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HS Code |
572600 |
| Productname | 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide |
| Casnumber | 1429777-45-2 |
| Molecularformula | C8H5BrF4 |
| Molecularweight | 257.03 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically >= 98% |
| Density | 1.65 g/mL at 25°C (approximate) |
| Refractiveindex | n20/D 1.481 (approximate) |
| Smiles | C1=CC(=CC(=C1CBr)F)C(F)(F)F |
| Inchikey | QAPMCZXAKSVXHE-UHFFFAOYSA-N |
| Storageconditions | Store at 2-8°C, protect from light and moisture |
As an accredited 3-Fluoro-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, 25 grams, with tamper-evident seal, labeled with chemical name, CAS number, and hazard warnings, tightly packed. |
| Shipping | 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide is shipped in tightly sealed, chemically resistant containers, clearly labeled and cushioned to prevent breakage. Transport complies with all relevant hazardous material regulations, including documentation for safe handling. Recommended shipping is via ground or air courier services certified for chemical transport, with temperature control if required. |
| Storage | Store **3-Fluoro-5-(trifluoromethyl)benzyl bromide** in a cool, dry, well-ventilated area, tightly sealed in a corrosion-resistant, clearly labeled container. Keep away from moisture, heat, light, acids, bases, and incompatible materials. Use secondary containment to prevent leaks. Handle only in a chemical fume hood, and store separately from oxidizing agents and strong reducing agents. Employ appropriate personal protective equipment (PPE). |
Applications of 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide in Industrial ManufacturingAs the direct producer of 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide, we supply this advanced chemical intermediate to manufacturers operating across highly specialized sectors. Below we summarize genuine industrial applications, detailing integration points, compliance requirements, and downstream product outputs specific to each use case. 1. Pharmaceutical Intermediate for Novel Active Pharmaceutical Ingredient (API) SynthesisIn pharmaceutical production, this compound functions as a key building block in the synthesis of select fluorinated drug molecules, especially in anti-inflammatory, CNS, and antineoplastic research pipelines. Developers use its activated benzyl bromide group for nucleophilic substitution reactions, facilitating the introduction of the unique trifluoromethyl and fluorine motifs into molecular scaffolds. Its precise reactivity profile supports complex multi-step synthesis with strict impurity control. Industry compliance standards
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2. Agrochemical Synthesis for Advanced Herbicide and Fungicide MoleculesThe molecule acts as a core intermediate in the agrochemical sector where its unique benzyl bromide functionality enables efficient linking to heterocyclic and carboxyl synthons. Its use is prominent in research and production of modern, fluorine-containing herbicides and fungicides, where enhanced metabolic stability and bioactivity profile are critical for regulatory acceptance and market performance. Industry compliance standards
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3. Specialty Polymer Additive Synthesis for High-Performance FluoropolymersWithin the specialty polymer industry, this compound meets the demand for tailored monomer introduction of fluorinated aromatic moieties, which impart enhanced chemical resistance, high dielectric stability, and reduced surface energy to advanced polymer matrices. It is typically consumed by polymer manufacturers in the production of custom fluoropolymer modifiers and crosslinking agents. Industry compliance standards
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4. Fine Chemical Synthesis for Liquid Crystal IntermediatesThe compound is adopted by advanced materials companies developing tailored liquid crystal molecules, where its combination of fluorine substituents and a reactive benzylic site enables selective construction of mesogenic units. These unique chemical features strengthen rigidity, reduce viscosity, and support wider temperature stability ranges in liquid crystal display (LCD) applications. Industry compliance standards
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5. Laboratory Reference Standard and Analytical Derivatization AgentChemical analysis laboratories and organizations engaged in method validation rely on this compound as a derivatization agent for mass spectrometry or NMR trace analysis, due to its high reactivity and distinctive fluorine-containing signals. It serves as a specialty standard for the development and calibration of analytical protocols, especially in complex matrix assessment in the pharmaceutical, agrochemical, and polymer sectors. Industry compliance standards
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Our close work with aromatic building blocks led us to manufacture 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide under strict process controls developed over years of chemical synthesis experience. We refer to it in our records as Model FTFM-BB03, and this isn’t just a code — it encapsulates a nuanced history of solvent handling, fluorination safety, and real-time process adjustments. We originally scaled its production in response to chemists who needed both selective reactivity and robust shelf life in their benzyl bromides. The distinctive substitution pattern, with a fluorine atom on the third ring position and a trifluoromethyl group on the fifth, brings changes in electron distribution that we could measure both in the lab and at scale.
