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HS Code |
862595 |
| Chemical Name | 2-Fluoro-4-(Trifluoromethyl)Aniline |
| Cas Number | 71770-38-6 |
| Molecular Formula | C7H5F4N |
| Molecular Weight | 179.12 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Boiling Point | 99-101°C at 20 mmHg |
| Density | 1.39 g/cm³ (approximate) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | C1=CC(=C(C=C1N)F)C(F)(F)F |
As an accredited 2-Fluoro-4-(Trifluoromethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Fluoro-4-(Trifluoromethyl)Aniline, with tamper-evident cap and hazard labeling. |
| Shipping | 2-Fluoro-4-(Trifluoromethyl)Aniline is shipped in tightly sealed containers under dry, cool conditions, and protected from light. Handling follows standard hazardous chemical procedures. Packages comply with relevant transportation regulations, including proper labeling and documentation. Shipping may be restricted based on local regulations due to its hazardous nature; check for any required permits or declarations. |
| Storage | **2-Fluoro-4-(trifluoromethyl)aniline** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from light and moisture. Use appropriate protective equipment and store in a chemical-resistant, labeled container. Handle under fume hood if possible to avoid inhalation of vapors. |
Applications of 2-Fluoro-4-(Trifluoromethyl)Aniline in Industrial Manufacturing2-Fluoro-4-(Trifluoromethyl)Aniline serves as a key intermediate for manufacturers in advanced agrochemicals, pharmaceuticals, specialty dyes, functional materials, and liquid crystal compound synthesis. The following sections detail real-world integration across major industries, with insights into compliance requirements, process parameters, and end-use products. 1. Herbicide Intermediate for Agrochemical SynthesisMany leading agrochemical producers use 2-Fluoro-4-(Trifluoromethyl)Aniline as a nucleus in developing innovative herbicides targeting resistant weeds. The molecule’s unique substitution pattern can improve binding affinity to target enzymes such as acetolactate synthase. Synthesis chemists employ it in multi-step reactions to construct highly selective molecules for broad-acre farming. Downstream blending lines frequently operate on customized ratio settings, responding to seasonal active concentration demands. Industry compliance standards
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2. API Intermediate in Pharmaceutical ManufacturingPharmaceutical active ingredient manufacturers leverage the fluorinated aniline scaffold to construct advanced pharmaceutical intermediates, including kinase and protease inhibitor structures. The compound’s electronic properties allow medicinal chemists to modulate metabolic stability and bioavailability in third-generation drug candidates. Integration takes place under cGMP guidelines, and stringent process validation governs all scale-up activity from kilo-lab to commercial reactor. Industry compliance standards
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3. High-Performance Dye and Pigment PrecursorSpecialty colorant manufacturers apply this compound as an electron-rich aromatic building block to synthesize high-performance dyes for plastics, inks, and fiber applications. The electron-withdrawing trifluoromethyl group offers robust stability for lightfastness and bleed resistance. Synthesis chemists implement this intermediate in diazotization or coupling onto chromophore scaffolds, ensuring targeted color characteristics through precision stoichiometry and reaction monitoring. Industry compliance standards
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4. Liquid Crystal Intermediate for Electronic MaterialsElectronics manufacturers utilize this advanced fluorinated aromatic amine in synthesizing high-anisotropy mesogenic compounds for liquid crystal displays (LCDs) and related technologies. The compound’s structural asymmetry supports enhanced mesophase stability and low threshold voltage properties demanded by next-generation display and sensor design. Production runs take place under high-purity protocols, with real-time process analytics ensuring impurity levels remain within industry thresholds. Industry compliance standards
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5. Building Block in Advanced Polymer SynthesisFluorinated aromatic anilines play a vital role as monomer precursors for the polymer industry, where manufacturers employ them to generate specialty polymers exhibiting high thermal and chemical resistance. The inclusion of both fluoro and trifluoromethyl motifs enables the fabrication of polymers with improved dielectric properties and hydrophobic surface characteristics, particularly for applications in wire insulation and precision membranes. Industry compliance standards
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Every now and then, a particular aromatic amine brings fresh thinking to the field of specialty chemicals. 2-Fluoro-4-(Trifluoromethyl)Aniline stands among this new tier, embodying the union of fluorinated functionality with amine versatility. At our facility, chemists often remark on the subtle energy that fluorinated arenes lend to their downstream partners. The production line has shown that each batch of this compound can often spell the difference between an average and a top-tier synthetic route—especially in the realm of pharmaceutical intermediates and agrochemical discovery.
