Products

3,5-Bis(trifluoromethyl)aniline

    • Product Name: 3,5-Bis(trifluoromethyl)aniline
    • Chemical Name (IUPAC): 3,5-bis(trifluoromethyl)aniline
    • CAS No.: 328-84-7
    • Chemical Formula: C8H5F6N
    • Form/Physical State: Solid
    • Factroy Site: Nanbao Development Zone, Tangshan City, Hebei Province
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Tangshan Sanyou Group Co., Ltd
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    Specifications

    HS Code

    295272

    Chemical Name 3,5-Bis(trifluoromethyl)aniline
    Molecular Formula C8H5F6N
    Molecular Weight 229.13 g/mol
    Cas Number 328-70-1
    Appearance Colorless to pale yellow liquid
    Boiling Point 197-199 °C
    Melting Point 9-11 °C
    Density 1.439 g/cm3
    Refractive Index 1.437
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles FC(F)(F)c1cc(N)cc(C(F)(F)F)c1
    Inchi InChI=1S/C8H5F6N/c9-7(10,11)5-1-6(15)3-4-8(5,12,13)14/h1,3-4H,15H2

    As an accredited 3,5-Bis(trifluoromethyl)aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g 3,5-Bis(trifluoromethyl)aniline is packaged in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3,5-Bis(trifluoromethyl)aniline: approximately **14 metric tons (drums, pallets), ensuring secure and compliant chemical packaging**.
    Shipping 3,5-Bis(trifluoromethyl)aniline is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and must be transported according to relevant regulations (e.g., DOT, IATA). Suitable secondary containment and safety labeling are required. Ensure handling by trained personnel using appropriate personal protective equipment (PPE).
    Storage 3,5-Bis(trifluoromethyl)aniline should be stored in a tightly sealed container, protected from light, moisture, and sources of ignition. Keep it in a cool, dry, well-ventilated area, away from incompatible materials such as strong oxidizing agents. Ensure proper chemical labeling and access restricted to trained personnel. Follow all safety and regulatory guidelines when handling and storing this compound.
    Shelf Life 3,5-Bis(trifluoromethyl)aniline is stable under recommended conditions; shelf life is typically several years when stored cool, dry, and sealed.
    Application of 3,5-Bis(trifluoromethyl)aniline

    Purity 99%: 3,5-Bis(trifluoromethyl)aniline with 99% purity is used in pharmaceutical intermediate synthesis, where high chemical integrity ensures optimal reaction yields.

    Melting Point 45°C: 3,5-Bis(trifluoromethyl)aniline featuring a melting point of 45°C is used in agrochemical formulation processes, where predictable phase behavior supports stable blending operations.

    Molecular Weight 231.13 g/mol: 3,5-Bis(trifluoromethyl)aniline at 231.13 g/mol is used in organic electronic material development, where precise mass contributes to reliable material properties.

    Stability Temperature up to 120°C: 3,5-Bis(trifluoromethyl)aniline stable up to 120°C is used in high-temperature polymer synthesis, where stability under heat promotes consistent polymer formation.

    Particle Size <50 µm: 3,5-Bis(trifluoromethyl)aniline with particle size less than 50 µm is used in catalyst support manufacturing, where fine dispersion enhances catalytic efficiency.

    Water Content <0.1%: 3,5-Bis(trifluoromethyl)aniline containing less than 0.1% water is used in moisture-sensitive dye preparation, where low water content minimizes hydrolysis risks.

    Assay ≥98% (HPLC): 3,5-Bis(trifluoromethyl)aniline with assay ≥98% by HPLC is used in custom chemical synthesis, where high assay guarantees product consistency.

    Refractive Index 1.48: 3,5-Bis(trifluoromethyl)aniline with a refractive index of 1.48 is used in specialty optical coatings, where precise optical parameters optimize light transmission.

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    Certification & Compliance
    More Introduction

    3,5-Bis(trifluoromethyl)aniline: Experience, Focus, and Deep Insight from the Shop Floor

    Introduction to the Molecule

    Chemistry does not stand still. Every time our team works with 3,5-Bis(trifluoromethyl)aniline, we’re reminded of the progress and subtle skill woven through each step. The formula—with its dual trifluoromethyl groups—catches attention not just from a structural viewpoint but from its track record in applications that demand reliability and repeatability. Those twin CF3 groups at the meta positions on the aniline ring lend this molecule a character that chemists in pharmaceuticals, specialty agrochemicals, polymer modification, and dye manufacture often ask about directly.

