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4-(Trifluoromethyl)Benzylamine

    • Product Name 4-(Trifluoromethyl)Benzylamine
    • Alias 4-(Trifluoromethyl)phenylmethanamine
    • Einecs 249-705-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    VTB
    Specifications

    HS Code

    996449

    Iupac Name 4-(Trifluoromethyl)benzylamine
    Molecular Formula C8H8F3N
    Molecular Weight 175.15 g/mol
    Cas Number 214759-28-9
    Appearance Colorless to pale yellow liquid
    Boiling Point 95-97°C at 16 mmHg
    Density 1.204 g/mL at 25°C
    Refractive Index n20/D 1.482
    Solubility Soluble in organic solvents (e.g., ethanol, DMSO); limited water solubility
    Smiles FC(F)(F)c1ccc(cc1)CN
    Inchi InChI=1S/C8H8F3N/c9-8(10,11)7-3-1-6(2-4-7)5-12/h1-4H,5,12H2
    Synonyms 4-(Trifluoromethyl)benzylamine; p-(Trifluoromethyl)benzylamine
    Storage Conditions Store at 2-8°C, tightly closed
    Purity Typically >98%

    As an accredited 4-(Trifluoromethyl)Benzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with a sealed cap, labeled "4-(Trifluoromethyl)Benzylamine," displaying hazard warnings and chemical details.
    Shipping 4-(Trifluoromethyl)Benzylamine is shipped in tightly sealed containers under standard ambient conditions. It should be protected from moisture, heat, and direct sunlight. The packaging must comply with local regulations for hazardous chemicals to ensure safe transportation. Appropriate labeling and documentation are required according to international shipping standards for chemicals.
    Storage 4-(Trifluoromethyl)Benzylamine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. It should be kept separate from strong oxidizing agents and acids. Proper labeling and chemical safety protocols must be followed, and personal protective equipment should be used when handling the chemical to prevent exposure.
    Application of 4-(Trifluoromethyl)Benzylamine

    Applications of 4-(Trifluoromethyl)Benzylamine in Industrial Manufacturing

    4-(Trifluoromethyl)Benzylamine serves as a specialized intermediate in several advanced manufacturing sectors, notably agrochemical synthesis, active pharmaceutical ingredient (API) production, specialty polymer modification, and development of performance coatings. Its use leverages precise reactivity profiles and regulatory compliance, supporting high-value downstream processes focused on differentiated end products.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical manufacturers employ this molecule as a building block in the construction of selective herbicides and insecticides featuring aromatic amine structures for enhanced biological activity. Its integration occurs primarily during the assembly of complex substituted aniline cores, critical for target-specific agrochemical agents designed to meet evolving resistance management strategies. End users adjust addition protocols to comply with regional and international residue and toxicity control, driving stable downstream compound synthesis aligned with contemporary stewardship requirements.

    Industry compliance standards

    • FAO/WHO JMPR pesticide specification guidelines
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • US EPA pesticide registration standards (40 CFR Parts 152 and 180)
    • China GB 2763 Maximum Residue Limits for Pesticides

    Typical usage ratio

    • 1.5–4 wt% of total batch, calculated as a function of reaction scale and product selectivity requirements; formulators optimize input to balance target activity and downstream yield.

    Downstream process integration

    • Introduced at nucleophilic aromatic substitution (NAS) or reductive amination step after halogenation of primary aromatic ring; typically used pre-formulation, prior to salt/crystal isolation and formulation stabilization.

    Final product types

    • Aromatic aniline-based herbicides (e.g., trifluoromethyl-substituted phenylureas)
    • Phenylpyridine-based fungicides
    • Selective insecticidal active agents
    • Seed coating protection ingredients

    2. Pharmaceutical Intermediate in API Manufacturing

    Custom synthesis groups and leading pharmaceutical companies utilize this compound as a key intermediate during the construction of central nervous system (CNS) drug candidates, anti-inflammatory APIs, and certain anti-viral scaffolds. The amine function serves as a precursor in amide coupling or cyclization steps under strict GMP conditions, with traceability from raw material inventory through to validated batch release and quality control, requiring complete documentation per ICH guidelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for APIs
    • US Pharmacopeia (USP) monograph cross-reference
    • European Pharmacopoeia (Ph. Eur.) intermediate declaration
    • 21 CFR Part 211 (US FDA cGMP regulations)

    Typical usage ratio

    • 0.8–2.2 molar equivalents relative to core API precursor; the adjustment depends on process yield tracking and impurity control through downstream purification.

