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HS Code |
775936 |
| Cas Number | 2402-77-9 |
| Molecular Formula | C5H2Cl3N |
| Molecular Weight | 198.44 g/mol |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 54-58°C |
| Boiling Point | 244-246°C |
| Density | 1.532 g/cm3 |
| Solubility In Water | Slightly soluble |
| Flash Point | 108°C |
| Purity | Typically ≥98% |
| Iupac Name | 2,3,6-trichloropyridine |
| Refractive Index | 1.589 (20°C) |
As an accredited 2,3,6-Trichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams, sealed with a screw cap; labeled with hazard symbols, chemical name, and batch details. |
| Shipping | 2,3,6-Trichloropyridine is shipped as a hazardous chemical, typically in sealed, labeled containers compliant with safety regulations. It should be packed to prevent leaks and protected from physical damage. The shipment must include appropriate documentation, hazard labels, and be handled by trained personnel in accordance with local and international transport regulations. |
| Storage | 2,3,6-Trichloropyridine should be stored in a tightly sealed, labeled container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Avoid moisture and sources of ignition. Store at room temperature and ensure appropriate spill containment. Use corrosion-resistant shelves and equipment, and keep away from heat and open flames. |
Applications of 2,3,6-Trichloropyridine in Industrial Manufacturing2,3,6-Trichloropyridine serves as a pivotal intermediate for advanced chemical synthesis across multiple downstream industries. Its use lies primarily in processes where controlled chlorination and pyridine scaffolding are required for high-purity specialty compounds. We supply 2,3,6-Trichloropyridine directly to manufacturers operating high-throughput production lines with exacting demands for regulatory traceability, process consistency, and end-product performance. Below, we outline the material’s application across established industry segments, specifying relevant technical criteria based on operational experience. 1. Agrochemical Synthesis: Herbicide IntermediateAgricultural chemical producers source 2,3,6-Trichloropyridine as a core building block in the synthesis of selective herbicides such as fluroxypyr and picloram. Chlorination of the pyridine base provides the reactive sites necessary for coupling reactions, ensuring molecular integrity under continuous-flow and batch synthesis regimes. Precision in dosing directly impacts downstream yield and impurity control, especially under high-pressure hydrogenation or amination conditions used in commercial herbicide precursor production. Industry compliance standards
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2. Pharmaceutical Intermediate Manufacturing: Antiviral and Antihypertensive APIsProducers of active pharmaceutical ingredients rely on 2,3,6-Trichloropyridine for its unique substitution pattern facilitating controlled functional group insertion in the synthesis of antiviral and antihypertensive agents. The compound enables concise route design for pyridine-derived scaffolds, with controlled introduction during pharmaceutical-grade nucleophilic substitution or Suzuki coupling. Stringent compliance and trace metal analysis are maintained from input through final API isolation to meet international pharmacopoeial standards. Industry compliance standards
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3. Dye and Pigment Manufacturing: Pyridine-Derived ColorantsManufacturers in the colorants sector utilize 2,3,6-Trichloropyridine as a reactive intermediate in the formulation of specialty dyes and pigments, particularly for synthetic fibers and plastics. Its chemical structure imparts specific hue modulation and improves fastness properties, while the controlled introduction of chlorinated moieties allows downstream substitution in azo and metal-complex dye synthesis. Production lines incorporate robust material batch validation to ensure compliance for use in regulated applications such as food packaging inks and medical device housings. Industry compliance standards
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4. Veterinary Drug Intermediate ProductionVeterinary pharmaceutical companies employ 2,3,6-Trichloropyridine as a fundamental precursor in the synthesis of pyridine-containing veterinary actives, especially for antiparasitic and antimicrobial agents. The compound facilitates access to stable, well-characterized intermediate structures via high-yield nucleophilic aromatic substitution. Strict process monitoring, as well as batch traceability, align with authorities regulating animal drug supply chains, with continuous verification extending through both synthesis and downstream formulation. Industry compliance standards
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5. Fine Chemicals: Agrochemical Co-formulant ProductionProducers of adjuvants and co-formulants for agrochemical formulations use 2,3,6-Trichloropyridine as a customized intermediate for the creation of specialty surfactants and stabilizers compatible with pesticide formulations. Its specific substitution pattern allows tailored lipophilicity and binding functionality essential for optimizing spray properties, emulsion stability, and tank-mix compatibility in modern pesticide products. Material validation links directly to customer specification and regulatory notification for new formulation ingredients. Industry compliance standards
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6. Advanced Material Synthesis: Specialty Polymer Additive IntermediateProducers of advanced polymeric materials draw on 2,3,6-Trichloropyridine as an intermediate for the development of reactive additives enhancing heat resistance, UV stability, and mechanical properties in engineering plastics. It enters into substitution reactions for the preparation of functional monomers, providing chemical tunability required by manufacturers at the forefront of automotive, electronics, and specialty film production. Batch consistency offers predictable integration into downstream polymerization lines, with full documentation for client audit. Industry compliance standards
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Work inside the chemical plant runs on a mix of routine and vigilance, especially where chlorinated pyridines are involved. Among these, 2,3,6-Trichloropyridine sees steady orders from regular customers in both pharmaceuticals and agrochemicals. This compound doesn’t sit on a shelf for long; each drum or bag picked up tells a story of careful synthesis and adjustment, guided by the demands we see in today’s market.
