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4-Fluoro-2-(Trifluoromethyl)Benzylamine

    • Product Name 4-Fluoro-2-(Trifluoromethyl)Benzylamine
    • Alias 4-Fluoro-2-(Trifluoromethyl)Benzenemethanamine
    • Einecs 629-018-5
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    579226

    Productname 4-Fluoro-2-(Trifluoromethyl)Benzylamine
    Casnumber 886762-58-1
    Molecularformula C8H7F4N
    Molecularweight 193.14
    Appearance Colorless to pale yellow liquid
    Purity Typically >97%
    Boilingpoint 73-74°C at 14 mmHg
    Density 1.327 g/cm3 at 25°C
    Refractiveindex n20/D 1.477
    Solubility Soluble in organic solvents (e.g., DCM, methanol)
    Synonyms α-(Aminomethyl)-4-fluoro-2-(trifluoromethyl)benzene
    Storagecondition Store at 2-8°C, tightly sealed
    Smiles C1=CC(=C(C=C1F)C(F)(F)F)CN
    Inchikey IMBDJYQPGYJYJB-UHFFFAOYSA-N

    As an accredited 4-Fluoro-2-(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 containing 10 grams of 4-Fluoro-2-(Trifluoromethyl)Benzylamine, with tamper-evident cap and hazard labeling.
    Shipping 4-Fluoro-2-(Trifluoromethyl)Benzylamine is shipped in tightly sealed, chemically-resistant containers to prevent leaks and contamination. It is packaged according to regulatory guidelines for hazardous chemicals, with clear labeling and material safety data included. Shipments are handled by certified carriers, ensuring safe transit under temperature-controlled and secure conditions.
    Storage Store 4-Fluoro-2-(trifluoromethyl)benzylamine in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as acids and oxidizers. Keep the container tightly closed and protected from moisture. Store under inert gas, if possible, and avoid direct sunlight. Follow all safety regulations, including proper labeling and secondary containment to prevent leaks or spills.
    Application of 4-Fluoro-2-(Trifluoromethyl)Benzylamine

    Applications of 4-Fluoro-2-(Trifluoromethyl)Benzylamine in Industrial Manufacturing

    4-Fluoro-2-(Trifluoromethyl)Benzylamine serves as a key intermediate in several specialized areas of industrial chemistry. As the original manufacturer, we supply this advanced amine compound to stringent pharmaceutical, agrochemical, and materials sectors, supporting process integration from pilot to full-scale operations.

    1. Pharmaceutical API Synthesis

    This amine acts as a critical building block for advanced pharmaceutical intermediates, especially in the synthesis of selective kinase inhibitors and fluorinated analgesics. Manufacturers use it to introduce specific fluoroalkyl groups during stepwise assembly of complex APIs, supporting targeted drug design and improving metabolic stability. Handling and usage require strict adherence to validated GMP production workflows to ensure purity and traceability.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 for finished pharmaceuticals
    • European Pharmacopoeia Monographs
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Utilized at 0.3–1.2 molar equivalents depending on the target API structure; process chemists adjust the ratio to minimize byproducts and match the downstream coupling partner.

    Downstream process integration

    • Added during the amidation or reductive amination stages; typically introduced following hydrolysis or protection group removal, depending on route design and impurity profile control.

    Final product types

    • Fluorinated kinase inhibitors
    • CNS-active pharmaceuticals
    • Specialty antivirals
    • Oral dosage and parenteral form API intermediates

    2. Agrochemical Intermediate Production

    Producers of advanced crop protection agents incorporate this amine as a core intermediate in the development of novel herbicides and selective insecticides. Its unique fluorinated aromatic structure enables the synthesis of active molecules for seed coatings and foliar sprays, delivering increased stability against UV degradation and enhancing bioactivity in field formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Phase I-II Testing Guidelines for Agrochemicals
    • ISO 9001:2015 Process Documentation
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • Typically utilized at 0.5–1.5 molar equivalents in condensation or cyclization reactions, dependent on target molecule structure and crop protection grade requirements.

    Downstream process integration

    • Joined at heterocyclic core-forming steps or appended to aromatic precursors by nucleophilic substitution, scheduled after raw material QC and prior to blending with other agrochemical actives.

    Final product types

    • Herbicidal concentrate intermediates
    • Selective insecticide active ingredients
    • Seed treatment actives
    • UV-stable agricultural adjuvants

    3. Fluorinated Material Monomer Manufacturing

    The electronics and advanced plastics sectors demand high-purity aromatic amines for synthesizing specialty fluorinated monomers. This compound provides a functional group for copolymerization, supporting the development of dielectric films, high-performance resins, and liquid crystal alignment layers. Accurate dosing and impurity control allow consistent performance in demanding thin-film and engineered polymer applications.

