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HS Code |
567154 |
| Cas Number | 461-82-5 |
| Molecular Formula | C8H8F3NO |
| Molecular Weight | 191.15 |
| Iupac Name | 4-(Trifluoromethoxy)benzylamine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 98-100°C at 15 mmHg |
| Density | 1.33 g/cm3 |
| Solubility | Soluble in organic solvents like DMSO, methanol |
| Smiles | C1=CC(=CC=C1CN)OC(F)(F)F |
As an accredited 4-(Trifluoromethoxy)Benzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, with tamper-evident screw cap; labeled with chemical name, molecular formula, and hazard warnings. |
| Shipping | 4-(Trifluoromethoxy)Benzylamine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is transported according to regulations for organic chemicals, typically at ambient temperature, with appropriate hazard labeling and documentation. Protective packaging ensures safe handling and compliance with international shipping standards for laboratory and industrial chemicals. |
| Storage | Store **4-(Trifluoromethoxy)benzylamine** in a tightly sealed container, under an inert gas such as nitrogen, in a cool, dry, and well-ventilated area. Protect from direct sunlight, moisture, heat, and sources of ignition. Keep separate from incompatible substances such as strong oxidizing agents and acids. Ensure all handling follows appropriate chemical hygiene and safety protocols. |
Applications of 4-(Trifluoromethoxy)Benzylamine in Industrial Manufacturing4-(Trifluoromethoxy)Benzylamine serves as a specialized intermediate in several high-value industrial sectors, where its functional properties support advanced synthesis routes and formulation practices. The following application scenarios demonstrate its distinct role in select downstream manufacturing processes. 1. Pharmaceutical API SynthesisThis compound plays a key role in the synthesis of active pharmaceutical ingredients, especially in selective serotonin reuptake inhibitor (SSRI) analogs and CNS-targeted drugs, where the trifluoromethoxy group modulates biological activity and receptor selectivity. Manufacturers introduce this material at the coupling stage with carboxylic acid derivatives under controlled temperature and solvent conditions, ensuring high-yield amide formation. Compliance with contamination control minimizes cross-reactivity, and continuous in-process monitoring supports reproducible batch production for regulated markets. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingDownstream agrochemical producers apply this amine for synthesizing crop protection agents, including pyridine and benzamide herbicide classes. The material participates in nucleophilic substitution and amide bond formation, benefiting from the stability and electron-withdrawing nature of the trifluoromethoxy group. Precision weighing and staged addition in jacketed reactors ensure process safety and consistent conversion rates, which are critical for meeting multi-country regulatory submission standards. Industry compliance standards
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3. Development of Liquid Crystal IntermediatesManufacturers of advanced materials employ this building block for the synthesis of high-performance liquid crystal intermediates, where the trifluoromethoxy moiety imparts improved thermal and electro-optical properties. The compound is introduced during the late-stage derivatization or ether bond formation steps, under strictly controlled moisture levels to avoid hydrolysis. Process engineers track integration with real-time FT-IR and NMR validation to ensure product identity for downstream compounding. Industry compliance standards
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4. Fluorinated Polymer Modifier SynthesisProducers of specialty polymers use this amine derivative as an end-cap or chain modifier in copolymerization or grafting reactions, especially for fluoroacrylate and fluoropolyether systems that require precise surface energy or dielectric characteristics. Operators meter the compound during the chain-terminating phase at elevated temperatures, employing automated dosing to achieve consistent polymeric functionalization. Downstream analytical characterization includes GPC and fluorine content validation to confirm specification adherence. Industry compliance standards
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5. Synthesis of Advanced Dyes and Pigment IntermediatesDyestuff manufacturers use this compound to introduce trifluoromethoxy-substituted benzyl groups into aromatic systems, boosting color strength and fastness in specialty dyes for textile and plastics applications. Integration occurs via reductive amination or direct coupling with aromatic nitro compounds in solvent-based processes using standardized agitation and heat profiles. Process stewardship prioritizes the capture and recycling of residual amines in accordance with strict environmental guidelines. Industry compliance standards
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As a chemical manufacturer, we handle a wide range of specialized building blocks supporting pharmaceutical, agrochemical, material science, and research applications. 4-(Trifluoromethoxy)benzylamine ranks as one of those compounds earning more attention in recent years. Based on our experience in both large- and small-scale production, we see this amine-based intermediate stand out for its unique structure and chemical properties. Its CAS number, 461-82-5, identifies it across scientific literature, but there's much more to this molecule than an entry in a database.
