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HS Code |
894432 |
| Chemical Name | 2,6-Dibromo-4-(Trifluoromethyl)Aniline |
| Molecular Formula | C7H4Br2F3N |
| Molecular Weight | 333.92 g/mol |
| Cas Number | 328-72-1 |
| Appearance | White to off-white solid |
| Melting Point | 88-91°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | 2,6-Dibromo-4-(trifluoromethyl)benzenamine |
| Smiles | C1=C(C=C(C(=C1N)Br)Br)C(F)(F)F |
| Inchi | InChI=1S/C7H4Br2F3N/c8-4-1-5(7(10,11)12)3-6(9)2-4(13)7/h1-3H,13H2 |
| Storage Temperature | Store at 2-8°C |
As an accredited 2,6-Dibromo-4-(Trifluoromethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a tamper-evident cap, labeled with hazard warnings and product information. |
| Shipping | 2,6-Dibromo-4-(Trifluoromethyl)Aniline is shipped in tightly sealed containers, protected from light, moisture, and incompatible materials. It is handled as a hazardous chemical, conforming to local, national, and international transport regulations (such as DOT, IATA, or IMDG). Package labeling includes relevant hazard and safety information for secure and compliant transit. |
| Storage | 2,6-Dibromo-4-(trifluoromethyl)aniline should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it away from incompatible substances such as strong oxidizers and acids. Store at room temperature and ensure proper labeling. Use appropriate personal protective equipment when handling and minimize exposure to dust and vapors. |
Applications of 2,6-Dibromo-4-(Trifluoromethyl)Aniline in Industrial ManufacturingOur facility produces 2,6-Dibromo-4-(Trifluoromethyl)Aniline to meet the demanding requirements of advanced industrial customers. This compound serves as a critical intermediate for several high-value chemical synthesis pathways in pharmaceutical, agrochemical, and specialty material sectors. The following scenarios illustrate documented end-uses, with precise technical details for each application route. 1. Pharmaceutical Intermediate for Active Ingredient SynthesisIn the pharmaceutical sector, this aniline derivative enables the synthesis of high-purity APIs, particularly in the development of fluorinated and brominated drug molecules that require stringent impurity profiles and consistent molecular structure. Manufacturers incorporate this compound at a defined step during heterocyclic assembly or aromatic substitution, utilizing its unique substitution pattern for structure-activity optimization in patented medicinal products. Industry compliance standards
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2. Agrochemical Active Ingredient PrecursorMajor agrochemical innovators use this material in the synthesis of herbicide and fungicide ingredients. Its brominated, trifluoromethylated aniline core facilitates subsequent transformation into bioactive molecules characterized by improved soil stability and pest-specific activity. Compound is weighed precisely and integrated into multi-step syntheses for crop protection products with regulatory approval tracks in multiple regions. Industry compliance standards
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3. Intermediate for Specialty Dye and Pigment ManufacturingPigment and dye producers employ this aniline compound in the creation of high-performance colorants, especially for plastics, fibers, and specialty coatings requiring strong thermal and photostability. The electron-withdrawing trifluoromethyl and bromine substituents enable precise shade development and enhance colorfastness in demanding polymer processing conditions. The compound is typically charged into closed reactors where multistep functionalization occurs under controlled temperatures and reagent concentrations. Industry compliance standards
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4. Raw Material for Advanced Electronic Material SynthesisManufacturers specializing in organic electronic materials, such as OLED emitters and advanced semiconducting lattices, leverage this compound for precisely substituted aryl amine building blocks. The tailored halogen and trifluoromethyl pattern promotes uniform film formation and influences charge transport properties critical to device efficiency and stability. Integration occurs under anhydrous, rigorously excluding air and moisture, to maintain batch consistency and downstream processing reliability. Industry compliance standards
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5. Building Block in Fluorinated Fine Chemicals ProductionLeading producers of fluorinated fine chemicals rely on this intermediate for its high reactivity in introducing both bromo and trifluoromethyl groups in custom syntheses. Precision is paramount in this context, as customers in the electronics and pharma sectors demand minimal cross-contamination and lot-to-lot consistency. The compound is metered into anhydrous reactors for nucleophilic aromatic substitution or used as a synthon in library screening for novel molecule design. Industry compliance standards
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Working every day at the chemical manufacturing site, we handle a range of specialty organics, but 2,6-Dibromo-4-(Trifluoromethyl)Aniline truly stands out for both its reactivity and purity requirements. Over the years, our production experience with this compound has shown how its unique structure, blending bromine, trifluoromethyl, and aniline moieties, creates unusual opportunities for pharmaceutical and advanced materials projects.