    Downstream process integration

    • Applied at amidation or condensation reaction phase, especially in Suzuki or Buchwald–Hartwig coupling routes once initial molecular framework is established; its integration precedes API-crystallization and final purification.

    Final product types

    • Fluorinated CNS drug candidates (e.g., antidepressants, antipsychotics with trifluoromethylphenyl motifs)
    • Non-steroidal anti-inflammatory drug (NSAID) intermediates
    • Antiviral lead compound precursors
    • Small-molecule research batch compounds for clinical trial supply

    3. Polymer Modification for Advanced Material Performance

    Innovators in specialty polymer manufacture select this amine for its ability to introduce controlled trifluoromethyl aromatic side chains into polyamide and polyimide matrices, enhancing chemical resistance, hydrophobicity, and dielectric performance. It is specifically valued for formulations demanding low extractables and high temperature stability, with process documentation supporting automotive, electronics, and aerospace regulatory filing.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management System
    • UL 94 (flammability standards for plastics)
    • ASTM D543 Chemical Resistance of Plastics
    • RoHS (Restriction of Hazardous Substances Directive, EU 2011/65/EU)

    Typical usage ratio

    • 0.3–1.2 mol% as a co-monomer; dosage optimization is performed by melt rheology analysis and downstream electronic property testing.

    Downstream process integration

    • Co-reacted via step-growth polymerization or end-group functionalization, commonly in solvent-assisted or melt-phase synthesis; integration occurs before extrusion or casting cycle, following molecular weight adjustment and purification.

    Final product types

    • High-performance polyimide films for flexible electronics
    • Polyamide blend components for precision automotive parts
    • Dielectric polymers used in advanced circuit insulation
    • Protective surface coatings for specialty engineering components

    4. High-Durability Industrial Coatings

    Paint and coatings formulators integrate this material into hardener components and curing agent blends, taking advantage of the electron-withdrawing trifluoromethyl group for film hardness, stain repellency, and solvent resistance. Its incorporation improves crosslinking in epoxy and polyurethane systems, especially where anti-graffiti or chemically resistant finishes are critical in public infrastructure or industrial environments, where performance testing drives compliance.

    Industry compliance standards

    • ISO 12944 Corrosion Protection of Steel Structures by Protective Paint Systems
    • REACH Regulation (EC) No 1907/2006 Substances of Very High Concern (SVHC) assessment
    • ASTM D4060 Abrasion Resistance of Organic Coatings by Taber Abraser
    • US Green Building Council LEED V4 Material Ingredients disclosure

    Typical usage ratio

    • 0.5–2 wt% in epoxy or polyurethane curing blend; precise proportion set by application performance testing, including abrasion and solvent rub resistance.

    Downstream process integration

    • Mixed with polyol or epoxy prepolymer before addition of crosslinker and solvent; the compound reacts during final film formation, after substrate preparation and before oven or ambient cure.

    Final product types

    • Anti-graffiti coatings for urban infrastructure
    • Chemical-resistant industrial floor finishes
    • Protective coatings for laboratory equipment
    • Architectural metal coatings subject to public wear
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    Certification & Compliance
    More Introduction

    Insights From the Production Floor: Introducing Our 4-(Trifluoromethyl)Benzylamine

    A Close-Up Look at a Key Intermediate

    Years of hands-on manufacturing have shaped the approach our team takes with every specialty chemical released from our facility. 4-(Trifluoromethyl)Benzylamine stands out on our production schedule for much more than its challenging raw materials or the rigorous safety practices it demands. The molecule carries both a trifluoromethyl group and a benzylamine backbone, a combination that creates real advantages, especially for advanced pharmaceuticals, agrochemical synthesis, and specialty materials development.

