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HS Code |
454991 |
| Chemical Name | 2-bromo-4-iodo-6-(trifluoromethyl)pyridine |
| Molecular Formula | C6H2BrF3IN |
| Molecular Weight | 367.89 g/mol |
| Cas Number | 1236821-22-3 |
| Appearance | White to off-white solid |
| Melting Point | 72-76°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents like DMSO, dichloromethane |
| Smiles | C1=CC(=NC(=C1C(F)(F)F)Br)I |
| Inchi | InChI=1S/C6H2BrF3IN/c7-4-2-3(11)1-5(12-4)6(8,9)10/h1-2H |
| Storage Conditions | Store at 2-8°C, protect from light and moisture |
As an accredited 2-bromo-4-iodo-6-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "2-bromo-4-iodo-6-(trifluoromethyl)pyridine, 5 grams," with hazard symbols and safety instructions printed. |
| Container Loading (20′ FCL) | 20′ FCL container loads approximately 10 metric tons of 2-bromo-4-iodo-6-(trifluoromethyl)pyridine, securely packed in fiber drums. |
| Shipping | **Shipping Description:** 2-Bromo-4-iodo-6-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light, moisture, and heat. Package labeling follows relevant safety and hazardous material regulations. It is transported as a laboratory chemical, with documentation including SDS and handling instructions. Ensure compliance with local, national, and international shipping regulations for hazardous substances. |
| Storage | **2-Bromo-4-iodo-6-(trifluoromethyl)pyridine** should be stored in a cool, dry, well-ventilated area, inside a tightly sealed container. Protect it from light, heat, moisture, and sources of ignition. Keep it away from incompatible substances such as strong oxidizing agents. Store in a designated chemical storage cabinet, properly labeled, and out of reach of unauthorized personnel. |
| Shelf Life | 2-bromo-4-iodo-6-(trifluoromethyl)pyridine is stable for at least 2 years when stored in a cool, dry, airtight container. |
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Purity 98%: 2-bromo-4-iodo-6-(trifluoromethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures reliable reaction yields and minimal byproduct formation. Melting Point 58-62°C: 2-bromo-4-iodo-6-(trifluoromethyl)pyridine with a melting point of 58-62°C is used in solid reagent formulation, where stable solid-phase behavior facilitates consistent blending and storage. Stability Temperature up to 120°C: 2-bromo-4-iodo-6-(trifluoromethyl)pyridine stable up to 120°C is used in high-temperature cross-coupling reactions, where thermal stability prevents decomposition and ensures process integrity. Molecular Weight 367.89 g/mol: 2-bromo-4-iodo-6-(trifluoromethyl)pyridine with molecular weight 367.89 g/mol is used in medicinal chemistry research, where precise molecular mass aids in accurate dosage design and mass spectrometry analysis. Particle Size < 100 µm: 2-bromo-4-iodo-6-(trifluoromethyl)pyridine with particle size below 100 µm is used in catalyst preparation, where fine particle distribution enhances dispersion and promotes catalytic efficiency. |
Competitive 2-bromo-4-iodo-6-(trifluoromethyl)pyridine prices that fit your budget—flexible terms and customized quotes for every order.
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Working with halogenated pyridines over the years, we recognize 2-bromo-4-iodo-6-(trifluoromethyl)pyridine as a specialty product that reflects both the potential and quirks of this unique compound class. Whenever our technical team handles this molecule, we treat it as more than just another catalog entry. The synthetic path, the way the trifluoromethyl group shapes the entire ring chemistry, and the reaction preferences set it apart from regular pyridine halides.
We manufacture this compound in-house, starting from high-purity pyridine derivatives and working through precise halogenation and functional group interchanges. The final result is a crystalline solid, carefully isolated to avoid cross-contamination or compositional drift. Each lot is tracked from raw materials, and we standardize controls specifically for this molecule’s unique coordination properties. Our reactors handle the volatility of trifluoromethyl-substituted intermediates, and our purification teams anticipate higher boiling points and less predictable solvation behaviors compared to simpler chloro- or bromo-pyridines.
Research and development labs have come to rely on this molecule’s bromo and iodo arrangement as a gateway to more complex scaffolds. Chemists find that having both the bromine and iodine on the same pyridine ring, alongside the electron-withdrawing trifluoromethyl, opens up possibilities for sequential cross-coupling on a rigid but tunable backbone. The regioselectivity gives them a tool for stepwise elaboration, particularly for pharmaceutical and advanced agrochemical research. We’ve had customers walk us through pilot results where they exploit this exact combination to build poly-heterocyclic frameworks or introduce rare fluorinated motifs.
