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HS Code |
874420 |
| Cas Number | 401-21-0 |
| Molecular Formula | C7H4F4 |
| Molecular Weight | 164.10 g/mol |
| Iupac Name | 1-fluoro-4-(trifluoromethyl)benzene |
| Appearance | Colorless liquid |
| Boiling Point | 102-104 °C |
| Melting Point | -28 °C |
| Density | 1.338 g/cm³ at 25 °C |
| Refractive Index | 1.426 at 20 °C |
| Flash Point | 26 °C (closed cup) |
| Solubility In Water | Insoluble |
| Vapor Pressure | 25 mmHg at 25 °C |
As an accredited 4-Fluorobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 500 mL amber glass bottle with a secure cap, hazard labels, and product details for 4-Fluorobenzotrifluoride (CAS 402-44-8). |
| Shipping | 4-Fluorobenzotrifluoride is shipped in tightly sealed containers to prevent leaks and contamination. It should be transported in compliance with relevant regulations, such as DOT and IATA guidelines for hazardous chemicals. The containers must be clearly labeled, and the shipment should be accompanied by appropriate safety and handling documentation. |
| Storage | 4-Fluorobenzotrifluoride should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container protected from direct sunlight and sources of ignition. Store away from heat and open flames. Ensure proper labeling and prevent static discharge by grounding equipment. Use only with adequate ventilation and avoid moisture exposure. |
Applications of 4-Fluorobenzotrifluoride in Industrial ManufacturingAs a direct production manufacturer specializing in halogenated aromatics, we supply 4-Fluorobenzotrifluoride for high-value synthesis in advanced chemical sectors. This material sees stable, well-documented downstream use in specific industrial segments. Below we detail actual application scenarios, reflecting typical compliance regimes, recommended formulation ratios, practical process integration points, and downstream market products resulting from direct customer manufacturing operations. 1. Agrochemical Intermediate Synthesis4-Fluorobenzotrifluoride is extensively utilized as a key aromatic building block for crop protection molecule synthesis. The electron-withdrawing trifluoromethyl and fluorine substituents provide this raw material with the attributes necessary for nucleophilic substitution, making it an essential feedstock in producing several modern herbicide and fungicide actives. Our customers integrate it at the initial condensation stage, often in the presence of copper or palladium catalysts, to construct complex aromatic scaffolds required for selective agrochemicals development. Industry compliance standards
Typical usage ratio
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2. Pharmaceutical Intermediate ManufacturingLeading pharmaceutical synthesis operations employ 4-Fluorobenzotrifluoride in the formation of fluorinated benzene rings within APIs and advanced intermediates. Its controlled reactivity profile is essential in multi-step protocols requiring selective aromatic substitutions, notably for anticancer, CNS-active, and antiviral drugs. The product is handled under strict batch protocols, often with in-process QC monitoring for trace halogenated side products. Industry compliance standards
Typical usage ratio
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3. High-Performance Polymer Additive SynthesisProducers of specialty polymers use 4-Fluorobenzotrifluoride as a monomeric additive to introduce chemical resistance and thermal stability in resin backbones. The compound’s unique substitution pattern enables it to co-polymerize or react as a modifying group in high-value fluoropolymer chains, such as in advanced engineering plastics, cable insulation, and microelectronics substrate coatings. Usage demands precise weighment and strict atmospheric control during polymerization to preserve its fluorinated functionality. Industry compliance standards
Typical usage ratio
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4. Specialty Coating & Surface Treatment ManufacturingManufacturers of high-durability coatings utilize 4-Fluorobenzotrifluoride as a specialty intermediate to improve surface hydrophobicity and chemical resistance in architectural and industrial finishes. Due to its trifluoromethyl-fluorine configuration, formulating chemists add this raw material at controlled stages to boost stain resistance and adhesion performance, particularly for outdoor metallic substrates exposed to aggressive weathering or industrial chemicals. Industry compliance standards
Typical usage ratio
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5. Chemical Vapor Deposition (CVD) Precursor in ElectronicsFabricators in the electronics sector select 4-Fluorobenzotrifluoride as a specialty fluorinated precursor for CVD processes applied to semiconductor substrates. Its volatility and reactivity facilitate the deposition of ultra-thin fluoropolymer layers, contributing to advanced dielectric barriers and low-k insulating interfaces in integrated circuits and printed circuit boards. The material’s purity and vapor-phase behavior are strictly monitored under cleanroom protocols to achieve defect-free film growth. Industry compliance standards
Typical usage ratio
Downstream process integration
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Our experience in bulk production of 4-Fluorobenzotrifluoride (CAS Number 402-46-0, molecular formula C7H4F4) has given us a direct perspective on what makes this aromatic fluorinated compound essential for both specialty and large-scale chemical synthesis. The structure of this molecule, featuring both fluorine and trifluoromethyl functional groups on a benzene ring, gives it a set of characteristics that set it apart from similar halogenated aromatics. As a manufacturer, we focus heavily on consistency in purity, controlled synthesis, and traceability of every batch, due to the compound’s sensitive applications in the pharmaceutical, agrochemical, and polymer sectors.