    What Sets 3,5-Bis(trifluoromethyl)aniline Apart

    Real hands-on experience shows us the differences between compounds are rarely academic. They play out in reactors, in the yield tray, and downstream—showing up as smoother runs, less risk of side products, or an easier purification step. This molecule stands out particularly among aniline derivatives. The two trifluoromethyls bring steric bulk and immense electron-withdrawing character to the ring. What lands on the bench is a colorless to slightly yellowish liquid that holds its shape in the face of tough process conditions and resists unwanted side reactions better than unsubstituted aniline or mono-substituted analogs.

    Handling this compound shows a notable drop in oxidative side-products compared to standard anilines. That means a cleaner reaction finish, easier downstream work, and less time troubleshooting post-reaction mixtures. Customers report batch-to-batch consistency with our material thanks to a fine-tuned distillation process and years spent refining our purification approach.

    Specifications Through a Practitioner’s Eyes

    In this factory, product models and specs aren't theoretical—they're checked every run. Our typical batch of 3,5-Bis(trifluoromethyl)aniline achieves a high purity, usually above 98% by GC. Trace residual solvents or metallic contaminants lag significantly below generally accepted thresholds for pharmaceutical or advanced material applications. Commonly, moisture levels are held well below 0.1%, based on direct feedback from teams that have faced real trouble from hydrolysis or crystal formation during storage or synthesis.

    Most shipments move as liquid in drums or HDPE containers designed for both safe handling and streamlined decanting. Our technical staff run melting point, refractive index, and GC-MS checks on the fly—not because an inspection checklist says to, but because real-world outcomes matter more than a piece of paper. We have set up targeted spot checks after feedback from long-term partners, especially those scaling up from pilot to commercial scale.

    From the Factory: Key Usage Areas

    Stories from our process line tell a lot about where this compound ends up. Bulk of our volume supports manufacturers of advanced pharmaceutical intermediates. Medicinal chemists often use 3,5-Bis(trifluoromethyl)aniline as a scaffold for more complex heterocycles or as a building block in fluorinated aromatic rings, which help tune the bioactivity and metabolic stability of a drug candidate.

    We regularly hear from agrochemical teams. Applications in newer herbicides or fungicides often depend on the unique electron-pulling nature of both CF3 groups, because the final molecule is harder for pests or fungi to metabolize, resulting in better field persistence. This value doesn’t come from marketing—it’s shared directly by users who measure effectiveness on large acreage, not just in the lab.

    Some smaller, highly specialized orders end up in the hands of teams working on advanced polymers and specialty dyes. The thermal stability and the low reactivity of the ring under oxidative or photolytic conditions mean new materials last longer. That kind of real-world stability comes up repeatedly in feedback, especially from users trying to push boundaries with UV-resistant coatings or specialty pigment synthesis. Each year, we field more questions about this molecule’s value in functional silanes and macromolecular design than about basic specs.

    Personal Experience: Batch Diversity and Consistent Output

    Not all 3,5-Bis(trifluoromethyl)aniline is created equal. It’s tempting to treat chemical product as generic across suppliers. We’ve learned that real consistency starts with raw material traceability and plant practice on the day the batch is made. Sourcing high-grade trifluoromethyl precursors has meant the difference between a batch that runs smoothly and one that causes headaches downstream. Each time a team calls back about a “strange” impurity or an unexpected reaction profile, our technical hands trace it to subtleties in source materials or storage conditions along the chain.

    Some users move between several vendors to chase price. Those who come back tell us the cost of process troubleshooting trumps the price difference per drum when a batch fouls their columns or leaves residue issues. Shortcuts carry risks—the most common involve invisible byproducts that spike in long-term storage or upon heating. We routinely focus on this during pilot runs for new customers. That real communication loop—chemists talking directly to plant operators—has helped head off process changes that could have caused havoc at scale.

