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HS Code |
154802 |
| Product Name | 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine |
| Cas Number | 887267-93-6 |
| Molecular Formula | C6H2ClF3IN |
| Molecular Weight | 323.45 |
| Appearance | Light yellow to brown solid |
| Melting Point | 42-46°C |
| Density | 2.13 g/cm3 (estimated) |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents such as DMSO and DMF |
| Smiles | C1=CN=C(C(=C1I)C(F)(F)F)Cl |
| Inchi | InChI=1S/C6H2ClF3IN/c7-5-2-11-3(1-4(5)12)6(8,9)10/h1-2H |
As an accredited 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine is supplied in a 5-gram amber glass bottle with a tamper-evident seal. |
| Container Loading (20′ FCL) | 20′ FCL can load about 12 metric tons of 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine, packed in 25kg fiber drums. |
| Shipping | 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. It is transported as a hazardous material, following all local and international regulations for hazardous chemicals. Appropriate labeling, documentation, and safety measures—including secondary containment—are used to ensure safe delivery. Store in a cool, dry, well-ventilated area upon receipt. |
| Storage | Store 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep away from incompatible substances such as strong oxidizers and bases. Ensure proper labeling and adhere to local regulations for hazardous chemicals. Use appropriate personal protective equipment when handling to avoid inhalation or contact. |
| Shelf Life | 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine is stable under recommended storage conditions; typically, its shelf life exceeds two years. |
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Purity 98%: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield reaction efficiency. Melting Point 62°C: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine with a melting point of 62°C is used in chemical research, where it offers controlled thermal behaviour during compound formulation. Moisture Content <0.2%: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine with a moisture content below 0.2% is used in agrochemical development, where it prevents unwanted hydrolysis and improves product stability. Stability Temperature 25°C: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine with stability at 25°C is used in laboratory storage conditions, where it maintains chemical integrity over extended periods. Molecular Weight 327.45 g/mol: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine of molecular weight 327.45 g/mol is used in heterocyclic compound synthesis, where it allows for precise stoichiometric calculations. LCMS Purity ≥99%: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine with LCMS purity of 99% or greater is used in analytical reference standards, where it guarantees reliable quantitative analysis. Particle Size <10 μm: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine with particle size less than 10 μm is used in advanced material formulation, where it enables superior dispersion in solvent systems. Residual Solvent <500 ppm: 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine with residual solvent content under 500 ppm is used in electronic chemical manufacturing, where it reduces risk of contamination in sensitive processes. |
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Experience in the factory has taught us there’s a difference between a product you meet on paper and the one you see every day on the line. With 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine, the distinction goes beyond raw numbers or phrases you’d find in a catalog. In the plant, every batch gives us a close look at how the right molecular choices can support tough projects in pharmaceutical and agrochemical research. As specialists in halogenated heterocycles, we produce this compound to meet the real-world challenges scientists face in late-stage functionalization and core scaffold design. Handling and producing this material in bulk or small scale brings its own lessons, and we carry those into the way we deliver consistent quality from drum to drum.
Everything starts with an understanding of what matters in the lab and the field. Years working on pyridine derivatives have shown us that bringing together multiple halogen substitutions on a single ring can open up unique reactivity patterns. The combination of chlorine and iodine atoms in distinct positions on the pyridine ring provides chemists with versatile sites for further coupling or halide exchange. The trifluoromethyl group introduces steric and electronic effects that can't be replicated by simple methyl analogs. Our customers often discuss how the interplay between these functional groups can drive selectivity in cross-coupling reactions or extend the lifespan of active pharmaceutical ingredients through fluorination. Bringing reproducibility to the synthesis process makes a difference in how you tackle SAR projects or scale up pilot runs.
On the shop floor, equipment handles different solvents and temperatures well only when every parameter is controlled. We've found that issues commonly crop up if the starting material purity drops or reaction work-up procedures aren't rigorous. We use high-purity starting reagents, continuous monitoring by HPLC and NMR, and regular in-process controls. When scales shift from grams to kilograms, stirring speed, reagent addition rate, and in-process checks become even more critical. There’s no hiding behind standard sheets — you notice small shifts in color or exotherm and act immediately, because any minor variation can cause unwanted impurities or reduced yield.
We judge performance by results, not slogans. Our batches of 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine typically achieve purity specifications over 98% by HPLC, with iodide and chloride confirmed by established chemical testing methods. Every shipment’s analytical data is available for customer review, taken from real production strips, not stock photos or cut-and-paste spreadsheets. Instead of using speculative or generic claims, we connect directly with our partners about methods, troubleshooting, and scale needs when they arise. Over the years, this has earned us long-term collaborations with large and small research teams, many of whom return for repeat orders.
