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HS Code |
670668 |
| Cas Number | 65856-15-5 |
| Molecular Formula | C7H5F4N |
| Molecular Weight | 179.12 |
| Iupac Name | 2-fluoro-3-(trifluoromethyl)aniline |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 180-182°C |
| Density | 1.398 g/cm3 |
| Refractive Index | 1.478 |
| Purity | Typically ≥97% |
| Smiles | C1=CC(=C(C(=C1)N)F)C(F)(F)F |
| Inchi | InChI=1S/C7H5F4N/c8-5-3-2-4(7(9,10)11)1-6(5)12/h1-3H,12H2 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | 2-Fluoro-3-(trifluoromethyl)benzenamine |
As an accredited 2-Fluoro-3-(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, sealed with a screw cap, labeled with chemical name, CAS number, hazard symbols, and handling instructions. |
| Shipping | 2-Fluoro-3-(Trifluoromethyl)aniline is shipped in tightly sealed containers, typically under cool, dry conditions to ensure stability and prevent degradation. Packaging complies with hazardous material regulations, using approved containers and labeling. Shipping is conducted by certified carriers, with accompanying safety data sheets (SDS) to ensure safe handling and compliance with regulatory requirements. |
| Storage | 2-Fluoro-3-(trifluoromethyl)aniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, ignition sources, and incompatible materials such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store in a designated chemical storage cabinet, preferably for organofluorine compounds, and follow standard laboratory safety protocols to prevent exposure. |
Applications of 2-Fluoro-3-(Trifluoromethyl)Aniline in Industrial Manufacturing2-Fluoro-3-(Trifluoromethyl)Aniline serves as a specialty intermediate for a range of advanced chemical production sectors. As the direct manufacturer, our technical expertise supports downstream users with high-purity grades, custom packing, and integrated supply for demanding industrial applications. Here we give detailed insights into key market uses based on specific process requirements, actual formulation ratios, and regulatory protocols followed by leading industrial clients. 1. Synthesis of Advanced Pharmaceutical IntermediatesPharmaceutical API manufacturers employ 2-Fluoro-3-(Trifluoromethyl)Aniline as a core building block in the creation of targeted fluoroaromatic scaffolds and small-molecule actives, including kinase inhibitors and anti-infective candidates. The specific substitution pattern achieves precise molecular architecture during multi-step synthesis routes, supporting regulated drug development from advanced intermediates to GMP-compliant bulk APIs. Production teams incorporate this fine chemical through established aniline derivatization and coupling reactions that require careful stoichiometry management and trace impurity control. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingProducers in the crop protection sector use 2-Fluoro-3-(Trifluoromethyl)Aniline for synthesizing key herbicide and insecticide actives. Its unique substitution facilitates the creation of highly potent fluorinated ring systems that deliver improved biological activity and rain-fastness. Plant operators add this compound during early-stage cyclization or condensation in pilot and large-scale agrochemical production, under strict regulatory controls to ensure final residue safety and batch-to-batch uniformity. Industry compliance standards
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3. Specialty Dye and Pigment SynthesisManufacturers of specialty dyes and high-performance pigments utilize 2-Fluoro-3-(Trifluoromethyl)Aniline to introduce robust fluorinated aromatic units, critical for enhancing chemical resistance, photostability, and brilliance in organic pigment systems. The material enters production during diazotization or nucleophilic aromatic substitution stages, with strict analytical QC to ensure high batch purity suited for downstream pigment and dyehouse approvals. Industry compliance standards
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4. Electronic Chemical Intermediate for OLED and Display MaterialsProducers of advanced display and electronic materials deploy 2-Fluoro-3-(Trifluoromethyl)Aniline to construct tailored fluorinated aromatic linkers and hole-transport building blocks. The molecular profile supports downstream integration in OLED emitter molecule synthesis and specialty semiconducting polymers, where trace metal and halogen levels must meet ultra-pure electronics standards. The material is input at key fine chemical stages such as Buchwald–Hartwig amination or Suzuki coupling, with close process control over intermediates and polymerization feedstocks. Industry compliance standards
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5. Fluorinated Polymer Crosslinker PrecursorPolymer additive and specialty resin manufacturers rely on 2-Fluoro-3-(Trifluoromethyl)Aniline to introduce stable fluoroaromatic content into advanced fluoropolymer matrices. Its chemical structure allows ring-functionalization and crosslinking with high weatherability and chemical resistance, essential for demanding applications such as protective coatings, membranes, and adhesives. Blending occurs during bulk monomer formulation and crosslinking reaction set-up, typically under inert atmosphere to maintain functional group integrity. Industry compliance standards
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Walking through our lab and plant floors on any given day, the nuanced aroma in the air often signals more than just work in progress. Hidden in that bouquet, 2-Fluoro-3-(Trifluoromethyl)Aniline often stands out. After years of synthetic research and development, we’ve learned that no two aromatics behave exactly the same, and this compound exemplifies that difference. What may seem, on paper, just another substituted aniline, reveals itself in process by offering new synthetic pathways, practical efficiencies, and safety challenges that keep longtime chemists both cautious and hopeful.
