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2-Fluoro-3-(Trifluoromethyl)Benzylamine

    • Product Name 2-Fluoro-3-(Trifluoromethyl)Benzylamine
    • Alias 2-F-3-CF3-BnNH2
    • Einecs 629-851-2
    • 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

    238057

    Product Name 2-Fluoro-3-(Trifluoromethyl)Benzylamine
    Cas Number 886372-17-0
    Molecular Formula C8H7F4N
    Molecular Weight 195.14
    Appearance Colorless to pale yellow liquid
    Boiling Point 57-59°C at 13 mmHg
    Purity ≥97%
    Density 1.32 g/cm³
    Smiles C1=CC(=C(C(=C1)F)C(F)(F)F)CN
    Inchi Key RZYTWZQPLXWBRJ-UHFFFAOYSA-N

    As an accredited 2-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 containing 5 grams of 2-Fluoro-3-(trifluoromethyl)benzylamine, sealed with a screw cap and tamper-evident label.
    Shipping 2-Fluoro-3-(Trifluoromethyl)benzylamine is shipped in secure, airtight containers to prevent contamination and moisture exposure. The product is labeled according to regulatory requirements and packed with protective material to minimize risk during transit. Shipping is conducted via regulated carriers, with accompanying safety data sheets to ensure safe and compliant handling and delivery.
    Storage Store 2-Fluoro-3-(trifluoromethyl)benzylamine in a tightly closed container, in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep at room temperature or lower, and protect from moisture. Use appropriate chemical storage cabinets, wear suitable protective equipment when handling, and ensure the container is clearly labeled.
    Application of 2-Fluoro-3-(Trifluoromethyl)Benzylamine

    Applications of 2-Fluoro-3-(Trifluoromethyl)Benzylamine in Industrial Manufacturing

    As a direct manufacturer, we supply 2-Fluoro-3-(Trifluoromethyl)Benzylamine with strict adherence to industry requirements. Our material integrates into advanced chemical synthesis processes across several defined industrial sectors. The following application scenarios detail how downstream users incorporate our amine derivative into their production, including regulatory standards, typical dosage, process entry point, and end product outputs.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Many pharmaceutical manufacturers employ this amine as a functional group source for synthesizing selective central nervous system agents and novel anti-inflammatory drugs. Its electron-withdrawing groups contribute to specific reactivity and stability, allowing accurate modifications during multi-step synthesis, especially in the preparation of protected or derivatized benzylamine cores. This intermediate has been incorporated into scale-up projects for innovative small molecule APIs, requiring strict quality and purification controls at each step of the synthetic path.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) guidelines for raw material source verification
    • 21 CFR Part 211: U.S. FDA Current Good Manufacturing Practice for Finished Pharmaceuticals
    • REACH (EC 1907/2006) registration for chemical raw materials used in pharmaceuticals within the EU

    Typical usage ratio

    • 0.5–2.5 molar equivalents as a step-specific reagent, adjusted based on the target molecule’s substitution pattern and protecting group strategy
    • Adjustment justified by desired reaction completeness and minimization of impurities during coupling or reductive amination steps

    Downstream process integration

    • Introduced at secondary or tertiary building block coupling stage
    • Fed into amide or urea formation after upstream halogenation or nitration processes
    • Purified via chromatography or crystallization prior to API condensation

    Final product types

    • API intermediates for neurological disorder therapeutics
    • Semi-synthetic anti-inflammatory agents
    • Small-molecule kinase inhibitors for oncology research

    2. Agricultural Crop Protection Synthesis

    Downstream agrochemical formulators select this amine for incorporation into the synthesis of novel fluorinated herbicide and fungicide active substances. Its electron-rich aromatic ring plays a vital role for chemists aiming to boost environmental persistence and selectivity of crop protection molecules. In pilot and industrial-scale reactors, it enables high-yield coupling and subsequent chlorination or oxidation reactions, generating intermediate scaffolds for regulated pesticides and plant health products.

