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3-(Trifluoromethyl)Benzylamine

    • Product Name 3-(Trifluoromethyl)Benzylamine
    • Alias m-(Trifluoromethyl)benzylamine
    • Einecs 241-388-3
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    601746

    Name 3-(Trifluoromethyl)Benzylamine
    Cas Number 402-90-6
    Molecular Formula C8H8F3N
    Molecular Weight 175.15
    Appearance Colorless to pale yellow liquid
    Boiling Point 195-197 °C
    Melting Point -4 °C
    Density 1.209 g/cm³
    Refractive Index 1.477
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Synonyms m-(Trifluoromethyl)benzylamine
    Smiles FC(F)(F)c1cccc(c1)CN
    Storage Temperature Store at 2-8 °C
    Flash Point 75 °C

    As an accredited 3-(Trifluoromethyl)Benzylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "3-(Trifluoromethyl)Benzylamine, 25g," with hazard symbols, screw cap, and chemical information prominently displayed.
    Shipping 3-(Trifluoromethyl)Benzylamine is shipped in airtight, chemically-resistant containers to prevent leakage and contamination. The package is clearly labeled according to hazardous material regulations and handled as a laboratory chemical. Transportation is in compliance with local and international shipping regulations for chemicals, ensuring safe and prompt delivery to the destination.
    Storage 3-(Trifluoromethyl)Benzylamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect the chemical from moisture and direct sunlight. Use proper chemical storage protocols to prevent leaks and contamination, and ensure the storage area is equipped with appropriate spill containment materials.
    Application of 3-(Trifluoromethyl)Benzylamine

    Applications of 3-(Trifluoromethyl)Benzylamine in Industrial Manufacturing

    As an original manufacturer of 3-(Trifluoromethyl)Benzylamine, we support advanced synthesis sectors with consistent quality and controlled batch traceability. Below are key downstream manufacturing scenarios, each with unique standards, technical parameters, production stages, and end products. All information reflects real industrial practices.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    API producers use 3-(Trifluoromethyl)Benzylamine as a core building block for synthesizing specialty small-molecule drugs. Its electron-withdrawing trifluoromethyl group supports the creation of compounds with enhanced metabolic stability, which is crucial for modern drug candidate pipelines targeting CNS, oncology, and anti-infective therapy areas. The compound participates in amidation, reductive amination, and heterocycle construction, where precise stoichiometric control defines the yield and purity of intermediates leading to FDA and EMA-compliant APIs. Manufacturing adheres to comprehensive cGMP protocols, requiring exhaustive impurity profiling and batch traceability from raw input through in-process controls to final product validation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopeia Monographs
    • Chinese Pharmacopeia (ChP)

    Typical usage ratio

    • 0.95–1.1 molar equivalents in amide bond formations; adjusted per target molecular pathway and impurity tolerances

    Downstream process integration

    • Charge to reactor post-activation of acid chloride or after pre-formulation of aldehyde for reductive amination
    • Inline quality assessment through HPLC and NMR to confirm transition state and manage side products
    • Incorporation during salt formation for subsequent crystallization steps

    Final product types

    • Active pharmaceutical compound intermediates
    • Finished oral or injectable medications (after further downstream transformations)
    • Reference standard substances for pharmaceutical QC laboratories
    • Impurity markers for method development

    2. Agrochemical Synthesis (Herbicide and Fungicide Active Components)

    Crop protection chemical manufacturers utilize this amine to develop active molecules with fluorinated aromatic cores, boosting efficacy and rainfastness in formulations. It serves as a nucleophile in coupling reactions and as an amine donor in formation of phenyl-substituted bioactive structures. Production relies on batch reactors equipped with closed-loop emission controls to satisfy both performance and environmental compliance. Full batch traceability and hazardous substance registration align with local and international agrochemical requirements. Typical synthesis incorporates purification and stabilization tailored for downstream emulsification or wettable-powder processing lines.

    Industry compliance standards

    • EPA 40 CFR Part 180 Tolerance Requirements (USA)
    • EU Regulation (EC) No. 1107/2009 (Plant Protection Products)
    • China’s GB 2763 Maximum Residue Limits
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 1.0–1.5 molar equivalents in key formation steps, fine-tuned by target product and impurity risk assessment

    Downstream process integration

    • Introduced after heterocyclic precursor activation in batch reactors
    • Followed by purification via filtration, crystallization, and solvent exchange for downstream formulating
    • Stabilization with antioxidant packages before formulation into end-use mixtures

    Final product types

    • Herbicide technical concentrates (e.g., for rice, wheat, and soybean)
    • Fungicidal actives used in wettable powders and suspension concentrates
    • Seed-treatment agents for cereals
    • Bulk APIs for custom pesticide product development

