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HS Code |
985672 |
| Productname | 2-chloro-3-(trifluoromethyl)-4-iodopyridine |
| Casnumber | 1211510-84-1 |
| Molecularformula | C6H2ClF3IN |
| Molecularweight | 307.44 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 42-46°C |
| Purity | Typically ≥97% |
| Smiles | C1=CN=C(C(=C1I)C(F)(F)F)Cl |
| Inchi | InChI=1S/C6H2ClF3IN/c7-4-2-11-3-5(12)6(4)1(8,9)10/h2-3H |
| Solubility | Soluble in DMSO, dichloromethane |
| Storageconditions | Store at 2-8°C, in a dry and dark place |
| Synonyms | 4-Iodo-2-chloro-3-(trifluoromethyl)pyridine |
As an accredited 2-chloro-3-(trifluoroMethyl)-4-iodopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 5 grams, tightly sealed with a screw cap, labeled with "2-chloro-3-(trifluoromethyl)-4-iodopyridine" and safety information. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packed drums of 2-chloro-3-(trifluoroMethyl)-4-iodopyridine, ensuring safe, moisture-free transportation. |
| Shipping | 2-Chloro-3-(trifluoromethyl)-4-iodopyridine is shipped in tightly sealed, chemically resistant containers, under dry and cool conditions. It is classified as a hazardous material due to halogen content; packaging ensures protection from moisture, heat, and light. Appropriate labeling and documentation are included, and transport complies with all relevant regulatory guidelines. |
| Storage | 2-Chloro-3-(trifluoromethyl)-4-iodopyridine should be stored in a cool, dry, and well-ventilated area, tightly sealed in a compatible container. Keep away from heat, ignition sources, and incompatible materials such as strong oxidizers or acids. Store under inert atmosphere if possible. Label clearly, and restrict access to trained personnel only. Avoid exposure to moisture and direct sunlight. |
| Shelf Life | 2-Chloro-3-(trifluoromethyl)-4-iodopyridine is stable for at least 2 years when stored cool, dry, and in tightly sealed containers. |
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Purity 98%: 2-chloro-3-(trifluoroMethyl)-4-iodopyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal by-product formation. Melting point 68°C: 2-chloro-3-(trifluoroMethyl)-4-iodopyridine with a melting point of 68°C is used in organic process development, where it facilitates controlled crystallization and reproducible batch quality. Molecular weight 325.47 g/mol: 2-chloro-3-(trifluoroMethyl)-4-iodopyridine at molecular weight 325.47 g/mol is used in medicinal chemistry programs, where it enables accurate stoichiometric calculations for target compound synthesis. Solubility in DMSO 50 mg/mL: 2-chloro-3-(trifluoroMethyl)-4-iodopyridine with solubility in DMSO at 50 mg/mL is used in high-throughput screening libraries, where it supports effective compound dispersion in assay systems. Stability temperature 25°C: 2-chloro-3-(trifluoroMethyl)-4-iodopyridine with stability at 25°C is used in storage and logistics for chemical reagents, where it maintains product integrity during ambient handling. |
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Developing 2-chloro-3-(trifluoroMethyl)-4-iodopyridine at manufacturing scale presents technical hurdles and satisfaction few outside the plant floor can imagine. Our chemists, equipped with hard hats and process histories, know firsthand what it takes to bring such a specialty pyridine derivative past bench scale and into consistent large-batch output. We navigate complexities beyond chemical equations: reaction temperature swings, exotherms unique to halogenated pyridines, waste stream toxicity, and the finicky habits of intermediates bearing both iodine and trifluoromethyl groups.
Chemical producers who fabricate these molecules routinely—rather than simply move drums—bring a level of practical insight shaped by experience. Operational tweaks are not just theoretical; they become hard-won process adjustments that drive yield and reduce impurity carryover. In a recent campaign, we tracked the influence of subtle moisture changes on halogen exchange. By tuning our solvents and monitoring every kiloliter, we caught issues that would otherwise result in colored off-spec product. These are challenges distributors rarely face, but every batch number represents hundreds of such interventions and validations.
