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HS Code |
974137 |
| Name | 2-Trifluoromethylaniline |
| Cas Number | 351-72-4 |
| Molecular Formula | C7H6F3N |
| Molecular Weight | 161.13 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 190-192 °C |
| Melting Point | -17 °C |
| Density | 1.272 g/cm3 |
| Refractive Index | 1.525 |
| Flash Point | 70 °C |
| Smiles | c1ccccc1C(F)(F)F |
| Solubility In Water | Slightly soluble |
| Synonyms | 2-(Trifluoromethyl)aniline, o-Trifluoromethylaniline |
As an accredited 2-Trifluoromethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Trifluoromethylaniline, 100g, is a sealed amber glass bottle with a tamper-evident cap and safety labeling. |
| Shipping | 2-Trifluoromethylaniline should be shipped in tightly sealed containers, kept upright, and properly labeled. Transport in accordance with local, national, and international regulations for hazardous materials. Protect from heat, direct sunlight, and moisture. Ensure compatibility with container materials and include safety documentation (SDS) with shipment. Handle by trained personnel only. |
| Storage | 2-Trifluoromethylaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store under an inert atmosphere if possible, and ensure proper labeling to prevent accidental misuse. Use secondary containment to avoid spills. |
Applications of 2-Trifluoromethylaniline in Industrial Manufacturing2-Trifluoromethylaniline serves as a highly specialized chemical intermediate in several industrial value chains, particularly in the synthesis of advanced agrochemicals, pharmaceuticals, dye intermediates, and specialty coatings. Below, we detail major downstream applications based on real manufacturing usage, compliance requirements, typical incorporation ratios, integration stages, and end product types. 1. Agricultural Herbicide SynthesisManufacturers leverage 2-Trifluoromethylaniline as a core building block in the production of advanced herbicide actives. Its trifluoromethyl group provides enhanced metabolic stability, critical for field performance and regulatory approvals. During process scale-up, QC teams must monitor for trace aniline and ensure controlled substitution patterns to match EU and US crop chemical standards. The compound typically reacts during the amide or sulfonamide coupling stage, following strict environmental control protocols to minimize residual by-products. End solutions focus on post-emergent selective herbicides for cereal and oilseed crops. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate for CNS AgentsIn pharmaceutical synthesis, 2-Trifluoromethylaniline is frequently used as a precursor in multiple CNS-active agent routes, including selective serotonin reuptake inhibitor (SSRI) scaffolds. Its electron-withdrawing group provides essential pharmacokinetic properties, supporting molecular designs that comply with both European and US API standards. Formulators introduce it in the core aniline condensation step, usually under anhydrous conditions, requiring dedicated cleaning validation to prevent cross-contamination. Manufacturers perform batch tracking through all stages to comply with stricter traceability rules for regulated final actives. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Organic Dye and Pigment Manufacturing2-Trifluoromethylaniline finds specific application in azo and anthraquinone dye synthesis where it serves as a diazo component or as a substitution base to adjust chromatic properties. Its integration allows pigment manufacturers to engineer shade, fastness, and substrate compatibility according to precise textile and plastics standards. The compound enters coupling reactions typically under acidic conditions, with close colorimetric QC at each stage to maintain consistent hue and purity tolerances throughout successive production runs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymer Additives and Coatings2-Trifluoromethylaniline is used by industrial clients as a functional group modifier for specialty polymer additives, boosting chemical resistance and thermal stability. Process engineers typically introduce it during polymerization or prepolymer modification, often using free radical or condensation polymer chemistry to ensure compatibility with engineering resins, fluoropolymers, or functional coatings. Material traceability, impurity control, and VOC reporting play a crucial role to satisfy end-use compliance in automotive, electronics, and heavy-duty equipment markets. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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At our plant, 2-Trifluoromethylaniline, model reference CAS 350-46-9, earns its reputation by performing in some of the toughest synthetic environments. We started producing this compound more than a decade ago, driven by demand from customers working on advanced agrochemical frameworks and specialty pharmaceuticals. Over the years, orders came in not just for kilogram batches, but eventually for metric tons—a sign the product had found its place in both research and large-scale production.
The structure combines a trifluoromethyl group at the ortho position of the aniline ring. This arrangement gives 2-Trifluoromethylaniline a unique electronic profile, setting it apart from standard anilines and their para- or meta-substituted cousins. With its chemical formula C7H6F3N, and a molecular weight of 161.13 g/mol, it offers both steric and electronic tuning that synthetic chemists rarely achieve through simple aniline derivatives. That –CF3 functionality does more than tweak reactivity—its sheer electronegativity can block side-reactions and control regioselectivity at a level plain aniline just cannot.
Our earliest clients came with requests for a trifluoromethylaniline designed specifically for challenging couplings and as a precursor for fluorinated heterocycle rings. In daily production, achieving consistent, high-purity material became a primary focus. Some customers ran into color instability and high water content from early samples sourced elsewhere, but by refining our purification sequence and using high-vacuum distillation setups, we soon delivered batches where color and impurity levels matched or exceeded strict regulations from major pharmaceutical multinationals.
