Products

2,6-Dichloro-4-Trifluoromethylaniline

    • Product Name: 2,6-Dichloro-4-Trifluoromethylaniline
    • Chemical Name (IUPAC): 2,6-dichloro-4-(trifluoromethyl)aniline
    • CAS No.: 439-92-5
    • Chemical Formula: C7H4Cl2F3N
    • Form/Physical State: Powder
    • Factroy Site: No.777 Mingyue Road, Huangdao District, Qingdao, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Qingdao Bright Moon Seaweed Group Co., Ltd
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    Specifications

    HS Code

    179447

    Cas Number 439-92-5
    Molecular Formula C7H4Cl2F3N
    Molecular Weight 230.02
    Iupac Name 2,6-Dichloro-4-(trifluoromethyl)aniline
    Appearance Off-white to light brown solid
    Melting Point 54-56°C
    Density 1.51 g/cm³ (estimated)
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Flash Point 132°C (closed cup, estimated)
    Smiles C1=C(C=C(C(=C1Cl)N)Cl)C(F)(F)F
    Synonyms 2,6-Dichloro-4-(trifluoromethyl)benzenamine

    As an accredited 2,6-Dichloro-4-Trifluoromethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g amber glass bottle with tamper-evident seal, chemical-resistant label displaying hazard symbols, product name, and handling precautions.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2,6-Dichloro-4-Trifluoromethylaniline: Typically 12-14 metric tons packed in fiber drums or HDPE barrels, securely palletized.
    Shipping 2,6-Dichloro-4-Trifluoromethylaniline should be shipped in tightly sealed containers under dry, cool conditions. Label containers with appropriate hazard warnings. Comply with international and local regulations for hazardous chemicals, ensuring protection against physical damage and incompatible substances during transit. Transport by approved carriers, following all chemical safety and documentation requirements.
    Storage 2,6-Dichloro-4-Trifluoromethylaniline should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Clearly label the container, and store it in a designated chemical storage cabinet, ideally with secondary containment to prevent leaks or spills.
    Shelf Life 2,6-Dichloro-4-Trifluoromethylaniline is stable under recommended storage conditions and has a typical shelf life of several years.
    Application of 2,6-Dichloro-4-Trifluoromethylaniline

    Purity 99%: 2,6-Dichloro-4-Trifluoromethylaniline with Purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures consistent yield and product quality.

    Melting Point 52°C: 2,6-Dichloro-4-Trifluoromethylaniline with Melting Point 52°C is used in agrochemical formulation processes, where defined thermal properties facilitate efficient solid handling and integration.

    Molecular Weight 230.02 g/mol: 2,6-Dichloro-4-Trifluoromethylaniline with Molecular Weight 230.02 g/mol is used in specialty dye manufacturing, where predictable molecular characteristics allow precise formulation.

    Particle Size <75 µm: 2,6-Dichloro-4-Trifluoromethylaniline with Particle Size <75 µm is used in advanced material coatings, where fine particle dispersion provides homogeneous surface coverage.

    Stability Temperature up to 120°C: 2,6-Dichloro-4-Trifluoromethylaniline with Stability Temperature up to 120°C is used in polymer additive applications, where high thermal stability enhances product durability under processing conditions.

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    Certification & Compliance
    More Introduction

    Introducing 2,6-Dichloro-4-Trifluoromethylaniline: From Our Manufacturing Floor to Your Process

    Our Commitment to Consistency and Reliability in Specialty Chemicals

    Day in and day out, we work with specialty aromatic compounds that underpin everything from crop protection agents to advanced polymers. Among the materials with a rising demand in fields like agrochemicals and pharmaceuticals, 2,6-Dichloro-4-Trifluoromethylaniline stands out with its unique reactivity and clean profile. Every batch that leaves our reactors comes backed by routine in-process monitoring, drawn from years of experience handling chlorinated aniline derivatives. This is not a commodity chemical, and treating it that way undermines the technical precision many applications require.

    Why This Molecule Matters for Formulation and Synthesis

    The structure of 2,6-Dichloro-4-Trifluoromethylaniline brings together two chlorine substituents and a trifluoromethyl group on an aniline ring—an arrangement that tailors its electronic properties for very specific downstream uses. We don’t see this molecule merely as a raw input, but as a building block that influences the performance and cost of many finished products. We have honed an approach that balances production scale with the careful handling needed to avoid discoloration, hydrolysis, or trace metal contamination—factors that can ripple through your process if not managed at the source.

