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4-Fluoro-3-(Trifluoromethyl)Benzylamine

    • Product Name 4-Fluoro-3-(Trifluoromethyl)Benzylamine
    • Alias 4-F-3-CF3-BnNH2
    • Einecs 629-729-9
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    938201

    Productname 4-Fluoro-3-(Trifluoromethyl)Benzylamine
    Casnumber 883500-72-7
    Molecularformula C8H7F4N
    Molecularweight 193.14
    Appearance Colorless to pale yellow liquid
    Purity Typically >98%
    Smiles C1=CC(=C(C=C1F)C(F)(F)F)CN
    Inchi InChI=1S/C8H7F4N/c9-6-2-1-5(4-13)3-7(6)8(10,11)12/h1-3H,4,13H2
    Synonyms α-(Aminomethyl)-4-fluoro-3-(trifluoromethyl)benzene
    Solubility Soluble in organic solvents
    Storageconditions Store at 2-8°C, tightly closed

    As an accredited 4-Fluoro-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, 5 grams, tightly sealed with a tamper-evident cap, labeled with chemical name, formula, hazard pictograms, and batch number.
    Shipping **Shipping Description:** 4-Fluoro-3-(trifluoromethyl)benzylamine is shipped in securely sealed, chemical-resistant containers, compliant with all relevant regulations. The package is labeled with hazard and handling information, protected from moisture, heat, and direct sunlight. Shipping is via approved carriers specializing in hazardous materials to ensure safety and material integrity during transit.
    Storage Store **4-Fluoro-3-(trifluoromethyl)benzylamine** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep the container under an inert atmosphere, if possible. Avoid moisture, heat, and ignition sources. Clearly label the storage container and ensure access is restricted to trained personnel.
    Application of 4-Fluoro-3-(Trifluoromethyl)Benzylamine

    Applications of 4-Fluoro-3-(Trifluoromethyl)Benzylamine in Industrial Manufacturing

    As a dedicated manufacturer with deep expertise in aromatic amine synthesis, we supply 4-Fluoro-3-(Trifluoromethyl)Benzylamine primarily to specialized chemical industries where high fluorine-content intermediates are essential. This unique raw material integrates into high-demand downstream segments, supporting the precise synthesis of advanced agrochemical actives, pharmaceutical intermediates, specialty polymers, and novel liquid crystal compounds. The scenarios below detail real-world adoption and formulation in industrial production contexts.

    1. Agrochemical Active Ingredient Synthesis

    Producers of selective herbicides and insecticides rely on this fluorinated benzylamine to introduce both fluorine and trifluoromethyl functionalities into final crop protection molecules. Factories integrate the amine group via nucleophilic substitution or reductive amination, using the material as a building block for phenylurea and aniline-based active ingredients. Formulators select application rates based on targeted conversion of specific aromatic core intermediates, adjusting to batch or continuous process scales. With strict residue and purity requirements in modern agricultural chemical manufacture, this material's high quality helps ensure target molecule traceability from input to field application.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • European Directive 91/414/EEC for Pesticide Registration
    • ISO 9001 for Quality Management Systems
    • REACH Registration for Hazardous Chemical Intermediates (EC 1907/2006)

    Typical usage ratio

    • Ranges from 0.8 to 1.2 molar equivalents relative to target halogenated aromatic core, with adjustment based on the required yield and conversion efficiency in multistep syntheses.

    Downstream process integration

    • Added at the key condensation or ring substitution step in intermediate active ingredient production, often under closed system with in-line process analytics for purity and conversion monitoring.

