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HS Code |
226412 |
| Cas Number | 17668-58-1 |
| Molecular Formula | C6H2Cl3NO |
| Molecular Weight | 224.45 g/mol |
| Iupac Name | 2,6-dichloropyridine-4-carbonyl chloride |
| Appearance | White to off-white solid |
| Melting Point | 63-65°C |
| Density | 1.63 g/cm³ |
| Solubility | Soluble in organic solvents such as dichloromethane and chloroform |
| Purity | Typically ≥ 97% |
| Smiles | C1=CC(=NC(=C1Cl)C(=O)Cl)Cl |
| Inchi | InChI=1S/C6H2Cl3NO/c7-4-1-3(6(10)11)2-5(8)9-4/h1-2H |
| Storage Conditions | Store under inert atmosphere, in a cool, dry place |
As an accredited 2,6-Dichloropyridine-4-carbonyl chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle with a secure screw cap, clearly labeled with the chemical name, hazard symbols, and handling instructions. |
| Container Loading (20′ FCL) | 20′ FCL loads **2,6-Dichloropyridine-4-carbonyl chloride** in sealed drums, total 16MT (net) per container, ensuring dry, ventilated storage. |
| Shipping | **Shipping Description:** 2,6-Dichloropyridine-4-carbonyl chloride should be shipped in tightly sealed, moisture-proof containers and clearly labeled. It must be handled as a hazardous chemical, compliant with local and international regulations (e.g., UN3261), and protected from heat and incompatible substances. Shipment should include relevant safety data and documentation for safe transport and handling. |
| Storage | Store 2,6-Dichloropyridine-4-carbonyl chloride in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as bases, alcohols, and strong oxidizers. Protect from direct sunlight and sources of ignition. Use under a chemical fume hood, and ensure appropriate secondary containment to prevent accidental release. |
| Shelf Life | Shelf life of 2,6-Dichloropyridine-4-carbonyl chloride: Store in a cool, dry place; stable for at least two years unopened. |
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Purity 98%: 2,6-Dichloropyridine-4-carbonyl chloride with purity 98% is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side reactions and increased yield of target compounds. Melting point 108°C: 2,6-Dichloropyridine-4-carbonyl chloride with melting point 108°C is used in fine chemical manufacturing, where controlled melting behavior facilitates precise processing conditions. Moisture content ≤0.5%: 2,6-Dichloropyridine-4-carbonyl chloride with moisture content ≤0.5% is used in agrochemical active ingredient formulation, where low moisture prevents hydrolytic degradation and maintains chemical integrity. Stability temperature up to 40°C: 2,6-Dichloropyridine-4-carbonyl chloride with stability temperature up to 40°C is used in sensitive reaction setups, where thermal stability supports consistent performance during storage and handling. Particle size ≤50 μm: 2,6-Dichloropyridine-4-carbonyl chloride with particle size ≤50 μm is used in high-efficiency catalyst preparation, where fine particle distribution enhances reactivity and surface contact. |
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Every product carries a story within our operation lines, and 2,6-Dichloropyridine-4-carbonyl chloride stands out for the challenge and satisfaction it brings to our team. Producing this compound means controlling each step, bringing precision to a sector where demands continue to rise for pharmaceuticals, agrochemicals, and advanced materials. Over the years, we have refined our processes, placing consistency and quality above all else, knowing that downstream applications rest on our reliability.
2,6-Dichloropyridine-4-carbonyl chloride comes from a family of building blocks prized for selective chlorination and the introduction of reactive acyl chloride functionality. Its structure allows for transformation in synthesis pathways that contribute directly to active pharmaceutical ingredients and research compounds. The real value lies in how the molecule bridges between core pyridine chemistries and modern, targeted synthesis routes. This isn’t a generic intermediate; controlling each batch to meet tight purity and contamination standards is critical due to its subsequent uses in regulated and heavily scrutinized sectors.
Few in the field have taken on the task of making this compound in larger quantities. The pathway seems straightforward on paper, but our engineers know the sticky details of reagent quality, temperature management, and handling of corrosive materials make all the difference. For us, a lot goes into reliable isolation and crystallization. We have invested in closed-loop systems and specialty glass-lined reactors, limiting exposure and preventing off-spec batches that could cause cascading problems in formulation or research labs relying on strict downstream reactivity.
Every kilogram produced passes through a full panel of analytical checks—HPLC, NMR, and GC-MS. The real test is consistency over time, not a single number. Each campaign is informed by feedback from users and our continuous in-process testing. By listening to end-users, whether in drug discovery or materials innovation, we tweak our protocols to avoid familiar pitfalls: moisture ingress turning batch contents into sludge, excessive byproduct content throwing off stoichiometry, or packaging that allows loss of reactivity over storage and transport.