    Building this material calls for close control over temperature and moisture — the amine is reactive, and every step from the charged reactor to the storage drums has to run in smooth order. The goal is not just to make a solvent-wet mass; it’s to achieve highly pure, stable amine that stays free-flowing and consistent from lot to lot. No two batches ever seem quite the same, and the experience of handling each one builds confidence that our protocols—not just our paperwork—keep quality high.

    Breaking Down the Chemistry

    Several years ago, routine preservation and routine formulation work with 4-(Trifluoromethyl)Benzylamine reminded us just how much the trifluoromethyl group changes the properties. The group itself adds significant electron-withdrawing capacity, shifting the amine’s reactivity away from that of common benzylamine. This means it has a lower pKa, and the difference shows up in downstream reactions. As a result, medicinal chemists often use this amine when they need to dial in reactivity for precise functionalization—especially where metabolic stability or enhancement of a lead compound’s pharmacokinetics could set their project apart.

    We supply the product as a colorless to pale yellow liquid in drums or smaller containers, depending on project need. Each lot ships with full trace analytics, with GC-MS and NMR confirmation. From experience, our plant operators know the synthesis route often introduces minor impurities if reaction atmospheres aren’t dry or if the base is added too quickly. Our standards require every batch to fall under strict purity thresholds; the amine is never diluted to mask defects, and purity figures reflect real output, not laboratory best-case.

    Key Applications Drawn From the Field

    Most of our regular customers produce either active pharmaceutical ingredients, advanced monomers, or specialty agrochemicals. In pharmaceuticals, 4-(Trifluoromethyl)Benzylamine is popular as a building block for molecules that need better metabolic resilience. The trifluoromethyl group can slow degradation in vivo, and medicinal chemists use this characteristic to help design longer-acting drugs. The difference from simple benzylamine lies in how the molecule distributes electron density—directly impacting how it reacts in biological and industrial settings.

    Custom material scientists have explored its use when traditional amines don’t deliver the thermal or acid resistance required. In fluorinated polymer design, adding a trifluoromethyl benzylamine fragment has delivered new performance levels, especially where polarity or resistance to environmental stressors was lacking. Here, our own test formulations for coatings and specialty electronic layers have proven the value—the difference between standard and fluorinated amines translates directly to resistance against degradation, yellowing, and surface energy tuning.

    Crop protection is another fast-changing area. Formulators need molecules stable under UV and oxidative stress. The trifluoromethyl group is more than an academic curiosity; it shunts reactivity in directions that affect not just activity but also shelf life and field performance. Teams working with plant growth regulators or fungicidal agents use our 4-(Trifluoromethyl)Benzylamine for these reasons, drawing on our documented quality controls to manage their regulatory filings.

    From Routine to Real-World: Handling and Integration

    Production teams can spot the differences between trifluoromethyl and regular benzylamine even before analytics come in. This chemical gives a somewhat sharper odor, and the vapor profile demands well-maintained extraction at every step. In the plant, contamination between this and more reactive amines can cause issues with cross-reactivity. That’s why rigorous dedicated lines are used for this production. Even successful scale-up doesn’t mean process engineers can relax—each barrel must be handled as if it’s going directly into a sensitive downstream intermediate.

    In practice, our customers report that the higher purity, lower water content, and consistent analytical results keep run-to-run variability within narrow bands. One quality-focused client recently commented that their palladium-catalyzed amination reactions showed improved selectivity and reduced byproduct when switching from commercial, lower-purity stocks to ours. It matches our experience: controlling process variables from synthesis to packaging brings real advantages, especially at larger scale, where impurities quickly multiply downstream costs.

    Technical service calls almost always revolve around integration. Our team has learned to provide not just a product but a set of recommendations grounded in years of accumulated small wins—and some instructive mistakes. For example, the high volatility relative to unsubstituted benzylamine requires careful degassing, while the increased surface activity can impact formulation homogeneity in solvent blends. Small differences in storage conditions can tip the balance between a day’s worth of reliable synthesis and a drum of unusable material.

