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HS Code |
987231 |
| Productname | 4-Bromo-3-Fluorobenzotrifluoride |
| Casnumber | 401-91-0 |
| Molecularformula | C7H3BrF4 |
| Molecularweight | 243.00 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 154-156°C |
| Meltingpoint | -4°C |
| Density | 1.70 g/cm3 |
| Refractiveindex | 1.485 |
| Purity | ≥98% |
| Flashpoint | 62°C |
| Smiles | FC1=CC(C(F)(F)F)=C(Br)C=C1 |
| Synonyms | 1-Bromo-2-fluoro-4-(trifluoromethyl)benzene |
| Solubility | Insoluble in water; soluble in organic solvents |
| Storagetemperature | Store at 2-8°C |
As an accredited 4-Bromo-3-Fluorobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 4-Bromo-3-Fluorobenzotrifluoride is supplied in a sealed amber glass bottle with a chemical-resistant screw cap. |
| Shipping | 4-Bromo-3-Fluorobenzotrifluoride is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified as a hazardous material and requires appropriate labeling, documentation, and handling in compliance with international transport regulations. Shipping typically occurs via ground or air freight with secondary containment to prevent leaks or spills. |
| Storage | 4-Bromo-3-Fluorobenzotrifluoride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizers. Keep it away from sources of heat, sparks, and ignition. Protect from moisture and direct sunlight. Always follow local regulations and use appropriate secondary containment to prevent spills or leaks. |
Applications of 4-Bromo-3-Fluorobenzotrifluoride in Industrial ManufacturingAs an advanced manufacturer specializing in substitution fluorinated aromatics, we support global B2B clients in multiple sectors. 4-Bromo-3-Fluorobenzotrifluoride functions as an essential intermediate in fine chemical synthesis, particularly where both halogenation and fluorination impart performance advantages. The following sections detail industry-specific application scenarios validated by real-world downstream practices. 1. Agrochemical Active Ingredient SynthesisOriented chemical manufacturers utilize this raw material in the development of novel agrochemicals such as herbicide and fungicide actives. The trifluoromethyl and bromo-fluoro substitutions provide the precursor backbone for target molecules requiring selective reactivity and environmental stability. Synthesis processes typically employ it in the key halogen-exchange or Suzuki-Miyaura coupling step, enabling efficient downstream molecule construction. Industry compliance standards
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2. Pharmaceutical Intermediate for Specialty APIsDownstream pharmaceutical producers rely on this compound as a halogenated building block during multi-step synthesis of APIs, particularly in fluorinated aromatic drugs where metabolic stability and bioavailability depend on precise substitution patterns. It is typically involved following aromatic bromination and is key for subsequent nucleophilic substitution or Buchwald–Hartwig amination. Industry compliance standards
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3. Advanced Material Monomer ProductionManufacturers serving the electronics and specialty coatings markets use this intermediate to engineer fluorinated aromatic monomers, enhancing insulation properties and chemical resistance in end applications. Its selection enables fine-tuning of monomeric units for high-performance films and engineered resins, with the compound introduced via aromatic substitution or Grignard coupling methodologies. Industry compliance standards
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4. Liquid Crystal Intermediate ManufacturingProducers of advanced liquid crystal materials incorporate this compound into synthesis protocols for high-anisotropy aromatic cores. Its trifluoromethyl and halogen profile promotes superior electro-optic switching speeds and voltage hold, especially in display panel manufacturing. Process chemists utilize it in halogen exchange routes for LC functional group introduction. Industry compliance standards
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5. Synthesis of Fluorinated Aromatic Dyes and UV AbsorbersDye and pigment manufacturers select this intermediate to yield light-fast, chemically durable chromophores, leveraging the unique substituent effects of the trifluoromethyl-bromofluoro motif. The compound facilitates structural modifications and ring substitutions that enhance solubility and UV absorption in high-end coatings and polymer films. Industry compliance standards
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From years spent on the plant floor, overseeing the reactors as they transformed raw precursors into fine chemicals, some products stand out not just for their chemical data but for the role they play in shaping industries. 4-Bromo-3-Fluorobenzotrifluoride sits in that category. It offers a unique balance of reactivity and selectivity that many research chemists and commercial producers seek, yet few molecules deliver with the same confidence. Real, lasting product value shows up in the details: purity that saves downstream headaches, predictable performance batch after batch, and physical properties that allow for straightforward handling in scale-up or lab work.
Let’s talk about the chemical itself. The structure—where a bromine and a fluorine attach to a benzene ring that’s also substituted with a trifluoromethyl group—inspires a reaction profile not found in more common building blocks. Model MF-4BF317 consistently shows up at over 99% purity fresh off the line, supported by robust GC and NMR analysis. What you see is a pale, free-flowing liquid, easy to pour, easy to weigh, and unlikely to stick or cake in cold storage. Product stability matters in multi-week shipments or extended inventory holds, and this compound holds up without unusual color shift or precipitate compared to earlier tries with similar molecules.