    Industry compliance standards

    • RoHS 3 Directive 2015/863/EU for restricted substances
    • IPC-4101 for base materials in printed circuit laminates
    • ISO 14001:2015 Environmental Management Systems
    • UL 94 Flammability certification for polymers

    Typical usage ratio

    • Dosed at 1.0–4.0% w/w relative to total monomer content; ratio calibrated based on desired fluorine content and dielectric property targets.

    Downstream process integration

    • Charged to pre-polymerization reaction mixtures, commonly with anhydrides or isocyanates, prior to chain initiation and followed by post-polymerization purification to maintain electrical grade quality.

    Final product types

    • Low-permittivity dielectric films
    • Photolithography resins
    • Alignment films for LCD panels
    • High-frequency circuit board materials

    4. Specialty Chemical Intermediate for Fine Chemicals

    Manufacturers of fine chemicals employ this fluorinated amine in multi-step synthesis of specialty dyes, functional additives, and analytical reagents. Its precise structure supports regioselective reactions, enabling downstream transformation into labeled probes, fluorinated surfactants, and advanced imaging compounds for research and diagnostics.

    Industry compliance standards

    • ISO 17025:2017 for laboratory reagent production
    • IUPAC nomenclature and substance traceability documentation
    • Chemical Storage and Handling OSHA 29 CFR 1910.1200
    • REACH SVHC (Substances of Very High Concern) notification for specialty applications

    Typical usage ratio

    • Employed at 0.1–0.8 equivalents, chosen based on the labeling or additive function required, with batch records specifying lot usage per protocol.

    Downstream process integration

    • Introduced during nucleophilic aromatic substitution or as an amine donor in functionalization steps, typically before end-stage purification and crystallization.

    Final product types

    • Fluorinated dye intermediates
    • Imaging calibration reagents
    • Surface-active labeling compounds
    • Fine chemical building blocks for analytical reference standards
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    Certification & Compliance
    More Introduction

    Deep Dive: 4-Fluoro-2-(Trifluoromethyl)Benzylamine from an Experienced Chemical Manufacturer

    Crafting the Unusual—Our Journey with 4-Fluoro-2-(Trifluoromethyl)Benzylamine

    Every chemist knows certain synthons unlock new pathways in organic synthesis. In our facility, 4-Fluoro-2-(Trifluoromethyl)Benzylamine stands out. Not because its name twists tongues, but because it solves problems where other building blocks start to fall short. Over the years, our team has seen interests in this fluorinated benzylamine grow, mostly because research environments keep asking for it. So today, let’s lay out what makes this compound different, why laboratories come back for it, and what a manufacturer faces during scale-up.

    Understanding 4-Fluoro-2-(Trifluoromethyl)Benzylamine—A Unique Structure

    The molecule combines a benzylamine backbone with two impactful substituents: a fluorine at the 4-position and a trifluoromethyl at the 2-position. These tweaks might look simple on a drawing, but in synthesis, small changes like these steer properties in ways most newcomers underestimate. The electronic effects, together with distinct steric bulk from the trifluoromethyl, make this compound stubborn in many reactions. Our process chemists spent dozens of trials refining reaction conditions to reach reproducible yields without runaway impurities.

    Most other benzylamines lack this level of site-specific fluorination. As a manufacturer, we notice that this substitution pattern gives the compound a niche, not just as a routine chemical but as a lever arm for molecular design. When our QC team runs NMR, IR, and MS profiles, the fingerprint turns out sharper and more unique compared to regular benzylamines—a direct result of these substituent effects. For researchers needing a solid fluorinated anchor in their synthesis, this matters far more than it might seem from catalog descriptions.

    Why Specification Matters—A Manufacturer’s Eyes

    We produce this compound primarily for the pharmaceutical sector and specialty research, so batch-to-batch consistency draws plenty of attention. Customers usually ask for material in the form of a colorless to pale yellow liquid, with purity over 98% by HPLC. Even trace contaminants impact downstream reactions, especially in drug discovery. Over time, we've mapped out how different solvents during purification introduce distinct impurity profiles and residual solvents, which can be invisible to buyers unless pointed out. We've focused on reducing these remnants to trace levels, as it reflects both on our process hygiene and the reliability of clients’ experiments.

    Packaging sounds trivial, but benzylamines tend to absorb moisture and even develop coloration if left in poorly-sealed vials. To counteract this, we flush with nitrogen and use fluoropolymer linings for longer term supply. Tracking bottle age, storage temperature, and headspace composition gives us data we use to offer real storage advice, not just a “keep in a cool dry place” slogan. These details draw from hard-earned experience, not what’s copied off a generic spec sheet.