Any chemist who has faced the downstream effects of trace contaminants in starting materials knows how a difference in synthetic route can change the outcome of a project. Our process uses high-purity starting materials and closed-loop reactor setups to minimize byproduct formation. Each batch of 4-Fluorobenzotrifluoride goes through a set of analytical verifications, such as GC-MS and NMR, designed to spot even minor impurities. Consistent purity—typically greater than 99.5% based on GC analysis—has proven essential for customers relying on this compound as a building block in further halogenation, cross-coupling, and nucleophilic aromatic substitution reactions. Low moisture and metal content enables cleaner reaction courses and less unwanted side product formation, especially in catalytic and organometallic chemistry.
Years working directly with the material taught us that 4-Fluorobenzotrifluoride requires a specific approach to storage and transfer. Although stable enough for standard warehouse conditions, the molecule’s volatility and its tendency to absorb onto surfaces call for lined drums and specific stainless steel contact points. We maintain our drums under nitrogen blanketing to avoid moisture seeping in, which can catalyze unwanted hydrolysis, particularly during long-term transit or outdoor storage situations.
A significant portion of our shipped product goes to advanced intermediates in active pharmaceutical ingredient synthesis. The electron-withdrawing nature of the trifluoromethyl and fluoro substituents make 4-Fluorobenzotrifluoride a favorite for those looking to produce aryl fluorides, phenols, and other functionalized benzenes through directed ortho-metalation or substitution. This molecule serves as a skeleton for fungicide and herbicide development, supporting direct scaling of milligram screening hits up to commercial runs of hundreds of kilograms. In the polymer sector, the unique substitution pattern gives 4-Fluorobenzotrifluoride a distinct reactivity compared to chlorinated or brominated analogs, delivering polystyrene derivatives with valuable dielectric and surface properties. We have also seen an uptick in requests for this compound as a solvent or intermediate for specialty electronic chemicals, owing to its low reactivity toward many normally aggressive reagents.
In our daily manufacturing work, meeting generic specifications does not cut it. No two applications treat this material exactly the same. As a result, we engineered flexibility into our purification process, enabling tighter control over factors such as residual acidity, organic chloride, and water content. Some customers request extra low aromatic impurities for use in sensitive photoinitiator synthesis or in electronics processing where outgassing matters. We accommodate these requirements by extending the purification cycle or increasing the number of distillation passes. This experience highlights the difference between material made to order and generic blends sourced through multiple traders—a variable many buyers overlook until a process issue arises.
Decades of manufacturing both this molecule and a range of substituted benzenes have made the differences abundantly clear. 4-Fluorobenzyl derivatives and compounds like 4-chlorobenzotrifluoride or 4-bromobenzotrifluoride each bring their own unique reactivity. 4-Fluorobenzotrifluoride stands out due to the positioning of the fluoro group, which draws electrons and influences subsequent aromatic substitution in a predictable manner, giving chemists valuable control over downstream transformations. Where chlorine or bromine analogs often trigger more side reactions—especially during transition-metal-catalyzed cross-coupling—the fluoro group’s stability can mean less clean-up and fewer catalytic poisonings. In processes demanding tight mass balances and reliable product isolation, this seemingly small substitution makes a marked difference.