    Final product types

    • Herbicide actives (e.g., fluorinated phenylureas)
    • Systemic insecticide molecules
    • Pre-emergence weed control agents

    2. Pharmaceutical Intermediate Synthesis

    API manufacturers use this fluorinated benzylamine to introduce metabolically stable fluoroaromatic groups into advanced intermediates for central nervous system and oncology drugs. Its presence in the synthesis enables the tuning of pharmacokinetic properties and improved receptor binding. The amine serves as a nucleophile in amide bond formations and reductive aminations, supporting both batch and continuous manufacturing of regulatory-compliant pharma intermediates. Exact molar input aligns to the stoichiometry of the target API, with residual controls monitored through validated HPLC and GC methods to meet global GMP standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) General Chapters
    • European Pharmacopoeia (Ph. Eur.) Monographs for Intermediates
    • Chinese Pharmacopoeia (CP) for registered intermediates

    Typical usage ratio

    • Applied at 1.0–1.3 equivalents depending on reductive amination or coupling step, precisely titrated to minimize unreacted amine in final intermediate.

    Downstream process integration

    • Charged during the intermediate construction phase, forming critical C–N bonds or substituted aromatics directly incorporated into final APIs after further elaboration and purification.

    Final product types

    • Oncology drug intermediates (e.g., kinase inhibitors)
    • CNS small molecule precursor compounds
    • Fluorinated pharmaceutical building blocks used in downstream API assembly

    3. High-Performance Polymer Modification

    Engineering polymer producers select this raw material to modify polyimides or polyamides, introducing fluorinated groups that alter thermal, chemical, and dielectric properties in finished resins. This benzylamine is typically incorporated via nucleophilic aromatic substitution or addition during the oligomer and prepolymer stage, resulting in enhanced polymer chain structure and increased hydrophobicity. The fluorinated segment plays a critical role in tuning glass transition temperature and resistance profiles, and input ratios correspond to the targeted degree of substitution within the monomer matrix.

    Industry compliance standards

    • ASTM D5207 for Polyimide Resin Quality
    • ISO 9001 Certified Production Facilities
    • RoHS Directive 2011/65/EU for Electronic Polymers
    • UL 94 Flammability Standard for Plastic Materials

    Typical usage ratio

    • Incorporated at 3–7 weight percent of total monomer feed, adjusted based on molecular weight target and intended final product dielectric performance.

    Downstream process integration

    • Added during polycondensation or reactive extrusion stage of high-performance resin synthesis, allowing covalent bonding into polymer backbone and ensuring uniform fluorine distribution.

    Final product types

    • Low-dielectric constant polyimide films
    • Fluorinated engineering plastics for electronic and aerospace insulation
    • Thermally stable coatings for microelectronic fabrication

    4. Liquid Crystal Intermediate Manufacturing

    Liquid crystal material suppliers utilize this compound to synthesize highly anisotropic aromatic intermediates required for advanced display and sensor technologies. The amine reacts via condensation or coupling reactions to yield mesogenic cores with superior thermal stability and specific dielectric anisotropy, driving the optical properties of the final display liquid crystals. This material's introduction is carefully controlled based on the geometric configuration of the target mesogen, with rigorous batch tracking and purity analysis standard in this segment.

    Industry compliance standards

    • ISO 14644-1 Cleanroom Standards for Electronic Chemical Manufacture
    • Japan Electronic Industry Development Association (JEIDA) Standards
    • RoHS/REACH Compliance for Display Chemicals
    • IEC 61249-2-21 for Halogen Content in Electronic Intermediates

    Typical usage ratio

    • Employed at 0.5–2.5 molar equivalents in targeted mesogen synthesis, adjusted for degree of molecular alignment and nematic phase properties required for specific LCD or OLED displays.

    Downstream process integration

    • Added during early-stage mesogen coupling and ring extension steps, ensuring precision incorporation into liquid crystal matrix precursors prior to final formulation and blending.

    Final product types

    • Twisted nematic and in-plane switching (IPS) display liquid crystal compounds
    • High-temperature-resistant liquid crystals for automotive and industrial panels
    • Specialty mesogenic intermediates for sensor or photonic applications
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    Certification & Compliance
    More Introduction

    4-Fluoro-3-(Trifluoromethyl)Benzylamine: The Value of Purity in Synthesis

    Introducing Our Experience with 4-Fluoro-3-(Trifluoromethyl)Benzylamine

    As a manufacturer in the chemicals industry, we encounter a flood of molecules, each with quirks and characteristics that show their true colors only during production runs and real-world applications. 4-Fluoro-3-(trifluoromethyl)benzylamine has made its way through our reactors and purification columns many times. We're familiar with its personality—the sharp hints from its aromatic ring, the electron-withdrawing power of its fluoro and trifluoromethyl groups, and the practical challenges that come from bringing a compound with this level of fluorination to high purity.

