|
HS Code |
656873 |
| Cas Number | 16063-70-0 |
| Molecular Formula | C5H2Cl3N |
| Molecular Weight | 198.44 g/mol |
| Appearance | White to pale yellow crystalline powder |
| Melting Point | 53-57°C |
| Boiling Point | 235-237°C |
| Density | 1.57 g/cm³ |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Synonyms | 2,3,5-Trichloro-1H-pyridine |
| Smiles | C1=NC(=C(C=C1Cl)Cl)Cl |
| Refractive Index | 1.604 (at 20°C) |
| Flash Point | 99°C |
| Storage Conditions | Store in a cool, dry place |
| Hazard Class | Irritant |
As an accredited 2,3,5-Trichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, tightly sealed with screw cap, labeled "2,3,5-Trichloropyridine, 100g," includes hazard warnings and safety instructions. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2,3,5-Trichloropyridine: typically 160 drums (200kg each), totaling 32 metric tons per 20-foot container. |
| Shipping | 2,3,5-Trichloropyridine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. During transit, it must be protected from moisture and incompatible substances, and handled according to hazardous material regulations. Proper labeling is mandatory to ensure safe identification, with transport typically conducted by certified chemical carriers. |
| Storage | 2,3,5-Trichloropyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat and incompatible substances such as strong oxidizing agents. The storage area should be clearly labeled, chemical-resistant, and protected from direct sunlight. Personal protective equipment (PPE) should be worn when handling to prevent inhalation, ingestion, and skin or eye contact. |
| Shelf Life | 2,3,5-Trichloropyridine typically has a long shelf life when stored in a cool, dry place, tightly sealed, and protected from light. |
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Purity 99%: 2,3,5-Trichloropyridine with purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures efficient reaction yields. Melting Point 64°C: 2,3,5-Trichloropyridine with a melting point of 64°C is used in agrochemical manufacturing, where its phase stability enhances formulation consistency. Stability up to 120°C: 2,3,5-Trichloropyridine with stability up to 120°C is used in dye production processes, where thermal stability maintains product integrity during synthesis. Moisture Content <0.2%: 2,3,5-Trichloropyridine with moisture content below 0.2% is used in specialty chemical formulation, where low water content prevents unwanted hydrolysis reactions. Particle Size <50 μm: 2,3,5-Trichloropyridine with particle size under 50 μm is used in catalyst preparation, where fine granularity improves dispersion and catalytic activity. Color Index ≤20 APHA: 2,3,5-Trichloropyridine with a color index not exceeding 20 APHA is used in electronic chemical applications, where low coloration ensures minimal impurity interferences. Refractive Index 1.590: 2,3,5-Trichloropyridine with refractive index of 1.590 is used in optical material development, where precise refractive properties are crucial for product performance. Boiling Point 230°C: 2,3,5-Trichloropyridine with a boiling point of 230°C is used in polymer additive synthesis, where high volatility allows controlled volatilization during processing. |
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2,3,5-Trichloropyridine pops up in more conversations between chemists than most folks might guess. Setting out to answer the ever-persistent need for particular halogenated pyridine derivatives, this compound fills a niche—and does it well. What I see in today’s industry is a growing demand for intermediates that lend reliability in both reactivity and purity, especially as pharmaceutical and agrochemical syntheses ramp up their complexity. With its three chlorine atoms precisely tagged onto the pyridine ring, this chemical offers a springboard for creative molecular design.
The trend in manufacturing leans hard on the ability to control reaction mechanisms. Bench chemists crave chemicals that cut down on purification steps and unpredictable by-products. In that context, 2,3,5-Trichloropyridine gives a consistent output. It brings to the table a molecular formula of C5H2Cl3N, and its physical form—usually presenting as a pale solid or crystalline powder—lets it blend easily into various solvents compatible with both small and large-batch operations. From experience, that flexibility takes a good chunk of frustration off any project leader’s desk.
If you open up a bottle of 2,3,5-Trichloropyridine, what you’ll notice first is that sharp, distinctive whiff typical of halogenated aromatics. It registers a melting point around 64-68°C and boils around 224-228°C. That’s squarely in the range needed for controlled distillation and crystallization, making it a manageable choice for multi-step reactions. Purity often clocks in over 98% by GC or HPLC, which isn’t a trivial achievement when producing at scale. A lab partner once told me that dropping purity a single notch brings headaches later—with this compound that frustration rarely comes up.
