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HS Code |
936944 |
| Chemical Name | 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide |
| Cas Number | 867363-85-9 |
| Molecular Formula | C8H5BrF4 |
| Molecular Weight | 257.02 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Density | About 1.63 g/cm³ at 25°C |
| Refractive Index | n20/D ~ 1.500 |
| Smiles | C1=CC(=C(C=C1F)C(F)(F)F)CBr |
| Synonyms | α-Bromo-5-fluoro-2-(trifluoromethyl)toluene |
| Storage Conditions | Store at 2-8°C, tightly sealed |
As an accredited 5-Fluoro-2-(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, 25g, with tamper-evident cap and chemical label detailing name, structure, hazard symbols, lot number, and storage instructions. |
| Shipping | 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide is shipped in tightly sealed chemical-resistant containers, protected from moisture and light. It is packed in accordance with relevant hazardous material regulations (e.g., UN numbers, Class 6.1), with appropriate hazard labels and documentation. Shipments are handled by certified carriers, ensuring safe transit and regulatory compliance. |
| Storage | 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong bases and oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a dedicated chemical storage cabinet. Protect from light and sources of ignition. Store at temperatures recommended by the manufacturer, usually at or below room temperature. |
Applications of 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide in Industrial ManufacturingThis section covers specialized industrial applications for 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide. As the producer, we detail how leading sectors integrate this intermediate by process stage, compliance considerations, formulation specifics, and final product types. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) SynthesisProcess engineers in pharmaceutical plants utilize this compound as an electrophilic building block for advanced small-molecule synthesis. The benzyl bromide structure supports introduction of fluorinated motifs into target molecules, crucial for enhanced bioavailability and metabolic stability in drug candidates. Operators perform direct alkylation during late-stage intermediate synthesis, under tightly monitored GMP conditions, with the material frequency determined by the specific synthetic route and purification under cGMP or ICH Q7 guidance. End uses focus on fluorinated drug candidates within the cardiovascular and oncology therapeutic areas. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate for Selective Herbicide ProductionAgrichemical formulators deploy this compound for synthesis of novel fluorinated aryl derivatives, supporting production of advanced herbicide molecules with improved field persistence and target crop specificity. The compound’s reactivity allows selective introduction into backbone frameworks during manufacture in compliance with agrochemical synthesis standards. Usage ratios depend on the desired substitution pattern and require controlled process validation to minimize residual bromide content in the final product. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Advanced Material Synthesis for Liquid Crystal Display (LCD) ComponentsManufacturers of specialty electronic materials integrate this benzyl bromide derivative in the fine chemical synthesis of high-performance liquid crystal monomers, where the electron-withdrawing trifluoromethyl and fluoro substituents modulate dielectric anisotropy and optical transparency. The compound enters production as a core precursor for subsequent coupling reactions carried out in GMP or ISO-certified cleanrooms, supporting device-grade material specs critical for leading panel producers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fine Chemical Building Block for Advanced Polymer Performance ModifiersPerformance polymer manufacturers use 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide to synthesize specialty additives that impart enhanced hydrophobicity, chemical resistance, and fluorine content to engineering polymers such as high-performance resins and coatings. In industrial reactors, the material undergoes controlled functionalization onto macromolecular backbones, ideally suited where stringent control of migration and leaching is mandated for end-user safety and regulatory compliance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Custom Intermediate for Advanced Organic Synthesis and Chemical R&DContract research organizations (CROs) and in-house R&D teams apply this compound in multi-step organic syntheses, targeting fluorinated aromatic structures for innovative molecular libraries. Chemists use the high selectivity of benzyl bromide chemistry to introduce unique fluorinated side chains under controlled laboratory or pilot plant conditions, with precise adaptation of reagent quantities based on the target scaffold and downstream purification requirements for analytical-grade intermediate standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Chemical progress relies on more than just formulas. As a manufacturer with decades of hands-on experience in halogenated aromatics, we understand the value of every process step, every purification, every final test that determines the quality of an intermediate. 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide has proven, over the years, to be one of those specialty compounds that test the capabilities of a chemical producer—not just because of its reactivity, but because of the fine balance between purity, stability, and reliability. Our team approaches each batch with awareness that every molecule matters, especially when projects hinge on trace consistency and uncontaminated supply chains.