We put immense effort into managing purity and moisture content. Unwanted moisture locks up reactivity, and trace colored impurities can drag down the yield of final products. 2-Trifluoromethylaniline that we supply typically achieves a purity level of at least 99.5% by GC, with moisture below 0.2%. That standard didn't come from marketing. It evolved through laboratory feedback—one batch with moisture slightly above spec translated directly into sluggish reaction rates at one customer’s pilot facility. They sent the batch back, and we learned quickly that peak dryness and colorless-to-pale yellow appearance, along with minimal residual solvents, were non-negotiable.
A lot hinges on packaging too. We ship in coated steel drums and pure HDPE containers with nitrogen padding to keep out ambient moisture and contamination. More sensitive applications receive material double-sealed in smaller containers, which almost eliminates risk during long sea or land travel. We store this product away from heat sources and light, in a nitrogen-filled environment, limiting oxidation or color darkening.
Most manufacturers offer ortho-, meta-, and para-trifluoromethylanilines. Yet only the ortho version—2-Trifluoromethylaniline—delivers the balance between reactivity and selectivity that several classes of coupling reactions demand. Unlike para derivatives, which feature a symmetrical charge distribution and generally allow less precise control over amine reactivity, the ortho isomer imposes steric constraints that often make it the chemist’s tool of choice for fine-tuning catalyst systems. The CF3 group at the 2-position can moderate the electron-donating properties of the aniline, which is essential for certain aromatic substitutions and C-N couplings.
2-Trifluoromethylaniline bridges the gap for manufacturers scaling up complex molecules—like fluorinated intermediates in herbicide design or for next-generation materials, including OLED precursors. Our direct customers—most of whom switch from other suppliers—report sharper, cleaner conversions and higher yields where positional isomerism makes or breaks the process. The difference between ortho and meta or para isn’t academic. Every batch we send out reminds us: stereochemistry at the bench impacts the bottom line at scale.
Market demand for 2-Trifluoromethylaniline climbs every year, especially in North America and Europe, where regulatory standards push for cleaner, more efficient synthesis. In agrochemical development, this isomer forms the backbone for several fungicide and pre-emergent herbicide programs. Many process chemists value it as a protected aniline for subsequent C-H activation, borylation, or Suzuki couplings—transformations that often stall or yield unwanted byproducts with unsubstituted aniline.
On the pharma side, discovery groups turn to this compound when they're sourcing novel scaffolds for small molecule drugs, especially analgesics and CNS agents. Here, the trifluoromethyl group lends metabolic stability and improved lipophilicity. End-users trace it all the way from grams on the benchtop into pilot and commercial scales. Every project brings new quirks; one pharmaceutical customer’s N-alkylation route yielded better selectivity and cleaner GC traces simply by switching to our material versus others from generalized traders.
Materials science teams order it, too. Electronic substrates and specialty polymers often need the specific properties imparted by the ortho-trifluoromethyl group for thermal stability or tuning dielectric properties—a demand that’s doubled in the past five years as consumer electronics shrink and performance requirements rise.
Anyone familiar with aniline chemistry knows that strong amines come with a set of safety challenges—fuming, odor, sensitivity to light and air. 2-Trifluoromethylaniline sports a boiling point in the low 200s Celsius, with a clear, persistent odor that signals its identity even in the lab. We’ve engineered our process runs to minimize fugitive emissions and capture any stray vapors using carbon filtration, which helps maintain a safe workplace on the production floor and in downstream warehousing.
Every lot undergoes rigorous QA testing. We deploy gas chromatography, 1H and 19F NMR, and headspace GC-MS to detect even low-level trace contaminants—a direct consequence of pharma and fine chemical partners demanding traceability and audit trails. Some years back, an entire lot flagged on NMR for a minor aromatic impurity introduced during a short maintenance shutdown. The trace didn’t impact most applications, but for one high-end user, it stopped their run. That event triggered new in-line sensors and an update of our lot release process. Customers want consistent, reliable material, but they also expect the underlying human oversight that closes the feedback loop between batch quality and end-use reality.
The pressure is mounting across the chemical sector to trim back hazardous byproducts and shift toward process intensification. In our own facility, a big leap forward came with solvent recycling loops and a swap from chlorinated to greener solvents where possible. By optimizing the amination step and using improved catalytic hydrogenation, we cut total byproduct volumes and improved atom efficiency by more than 15%. Yet, we still reach out to customers for feedback—rethinking waste reduction is not a one-off fix.
Several years ago, discussions with a pharmaceutical customer led to a co-developed protocol for in-line solvent recovery. Instead of disposing of used THF after recrystallization, they piped it back into our recycling loop. Costs dropped on both ends, and our environmental audit scores improved. The lesson stuck: progress comes from collaboration as much as from automation.
We keep our ears open to developments in catalytic amination, specifically new ligand designs that lower reaction temperatures and minimize hazardous waste. Emerging demand from medical device and energy storage companies has us revisiting both the specs of our product and safety data sheets to meet new purity targets. While traditional uses in fine chemicals remain the backbone, cross-industry requirements keep pushing us to think about long-term investments—in new reactors, better VOC control, training for our teams, and digital tracking across every drum shipped.