The intricacies of this molecule lie in its asymmetry and substitution pattern. Unlike simpler mono-halogenated pyridines, which can flood the market by volume, our compound delivers both a strong electron-withdrawing group and two halogen handles for increased reactivity. In Suzuki–Miyaura or Buchwald–Hartwig couplings, researchers have reported sharper yields and higher reliability compared to single-halogen analogs. Many of our customers prefer it because of better substrate control when building more complicated libraries for structure–activity relationship studies. Feedback we get stresses that the presence of both iodine and chlorine atoms permits orthogonal chemistry, which allows stepwise functionalization strategies that speed up the discovery process.
Any manufacturing company will promote high purity as a selling point. What matters more is how purity impacts downstream chemistry. Our reviews with synthetic chemists consistently note that even trace levels of non-pyridine impurities or unreacted halide can block tough coupling reactions or cause costly side-products. The usual suspects, such as bipyridine contaminants or incomplete halogenation side chains, receive special attention in our workup process. Beyond instrument readouts, experienced staff routinely test small trial reactions with every batch, catching any real-world differences early and making refinements before the product leaves the plant.
Researchers tackling modern drug or crop protection projects turn to 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine for its proven performance as a reliable intermediate. Over the past decade, the demand for highly functionalized building blocks has grown as new targets and regulatory requirements shape the future of chemical development. Compared with less substituted pyridines, this compound stands out in high-throughput and diversity-oriented synthesis, where orthogonality is a must.
Our clients have used it in key steps for pharmaceuticals such as kinase inhibitors or antifungals, leveraging the robust halogen exchanges and stability under both acidic and basic conditions. In crop science, research groups appreciate its ability to anchor bioactive fragments while providing multiple points for later derivatization. The trifluoromethyl group adds metabolic stability, a common request from teams involved with lead optimization projects.
We regularly hear from labs that the compound’s reactivity profile saves them weeks in hit-to-lead programs. They cite how standard mono-functionalized analogs require additional protection/deprotection steps, wasted time, and yield losses. Our product answers these concerns by providing a direct entry point to cross-couplings, halogen-exchange, and palladium-catalyzed aminations without added synthetic gymnastics. One of the main requests we supported in the early days was the transition from time-consuming, multi-step lab synthesis to straightforward stockroom access.
Seeing the same compound produced by different manufacturers, experienced chemists can tell who's serious from batch consistency and transparency. We don’t cut corners by using recycled reagents or inferior solvents. Instead, we invest in robust purification methods such as chromatography and fractional crystallization for each lot, going beyond the basic single-pass trituration used by generic producers. Our facility operates with closed-system handling for hazardous iodinated intermediates, which reduces cross-contamination and loss, especially for sensitive halogen stocks. Temperatures and stir rates are logged for transparency, and all operators remain trained in the specifics of pyridine handling to prevent drift in product specification over time.
Comparing with competitors’ materials, the difference comes up not only in purity percentage but also in real-life performance. For instance, while some third-party sources offer similar molecules (like 2-chloro-5-(trifluoromethyl)pyridine or 2-iodo-5-(trifluoromethyl)pyridine), these lack the dual reactivity sites and don’t facilitate as much flexibility in sequential transformations. Chemists needing to introduce amine, aryl, or alkoxy groups at precise positions find they avoid dead ends or rearrangement risks by using our dual-halogen compound. Rapid and predictable halogen exchange or oxidative coupling becomes routine, which gives projects dependable throughput.
Differentiation isn’t a marketing game for us: it’s the result of careful process stewardship and feedback from continuous use in diverse application settings. Several partners have run side-by-side pilot tests, measuring reaction performance and downstream impurity profiles. Results have consistently favored our batches due to lower ppm levels of common side-products, which streamlines purification and regulatory compliance during scale-up. The traceability and open communication we provide, from synthesis protocol to lot history, underpin these real differences.
Reliable supply of halogenated heterocycles doesn’t happen by chance. Over the years, our team has refined process controls to address bottlenecks that frequently challenge the industry. The synthesis requires careful control of temperature and timing to avoid over-halogenation or side-product buildup. Each lot faces quality reviews for not just the main compound, but byproducts and trace organohalides, using mass spectrometry and NMR as part of our standard battery of checks. Sometimes a shift as minor as source variation in the iodine can introduce batch-to-batch inconsistency, which we catch and resolve through early supplier audits and materials testing on-site.
Scaling up halogenated pyridines comes with its own risks. For example, exothermic steps in the halogen exchange stages can become runaway if the reactant flow isn’t metered with care. Our technical staff manage these transitions manually and through automated monitoring, preventing dangerous heat-up scenarios and ensuring reproducibility for every kilogram produced. Every production run generates a full reaction log retained for audit and review. Assembly-line knowledge, built from dozens of repeated cycles, strengthens our ability to solve problems before they affect the end-user.
Another common problem arises during crystallization and drying. Products like this can attract atmospheric moisture or trap residual solvents. Routine testing after workup checks water content and residual solvent levels, ensuring the material leaves the factory shelf-stable and suitable for direct use in bench chemistry. Customers expect that each shipment opens to the same crystal free-flow as in their last order. If practical concerns surface, such as clumping during transport or minor color variation, our team investigates root causes and refines downstream processing, sometimes adding secondary sieving or blending steps. Feedback loops remain direct, practical, and responsive.