Repeated handling of this molecule unfolds the story beyond a list of chemical properties. Technically, you’ll know it as an aromatic amine, a benzene ring studded with a fluorine at the 2-position and a trifluoromethyl group at the 3-position, alongside the amino functionality. In our hands, it shows a tendency to resist typical side reactions you might face with other halogenated anilines, mostly on account of its electron-withdrawing groups. We watch batch stability, reactivity toward other reagents, and subtle details like product color and odor development—because our customers, both from pharmaceutical and agrochemical pipelines, notice such markers. Their production yields and downstream activity depend on how cleanly and predictably the molecule behaves, and so does ours.
From a manufacturing standpoint, the journey starts with careful selection of starting materials. Over the years, we have seen how impure or varied fluorobenzene suppliers complicate purification and make final product consistency a non-trivial challenge. Early process steps involve meticulous halogenation, and the introduction of the trifluoromethyl group transforms the compound’s physical and chemical behavior. By the time reduction and amination come into play, the reaction medium must be adapted to the compound’s moderate volatility and sensitivity to both heat and excess acid. Our teams learned this lesson more than once when seeing yield drift due to inconsistent temperature ramping or solvent traces unresolved during workup.
We typically produce 2-Fluoro-3-(Trifluoromethyl)Aniline under tightly-controlled conditions to reach high chemical purity. Each year brings another tweak—new in-process controls, finer analytical instrumentation, and, of course, endless conversations between QA and synthesis teams. Most recent stock averages over 99% by GC analysis, in line with what our pharma partners lean on for advanced intermediates. Among the distinguishing features, we keep a close watch on residual water content and byproduct levels, as these have repeatedly shown to affect subsequent coupling or condensation steps. We consider it a decent feat to deliver reliable low-ppm moisture and minimize unknown peaks, even at scale, given how reactive some batches of starting halides can turn out.
Every batch passes through a multi-stage filtration and crystallization procedure before drying. Each step shows us a slightly different story about solubility and impurity profile, reminding us that commercial-scale chemistry is never “plug and play.” Dense, clear white to off-white crystals roll out at the end, packing easily and showing expected melting behavior. In the lab, chemists handling it repeatedly comment on the sharp and faintly medicinal odor—another sign that this isn’t just “any” aniline. From weighing to blending, the way it flows, cakes, and responds to agitation tells us a lot about the subtle differences in each run.
Years ago, general substitutions on aromatic rings felt like more of an exercise in academic curiosity than necessity. Today, nearly every pharmaceutical candidate or agrochemical screening set faces scrutiny about metabolic stability, toxicological profile, and selectivity. The presence of both a fluorine atom and a trifluoromethyl group in this aniline configuration changes not only the molecule’s electronic character, but also its fate once deployed in a synthesis or biological system.