2-chloro-3-(trifluoroMethyl)-4-iodopyridine carries the formula C6H2ClF3IN. Both the electron-withdrawing trifluoromethyl group at the 3-position and the bulky iodine at the 4-position make this pyridine more than just another halopyridine. Nucleophilic substitution reactions behave differently here. The placement of each functional group influences not just reactivity but also physical handling: volatility, solubility, and even odor mark the difference between a well-made product and a batch destined for reprocessing.
We control air moisture and select non-reactive glassware—our engineers know halogenated intermediates demand thorough purging between runs or previous residues shift kinetics and color. Experience dictates how to scale up—using the right agitation, monitoring hydrogen fluoride byproducts, and filtering with caution. Fluctuations visible in the lab magnify exponentially with scale, impacting isolation efficiency and recovery of high-purity product. Over years, our R&D and plant operators have exchanged notes, fine-tuned batch records, and invested in controls to push yields well above what can be quoted from textbook procedures.
This compound’s combination of a trifluoromethyl group and an iodo substituent gives it a rare reactivity profile. Many pyridine derivatives use only lighter halogens, leading to differences in downstream applications and process safety. Handling molecular iodine, at scale, brings distinctive logistics. The resulting compound’s density, melting range, and reactivity with aryl boronic acids take a separate approach than common dichloro- or difluoro-pyridines. Our plant teams have repaired heated lines frozen by accidental iodine precipitation—problems seldom seen in lighter analogues.
Comparing with methylated or only fluorinated pyridines, 2-chloro-3-(trifluoroMethyl)-4-iodopyridine offers not just alternate reactivity but also unique synthetic routes: palladium-catalyzed couplings, site-selective metalations, and functional group interconversions. The steric bulk and electron-withdrawing effect make possible Suzuki-Miyaura and Buchwald–Hartwig reactions that fail for related structures. Medicinal chemistry teams often come to us after high-throughput screening, frustrated with failed analogues. We work together to examine the product’s spectral identity, batch contaminants, and how these influence subsequent cross-couplings. Every new active ingredient synthesized downstream becomes a testament to the compound’s laboratory and plant history.
Quality isn’t a promise written on a data sheet; it’s the product of process control sheets stained by time on the production floor. Spectroscopic purity above 98% by HPLC, water content tailored below 0.2%, and single-digit ppm heavy metals—these numbers mean something only when they stand up to actual process and customer feedback. Fulfilling a custom kg-scale order with exceptionally low residual chloride content took us six trial batches, several nights’ overtime, and countless communication loops between process, QC, and logistics. The solution, as always, emerged from direct engagement with both equipment and chemist.
Batch homogeneity and impurity profiles are informed by dozens of GC and NMR profiles we’ve accumulated. Spectroscopic quirks—trace impurities from incomplete halogen exchange, unexpected peaks near 7.4 ppm—draw our attention every cycle, since even minor contaminants can sabotage catalysts later. One advantage comes from the way we maintain plant discipline. By dedicating glass-lined vessels to pyridine halide syntheses, cross-contamination is kept under control better than in plants that switch from commodity products to specialties week by week. QC technicians sample at every stage. They’re not just following SOPs but responding in real time—changing solvent ratios or altering purge routines based on smell, color, or foam in the sample jar.
Most buyers of 2-chloro-3-(trifluoroMethyl)-4-iodopyridine run sophisticated, multi-step syntheses. Medicinal and agricultural chemists seek out this compound for late-stage functionalization of lead molecules, often using cross-coupling reactions. Some apply it as a precursor for kinase inhibitor development or in discovering new pesticide scaffolds. Our involvement rarely ends at the invoice. We are called upon to troubleshoot formation of side products, advise on solvent swaps, and share samples analyzed by our own LCMS. It’s not uncommon for us to adjust our process in direct response to customer feedback—each application suggesting ways to shave down byproducts or fine-tune the particle size for specific filtration setups.
Unlike distributors with standard offerings, our batch records form the basis for process audits and regulatory filings by our clients. It’s a point of professional pride to supply not just material, but a record—raw data, full spectral prints, stability notes from real-time storage studies—to support IND or regulatory submissions. We document even minor irregularities, not because the form requires it, but because these observations help our customers avoid expensive reruns and surprises at developmental scale. In one global agrochemical project, sharing our GC-MS profile helped downstream partners eliminate a persistent impurity that had plagued screening efforts for months.