Crystallizing this product demanded tighter controls than older halogenated benzyl derivatives. Even small tweaks in temperature curves changed the purity profile. We leaned on tried-and-true distillation tricks and kept an eye on trace contaminants with every batch. The crystalline solid we produce shows purity above 98 percent by HPLC, because the presence of that trifluoromethyl group ups the volatility and reactivity. Besides purity, our crews verify each lot with proton and carbon NMR, and we've calibrated our GC systems to distinguish the faintest byproducts, especially those from incomplete substitution. Only batches matching both spectrometric and chromatographic standards leave our site. Our plant has handled aromatic brominations for more than two decades, so we’re alert to the quirks of each raw material — whether a new batch of pyridine throws the reaction off, or a tiny moisture pickup affects handling.
We see a wide gulf between this molecule and more typical benzyl bromides. The pairing of fluorine and trifluoromethyl groups dramatically tunes the compound’s reactivity. Customers tell us their alkylation steps run with higher selectivity and cleaner conversion, which often means faster purifications and fewer chromatographic passes. As plant chemists, we note that the extra electron-withdrawing power grants a more stable benzylic bromide that can participate in both nucleophilic and radical-based organic synthesis.
For chemists working on pharmaceuticals, agrochemicals, or specialty materials, the region-selective substitution offered by this compound opens building blocks that are hard to prepare with less functionalized benzylic species. That’s why some medicinal chemistry routes achieve higher yields or shorter step counts by plugging this molecule into their convergent syntheses. We’ve watched colleagues in crop protection harness these features to build insecticides where the metabolically stable trifluoromethyl moiety saves months of oxidation testing.
Details make a difference in this business, so our manufacturing tolerances never come from guesswork. Typical batches run as a white to pale yellow solid with a molecular weight of 267.02 g/mol and melting points in the 54–57°C range, observed under nitrogen atmosphere to avoid ambient hydration. Most laboratory notes reflect faint aromatic odors; no strong off-notes signal stable containment. Density testing (1.6–1.7 g/cm³ at room temperature) gives a quick cross-check on composition.
Every lot we ship has passed rigorous GC and HPLC analyses. We sample product regularly throughout synthesis, not just at the endpoint. Minute levels of ortho-brominated side products or dibromo aromatic residues could hinder downstream reactions, and we know our best customers are measuring with the same discipline. Infrared analysis shows characteristic C–F and C–Br stretches — confirming the right structure and verifying that no hydrolysis has occurred during packing.
We pack this compound in high-density polyethylene bottles with foil liners to block moisture and air ingress. Over the years, surface crystallization, caking, and particulate formation have all been traced back to poor storage. We shifted our protocols to keep the product flowable, even at the end of shelf life. Each drum includes tamper-evident seals and batch-specific documentation, showing traceability back to each raw material and operator shift.
The benzyl bromide motif remains a backbone in organic synthesis, but once you add fluorine and trifluoromethyl groups, the applications broaden. Our customers order 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide for key steps in medicinal chemistry, particularly for building fluoroalkylated phenethylamines, benzylamines, and substituted aromatic ethers with metabolic resistance. We’ve collaborated with API plants who found fewer byproducts formed when using our material in alkylation or nucleophilic substitution, compared to non-fluorinated versions.
Those in crop protection research tap into the unique profile for synthesis of agrochemicals — especially where resistance to oxidative or enzymatic degradation is essential. Material scientists and polymer chemists have asked about scale-up for incorporating trifluoromethylbenzylic arms into polymer backbones, chasing durability and lower surface energy in finished materials.
On our plant tours, visiting chemists often point out the transformation in downstream processing: aqueous quench steps show notably fewer emulsions, extraction phases complete with fewer transfers, and color purity stays higher. Data from recent customer runs demonstrated that impurities associated with dehalogenation sit below detection limits more often, shortening their overall synthesis cycle.
Manufacturing halogenated aromatics comes with heightened risks. With this molecule, our first challenge emerged in bromination exotherms. Over the years, we’ve designed jacketed reactors that can manage the heat and mitigate any runaway hazards. Scrubbing systems neutralize both bromine and hydrogen fluoride releases, preventing problems shown in older-generation plants.
Our site’s permitted for handling organobromide emissions, and we invested in state-of-the-art ventilation and effluent management. Teams regularly test containment for leaks — a compound with this much halogen content brings extra scrutiny. Waste from synthesis, packed with spent bromide and unreacted aromatics, routes through verified incineration or secure landfill, based on local environmental codes. We’re responsible for keeping these pathways safe, so we take no shortcuts with storage or transport, logging every drum’s journey from filling to delivery.
We offer training and practical guidance to each customer on storing and using the product. Our chemists have spent years handling fluorine-rich organics, and we share best practices openly: avoid prolonged light exposure, keep the material sealed under nitrogen or argon, and flush glassware thoroughly to prevent surface accumulation.