Running multi-ton continuous reactors, we learned the biggest bottlenecks occur in handling off-spec batches stemming from trace contamination or inconsistent reaction conditions. Automation and inline analytics improve reliability, but worker training and direct oversight remain irreplaceable. For instance, 4-Fluorobenzotrifluoride distills cleanly at around 102–106°C under reduced pressure, but without strict temperature control or carefully tuned reflux times, carryover of heavier aromatic impurities leads to significant off-hours in reprocessing, increasing cycle costs. We document these lessons and apply traceability to every run, so customers get the batch and purity they expected every time—a key advantage over loosely managed facilities.
Packaging is more than just an afterthought. The fluoroaromatic chemistry of this molecule calls for materials that don’t introduce leachables or react with stored product. We employ fluoropolymer linings or compatible stainless-steel drums, with a policy of full traceability on seals and liners to minimize the risks of cross-contamination or degradation in transit. The low moisture uptake gives an edge, especially in tropical port environments or during long sea journeys.
While specialty pharma synthesis commands much of the attention, we see this product move across into electronics, agricultural, and even surface coatings work. Our partnerships extend from boutique R&D firms to industrial-scale manufacturers looking for reliable monthly supply. Successful scaling or daily “just-in-time” deliveries require constant technical support, not just a generic spec sheet, so we keep expert process chemists accessible right through to our loading bays. Detailed certificates of analysis accompany every shipment, with batch-specific data drawn from the actual analytics—never a copy-paste from master data files.
Reacting to customer demand pushed us to examine greener alternatives in our purification and waste handling. Standard fluorinated aromatics can generate tough-to-manage waste streams, given the stability of C–F bonds. We invested in solvent recovery and advanced scrubbing systems to reduce both ecological and regulatory burdens. On the research end, we are probing selective catalytic fluorination routes to potentially streamline synthesis, lower reagent usage, and improve atom economy, since the traditional routes using strong halogenating agents leave little room for error and tend to create persistent byproducts.
Our commitment to traceable, verifiable analytics extends back to raw material sourcing. Each solvent, reagent, and additive gets tracked through ERP-integrated batch codes. This attention to detail is not academic; downstream users often report back that tighter impurity profiles in their 4-Fluorobenzotrifluoride batches directly reduce clean-up costs and improve batch-to-batch reproducibility for their finished products. Our technical support staff notes the most frequent questions involve solvent residue, heavy metals, and trace organic content—metrics we report transparently and in detail, not just aggregate values.
We spend as much time with compliance teams as in the reactor bays. The molecule itself does not fall under controlled substance lists in most regions, but end-use declarations, REACH pre-registration, and product stewardship protocols underpin long-term global supply. Our regulatory staff ensure each MSDS, COA, and other product documentation reflects the exact batch parameters, and integrates customer feedback and requirements, not just minimal regulatory compliance. This hands-on approach supports responsible manufacturing and builds trusted relationships.
We routinely incorporate suggestions from regular users, whether it’s requests for custom packaging sizes, lower impurity thresholds, or modifications in labeling for automated warehouse integration. One of the recurring themes in customer site visits: unexpected side reactions due to off-brand substitutions—a scenario often avoided by long-term buyers who recognize the manufacturing origin matters. It is not unusual for us to tweak a production parameter or schedule extra QC checks based on input from a client scaling from pilot to full production.
Years spent troubleshooting reactor issues, negotiating logistics delays, and adjusting purification have clarified what differentiates truly consistent bulk chemical suppliers from generic intermediaries. Success with 4-Fluorobenzotrifluoride depends on direct communication, agility in technical adjustments, and deep process understanding. We treat each order as a long-term relationship investment, not a one-off sale. Our technical, warehouse, and regulatory teams respond quickly to evolving needs—not because of contractual obligation, but from an understanding that reliability is earned, not assumed.
In the crowded space of fluorinated building blocks, end users quickly learn that manufacturing quality makes or breaks a process. The impact shows up in purification columns running cleaner, reactors generating less fouling, and final products hitting target specs with less post-processing. Our accumulated process control—from raw material bulk unloading through to analytical batch release—remains a differentiator for teams seeking reliable input materials for their proprietary chemistries.
Work with 4-Fluorobenzotrifluoride has reinforced how value builds not only from high purity and consistent packaging, but from adaptability to real-world process needs. Our manufacturing systems, people, and problem-solving approach have proven their worth in fields as diverse as pharmaceuticals, electronics, and advanced materials research. We continue to refine our production and analytical controls, because every batch delivered carries the reputation we have built—and every user counts on us to lock in those advantages for their innovations downstream.