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HS Code |
413382 |
| Product Name | 2-Chloro-5-(Trifluoromethyl)Benzyl Bromide |
| Cas Number | 85118-22-9 |
| Molecular Formula | C8H5BrClF3 |
| Molecular Weight | 273.48 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.67 g/cm3 (approximate) |
| Purity | Typically ≥97% |
| Synonyms | α-Bromomethyl-2-chloro-5-(trifluoromethyl)benzene |
| Smiles | C1=CC(=C(C=C1CBr)Cl)C(F)(F)F |
As an accredited 2-Chloro-5-(Trifluoromethyl)Benzyl Bromide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with secure screw cap; labeled "2-Chloro-5-(Trifluoromethyl)Benzyl Bromide, 25g" with hazard symbols and safety instructions. |
| Shipping | 2-Chloro-5-(trifluoromethyl)benzyl bromide is shipped in tightly sealed, chemical-resistant containers, protected from moisture and light. It should be handled as a hazardous, irritant substance under UN shipping regulations. Appropriate labeling, documentation, and compliance with all local, national, and international transport regulations are required during shipping to ensure safety. |
| Storage | Store 2-Chloro-5-(trifluoromethyl)benzyl bromide in a tightly sealed container, away from moisture and incompatible materials such as strong bases and oxidizers. Keep in a cool, dry, well-ventilated area, preferably in a chemical fume hood. Protect from direct sunlight and sources of ignition. Properly label and handle with appropriate personal protective equipment due to its hazardous nature. |
Applications of 2-Chloro-5-(Trifluoromethyl)Benzyl Bromide in Industrial ManufacturingAs a direct producer of 2-Chloro-5-(Trifluoromethyl)Benzyl Bromide, we support key chemical sectors that require advanced intermediates with high purity and strict batch-to-batch consistency. Below are specialized downstream applications where this compound plays a critical role in formulation and production, together with compliance protocols, typical dosing, integration stages, and resultant end products. 1. Agrochemical Active Intermediate SynthesisMajor crop protection and seed treatment solution manufacturers employ this compound as a benzylic halide intermediate in the synthesis of complex herbicidal and fungicidal actives. Its electron-withdrawing groups facilitate nucleophilic substitution to yield customized active ingredients for region-specific agricultural threats. Feedstock traceability, compatibility with automated batch reactors, and impurity control are essential. Precise charge-in determines consistent final actives and minimal byproduct formation. Industry compliance standards
Typical usage ratio
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2. Pharmaceutical Intermediate for Antiviral Compound DevelopmentThis halomethyl benzyl substrate is integral in small-molecule pharmaceutical pipelines, particularly for manufacturing intermediates used in anti-influenza and hepatitis compound synthesis. The material’s precise halogen and trifluoromethyl positioning enhances the building block properties for targeted nucleoside or arylamine integration. Full batch documentation and supplier GMP adherence are critical for audit trails and pharmaceutical registrations. Industry compliance standards
Typical usage ratio
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3. Fluorinated Aromatic Polymer ModifierIn advanced polymer material manufacturing, this raw material serves as a chain-modifying agent for specialty fluorinated and chlorinated aromatic polymers designed for high-performance membranes and coatings. Its molecular structure brings enhanced hydrophobicity, solvent resistance, and dielectric stability required in electronics and industrial filtration. Precise stoichiometry during addition is crucial for reproducible mechanical and thermal properties in finished resins. Industry compliance standards
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4. Intermediate for Liquid Crystal Material SynthesisLeading liquid crystal material formulators use this substituted benzyl bromide to construct highly ordered, fluorine-containing mesogenic structures providing tunable birefringence and chemical stability demanded by TFT-LCD and OLED displays. Formulators require ultra-low metal ion content and minimal residual solvents, with full traceability from feedstock to final alignment layer deposition. Industry compliance standards
Typical usage ratio
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Nobody working in fine chemicals has endless patience for labor-intensive syntheses or low-purity results. Over the years, the need for smoother reactions and consistent quality led us down the path toward halogenated benzyl intermediates. Among those, 2-Chloro-5-(trifluoromethyl)benzyl bromide stands out in our lineup. We’ve engineered this compound to address the practical needs of pharmaceutical labs, agrochemical research, and speciality material producers who depend on reliable electrophilic benzyl halides.
Our batches of 2-Chloro-5-(trifluoromethyl)benzyl bromide consistently meet high-assay specifications. At the core sits a benzyl ring, bearing a chloro group at the ortho position and a trifluoromethyl at the meta, finished off with a reactive benzyl bromide handle. Over years of refining the production route, we noticed subtle shifts in impurity profiles based on solvent selection during bromination. Pure crystallization, scrupulous handling, and targeted purification steps allow us to keep side-product levels minimal, which directly supports higher downstream reaction yields.