Physical data shows a boiling point near 174°C, with a refractive index making it easy to track purity during QC. We have noticed that, unlike some halogenated benzenes, it stays clear and pure for notable periods, as long as the storage drum seals properly. The molecular weight sits at 259.01 g/mol—firmly into the “workhorse” category without going heavy enough to trigger handling surcharges at logistic checkpoints. With a density just above 1.6 g/cm³, transfer and metering always stay accurate, giving researchers predictable conversion yields. Every operator on the line knows that these details avoid cost overruns and rework caused by product variability.
This trifluoromethylated aromatic has carved out a reputation as a valued intermediate in pharmaceutical and agrochemical syntheses. When downstream developers need to introduce both halogens and electron-withdrawing groups, 4-Bromo-3-Fluorobenzotrifluoride saves time in route design. Medicinal chemists often call for this structure because the electron-withdrawing trifluoromethyl can tune the activity of APIs, while the bromo and fluoro allow further coupling or substitution. Attempts to substitute this with simpler fluorinated benzenes usually push the process into lower yields or introduce purification hurdles.
Crop protection labs reach for this compound when screening new actives, especially when early biological activity hints that a fluorine or trifluoromethyl moiety could stabilize target interactions. At no small cost, development pipelines show bumps or delays when trying to “mix and match” less specific halogenated aromatics. We hear from end-users frustrated by solvents picking up colored impurities from lesser-grade intermediates. Sitting in on calls with medicinal chemistry teams, their feedback circles back to the theme of time saved by avoiding redistillation or re-purification.
As a manufacturer, attention falls on what goes into a bottle, not just what’s written on a spec sheet. The fluorination and bromination stages demand constant monitoring. Halogenated aromatics can give off tricky byproducts, and only persistent in-process verification keeps odorous or impure fractions in check. Operators see that switching just the order of substitution or the temperature ramp yields different impurity profiles. Our batches leave the plant only after clearing a screen for residual solvents and side products—verification that often flags problems the moment they arise.
Packing matters just as much. Shipping standards built up over hundreds of barrels reveal which seals last months and which caps let in enough air to yellow the product. After seeing returns due to pitting from incompatible plastics, our team moved to thicker, fluoropolymer-lined containers, recognizing that only real-world experience distinguishes theoretical compatibility from dependable performance. Customers notice the difference: one less source of batch-to-batch variation, easier melting, and less crystallization at the lab bench.
Anyone with a catalog can spot dozens of halogenated benzenes. The question always lands on why go with this particular scaffold rather than defaulting to a simple trifluoromethylbenzene or plain bromobenzene. Subtle electronic effects dictate much of the value. The combined bromine and fluorine positioning on the ring gives cross-coupling and substitution reactions a site-selective advantage, translating into higher yields, milder conditions, and reduced byproduct generation in most lab or pilot plant settings.
After regular feedback cycles from research and process customers, our teams recognize that using a mono-substituted or symmetrical molecule usually means longer synthetic routes, increased separation costs, and slower scale-up. Growth in demand for molecules with defined substitution patterns owes much to time lost in cleaning up side reactions from non-specific intermediates. We’ve seen pilot plant campaigns trimmed by entire purification steps after upgrading from commodity halogenated benzenes to 4-Bromo-3-Fluorobenzotrifluoride. Combined with its physical resilience during transit and storage, this means fewer headaches and more reliable project timelines for users.
Scaling-up a compound with multiple halogens introduces unique hurdles. Trace metals and catalysts must clear strict limits, especially for pharma-bound product. The powders and solutions we generate must handle the repeated refilling of synthesis lines, as residue from one batch can affect the next. Night shifts have taught our teams the small tricks, like opening fill lines with dry nitrogen and staging product drums near the warehouse edge to avoid condensation. No bench-scale lesson matches what comes from running 2,000 liters through jacketed reactors.
Consistent product emerges from patience and repetition. Early experiments struggled with micro-batch exothermic spikes; data logging, stirrer redesign, and operator retraining pulled batch yields close to the theoretical maximum. Repeated practice taught which sources of precursors keep impurities below actionable thresholds. Having internal method validation, and not relying on third-party checks, gives us confidence that what leaves the plant will meet the application needs of highly regulated industries.
Year after year, requests for custom and scalable halogenated aromatics push our teams to stretch what is possible with existing infrastructure. Researchers bring new coupling reactions or catalytic techniques to us, looking for intermediates that won’t degrade or react prematurely. 4-Bromo-3-Fluorobenzotrifluoride, by virtue of its structure and robustness, keeps outperforming newer designer compounds in a number of test reactions.
