists fueled with up-to-date literature and real-world case studies. Continuous improvement has taken root, making workshop suggestions part of annual reviews and rewarding staff for process optimization that trims waste or speeds up loading and transfer.
Several times, customers challenged us to push beyond the familiar by adjusting key process variables—whether switching solvents, trying non-standard coupling agents, or adjusting temperature ramps for exotic intermediates. Our in-house R&D group, equipped with pilot-scale glassware and simulation tools, regularly replicates those conditions, looking for points where the dichloride excels or alerts to unexpected hazards. Each new variant, each process tweak, is recorded, discussed, and tested, with updates making their way not only to safety sheets but into training for experienced hands and newcomers alike.
Chemicals as particular and versatile as 2,6-pyridinedicarbonyl dichloride rarely become mainstays unless supported by steady, knowledgeable production. The flexibility built into our manufacturing methods allows us to tune particle size, packing, and batch purity to meet hard metrics provided by development chemists working at the edge of new polymer or pharmaceutical applications. Repeatedly, we’ve seen projects require rapid adjustments: custom drum sizes, non-standard moisture specs, or one-off analytical runs to clear regulatory questions for a novel synthesis route. Long hours and tight timelines mean adjustments ripple up the supply chain, but those commitments convert to lasting relationships with scientists and engineers who remember fast action and sound technical knowledge.
As advanced synthesis keeps evolving, versatility and reliability only become more important. The dichloride’s compatibility with modern coupling agents, ability to operate in diverse solvents, and predictable reaction patterns continue to win it a place in everything from university research labs to high-throughput manufacturing sites. Its lower tendency for unexpected side reactions, straightforward waste management, and proven performance in both classic and modern synthetic routes provide daily value to production chemists balancing yield, safety, and cost pressures.
Years of direct experience tell us that the best chemical intermediates aren’t just defined by their datasheets or purity specs—they’re marked by the reliability felt during each transfer, the confidence they inspire during high-stakes syntheses, and the technical expertise available when questions arise. The story of 2,6-pyridinedicarbonyl dichloride isn’t shaped by slogans or marketing catchphrases, but by the accumulated lessons of thousands of reaction vessels, decades of troubleshooting, and the deep trust built up between manufacturers, chemists, and innovators around the world.