Users in process chemistry describe the reaction behavior as “predictable”—not every benzyl bromide on the market can claim that. Trace by-products, out-of-spec impurities, or batch-to-batch variations introduce noise into screening results and, ultimately, scale-up headaches. We’ve spent a lot of time monitoring halide distribution using GC and NMR, since even small spikes in residual precursor chloromethyl or dibrominated by-products can trip up late-stage synthesis. Our plant design and QC approach tackle these issues by tightening up exotherm control and using staged phase separations.
Traditionally, benzyl halides see heavy use for introducing substituted benzyl groups through nucleophilic substitution, especially in creating ethers, esters, and amines. What we’ve found, as manufacturers handling multi-ton batches, is that the electron-withdrawing trifluoromethyl and chloro groups uniquely tune the substrate for reactivity and selectivity. Competing benzyl bromides without these substituents often react too fast or unpredictably with delicate nucleophiles, producing generous helpings of side products. Our experience has shown that this exact combination of substituents slows the nucleophilic attack just enough to let you steer the outcome, particularly when working with complex heterocycles or chiral auxiliaries.
Customers report a much lower rate of undesired benzylic rearrangements compared to unsubstituted analogues. We attribute this to the electron-withdrawing effects which reduce carbocation-like intermediates, making the compound a solid pick for workups requiring clean lines and minimal column time. Pair this with spectral evidence—FTIR and HPLC results we supply upon request—and scientists see with their own eyes the tight specifications across each container, matched to the job at hand.
Safe, predictable manufacturing processes save time and resources every season. From the first day we added 2-Chloro-5-(trifluoromethyl)benzyl bromide to our product portfolio, our plant workers flagged concerns about fume containment and reagent compatibility with standard gaskets. This drove us to install vent sensors on reactors and use PTFE-lined stirrers instead of simple elastomers. Alongside dedicated containment, our teams found it important to keep operator exposure low, not just for regulatory compliance but also for protecting the know-how that keeps our operation running.
Once filled and sealed, drums containing this compound don’t leach or off-gas under typical storage conditions. We maintain strict controls over temperature and light exposure by using opaque, lined drums in all outbound shipments. Years of monitoring container returns and customer feedback taught us that a little extra attention in packaging pays off, especially when summer temperatures climb or shipments cross time zones.
Every year brings new questions from R&D labs: “Will your batch survive a scale-up to our flow reactor?” “Can I alkylate my heterocycle without deep-freezing the mixture?” These are not hypotheticals. One European partner reported seeing much tighter conversion rates and fewer work-up headaches after switching to our product from a cheaper source. They highlighted smoother phase separations and easier downstream purification. The feedback loop between our technical specialists and customers directly influences how we tweak process parameters season to season.
Our staff fielded requests for trail samples tailored for library synthesis in small vials. Each batch carries documentation on residual solvents, water content, and halide speciation. Analytical chemists in one major pharmaceutical group told us that minimizing unknown peaks during scale-up matters just as much as getting a competitive price. Reducing post-reaction chromatography time shortens project cycles, frees up bench space, and lessens waste disposal costs. A few users tried to swap in cheaper analogues with less purification, only to end up spending more time salvaging their products.
Material scientists have embraced this intermediate for building high-performance materials, noting the stability and reactivity window. Application journals frequently report using it for synthesizing specialty monomers, liquid crystals, and some pesticide candidates. Word has spread that our controlled impurity specifications help researchers avoid re-optimizing synthetic routes with every batch.
In practice, we sometimes field requests for 2-chlorobenzyl bromide or 2-trifluoromethylbenzyl bromide as lower-cost alternatives. What customers learn—usually after a few failed reactions—is that dropping either substituent affects selectivity and stability. The combined presence of chlorine and trifluoromethyl on the aromatic ring does more than shift electronic character; it influences reaction rates and the range of compatible solvents. No other product in our line delivers the same performance for certain ring-alkylation reactions, especially where electron density and steric profile matter.
Some buyers ask whether they can achieve similar results by blending or substituting with less pure or slightly different analogues already on hand. Reaction screenings run at kilo scale tend to reveal the real limitations: off-flavor byproducts, poor conversion yields, and less stable intermediates that don’t stand up to extended storage. Skimping on the right intermediate rarely proves worthwhile, measured by whole-project success.
Manufacturing tight-spec benzyl bromides never comes down to “set it and forget it” process chemistry. Small variations in bromination rate, temperature gradients, or purification cycles add up fast. Our teams draw on a mix of automated monitoring and plain experience to spot process drift early and intervene before a batch slides out of spec. The upshot: reliable quality, fewer returns, and more predictable results for users dealing with ambitious synthesis projects.