2,6-Dichloropyridine-4-carbonyl chloride often appears with demanding purity specifications—usually exceeding 98% by assay, with water and contamination thresholds well under 0.5%. Through close control of chlorination and workup conditions, we keep undesirable chloride byproducts to a minimum. During scale-up, small changes in reagent source or mixing rates leave a trace in product quality, detected in sharp-eyed QC checks. What we learned early on: a good method becomes better only through continuous improvement and a hands-on approach. Minor changes upstream, such as solvent quality, can have a drastic effect on the yield and cleanliness of final product, as even non-obvious impurities alter both reactivity and handling safety.
We ship the product in sealed, inert-lined containers. The reason is simple: moisture intrusion ruins batches, causing acid hydrolysis and lowering shelf life. Technicians who have handled hydrolyzed material know the frustration—fuming, irritant fumes, and the wasted work as contaminated product can't reach downstream synthesis objectives. Our packaging choices come after repeated stress trials and consultation with major users, who flagged prior issues with traditional drum liners or basic sealing. We adjusted—and reliability increased.
Many researchers and developers depend on this compound as both a stand-alone building block and as a key node in more elegant synthesis strategies. Its appeal lies in the possibilities unlocked by the combination of two ortho chlorine atoms and the activated ring. In the pharmaceutical sector, it enables rapid coupling and derivatization, giving chemists leverage to modify molecular scaffolds with precision. More than one customer story returns to us, reporting how a consistent supply allowed reductions in step count for complicated molecules, translating to months saved in late-stage R&D projects.
On the agrochemical side, this compound often forms part of active ingredient backbones or intermediate stages in selective herbicide or fungicide design. Given the regulatory scrutiny of these end uses, we have always emphasized transparency in both residual solvent content and exact specification disclosure. We know formulations in this space must pass through battery after battery of stability and tox panels—a leaky or out-of-spec intermediate halts projects cold. Reliable supply and minimal deviation from the agreed specification let users focus on innovation, not rework or troubleshooting.
Other chloropyridine derivatives appear on the market in a spectrum of purities and substitution patterns. What makes 2,6-Dichloropyridine-4-carbonyl chloride unique isn’t just its substituent log—it’s the fine balance between reactivity and selectivity. Chlorination at the 2 and 6 positions brings a degree of resonance stabilization, making certain transformations more predictable. The 4-carbonyl chloride group, reactive yet susceptible to hydrolysis, must be produced and handled with greater care than straightforward acid chlorides or less-substituted pyridines.
Our facility also produces related compounds with single-chlorine or with substitution at the 3 or 5 positions, but end-user feedback remains consistent—no substitute allows for the same flexible extension of the heterocycle onto bioactive molecules without increased burden during downstream handling. Alternate acyl chlorides based on benzene or even less halogenated pyridines present fewer challenges in reactivity but ultimately require more steps or show lower yields in key coupling reactions.
Working with these alternatives highlights trade-offs: lower cost per kilogram can mean higher processing costs after delivery, either due to clean-up, excessive byproduct work-up, or greater labor needs. For innovators designing around exacting regulatory or methodological endpoints, these few percent differences in purity and chain-of-custody record add up fast across development timelines measured in months and years.
Most people only see the finished product, rarely appreciating what stays unseen behind closed reactor doors or in procedure logs. To reach the required purity, our operators keep a sharp watch on each parameter, especially during chlorination and subsequent phase separations. Deviations bring in off flavors—literally, sometimes, in pyridine chemistry, with odors hinting at over-reaction or excessive byproducts. We have learned that training is as good as technology: skilled technicians understand subtle shifts in color, viscosity, and exotherm profiles before instruments do.
Supply interruptions sometimes hit markets for specialty intermediates, especially when regulations tighten for certain feedstocks or when international logistics disrupt raw material flows. We built diversification into our sourcing from early on—in practice, it meant extra work and tighter inventory management, but we saw that users depended on us for regular shipments. By pushing for redundancy in both our upstream partners and on-site storage, we stepped in to fill gaps when others couldn’t, scoring points for reliability when every week counts in a development program.
Handling this particular compound forced us to rethink legacy approaches to operator safety and environmental controls. We implemented dual-containment filling and automated ventilation to minimize exposure during packaging and transfer—this earned us both peace of mind and local regulatory wins, but more importantly, it gave new operators confidence working with potent reagents. We recall early incidents in the sector where cut corners led to reactivity incidents, causing both injuries and unscheduled downtime. For us, lessons learned never get ignored: each update to our procedures absorbs feedback and new science, and every operator’s input shapes our practices.