The trifluoromethoxy group attached to the para position on the benzylamine backbone introduces a significant electron-withdrawing effect. Instead of just yielding a variation on a common amine, this substituent shapes the reactivity and ultimate performance when the compound enters further synthetic steps. Over the years we refined our synthesis methods, using well-sourced feedstocks and robust purification so each batch remains consistent.
From a practical standpoint, our 4-(Trifluoromethoxy)benzylamine arrives as a colorless to pale yellow liquid. This might sound trivial, yet during storage and use, its low volatility, manageable viscosity, and predictable solidification point remain a big part of its appeal in the lab or plant. By focusing on real-world handling, we cut down on waste and help customers avoid the typical headaches with more sensitive or unstable analogues.
During our time supplying this material, we've learned what chemists and formulation specialists care about. Compared to standard benzylamine, adding the trifluoromethoxy group gives the molecule a distinct profile. The fluorine atoms grant enhanced metabolic stability, making it a better fit in medicinal applications where biotransformation can degrade simpler structures too fast. In recent projects involving kinase inhibitor scaffolds and CNS target modulators, this group brings crucial lipophilicity combined with improved resistance to oxidative metabolism.
For customers accustomed to para-halogenated or alkoxy-substituted benzylamines, 4-(Trifluoromethoxy)benzylamine consistently delivers a higher degree of chemical inertness where side reactions threaten yields. In cross-coupling, reductive amination, or amide bond–forming protocols, users often report fewer byproducts and easier purifications. Our experience validates these claims, with in-process analytics showing tight profiles and cleaner isolate batches.
Our main product grade strictly follows the most widely referenced analytical standards, with purity regularly measured by both HPLC and NMR techniques. Although specifications depend on the intended project, typical lots reach 98% or greater purity, with minimal presence of isomeric or oxidized impurities. Clients integrating the amine into API candidates or advanced intermediates depend on maximum reproducibility, which shapes our production decisions. We avoid overprocessing, striking a balance favoring yield and straightforward filtration rather than only maximizing purity numbers.
Within the factory, each kilo batch follows a single fitted protocol, not just a generic benzylamine process. We use chilled, anhydrous reaction conditions and a careful distillation system, cutting out routes prone to byproduct buildup. Because some impurities persist in earlier stage syntheses, we've adopted adaptive workups and fractional distillations, reducing the risk of later process snags. Any adjustments in feedstock quality or process temperatures are quickly tracked and documented, helping us support repeat orders with the same reliability.
Feedback from users highlights how easier storage translates into smoother operations. Our experience storing this compound mirrors much of the industry: sealed drums or amber bottles kept in cool rooms for extended periods, with only moderate precautions needed to avoid hydrolysis or air oxidation. While more reactive amines require elaborate blanketing or refrigeration, 4-(Trifluoromethoxy)benzylamine holds up well in ordinary chemical stores, a fact that gets overlooked until someone deals with bulk supply at scale.
Repeated orders from customers in both humid and arid environments show that moisture ingress or temperature swings rarely cause any measurable drop in purity or physical form—provided sensible packing and decanting routines are followed. We’ve seen the pitfalls of poor drum seals or careless transfer in the past, so we provide instructions shaped by these lessons rather than just generic guidance lifted from textbooks.