One partner recently requested a custom grade—a 2-Trifluoromethylaniline variant with ultra-low trace metal content. Serving that project meant tweaking upstream synthesis, investing in a new purification line, and running extra analytical work to validate the results. We don’t sell a “one size fits all” product. Each specification shift sparks fresh learning and a new round of process validation.
Our team includes seasoned batch operators, chemical engineers, and analytical chemists, some of whom have been overseeing the same reactor line since our earliest deliveries. They recognize subtle shifts in color or odor that outpace any instrument. Training and mentorship happen on the floor as much as in classrooms. New hires learn quickly that one off-grade batch can ripple through an entire supply chain—delaying research, costing money, even shutting down pilot lines. We make decisions with this in mind every day.
Behind every specification sheet and COA sits a story of troubleshooting and innovation. When a client’s route crashed due to trace iron—picked up from a worn reactor valve—we rolled out extra filtration and swapped components, then revised SOPs to prevent recurrence. That experience, and many others, shape our standards.
Chemical procurement teams want more than a certificate stating “meets 99% purity.” They need straight answers on batch consistency, impurity profiles, and long-term supply security. Over the years, we’ve developed relationships built on transparency and technical consultation—responding to urgency in R&D as much as to JIT manufacturing spikes. Supporting a major crop science leader during a sudden surge in demand taught us about flexibility: scaling from our usual monthly tonnage to triple output in less than six weeks, without compromising quality, forced us to fine-tune logistics, retrain staff, and run around-the-clock analytics.
Open channels with R&D leaders shape improvements both in-house and downstream. Regular feedback from end-users—everything from “GC trace looks clean” to “color slightly off this run”—feeds back into our control system and adjustment cycles.
Supplying specialty fluoroaromatics like 2-Trifluoromethylaniline is more than throughput or scale. It demands ongoing dialogue with technical partners. Once, during an early launch with a biotech client, their synthesis hit a roadblock after scale-up—reaction rates tanked and product yield dropped. Their team shared analytical details, and our process chemists worked together, tweaking drying times and switching to a fresh packaging format. The recovery restored the project’s timeline and even exposed small process improvements that benefitted our own operation.
Technical support carries through to logistics. Clients often call with storage questions, regulatory paperwork needs, or last-minute export documentation. Experienced staff respond rapidly—drawing on direct operational knowledge rather than boilerplate answers. A shipment stuck at a customs checkpoint prompted us to redesign our label format to match new GHS regulations, sidestepping weeks of delay in future runs.
Some may ask why a process group would stretch their budget to use a specifically substituted ortho-trifluoromethyl variant over other anilines. Simple: performance per gram matters at commercial scale. Subtle differences in electron-donating capacity, steric hindrance, and solubility determine the success of multistep syntheses and final product purity. That –CF3 group at the 2-position means faster reaction rates for nucleophilic aromatic substitution, and prevents unwanted ortho coupling, compared to the more commonly used para version. Fewer byproducts mean simpler downstream purification—translating to real cost savings, not just theoretical yield gains.
Several research groups report that meta and para isomers often fail to deliver equivalent selectivity, sometimes initiating irreversible side-reactions or premature deactivation of expensive catalysts. One long-term customer presented us with data showing a 6% yield bump after switching from the para- to our ortho-isomer in their agrochemical intermediate production. On the manufacturing end, that yield edge ripples out to reduced waste—and dozens of kilograms saved per batch.
Global compliance pressures keep evolving. Many of our customers now operate under ICH Q7 and ISO 9001:2015 regimes, with direct audits of our plant and supply chain. Every year, quality management systems undergo rigorous updates not just for paperwork’s sake, but to address feedback from real-world failures and near-misses. For products like 2-Trifluoromethylaniline, staying ahead of regulatory change is not a box-ticking exercise—it keeps export channels open and makes sure that a customer’s finished product stays in compliance.
Our experience also shows that integrating digital traceability—QR-coded drums, blockchain signing where required, SOP documentation—matters for trace-back and recall. Years ago, a lab-scale lot flagged for a packaging anomaly. Rapid response and traceable batch records narrowed the scope, scrapped suspect stock, and restored trust fast.
Reliable supply of 2-Trifluoromethylaniline makes a visible difference not just in the lab but at commercial scale. From blending in process liquors to isolation of critical intermediates, performance relies on more than numbers on a COA. Every specification has a backstory—real people running, sampling, analyzing, double-checking.
Supplying this key intermediate brings constant challenge and learning. The market never stops pushing for higher purity, cleaner batches, more sustainable production, and greater logistics reliability. We keep challenging our own procedures, working directly with customers, and investing in staff development and process modernization—because each incremental improvement doesn’t just help us, it keeps the entire supply chain delivering better products, smarter processes, and tangible cost savings.
We invite collaboration—problem-solving and mutual development—because that’s how both our team and our partners move ahead in a competitive, rapidly-changing sector. Our commitment to close quality control, technical dialogue, and continuous process improvement ensures that with every drum of 2-Trifluoromethylaniline leaving our plant, customers get more than raw material—they gain a partner invested in their long-term success.