    The Value of Knowing the Source and Process

    Users of specialty amines get real peace of mind from single-source manufacturing. Traceability remains important, not just for regulatory reasons but for genuine process troubleshooting. We keep samples from each lot and track every raw material’s supplier through a backward chain, confirmed by certificates of analysis stored for years. Early in our years making this compound, a minor change in our supplier’s bromine grade introduced an impurity; detecting and eliminating it taught the importance of controlling the full supply chain—not just the final product.

    The origin of water in the process is just as critical. Moisture-sensitive reactions require that the amine ship out below a strict moisture ceiling, so we actively monitor both reactor headspace and condensation traps during synthesis. By tuning distillation points and reactor charges, our technicians have eliminated the chronic haze and color changes that plagued early lots from less controlled plants. These small improvements translate into fewer re-tests, less off-spec waste, and most importantly, the ability to promise and deliver what the data say each barrel can do.

    How This Product Stands Out

    Compared with other benzylamine derivatives, this material stands apart for more than just a trifluoromethyl label. The synthesis process incorporates additional protection and deprotection steps uncommon with simpler amines. The resulting purity profile consistently shows lower levels of halide and residual organics—particularly important for customers using the amine as a pharmaceutical precursor. Raw material selection, solvent purity, and in-process controls together produce a product where batch-to-batch variations get minimized, supporting continuous operations without unexpected downtime.

    Some manufacturers chase cost reductions by shortening purifications. Our experience shows that skipping these steps leads to poor reactivity or off-specification side reactions in downstream chemical synthesis. By maintaining the purification layer, not only do we improve shelf life, but customers gain additional months of storage stability even under global shipping conditions. The color, clarity, and reactivity remain closely matched, even after extended transport—a factor that matters more as supply chains grow more complex.

    Comparing 4-(Trifluoromethyl)Benzylamine to non-fluorinated variants reveals differences in volatility and base strength, as well as greater chemical resistance. The combined effect means that for some applications—such as advanced resin crosslinking or new fluoropolymer architectures—using the trifluoromethyl-substituted version unlocks performance impossible with trading-house benzylamines or bulk commodity grades. Our team has worked side-by-side with customers conducting pilot runs, troubleshooting purification hold-ups, and finding solvent systems that maximize yield without causing fouling or resin precipitation.

    Direct Production, Not Just Replication

    Many end users find out too late that their material comes through a long chain of traders or warehouse consolidators. This disconnect between source and accountability often surfaces as inexplicable variations between lots, unexplained residues, or compliance headaches. As primary producers, we take responsibility for both process and product. Our QC team signs off on every output; if a deviation arises, we contact all affected clients with mitigation plans, not just batch records. Having walked the plant floors ourselves and handled every step from raw material receipt to finished product, our crew makes decisions based on institutional memory—not just a manual or a third-party spec.

    During supplier audits, clients often remark on our documented process history. The origin of every bottle or drum can be traced, not merely for marketing, but to support pharmaceutical or restricted-use agrochemical registrations worldwide. Our involvement doesn’t stop at shipping; many long-term relationships involve troubleshooting novel synthesis pathways, scaling up new intermediates, or verifying compatibility with innovative catalysts. These projects routinely rely on us because we don’t just supply, we support with specific know-how, born from owning each stage of production.

    Challenges and Practical Solutions in Synthesis

    Synthetic chemistry rarely follows a straight path. Making 4-(Trifluoromethyl)Benzylamine at production scale means troubleshooting reactor fouling, competing side-reactions, and tight thermal profiles that can lead to rapid exotherm if left unchecked. Over the years, in-house pilot runs have taught our chemists and operators to favor slower reagent addition and more robust pressure controls. The initial investment in advanced process controls pays off every day through safer, more reliable operations and dramatically lower waste volumes.