    Industry compliance standards

    • ISO 9001:2015-certified production for agrochemical inputs
    • US EPA 40 CFR Part 169: Reporting for pesticide chemical manufacturing
    • European Regulation (EC) No 1107/2009: Plant protection product ingredient assessment
    • China National Standard GB 2763 for pesticide use safety

    Typical usage ratio

    • 0.8–1.5 equivalents for initial active intermediate formation, depending on downstream halogenation cycle requirements
    • In multicomponent assemblies, slightly higher ratios prevent unreacted starting material carryover; controlled via in-process HPLC

    Downstream process integration

    • Inserted in the first or second step of heterocyclic ring formation
    • Subjected to acylation or N-alkylation prior to specific active ingredient derivatization
    • Blended with other fluorinated building blocks in campaign-based synthesis schedules

    Final product types

    • Fluorinated triazole fungicide intermediates
    • Novel diphenyl ether herbicide scaffolds
    • Seed treatment precursor compounds

    3. Advanced Material Monomer Customization

    Producers of specialty materials integrate this compound as a monomer modifier while engineering high-performance fluorinated polymers and liquid crystal intermediate mixtures. Its unique benzylamine backbone enhances chemical resistance, dielectric properties, and solubility profiles of resultant materials. Process engineers precisely meter the amine during polymerization, governing molecular weight and tuning chain-end functionalities for downstream electronics, optics, or advanced coatings industries.

    Industry compliance standards

    • RoHS 2011/65/EU and 2015/863: Restriction of hazardous substances in electrical/electronic equipment
    • IATF 16949:2016 for automotive-grade polymer raw materials
    • ASTM D4329: Accelerated aging compliance for plastics under UV exposure
    • ISO 14001: Environmental management of industrial inputs

    Typical usage ratio

    • 0.2–1.0 wt% as a functional additive in fluoropolymer resin feeds
    • For custom LC mixtures, 2–15 mol% blended with other aromatic amine monomers; optimized by end-product dielectric or refractive index targets

    Downstream process integration

    • Added at the in-situ polymerization or monomer blending phase
    • Used as a reactive diluent to modulate cure times in prepolymer syrup processing
    • Participates in surface modification and finishing for hydrophobic layer deposition

    Final product types

    • Fluorinated polyimide films for flexible displays
    • Dielectric specialty coatings for semiconductors
    • Liquid crystal intermediate formulations

    4. Specialty Dye and Pigment Manufacture

    Our industrial clients employ this fluoro-trifluoromethylated amine as a reactive amine donor in the synthesis of high-stability fluorinated azo and anthraquinone dyes. Its influence on color fastness, light resistance, and shade control supports advanced pigment production for applications in technical textiles, plastics coloration, and security inks. Downstream facilities leverage the amine’s nucleophilicity at the initial diazotization or conjugation stages, maximizing batch-to-batch consistency of pigment performance.

    Industry compliance standards

    • OEKO-TEX Standard 100: Restricted substances in textile dye components
    • EN 71-3:2019 for heavy metals and amine safety in toys and pigments
    • REACH Annex XVII: Restrictions on certain amine dyes
    • ISO 18314-2 Colorimetry for industrial color preparation QC

    Typical usage ratio

    • 0.5–1.2 equivalents in diazotization reactions, adjusted for target chromophore depth
    • For pigment dispersions, amine content controlled to less than 8% of total colorant mass by finished product safety thresholds

    Downstream process integration

    • Feeds into azo coupling as the primary amine source
    • Undergoes condensation in anthraquinone pigment synthesis prior to sulfonation or halogenation
    • Handles batchwise with in-process FTIR monitoring to verify conversion

    Final product types

    • Fluorinated azo textile dyes for synthetic fibers
    • High-performance anthraquinone pigments for engineering plastics
    • Security and anti-counterfeiting ink formulations
    Free Quote

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    Certification & Compliance
    More Introduction