    Understanding the Structure that Drives Performance

    4-Fluoro-3-(trifluoromethyl)benzylamine stands out because its backbone draws on two strong trends in modern chemistry: fluorine incorporation and amine functionality. From decades of working in multi-purpose plants, we’ve seen that trifluoromethyl groups and their neighboring fluorines shift a molecule’s reactivity, solubility, and bioavailability in predictable ways. That’s not just marketing talk. The electron-rich amine balances out the electron-withdrawing influence of the fluorines. This adjustment translates into unique reactivity when chemists use it as a building block—the core reason for its growing popularity in pharmaceutical and agrochemical research.

    The chemical structure lends itself to both robustness and tunability. In our operations, we carefully control temperatures and pressures to maintain the sensitive amine group while introducing the aggressive fluorine atoms. After many batches, we’ve found that minor changes in reaction environment can make a world of difference in both yield and purity.

    Production Nuances that Matter

    Our hands-on experience points to the inherent challenges of producing benzylamines with heavy fluorination. The trifluoromethyl group withstands harsh conditions, but the introduction of the amine means moisture and air control become front and center issues. Running a reactor at scale, all the small leaks and contamination pathways show up quickly. Over the years, we’ve invested in purification steps beyond conventional crystallization—high-vacuum distillation, multiple columns, analytical monitoring at every step—to hold a purity level that makes downstream reactions less trouble.

    4-Fluoro-3-(trifluoromethyl)benzylamine production doesn’t see the yield or simplicity of a classic benzylamine synthesis. The fluorines complicate every stage. We’ve needed to redesign reactor linings and choose specialized seals to resist corrosion. Our logistics team invests extra care into packaging to avoid product degradation. Controlled humidity in packaging and clean handling zones during filling are part of the routine now.

    From the Plant to the Lab: Real-World Use Cases

    The majority of requests we receive come from labs working in drug discovery, specialty chemical design, or advanced materials. In these areas, chemists rely on intermediates with high integrity because a single contaminant can ruin an entire synthesis project. We’ve lost count of the stories where a subpar benzylamine side product clogged up columns or showed up in mass-spec runs, costing weeks of delay and frustration. We keep those failures in mind every time the team signs off on a new batch.

    What gives 4-Fluoro-3-(trifluoromethyl)benzylamine its edge isn’t simply the presence of the amine. The combined electronegative groups produce distinct reactivity, which synthetic teams value for introducing diversity into analog libraries. In our feedback from customers, the selectivity in nucleophilic substitution and the stability in demanding catalytic conditions are often cited. Bench chemists also mention that our higher-purity material doesn’t leave behind the trace halide salts or unknown impurities that can block downstream reactions. Our analytical team often runs additional NMR and LC-MS tests to confirm that non-target isomers or heavy-metal residues do not sneak through.

    What Sets It Apart from Other Alkylated Benylamines

    Having synthesized a broad range of benzylamines over the years, some clear differences emerge. Plain benzylamines tend to react predictably but lack the subtle electronic effects that come from heavy fluorination. Add a trifluoromethyl group and positioning of a fluorine, and suddenly there’s more than just steric hindrance and solubility at play—the molecule shows both increased metabolic stability and shifts in basicity, which directly affect activity in pharma targets or polymers.

    In our experience, analogs like 4-chlorobenzylamine or even 3-(trifluoromethyl)benzylamine demand less stringent process controls. 4-Fluoro-3-(trifluoromethyl)benzylamine asks more from equipment, personnel, and downstream logistics. There is no room for shortcuts. Handling this compound is a test of production discipline. Our quality assurance protocols for this molecule are more intensive than for standard benzylamines; we check for residual acids from the CF3 introduction and for possible by-product amines resulting from incomplete fluorination. These steps help build trust, especially for partners in regulated industries.

