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HS Code |
416146 |
| Cas Number | 349-20-2 |
| Molecular Formula | C7H6F3N |
| Molecular Weight | 161.13 |
| Iupac Name | 2-(Trifluoromethyl)aniline |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 175-177 °C |
| Melting Point | −12 °C |
| Density | 1.299 g/cm³ |
| Solubility In Water | Slightly soluble |
| Refractive Index | 1.498 |
| Flash Point | 70 °C |
| Synonyms | 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 | Amber glass bottle containing 100 mL of 2-Trifluoromethylaniline, securely sealed with a screw cap and labeled with safety precautions. |
| Shipping | 2-Trifluoromethylaniline should be shipped in tightly sealed, clearly labeled containers, compliant with all local, national, and international regulations for hazardous chemicals. Ensure packaging prevents leaks and protects from physical damage. Transport with proper documentation, avoiding extreme temperatures, direct sunlight, and ignition sources due to possible flammability and health hazards. |
| 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. Ensure proper chemical labeling and keep away from heat sources. Personal protective equipment should be used when handling to avoid exposure. |
Applications of 2-Trifluoromethylaniline in Industrial ManufacturingWe manufacture 2-Trifluoromethylaniline for direct use in specialized chemical synthesis across regulated downstream sectors. This section presents application methods, formulation parameters, and compliance insights specific to advanced chemical production lines, based on verified usage in global industry segments. 1. Agrochemical Intermediate Synthesis2-Trifluoromethylaniline serves as a building block for constructing active ingredients in selective herbicide and fungicide formulations. Its unique trifluoromethyl aniline structure enables downstream synthesis of pyridine and triazole derivatives required for next-generation crop protection chemicals. Our customers introduce it during the initial coupling step, benefitting from controlled reactivity in multi-step reactions. The incoming raw material’s impurity profile directly affects downstream activity and regulatory dossier acceptance. Industry compliance standards
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2. Pharmaceutical Advanced Intermediate ProductionIn pharmaceutical manufacturing, 2-Trifluoromethylaniline is essential in multi-step production of prescription active pharmaceutical ingredients (API). Its electron-withdrawing trifluoromethyl group facilitates nucleophilic aromatic substitution and regioselective coupling during core intermediate formation. Production lines demand traceability and batch consistency to comply with strict pharmacopeial validation. The material is typically dosed during amidation or urea formation stages where critical functionalization is required for later-stage transformation into final API molecules. Industry compliance standards
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3. Dye and Pigment Synthesis for Specialty ApplicationsThis raw material is deployed in the synthesis of high-stability dyes and pigments, where the trifluoromethyl group improves lightfastness and chemical inertness. Downstream manufacturers use it in diazotization, coupling, or condensation reactions to functionalize azo, anthraquinone, and phthalocyanine frameworks needed for inks, plastics, and coatings. Incoming lot color consistency and absence of trace metal contaminants are crucial for reproducible shade development and regulatory labeling. Industry compliance standards
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4. Electronics and Performance Polymer ModifiersProcessors rely on 2-Trifluoromethylaniline as a monomer or chain extender modifier for high-performance fluorinated polymers. Its molecular structure contributes to improved dielectric properties and hydrolytic stability, catering to the precise requirements of electronics encapsulation and specialized films. Manufacturers require batch traceability to maintain electrical and mechanical uniformity across production lots. The material enters reaction vessels in the polycondensation stage, where reaction efficiency is sensitive to both impurity levels and exact molar ratios. Industry compliance standards
Typical usage ratio
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As long-time manufacturers specializing in aromatic amines, we recognize how niche yet crucial 2-Trifluoromethylaniline has become in laboratories and factories worldwide. The story behind this compound goes well beyond catalog numbers or market trends—over years on the production floor, we have witnessed shifts in demand, refinements in synthetic routes, and increasing scrutiny on both purity and regulatory thresholds. The molecule itself—composed of an aniline ring with a trifluoromethyl group at the ortho (2-) position—sits at the intersection where reactivity meets stability, making it both versatile and reliable for diverse chemistries.
We focus on the analytical purity of each batch. 2-Trifluoromethylaniline, with its clear to pale yellow liquid appearance and characteristic aromatic odor, is more than its CAS number. Our in-plant experience underscores the necessity of strict control over residual solvents, so GC purity consistently exceeds 99%. We ship it after passing both NMR and GC-MS analyses. Moisture and iron content receive particular consideration, since uncontrolled trace contaminants trigger costly side reactions in pharmaceuticals and electronic intermediates. Anyone who’s worked on multi-step syntheses knows an unreliable starting material slows down projects and raises costs.
Storage conditions count as much as purity. The compound’s boiling point, around 180–182°C, means that bulk stock remains stable under nitrogen at room temperature, but we always urge developers to take precautions against prolonged light exposure or moisture ingress. We actively monitor for peroxide formation; we have found that using amber bottles mitigates risk, especially for R&D-scale deliveries.