    2-Fluoro-3-(Trifluoromethyl)Benzylamine: Insights from the Manufacturing Floor

    Understanding 2-Fluoro-3-(Trifluoromethyl)Benzylamine from a Manufacturer’s Standpoint

    Working directly with 2-Fluoro-3-(Trifluoromethyl)Benzylamine, known among our team as a reliable intermediate in the synthesis of diverse novel compounds, teaches a manufacturer certain facts—ones that don’t always filter through supply chains or secondary writeups. We engage with every stage of this product’s lifecycle, from raw starting materials to the purity analysis that closes off each batch. With years of firsthand experience handling fluorinated aromatics, we’ve learned why each tweak in synthesis or handling matters in daily production and why this molecule holds weight in the eyes of process chemists and R&D specialists.

    What We Aim For in Every Batch

    We don’t just read chemical specifications—we work to achieve them as a matter of course. In our plant, each portion of 2-Fluoro-3-(Trifluoromethyl)Benzylamine emerges from a carefully sequenced process. Stringent controls at each reactor stage and cleaning procedures let us consistently reach an assay over 98% by HPLC, a necessity for pharmaceutical or crop-protection labs. Trace moisture, low residual solvents, and tight control of other aromatic amines keep our product’s performance predictable, so you don’t encounter surprises downstream. The color, clarity, and odor, minor details for some, can signal trouble for those working in organofluorine chemistry—they give an early warning about any anomaly the eye can spot before an instrument even samples it.

    What Sets This Building Block Apart

    If you’ve run syntheses with benzyl amines, you know there is no shortage of choices with subtle structural features. Our experience teaches us that the dual substitution—a single fluorine at the ortho position, plus a trifluoromethyl at the meta—endows 2-Fluoro-3-(Trifluoromethyl)Benzylamine with a unique reactivity profile. The electron-withdrawing effect modifies its nucleophilicity and, in several cross-coupling or amide bond formations our partners attempt, these substitutions minimize unwanted side reactions. You trade a small reduction in basicity for improved selectivity. Letting you coax out target compounds in higher yield with fewer purification steps has become a consistent point of feedback from teams working in drug discovery or advanced material synthesis.

    While other benzylamines may promise similar profiles, variants lacking the ring’s trifluoromethyl or fluorine groups show a tendency toward either excessive reactivity or instability, especially once exposed to elevated temperatures or strong bases. We often field requests from labs needing a balance between chemical robustness and selectivity not present in unsubstituted or simply mono-fluorinated benzylamines. That’s where the 2-fluoro, 3-trifluoromethyl structure carves out its niche. We don’t push the market with any molecule; repeated orders and scale-ups from the same process teams tell us where the value lies.

    Practical Experience Matters on the Production Line

    Producing 2-Fluoro-3-(Trifluoromethyl)Benzylamine needs close attention to safety protocols, precise temperature regimes, and smart waste management. These aren’t secondary to cost or speed. Our chemistry team tracks each reaction’s exotherm, and years of pilot-batch mishaps have taught us not to underestimate the volatility of some intermediates. We take pride in batch records that go deep, logging not just the yields but the hints of deviation from routine—a faint change in the gas-chromatography retention time, a shift in UV absorption suggesting minor by-products.

    This attention pays dividends for teams relying on downstream chemistry to run without hitches. Books teach procedural chemistry, but running 500-liter reactors over years teaches you about what happens when a slight impurity sneaks through—lost product, fouled purification columns, unnecessary head-scratching in development labs. We invest more in analytical quality control than any protocol could strictly require, because we’ve seen what happens outside of specs.

    Supporting Innovation Across Sectors

    Behind every kilo of 2-Fluoro-3-(Trifluoromethyl)Benzylamine, there’s someone using it to make a leap in their own research. Medicinal chemistry teams look to this molecule for better metabolic stability in lead drug candidates. The electron-deficient ring system, shaped by its fluorinated groups, has a noticeable impact on in vivo performance—something we’ve heard about in project wrap-up calls with researchers. In the realm of agrochemicals, creative use in linker chemistry delivers selectivity or persistence when older scaffolds fall short. Our product lets formulation chemists push designs that can stand up to environmental stressors or enzymatic breakdown.