After supplying dozens of aryl-substituted benzylamines, the specific advantages of the trifluoromethoxy derivative stand out. The group behaves differently than classic methoxy, ethoxy, fluoro, or chloro analogues. Chemically, its electron-withdrawing nature pushes reactivity in predictable ways, affecting nucleophilicity at the amine and ring. The resulting product works better in some metal-catalyzed reactions, particularly where overalkylation or ring substitution tend to cause bottlenecks.
Some clients transition to this product after trouble using 4-methoxybenzylamine, finding the improved resistance to oxidative degradation particularly valuable in drug discovery efforts. The bulkier trifluoromethoxy group fills out the receptor-binding space, which can be favorable or not depending on the target—but this deliberate shift often resolves issues caused by too much polar surface area or metabolic lability. For process chemists, the trifluoromethoxy’s bulk also supports improved crystallization and less oiling in isolation steps.
Comparing storage and shelf life, most closely related amines show similar stability at lab scale. Yet, from the manufacturer’s angle, 4-(Trifluoromethoxy)benzylamine’s clear handling advantages come into play at the kilo or greater scale. Simple packaging, lower risk of self-condensation, and minimal odor make logistics more straightforward—an advantage when multiplied across a busy warehouse. For downstream chemistry, the absence of extraneous substituent reactivity keeps side product formation to a minimum, so purification proceeds with less reliance on chromatography.
We routinely support pharma and biotech groups investigating CNS, oncology, or inflammation targets. The trifluoromethoxy group’s metabolic stability proves especially useful where rapid in vivo clearance ruins efficacy data, or where oxidative metabolites could lead to adverse effects in advanced preclinical stages. We’ve seen teams achieve higher plasma exposure in animal models simply by swapping out a previous amine for our compound. The structural rigidity and low basicity also help limit off-target effects—a major challenge with other benzylamine derivatives.
In custom manufacturing for research clients, the compound often enters reductive amination or Suzuki–Miyaura coupling workflows. Each step benefits from reliable amine input, and we’ve watched yields edge up when users upgrade from less pure or less stable analogues. In some cases, material scientists use this benzylamine to introduce fluorine-rich moieties into polymers, impacting hydrophobicity and chemical resistance. Other specialty areas include developing functional surfactants, ion-exchange resins, or probing agents for analytical chemistry, though these demand rigorous batch-to-batch consistency—a standard we adhere to.
Ensuring purity and batch uniformity comes from hands-on monitoring. We build each run around in-process checks, NMR spot tests, and tailing offside peaks by iterative distillation. This limits the presence of p-toluidine, benzylamine, or formaldehyde-related side products that plague less selective reactions. Regular shakedowns at the filtration and packaging stages catch early warning signs of instability, especially considering air- and light-sensitivity at the micro trace level. We’ve invested in early-warning quality monitoring, which lets us identify and resolve anomalies before they scale up.
Over several years of scale-up and repeat production, we’ve tweaked our approach to avoid the common problems of co-distillation residue or water ingress. Each lot comes with a full analytical packet, but reliability really tracks back to our experience managing upstream reagents, prompt filtration, and thoughtful choice of solvents. We realize that a gap of even a fraction of a percentage point in purity can domino into a failed series of reactions, so process discipline becomes a habit, not just a regulatory line on a document.
Shipping and supply chain logistics matter almost as much as chemistry. Unlabeled, inadequately sealed, or mixed-up containers lead to more lost time than most labs expect. Based on those hard lessons, our warehouse teams build packaging and documentation around the real disruptions we’ve faced—heat cycles in transit, moisture entry after long customs holds, and variations in secondary shipping routes.
Customers notice the difference between thoughtfully packaged benzylamine and careless shipments only after one or two bad experiences. We’ve responded by shifting to UV-protective containers, inert gas top-offs for larger drums, and more robust seals. Every time a client opens a fresh drum untainted by discoloration or volatile impurities, that’s the real proof our process choices work.