The structure—anchored by a fluorine atom at position 2 and a trifluoromethyl group at position 4 of the aniline ring—yields distinct chemical behaviors compared to more basic anilines. With these electron-withdrawing groups, we see marked differences in reactivity, stability, and how it couples or transforms under common laboratory conditions. Many synthetic chemists long for a route that can handle tough coupling reactions or amide bond formations without excessive by-products. Over years of running kilo labs and pilot plant campaigns, we’ve confirmed that judicious introduction of fluorine—both mono and trifluoromethyl—often tunes the electron density just enough to deal with stubborn functional groups, or to force a clean conversion in otherwise sluggish systems.
The engineering team worked closely with our R&D staff to streamline the process and minimize material loss. Unlike unsubstituted aniline, 2-Fluoro-4-(Trifluoromethyl)Aniline resists atmospheric oxidation and offers a seductive stability profile—something one rarely finds in more basic aromatic amines. The typical batch, after purification, gives a pale-colored free-flowing solid or viscous oil, depending on temperature and storage. Residual solvents are kept below detection limits through extended vacuum treatment. Each shipment leaves the plant sealed in certified fluoropolymer or HDPE containers, not only for compliance but because these vessels have stood up best in long-haul shipment and seasonal temperature swings.
Across dozens of kilo runs, process reproducibility remains a strong suit. Titration assays nail the primary amine count, and NMR spectra show resolute single peaks for the desired aromatic core and heavy fluorination. These results set it apart from anilines with alkyl or single-fluoro substitution, where isomers can still creep in from side-reactions. Here, the robust steric and electronic shielding from fluorine delivers a product that rarely sees major side impurities.
Rarely does a week go by without an inquiry from advanced materials teams or synthetic R&D groups seeking a compound that offers both positional selectivity and robust stability under heat, acid, or base. The 2-fluoro and 4-trifluoromethyl dual substitution dramatically reduces amine oxidation, making it a steady partner in conditions that would otherwise ravage plain aniline. In our hands, this durability opens doors for scale-up campaigns in continuous reactors—often outpacing many simple mono-substituted anilines in both yield and process simplicity.
Typical customers use this molecule as a core intermediate in drug discovery, where tweaking the electronics of the aromatic moiety nudges entire synthetic campaigns toward new biological leads. The story echoes in the agrochemical sector, too. Researchers find this molecule an ideal ‘skeleton’ for assembling high-potency crop protection compounds. Its kinetic profile doesn’t just reshape a few steps in the route; it often slashes entire purification steps because unwanted by-products simply don't form at the same rate.
In the manufacturing world, efficiency means everything. Using 2-Fluoro-4-(Trifluoromethyl)Aniline, customers report shorter reaction times and higher selectivity in electrophilic aromatic substitution reactions. The increased resistance to hydrolysis, owing to the combined inductive effect of both fluorinated groups, yields practical advantages for both bench-top and continuous manufacturing, permitting harsher or more variable process conditions without the batch variability that haunts basic anilines.
Our process engineers build every kilogram with a strong respect for the nuances that come from live plant experience. One fundamental lesson: even slight changes in catalyst or solvent choice quickly translate into shifts in isomer ratios. Where older protocols might suffer from uncontrolled ring substitution, this molecule’s particular substitution pattern gives sharply defined products—fine-tuned through exacting temperature and pH tracking.