    Why This Molecule Matters for Applied Synthesis

    Practical chemistry pushes teams to seek tools that add functional handles without making new problems. 3,5-Bis(trifluoromethyl)aniline’s structure makes it more than a curiosity. Those two meta CF3 groups drop the basicity of the amine substantially. Processes involving electrophilic aromatic substitution, diazotization, or urea formation gain a level of selectivity that’s tough to reach with less substituted analogs.

    Feedback from users running route optimization highlights cleaner conversions, fewer tarry residues, and easier work-ups. For chemists designing library syntheses or cranking out several analogs at once, those saved hours add up. We’ve witnessed pilot teams move from standard aniline starting points to this advanced derivative, reporting shorter purification cycles, less silica, and lower overall solvent loads.

    Even in less sensitive runs, the added bulk from dual trifluoromethyl groups helps tune the ring’s steric profile. That delivers side-product suppression, especially in cases where ortho-attack from nucleophiles poses a problem. These are not theoretical improvements—they’ve been measured by our customers running real-world costings and clean-up tracking.

    Tracking Quality: Insights from Experience

    Delivering a consistent molecule means more than hitting purity numbers. We have learned the hard way through a few missteps: what sits in the certificate isn’t always what goes into a reactor a month later. Firms working across continents sometimes misunderstand how transport, exposure to high humidity, or poor drum seals change a material’s handling profile by the time it reaches a plant floor. Our answer has been to invest directly in better containers and moisture-barrier liner upgrades, plus regular re-analysis after storage.

    Recently, we caught a batch showing trace peroxide formation due to storage over an extended period. We adjusted our packing protocol and offered replacement material before customers even filed a complaint. Cost of this response was measurable in the short term, but in the long run, keeping plant managers and chemists confident in material quality paid deeper dividends. Our analysis techs have become experts at sniffing out sources of silent impurities. This hand-on, plant-level approach comes from years working through actual product returns and tracing back issues to fork-lifts, drum seals, or stray residual acid in the plant air.

    Comparisons: What Makes 3,5-Bis(trifluoromethyl)aniline Different?

    Over time, we’ve seen companies shift from basic aniline to mono-trifluoromethyl analogs, and then on to this difluorinated material. Each upgrade wasn’t just about more fluorine atoms; users gained new levels of performance, stability, or process simplicity. Compared to 3-trifluoromethylaniline or 4-trifluoromethylaniline, the bis variant demonstrates higher resistance to oxidation and less tendency to polymerize under basic or acidic catalytic conditions.

    Standard aniline, though cheaper, creates more cleanup work after advanced coupling or diazotization steps. Early batches of mono-trifluoromethyl anilines sometimes struggled under thermal stress. By contrast, this bis-variant holds up better in extended heating or recycling, saving time and expense for teams running multi-stage processes.

    It also differs in how it enters final molecules. Some pharmaceutical clients report improved pharmacokinetic properties in their active ingredients, thanks to altered lipophilicity delivered by the dual trifluoromethyl groups. Material scientists have flagged its impact on glass transition and melting points in specialty polymers, which could not be achieved using simpler ring structures.

    Meeting Evolving Needs: Listening to the End User

    We thrive on honest, direct feedback. Many industry chemists who purchase our 3,5-Bis(trifluoromethyl)aniline come from backgrounds in large-scale drug synthesis, specialty monomer development, or dye research. They consistently tell us transportation issues and storage stability sway their buying decisions more than any minor price delta.

    Clients with detailed analytical capabilities sometimes share their own impurity profiles or side product analyses, giving us real-world data that often leads to incremental improvements at our site. After repeated suggestions, we now include optional re-analysis kits for long-term storage and provide rapid application support. Getting the most from this molecule usually depends on planning, temperature controls, and knowing what to watch out for—details we’re glad to share openly through technical notes, not just datasheets.

    Troubleshooting and Real-World Solutions

    Every chemical production plant faces snags. We’ve seen rare but real issues with product turning slightly off-color on long-haul journeys, typically traceable to minute exposure to sunlight or excess headspace in drums. Offering amber packaging and robust drum purging has cut these cases to near zero. Tight closure protocols and foiled liners—upgrades prompted by dialogue with daily users—make the greatest difference in field performance, not spec sheets.