When we commit to producing a compound such as 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide, we rely on a blend of practiced process controls and granular recordkeeping. The backbone of our approach involves tracing every lot of raw material, from halogenated benzene derivatives to reagents and solvents. We only proceed with suppliers who pass our threshold for contaminant audits and impurity profiles—one of the fastest lessons in this business comes when even a minor deviation in feedstock leads to costly purification reruns or—worse—unsatisfactory product that never leaves the plant floor.
Over years of trial and refinement, we’ve landed on a route that produces a bright, low-yielding intermediate initially, which we then subject to a series of treatments, drying steps, and final distillation to achieve batch-to-batch repeatability. Our chemists never “set and forget” at the reactor stage. They’re in the control room watching pressure, flow, and color, ready to adjust on the fly. If a process shift threatens the expected bromination selectivity, they intervene. Because we manufacture, not trade, every kilogram carries our direct oversight.
Among benzylic halides, 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide stands out. Its structure, with both an aromatic fluoro substituent and a strongly electron-withdrawing trifluoromethyl group, grants it reactivity and selectivity rarely matched by simpler analogs. In the lab, chemists tell us it’s the go-to choice where both nucleophilic substitution and site-specific arylation are needed. It brings a combination of steric and electronic bias that ordinary benzyl bromides lack.
When putting it up against traditional benzyl bromide, differences become evident at the bench scale. The trifluoromethyl group does more than just increase volatility—it modulates electron density so that reaction conditions need tuning. Using this compound demands a thicker gloves-on approach to handling: volatility climbs, odor becomes sharper, and accidental volatilization is a genuine issue in poorly ventilated setups. Yet this same feature allows more predictable kinetic control in sulfonamide protection or etherification steps, where the risk of carbocation rearrangements generally rises with more basic bromides.
Synthetic teams in the pharmaceutical sector often report higher yield reliability when this compound is used for late-stage functionalization. Agrochemical researchers comment that fewer by-products form, saving them several cleanup columns. We hear directly how the tightness of our impurity profile helps researchers skip unnecessary recrystallization—every impurity, especially isomeric bromides or persistent organic residues, can introduce risk in scale-up. Meeting those standards is not just a matter of pride for us; it’s what establishes long-term trust.
5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide finds its way mainly into custom synthesis of drug candidates, specialized ligands, and advanced materials. Direct feedback from process chemists shows it behaves best under carefully anhydrous conditions. Once, a pharmaceutical team shared how switching from a generic grade to our product slashed their purification footprint. They noted less discoloration, lower halide by-products, and a dramatic cut in GC-visible impurities. This move allowed them to move faster from milligram screens to kilogram pilot batches—proving out a medicinal chemistry hypothesis that required tight analytical tolerances.
Our insight into the market tells us that researchers using this compound for securing chiral amines via nucleophilic substitution prefer material free from isomeric or dibromo contaminants. Some competitors, especially third-party resellers, push batches with wider impurity loads. We answer to our own standard since back-integration opens up our entire production record. Over time, we’ve noticed increasing numbers of inquiries about scale-up potential, especially from labs engaged in optimizing fluorinated intermediates for API synthesis. Each of these requests ends up with our production managers, who assess the feasibility of fit—our reactors, safety protocols, and timelines tailored to the needs of scale-up chemists already familiar with the compound.
Manufacturing at scale entails more than just mixing and reacting chemicals. Several properties make this molecule a handling challenge: its volatility, aggressive bromine content, and tendency to undergo side reactions if storage isn’t tightly controlled. Our protocols go deeper than broad-brush recommendations. After purification and fractional distillation, the compound is filled under inert gas, then sealed in specialized fluorinated containers. Over the years, we’ve seen what happens to lesser grades packaged in generic glass or untreated plastics—the material loses mass, residue builds up on closures, and end users complain about odd chromatographic fingerprints.