The typical product model from our production line delivers material with a purity exceeding 98%, meeting the expectations of pharmaceutical researchers and custom synthesis teams. By keeping strict control over moisture levels and trace impurities, our process helps customers avoid common setbacks found with lower-grade anilines, particularly those sourced from less precise or inconsistent synthesis routes. We have learned that careful handling at every step, from raw-brine selection through drying and packaging, can dramatically reduce batch rejection rates for partners synthesizing active pharmaceutical ingredients or high-performance intermediates.
We have dealt with many challenges around the stability of halogenated anilines. 2,6-Dibromo-4-(Trifluoromethyl)Aniline sometimes attracts moisture, and small traces of iron or copper can catalyze decomposition if process controls slip. To maintain quality, we run periodic stress-tests under lights and humidity far above normal storage conditions, learning to detect problematic lots before they leave the plant. Our experience shows that weak spots often come from plant upsets at the crystallization step. Because of this, we work on continuous feedback between lab and operations, shifting solvent volumes or adjusting temperature in real time, so quality remains stable even across scale-up runs or harsh weather swings.
Unlike bulk aromatic amines, this product requires equipment fully isolated from chlorinated solvent residues. Any slip—trace amounts of chlorinated byproduct above our internal threshold—can throw off yields for clients in arylation reactions. As a result, we cleaned and relined our reactors after several cases where repeat customers found unexpected residues. Over time, experience running hundreds of lots taught us that details beyond the bench—right down to filter paper quality—change the game for users running late-stage or regulatory-critical syntheses.
Research teams and pilot-scale plants value 2,6-Dibromo-4-(Trifluoromethyl)Aniline as a building block for coupling and substitution reactions. Its dual bromines open up positions for Suzuki and Buchwald-Hartwig cross-couplings, making it easier to create libraries of arylamine derivatives. The trifluoromethyl group adds electron-withdrawing power, offering pathways researchers cannot access with unsubstituted or mono-halogenated anilines. Our own R&D collaborations have shown how this group supports increased metabolic stability or improved target binding, which matters to formulators designing next-generation pharmaceuticals or crop protection agents.
Compared to simpler halo-anilines—such as 4-Trifluoromethylaniline or 2,6-Dichloroaniline—we notice sharper reactivity and selectivity in high-throughput screening runs. Clients synthesizing advanced intermediates report better performance, lower byproduct formation, and cleaner isolations using high-purity material sourced directly from controlled plants. Engineering staff at our facility have helped troubleshoot applications ranging from fluorinated biphenyls to pyridine or pyrazole derivatives, and each time, the full trio of functional groups allows more controlled entry into complex molecules, especially in steps where precise electronic and steric control determine overall project success.
Another advantage became clear over the years—2,6-Dibromo-4-(Trifluoromethyl)Aniline stores and ships much more stably than more oxidizable derivatives like 4-Amino-2,6-dibromotoluene, provided proper handling is used. The trifluoromethyl group, rather than a methyl or other alkyl, delivers both chemical and shelf-life benefits under regular warehouse conditions—something we have measured with open-drum trials and aging tests.
