|
HS Code |
560434 |
| Chemical Name | 2-(Trifluoromethyl)aniline |
| Molecular Formula | C7H6F3N |
| Molar Mass | 161.13 g/mol |
| Cas Number | 88-17-5 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 182-184 °C |
| Density | 1.283 g/cm3 |
| Refractive Index | 1.509 |
| Flash Point | 72 °C |
| Solubility In Water | Slightly soluble |
| Smiles | CC1=CC=CC=C1N |
| Inchi | InChI=1S/C7H6F3N/c8-7(9,10)6-4-2-1-3-5(6)11/h1-4H,11H2 |
| Synonyms | o-(Trifluoromethyl)aniline, 2-Aminobenzotrifluoride |
As an accredited 2-(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 100 g of 2-(Trifluoromethyl)aniline, tightly sealed with a screw cap, labeled with hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL container loads approximately 12–14 metric tons of 2-(Trifluoromethyl)aniline, securely packed in drums or IBCs for export. |
| Shipping | 2-(Trifluoromethyl)aniline is shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous chemical, with appropriate labeling and documentation. Transport must comply with relevant regulations for flammable liquids, ensuring secure packaging to prevent leaks or contamination. Personal protective equipment is recommended during handling and transport. |
| Storage | **2-(Trifluoromethyl)aniline** should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Keep the container protected from moisture and direct sunlight. Properly label and segregate the storage area, and ensure suitable spill containment measures are in place. |
| Shelf Life | 2-(Trifluoromethyl)aniline has a shelf life of 24 months when stored tightly sealed at 2–8°C, protected from light. |
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Purity 99%: 2-(Trifluoromethyl)aniline with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting Point 13°C: 2-(Trifluoromethyl)aniline with a melting point of 13°C is used in agrochemical manufacturing, where it enables precise incorporation into reaction mixtures. Molecular Weight 161.13 g/mol: 2-(Trifluoromethyl)aniline of molecular weight 161.13 g/mol is used in organic electronics research, where consistent mass facilitates reproducible device fabrication. Stability Temperature 120°C: 2-(Trifluoromethyl)aniline with stability temperature up to 120°C is used in high-temperature polymer synthesis, where it maintains structural integrity during processing. Water Content <0.2%: 2-(Trifluoromethyl)aniline with water content less than 0.2% is used in fine chemical reactions, where low moisture content prevents side reactions and maximizes purity. Refractive Index 1.511: 2-(Trifluoromethyl)aniline with refractive index of 1.511 is used in specialty optical material production, where it contributes to precise optical properties. GC Assay 99.5%: 2-(Trifluoromethyl)aniline with GC assay 99.5% is used in dye precursor synthesis, where it delivers consistent color intensity and quality. Residual Solvent <500 ppm: 2-(Trifluoromethyl)aniline with residual solvent below 500 ppm is used in pharmaceutical formulation, where it meets stringent purification standards for safety. |
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2-(Trifluoromethyl)aniline, sometimes referred to in trade as o-(Trifluoromethyl)aniline, is a building block that has earned its place across industries. On the manufacturing floor, workers know it for its chemical formula C7H6F3N, bringing together an aniline backbone with a trifluoromethyl group in the ortho position. The product arrives as a colorless to pale yellow liquid, noticeable for a sharp, pungent aroma. Over the years, repeated batches through our reactors have taught us that purity matters; we hold specifications to a minimum of 99.0%, verified with gas chromatography after every run.
Our process operators encounter this molecule day in and day out. We measure boiling range and water content as routine. The boiling point sits between 172 and 174°C at atmospheric pressure. The density comes in at about 1.282 g/cm³, checked at ambient temperature—there are no surprises, whether you pour from a flask in a research lab or draw samples at scale in an IBC. Hydrochloric acid residue and solids get filtered out early and often; trace levels mean trouble in downstream use, so we actively manage our line cleaning and reaction quench steps.
You work with chemicals for long enough, and you see how a small change in structure transforms usage. In practice, our customers differentiate ortho-trifluoromethyl substituted aniline from its para- and meta- isomers with good reason. Ortho substitution introduces steric effects close to the amino group, changing electronic features and reactivity. In pharmaceutics, that makes 2-(Trifluoromethyl)aniline particularly valuable for selective syntheses, where other isomers lead to different activity or entirely different byproducts.