    Comparing Bench and Plant Experiences

    At the bench scale, synthesis of 4-Fluoro-3-(trifluoromethyl)benzylamine feels manageable. Small glassware and fresh reagents minimize exposure to air and moisture. On the plant floor, the difference is clear. Scaling up introduces new challenges—mixing, temperature gradients, and long transfer lines all put the molecule’s stability to the test. Even the storage drums—lined and sealed with moisture barriers—must match the standard set by downstream users. Suppliers who lack deep production experience often cut corners here, causing headaches later on. We’ve learned that consistency, not just claimed purity, makes all the difference for our customers.

    Comparing with other fluorinated benzylamines or aromatic amines, this compound amplifies process hazards. The by-products—if uncontrolled—can introduce hydrofluoric acid or other challenging residues, requiring familiarity with both chemistry and plant operations. Our teams regularly audit process safety and environmental management, ensuring we can handle every kilo responsibly from synthesis to delivery.

    Impact on Medicinal Chemistry and Functional Materials

    Years of working with leading pharma and materials science teams have taught us where this compound shines. Medicinal chemists use 4-Fluoro-3-(trifluoromethyl)benzylamine to fine-tune ADME profiles, aiming for a balance of solubility, metabolic resistance, and receptor specificity. The molecule’s carefully chosen pattern of fluorines delivers distinct lipophilicity and electron density profiles—a fact borne out in peer-reviewed research.

    Functional materials designers value these same effects. The amine allows for coupling to a range of scaffolds, while the fluoro and trifluoromethyl groups lend chemical and thermal stability, important in coatings and electronic components. Over multiple production campaigns, we’ve supported collaborations where only this specific substitution pattern unlocked a desired function—whether in a new OLED material or a surface-modifying agent. We keep careful records and document performance parameters, as feedback always triggers another process optimization round.

    Trust Built Through Direct Manufacture

    Many end users ask if we make the compound ourselves or source from third parties. Having been on both sides, we make it a point to manufacture all batches in-house. Direct production control lets us guarantee batch-to-batch consistency—something importers or resellers often lack. Whenever a deviation appears, our analytical team can trace its source and fix it right away, not weeks later after complaints. Over time, this approach has built a sense of mutual trust with research labs and industrial clients, who come back to us repeatedly after trying less reliable sources.

    One key lesson has been the importance of honest feedback and problem solving. If a client reports an issue with crystallinity, solubility in a non-standard solvent, or even unexpected reactivity, our chemists dig into the operational data, then run checks on retained samples. This closed feedback loop drives both process improvements and renewed confidence in the quality of supply. We do not rely on generalized assurances—we back up every certificate with real-time data collected through the process, and share this when requested.

    Safe Handling and Storage Draw on Production Experience

    We have learned through experience not to underestimate the impact of fine details in handling. Benzylamines with multiple fluoro groups can react with atmospheric moisture—sometimes in ways that remain invisible to the naked eye but show up on analytical methods. Storage logistics require real investment in inert-gas packaging, multi-layer barriers, and continuous monitoring for any signs of decomposition.

    Early on, our logistics team took advice from warehouse operators, not just chemists, and refined our drum and bottle filling protocols. Every transfer process now operates in a laminar flow hood, and all containers ship with detailed timestamps and lot tracking. These steps came from lessons learned the hard way—batch recalls, field complaints, and delayed projects. Now, we operate with an awareness that even one contaminated sample can undermine weeks of research for our customers.

    Collaborative Solutions for Formulation and Scale-Up

    Our partnerships with downstream users often turn into collaborative problem-solving efforts. A pharma group once reached out, reporting issues in forming stable salts of 4-Fluoro-3-(trifluoromethyl)benzylamine despite following published methods. Together, we dug through process records, assessed the secondary impurities, and fine-tuned the pH adjustment protocol in real time. Within days, we delivered a tailored solution and helped redesign their purification sequence.