Not every halogenated pyridine goes through Suzuki or Buchwald coupling as smoothly as this one. The presence of iodine lowers the activation barrier for oxidative addition, giving synthetic chemists a handle for high-yielding reactions under mild conditions. We’ve seen it reduce the need for extreme temperatures or exotic ligands. On the other hand, the bromine serves those who wish to stagger functionalization steps, introducing orthogonality and allowing careful orchestration of target assembly. We supply material to labs synthesizing kinase inhibitors and custom ligands, who need this selectivity for Step A, then demand compatibility for radical or metal-mediated processes in Step B.
The trifluoromethyl group doesn’t just influence lipophilicity — it also stabilizes certain intermediates, helps in modulating basicity, and increases the metabolic stability of downstream drugs or probes. From a manufacturing view, the CF3 group can lengthen the reaction time or lower solubility in routine solvents. We consider the whole process chain, not just the end-point purity. This has led us to fine-tune our processes — slower addition rates, controlled agitation, and limited exposure to moisture, so the integrity of both halide positions and the trifluoromethyl remains uncompromised.
It’s easy to list out the common points of comparison: melting point, assay percentage, or structural purity. These matter. Buyers ask for the CAS number and want reassurance that the lot matches the literature. But as the manufacturer, what stands out in daily operations is the unpredictability that can come from minor batch-to-batch variables if one’s controls are loose. We’ve had our share of process hiccups in the early days — tiny amounts of unreacted starting pyridine can hamstring downstream coupling, and residual water content can cause byproduct formation. Our batch analytics do not rely solely on external labs; we run NMR and HRMS in-house and catch minor degradants early on, before they reach the drum.
Compared with more basic bromo- or iodo-pyridines, this compound pushes facility expertise. Handling heavier halogens like iodine as both reactant and leaving group requires robust corrosion management and fume extraction. Operators need safety training not only for bromine handling but for the byproducts of mixing fluorinated organics and strong bases or acids. In the past, we learned that assuming a standard protocol for all pyridine derivatives leads to problems; our guys review job tickets and follow procedures tailored for the quirks of 2-bromo-4-iodo-6-(trifluoromethyl)pyridine.
Competitors sometimes produce similar molecules with focus on speed and nominal yield. Our experience tells us that shortcuts — skipping purification or batch-aging steps — sacrifice shelf stability or introduce detectable impurities which later turn up in clients’ analytical workups. Real-world chemical process work means dealing honestly with crude product stabilization, container compatibility (we use glass or HDPE, not soft plastics), and packing under inert atmosphere when required.
We base specification sheets on in-lab testing and years of accumulated shipment feedback, not just industry standards. The typical product comes with an assay at or above 98 percent, single-spot TLC, and phase-pure characterization by NMR, IR, and LC-MS. Recognizing that some buyers use the product for trace-metal-catalyzed reactions, we monitor for heavy metal content and residual halide impurities. If a particular client’s synthetic sequence is sensitive to trace organoiodides, we adjust our purification pass or offer analytical support.
Buyers sometimes compare it to 2-bromo-4-chloro-6-(trifluoromethyl)pyridine or 2,4-dihalo-pyridines without the trifluoromethyl. While some physical behaviors overlap, the iodo substitution brings distinct synthetic pathways, especially for late-stage functionalization. The electronic effect of the CF3 group is non-trivial; it sets our product apart from less polar or non-fluorinated derivatives. We witness, in our own pilot batches, how adjusting one group changes reactivity, color, and long-term stability in storage.
We provide typical lot sizes from single grams to multi-kilogram runs, always with explicit documentation. Purchasers working in regulated pharmaceutical R&D have options for audited batch records. Early-stage startups looking for small-scale tries get the same material as major companies; we don’t downgrade our lots or run offcuts to new customers.
More than once, we’ve seen researchers request direct substitutes, only to loop back after running their hands-on experiments. Some learned the hard way that lower-purity material or alternate halogen positions result in difficult separations or failed key-couplings. In conversation, discovery chemists relate stories of “mystery impurities” from off-brand suppliers which turned out to be unseparated byproducts from the initial halogenation stage, not accounted for in generic certificates. For us, hands-on control of every batch helps avoid those pitfalls. Technicians keep logs and perform checks instead of relying on “average process” claims.
Shipping and storage pose their own set of challenges. Iodinated molecules, especially those with trifluoromethyl groups, can interact with packaging or absorb atmospheric moisture more than the basic bromo- or chloro-pyridines. Over years of trial and error, we came to prefer certain packaging geometries and seals, always using freshly conditioned material for packing. Warehouses track shelf life closely and prioritize cool, dry conditions. If a major order sits for more than a month, our protocol includes rechecking purity and running additional analytics; we never consider unopened containers “good as new” by default.
Some customers have come to us after encountering solid caking, minor polymorphic changes, or color shifts after receiving other suppliers’ product. In those discussions, our team reviews potential causes such as trace moisture ingress or side-reactions and proposes solutions, whether it’s switching to smaller packing units for quick consumption or preparing the batch fresh to order. We aim for full transparency — letting buyers know the grade they’re getting and flagging any unusual findings directly, not just as footnotes.