There are plenty of benzyl bromides, but few carry the fluorinated pattern seen here. Many alternatives, such as plain benzyl bromide or para-substituted trifluoromethylbenzyl bromide, simply lack the combined electronic effects that drive clean reactivity and selectivity. In our hands, even minor pattern shifts cause reaction rates and product profiles to diverge; the position of the fluorine and trifluoromethyl groups guides the intermediate’s fate.
Traditional benzyl bromide can overalkylate or set off multiple side reactions, especially in bases or at higher temperatures. The 3-fluoro-5-(trifluoromethyl) version, as produced here, resists these pitfalls, giving higher monosubstitution yields and leaving less tar formation. For biologists tracing metabolites, these changes translate to less ambiguity in final product profiles.
We see this difference play out in scale-ups as well. With other benzyl halides, controlling dusting, caking, and storage degradation remains a headache. The presence of the two fluorinated groups actually increases long-term shelf stability and reduces off-odors — something you notice straight away on the filling line. These properties let our customers store material for longer, use it more flexibly, and minimize waste in development campaigns.
Few things matter more than continuity — from batch quality to shipment scheduling. Our teams log every process variable, not for bureaucracy, but because running a multi-step synthesis at scale means surfacing potential problems before they hit the next reactor. Gas feeds, pressure controls, reaction quench timing: seasoned line workers know how small changes ripple through a batch, affecting purity or causing downtime.
Supply chain upsets — from solvent delays to regulatory shifts — pose big risks for tight schedules. We don’t rely on a single source for key raw materials, and our warehouses keep contingency stocks on site. COVID-era disruptions underlined how valuable this is; we kept our customers running even as international logistics stuttered.
We’ve heard horror stories from buyers whose production lines halted due to inconsistent deliveries or quality swings from other suppliers. Years of close partnerships with process chemists, logistical planners, and regulatory experts mean our shipments show up as committed, packaged safely, and with documentation you can trace back to origin. Our customer service team — many with chemistry degrees and plant experience — can answer process questions live, not just send generic sheets.
No chemical synthesis stays static. Feedback from customers, new regulatory guidelines, and internal audits push us to tune every detail. We regularly run bench-scale simulations before rolling out plant-wide changes. Minor adjustments — like a slower addition of bromine or a deeper distillation cut — led to five percent higher yields in the last review cycle.
On waste minimization, we switched to closed-loop solvent recovery a few years ago, capturing even more of the dichloromethane and acetonitrile used in process steps, and slashing our annual halogen discharge. Operators join rapid-response training each quarter to refresh hazard mitigation; nobody takes shortcuts on this site, because accidents happen fastest when systems grow familiar.
We review every customer complaint or query, whether it’s about a faint color shift or a question from an analytical lab. Patterns from these lessons prompted minor formula changes — and caught a rare batch contamination before it left the plant floor. In the end, long-term trust rests on not just hitting minimum standards, but exceeding what the lab and market expect.
Chemicals don’t stand alone. They rely on upstream raw material supply and downstream logistics out of the plant to user labs. We lay out all sources and intermediates as part of our documentation. This transparency helped a pharmaceutical customer secure their regulatory filing by showing, lot-by-lot, that each input met stringent standards at every step.
Auditors regularly challenge us with deep tracing of batches, from receipt of fluorobenzene starting materials to the bottling room. We learned to keep these records digital, time-stamped, and indexed to avoid lost paperwork or missed reviews. Complying with global standards keeps our teams vigilant — documentation isn’t just bureaucracy, it’s risk reduction.
Trends in pharmaceuticals, crop protection, and materials science drive continued interest in fluorinated building blocks. Drug developers pursue molecules with better metabolic profiles; crop scientists seek durable, weather-resistant actives; engineers explore polymers with low surface energies. We see orders for smaller pilot lots from research teams, then calls for larger drums as projects scale from lab to plant.
We invest in research collaborations with universities and development labs, sharing both process insight and product samples. Some breakthroughs have come from cross-industry conversations — a method designed for pharmaceuticals now finds use in next-generation electronics materials. Every inquiry, from gram-scale to multi-ton, brings new challenges and feedback that help us refine what we do.
Requests for cleaner, greener synthesis echo across customer calls. Reducing waste, limiting halogen byproducts, and capturing solvent emissions remain active projects for our site chemists. Our aim holds steady: reliable product, safe manufacture, full traceability, and openness with all partners.
Years of manufacturing 3-Fluoro-5-(Trifluoromethyl)Benzyl Bromide taught us how small molecule differences reshape everything from reaction time to waste profile. It’s more than a fine chemical — it’s proof that attention to detail, discipline at the operator level, and honest communication with the end user shape positive results. As new applications arise, we dig into the data, talk openly with researchers, and adapt our process. If there’s a better way to produce, contain, or apply this compound, our teams are listening — because that’s how you build both better chemistry and lasting trust.