Handling is straightforward with routine safety standards—avoid inhalation, keep bottles tightly sealed, and use gloves and goggles. The low water solubility puts it in a favorable spot for organic-phase reactions. In my past projects, the chemical proved easy to portion by weight without clumping or absorbing humidity.
Some might measure success by how many steps a compound can shave off a full synthesis route. Lab teams find themselves coming back to 2,3,5-Trichloropyridine for this very reason. Its stable molecular structure holds up under diverse conditions, allowing selective substitutions or further halogenations with high yields. The ability to avoid side reactions is a big part of why it’s chosen over compounds with less predictable profiles.
One of the key talking points about 2,3,5-Trichloropyridine lies in its broad usage. I’ve watched research groups seek out multi-chlorinated pyridines as building blocks for novel herbicides, fungicides, and pharmaceuticals. A compound crossing into different industries shows staying power, and this one does just that. Agrochemical synthesis often needs intermediates that won’t interfere with thermal stability or environmental fate. Here, the triple-chlorine signature opens possibilities that a mono- or dichloro analog just can’t.
In the pharma industry, the necessity for well-defined intermediates takes on added significance. Drug development depends on controlling every aspect of structure–activity relationships. With 2,3,5-Trichloropyridine as a starting point, one can build nitrogens or modify ring positions without awkward detours. Several antihistamines, anti-inflammatory agents, and even kinase inhibitors have chemical ancestry tracing back to chlorinated pyridines.
Veterinary medicine circles around the same core requirements, needing robust intermediates for compound libraries. Agricultural scientists, meanwhile, count on this compound to support next-generation pesticides. Traceability and reproducibility matter; inconsistencies at this stage ripple through entire supply chains. Here’s the crux—a consistent batch of 2,3,5-Trichloropyridine helps keep timelines and results predictable.
Experience working with a range of halogenated pyridines taught me a few simple truths. Minor changes in substitution patterns on the pyridine ring have outsized impacts on how a compound behaves. For example, 2,3,5-Trichloropyridine often outperforms its 2,4,6-trichloro sibling in cross-coupling reactions, especially under milder catalytic conditions. Its unique arrangement of chlorines leaves certain positions open for selective nucleophilic attack, letting chemists get more creative with less risk of unwanted rearrangements.
Physical properties also matter in practice. Some similar compounds form sticky oils, or draw moisture from air, complicating storage and. In day-to-day lab work, no one wants chemicals that change texture between weighing and mixing. 2,3,5-Trichloropyridine stays stable, doesn’t clump, and pours easily. That might sound like a minor perk, but in a production environment juggling tight deadlines, it matters a lot.
Drilling down into cost-effectiveness, another factor sets this compound apart. The process routes for making 2,3,5-Trichloropyridine require less harsh reagents than some other trichlorinated variants. This cuts back not just on raw material expenses, but also on waste disposal costs—a growing focus area for sustainability managers and regulatory bodies. Over the years, regulatory oversight for chemical intermediates deepened, with demands for transparency and auditability. Compounds produced through gentler methods stand out, not just for the feel-good narrative but for clear, trackable impacts on compliance.
No chemical, no matter how reliable, comes without its complications. One issue often raised in procurement is batch-to-batch consistency. Many suppliers claim high purity but can’t always back that up if you request independent verification. We ran into this gap during a contract synthesis, where a batch variation threw off downstream steps. 2,3,5-Trichloropyridine, when sourced from established production lines, keeps such incidents to a minimum. Producers with robust purification processes, and good quality control, allow research teams to breathe easier.
Scaling up from bench to pilot plant introduces its own headaches. Reaction exotherms and solvent management climb up the list of concerns for multi-kilo batches. 2,3,5-Trichloropyridine’s standard process tolerates a bit more heat than analogs, meaning plant operators can avoid unplanned shutdowns. At a time when many facilities run lean on experienced technicians, the margin of error makes a real difference.
Whenever I step into a production meeting, I see how often the question comes up: can a critical intermediate, like 2,3,5-Trichloropyridine, be supplied on short notice? Global logistics wobbled during recent years, highlighting the risk of relying on single-source suppliers. Chemical buyers know this and have grown more detailed in their vetting. The best-equipped suppliers offer clear traceability, thorough documentation, and stable lead times. Chemicals that hit those marks—this one included—move to the front of the line.
