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HS Code |
565511 |
| Product Name | 3-Methyl-5-Trifluoromethylaniline |
| Cas Number | 261952-29-6 |
| Molecular Formula | C8H8F3N |
| Molecular Weight | 175.15 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 208-210°C |
| Density | 1.217 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Refractive Index | 1.494 |
| Smiles | CC1=CC(N)=CC(C(F)(F)F)=C1 |
| Synonyms | 3-Amino-5-methylbenzotrifluoride |
As an accredited 3-Methyl-5-Trifluoromethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g amber glass bottle features a secure screw cap, hazard labeling, and clear identification of 3-Methyl-5-Trifluoromethylaniline. |
| Shipping | 3-Methyl-5-Trifluoromethylaniline ships in tightly sealed containers to prevent leakage and contamination. It is transported under standard chemical shipping regulations, typically at ambient temperature, with clear hazardous material labeling. Ensure compliance with local regulations and use appropriate protective packaging to avoid exposure and environmental release during transit. |
| Storage | Store **3-Methyl-5-Trifluoromethylaniline** in a tightly sealed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances like strong oxidizers and acids. Protect from direct sunlight and moisture. Use appropriate chemical-resistant storage solutions and label containers clearly. Follow all relevant safety and local regulatory guidelines for storage of hazardous chemicals. |
Applications of 3-Methyl-5-Trifluoromethylaniline in Industrial Manufacturing3-Methyl-5-Trifluoromethylaniline serves as a key intermediate in several established chemical production sectors. As an experienced manufacturer, we support global partners in integrating this specialty amine into advanced synthesis workflows. Below, we detail actual downstream scenarios that rely on our material, delineating regulatory standards, precise formulation ratios, processing stages, and the finished products used in professional applications worldwide. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisLeading pharmaceutical manufacturers select this compound for constructing core heterocyclic motifs during early-stage API synthesis, particularly in fine-tuned multi-step flows for fluorinated drug development. It delivers unique electron-donating and -withdrawing character, influencing reactivity profiles essential for high-purity amide and urea derivatives in small-molecule drugs. Industry compliance standards
Typical usage ratio
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2. Agrochemical Synthesis for Herbicide and Fungicide ActivesCustom agrochemical compounders incorporate this aromatic amine in synthesizing novel triazine and pyridine-based herbicides, as well as key fungicide precursors, leveraging its trifluoromethyl group to impart environmental stability and soil mobility control in the end formulation. Industry compliance standards
Typical usage ratio
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3. Specialty Dye Manufacture for Electronics and Laser ApplicationsLeading pigment and dye producers integrate this aromatic amine into their molecular design platforms for synthesizing high-contrast, electronically stable dyes and laser marking materials. The combination of methyl and trifluoromethyl groups yields chromophores ideal for print electronics and laser-emitting components. Industry compliance standards
Typical usage ratio
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4. Advanced Polymer Additives for High-Performance CoatingsMajor resin formulators include this specialty amine in synthesizing bespoke benzoxazine and polyimide monomers, enabling coatings with superior chemical resistance and UV durability. The molecular profile supports polymer chain modification aimed at high-heat industrial coating applications. Industry compliance standards
Typical usage ratio
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5. Fine Chemical Building Block for Liquid Crystal Display (LCD) IntermediatesKey LCD material developers utilize this aniline derivative to build highly substituted aromatic systems, which are then incorporated into advanced mesogenic compounds. Its unique structure offers improvements in dielectric properties and thermal stability required for next-generation liquid crystal formulations. Industry compliance standards
Typical usage ratio
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Years of producing 3-Methyl-5-Trifluoromethylaniline (often referenced in scientific work by its CAS number 328-74-5) have taught those on the manufacturing floor what makes a building block worth choosing over another. This compound houses a trifluoromethyl group, which means you get distinct electron withdrawing power that can tune how your molecular structure reacts. Technicians who spend their days hunched over reactors know the difference a methyl group’s positioning makes. In 3-Methyl-5-Trifluoromethylaniline, it sits in the right spot to make reliable intermediates for agrochemical and pharmaceutical researchers. These groups, paired together on the aniline core, let downstream chemists explore transformations like amide coupling or selective substitution that would be trickier with more basic anilines.
While many on paper might compare it to 4-methylaniline or trifluoroaniline, only someone formulating hundreds of kilograms at a time knows the distinction in purity, batch consistency, and how the raw material’s trace moisture levels or residual impurity can derail a pilot process. Our engineers, who oversee each batch, use vacuum distillation and storage protocols that fit what downstream chemists need: not just to meet numbers on a certificate, but to keep their yields predictable and their reactions free from byproduct headaches.