    Tightened emission controls and stricter worker safety obligations have also changed how this product is handled and monitored. In our experience, higher volatility means exhaust systems and containment must function within narrow bands, with regular equipment checks and redundant alarms in place. Failing to keep control results not just in lost product but in genuine personal risk for everyone on-site. Since moving to these tighter controls, downtime events and safety incidents linked to amine processing have declined, and employees are far more engaged in ongoing training and incident reviews.

    Another point of difference in our operation is the approach to raw material qualification. Suppliers undergo transparent checks and materials are regularly spot-checked against multiple reference standards. This prevents the costly side-effects caused by off-grade starting materials, which too often surface only once product reaches customer lines. We consider this diligence part of our role—not just factory routine, but a direct service to our customers whose end products depend on every detail.

    Serving Evolving Research and Regulation

    Our manufacturing team stays connected to the front lines of research. Regulatory standards, customer formulation goals, and the chemistry field itself keep moving. Adjusting to changing European substance requirements, for instance, has led us to expand analytical testing. Increased scrutiny of nitrosamine precursors and other trace contaminants has pushed us to develop new, more sensitive detection protocols. We engage with customers’ analytical teams directly, bridging any gap between their in-lab requirements and industrial-scale delivery.

    Development teams working in pharmaceuticals and agchem pay close attention to impurity profiles, toxicological clearances, and consistent regulatory documentation. We consider it our job to support their development timelines, not disrupt them with unreliable information or shifting analytical results. In practice, this means rapid response to material data inquiries, transparent reporting on lot analytics, and full access to technical support for integrating our amine into complex multi-step synthesis.

    Experience Shapes Every Batch

    The lessons learned from years of hands-on manufacturing show clearly in each barrel we ship. Subtle improvements—adjusting reactor ramp rates, changing glassware treatments, and qualifying new drum liners—have led to greater reliability. While technical bulletins and specifications tell part of the story, nothing can replace the shared experience of operators who have solved the same problems, batch after batch, and who genuinely care about consistent, high-quality output.

    Customer demands rarely fall into neat categories. Projects jump from exploratory lab scale to pilot-scale synthesis, each posing new requirements. Our team provides advice on dilution, storage, and integration, not as theoretical best practices but as methods that have protected countless kilos from avoidable spoilage, degradation, or misformulation. By listening closely and responding flexibly to a wide variety of requests, we help scientific teams push the boundaries of what’s possible, and do so safely.

    End users evaluating 4-(Trifluoromethyl)Benzylamine have more than one supplier option. Still, the difference between factory-direct output and intermediates sourced piecemeal from traders or stockists is clear when performance matters. Our production approach—combining deep process expertise, strict analytical controls, and a culture of continuous improvement—offers reliability that enables careful research, successful new product launches, and true scale-up. The product offers distinctive reactivity and stability; the people making it bring thousands of hours of hands-on experience to every order.

    Building Partnerships, Not Just Delivering Barrels

    Working as a manufacturer isn’t just about making molecules. It’s about making promises and keeping them. For us, supplying 4-(Trifluoromethyl)Benzylamine builds on years of trust between chemists, engineers, and end users who rely on predictable results. Our relationships with partners in advanced materials and life science labs have produced new syntheses, untangled bottlenecks, and solved problems other suppliers dismissed as unsolvable.

    Open lines of communication, continual product support, and the willingness to troubleshoot side-by-side with end users make a measurable difference in product quality and customer satisfaction. We know most of our partners by name, having walked the lab floors together and traded experience over more project meetings than we can count. Our culture reflects a commitment to continuous learning and a practical focus on solutions. If problems arise, both process and product knowledge combine to deliver answers rooted in manufacturing reality, not just theory.

    4-(Trifluoromethyl)Benzylamine remains more than just a catalog entry; it represents years of cumulative experience, the dedication of a skilled team, and the belief that every drum delivered shapes our shared future in specialty chemistry. Lab, pilot, or commercial plant—our commitment runs through every scale, every lot, every order placed. Direct manufacturing experience, tested with every challenge met, continues to define what our customers receive, day after day.