We constantly field technical questions from process chemists: why start with this molecule rather than a more basic aniline or a singly-substituted derivative? The fluorine at the ortho position significantly slows down oxidative degradation, which elongates half-life in both synthetic and biological contexts. When reacting in nucleophilic aromatic substitutions or cross-couplings, these groups modulate the reactivity of the amino position, providing routes toward less common heterocyclic scaffolds. Medicinal chemists often look for this fine-tuning, hunting for that balance between desired potency, protein binding, and metabolic fate.
On the agricultural side, we see a different set of priorities—compound persistence in the environment, activity against resistant targets, and manageable toxicity to non-target species. Here, the combination of substitutions offers leads that survive sunlight, moisture, and pH shifts. Developers tell us that the electron-withdrawing strength imparts stability without turning the molecule into an environmental headache.
No conversation about specialty aromatics like this would be real without a plain discussion of safety and logistics. We move every kilogram behind local ventilation and personal protective gear, with operators trained on both chemical handling and the realities of working alongside potentially sensitizing anilines. Our own experience taught us that even minor skin contact produces irritation in some workers, so our packing lines use reinforced containment and clear spill response plans.
Packing this compound contends with moderate volatility and the faint, but persistent, tendency to creep out from less-than-perfect seals. We select high-integrity containers and place added indicators for humidity and seal status. Shipping routes favor rapid transit and climate-stable carriers. Customers in distant geographies sometimes ask about shipment delays, but in our experience, even short-term delays rarely affect compound quality if containers remain unbreached and dry.
Over time, thorough labeling and digital traceability proved invaluable. Once, a downstream user found trace contaminants arising not from our own process, but from a poorly cleaned tote used further down their supply chain. Every unusual customer report now triggers a root-cause loop here, squashing even low-probability routes of cross-contamination. None of this appears on a datasheet, but our staff know the stakes are larger than “acceptable ppm levels.” Trust comes from direct responsibility—and our entire team feels it, batch after batch.
Compared to other substituted anilines, 2-Fluoro-3-(Trifluoromethyl)Aniline both stands out and fits in awkwardly. Manufacturers struggle to balance performance, hazard profile, and accessibility. Take plain 3-(Trifluoromethyl)Aniline—a recognizable cousin: it offers reactivity, but not the fine-tuned stability and selectivity that medicinal chemists wring from the fluorine group's presence at the ortho position. Other fluorinated anilines show differing reactivities, but trifluoromethyl inclusion at the meta position leads to more pronounced lipophilicity and binding properties.
In trial syntheses, our own teams have learned how this dual substitution opens up novel routes to otherwise hard-to-access phenyl-substituted scaffolds. With paired fluorine and trifluoromethyl, electron-withdrawing character alters nucleophilicity and resonance in a way that makes certain palladium-catalyzed couplings and directed-lithiation routes higher-yielding, compared to monosubstituted variants. Where regioselectivity of further functionalizations is critical—especially when constructing heterocycles or fine-tuning bioactivity—this profile proves its worth.
Contrast this molecule with those bearing only alkyl or halogen substituents. The electron density at the ring and the amino group’s modified basicity change hydrogen-bonding patterns and solubility profiles, ultimately dictating formulation strategies for downstream users. In one memorable scale-up, a partner described how swapping in a non-fluorinated analog destroyed the shelf life of their candidate API. Minute differences matter, and inside our plant, nobody underestimates the stubborn selectivity that these groups enforce.
Many journeyed into this field as small-scale research chemists, toiling with gram-scale reactions and endless chromatographic runs. Bringing 2-Fluoro-3-(Trifluoromethyl)Aniline into commercial realization required a leap not only in vessel size but in mindsets. Each move—from degassing solvents to carefully managing heating cycles—brings fresh room for missteps and improvements. Quality assurance means more than confirming identity or purity; it means anticipating seasonal inconsistencies in raw materials, varied transportation climates, and the occasional hiccup in global supply chains.