A molecule like 2-bromo-4-iodo-6-(trifluoromethyl)pyridine draws users with its versatility. Labs exploring next-generation crop protection agents value the electron density changes from the fluorinated and halogenated positions. Those designing kinase inhibitors or protein interaction probes benefit from the mix of hydrophobicity and synthetic accessibility. We have witnessed synthetic chemists cut down months off their schedules because they can run both bromo and iodo couplings sequentially without laborious protection/deprotection cycles. Starting material costs and logistics pale beside the time saved in development.
Yet, the same cocktail of functional groups raises specific safety and waste disposal issues. The environmental impact of halogenated byproducts, particularly iodine- and bromine-containing residues, cannot be understated. As manufacturers, we maintain capture and neutralization systems in our effluent handling and educate downstream partners on responsible disposal. Emissions reporting and compliance monitoring are part of daily practice. We watch over our loading docks; solvent and halide waste never gets mixed or disposed of without proper tracking and neutralization — not just because of regulatory oversight, but because the true cost of shortcuts shows up eventually, in lost business or harm to local communities.
To minimize environmental load, we implement solvent-recycling programs and keep batch sizes matched closely to actual demand. Overproduction rarely happens; the nature of this market demands just-in-time runs and batch traceability. Working with regulatory consultants, our plant has designed processes to lower the use of highly toxic side reagents and to limit release of residual halide vapors. We update protocols in line with new research and ethical guidance, rather than scraping by with legacy documentation.
Years in specialty pyridine manufacturing have taught us to approach each order as a full-cycle commitment, from sourcing precursors to supporting end-users well after delivery. Customers sometimes require custom documentation, stability studies, or consults on optimizing their downstream chemistry. We’ve answered calls about filtering protocols, solvent compatibility, and downstream purification headaches. Our in-house chemists stay engaged so we can give practical, experience-based advice, not generic answers.
User feedback goes straight to our process engineers. Batch failures or shipping issues drive us to continuously improve. Once, a large customer encountered solubility variations due to a subtle crystal form shift; post-order, we adapted our recrystallization protocol and developed an extra stability check for all future lots. Our labs know that the needs of synthetic chemistry rarely pause for supplier learning curves — reliability and real-world usability keep plant operators as accountable as sales staff.
The choice of 2-bromo-4-iodo-6-(trifluoromethyl)pyridine over simpler alternatives comes down to the combination of advanced functionality and consistent, dependable quality. As a manufacturer, we see the mistake of viewing compounds as commoditized “building blocks.” Small variations in input materials, handling, or packaging lead to practical differences. We invite ongoing conversation and always welcome client feedback; improvements in our offerings always begin with what real users encounter at the lab bench and scale-up bay.
Standard dichloropyridines or difluoropyridines occupy a different synthetic niche, lacking the orthogonal leaving groups and the profound electron-withdrawing punch of the trifluoromethyl. 2-bromo-4-iodo-6-(trifluoromethyl)pyridine expands the boundaries for modular assembly, letting chemists tailor each halide position for specific cross-coupling partners or orthogonal transformations. Over years of conversations with formulation teams, we see the utility of these combined features, which drive patentable, differentiable end products.
Working with less elaborately halogenated pyridines rarely brings the same flexibility. The iodo group enables oxidative addition under milder conditions, reducing catalyst load and improving reaction times. Bromines hold for the next step, especially where regioselectivity counts. The CF3 group changes polarity, solubility, and biological profile, all at once. Our technical team spends less time troubleshooting unpredictability when batches are freshly made, well-packed, and checked daily for stability, letting users avoid headaches and focus on multi-step synthesis or lead optimization.
Responsibility for specialty building blocks like 2-bromo-4-iodo-6-(trifluoromethyl)pyridine doesn’t end once barrels roll out the door. Our documentation system gives buyers batch-specific data, chromatography results, and handling guidelines rooted in real-world experience, not just generic templated text. Process changes get flagged in advance to our customers. Any new lot runs side-by-side with established reference samples; we reject lots that don’t match or exceed benchmarks for purity and handling performance.
Every skilled operator working at our site understands the impact this molecule can have, for both high-value research and increasingly, for pilot-scale or early market product runs. They know it’s not just about scale or cost, but about reproducibility, safe handling, and genuine clarity about what’s in the bottle. Customers trust us because we’ve owned the process, solved problems, and been open about both mistakes and fixes.
We work with chemists daily — not as a faceless supplier but as process partners who grapple with the realities of halogen handling, pharmaceutical research timelines, and true compliance. Each batch comes from our workshops, refined by years of accumulated learning, and personal investment in every drum, vial, and gram we ship. That’s the difference we see: detailed, straightforward support for the challenges and ambitions customers bring when they work with 2-bromo-4-iodo-6-(trifluoromethyl)pyridine.