On our main line, the pyridine ring forms the backbone of several manufacturing steps. Chlorination at the 2, 3, and 6 positions produces a pale to light yellow crystalline solid: 2,3,6-Trichloropyridine. We deliver it with a purity that consistently measures above 98% by GC, meeting the standards customers expect when making higher-value goods downstream. Appearance and melting point range get checked every shift, as does the moisture content—so clumping or caking rarely causes issues during handling.
Over the past decade, we’ve seen orders trace a cycle tied closely to the development of new crop protection products and active pharmaceutical ingredients. Chemists rely on this molecule as a building block for advanced heterocycles. Its chlorines lend themselves well to nucleophilic substitution, so it acts as an anchor in coupling reactions. Teasing out substitutions at the 3- or 6-position makes this intermediate a go-to choice for molecules requiring selectivity along the pyridine ring.
Companies working on herbicides, fungicides, and seed treatments favor this substrate for its predictable reactivity. Where competing molecules such as 2,6-dichloropyridine offer fewer points of functionalization, the extra chlorine at the 3-position in our product keeps routes open for molecular designers. This gives chemists more control in tuning the properties they want: solubility, biological target affinity, and metabolic stability.
Pharmaceutical researchers pursuing kinase inhibitors and other nitrogen-containing heterocycles request this intermediate to build structures where the residual chlorines serve as handles for further transformation. The unique arrangement allows for metal-catalyzed cross-coupling and SNAr conditions without the frustration of scrambling the skeleton—an issue that pops up during scale-up with some other blocked pyridines.
In the plant, quality control shapes every batch. We work with reactors lined for high chlorination resistance, because impurities can trigger shutdowns or slow reactions. The process brings its own challenges: balancing temperature to avoid over-chlorination, purging HCl safely, and timing the work-up stages to recover the right fraction. Operators check each cut for unreacted pyridine or over-chlorinated side products, returning anything not up to par for retreatment or recycling.
Once dried and ground, the crystals are bagged in sealed containers that block light and moisture. This matters because color changes—usually a result of light exposure or trace air moisture—can alter the apparent purity, even if the assay remains within specification. We instruct warehouse and shipping teams to store finished goods in cool, shaded conditions to minimize degradation and keep requalification to a minimum.
Being able to offer a guarantee on purity means end users can plan syntheses with fewer hiccups. During scale-up, we've seen customers reduce recrystallization steps and bring yields into commercial range, just by switching to our process or batch. Less time managing byproducts or running additional distillations frees up technical staff and tightens delivery schedules. It's one thing to promise quality; we've staked our reputation on delivering it with minimal batch-to-batch variability.
Wherever possible, we keep our process continuous, which preserves energy and shortens turnaround times. In one instance, a partner firm came to us after facing plugging issues with other grades. Their process involved a two-step amination that kept stalling due to slight increases in residual moisture. Our product’s low water content let their reaction run smoothly, solving the issue without modification of existing equipment.
Our plant handles several pyridine derivatives, but if you’re comparing options, key differences become clear. For instance, 2,3,6-Trichloropyridine introduces three reactive chlorines, compared to the more common 2,6-dichloropyridine or 2,3,5-trichloropyridine. With only two chlorines, the dichloro variant locks you into fewer substitution patterns and sometimes suffers from unhelpful isomer formation during further steps. Extra chlorination at the 3-position gives an advantage in customizing reaction pathways, especially where regioselectivity drives efficiency.
We’ve handled requests for higher-purity fractions, but have found 98% strikes the best balance. By avoiding extensive purification, we keep costs reasonable and batch sizes practical. Every additional percent brings a diminishing return, particularly if the main impurities stem from structurally similar byproducts that do not interfere with planned chemistry. Downstream teams often tell us that minor impurities do not pass into their final APIs due to strong downstream purification.