Crafting 2-Trifluoromethylaniline demands more than a reaction flask and reagents. Decades of scaling up from pilot batches to commercial delivery have taught us the importance of robust safety measures. Starting from fluoroaromatic feedstocks, we rely on a well-tested catalytic amination route. Our reactors feature double-sealed systems that prevent fugitive emissions, given both the cost and potential environmental impact of fluoro-compound leaks. Every synthesis run features in-process controls for temperature, pressure, and pH, allowing for reproducibility and minimizing impurity formation. We handle waste fluorides and solvent residues using industry-approved abatement equipment.
As regulations have tightened, especially in jurisdictions like the EU and Japan, we’ve adjusted protocols to satisfy evolving standards. We pre-qualify all raw material vendors and track solvent residues to ensure downstream regulatory compliance. Years of treating our operators as stakeholders—not just technicians—results in a safer, steadier product. For customers in high-purity markets, we dedicate reactor time for the exclusive preparation of specialty grade 2-Trifluoromethylaniline, providing documentation on trace impurities and full batch traceability.
We receive ongoing feedback from our customers, which has taught us the importance of transparency in where and how our product fits. 2-Trifluoromethylaniline shows up first as an intermediate, but its impact tracks downstream into several key sectors. Agrochemical R&D uses it for introducing trifluoromethyl groups without the harsh conditions required for late-stage fluorination. Several pharmaceutical firms, especially in North America and Europe, rely on our material for their kinase inhibitor programs; here, the electron-withdrawing trifluoromethyl group enhances both activity and metabolic stability profiles.
Dyestuff research and OLED developers approach us for the same molecular motif that makes the compound structurally unique. By leveraging the effect of fluorine, they access shifts in color and performance difficult to achieve through other substituents. Over the years, we have supplied 2-Trifluoromethylaniline to teams designing custom ligands for catalysis or new-generation herbicides, each time learning more about the interplay between structure and function. Given the increase in patent filings involving this scaffold, experience tells us its relevance will only broaden.
Talking to formulation chemists highlights how purity extends shelf-life and reproducibility, particularly in fine chemical syntheses where impurities linger through multiple steps. We back every delivery with analytical support, because we have seen upstream corners cut in other products, leading to destabilized formulations or regulatory headaches for our clients.
Our daily encounters with bulk and specialty aromatic amines put the unique features of 2-Trifluoromethylaniline in clear relief. Direct comparisons to unsubstituted aniline, para-substituted versions, or even other ortho-substituted derivatives such as 2-chloroaniline reveal points of divergence that matter beyond the bench. The trifluoromethyl group at the ortho-position increases lipophilicity and improves the resistance of the ring to oxidative degradation. This contrasts with 2-chloro- or 2-methylaniline, which lack the same metabolic stability—one reason why fluoroaromatics often replace less robust motifs in pharmaceutical scaffolds.
From the manufacturing standpoint, the physical handling of 2-Trifluoromethylaniline resembles other light aromatic liquids, but its volatility is lower than simple aniline due to the bulk and electron-withdrawing power of the trifluoromethyl group. Odor thresholds also differ; years of batch production exposed us to how even trace concentrations linger in poorly ventilated spaces, so we’ve invested in closed transfer technology that eliminates exposure risks and odor complaints.
Those new to fluorinated building blocks often ask about alternative routes to introduce CF3 groups at the ortho-position. In truth, many older methods bring along excessive cost or environmental hazards. Our current route suppresses HF release and hits a balance between cost, yield, and environmental safety. We routinely compare our batches with samples from non-fluorinated analogues, noting how downstream yields and reaction rates shift. Academic reports confirm what we find in practice: the trifluoromethyl group modifies the ring’s electronics in ways unattainable via other simple alkyl or halogen substitutions.
Chemical synthesis evolves rapidly, and we are in regular dialogue with R&D groups working on new chemical entities. 2-Trifluoromethylaniline appears in lead generation projects and specialty material prototyping. In our experience, customers sometimes need slight shifts in impurity profiles to suit catalytic or scale-up requirements. Rather than push a one-size-fits-all product, we adjust our purification, filtration, or storage protocols to deliver on non-standard needs—real life seldom aligns with textbook cases.
A leading pharmaceutical partner once developed a custom amide using our material, but noticed a decrease in crystallization yield. Collaborating with their team, our process engineers tweaked distillation cuts to cut trace sulfonic acid carryover. The result delivered both higher downstream yields and easier purification at the customer site. In another case, an OLED materials group flagged batch-to-batch variance in minor byproduct levels. Our internal QC process found the culprit in a minor distillation step—solving it led to consistent device performance at their end.
Key to these experiences has been a willingness to listen and adapt. Chemical supply requires more than shipment paperwork; it means treating each batch as a stepping stone for innovation, not just another barrel on the loading dock. We now supply small lots to academic groups, scale tons for industrial users, and always keep a technical team ready to troubleshoot at short notice.