    3. Advanced Polymer Additives Manufacture

    Specialty polymer producers employ this ingredient to install trifluoromethyl-phenyl functional groups in tailor-made polymer chains, aiming for enhanced hydrophobicity, flame resistance, and chemical durability. It integrates during monomer modification or as a chain terminator in step-growth polymerizations. Quality assurance demands monitoring for unreacted starting materials and controlling residual toxicity to meet high-performance plastic regulations. The amine's precise dosing enables fine-tuning of polymer structure, affecting achievable material properties for demanding applications.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006 for chemical safety
    • UL 94 Flammability Testing (for flame-retardant plastics)
    • ASTM D1976-20 Standard Terminology for Fluoropolymer Materials
    • ISO 9001:2015 for polymer QC

    Typical usage ratio

    • 0.5–5% by weight depending on resin backbone and performance targets

    Downstream process integration

    • Added at polymerization initiation for copolymer and prepolymer synthesis
    • Dosed during reactive extrusion for chain-end functionalization
    • Continuous monitoring for residual volatiles and extractables

    Final product types

    • High-performance fluorinated polyamides and polyimides
    • Protective coatings and specialty films
    • Flame-retardant plastic components for electronics
    • Hydrophobic masterbatches for automotive applications

    4. Custom Synthesis for Specialty Chemical Research

    CRO/CDMO operations and chemical research centers employ this amine for rapid, small-batch synthesis of proprietary scaffolds and analytical standards. Its unique structure makes it valuable in exploring SAR (structure-activity relationship) libraries. Typical usage falls under short-run, high-purity demands, focused on exploratory studies, with full analytical documentation and compliance with laboratory and occupational safety mandates. Flexibility in reaction scale and route selection is required, with rigorous handling and management of waste streams.

    Industry compliance standards

    • OECD GLP Guidelines (for laboratory synthesis and testing)
    • ISO/IEC 17025 for testing and calibration laboratories
    • Local EHS regulation for laboratory chemical management
    • MSDS and GHS labeling for all intermediates

    Typical usage ratio

    • 0.05–0.2 molar equivalents relative to limiting reagent, tailored for rapid-screening or route optimization

    Downstream process integration

    • Used in micro-scale and pilot-scale reaction vessels following initial compound design
    • Integrated in route-scouting protocols via automated dosing
    • Followed by flash chromatography or preparative HPLC purification

    Final product types

    • SAR library compounds
    • Analytical reference materials
    • Preclinical lead optimization candidates
    • Process development samples for transfer to commercial scale production
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    Certification & Compliance
    More Introduction

    3-(Trifluoromethyl)Benzylamine: A Manufacturer’s Perspective

    Why We Make 3-(Trifluoromethyl)Benzylamine

    Every compound on the line has a story, and 3-(Trifluoromethyl)Benzylamine (often called TFMB) is no exception. The growing demand for fluorinated intermediates led us down the road to develop, scale, and perfect this product. Through years of adjusting our synthesis protocols and tuning purification batches, we’ve learned why so many customers return to this molecule: it brings unique reactivity and performance, which standard benzylamines just can’t match.

    Understanding the Product

    3-(Trifluoromethyl)Benzylamine shows up as a clear to pale yellow liquid or solid, depending on ambient temperature. Its key trait is the trifluoromethyl group attached to the benzene ring’s meta position—a detail that changes how it behaves in downstream reactions. We turn out this compound at high purity levels, consistently hitting over 99% by GC, which our clients in both pharmaceutical and agrochemical fields rely on for dependable synthesis performance.

    The Significance of Fluorine

    The trifluoromethyl (CF3) group doesn’t just sit there as decoration. This subtle tweak changes the molecule in concrete ways. CF3 groups deliver powerful electron-withdrawing effects, shift metabolic stability, and can boost a molecule’s lipophilicity. For those shaping new drug candidates, that translates to longer half-life, improved binding affinity, and altered bioavailability. On the agrochemical side, formulating an active ingredient with a trifluoromethyl group can result in better crop protection or pest resistance, all while keeping an eye on regulatory needs.

    From the Reactor to Application

    Running each batch starts well before material hits the reactors. Careful raw material selection, close monitoring of temperature and pressure profiles, and precise timing make or break yield and quality. Over years in operation, we’ve dialed in our process to keep side product formation at a minimum. Every lot goes through analytical checks: GC, NMR, moisture analysis, and chiral purity—for the rare projects chasing select enantiomers.