Processes using this compound often produce active ingredients for herbicide or fungicide development, or certain APIs where a trifluoromethyl group stabilizes metabolic pathways or modifies receptor binding. We see demand from teams looking for a straightforward way to introduce a trifluoromethyl group to their scaffold, but with the amine kept reactive for further analog development. Other trifluoromethylanilines may compete for similar slots, but here, the 3-methyl adds solubility tweaks and can change hydrogen bonding. Such factors, though small on paper, emerge as bottlenecks later if overlooked during development.
Our batches of 3-Methyl-5-Trifluoromethylaniline meet the strict HPLC and GC purity targets demanded by regulated industries. But more than the numbers, it’s the stability and shelf storage—realities often overlooked—that push us to invest in moisture removal and packaging under inert gas. In our experience, even minor groundwater ingress can trigger color changes or early decomposition. Teams from analytical labs have called us to discuss lot-to-lot color, and over time, we have traced every shade shift to a process anomaly that could have been controlled with better QA or vessel cleaning. We check for residual solvents below one-tenth of regulatory minimums, trace any amine byproducts that sneak in during reductive steps, and rework every batch that doesn’t degas smoothly or give a clean baseline in its NMR.
Handling is straightforward in a plant built for it, but its vapor pressure and faint amine odor can drift through leaky seals if not packed right. Our floor managers inspect every drum for seal integrity, knowing how one loose cap can waste a good batch en route to a customer. The boiling point (usually noted around 185°C) supports most standard organosynthetic setups, and the compound’s low aqueous solubility means it works well where water-sensitive transformations run. You can’t gauge this value from a spec sheet—it emerges from hundreds of drum shipments where the difference in field performance often means the making or breaking of a project timeline.
For R&D teams pursuing patentable lead compounds, the 3-methyl contributes to selective molecular interactions, while the trifluoromethyl group boosts metabolic stability. Synthetic chemists reach for it to introduce aryl amines into heterocycle synthesis, especially when downstream halogenation or acetylation is intended. Peptide or small molecule developers rely on the amine’s nucleophilicity to couple a range of activated carboxylic acids or acid chlorides, often producing intermediates for CNS or oncology candidates. Those experienced in agrochemical design know the subtle difference a trifluoromethyl group brings—slower biodegradation, greater lipid solubility, and sharper differentiation from off-patent analogs.
As a manufacturer, we see where typical commercial batches fail: solvent residues or unstable byproducts can throw off pharmacological profiling assays or field trial formulations. This is not just academic; raw material flaws set off a cascade that piles up cost in lost time and re-qualification. Our teams double down on outbound QC to keep every canister within the defined limits, so our clients don’t wrestle with unknown variables at the formulation or preclinical stage.
On industrial scales, chemists use this aniline for functionalization, cross-coupling, or to make urea and sulfonamide derivatives. You can’t get the same substitution pattern, say with a meta-methyl and para-trifluoromethyl, from off-the-shelf anilines; regioselectivity and electronic tuning matter when climbing a multistep synthetic ladder. We supply kilo to metric ton quantities with attention to drum lining, palletization, and shielding from UV during transit, because product loss from sunlight or temperature spikes can wipe out margins, and everyone from shift supervisors to warehouse handlers knows the aftershocks of a mispacked shipment.
There is no substitute for hands-on, batch-by-batch experience when it comes to reliable supply. Our chemical engineers track each lot from catalyst preparation through final distillation. If a known impurity emerges during workup, adjustments aren’t guesses; they’re tested tweaks backed by years of plant data. Such nimbleness would not be possible through third parties, where feedback cycles lag and repeat quality issues fester. Custom orders using client-specified moisture levels or alternate solvents don’t require bureaucracy—they go straight to production planning. This is a supply chain difference that keeps partner projects on schedule and regulatory filings smooth.
We’ve been called for urgent fills when a competitor’s lot failed stability or an intermediate batch proved unusable. Our people talk to the chemists at the receiving end, asking which assay or formulation issue triggered the callback, and our fix is grounded in firsthand processing knowledge. If a process hiccup emerges—say, trace halides increase oxidation during one synth run—we document, adjust, and cycle in improvements. Academic chemists tell us about NMR multiplicity shifts, and our QC adapts accordingly, checking the next round for clues that something might disrupt a route. This ongoing feedback, translating field insight into plant practice, sets apart direct producers from those focused solely on logistics.
Many buyers compare 3-Methyl-5-Trifluoromethylaniline to simpler anilines like toluidine or para-trifluoromethylaniline. To anyone running an industrial synthesis, the difference often appears in product isolation and workup. A para-positioned trifluoromethyl usually provides higher oxidative stability but at the cost of lower reactivity in further substitutions. The meta-methyl in our product tweaks the ring’s electronic density, making certain cross-couplings more manageable, and avoids reaction bottlenecks common in more symmetrical structures.