Familiarity with the molecule means we can offer practical advice about purification, handling, and potential waste streams. On more than one occasion, teams from pharmaceutical partners have visited to trace an unexplained impurity to upstream solvent residues, resolved only through tweaks to the clean-in-place cycles and better distillation setup. Open feedback loops between manufacturing and end-users help refine each production run.
Handling halogenated products carries definite safety and environmental obligations. The legacy approach of venting or bulk incineration changes as regulations and best practices evolve. Our facility addresses these challenges by investing in improved ventilation, closed-loop solvent recovery, and advanced effluent treatment. These are not abstract commitments; they come from time spent responding to regulatory audits and internal reviews.
Operational updates have focused on precise inventory management to avoid overstock and prevent unnecessary product aging. Employee training emphasizes both safe handling and rapid response to contain spills, knowing accidents rarely happen under ideal circumstances. The raw experience of handling small releases has led to a protocol overhaul—improved absorbents, updated PPE policies, smarter emergency drills. Commitment to safety grows out of lived situations and ongoing investment, not slogans.
Real communication with clients builds more than transactions—it shapes product evolution. Technical service questions aren’t farmed out to remote experts; chemists who’ve synthesized the compound on scale guide conversations. Users describe synthesis plans, intended uses, or observed issues, and our staff shares practical fixes, based on what’s actually worked in our plant. A researcher looking to scale a route can rely on our experience with drum filling, transfer losses, or temperature stability rather than navigating anonymous technical notes.
Our teams stay engaged through the entire order process, troubleshooting issues such as shipment delays during customs checks or weather-related transit holds. We know that delays or material inconsistencies can disrupt schedules, trigger losses, or jeopardize product launches. By keeping production in-house and relying on repeatable, well-documented processes, we reduce these disruptions.
Choosing a building block for multi-step syntheses rarely happens in a vacuum. Multiple factors enter the calculus: purity, cost, reactivity, downstream compatibility, and supply security. From years on the ground, chemists appreciate that 4-Bromo-3-Fluorobenzotrifluoride assembles these attributes without serious trade-offs. Unlike split shipments from brokers, our material always reflects current batch data, handled by staff who regularly check in with user feedback.
Cost competitiveness improves as we streamline internal processes and scale batches up to meet fluctuating demand. The raw price of a kilogram tells only part of the story. The time and money saved on improved yields, purification, fewer side reactions, and stability over shelf-life makes a bigger dent in downstream budgets. Not all halogenated aromatic intermediates deliver these advantages outside of narrow, small-batch runs.
Feedback from longstanding customers points to repeatable success in established synthetic routes—whether making active pharmaceutical ingredients, pesticide actives, or advanced polymers. Unlike common trifluoromethylated or brominated benzenes, the studied balance of substituents delivers robust reactivity without requiring laborious process re-optimization at each scale. In tightly regulated settings, this means fewer surprises and closer adherence to approval guidelines.
Long production history shows where improvements have lasting benefit. Early runs showed drifting purity when holding times became too long; tighter schedule controls fixed that. Process upgrades, such as improved temperature control and in-line purity monitoring, raised yield and consistency. Technical staff documents every deviation and correction so future batches avoid the same pitfalls.
Advanced analytical methods like HPLC and FTIR supplement standard GC for impurity control. Routine data review sessions involve production, quality, and technical teams dissecting batch histories to anticipate and prevent future problems. This culture of openness and granular process review sustains high product integrity rather than relying on one-off “heroic” fixes. The end result for users is a consistent, predictable product that performs under real-world lab and plant conditions.
Demand for high-quality building blocks only grows as pharmaceutical and agrochemical research expands. Our investments extend to new reactor capacity, additional purification lines, and staff training—all aimed at producing not just more product, but better product. The combination of strong technical knowledge, hands-on production experience, and open communication underpins our consistent delivery of 4-Bromo-3-Fluorobenzotrifluoride.
Engagement with regulatory trends, sustainability targets, and evolving user requirements drives ongoing process adaptation. We review regulatory guidance on halogenated aromatic handling, environmental controls, and product stewardship, not as a box-ticking exercise, but as a chance to advance practice. Internal training adapts as staff face new hazards or efficiency tools, grounding development in both industry standards and daily plant realities.
Real quality in 4-Bromo-3-Fluorobenzotrifluoride comes not just from chemical structure or catalog entries, but from the habits and lessons accumulated by those who produce it at scale. Day-to-day familiarity with the molecule, attentive process controls, and frequent feedback create a product that busy teams can count on to advance research and build out supply chains. For chemists, formulators, and process managers who depend on reliability, traceability, and product purity, the difference lies not just in molecules set on paper, but in the deep experience brought by those who know this molecule inside and out. As demands shift and new applications surface, we stand ready to meet every challenge from a foundation built on practice, trust, and respect for the details.