    As more labs invest in fluorinated motifs to boost target binding or bioavailability, requests for this building block have grown. We keep our processes flexible to ensure that we can meet increasing or custom demand. Modifying pack sizes, shipment frequency, or documentation doesn’t just reduce downtime for other teams—it signals that we’re in step with their pace of discovery.

    Why Rigorous Sourcing Remains a Priority

    Strict controls over precursor sourcing and vendor selection let us sleep at night. Poor-quality feedstocks breed long-term headaches, not just minor cleanup. We don’t cut corners, even when market pressures drive buyers to cheaper alternatives, because problematic precursors multiply costs downstream—especially in critical applications where even a trace contaminant can derail a multi-step synthesis.

    A few years ago, sourcing teams flagged subtle shifts in aromatic starting material purity that translated into downstream chromatographic tails. Instead of dismissing it as a “supplier issue,” we reevaluated our internal purification and switched back to more reliable partners, despite the extra cost. The point is simple: shortcuts in procurement almost never pay off for a manufacturing operation that values its reputation.

    Real Consequences for Those Who Cut Corners

    The reality of synthetic chemistry, especially with specialty aromatics like 2-Fluoro-3-(Trifluoromethyl)Benzylamine, is that inconsistencies surface fast. We’ve heard more than one story of an end-user finding that trace metal residues, left unchecked by some producers, catalyze unintended byproducts or color changes in sensitive downstream reactions. These aren’t just anecdotal inconveniences—they sometimes translate into lost days or scrapped projects.

    We made our choice to invest in better purification of the product and to run comprehensive batch analytics—not out of regulatory necessity, but from a string of avoidable losses we faced years ago. Today, end-users who try a high-purity batch after struggling with bargain options usually don’t go back. Confidence in consistency breeds loyalty and, more importantly, gives their own teams more reliable experimental outcomes.

    Handling Demands from Both R&D and Production

    R&D requests rarely line up with what process teams need. One group wants 5 grams for a quick-and-dirty screen, another schedules a 100 kg campaign. We know that both must get exactly what they ask for—no more, no less. That takes production planning and logistics aligned closely with the synthesis schedule. Our operational team works on reducing lead times and building redundancy in the supply chain so one unexpected order doesn’t throw off fulfillment for others.

    We have also noticed surging customization demands: some groups want extra documentation on potential genotoxic impurities, others want anhydrous product with extra drying. We modify our post-synthesis steps, offer alternative solvents for final dissolution, and adapt packaging for cold-chain transport or inert-atmosphere storage—each adjustment grown from learning what really solves the user’s next problem.

    Engaging with Regulatory and Sustainability Challenges

    Manufacturing 2-Fluoro-3-(Trifluoromethyl)Benzylamine requires more than chemistry; it calls for anticipation of evolving regulations and closer scrutiny on EHS impact. Our decades on the front lines make us aware of the shifting landscape around permissible exposure levels, waste effluent standards, and transportation rules, especially for organofluorines. Proactivity matters: we update process documentation and internal audits to keep pace, not just react to inspections.

    Sustainability isn’t a catchword where energy, reagent, and waste costs hit the bottom line. In several process-improvement pushes, we retooled step yield and effluent treatment to reduce both direct and hidden environmental impacts. We take pride in the reduction of halogenated waste volumes and switch to greener solvents where compatible, but never at the expense of product quality or safety.

    Technical Support: Fixing Problems Before They Spread

    Support from a manufacturer means taking your customer’s problem as your own. We keep lines open between our technical, analytical, and production teams so any deviation—off-color samples, documentation gaps, process snags while scaling—gets a rapid response. Open communication with our key clients lets problems surface before they turn into costly mistakes. We don’t script responses or outsource initial troubleshooting. Our chemists step in, using their own hands-on knowledge of this specific product’s quirks, to tackle whatever comes up.