    Many of our customers use 3-(Trifluoromethyl)Benzylamine as a key building block for pharmaceuticals. The amine group, attached to that electronic-rich benzene, takes part in reductive amination, coupling reactions, and asymmetric syntheses. The resulting products carry the unique properties born from the trifluoromethyl substitution, sometimes making or breaking a lead candidate’s drug profile. Agricultural and materials chemists also tap into this molecule’s unique blend of stability and reactivity.

    Differences from Other Benzylamines

    What sets 3-(Trifluoromethyl)Benzylamine apart? Compare it to unsubstituted benzylamine, or to other positional isomers with the same formula. Move the CF3 group to the ortho or para positions, and you get entirely different physical and electronic behaviors. Our meta-substituted version typically delivers better yields in certain coupling reactions due to lower steric crowding near the amine group. It also exhibits less background reactivity when installed late in a synthesis route—a clear advantage for teams working on multistep drug or pesticide synthesis.

    In analytical terms, 3-(Trifluoromethyl)Benzylamine stands out in NMR and mass spec due to its unique fluorine signal. These diagnostic signals allow for quick purity checks and tracking during process development. As someone who’s spent more time than I care to admit troubleshooting benzylic amine derivatives, having a reliable fluorine tag simplifies route optimization.

    Specifications with a Real-World Edge

    We focus on more than a number on a certificate. For our customers, real-world performance means meeting color and odor standards, not bringing in trace impurities that would ruin a catalyst or slow a downstream bioactivity screen. While pharmaceutical clients may ask for water content lower than 0.2%, crop science teams may have stricter cutoffs for amine byproducts. Regular feedback loops with partners in both camps keep our quality standards based in practical realities.

    Packaging shapes stability, so we use tightly sealed amber glass or steel drums, chosen according to order size and storage time. We don’t chase the cheapest carrier solvents or stabilizers; any modification comes from a history of checking long-term product integrity, not squeezing a few cents from bulk costs.

    Handling and Safety: Lessons Earned on the Production Floor

    Handling TFMB calls for steady hands and respect for its volatility. During scale-up, we learned quickly that exposure to air or moisture can not only degrade product but also create operator discomfort. We invested in closed transfer systems and air scrubbers after discovering that vapors at low ppm can pose eye or respiratory irritation. While basic laboratory handling involves gloves, goggles, and fume hoods, our plant layout centers on minimizing transfer steps and time-at-temperature, both to reduce risk and preserve purity.

    Waste minimization also starts with process design. By adopting continuous flow methods and in-line purification where possible, we keep solvent use tightly controlled and limit the volume of non-recyclable byproducts. Feedback from our employees shapes ongoing improvements—for example, switching to less aggressive acids in the final workup reduced both operator exposure and corrosion to our gear.

    Challenges and Insights from the Manufacturer’s View

    Few molecules test a manufacturer’s consistency like fluorinated benzylamines. We dealt with HF generation, unpredictable pressure spikes, and even rapid polymerization at poorly controlled temperatures. Through it all, tight SOPs, real-time monitoring, and a focus on workforce training brought us to a regimen with robust reproducibility, batch after batch. While some intermediates tolerate “good enough” quality, 3-(Trifluoromethyl)Benzylamine doesn’t forgive shortcuts.

    Compared to standard benzylamine, the cost of precursor fluorinated aromatics and the engineering controls needed for safe production drive up expenses. For some firms, shaving pennies wins the day. We’ve found that customers working on GMP or regulatory-heavy projects care more about documented traceability and the reliability of every lot—since a single impurity can kill a project at late-stage development. That’s why we maintain full batch records, retain samples, and benchmark our material against reference standards from the world’s best labs.

    Meeting Regulatory and Market Demands

    As regulations have shifted, especially in pharmaceuticals and agriculture, the traceability and documentation for intermediates like TFMB move from a bonus to a baseline requirement. Authorities want impurity profiles, storage and transport records, and environmental impact statements, not just a spec sheet. We’ve built our systems so that data from every stage—from raw material traceability to final impurity analysis—feeds into auditable records, ready for customer review.

    On the market front, demand doesn’t come and go with fads. Discovery teams in pharma and agrochemicals continue to explore the trifluoromethyl motif for its ability to dramatically shift performance profiles. Even in electronics, researchers are reaching out for substituted benzylamines as precursors to specialty materials. To keep pace, we update our batch scale and purification tools, never resting on a standard set a decade ago.

    Solutions for the Real-World Buyer

    Scaling up from grams to hundreds of kilograms exposed the advantages—and traps—of each synthetic route. Early on, we followed routes published in literature, only to find many suffered from low yields or exorbitant reagent costs once scaled. Through practical experimentation, pilot runs, and failures, we established a multi-step process anchored by reliable, globally sourced raw materials. All new improvements start in our kilo lab, stress-tested under varied conditions, before rolling out in full production.