Back in production, routine audits spotlight process drift or slow degradation in yield. Instead of patching these up with last-minute purifications, we correct upstream sourcing, keep reactor conditions stable, and revalidate analytical methods at regular intervals. As scale increases for a new application—often from hundreds of grams to multi-kilo—a smooth production ramp-up relies on this discipline. The payoff shows in stable supply, fewer delayed syntheses, and less rework at the customer site.
In the last decade, trifluoromethoxy substituents crossed over from rare specialty chemicals to more widely used intermediates. Advances in fluorination chemistry and structure-based drug design drive this shift. For pharmaceutical clients, these motifs introduce specific absorption and metabolic features not easily reproduced by non-fluorinated alternatives. Our conversations with drug development partners suggest that trifluoromethoxy-substituted phenyl amines may see even broader uptake for both small molecule and linker chemistry.
We track patent activity and research interest across multiple therapeutic areas. Recent applications focus on kinase inhibitors, GPCR ligands, and PET imaging tracers. In materials, increased use of perfluorinated building blocks in coating polymers and advanced membranes requires this niche intermediate. Rising regulatory expectations for traceability and impurity documentation put pressure on us to improve analytical coverage, an area where we’ve invested consistently across equipment and training.
Every specialized product faces hurdles, and 4-(Trifluoromethoxy)benzylamine is no exception. Supply bottlenecks for certain fluorinating agents can ripple through the whole schedule, affecting delivery reliability. In the last few years, volatility in feedstock pricing—especially for fluoroaromatic raw materials—has sometimes forced us to negotiate delivery timelines. To manage this, we keep expanded inventory of both key reagents and final products, while deepening relationships with trusted upstream suppliers.
Another challenge lies in analytical verification. The trifluoromethoxy group introduces signals in NMR and mass spectrometry requiring properly tuned equipment. Without vigilant methods, labs risk missing low-level impurities that can scuttle high-cost synthesis steps. We’ve worked alongside clients to share validated protocols, provide authentic spectra, and consult on troubleshooting integration errors. This commitment to practical support helps labs avoid costly shutdowns and delays.
Downstream, handling and waste disposal require specific guidance. The introduction of fluorinated chemicals brings stricter control for both workplace safety and environmental management. Our factory maintains closed-system transfer and carefully managed waste streams, partners with licensed disposal vendors, and assists customers in developing responsible on-site practices. We keep lines of communication open to field technical queries, especially when labs transfer bench-scale work to pilot or commercial settings where the stakes are higher.
Supplying this benzylamine taught us that the small differences in manufacturing and handling quickly add up at scale or across multiple synthetic runs. The choice to improve reactor cooling, pack drums under nitrogen, or triple-check every analytical panel stems from experience with real-world disruptions—unexpected crystallizations, error-prone shipments, and import holdups. End users may only see the final product label, but decades spent producing, purifying, and shipping this compound shape every drum that leaves our plant.
Clients want not just a commodity molecule, but process insight and a partner who anticipates snags before they shut down a production line. We share this focus, supporting projects with firsthand troubleshooting and sharing lessons learned over thousands of deliveries. Experience navigating chemical supply even in unpredictable markets ultimately guarantees that researchers, scale-up teams, and procurement specialists see the results in reliable performance and consistent material quality.
Industry shifts mean staying ahead of demand with new production technologies and stronger cross-team communication. In our facility, ongoing upgrades to solvent handling, analytical throughput, and in-line purification drive both cost efficiency and tighter lot control. Regulatory and customer-expectation headwinds act as a forcing function toward ever-better documentation and traceability; rather than a burden, we see this as a path to better customer trust.
Continual learning from customer feedback, both good and bad, helps us spot process blind spots or anticipate the next round of regulatory scrutiny. In supplying 4-(Trifluoromethoxy)benzylamine, our plant teams work closely with R&D and quality assurance to adapt quickly. Each drum shipped represents hard-earned lessons and daily commitment, both to the science in the flask and the team relying on what comes through our doors.