    Similar stories echo in materials science. A client working on a new lubricant additive struggled with solubility and blending properties. Rather than offer generic advice, we volunteered to send small pilot lots with slightly varied moisture contents and performed stability tracking. These targeted adjustments allowed their R&D team to pinpoint the optimum tolerance range, speeding up their development cycle.

    This personal involvement—treating every production run as more than just another batch number—became a core company value. Users see the benefit not just in speed or documentation but also in the sense of partnership. As new applications for 4-Fluoro-3-(trifluoromethyl)benzylamine emerge, we keep our systems flexible to respond to unexpected hurdles, knowing that shared expertise carries real weight in high-value research or commercial production.

    Quality Control Rooted in Plant-Led Practices

    Measuring quality starts on the reactor floor, not in the lab report. Our operating team pulls samples at every key transition—after reaction, before work-up, following each purification step. By analyzing trends over years of production, we’ve isolated minor shifts that can predict off-spec product before it makes it to final fill. Analytical methods run alongside production, not after the fact. Every critical impurity is qualified using internal benchmarks set higher than minimum regulatory standards.

    Real quality control also means transparent records. Every customer gets access to full spectral data and analytical reports, not just a paper certificate. If a batch’s water content or residual solvent goes out of established norms, we recall, reject, or reprocess it without delay. Our plant team learns from every deviation. These small but steady process tweaks show up as long-term improvements—better yields, increased consistency, and tighter specifications that our clients notice.

    Environmental and Safety Commitment Informed by Day-to-Day Operations

    Our journey in making fluorinated benzylamines has taught us about stewardship—safety in the workplace and minimizing emissions in the community. Processing dense fluorinated molecules brings waste streams we can’t ignore; our waste management protocols include multi-stage scrubbing of off-gases and closed-loop recovery of volatile solvents. Byproducts and side streams receive as much monitoring as main products—our philosophy is to treat every kilo as a responsibility, not just an economic asset.

    On safety, we emphasize regular team training based on what really happens during scale-ups, not just textbook emergencies. Operators rotate between lab and plant work to build respect for both process variability and personal safety. Every incident, whether near-miss or actual event, leads to a process review and equipment upgrade if needed. Over multiple years, this approach has sharply reduced downtime and accident rates. Our employees carry the ethos that high standards protect both people and science.

    Pushing Forward in an Evolving Market

    Markets shift, new research creates demand spikes, and regulatory standards tighten year by year. Our strategy for keeping pace rests on flexibility in production scheduling and rapid integration of feedback from clients. For each new batch of 4-Fluoro-3-(trifluoromethyl)benzylamine, our R&D team tracks emerging literature and benchmarks against the best-in-class production protocols, not just our own past practice.

    We invest in pilot batch studies and side-by-side stability tests using actual customer SOPs, not just idealized conditions. If a downstream process illuminates previously unnoticed degradation or incompatibility, we trace the cause and upgrade the process without delay. Production changes move quickly from pilot to full runs, supported by documentation accessible to all our partners.

    Real-World Lessons from Manufacturing Experience

    Every batch of 4-Fluoro-3-(trifluoromethyl)benzylamine that meets a client’s needs carries forward hard-won lessons—a process tweak that fixed an impurity, a packaging upgrade that controlled shelf life, a risk assessment that averted a production delay. These changes set our product apart in tangible ways, not just in technical terms but in day-to-day reliability and demonstrated respect for the user’s work.

    Synthesis of organofluorine compounds like this benzylamine is not just theory on a page. It is long days in the plant, learning from small failures and finding real solutions. Our dedication comes from years spent facing challenges alongside our staff and clients—building trust batch by batch, driven by a clear commitment to both science and safety. By delivering 4-Fluoro-3-(trifluoromethyl)benzylamine with the highest possible quality, we aim to be genuine partners in our clients’ continued innovation and success.