    Customers sometimes encounter shifts in solubility or viscosity compared to other commercial sources. In our own experience, these changes usually result from minute shifts in trace byproduct levels—details that don’t always show in basic analytical scans but stand out during repeated syntheses or surface modification work. Our ability to dig into production records and share honest answers—even when things go less smoothly—lets users adjust process parameters and avoid lost time.

    Direct user calls sometimes flag entirely new usages or suggest tweaks, such as specialized filtration or an extra re-crystallization step for high-sensitivity polymer projects. Chemists developing new color-fast dyes recently walked us through their proprietary solvent systems, highlighting how smart solvent choice combined with our high-purity batches unlocked vital stability for their latest product line. We don’t insulate these stories in a silo—they feed back to the line workers making each batch.

    Safety, Responsibility, and Sustainable Practice

    Experience teaches that safe handling means more than ticking boxes. 3,5-Bis(trifluoromethyl)aniline, like all reactive aromatics, demands informed attention at every stage. Plant veterans train new staff on ventilation, solvent selection for cleaning, and robust PPE—not because a manual says so, but because real slips cost time or worse.

    We follow both local and international guidelines for safe transport and storage, not just out of compliance, but because years of visits to customer sites have shown that thoughtful packaging and clear labeling cut incident rates. Shared, open dialogue about near-misses and proper response has led to continuous upgrades in documentation and on-drum instructions. We routinely visit customer plants, not just for audits but to observe how the chemical flows into production and gathers insight from frontline operators.

    Waste minimization forms another core element of our practice. Fluorinated compounds bring special concerns, so we stay abreast of evolving disposal and reclamation methods. Several of our clients have set up solvent recovery streams or material return programs thanks to open, technical dialogue about what truly works. We also continuously refine our reactor cleaning and waste handling so that the fluoro-content of our effluents is held below regulated levels, securing both environmental and occupational peace of mind.

    Where Experience Meets Need: Honest Lessons from the Bench

    Over decades, we’ve seen demand for 3,5-Bis(trifluoromethyl)aniline slowly shift from high-volume dye intermediates to more targeted uses in pharmaceuticals and advanced materials. That means buyers today are smarter, more technically aware, and focused on data-driven decisions instead of marketing stories. We respond to this shift with transparency—sharing batch histories, fielding customer audits, and posting representative analytics from recent runs, not pie-in-the-sky values from outsourced labs.

    The best feedback comes from case studies where a client’s innovation meets our consistent product. At one polymer research facility, an uptick in mechanical stability and weather resistance for new fluorinated films led back to a key substitution involving our compound. Adjusting the ratio mid-run, informed by our on-call chemists, meant the research group met deadline and published on schedule. These stories cross our desks almost monthly, reminding us why honest, hands-on practice matters more than sales claims.

    Making the Future of Advanced Aromatic Chemistry Tangible

    The market for 3,5-Bis(trifluoromethyl)aniline moves quickly, shaped by changing regulatory stances, advances in fluorinated chemistry, and rising global material needs. As direct makers, we adapt production runs within weeks to meet surges or new purities dictated by client specs, laboratory breakthroughs, or industry shifts.

    Hearing what works and what doesn't—direct from teams pouring, measuring, and experimenting—steers our investments. Last year, an uptick in demand for nearly solvent-free product led us to expand vacuum distillation columns and recalibrate storage protocols, responding to field data on downstream solvent sensitivity.

    We’ve survived and grown through clunky pilot batches, customer complaints, and experimental dead-ends. The ground truth: only consistent manufacturing, open technical exchange, and the humility to fix what isn’t perfect keep this molecule relevant and trusted by real-world chemists, not just procurement officers or catalog sorters.

    Real Value, Long-Term

    Each drum of 3,5-Bis(trifluoromethyl)aniline that leaves our gates brings with it the effort, hard-won skill, and feedback from hundreds of hours at the reactor, in QA, and at customer sites. Those looking to push the limits of medicinal chemistry, functional dye performance, or advanced materials science count on a molecule that’s more than a catalog number—it’s a product refined through direct experience and a long-standing commitment to safety, performance, and open technical partnership.