Making advanced intermediates often means complex waste streams and logistical challenges. For 2,6-Dichloropyridine-4-carbonyl chloride, we designed our process from the ground up with recovery and minimization strategies built in. Where older methods vented chlorinated gases or dumped unreacted material, our system recaptures and neutralizes byproducts, both reducing our local discharge and cutting costs.
By monitoring every batch with linked sensors and predictive maintenance schedules, we've cut chemical losses that once seemed inevitable. We also work with downstream users to collect packaging for safe recycling or high-temperature destruction, closing the loop instead of leaving waste management up to chance. These changes take coordination and a willingness to sometimes spend more at the outset—but our experience shows the payoff comes in regulatory compliance and long-term customer confidence.
Chemists in pharmaceuticals and crop science look for intermediates offering robust coupling, clear analytical signatures, and clean exit after the target transformation is complete. During hundreds of feedback cycles, we have adjusted our process to improve the compatibility of our 2,6-Dichloropyridine-4-carbonyl chloride with advanced coupling reagents, catalysis protocols, and emerging green chemistry workflows.
One striking advantage, confirmed by client project outcomes, appears during scale-up stages of new molecule synthesis. Our tighter impurity profile minimizes side-product formation, so teams spend less time debugging or purifying downstream intermediates. Reliable lot-to-lot consistency smooths handoffs between teams: a difference that rarely makes headlines but is felt in cut-down lead times and more successful runs.
Some partners work under full cGMP oversight; others are fast-moving R&D units racing to proof-of-concept. Our role extends into technical consultation—open channels let us refine the offering based on changing research directions or new regulations. On occasion, close work with users revealed surprising new reaction conditions, prompting us to re-examine our product finishing or drying techniques to avoid bottlenecks from moisture pickup or micro-level contamination.
Manufacturing a complex intermediate isn’t just a matter of running a dossier and shipping drums. The hands-on knowledge our chemists and production engineers bring comes from years on the plant floor—troubleshooting crystallization fouling, fending off runaway reactions, or identifying sources of persistent trace contamination that eluded basic QA.
We learned long ago that partnering directly with users brings benefits on both sides, from correcting small errors in use instructions to sharing insights about what’s possible in scale-up. Our teams field questions on reactivity, storage, and application, offering fixes that derive from first-hand problem-solving, not speculation. More than once, shared testing protocols or customized documentation have saved users from repeating costly errors or abandoning projects in late stages.
This direct visibility and willingness to adapt comes from being a manufacturer instead of a middleman. We have no layers of intermediaries muddying communication, so changes in market requirement or process chemistry gets fed straight back into action. The relationships built through candor about what works and what doesn’t last longer than any contract—and these connections foster real innovation.
Market demands for fine chemicals evolve rapidly, driven by global innovation and new frontiers in medicine and agriculture. Down cycles and sudden spikes in demand test the agility of even the most seasoned manufacturers. With 2,6-Dichloropyridine-4-carbonyl chloride, those cycles tend to track discovery pipelines—one breakthrough in medicinal chemistry or a regulatory nod for a new active molecule and demand triples.
Anticipating those changes, we scaled in modular fashion, expanding batch sizes without sacrificing control or needing full redesigns between lots. Instead of pursuing headlong expansion for its own sake, planning stays linked to reliable feedback about end-user projects and the regulatory landscape. For example, ongoing reviews of allowable impurity thresholds or trace contaminant monitoring standards in pharmaceuticals push us to upgrade analytics well before users ask for it. Advanced automation in our workflow allows us to stay ahead of datalogging and documentation requirements, making compliance routine rather than a hurdle.
Meanwhile, international shifts in chemical control regulations—such as new limits for certain byproducts or stricter shipping classification—never come as a surprise. Our membership in technical consortia and close tracking of regulatory bulletins keep us prepared. Routine audits and practice drills ensure staff remains current in emergency protocols, providing users with an extra layer of reassurance about supply chain security.
For us, manufacturing 2,6-Dichloropyridine-4-carbonyl chloride means more than making a product for sale. It’s a process of continual engagement—sharing knowledge, adapting procedures, investing in capability and resilience. Engagement with end users, from multinational pharma to university research teams, informs every tweak, upgrade, and service enhancement. There’s pride in knowing a small building block molecule produced with care may find its way into better medicines or more sustainable crop production.
We keep our doors open to feedback and collaboration, welcoming projects both large and small. If there’s a specific request—an altered particle size, a new solvent system, or stricter handling guidance—we welcome the challenge. Our goal is to stay not just a supplier but an indispensable partner for chemists and developers pushing boundaries.
For those working with 2,6-Dichloropyridine-4-carbonyl chloride, we promise direct answers and steady commitment to making every batch count. Behind each shipment rests decades of know-how, hard-won by people who care about getting the chemistry just right.