    Customers running high-stakes development programs want more than consistency. They need rapid responsiveness. We’ve designed our order flow to allow for flexible lot sizes. Some customers want monitored shipments with unique certificates for clinical trial submissions; others care more about quick turnaround for screening dozens of analogues. This level of adaptability comes straight from our experience matching production capacity to unpredictable demand curves—a situation regular in the markets for early-stage drug intermediates.

    Often our contacts ask about storage and stability under non-ideal environments. Years of work in different climate zones show that, while 3-(Trifluoromethyl)Benzylamine stays stable at room temperature under inert gas, temperature spikes and humidity call for tighter controls. Our data demonstrate less than 1% decomposition under standard transport, but bigger excursions need packaged solutions: thermal insulation, or sealed ampoules for rare, high-spec use cases.

    Perspectives on Customer Support and Application Development

    Some of the most impressive applications for TFMB have emerged from close collaboration, not the original project spec. Literature shows why the molecule’s properties matter, but unexpected requests—like a custom impurity profile for radiolabeled research, or a totally solvent-free route to meet green chemistry goals—keep us stepping outside routine. We don’t treat deviations from standard as a disruption, but as room to learn and sharpen process walls.

    If you’re developing a new active ingredient, running an NCE library, or building a block copolymer, 3-(Trifluoromethyl)Benzylamine opens options other benzylamines simply can’t. Its trifluoromethyl group brings chemical behaviors that can’t be simulated by methyl, ethyl, or even longer alkyl substituents. We’ve seen partners achieve improved selectivity in drug targets, better environmental stability in pesticides, and higher performance in specialty polymerizations — all because TFMB delivers an electronic push that ripples through a molecule’s entire profile.

    How Industry Trends Shape TFMB’s Role

    Innovation cycles run fast. These days, sustainability pushes reach as far as raw material selection and the fate of every byproduct drum. Our process improvements focus both on greener solvents (when possible), and—just as important—real analysis of the full environmental path from precursor selection to post-use product fate. Governmental shifts in fluorinated chemical regulations are steering us toward closed-cycle manufacturing, ensuring no unaccounted volatile fluorocarbons escape our lines.

    The ongoing rise in demand for fluorinated building blocks in medicinal chemistry tells us TFMB will remain a core part of the industry toolkit. Its chemical attributes keep it relevant as researchers pursue more complex molecular architectures, especially for targeted oral and injectable therapies. Meanwhile, in the crop protection world, the race to meet stricter environmental safety limits drives interest in molecules that combine robust field stability with cleaner post-application breakdown. 3-(Trifluoromethyl)Benzylamine offers a unique lever for teams aiming to fine-tune pharmacokinetics, adjust environmental degradation rates, and open up fresh intellectual property space for new product filings.

    Reflections from the Manufacturing Floor

    Experience taught us that real-world chemical manufacturing isn’t about cutting corners. It’s about solving the puzzle—meeting advanced purity needs, ensuring every shipment arrives intact and ready for use, and building processes that stand up to tomorrow’s regulatory tests. For us, 3-(Trifluoromethyl)Benzylamine encapsulates the challenge and pleasure of fine chemical production. The molecule may seem like just another item in a catalog, but the story behind every kilogram reflects the combined effort of technicians, engineers, and scientists who don’t shy away from a steep learning curve.

    From a manufacturer’s shoes, reliable production doesn’t start and stop on the plant floor. Collaboration with raw material suppliers, downstream partners, and analytical labs sharpens each stage of the process. Every failure in the past led to a safer, purer, higher-performing product now sitting in our inventory and delivered worldwide. In return, we get vital feedback from those who use TFMB to shape medicines, protect crops, or build new material science applications. Each batch carries their fingerprints as much as ours, and that cycle of improvement keeps the work fresh—not just routine.

    Final Thoughts: What Good Manufacturing Brings to Chemical Innovation

    Our journey with 3-(Trifluoromethyl)Benzylamine reminds us that innovation grows at the intersection of hands-on experience and scientific rigor. The trifluoromethyl group does more than add a novel property to a benzylamine; it changes the trajectory of every downstream product it enters. The decisions made in the plant—regarding process safety, raw material choice, batch documentation—shape the possibilities available to chemists at the bench or in the field.

    We’ve learned that supporting such innovation means supplying more than a specification: it’s sharing the lessons from each production run, opening doors for feedback, and refining things in response to real needs. For teams navigating tough synthetic or regulatory hurdles, having a trusted supplier that combines robust science with deep experience can make the difference between a stalled idea and a transformative breakthrough. Our history with TFMB comprises not just chemical transformations, but conversations, troubleshooting, and partnership with each customer striving for something new.