Team members often recount the first commercial-scale synthesis: the earlier candidate, a meta-fluoro or para-trifluoromethyl analog, always suffered from tedious distillation and intractable tar formation. Adopting the ortho-fluoro and para-trifluoromethyl approach changed the yield curve and improved batch-to-batch consistency. Instead of having to run multiple chromatographies or settle for half-pure material, customers now build their syntheses atop a reliable platform, dramatically reducing time in the analytical lab.
We also recall one customer’s pursuit of an advanced therapeutic target that failed due to excessive deamination in the presence of strong oxidants. Swapping in our 2-Fluoro-4-(Trifluoromethyl)Aniline, the problem evaporated. The compound’s resistance to oxidative decommissioning meant more grams of precious product were isolated, with less reprocessing. This feedback from the field mirrors what our internal R&D operations found as well: thoughtfully fluorinated aromatics often take more punishment—and deliver more reliable end-products—when real manufacturing pressures come into play.
Much discussion in the specialty chemical trade centers on listed numbers—assay, moisture, identification by NMR or HPLC. From our perspective as a manufacturer, these figures tell only half the story. In daily practice, shelf life, color stability, and ease of handling carry weighty importance. This product, even under humid summer warehouse conditions, clings to its integrity. We examine every drum visually and with spot analysis; rarely does one meet a darkened or decomposed lot if stored with sensible precautions.
Melt-point consistency matters to downstream formulating labs. Finely distributed fluorine content confers a higher, sharper melt-point ceiling than is seen in comparable mono-fluoro or simple methyl anilines. Analytical teams in our plant pick up on these differences right away, making process control easier and troubleshooting more straightforward. Whenever we run three consecutive campaigns, the appearance, melting profile, and purity remain almost indistinguishable—something not always true for less sterically protected amines.
Packaging also makes a difference: it’s not just regulatory compliance but a nod to years of lessons. Polyethylene containers outlast glass for certain customers due to impact resilience, yet preserve the low vapor pressure and oxygen exposure vital to aromatic amines. We never standardize on packaging simplistically; field returns and customer audits feed back into our SOPs, ensuring the packaging of 2-Fluoro-4-(Trifluoromethyl)Aniline matches the purity and stability baked in during synthesis.
Ask any plant operator about running a batch of unsubstituted aniline, and stories soon fill the air with problems: rapid oxidation, color drift, unpredictable pH swings, tough cleanup. By contrast, the product in focus here—with both 2-fluoro and 4-trifluoromethyl substitutions—avoids many of these pitfalls. Through a dozen production cycles, our logs show this molecule holds its color and minimizes resinous by-product formation.
We’ve tested related products such as mono-fluoro, methyl, chloro, and even nitro-anilines. Not one offers the same collision of stability and tuned reactivity. Where other amines stain containers or degrade in the presence of trace acids, this molecule powers through both strong mineral acid and moderate heat, giving more latitude in purification and reaction setup. Customers seeking ortho-selective coupling or meta-directed transformations typically see a smoother run-up with this product than with any singly fluorinated analog.
Many non-manufacturers only see a product at the point of purchase. For the teams who work in close quarters with these substances, everything from the aroma upon opening a drum to the flow of bulk powder counts toward operational safety and efficiency. 2-Fluoro-4-(Trifluoromethyl)Aniline offers lower vapor pressure, reducing inhalation risks compared to many other anilines. This brings direct benefits to plant safety and long-term worker health.
Regular check-ins with core customers reveal a pattern: end-users in pharmaceutical R&D value this material for its role in synthesizing kinase inhibitors and other drug leads with heavy fluorine footprints, while agricultural researchers leverage its stable amine group to build pre-emergent herbicides that resist field degradation. Neither group reports issues with background reactivity or isomeric impurities, a pattern that matches our findings from process development.