Raw material teams regularly ask if anilines with fewer or different substituents work in a given process. Our experience tells us that trace differences—like a methyl in the wrong ring position—can throw off LC purities by single-digit percentages, turning a scale-up run into scrap. With years spent on optimizing workups and minimizing labor-intensive extractions, we keep our products tailored to the needs of synthetic chemists who rely on predictability and minimal waste. This isn’t a minor point; cleanup steps and waste disposal cost labs valuable hours and resources, and suppliers delivering batch-to-batch variation make this worse. Direct production, with in-line monitoring of impurity levels, sidesteps these risks.
More basic anilines, like simple toluidine, might serve in unregulated uses, but they fail when regulatory filings demand thorough impurity mapping. Our teams track every batch’s byproducts and keep analytical archives for those preparing files for regulatory bodies or IP protection. It isn’t just about ticking boxes; from cleaning reactors to minimizing carryover, we streamline processing to help innovation-driven labs speed up their projects. Our QC handles not just standard chromatographic purity but stability under accelerated aging and exposure to typical lab and plant stresses, based on years of returned sample analysis.
The stricter the market’s environmental and safety requirements get, the more it matters that manufacturing controls product quality from raw material selection through final dispatch. We use closed-system reactors with emission capture and solvent recycling. Years ago, we recognized that uncontrolled venting leads to operator complaints and neighborhood issues, so newer production lines include air scrubbing and in-line neutralization. Handling is set up to keep worker exposure within current TLVs, not just regulatory minimums. As demand increases from Europe and North America, with their tighter controls, we invested in storage, drum lining, and tracking technologies to avoid heat or moisture events that can ruin whole shipments.
By making the product ourselves, we record every step and document every process adjustment. This isn’t just about paperwork; it lets us follow any field issue back to a sawing shift or a pH blip during workup. Our engineering and QA teams meet regularly to assess root cause, making the product safer for downstream compounding and use. Storage rooms run on positive air pressure with nitrogen blankets for long-term inventory. We learned that even minor lapses in drum closure, caused by hasty loading, lead to more waste than mismeasured chemicals.
Our approach to sustainability includes both process improvements and waste minimization. We reduce solvent use wherever practical, and recycle to the greatest extent allowed by product purity requirements. Discharge water from the site goes through on-site treatment, and we divert usable heat from exothermic reactions into plant operations. These are practical, under-the-hood changes that add up to measurable environmental benefit and lower operational risk for our partners.
One challenge for any chemical developer is juggling scalability and regulatory compliance. We provide full analytical support, not just for regulatory files but for customers’ in-house troubleshooting. Every batch is archived with its synthesis route and test data for years, so returning to any point of failure is practical. Several customers have come to us with scale-up failures traced to supplier inconsistency on positional isomer content or tin catalyst carryover. Our analytical team partners with process chemists, swapping field notes so QA can adjust ranges on in-process standards, minimizing delay between pilot and production.
We actively encourage pilot feedback—what passed a bench-scale assay might gum up a production filter, and chemists have flagged issues like emulsion formation or unexpected color. Years of reviewing these notes have taught us that robust customer communication loops catch problems early. Instead of waiting for quarterly feedback, our sales and QA review returns weekly, feeding insights straight to the plant floor. Some of our process changes—like using double filtration or secondary washing—came from seeing repeated questions from R&D teams about trace boehmite or tin salts in reactions. None of these fixes happen if the only experience with the product sits in a warehouse inventory spreadsheet.
3-Methyl-5-Trifluoromethylaniline earns its keep as a bridge between generic anilines and highly specialized, custom-functionalized blocks. It’s most often used by teams aiming to adapt an established process, upgrade a side chain, or prepare intermediates for screening against lead targets. The product’s structure, with its methyl and trifluoromethyl groups in well-chosen positions, makes it a mainstay for those walking the line between commodity pricing and novel synthesis.
Field experience—and the collective wisdom of those making and shipping product every day—shows that the difference between “fit for purpose” and “costly headache” comes from intimate process knowledge. Whether in batch filtration, powder handling, or final distillation, the gritty details make or break reproducible chemistry. An experienced manufacturer sweats over every assay, tweak, and shipment, having seen firsthand how failed deliveries ripple down the supply chain, affecting not just today’s product but next quarter’s innovation.
The manufacturing floor is not a place for speculation. Customers return to us because we deliver more than a spec sheet; we provide a reliable partnership, with full transparency from raw material to drum shipment. This commitment—reflected in traceability procedures, QA at every step, and willingness to adjust quickly—has helped us keep pace with regulatory updates and shifting global demand. Every improvement in process control, environmental protection, and worker safety circles back to the product itself, ensuring that R&D teams, production chemists, and analysts get consistent material for their needs.
Anyone who has worked at scale knows that chemistry doesn’t happen in a vacuum, and every bottle or drum tells a story about attention to process, speed of feedback, and commitment to customer goals. Our track record in producing 3-Methyl-5-Trifluoromethylaniline comes from not just technical know-how but the willingness to learn from every hiccup and batch improvement. This kind of direct manufacturing experience is what customers remember long after the last drum leaves the warehouse.