To address this, regular QA checks monitor not only product content but also headspace composition and micro-residuals. We test stability over real storage periods, not just theoretical timeframes. If an issue with bromide off-gassing flags during aging—such as a faint yellowing or increased peroxide risk—we halt distribution and retrace our storage regimen. Our shipping team, familiar with the sensitivity of this molecule, knows to train partners in safe unpacking, immediate transfer to cool storage, and protocols for post-shipment testing. Field failures are both costly and damaging—our team avoids them by closing the loop between shipping, end user, and root cause analysis.
Our plant personnel have learned, sometimes the hard way, that even subtle changes in ambient humidity during filling can introduce enough water to degrade product. For this reason, our filling rooms run dry air circulation and use non-reactive liner materials to avoid side reactions. Years ago, after several customer complaints about material degrading or failing key purity checks, we changed our plant design to include dedicated transfer lines, which get traced for every production. This attention to process details keeps the product consistent and reassures our industrial clients who risk major project delays from subpar intermediates.
Some buyers hesitate when comparing this product to more broadly available benzylic bromides. It’s a fair question: why pay premium for a fluoro-trifluoromethyl-substituted grade when other derivatizable benzyl bromides exist at lower cost? Our experience shows nuanced advantages. During scale-up runs in contract synthesis projects, intermediates derived from this molecule tend to undergo fewer side reactions, especially in the presence of nucleophilic bases. For challenging arylations or coupling steps, the electronic effects from the trifluoromethyl and fluoro substituents increase selectivity, raise yields, and, most importantly, decrease byproduct formation during subsequent transformations.
On the downside, users notice higher sensitivity to storage and handling compared to simpler analogs. We never downplay this factor. In real-life scenarios, researchers unfamiliar with this molecule risk generating false negatives on yield or purity if they use basic processing conditions. But users who stick to well-controlled setups, as we do here in production, consistently report higher reliability and less downstream troubleshooting.
Our chemists, trained in late-stage fluorination techniques, prefer this intermediate due to its utility in embedding fluorine atoms into complex architectures. The pharmaceutical industry, with its unending drive for bioavailable, metabolically stable compounds, finds this group’s balance of size and electronegativity uniquely useful. Colleagues from material science labs mention how the compound’s attributes open the door for tailor-made polymers, especially where resistance to hydrolysis and oxidative degradation is critical.
Over several years, close partnerships with top pharmaceutical R&D units have shaped our understanding of this compound’s real-world effects. One instructive case involved a custom synthesis project for a major client, whose scale-up team struggled with inconsistent yields using commodity grades. After switching to our tightly-controlled batches, they found chromatograms clearer, reaction times shorter, and overall throughput increased as byproduct trapping requirements diminished. The result: a pilot batch that translated to fewer column runs, less waste, and greater confidence at the next development milestone.
From another sector, an agrochemical collaborator shared their experience using our fluorinated benzylic bromide for innovative crop protection compounds. Their own screening compared six vendors, but only our grade allowed them to hit both purity and thermal stability thresholds. They reported that our documented impurity breakdown expedited their method validation, saving several weeks in project ramp-up. This kind of feedback cycles right back to our R&D and production teams, reinforcing the practices that distinguish our operation.
Learning from our own process and customer engagement, we make a point to run post-mortem reviews after every large-scale batch. Each incident—good or bad—contributes to our internal library of lessons, capturing the minutiae: reactor jacket malfunctions, aberrant titration results, and even weather effects on plant stability. These are the practical realities that surface never make it onto a typical datasheet or outsider’s datasheet blurb, but experienced users see the results in consistent product delivered on time.
All production involving halogenated intermediates must take environmental impact and local compliance seriously. Our chemists and engineers don’t just aim for product throughput. Every process step undergoes review for waste minimization and safe treatment of effluent streams. During bromination, byproduct recovery is prioritized—eliminating uncontrolled venting and secondary pollution. The plant’s on-site remediation system neutralizes spent bromine, collects benzylic residue, and sends all non-recoverable waste for compliant disposal.