We keep logs on every customer’s feedback, especially around lot-to-lot consistency and challenges in downstream coupling. Over the years, users of less sophisticated anilines have reported batch failures due to air sensitivity or unplanned color changes. With this product, consistent batch outcomes remain a recurring theme, even in challenging environments. A North American client notes a 25% reduction in time needed for their key synthetic steps after switching to our material—a fact that highlights the sometimes-hidden value of improved starting reagent quality.
From a handling point of view, the compound retains more resistance to hydrolysis and oxidation than the sum of its fluorine substituents would suggest. Most plant operators prefer working with it over the simpler anilines or meta-fluorinated cousins, noting the dramatic drop in container residue and easier handling requirements. Gloves and local exhaust suffice for safe operation, and the absence of noxious by-products contributes to a safer, more controlled work environment.
Even in bulk, we haven't faced routine issues with compaction, static cling, or problematic dust—frequent complaints with other aminated aromatics. Most notably, returns or complaints due to shelf-life failure scarcely register. Shipping partners report no leakage or decomposition over long hauls in either cold northern winters or humid tropical climates.
We have seen a strong trend toward safer, more sustainable fluorination methods in recent years. Direct sourcing of fluorinated reagents from established partners ensures traceability. Unlike older days relying on hazardous reagents, our newer flow-chemistry setups reduce both solvent burden and operator risk. Waste minimization strategies, combined with in-line monitoring, keep environmental releases below the tightest local standards.
Our operations blend practical safety with ongoing innovation. For example, plant upgrades now channel off-gassed volatiles into scrubber systems. Secondary containment has ended almost all risk of spills or leaks, and our on-site teams regularly audit process steps to keep emissions ultra-low. Electronic batch records and routine peer review embed both accountability and quality into every step.
Field reports from advanced manufacturers validate the effort. As more pharmaceutical projects chase green chemistry benchmarks, having a reliable, low-impurity fluorinated aniline supports initiatives to simplify waste management and minimize the need for rework. This theme repeats across our customer base: process chemists get higher throughput with fewer headaches, QC managers document fewer deviations, and EHS teams sleep more soundly.
Why has 2-Fluoro-4-(Trifluoromethyl)Aniline earned favor among demanding synthetic chemists and production planners? Reliable performance, measurable gains in yield, and predictable behavior in both bench and industrial environments. Published studies and internal benchmarking show that electron-deficient aromatics like this one routinely outlast others in both storage and active process steps. In practical terms, switching from plain or mono-substituted anilines results in lower waste, cleaner product streams, and more robust purification options.
Ongoing innovations help lower unit costs by reducing energy consumption, improving throughput, and enabling new process windows. Our teams work jointly with customer R&D to debug scale-up puzzles on-site. We have documented repeated success in collaborative process troubleshooting: bottlenecks linked to poor conversion or side-reaction profiles have vanished when using our refined fluorinated aniline. The evidence accrues with every successful downstream campaign.
If trends toward more sustainable and safe chemistry persist—and all signs suggest they will—materials like 2-Fluoro-4-(Trifluoromethyl)Aniline will play a bigger role in defining what excellence looks like in both specialty chemicals and high-growth application areas.
Decades of collective manufacturing experience have shown us that reliable supply, transparency around quality, and a hands-on approach to customer support matter just as much as any specification listed on a paper. 2-Fluoro-4-(Trifluoromethyl)Aniline emerges not only as a high-purity intermediate but as a practical solution to persistent synthetic bottlenecks. It stands apart not just by numbers but because, time and again, it has delivered in the most demanding conditions. That’s why plant managers, chemists, and innovation leads across sectors look to it for unlocking greater efficiency, stronger safety margins, and more reliable outcomes. Our promise up and down the value chain hinges on the value that this material brings from first synthesis to final product—and we stand ready to face the next challenge, with the lessons of hands-on experience guiding each batch.