Regulatory requirements act as both a bar and a guide. We routinely provide full product dossiers documenting batch traceability, analytical methods used, and all impurity screens. Decades of dialogue with regulatory agencies and customer auditors keep us aligned with current Good Manufacturing Practices. Many clients leverage our documentation for their own regulatory filings, since they require ironclad provenance not only for active ingredients, but also key intermediates.
Our statistical process controls bring reproducibility, but achieving “the same” 2-Trifluoromethylaniline for pharmaceutical agents demands validated cleaning and split sampling. Regulatory inspectors have visited our lines, looking for systems to prevent cross-contamination with other anilines or reactive contaminants. We have invested in dedicated glass-lined reactors and air scrubbers. This helps not just with compliance paperwork—it minimizes unscheduled production downtime and cuts waste, with cost savings passed on in pricing and reliability.
Documentation extends to shipment—every drum or bottle shipped receives printed and electronic checks, ensuring all labeling, safety, and transport documentation aligns with current international law. High-value batches receive protective secondary containment both inside and outside the drum, tuned in response to customer feedback about rough handling at customs. By shipping with overpacking and positive ID tags, we’ve seen claims for leakage or product mix-up drop to near zero.
By controlling production and shipment, we reduce uncertainty for end users. Years ago, many would source this compound via traders or bulk blenders, introducing risk with delays and variable batch quality. With our in-house manufacturing, we offer firm delivery timelines, batch reservation for large projects, and customized packaging options directly from the plant.
Our engineering staff respond to technical queries, including compatibility evaluations for reactors, solvent systems, and waste treatment. Having met in person with researchers troubleshooting issue with scale-up, we know how important it is to connect sharply with the technical team behind the product. Few things sap research budgets faster than procurement errors or impurity surprises, especially as development cycles become more compressed.
We maintain open lines with process and formulation scientists—sometimes the best solutions come from a short call rather than a sales brochure. Customers planning new product launches have included us early in their workflows, allowing us to provide custom samples, recommend storage solutions, or even suggest alternative shipping schedules. Years spent in the supply chain taught us that reliability stems not just from the molecules, but from the partnership built with producers and users.
Increasingly, sustainability drives choices in raw materials and processes. While trifluoromethylated compounds present challenges in waste treatment, we back up every batch with a closed-loop waste management plan that complies with local and global regulations. Our reactor designs prioritize solvent economy and byproduct minimization. We work with licensed waste handlers to ensure fluorinated wastes receive proper treatment, mitigating downstream environmental load.
Supply chain transparency matters, particularly as more end-users need Life Cycle Analyses or third-party audits. On annual basis, we review our suppliers and update our environmental impact statements. Lessons learned from years on the shop floor have pushed us toward more recyclable packaging and minimized secondary containment for domestic shipments, without cutting corners on safety. Customers seeking carbon impact declarations or detailed chain-of-custody can access this data without hidden fees or delays.
One benefit of direct manufacturer relationships—especially in markets where compliance audits carry teeth—is clarity in environmental and quality performance. Our commitment stands not just in words, but in long years of audited performance, site visits, and open technical files. As regulations evolve and stewardship expectations become more demanding, we view our investment in sustainable operations as not just a box checked, but a means of competitive differentiation.
The last decade has brought step changes both in demand for 2-Trifluoromethylaniline and the standards demanded by downstream industries. Advances in medicinal chemistry, electronic materials, and custom catalyst design keep pressing for variants with new features—higher purity, specialized packing, documentation mapped to regulatory frameworks. We constantly invest in our own process technology: refining distillation, exploring greener chemistry for aromatic substitution, and tightening QC at every turn.
Feedback from clients—whether working on a drug candidate in preclinical studies or scaling up a new optoelectronic material—points in the same direction: the role of a specialty chemical producer extends beyond manufacturing. We now regularly collaborate on technical workshops, share anonymized case studies on impurity troubleshooting, and take supplier audits as opportunities to strengthen our processes. New routes to trifluoromethylated arenes, including those based on catalytic C–H activation or photo-induced methodologies, are on our R&D horizon, aiming for greener, higher-yielding preparations.
We see our job today as bridging between advancing synthetic technologies and practical delivery of reliably pure products. Market signals point to growing application in next-generation pharmaceuticals and materials science. Our unique experience—not just in making the product, but in understanding every layer from raw material to end-user process—will continue to drive improvements in quality and responsiveness.
Working hands-on with 2-Trifluoromethylaniline has shown us that value comes from real, technical engagement at every step. Every kilo we deliver reflects cumulative years of handling, problem-solving, and listening. The difference between a commodity chemical and a specialty intermediate often lies in unglamorous details—trace moisture control, batch-to-batch reproducibility, and proactive technical support. Competing products on the market can appear identical at a glance, yet missed details in synthesis or finishing stages ripple downstream, impacting costs, project timelines, and regulatory filings.
For customers who need more than a label, our open technical lines, documentation archives, and flexibility distinguish us in the market. 2-Trifluoromethylaniline may anchor a reaction, but it relies on the hard-won knowledge and commitment of experienced producers. This mindset builds both product quality and trust—not just in what gets delivered, but in the people and processes behind it.