Fluorinated intermediates attract regulatory scrutiny, especially as per- and polyfluoroalkyl substances face closer examination worldwide. Our compliance team stays updated on evolving standards, ensuring our process lines operate below permit thresholds and all shipments can be traced for origin and ingredient breakdown. Material Safety Data Sheets are regularly updated, reflecting the latest toxicological and environmental findings. Several years ago, a shift in local groundwater monitoring requirements led us to update secondary containment around our production vessels—even though no leak had ever occurred. This approach, while resource-intensive, minimizes both our environmental burden and business risk from non-compliance.
Responsible handling means more than ticking boxes for certification. Our process safety teams conduct quarterly reviews, including emergency response drills for accidental release scenarios. This investment translates directly into security for our partners—no surprises, no interruptions to your research schedules. It also drives internal process improvements: captured solvent waste turns into feedstock for other business lines, and ongoing audits keep inefficiencies from escalating into compliance headaches.
For many teams, 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide isn’t just another halogenated building block—it serves as a pivotal intermediate in constructing new molecular scaffolds. Small differences in impurity content or isomeric ratios ripple through entire development pipelines. Our focus, shaped by years of dialogue with drug discovery, biotech, and material science teams, remains on providing a product with verified, transparent analytical data. Each lot ticket links to a batch record that spells out every process, every analytical method, and every deviation logged so project chemists know exactly what their reactions start with, run after run.
Academic and start-up clients, especially those running lean teams, often mention how unreliable supply chains or material variability have delayed critical experiments in the past. They’ve come to depend on our ability to maintain continuity—and transparency—to prevent development setbacks arising from unexpected product shift. We’re not traders or brokers with a stack of certificates—we’re the operators behind the reactor controls, supervising purification and packaging, troubleshooting at two a.m. if a run veers off profile.
One of our core priorities remains investment in modern process technology. Over the last decade, we upgraded from batch reactors susceptible to local heat gradients to fully automated, continuous flow systems. This shift has paid off in better control, lower impurity levels, and greater confidence for clients scaling from grams to multi-kilos. Inline monitoring catches deviations early, addressing problems before they translate into whole-batch rejects. Our operators, experienced in manual controls, now harness the best of both worlds—human expertise augmented by digital oversight, with the ultimate beneficiary being research teams counting on “no surprises” chemical inputs.
Looking ahead, the trend towards more complex, heavily substituted aromatic building blocks isn’t slowing down. Customers expect new functionalities, tighter tolerances, and reliable environmental compliance. In response, we push ongoing R&D investments. Several collaborations with leading chemistry institutes focus on developing safer, greener bromination alternatives—initiatives aimed at reducing reliance on hazardous reagents and minimizing generated waste. We also prototype advances in recycling spent containers, increasing reuse rates while maintaining purity requirements.
Rather than focusing solely on throughput, our philosophy remains grounded in end-user outcomes. We invite feedback, document the specifics, and work directly with partners to remove not just technical, but also logistical friction. Each new challenge raised by a research partner—whether a dosing anomaly, a need for custom particle sizing, or a request for a tailored impurity fingerprint—becomes an opportunity for us to apply both our experience and our flexibility as a direct manufacturer.
We never rely purely on theoretical specs or abstract claims about our chemical products. Every detail in the production and delivery of 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide draws from real manufacturing experience, hard-earned lessons from years on the plant floor, and candid feedback from the field. What distinguishes our approach is the conviction that reliable supply means more than target percentages and clean certificates. It’s the sum of fastidious recordkeeping, rigorous process control, and transparent communication with the end user.
Discovery and innovation depend on a steady foundation. We take pride in being part of that foundation, working side by side with leading minds in synthesis, adjusting and improving based on direct dialogue, not just market trends or standard protocols. Each batch of 5-Fluoro-2-(Trifluoromethyl)Benzyl Bromide reflects a commitment to consistency, utility, and quality—delivered with clarity and personal accountability, because we know exactly how much depends on each molecule we send out our doors.