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HS Code |
605213 |
| Product Name | 5-(Bromomethyl)-2-(trifluoromethyl)pyridine |
| Cas Number | 161311-54-0 |
| Molecular Formula | C7H5BrF3N |
| Molecular Weight | 240.02 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥97% |
| Density | 1.638 g/cm3 (at 25°C, estimated) |
| Smiles | C1=CC(=NC=C1CBr)C(F)(F)F |
| Refractive Index | 1.500 - 1.520 (estimated) |
| Flash Point | 79°C (estimated) |
As an accredited 5-(Bromomethyl)-2-trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g chemical comes in a sealed amber glass bottle, labeled with product name, purity, CAS number, and hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL: Securely packed 160–200 drums (25 kg each) of 5-(Bromomethyl)-2-(trifluoromethyl)pyridine, on pallets, inside a 20-foot container. |
| Shipping | **Shipping Description:** 5-(Bromomethyl)-2-(trifluoromethyl)pyridine is shipped in tightly sealed containers, protected from light and moisture. Classified as a hazardous material, it is transported according to international regulations, ensuring proper labeling. The chemical is shipped under ambient temperature unless otherwise specified, with appropriate documentation and safety data included. |
| Storage | 5-(Bromomethyl)-2-(trifluoromethyl)pyridine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent accidental release or exposure. Use appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life of 5-(Bromomethyl)-2-(trifluoromethyl)pyridine is typically 2 years if stored cool, dry, and tightly sealed. |
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Purity 98%: 5-(Bromomethyl)-2-trifluoromethyl)pyridine with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and minimal side-product formation. Molecular weight 260.04 g/mol: 5-(Bromomethyl)-2-trifluoromethyl)pyridine of molecular weight 260.04 g/mol is used in agrochemical development, where it facilitates accurate stoichiometric calculations. Melting point 42-45°C: 5-(Bromomethyl)-2-trifluoromethyl)pyridine with a melting point of 42-45°C is used in solid formulation processes, where its defined thermal behavior provides consistent crystallization. Residual solvent <0.5%: 5-(Bromomethyl)-2-trifluoromethyl)pyridine with residual solvent content below 0.5% is used in material science research, where it reduces contamination risk in sensitive analytical applications. Storage stability ≤25°C: 5-(Bromomethyl)-2-trifluoromethyl)pyridine exhibiting storage stability at or below 25°C is used in reagent stock solutions, where it maintains chemical integrity over extended periods. Reactivity profile: 5-(Bromomethyl)-2-trifluoromethyl)pyridine with high reactivity is used in nucleophilic substitution reactions, where it enables efficient introduction of pyridyl groups into target molecules. Particle size <100 μm: 5-(Bromomethyl)-2-trifluoromethyl)pyridine with particle size less than 100 μm is used in automated dispensing systems, where it allows for precise dosing and uniform mixing. |
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Every chemist working in the synthesis of pharmaceuticals, agrochemicals, or specialty materials knows the critical role that structurally complex pyridine derivatives play in modern research and manufacturing. As a chemical manufacturer with direct hands-on experience in scale-up, synthesis pathway design, and quality control, I’d like to share practical insights into one of the star performers in pyridine chemistry—5-(Bromomethyl)-2-(trifluoromethyl)pyridine.
This compound features two impactful substituents on the pyridine ring: a trifluoromethyl group attached at the 2-position and a bromomethyl group at the 5-position. Each brings a specific benefit to the table. The trifluoromethyl group is valued for increasing metabolic stability, fine-tuning electronic effects, and improving bioavailability in active pharmaceutical ingredients. The bromomethyl moiety offers a handle for further functionalization via nucleophilic substitution, allowing it to serve as a key intermediate—or a versatile “building block”—in the transformation towards higher-value molecules.
Many pyridine derivatives exist commercially, but few balance selectivity, reactivity, and adaptability as precisely as this product. Some intermediates feature halogen atoms at the 3- or 4-positions, or lack the electron-withdrawing effect of trifluoromethylation, leading to divergent chemical behavior. By modifying both the electronic and steric properties of the core structure, this specific layout enables synthetic routes and molecular designs not possible with simpler analogs.