The chemical industry reached a turning point, where environmental compliance is no longer an afterthought. Halogenated compounds still draw scrutiny due to their persistence in ecosystems. As such, buyers examine both the synthetic steps and the waste treatment options for products like 2,3,5-Trichloropyridine. I’ve seen companies partner directly with suppliers to ensure closed-loop production, solvent recycling, and minimal discharge during manufacturing.
From a regulatory perspective, responsible partners make a habit of updating safety data sheets, labeling, and transport certificates. I’m convinced that proactive communication heads off most compliance puzzles. Finished products derived from 2,3,5-Trichloropyridine may enter animal feed, pharmaceuticals, or crop protection markets—places where regulators dig into provenance and impurity profiles. Foresight here means anticipating and adapting to tightening global standards, not scrambling reactively.
People working in labs and production plants expect—and deserve—products that check both boxes: high performance and low risk. Environmental-auditing teams request batch documentation, material origins, and disposal practices. Suppliers willing to share that data openly build trust fast. That transparency can make all the difference in an audit or market recall situation. From my time spent on compliance projects, I learned customers rarely forgive producers who treat documentation as an afterthought.
New chemical products fuel real advances in medicine and agriculture, but every discovery rides on the reliability of core intermediates. 2,3,5-Trichloropyridine, versatile and predictable, acts almost like a toolkit for chemists hunting for new pathways. Its layout on the pyridine ring makes it an excellent candidate for Suzuki coupling, Buchwald-Hartwig amination, and other essential transformations. Many teams favor it for these reactions because yields stay high and workups run cleaner than with more congested or less symmetric isomers.
I spent years working with development chemists who measured materials by their track record, not just a spec sheet. The trust earned by a compound like this comes in part from its track record on real-world projects: synthesizing crop-safe pesticides, generating lead-compound libraries for new pharma targets, or, just as importantly, providing a stable control reference to calibrate analytical equipment.
Longevity in the chemical market means adaptation. Suppliers who listen to what researchers want—tighter particle size distribution, custom packaging, tailored solvent recovery protocols—find repeat business. 2,3,5-Trichloropyridine continues to fit the evolving needs of chemical enterprises because its core benefits align with both traditional and next-generation production requirements.
For chemists looking to sidestep common pain points, one approach centers on robust supplier relationships. Instead of rotating between sources, teams that invest time in certifying one or two proven suppliers can negotiate for batch reservations, process insight, and support with regulatory paperwork. I’ve seen this pay off in time saved and headaches avoided down the line.
Another solution is investing in analytical redundancy. Relying on a single assay type sometimes lets minor impurities slide through. By developing a panel of analytical methods—GC, HPLC, and NMR—researchers can fingerprint each incoming batch, catching inconsistency fast.
On the sustainability front, forward-thinking labs evaluate greener synthesis alternatives. Organic chemists and process engineers now collaborate more than ever, iterating on pilot reactions to reduce overall chemical footprints. 2,3,5-Trichloropyridine, which already features less resource-intensive production, offers a good example for incremental gains—like switching to closed-loop wash systems or fine-tuning solvent recapture.
For those working to future-proof procurement, digital tracking stands out. Introducing digital batch tracking and automated certificate confirmation cuts manual error out and brings traceability sharply into focus. More players in the chemical supply chain are moving this way as regulatory demands and end-user expectations inch higher.
I can’t count how many teams I’ve seen slowed down by unreliable intermediates. In a world where new agrochemicals and pharmaceuticals need to clear higher bars for purity and documentation, leaning on proven, consistently pure chemicals saves both time and budget. 2,3,5-Trichloropyridine checks all the technical boxes—stable at room temperature, handles well in solution or in bulk, and behaves predictably even in novel synthesis protocols.
Set against other trichlorinated pyridine isomers, this one stands out for its combination of physical manageability and reactivity. While every synthetic pathway brings unique challenges, compounds that limit unwanted branching or troublesome by-products win favor with process chemists and auditors alike. My own work drove home the lesson again and again—having dependable access to key intermediates marks the difference between a stalled timeline and a breakthrough.
Looking ahead, the value of solid production and responsible sourcing will only grow. End-users now weigh more than just chemical performance—they look for supply resilience, environmental soundness, and solid documentation. 2,3,5-Trichloropyridine succeeds on these fronts by standing as a quietly indispensable piece of the broader industrial and research puzzle.