On the plant line, when blending or reacting 2-(Trifluoromethyl)aniline, operators report fewer issues with over-oxidation or uncontrolled side reactions compared to para-variants. A trifluoromethyl group at the ortho position stabilizes intermediates, and users who switch from the para- or meta- isomers note improved yields in their specific applications. In custom syntheses for agrochemical active ingredients, our partners have shared with us that the ortho isomer brings unique potential for site-selective functionalization. These first-hand accounts shape our priorities for maintaining product integrity batch after batch.
We send most of our 2-(Trifluoromethyl)aniline output to pharmaceutical and agrochemical synthesis. Medicinal chemists prize its electron-withdrawing trifluoromethyl group, which changes biological properties, membrane permeability, and metabolic profiles. Our technical teams often get calls for advice on scale-up protocols for API intermediate synthesis. In crop protection, makers draw on the stability that the trifluoromethyl group brings—a property critical in synthesizing herbicides and fungicides that have to stand up to sunlight and moisture in the field.
Other uses show up in specialty dye and pigment modifications. Color chemists tell us that the presence of the ortho-trifluoromethyl group shifts electron density, deepening color or improving resistance to fading under UV. A few manufacturers working with high-performance materials turn to this molecule in polymerization reactions to introduce fluorine atoms into backbones, which leads to highly robust, chemical-resistant plastics. This flexibility means our teams coordinate deliveries in drum, tote, or bulk tank truck form to meet the requirements of a spectrum ranging from gram-scale R&D to continuous campaign manufacturing.
Decades of chemical production teach you where impurities hide and how they surface. Our in-plant trials pinpoint the main troublemaker: ortho and para isomers’ separation, water content, and foreign amine residues. We triple-check identification on incoming raw materials, then rely on in-process controls to spot deviations early. Infrared spectroscopy and gas chromatography ensure each drum holds onto a singular, clear spectrum. We target less than 0.5% total impurities, since small increases in byproduct mean headaches for users down the line, especially in regulated spaces like pharma.
We have found that customers in high-stakes applications, from API intermediates to active molecules for crop protection, see their yields drop off if purity falls below 98.5%. We respond to audit requests freely; keeping our shot records detailed and updated pays off. Water content—often underestimated—attracts special attention. Any moisture above 0.2% can trigger unwanted hydrolysis in our customers’ reactors, and we use in-line Karl Fischer titration as standard. These investments don’t just reflect good documentation; they lower real-world risk and downtime.
Our crews know this product’s quirks firsthand. 2-(Trifluoromethyl)aniline wants dry storage, preferably in sealed, inerted containers. During summer runs, warehouse temperatures climb, so we stagger shipments and encourage customers to warehouse in cool spots. Spill management falls under protocols we’ve established over years; every worker on the line trains yearly with simulated incidents, ensuring that the odor and volatility do not sneak up on anyone.
Customers often ask about compatibility with common materials. Most polymers and elastomers handle short-term contact, though we advise stainless steel or glass for longer exposure. Some fluoropolymer-lined fittings have proven leak resistant for years. Reactivity with oxidizers and acids ranks among the product’s more notable concerns in both production and customer labs; keeping stock isolated from such reagents has become second nature to our shippers and warehouse teams.
Direct supply brings real advantages in the fine chemical world. Selling 2-(Trifluoromethyl)aniline straight from our tanks, we see where knowledge gained on the production line helps avoid the pitfalls of old or mishandled inventory. Customers working on tight timelines rely on fresh product, not year-old drums that have sat neglected in a warehouse. We guarantee quick turnover on each lot, which means fresher, more reliable material for sensitive syntheses.
Inconsistent quality from resellers rarely comes down to chance; every week of storage in poor conditions, or shipping through multiple hands, can mean degradation or contamination. We watch for the yellowing that signals breakdown, and we work closely with haulers so that temperature swings and rough handling don’t affect what arrives at the customer’s dock. This vigilance comes from being both chemists and manufacturers, taking pride not just in the chemical formula, but in the day-to-day repeatability our customers see. Direct relationships with end-users make for faster feedback and faster correction, leading to better material and fewer wasted runs in downstream labs.
Past experience shows that trends in health, agriculture, and materials science ripple straight through production schedules. Each time a new pesticide or a novel pharmaceutical cGMP route comes on the scene, we see spikes in demand for ortho-trifluoromethyl intermediates. Antiviral research or crop-resistant fungus drives usage upward; our batch records show strong seasonality tied to regulatory approvals and field trials.
More producers now ask for expanded data packages and more transparent traceability—requirements our teams accommodate without hesitation. Safety standards tighten every few years; regulatory authorities demand more granular impurity profiles, not just overall purity. Our QC team responds with more sensitive testing methods, keeping audit records ready to share. These realities mean we invest in lab upgrades and revalidation of every process change, which, in turn, keeps risk low for users who rely on us.