In the manufacturing space, laboratory scale doesn’t always translate smoothly to industrial output. Over the years, our team has worked through the bottlenecks that arise during the bromination of 2-(trifluoromethyl)pyridine, controlling exotherms and selective halogenation to yield the high purity demanded by downstream applications. Every batch faces rigorous purification steps including fractional distillation, crystallization, and chromatography, monitored at every point by advanced analytical equipment and experienced chemists.
Production starts by sourcing high-purity 2-(trifluoromethyl)pyridine, since any off-flavors in the starting material amplify during functionalization. The bromomethylation reaction follows well-mapped protocols but doesn't drive itself, especially at larger volumes. Timing the reagent addition, maintaining temperature profiles, and quenching with precision distinguish reliable industrial manufacturers from those gambling with side-product contamination. After isolation, quality control laboratories run NMR, GC-MS, and HPLC checks to confirm isomeric purity and rule out trace contaminants that can poison a reaction further down the supply chain.
Throughout the industry, subtle variations in production technique lead to differences that aren’t immediately obvious from a typical certificate of analysis. Inconsistent reaction control may leave high levels of byproducts like dibromomethyl or tribromides. Without robust purification, such impurities follow the intermediate into the next synthetic steps, resulting in yield loss, colored impurities, or regulatory rejections for pharmaceutical applications.
Our approach assumes that the user—the process chemist, the formulator, the research scientist—needs consistent reactivity and a transparent impurity profile. Each kilogram produced traces back through documented, repeatable process controls, proper waste handling, and consistent supply chain management. The product you receive maintains structural integrity, performs predictably in downstream substitutions or couplings, and doesn’t surprise you with erratic yields or unexpected chromatograms.
For comparison, similar brominated pyridines either lack the electron demand created by the 2-trifluoromethyl group or introduce more steric congestion, compromising the accessibility or reactivity at the bromomethyl site. By offering selective activation at a less-crowded location, our product adds design flexibility—a quality often asked for by those optimizing new medicinal or agrochemical leads.
We’ve heard from medicinal chemists frustrated by late-stage intermediates that underperform in key coupling reactions. In our own hands, 5-(Bromomethyl)-2-(trifluoromethyl)pyridine has enabled scalable synthesis of molecules ranging from antineoplastic candidates to anti-infectives. The ability to efficiently introduce a new substituent onto the pyridine ring at controlled locations opens up structure-activity relationship studies and lets teams optimize lead compounds with greater speed and certainty.
Process developers within the agrochemical industry leverage this intermediate to create selective herbicide or insecticide scaffolds featuring fluorinated heterocycles, prized for their environmental and metabolic profiles. Access to a consistent, clean bromomethyl group at the 5-position speeds up parallel syntheses, especially when trialing dozens of analogs in search of efficacy against resistant strains.
Academic researchers who work on organometallic catalysts or specialty materials also use this intermediate to introduce unique, fluorinated functional groups onto solid supports, ligands, or polymer chains. Tailoring reactivity for surface modification or tuning optoelectronic properties in conjugated materials often hinges on reliable access to electronically versatile and sterically accessible pyridine derivatives such as this one.
Building a good molecule isn’t only about purity numbers. It takes reproducibility from flask to tank. In our facility, each batch of 5-(Bromomethyl)-2-(trifluoromethyl)pyridine comes from processes validated at pilot and commercial scale, letting us serve both early-stage R&D and full-scale production. The product is typically delivered as a colorless to pale yellow liquid or low-melting solid, depending on storage conditions and ambient temperature. While other suppliers sometimes ship in less robust packaging, our experience with packaging engineering keeps the material stable, moisture-tight, and free from light-induced decomposition.
Meeting agreed-upon assay values and impurity thresholds is not simply a box to check. In pharmaceutical applications, the wrong grade—or a poorly characterized impurity—may compound regulatory risk and bring headache during validation. We continually monitor for residual solvents, halide contaminants, and known synthetic byproducts. Cost savings from shortcutting quality evaporate when facing batch rejection or process recalls.
Our in-house laboratories always retain representative samples of each batch for cross-checking and troubleshooting. These retained samples let us support customers backed by analytical evidence if a downstream issue arises, closing the feedback loop between bench and plant.
A handful of related brominated pyridine products see use as intermediates, substituting at different ring positions or modifying the fluorination pattern. A bromomethyl group at the 3-position, for example, offers different directivity for further substitution, often leading to divergent regioisomeric mixtures in the next reaction step. While other products drop the trifluoromethyl group, those lack essential resilience to oxidative metabolism—a top concern for pharmaceutical chemists designing stable drug candidates.