The route to 2-chloro-3-(trifluoroMethyl)-4-iodopyridine involves halogenated reagents, some of which pose environmental and health hazards if not controlled properly. As manufacturers, we move beyond legal minimums. We audit effluent regularly for iodine and fluorine release, investing in dedicated scrubber systems to neutralize emissions before discharge. Redesigning the quench process trimmed iodine loss by half after a year-long study. In parallel, we’ve trained every staff member handling reagents in spill drills—not because regulations stipulate it, but because a single careless moment can threaten both safety and reputation. Community health and long-term business both rise or fall with these disciplined practices.
Waste minimization presents ongoing challenges for halogenated organic syntheses. On multiple occasions, we’ve stopped a process mid-run to address reactors showing higher-than-expected color or thickening—often the precursors of problematic byproduct build-up. Fine-tuning reagent stoichiometry, pushing filtrates through custom-designed columns, and relentless record-keeping let us minimize off-spec output. When possible, spent iodide is collected for recovery and reuse, sparing both raw material costs and environmental impact. Our sustainability goals push us to stay abreast of green chemistry trends, but every improvement comes against real-world chemical and cost constraints. We put these lessons into new projects, always looking for the incremental gain—a lower ppm emission, a safer transfer method, another byproduct routed to recycling instead of incineration.
There’s a gulf between what’s published in journals and what works at scale. In development, theoretical yields rarely match the numbers that come off our plant floor. Every new scale-up begins with uncertainty: not just will the chemistry hold, but how will batch-to-batch variation, vessel material, and scale-dependent heat transfer affect the actual outcome? We study impurity drifts and product tendency to crystalliize unexpectedly at chilldown. Our staff’s years producing halopyridines let us anticipate bottlenecks that slow others: from insoluble byproduct layers that foul filters to unexpected color shifts suggesting trace oxidation. Each run teaches us something new about this compound’s temperament.
Learning what every parameter means in practical terms drives continuous improvement. Temperatures that seem trivial on the heat map turn process critical when a ten-degree bump doubles side reactions. Our veteran operators keep their eyes— and noses—alert to subtleties that don’t show up in electronic logs. Shifts in odor, foam, or color during solvent partitioning signal tiny changes that flag potential headaches downstream. Tracking this “soft data” alongside rigorous analytics generates a database of both human and machine wisdom—a resource few external stakeholders appreciate.
Many of our buyers run into challenges beyond their control: process shifts at scale, unplanned side reactions, regulatory questions. We act as technical partners to help untangle these issues. We don’t send anonymous samples; we send back annotated spectra and raw data, highlight the quirks in halogen balance in every lot, and offer batch-specific observations that arm process chemists with practical knowledge. This goes hand-in-hand with our commitment to problem-solving as new platforms or synthetic routes push the boundaries of what our old SOPs allow.
Feedback from the field regularly drives refinement. In one instance, a pharma customer’s struggles with poor palladium catalysis led to a collaborative effort. We examined minor impurity peaks, tested small changes in the carrier solvent, and ultimately made a process tweak improving cross-coupling conversion rates. Such interactions move both our QC and production teams forward, informing subsequent batches and sometimes shaping future SOPs. We benefit from sharing high-resolution identifiers and alerting clients to even marginal lot-to-lot drifts that might otherwise escape attention.
Experience as a manufacturer leaves no space for ambiguity. Each kilogram of 2-chloro-3-(trifluoroMethyl)-4-iodopyridine shipping from our site comes with a backstory of dozens of runs, hundreds of batch checkpoints, and constant engagement with the science behind the formula. We see this compound not as a simple reagent, but as an exercise in applied problem-solving: from raw material purity through emissions control to the subtle art of balancing yield against byproduct minimization.
Real-world production challenges, troubleshooting at scale, and the constant struggle to reconcile lab findings with operational practicalities build a product that meets high expectations in terms of both purity and reliability. These lessons—earned through sweat, mistakes, and collaboration—define our difference as a chemical manufacturer rather than a middleman. By sharing what we learn, adapting to specific customer feedback, and investing in sound process safety and environmental responsibility, we contribute meaningfully to the industries driving chemistry forward.
For those who require not just reliable material, but also direct access to the knowledge and discipline behind every bottle, our product and partnership stand ready for the next challenge.