    Physical and Chemical Characteristics We Control at Scale

    2,6-Dichloro-4-Trifluoromethylaniline is handled as an off-white to pale yellow crystalline solid. Our experience shows that purity—consistently measured by GC or HPLC above 99%—directly determines yield and selectivity in most downstream reactions. By maintaining tightly managed synthesis conditions and drying steps, we keep moisture content low and reduce handling losses. Packing and transportation involve nitrogen blanketing and lined drums to avoid degradation. Every processing step, from charging raw materials to crystallization and filtration, aims to eliminate variability and keep dust or trace impurity levels below the thresholds set by our most demanding customers.

    Application Insights Drawn from Daily Production Experience

    We produce this aniline derivative for clients who formulate advanced herbicides, fungicides, and intermediates for fine chemicals or pharmaceuticals. The core property users seek traces to how the trifluoromethyl group resists metabolic breakdown and enhances lipophilicity, which extends the reach of active ingredients into plant or animal tissues. Two chlorine atoms ortho to the amine group provide further stability in chlorination or coupling reactions. In classic synthesis pathways for fluorinated phenylureas, for instance, our material enables stepwise assembly with high selectivity. We have responded to many synthesis teams who found that subtle changes in impurity profiles—like residual toluene or halides—can trigger by-products or slow their downstream coupling. With extensive QC records to back us up, we can trace each batch’s history, satisfying even strict material vetting in regulated end uses.

    Comparing 2,6-Dichloro-4-Trifluoromethylaniline to Other Aromatic Amines

    Having worked with a broad portfolio of halogenated anilines, we recognize that every substitution—whether that’s exchanging one chlorine for a methyl group, or using a para- versus ortho-fluorinated ring—impacts the physicochemical properties and reactivity. Ordinary dichloroanilines lack the pronounced electron-withdrawing force and lipid solubility provided by trifluoromethyl incorporation; meanwhile, trifluoromethylanilines without the extra chlorines show less stability under oxidative conditions. By producing this specific combination, we give formulators control over both phase behavior and compatibility with a broader range of coupling agents and halogenation steps.

    Feedback from formulation researchers points to lower volatility and increased process window for coupling reactions involving our material, compared with closely related anilines. Fewer side reactions mean less need for purification at later stages, trimming cost and downtime. Success in one customer’s process frequently leads to changes in how entire product lines are manufactured, underscoring the ripple effect that small molecular differences can have.

    Pushing for Fewer Impurities: What Experience Has Taught Us

    Over the course of ramping up capacity, we’ve learned that even N-methyl impurities or traces of polychlorinated by-products—often measured in just a few dozens of ppm—can set off erratic color changes, plugging of downstream filters, or even unwanted reactivity. Automatic sampling, solvent cascade washes, and careful vacuum drying now define our standard production procedures. Rarely does a week go by without revisiting QC chromatograms, especially when a client prepares for registration or regulatory review of a new use. We stand ready to provide not just analytical results but also samples from specific lots for in-house verification, knowing that trace-level changes can have outsize consequences.

    Setting and Meeting Real-World Specifications

    Our product leaves the plant aligned with the requirements that matter for downstream efficiency: purity over 99%, specific melting range, moisture less than 0.2%, and trace metals such as iron or copper tightly controlled. Since our reactors have seen constant upgrades—whether in agitator design or advanced temperature monitoring—we've reached a place where batch-to-batch reproducibility is the rule, not the exception. We use sample retention and long-term trend tracking to spot any drift before it matters for your final product performance. Experience with export shipments has taught us to watch out for packaging stress or UV exposure during long transits, and we include stabilizer additions or light-resistant drums whenever needed, especially for high-value orders bound for custom chemistry lines.

    Downstream Impact: Saving Time and Cost Across the Value Chain

    Applications relying on 2,6-Dichloro-4-Trifluoromethylaniline have little margin for error. In agricultural chemistry, this intermediate often sets the backbone for herbicide molecules where regulatory approval hinges on avoiding off-spec by-products and minimizing residue. Our long history delivering to multinationals and small specialty shops alike means we anticipate upcoming compliance changes, whether they relate to EU REACH or other global standards. By delivering consistent product batches, we cut the preparative work formulators need to do—reducing requalification and trial runs, and supporting reliable scale-up without surprises.

    Beyond compliance, our technical team fields questions about reactivity under different solvents, compatibility with copper- or iron-catalyzed cross-couplings, and optimal conditions for N-acylation or sulfonation. Having walked through these reactions in our own process development labs, we offer perspective that stretches past the sales pitch—advising on solvent choice, mixing order, and even possible pitfalls in scale-up, such as subtle changes in exotherms or emulsion stability.