    Applications—Meeting Chemists Where They Work

    As a producer, we track where 4-Fluoro-2-(Trifluoromethyl)Benzylamine heads after leaving our warehouse. Most orders come from research groups working on medicinal chemistry, agrochemical intermediates, or material science. The compound acts as a key intermediate for making high-value amides, ureas, or other nitrogen-containing frameworks. By introducing both trifluoromethyl and fluorine atoms onto aromatic rings, synthetic chemists can boost metabolic stability or bioactivity in new candidate molecules. These features cause biological systems to “pause and think,” so to speak. This effect shows up in late-stage functionalization and in SAR libraries.

    In comparison, non-fluorinated benzylamines struggle to bring about the same pharmacokinetics, and mono-fluorinated ones rarely deliver enough change to justify their use over standard reagents. Our customers see real results with the regioselectivity our compound brings, especially as larger groups shift toward more fluorine-rich scaffolds. From the manufacturing side, seeing repeat orders for this specific benzylamine gives our team a satisfying sense of playing an important support role in both late-stage research and early pilot rounds.

    Making It in Volume—Lessons from the Factory Floor

    Sustaining high quality for 4-Fluoro-2-(Trifluoromethyl)Benzylamine takes more than following a recipe. Our earliest trials produced solid yields in the flask, but scale-up opened a dozen fresh headaches—solvent carryover, tough-to-separate isomers, and instability on heating. Every larger batch forced us to re-examine work-up conditions and clarify which parameters actually matter. We recall adjusting acid wash ratios by tiny increments, only to watch downstream impurities shift unpredictably. Only by logging every trial and cross-correlating results have we tuned the process into something robust.

    Handling fluorinated intermediates, especially at scale, also means dealing with tricky cleaning cycles in the plant. The residues don’t behave like those of plain aromatics, and pipes sometimes lock up unless flushed with a combination of polar and nonpolar washes. For each fresh order, a chain of inspections takes place to make sure residuals fall below strict limits—otherwise cross-contamination risks climb. Layers of in-process testing keep surprises low, but real vigilance only comes by understanding how fluorinated amines interact with everything from plastic tubing to stainless steel reactors. Our operators and QC chemists learn these details in the plant, not from textbooks.

    Safety and Operator Experience

    4-Fluoro-2-(Trifluoromethyl)Benzylamine brings stronger odors than many plain amines. This translates into more diligent ventilation practices during filtration, distillation, and packaging. We invested early in closed transfer systems to keep exposure low. Operators always wear appropriate PPE and work under exhaust, but these rules become obvious once anyone spends a shift with an olfactory sting that lingers. For transport, the compound’s sensitivity to air and light prompted us to adopt amber glass packaging sooner than required. While standard benzylamines might pass undisturbed through regular glass, fluorinated ones resist that convenience—they force us to rethink even simple storage conventions.

    From years working the floor, staff colleagues trade advice on what works for neutralizing spills and cleaning vapor traces. Dilute bleach sometimes causes more trouble, so we emphasize using specific neutralizers designed for amines, then carefully ventilate enclosed spaces before re-entry. These protocols evolved in response to direct feedback—a two-way channel between management and operators, not a one-off set of rules from a printout.

    Traceability—Following Each Batch’s Story

    Each unit of 4-Fluoro-2-(Trifluoromethyl)Benzylamine carries a unique batch identifier, not just for compliance but as part of our commitment to transparent supply chains. Over the last decade, regulatory expectations for fluorinated chemicals have risen. That means record-keeping covers everything from raw material source to temperature profiles during each production step. Some clients require data on solvent origins or even on non-chemical aspects like energy use.

    From our experience, traceability tools shine brightest when something unpredictable happens—a shipment delayed at customs or a QC query from a client’s own testing lab. Because our production logs stay detailed, we solve these bottlenecks quickly. Our batch records show not just numbers but full run notes, from observations in the plant to follow-up handling. Auditors who arrive on-site often remark on our practical ability to answer tough questions right away, a result only achievable by blending digital tracking with real-world attention to detail.

    Environmental Reflections—Fluorinated Chemistry’s True Cost

    As a direct manufacturer, we don’t get to ignore the environmental side of fluorination. Producing 4-Fluoro-2-(Trifluoromethyl)Benzylamine means careful waste segregation, scrubbing emissions from vented gases, and tracking each kilogram of fluorinated byproduct. We have invested in dedicated wastewater treatment to prevent fluorine-containing residues entering local systems. Partners down the chain expect proof of these measures—not just paperwork, but analytical results demonstrating compliance over time.

    Many researchers ask about overall sustainability and regulatory adherence before placing orders. In response, we share process improvements—from solvent recovery to better abatement technologies—that cut waste and raise process yields. Engineers constantly trial new columns and distillation settings, aiming to raise throughput while using less energy. These steps don’t make headlines, but they steadily trim both process costs and environmental footprint. We learned over years that successful fluorination chemistry blends practical risk control with long-term vision on resource responsibility.