Another point of comparison concerns the physical properties. The melting range of our product falls between 62 and 65°C. Powders store well and flow with ease, making them more convenient to handle than some trade-grade chlorinated pyridines, which can form sticky lumps after transport. We also design packaging for minimal tearing and accidental exposure, based on experience with customer complaints in years past.
Running chlorination reactions at production scale brings sharp environmental obligations. Our high-performance scrubbers scrub HCl off-gas to below legal discharge limits, and recovery systems channel as much material as possible into usable byproducts. Solvent recycling forms a core part of our cost control, and we keep a close eye on waste streams for anything that falls out of process tolerance. Our record with environmental regulators reflects that—routine inspections have driven us to bolster safeguards and fine-tune emissions sampling.
On the safety front, chlorinated heterocycles demand careful handling. 2,3,6-Trichloropyridine releases irritating vapors if mishandled; lab and plant workers receive annual training and carry detectors that give early signals of leaks. For all its value on the production line, the substance doesn’t belong outside controlled systems. Teams wear full PPE, and we run drills on containment and cleanup, since mishaps rarely offer second chances with this class of chemicals. Any spilled material gets neutralized promptly and removed before it can reach drains or mingle with incompatible substances.
Judging by order patterns, industry trends continue pushing toward greener synthesis methods. Some partners ask specifically about the origin of key raw materials or solvent systems. We source our pyridine ring structure from long-standing suppliers with robust documentation. We’ve also begun working on alternative chlorination methods that reduce byproduct formation and accelerate throughput. Incremental improvements in catalyst selection and solvent recovery keep our process leaner year after year.
Researchers in both pharma and crop science look for ways to streamline their pipelines. By maximizing the ratio of useable product to waste and improving the reactivity window, we help buyers cut their own resource use. Feedback loops run from the bench chemist who needs a trouble-free precursor, back through our technical teams, right to the operators loading reactors. Direct conversations with customers have inspired a round of minor formulation changes and have cut down on shipments sent back for rework.
We maintain field relationships with several major multinational groups and a growing list of smaller independent labs. Once, a process engineer from a European crop protection company visited our site, curious about how we handled scale-up bottlenecks. By walking through the reactors and purification lines with our foreman, he picked up tips on adjusting feed rates and troubleshooting color drift. These collaborative exchanges help cement technical trust—in this market, losing that edge makes retaining repeat business impossible.
Not every batch leaves our facility in perfect shape. A few years ago, we traced a tarnished shipment to thermal cycling during overseas transport. Investigating with the forwarder taught us to reinforce insulation and upgrade data loggers in our containers. Since then, we’ve seen customer complaints drop and shelf life extend, all from practical changes to packaging and logistics, rather than fiddling endlessly with purification specs.
Right now, chemical manufacturing faces broader scrutiny over carbon footprint and traceability. Every year, buyers pay more attention to supply chain transparency and the total resource burden of their processes. We’re increasing investments in digital batch records and predictive analytics. These tools flag anomalies sooner, helping avoid off-spec shipments and reduce the need for batch-by-batch paperwork.
The world’s demand for new pharmaceuticals and safer, more sustainable crop protection drives us to optimize not just for yield, but for reliability and eco-footprint. Every improvement in reactivity, waste reduction, and packaging safety makes that next innovation possible. Feedback from end users keeps the direction practical—each improvement grows out of actual production issues experienced on the shop floor or in customer plants.
We commit to keeping the line running with traceable raw materials and a chain of custody that withstands regulatory audits. Chemistry should empower new solutions, not introduce uncertainty. Our priority stays focused on delivering an intermediate that integrates easily with the evolving needs of manufacturing partners, and whose performance can stand up to close inspection, batch after batch.
Colleagues in process development tell us that no other trichloropyridine offers quite the same flexibility. The choice of substitution site influences final product characteristics. The direct experience of success in late-stage pharmaceutical intermediates—or in robust field-tested crop solutions—keeps 2,3,6-trichloropyridine on our production slate year after year.
Our continued focus rests not on just hitting a spec, but on meeting real-world challenges shared by every person making, shipping, or researching with this material. Close listening to feedback has led us to redesign hazards labeling, invest in independent third-party analyses, and tweak warehouse inventories to prevent cross-contamination from other pyridines. These steps may seem like incremental tweaks, but in a tightly regulated sector, the smallest change can ripple outward, helping end products meet tougher safety and environmental standards.
The story of this compound traces the larger story of modern chemistry: continuous adjustment, problem-solving, and hands-on learning. Working at the heart of the supply chain gives us perspective—we respond to operational headaches and evolving expectations not with generic claims, but with every ounce of technical experience built into our process. That’s how a staple like 2,3,6-trichloropyridine remains a reliable building block in tomorrow’s solutions.