Many clients have switched to 2,6-Dibromo-4-(Trifluoromethyl)Aniline after frustration with more common dihalogenated anilines. During scale-ups, traditional 2,6-dibromoaniline often develops troublesome color or impurity problems which slow downstream column work. Our team worked alongside formulators who spent days repeating chromatography to clear these up, only to find the trifluoromethyl variant sidestepped the major issues. We shared notes with chemists running multi-gram and pilot batches—they found smoother crystallizations, better phase separation, and consistent melting point confirmation when swapping in our product, even in challenging solvent blends.
Quality differences extend beyond the flask. On the production side, experienced operators see how the right raw materials at the aniline-coupling step make or break timelines for time-sensitive programs. Consistency from a plant that genuinely manages high-throughput halogen install—not just outsourcing or blending from inconsistent sources—results in fewer benchside headaches. People running kilo chemistry or setting up for GMP registration notice these effects in everything from lot-to-lot analytics to reaction scale reproducibility.
Traders and third-party warehouses sometimes circulate product that looks fine by appearance but hides process residues, color bodies, or even traces of other halo compounds. Our direct monitoring ensures each drum or sealed container retains color, flow, and performance batch after batch, so formulation scientists or analytical chemists know they receive what project documentation demands. Each year, we field urgent requests for rescreening analysis due to supply chain gaps or variable imports. The firsthand lessons our staff share with clients shortens these costly searches—nearly always, the root cause traces back to upstream purity and stable manufacturing practice.
One aspect we have come to appreciate is that collaboration builds the best process improvements. Custom molecule runs—especially for pilot or pre-commercial pharmaceuticals—often require fast turnaround and detailed documentation. From early contact through scale-up, our technical team works side by side with research chemists, responding quickly to questions about solubility, thermal stability, or integration into multistep sequences. We publish extended impurity profiles by request and supply analytical samples for method validation, based on actual production lots, not generic or repackaged material.
We also see the real world of chemical R&D is full of trial and error. Our plant engineers design process protocols so teams working with 2,6-Dibromo-4-(Trifluoromethyl)Aniline experience fewer delays and less troubleshooting time. It starts with precision at the bromination and trifluoromethylation steps—each controlled by in-process chromatography and strict endpoint monitoring. Each freshly packed lot undergoes both NMR and GC validation, a policy drawn from long experience with the project timelines that depend on stable, repeatable inputs. When questions arise on storage or re-purification, our process chemists respond with hands-on suggestions, built from actual batch history and problem-solving from the plant floor.
We constantly refine our approach as batch volumes and customer needs evolve. Years ago, we relied on more manual techniques for halogen installation and downstream work-up. Tightening up temperature profiles, switching to improved crystallization solvents, and investing in upgraded drying systems made a marked difference in both final appearance and impurity content. Many of these changes grew from responding to client feedback—especially when partners flagged sensitive impurities or difficulties during scale-up.
Material-handling logistics made a difference, too. We once packed drums in basic liners but learned that long-haul shipments suffered from static charge build-up and minute chipping. Now, upgraded containers with grounding and anti-static features preserve color and particle integrity for weeks or months of transit. We work directly with logistics teams so that production schedules, shipping arrangements, and customs documentation all align to uphold specifications that matter to analytical and formulation teams.
Another area where field feedback shaped operations involves storage. Warehouses sometimes subject organics to uncontrolled humidity and accidental sunlight exposure. High-value intermediates like 2,6-Dibromo-4-(Trifluoromethyl)Aniline need rigorous inventory control, regular stock rotation, and dedicated clamping systems during transit. By reviewing annual returns and customer complaints, we have identified and corrected sources of small but costly loss, ensuring project budgets and research timelines do not suffer from avoidable supply interruptions.
Chlorinated and halogenated aromatics come with significant process hazards, especially at scale. Building hands-on knowledge addressing spills, accidental contact, and air release proved essential in keeping operations both safe and reliable. Routine CO monitoring, local exhaust, and spill management stations across the plant have reduced unplanned downtime and met increasing regulatory checkpoints. These hard-won improvements keep not only the site team safe, but increase market confidence from customers whose own audits grow stricter every year.