Periodically, we swap notes with other manufacturing engineers about reactor coatings, agitation profiles, or product tank designs that reduce contamination. There’s no secret ingredient—consistency rests on scrupulous plant hygiene, raw material vetting, and on-the-fly troubleshooting. Human oversight and years of process tuning stand behind every shipment. In every production run, our operators record batch notes in detail, supporting troubleshooting and incremental process improvement.
International shipping can expose fine chemicals to rough conditions—rapid temperature swings, high humidity, or even short-term stacking in third-party warehouses. Early experience taught us to upgrade drum linings, inspect seals, and keep paperwork matched to regulatory shifts in transit regions. Our logistics partners receive hazard training, including real-world spill drills at depots.
Out in the field, buyers rarely want to think about packaging unless something goes wrong. Our job involves delivering the compound ready for use, with clear batch traceability woven into the documentation. There’s no margin for error; no research project benefits from learning the hard way that a shipment failed en route, or picked up contaminants from a faulty seal.
Responsible chemical manufacturing calls for more than just legal compliance. Over years of handling halogenated aromatics, we’ve overhauled our waste management program to safely neutralize halide residues and mitigate environmental impact. Residual bromide and fluoride pose particular demands on local treatment systems, so our operators collect all process washings for specialist handling. Transitioning to closed-loop handling setups and reusable PPE cut down on accidental emissions and disposal volumes.
In parallel, we work continuously with industry partners to discover greener routes to the same product. Current R&D efforts explore milder bromination protocols, solvent recycling, and potential catalysts that lower energy use per ton produced. The industry goal remains clear—reliable chemistry paired with a shrinking environmental footprint. Stepwise gains in waste reduction and emission controls have translated into safer working conditions and fewer permitting headaches.
Staying ahead of regulations means more than extra paperwork; it requires methodical change from the shop floor up. Each year brings fresh scrutiny over halogenated organics, worker exposure, and transportation risks. We maintain up-to-date registrations, run routine audits, and adapt storage protocols in-line with changing standards. This gives downstream users confidence that their supply chain rests on firm, transparent practices.
Our technical advisors often work one-on-one with customers to resolve documentation or certification questions before shipments cross borders. These relationships help teams on both sides plan timelines, choose the right grade, and avoid delays linked to compliance hiccups. Face-to-face discussions build practical trust, which makes all the difference once a project passes early R&D and moves to commercial scale.
Chemical manufacturing isn’t static. As demands for faster, more selective transformations grow, the role of specialty benzyl bromides continues to expand. Our teams keep pace by paying attention to both lab-based innovation and real plant-floor challenges. Efforts to improve product quality draw equally on analytical rigor and grounded practical feedback. The recent uptick in demand for more complex fused-ring and fluorinated building blocks only raises the bar for intermediate purity and batch consistency.
In research syntheses, our 2-Chloro-5-(trifluoromethyl)benzyl bromide handles challenging alkylations with a flexibility that general-purpose benzyl bromides can’t match. The uptick in requests from fields as diverse as medicinal chemistry and advanced polymer science shows just how versatile this compound can be. A new generation of chemists—many who cut their teeth scaling up small-batch reactions—demand both reliability and transparency from their suppliers. Our track record reflects that reality.
As manufacturers, everything we know about 2-Chloro-5-(trifluoromethyl)benzyl bromide comes from real production and real troubleshooting, not just catalog copy or tech specs. Our history handling kilos or tons each month brings a different perspective than a reseller or distributor can offer. Facility engineers, QC chemists, and logistics coordinators blend their expertise in all stages—yielding a product whose reputation stands on performance, not just marketing.
Every shipment carries with it a piece of our operation’s story, from raw material handling and batch notes to the final seal on the drum. We have seen how tight process control and in-depth customer service combine to solve problems before they grow. Years of feedback, operational tweaks, and hands-on experience shape our understanding of what makes this compound indispensable to so many real-world projects.
Working tightly with chemists, process engineers, and project managers has shown that the best solutions rarely come from isolation. By continuing to share lessons learned—about batch consistency, safe handling, or emerging best practices—we invest not just in business but also in the scientific community’s momentum. Our facility serves as a point of exchange, where observations feed future improvements, and customer insights sharpen our technical bench.
At the end of the day, 2-Chloro-5-(trifluoromethyl)benzyl bromide brings together thoughtful chemistry and operational experience. Every container reflects a commitment to quality, compliance, safety, and responsibility—kept grounded by countless hours in the plant, and shaped by real relationships across global chemical innovation.