    Advantages Over Alternative Synthetic Routes

    There’s more than one way to make chlorinated trifluoromethylaniline, but not all routes produce material with low impurity levels or reliable isomer ratios. After evaluating both chlorination of preformed trifluoromethylanilines and alternative Friedel-Crafts approaches, we settled on a sequence that uses an optimized set of catalysts and automated phase separation to keep side-product build-up at bay. This means higher chemical yield per pass and easier downstream processing, both for us and for those further down the value chain. We do not rely on recycled solvent systems from unrelated synthetic campaigns, sidestepping the risk of cross-contamination that sometimes plagues less specialized manufacturers.

    By focusing on redundant filtration and in-line crystallization, our operation maintains a close-to-theory purity and yield benchmark. This shows up in the low waste factor and sharp melting profile visible batch after batch—a reassurance for end users designing complex multi-step syntheses around consistent inputs.

    Handling, Storage, and Delivering Material Ready for Immediate Use

    Care from the minute raw materials come in carries through to packing and shipping. We store finished 2,6-Dichloro-4-Trifluoromethylaniline in conditions designed to keep out light, oxygen, and moisture. Logistics experience covering inland and sea freight gives us a window into increased risk from condensation, vibration, or customs holds. Our shipping team selects liners and seals optimized to prevent material loss or atmospheric ingress, helping end users reduce costly testing and rework. For high-throughput clients, drums leave us with batch traceability and chain-of-custody records, satisfying industry expectations for transparency and regulatory reporting.

    Small or packed-quantity orders receive the same care and documentation as bulk deliveries. Each drum’s closure receives a tamper-evident seal, and every shipment carries a full analytical history for batch-specific traceability. We commit to rapid, clear communication if material must be quarantined or fails to meet our internal release criteria, drawing on lessons learned over years navigating global trade disruptions and fast-evolving regulatory requests.

    Product Stewardship Informed by Real Manufacturing Experience

    Working with aromatic amines means more than just making and selling molecules. Our stewardship approach draws on stories passed down from generations working these plants—everything from slip prevention protocols and dust suppression measures to emission monitoring and employee training. As new downstream health and environmental guidelines emerge, we respond by evaluating every change for its implications, both to end users and to our own staff. Data tracking shows our ongoing investment in improved ventilation, monitoring exposure, and updating protective equipment, all to ensure that new risks haven’t slipped in through process tweaks or incoming materials.

    Questions sometimes arise about residual solvents, process side-products, or how small differences in impurity profiles can impact specific uses. We make it our practice to welcome audits from your teams and regulatory authorities alike, opening our plant records and historical lot files. Our engineering and analytic teams regularly update technical sheets, capturing both new external standards and our on-the-ground improvements. We encourage open conversations about process changes, because every tweak—from feedstock supplier to quench temperature—leaves a fingerprint on the final aniline product.

    Respecting End-User Innovation

    We know successful formulation doesn't happen in a vacuum, and every lab or manufacturing line using our dichloro-trifluoromethylaniline faces unique constraints. Our history working alongside synthetic chemists and process engineers means we respect the cycle of experimentation and failure that leads to industrial breakthroughs. We provide not just consistent material but also technical input honed through our own troubleshooting. Whether the issue lies in scaling up a batch or achieving the right coupling efficiency, we're a real partner, aligned with your targets for uptime and reproducibility.

    What We See Coming Next

    Growing emphasis on traceability, environmental performance, and downstream safety drives us to keep investing in process improvements. Whether this means more rigorous impurity fingerprinting, new solvent recovery systems, or advanced packaging that keeps contents stable for longer, we aim to stay a step ahead of regulatory and industry curves. Ongoing process control investments tie back to our real-world experience, allowing us to troubleshoot fast, iterate quality improvements, and ensure that what leaves our facility strengthens your process, not hinders it.

    The Value of Direct, Experienced-Based Supply

    Unlike traders or generic compounders, as a chemical manufacturer we see every kilogram through its entire lifecycle. This experience-based stewardship leads to practical know-how: seasonal changes in raw material characteristics, subtle batch-to-batch color differences before drying, or optimal purge gas flows to minimize product loss. Our teams bring real context to technical conversations—sharing what has worked, what hasn’t, and where even minor upstream changes caused surprises in the field.

    In our experience, the link between manufacturing diligence and downstream success is direct. We have built a supply record with companies pushing boundaries in crop protection, specialty polymers, and advanced intermediates—groups for whom reliability, transparency, and technical insight matter more than surface-level assurances. With every lot of 2,6-Dichloro-4-Trifluoromethylaniline, we do more than fill an order; we provide a foundation on which your process can advance with confidence and precision.