As a chemical manufacturer, we’ve grown to revere the straightforward and dependable above the flashy but unpredictable. Our commitment to traceability, in-process analytical controls, and rapid response to client feedback forms the bedrock of our approach. Over the years, supporting both small biotech start-ups and multinational agrochemical houses, we have learned to weigh the trade-offs on lead time, scale, and formulation needs in honest conversation with our customers. This spirit of partnership often guides how we plan production windows, manage batch reservations, and decide whether to hold inventory or prioritize made-to-order runs.
Those who have worked on the plant floor know the impact of a ten-minute deviation during crystallization or the consequences of a contaminated solvent delivery. We keep our heads clear and our eyes on the practical realities: the generation of consistent, high-quality material, the safe and secure transfer of product from our hands to the customer’s, and eliminating bottlenecks before they threaten timelines.
Consistency rarely receives the attention it deserves in glossy product brochures, but day-to-day, it remains a relentless pursuit. Even when chemistries appear robust on paper, small variables—humidity, stirrer geometry, thermal gradients—shape batch-to-batch outcome in the real world. We use continuous in-line monitoring, rapid on-site analysis of incoming raw materials, and invest in regular staff cross-training. After all, a well-practiced operator or shift team can catch a drifting pressure valve or an off-specification color tone long before it becomes a reportable deviation.
Scale-up sometimes reveals quirks that make or break commercial viability. Take the solvent choice: on kilo-scale, waste disposal, odor management, and safety become as important as yield. In more than one campaign, alternative solvents—once beloved for laboratory ease—turned out ill-suited for commercial work due to regulatory or waste-treatment hurdles. Our current workflow optimizes for both outcome and environmental impact, helping us reassure customers that their end-use will not be complicated by avoidable burdens.
The days of “make, ship, and forget” grew outdated years ago. Customers expect traceability and environmental stewardship while regulators press for lower emissions and minimized human exposure. Internally, we continue evaluating greener synthesis routes, with a particular focus on minimizing halogenated waste. We are studying continuous flow alternatives for certain steps, with the aim to both improve safety and reduce resource footprint. Small changes in energy use and waste recovery during workup, spread across many metric tons of production, quickly add up.
Downstream, end-users increasingly ask about the lifecycle of our products—the presence of residual solvents, potential for bioaccumulation, and compatibility with recycling or waste treatment streams. By staying ahead of such queries, we avoid unpleasant surprises for all parties and develop a more resilient relationship between our plant and those who trust our materials.
We also engage directly with new regulatory discussions, whether around perfluorinated compounds or new exposure limits. Our technical staff keeps pace with emerging toxicological data and shares relevant findings with our clients, aiming to inform their own R&D and compliance teams before small issues grow into major project delays. Long experience teaches that quiet communication and shared transparency pay dividends over time.
Nothing compares to firsthand reports from users. Our technical support team shares synthesis notes with partners, helping them troubleshoot isolation steps or interpret tricky NMR signals involving fluorinated aromatics. We welcome return samples for reanalysis when someone encounters a sticking point in a reaction or finds a variance in downstream product performance.
Customer collaboration helped us improve crystal form uniformity and packing, reduce anomalous color development, and eliminate trace odor issues in our shipments over the past decade. In one project, an overseas partner’s repacking of our material led to clumping after several months at high humidity. Our subsequent change in primary packaging materials reduced this risk for others. Each exchange sharpens our processes and opens new questions about how best to support emerging applications.
Nobody in chemical manufacture can afford complacency. We see this in every fresh demand for a new grade, or every client push for a greener process and higher consistency. 2-Fluoro-3-(Trifluoromethyl)Aniline offers value and challenge in equal measure: performance, stability, reactivity, and safety all demand close daily scrutiny. We deploy cross-functional teams, blending raw process intuition with hands-on analytical skill, aiming for better and more predictable output.
Policy, regulation, and customer expectations continue evolving, especially around fluorinated materials. We meet these realities not only with improved controls, but with a commitment to ongoing learning and collective responsibility across our shop floor. For those built for the long game, the challenges of mastering this molecule prove as rewarding as the most successful batch delivered to a valued client.