Long before governments set emission limits or workplace guidelines, plant operators understood the importance of safe work environments. 2-(Trifluoromethyl)aniline, like any aromatic amine, brings health and handling challenges. Our process design includes double containment on transfer lines, fume collection hoods over both reactors and drums, and ongoing air monitoring—lessons we’ve learned after more than one minor incident in the past. Paying attention to these risks pays off with fewer lost-time incidents.
Waste management, too, draws direct attention. Any aromatic amine waste, especially those with fluorinated groups, needs careful segregation to avoid cross-reactivity in standard incinerators. We maintain relationships with licensed processors, tracking all waste leaving the facility. Operators double-check each container, and solvent recovery runs on every campaign, not just for cost efficiency, but because the downstream impact of trace residues matters—especially for partner companies striving for greener profiles in their supply chains.
Complex syntheses often bring up unique technical hurdles. One scale-up partner struggled to displace residual water in high-purity 2-(Trifluoromethyl)aniline; we responded by trialing new drying columns, lending our engineers on the customer’s site, and modifying packing protocols. This kind of back-and-forth, driven by open, technical conversation, shapes our product continuously. The hard-won lessons from these shop floor collaborations pursue more than compliance—they lead to process improvements that benefit everyone, including downstream researchers and manufacturers across the globe.
We’ve also tackled physical handling issues: in colder months, increased viscosity and slower pour rates become an annoyance in high-throughput lines. By adjusting storage conditions and providing guidance on controlled warming before use, we help partners avoid slowups and sampling errors. Fielding these questions directly—not filtering them through layers of distributors—shortens the route to workable, real-world fixes instead of theoretical answers.
In research and production, it’s the combination of reactivity and stability that sets 2-(Trifluoromethyl)aniline apart. The electron-withdrawing trifluoromethyl group restricts excessive side reaction at the amino function, allowing for greater selectivity in both nucleophilic and electrophilic substitution. Synthesis teams capture higher yields with fewer secondary products, making purification simpler.
Comparing this compound to unsubstituted aniline or to para- and meta-trifluoromethyl versions shows genuine differences in reactivity. Direct feedback from formulation chemists confirms that the ortho variant supports unique reactivity patterns, such as ortho lithiation, unavailable with its isomers. This specificity translates to less waste and tighter process control on multi-step syntheses, both in pharmaceuticals and agrochemicals.
Every production cycle brings new information. Records from our in-house QC teams allow us to pinpoint process drift, keeping specifications tighter with each year. Modest changes in solvent composition or temperature ramp create measurable impact on impurity profiles; experience built from years of operational data and test runs helps us spot deviations quickly. This hands-on attention gives customers confidence, especially when switching from test batch to multi-ton scale.
We’ve worked closely with researchers experimenting on new catalysts; sharing small samples and collecting reaction feedback cycles investment back into future batches. These real-world partnerships drive changes, whether it’s improving filtrate clarity, reducing iron contamination, or amending storage protocols. The result is simple: more consistent, predictable performance in the hands of our users.
2-(Trifluoromethyl)aniline continues to see steady investments across research and industry. As regulatory oversight increases, requirements for product purity and chain-of-custody tracking will only grow tighter. Customers seek lower trace metal content, greater transparency on side-product profiles, and more competitive pricing without loss of quality. We build these improvements directly into our plant—upgrading reactors, automating data logging, and refining downstream purification steps.
Long-term, we expect applications to diversify. Demand from electronic materials, fluorinated polymer synthesis, and new classes of bioactive molecules continues to trend upward. As base chemistry gets pushed into new territory, we adapt formulary and logistics support, keeping material supply in sync with evolving needs. On the manufacturer’s side, the focus remains on responsiveness and technical support—helping innovators achieve more, with fewer obstacles and tighter timelines.
Many products claim to reinvent the wheel; 2-(Trifluoromethyl)aniline simply does its job, batch after batch. The chemistry is robust, the specifications defined, and the performance proven across industries. Our relationship with this molecule, as manufacturers, runs deeper than data sheets or catalog entries—it’s built on cycles of learning, troubleshooting, and honest feedback from people who rely on it to work right, every time. For those on the front lines of synthesis, medical discovery, or material innovation, sourcing direct means getting the best version—handled properly, regulated thoroughly, and supported by a team that knows both the chemistry and the realities of large-scale production.