Waste minimization and responsible effluent management matter. Instead of short-term solutions, our plant invested in thermal treatment and batch neutralization units focused on high-concentration side streams. Experience taught us that downstream purification routines benefit from pre-sorting at the synthesis step and that investing in closed-loop solvent recovery provides both cost and environmental benefits. Feedback from multinational clients—often under tough scrutiny—drove us to adopt and certify our processes to demonstrable compliance standards.
We continue to study and adapt to emerging international regulations for persistent organic pollutants and fluorinated intermediates. Keeping close relationships with regulatory bodies and updating material safety profiles ensures reliable, uninterrupted supply chains even as market and legislative pressures shift. Staff regularly attend technical exchanges, ensuring our plant remains a step ahead in both technical expertise and environmental stewardship for specialty aromatics.
We have seen how direct sourcing impacts research and production projects. Teams who work with us avoid the uncertainty and delays tied to secondary or brokered supply chains. They get product that matches documented specifications every shipment, with no surprises inside the drum. Repeat customers often discover they save both time and money downstream, cutting unnecessary rework or purification steps. Faster troubleshooting—thanks to direct access to technical staff—keeps project timelines on track.
Future-proofing projects matters, especially in regulated industries. Direct manufacturers like us stay ahead of shifting compliance expectations, tracking every input and process variable so stakeholders can trace each lot from raw material through final shipment. For complicated target molecules, knowing the true manufacturing background of each intermediate removes a layer of uncertainty and friction from quality assurance audits.
Building genuine customer relationships forms the core of our operation. We learn from each feedback cycle, adjusting batch parameters and operational timelines to fit both recurring and new project demands. This level of transparency and shared expertise, built from actual shop-floor experience, sets experienced manufacturers apart from resellers or generic trading platforms. The hands-on lessons learned producing 2,6-Dibromo-4-(Trifluoromethyl)Aniline transfer straight to customer results in the lab and the pilot plant.
Our work with research partners has shown that further value lies in integrating 2,6-Dibromo-4-(Trifluoromethyl)Aniline into new synthetic pathways. Current collaborations with university and industry teams explore broader catalytic coupling methodologies, developing catalyst systems that tolerate the unique electronic signature of both bromide and trifluoromethyl groups. These efforts promise to unlock entirely new families of advanced organic materials, addressing needs in bioactive screening, polymer engineering, and emerging electronics.
Early-stage user trials suggest that extended purity standards combined with ultra-low trace metal levels enhance both selectivity and reactivity in cross-coupling regimes. Using advanced purification techniques, our team continues to improve residual catalyst extractability, providing cleaner downstream intermediates that form the backbone for next-generation chiral and functionalized molecules. Ongoing investment in analytical technique upgrades—from high-resolution LC-MS to differential scanning calorimetry—further guarantees batch-to-batch uniformity at scales suited for both discovery and commercial ramp-up.
Process safety improvements and green chemistry advances remain at the top of our innovation roadmap. We work on integrating recyclable solvents, minimizing energy use, and developing real-time in-line monitoring to assure stable product attributes with reduced operator intervention. By bringing together practical factory knowledge, years of manufacturing metrics, and ongoing customer-driven project insights, we build more robust and flexible product platforms to meet industry demands.
Consistent success in manufacturing 2,6-Dibromo-4-(Trifluoromethyl)Aniline rests on a foundation of hands-on experience, responsiveness to customer needs, and continuous process improvement. Our team brings operational rigor and technical insight to the table—qualities that help customers solve tough synthetic challenges and stay ahead in competitive fields. For scientists and engineers, this means reliable access to a high-quality aromatic intermediate proven to support both advanced R&D and scale-driven programs.
We see every new project as an opportunity to learn, refine, and deliver better results, both in the plant and the end user’s lab. Customers who have worked with us notice the difference that true manufacturing expertise brings to specialty chemicals—whether it's clarity of supply, technical reliability, or practical advice grounded in real experience. This is the approach that has shaped our past and continues to guide our future with 2,6-Dibromo-4-(Trifluoromethyl)Aniline and beyond.