    Product Stability and Storage

    Storing 2-Fluoro-3-(Trifluoromethyl)Benzylamine correctly matters. Over the years, we’ve seen the difference cold-chain transport and proper inert-gas blanketing make in minimizing oxidation and preserving the amine’s color and odor profile. Our hands don’t leave a shipment until we know it can survive the haul and shelf storage—not just because a label says so, but because we’ve tracked the data batch after batch.

    Feedback That Drives Improvements

    Manufacturing is a two-way street. Each batch provides lessons not just from what goes right, but from what arrives in the form of customer feedback. Some of our best process innovations stem from requests or complaints—like minimizing halide residue, reducing water content for air-sensitive workflows, or boosting certificate detail for regulatory submission. Our openness to ground-level suggestions keeps us honest; it also gives our partners a sense that their future work drives our improvements, not just our own bottom line.

    Where We Stand on Authenticity and Transparency

    Our approach values transparency above all else. Every specification we list—be it assay, residual solvent, or impurity threshold—is based on actual batch analysis run right in our lab. No sales filter the picture, no inflated marketing. We find that by keeping this clear and inviting open audits of our analytics and manufacturing processes, we build trust with research teams whose own success depends on our reliability.

    Comparing with Other Benzylamines

    Labs with experience running benzylamine derivatives notice the difference right away between our product and less-substituted analogues. Higher polarity and distinctive NMR signatures mean you can track transformations with confidence, and the electron-withdrawing groups can quiet typical side-amine reactions. Scales over 50 kilograms go more smoothly when the intermediate resists breakdown, and product consistency batch-to-batch reduces revalidation burdens. Peers working with unsubstituted or mono-trifluoromethyl analogues tell us about higher volatility, unpredictable solubility, or more troublesome byproduct profiles. Such nuances only grow in importance as you scale past milligram libraries toward commercial-stage work.

    Application Highlights: Where 2-Fluoro-3-(Trifluoromethyl)Benzylamine Shines

    Medicinal chemists synthesizing kinase inhibitors or CNS-active molecules often turn to this building block for rapid scaffold elaboration. Its substituent-induced properties modulate biological activity and boost lead optimization campaigns. In agricultural screens, select teams work with it due to increased environmental resilience and breakdown rate control. Some material scientists even find value in embedding this moiety to enhance polymer or surface properties, leveraging the unique combination of hydrophobicity and reactivity imparted by the fluorinated benzyl group.

    Through every application, what stands out most from the manufacturer’s eyes is the demand for predictability. Those on the research front don’t want a surprise shift in impurity profiles or color from week to week. We stake our reputation and the viability of our customers’ next breakthroughs on that consistency.

    Looking Forward—And Listening to Evolving Needs

    Trends don’t stay put. Every quarter, we’re asked to provide more detailed impurity spectrums, adapt to new biopharma regulatory frameworks, and support more ambitious time-to-market demands. We adjust not by chasing fads, but by growing alongside our core partners and investing in upstream process control. Staying close to the realities of hands-on synthesis, environmental scrutiny, and the shifting scientific landscape, we see continued strong demand for 2-Fluoro-3-(Trifluoromethyl)Benzylamine—and work to ensure our manufacturing depth evolves in lockstep with those changing requirements.

    Final Thoughts from Where the Chemistry Gets Done

    Our experience tells us that making 2-Fluoro-3-(Trifluoromethyl)Benzylamine isn’t just about chemistry—it’s about appreciating the context in which real chemists use it, anticipating and preventing problems, and learning from every batch, every day. What matters more than any published property or data sheet is the confidence those downstream can have in every bottle, every shipment—a confidence that comes only from direct, hands-on manufacturing experience and a shared commitment to scientific progress.