Small changes on paper make big changes on the bench. Our experience in process troubleshooting shows that switching even between suppliers of the “same” compound—much less swapping positional isomers—leads to subtle but significant changes in reactivity, phase behavior, and crystallization profiles. Misalignment here can stall a project, blow the analytical budget, or spur regulatory questions.
By focusing on reproducibility and clear communication from manufacturing through to delivery, we provide a product that isn’t just another flask label, but a tool that consistently moves projects forward.
Not everyone in the sector produces their own intermediates. Some entities buy from trading houses or contract manufacturers, repack, and resell. Our business has invested directly in backward integration, starting with raw material evaluation and moving through every synthetic step to the final packaging.
This means complete accountability, not just for consistency but also for regulatory traceability, environmental impact (solvent recovery, waste disposal), and worker safety. Our plant layout and process design ensure that staff handle hazardous brominating reagents only within well-controlled environments, mitigating exposure and minimizing off-gassing. Reliable process engineering translates into secure supply and fewer surprises at the user’s site.
Customers doing scale-up work on their own end can rely on comprehensive data packages—spectra, impurity profiles, stability reports—because we collect and stand behind them, rather than fishing for partial data after customer complaints. If push comes to shove, we offer process troubleshooting support, since we know exactly how the molecule is made, rather than relying on layers of hearsay.
Research teams start their journey with gram samples. As projects move through hit-to-lead, lead optimization, and pilot plant evaluation, the need for reliable multi-kilogram or ton-scale supply separates real suppliers from those only offering catalog vials.
We build our process development around adaptable tooling and flexible scale, letting us offer rapid ramp-up on short notice. A decade of experience has taught us which process steps may need tweaking under heat or agitation at larger volumes, and which analytical methods flag issues before they escalate.
Teams using our material in scale-up projects have reported few deviations from their small-scale work, cutting down on months of backtracking and revalidation. Once a customer’s process moves into commercial production, regular supply relies on tight scheduling and transparent inventory management—a task we embrace by managing warehousing, batch reservation, and logistics directly, not through third-party intermediaries.
As with any halogen- and trifluoromethyl-containing intermediate, responsible manufacturers focus on containment, worker protection, and waste minimization. Our process installations use closed systems and negative-pressure ventilation to prevent escape of hazardous vapors, robust PPE and emergency drills keep staff protected, and solvent recovery units minimize waste volumes. These investments in safety and environmental stewardship aren’t just regulatory requirements, but reflect a deep-seated respect for both product safety and the community around our manufacturing operations.
Spent solvents and waste bromides find their way to approved regeneration partners, while internal audits keep our own practices up to international standards. Through these measures, we make sure our customers—and regulators—can trust the integrity and safety of every kilogram we ship.
Our best process improvements have often arisen from customer feedback—not just compliments, but tough questions about trace co-contaminants, packaging options, or reactivity in new transformations. Working as a team with global chemists, we’ve improved assay accuracy and reduced byproduct carryover through tighter process controls. We revalidate our procedures every time we spot an outlier in analytical results. Iterative improvements in product quality, not just splashy marketing, underpin our credibility in this tightly knit sector.
By maintaining close conversations with downstream process developers, we adapt packaging sizes, labeling formats, and even batch documentation to support industry shifts and regulatory updates. Reliable supply doesn’t just rest on chemical purity, but on every link in the customer’s workflow—from order through to consumption and return of drums for recycling.
For chemists and process engineers, 5-(Bromomethyl)-2-(trifluoromethyl)pyridine isn’t just a reagent, but a foundation for discovery and large-scale production alike. Manufacturing this intermediate in-house, under transparent quality systems and experienced chemical oversight, guarantees not only purity but security of supply, traceability, and process support.
In a crowded market, product differentiation rests on more than a chemical label. It takes hard-won expertise, direct responsibility for each synthetic step, and a willingness to adapt quickly as customer needs evolve or regulatory pressures tighten. Our journey with this pyridine derivative—and feedback from dozens of scale-ups and launches—has taught us that the right supplier enables seamless progress, reduces project risk, and gives downstream innovators every advantage as they build new medicines, agrochemicals, and advanced materials for a changing world.