Producing and moving halogenated organics comes with regulatory and safety responsibilities. We maintain compliance with local and international transport guidelines, particularly for hazardous materials and potential waste streams. In the last five years, tighter regulation of organofluorine and iodinated chemicals has increased the need for documented waste disposal and traceability. By staying updated with best practices, we lower environmental risk and assure continuous production, avoiding downtime or shipment delays caused by regulatory backlogs.
Solvent selection and recycling became key areas of improvement. Facilities deploy solvent recovery units for dichloromethane and acetonitrile, reducing the consumption of fresh solvents and minimizing emissions. Our plant layout keeps process streams separated to avoid cross-contamination, especially since trace residues of chlorine, iodine, and fluorinated byproducts carry their own handling and disposal protocols. Technicians train on spill response and correct personal protection to protect themselves and the environment. Each improvement reflects practical lessons learned across seasons, regulatory cycles, and changing product volumes.
Materials like 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine bring their own transport and storage rules, especially in larger-volume shipments. Correct labeling, secondary containment, and temperature management avoid issues like decomposition or cross-reactivity during transit. Downstream partners benefit from this diligence by receiving product ready for use, not compromised by preventable transport mistakes.
Many of our longest-standing relationships began as hands-on collaborations with research teams and manufacturing plants. It’s not rare to walk through a process issue or reaction optimization over the phone, in person, or through direct lab partnerships. Feedback on poorly performing reactions, unexpected side products, or storage challenges returns directly to our technical staff, who then mirror the same tests and conditions to track down the root cause.
We often share practical know-how with chemists launching pilot runs, troubleshooting palladium-catalyzed couplings, or examining post-reaction purification. Real insight doesn’t just come from reading specs, but from understanding why a batch may perform better in one coupling sequence versus another. For anyone starting out with this molecule, typical reaction sequences include direct arylations, aminations, or alkoxylations, each sensitive to minor contaminant levels or thermal history. Our track record rests on the trust that we’ll give more than a labeled bottle – we provide repeated, practical guidance based on our own production and use history.
No manufacturing journey is without its rough patches. Early production runs faced problems like inconsistent halide loading, crystallization failures, and occasional high-color fractions that worried some customers. Each challenge led to concrete improvements: switching to higher-grade reactants, adjusting solvent ratios, and refining physical handling to prevent caking or color drift. We invest in regular maintenance for all synth and post-synthesis equipment, and operators cross-train on both manual and automated systems. Batch records provide full transparency on temperature, reactant source, operator, and testing protocol.
We observed some customers attempted to adapt third-party materials for tough Suzuki or amination reactions, only to report problems such as variable solubility, incomplete conversion, or unexpected side products. Shared data from these cases became valuable for our own internal troubleshooting, and over several years, we cut both process impurities and lead times. These cycles of feedback, trial, and refinement remain central in our way of working.
Behind any specialty product, there are stories and people working long hours to get things right. Operators who handle synthesis and purification know by sight, smell, and process change when something isn’t up to par. Teams gather every week to review any batch deviations or customer notes, keeping the focus practical. Our approach gives an advantage, not only through advanced reactor systems or fancy analytics, but through staff who recognize the criticality of tiny details — a pH drift, a slight moisture uptick, a change in supplier reagent lots — and act immediately.
While automation and analytics grow every year, experienced technicians still make judgment calls that catch and fix issues before they reach a lab bench. Relying on this combination of technology and hands-on know-how has built resilience into the supply chain, reducing downtime and ensuring reliable, on-spec batches.
The market for complex halogenated pyridines keeps evolving, driven by demands for expanded functionality and compliance. As a manufacturer, agility and openness to new synthetic pathways prove vital. Our team regularly pilots new reagent strategies or purification methods to increase yield and reduce waste. Whether through continuous flow adaptation or “greener” solvents, the learning curve never really ends.
Several drug discovery groups now want customized substitutions or isotopic labeling for tracing and imaging applications. We work directly with them to scale up new derivatives or supply pilot lots tailored for fast-moving SAR studies. The ability to quickly shift or expand the range of available halogen patterns distinguishes real-world manufacturers from bulk-traders who simply buy and relabel.
The journey from raw materials to a bottle of high-purity 2-Chloro-4-iodo-5-(trifluoromethyl)pyridine is the product of practical experience and daily diligence, not just a set of numbers on a label. Real chemical manufacturing means every lot earns its reputation through repeated use, feedback, and adaptation. By pairing dual-halogen sites with a trifluoromethyl group in a single scaffold, this compound supports applications that simpler analogs can’t fulfill. The routine input from customers, process chemists, and plant operators keeps raising our own bar for performance. Our story with this product illustrates how tight focus on reliability, customization, and technical support leads to smarter research and faster discoveries — not by luck, but by experience at every step.