    Comparisons—What Sets This Compound Apart?

    Compared to standard benzylamines, 4-Fluoro-2-(Trifluoromethyl)Benzylamine changes the game in synthetic strategy. Chemoprotection improves, electronic tuning sharpens, and downstream derivatizations run smoother. Regular benzylamines without the fluorinated pattern fall short in certain coupling reactions, and their biological activity tends to waver after metabolic testing. Some competitors substitute only a fluorine or a methyl, but without the trifluoromethyl group, the balance between lipophilicity and reactivity shifts unfavorably for demanding research tasks.

    As a manufacturer, we feel the difference most during the packaging and storage phase. The compound’s stability under ambient conditions can’t be taken for granted, unlike some alternatives. Research teams hunting for rare effects in CNS-active compounds or advanced materials find the unique substitution pattern invaluable. Our feedback loop with clients reinforces this: the substitution unlocks activity profiles and synthetic steps that regular or mono-functionalized benzylamines simply don’t match. By making the compound at scale while holding down impurity levels, we enable customers to stretch the boundaries of their own work.

    Challenges in Customization and Scale

    Some clients order 4-Fluoro-2-(Trifluoromethyl)Benzylamine with tweaks—ultra-high purity, alternate solvents, or as salts. Every new request brings up plant logistics. Shifting from free base to a hydrochloride salt looks simple on paper, but moisture management, crystallization kinetics, and filtration change enough to force pilot runs. We work with clients to define realistic specs, explaining the trade-offs transparently instead of promising the moon. Repeatable production and real yield data trump marketing flourish in our business.

    Upscaling always pushes the limits. Raw materials may be globally sourced, and market volatility impacts supply lines. Our experience navigating these issues centers on maintaining credible supplier partnerships and engineering workarounds for lean times. From one season to the next, tightening up process flows or broadening reagent choices matters more than getting tied to single points of failure. By focusing on synthesis routes we control, we avoid surprise shortages and hold our QC standards constant.

    Feedback Loop—The Importance of Dialogue

    Manufacturing highly-substituted benzylamines isn’t a matter of shipping drums from a warehouse. Each client’s project shapes the tweaks we adopt on the production line. Feedback comes back to us in unexpected ways—a synthesis that worked at milligram scale failing once the chemist shifts to a preparative run, or an analytical spike showing up only after a downstream enzyme screening. We maintain a two-way channel, speaking plainly with research clients and troubleshooting not just our product, but sometimes, the project they pursue.

    Our technical support teams spend hours reviewing client HPLC chromatograms, offering advice drawn from our own work-up records. Sometimes, swapping a single process step—say, adjusting the final wash or shifting to a less-reactive drying agent—makes the difference between a stalled project and a breakthrough. This openness forms the backbone of trust, more so than any certificate or label ever could.

    The Why Behind the Work—Value Beyond the Product

    Producing 4-Fluoro-2-(Trifluoromethyl)Benzylamine takes more than equipment and reagents. Anyone can attempt the synthesis, but reliable manufacturing means seeing every link of the supply chain as a living part of the outcome. Each operator and chemist at our site brings practical wisdom shaped by years of failure and incremental victory. Every new order is another test of that know-how—keeping impurity levels low, tracking bottle age, and sharing storage best practices that actually work outside the lab.

    We see our product as a bridge to new science and technology. For all the complexity this compound brings us, the sense of purpose returns each time a new application takes shape—a drug hitting the next phase, a material gaining a patent, a client finding a solution in a place previously walled off by chemistry’s limits. In the industrial trenches, this simple amine stands as a reminder: the work is never just about molecules, but about helping people push science forward.

    Final Word—What We’ve Learned, and What Comes Next

    Working directly as a chemical manufacturer grants a perspective trading and distribution can't. Each batch of 4-Fluoro-2-(Trifluoromethyl)Benzylamine carries a history written in troubleshooting, hands-on trial, and transparent quality reporting. Our process adapts year by year, tracking new research applications and regulatory landscapes. Challenges—from scaling batch sizes to balancing environmental responsibility—sharpen the discipline needed to reliably supply a compound with such a specialized role.

    For us, the most valuable lesson is that successful supply of such chemicals depends as much on openness, feedback, and daily attention to real-world detail as it does on technical prowess. We’re committed to staying responsive, innovative, and above all, grounded in the experience only direct manufacturing can provide. The future will bring new challenges in fluorine chemistry—more environmental scrutiny, more complex synthesis demands, and tighter purity requirements. We’re already building the know-how and infrastructure to meet that future, and in every batch sent out, we see the next step in this ongoing journey with our partners in the lab and beyond.