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2,3,6-Trichloropyridine

    • Product Name 2,3,6-Trichloropyridine
    • Alias 2,3,6-Trichloropyridin
    • Einecs 218-665-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 2,3,6-Trichloropyridine

    Applications of 2,3,6-Trichloropyridine in Industrial Manufacturing

    2,3,6-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 Intermediate

    Agricultural 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

    • OECD Guidelines for Chemical Testing
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) requirements
    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001-certified quality management systems for agrochemical manufacturing

    Typical usage ratio

    • 0.85–1.10 molar equivalents per batch, adjusted according to target yield and impurity threshold defined by product specifications

    Downstream process integration

    • Enters as the chlorinated ring precursor during the cyclization and amination stages of herbicide active ingredient synthesis
    • Used prior to condensation with carboxylic acids or amines for specific pyridine-based herbicides
    • Added in a dedicated closed feed system to minimize occupational exposure and cross-contamination

    Final product types

    • Fluroxypyr acid and salts (selective systemic herbicides)
    • Picloram formulations (broadleaf weed control agents)
    • Intermediates for other pyridine-derived crop protection chemicals

    2. Pharmaceutical Intermediate Manufacturing: Antiviral and Antihypertensive APIs

    Producers 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

    • Current Good Manufacturing Practice (cGMP) as per ICH Q7
    • USP (United States Pharmacopeia), EP (European Pharmacopoeia) monographs for APIs
    • 21 CFR Part 211 (FDA Quality System Regulation)
    • ICH Q3D Guidelines (elemental impurities)

    Typical usage ratio

    • 0.92–1.05 molar equivalents in API synthesis; exact ratio defined by route design and required pyridine ring purity

    Downstream process integration

    • Charged as an initial intermediate in the early stages of multi-step synthesis for API core construction
    • Undergoes substitution and further heterocyclic modification under inert conditions
    • Integrated into high-containment suites to safeguard against cross-contamination with other highly potent intermediates

    Final product types

    • Antiviral agents featuring dichloropyridine or substituted pyridine substructures
    • Antihypertensive pharmaceuticals with modified pyridine rings
    • Precursors for registered generic and branded medicines

    3. Dye and Pigment Manufacturing: Pyridine-Derived Colorants

    Manufacturers 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

    • EN 71-3 (European safety standard for toy materials, migration of certain elements)
    • OEKO-TEX Standard 100 (Textile safety)
    • GMP for the manufacture of food-contact inks and pigments (EU Regulation No 2023/2006)
    • ISO 14001 (Environmental management for dye manufacturing)

    Typical usage ratio

    • 10–18% by mass in dye synthesis runs, varying by target hue and depth of the final pigment product

    Downstream process integration

    • Reacted at the primary coupling step of dye precursor formation, often under controlled pH and temperature
    • Subject to post-reaction purification to ensure residual chlorine is managed within allowable limits
    • Monitored during milling and blending to stabilize pigment particle distribution in bulk colorant batches

    Final product types

    • Specialty azo and pyridine-based dyes for polyester fibers
    • Pigments for food-grade inks and coatings
    • Color additives for polymer-based industrial goods

    4. Veterinary Drug Intermediate Production

    Veterinary 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

    • VICH GL 3 (GMP for Veterinary Medicinal Products)
    • Pharmacopoeia of the People’s Republic of China (ChP), Veterinary Section
    • USP Veterinary Drug Monographs
    • ISO 17025 for quality assurance laboratories

    Typical usage ratio

    • 0.87–1.13 molar equivalents as required by active ingredient target and allowable process impurity levels

    Downstream process integration

    • Introduced in the initial condensation step for veterinary active ingredient synthesis
    • Treated under high-stirring, inert atmosphere to produce stable intermediates usable in downstream salt formation
    • Sampled at multiple process points for residual chlorinated byproduct analysis

    Final product types

    • Antiparasitic veterinary actives containing dichloropyridine motifs
    • Antibacterial drugs for livestock (oral and injectables)
    • Premixes and veterinary finished formulations intended for regulated markets

    5. Fine Chemicals: Agrochemical Co-formulant Production

    Producers 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

    • EU Regulation (EC) No 1107/2009 (plant protection products)
    • EPA 40 CFR Part 180 (tolerances for pesticide chemicals in food, adjuvant requirements)
    • Chemical Control Law (Japan)
    • ISO 17034 (Reference Material Producers)

    Typical usage ratio

    • 3–8% by weight in batch processes for surfactant and stabilizer synthesis; dosing accuracy determined by performance testing and emulsion index targets

    Downstream process integration

    • Charged during the alkylation or condensation reaction step of co-formulant manufacture
    • Closely monitored for residual chlorinated byproduct removal during work-up and purification
    • Documentation aligned with customer submission packages for regulatory pre-registration

    Final product types

    • Nonionic and anionic surfactants for pesticide emulsions
    • Stabilizers tailored for water-dispersible granule (WDG) formulations
    • Emulsifiable concentrate (EC) co-formulants compliant with regional approvals

    6. Advanced Material Synthesis: Specialty Polymer Additive Intermediate

    Producers 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

    • ROHS (Restriction of Hazardous Substances Directive, EU)
    • UL 94 (Flammability tests for plastic materials)
    • ISO 9001 for fine chemical and additive manufacturing
    • TSCA (Toxic Substances Control Act) inventory verification

    Typical usage ratio

    • 5–12% by mass as an intermediate in batch or semi-continuous monomer production for additive-grade specialty polymers

    Downstream process integration

    • Added during initial polymer precursor formation, typically post-reactant blending phase
    • Subjected to purification and functional testing before integration into compounding and extrusion operations
    • Process includes downstream thermal analysis for additive compatibility

    Final product types

    • High-performance polymer additives for engineering plastics
    • Stabilizer systems for automotive electrical components
    • UV-stable films and functional coatings for electronics applications
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    More Introduction

    2,3,6-Trichloropyridine—A Closer Look at Our Proven Intermediate

    Practical Experience with 2,3,6-Trichloropyridine

    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.

    Trusted Reactions and Applications in Pharmaceuticals and Agrochemicals

    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.

    Production Realities and Quality Management

    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.

    Downstream Benefits: Process Efficiency and Reliability

    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.

    Understanding the Differences: How 2,3,6-Trichloropyridine Stands Out

    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.

    Environmental and Safety Realities in Manufacturing

    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.

    Supporting Sustainable Growth and Innovation

    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.

    Working with End Users: Field Data and Real-World Demands

    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.

    Future Outlook and Industry Shifts

    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.

    Why 2,3,6-Trichloropyridine Remains a Valued Choice

    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.