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HS Code |
375874 |
| Cas Number | 367-25-9 |
| Molecular Formula | C6H3F4N |
| Molecular Weight | 163.09 g/mol |
| Appearance | Pale yellow to brown solid |
| Melting Point | 41-45°C |
| Boiling Point | 182-184°C |
| Density | 1.49 g/cm³ |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | Nc1c(F)c(F)cc(F)c1F |
| Refractive Index | 1.497 (predicted) |
| Synonyms | 2,3,4,5-Tetrafluoro-1-aminobenzene |
As an accredited 2,3,4,5-Tetrafluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Supplied in a 100-gram amber glass bottle, 2,3,4,5-Tetrafluoroaniline features a secure, chemical-resistant cap and hazard labeling. |
| Shipping | 2,3,4,5-Tetrafluoroaniline should be shipped in tightly sealed containers, compliant with hazardous material regulations. Store in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling and documentation are required, and handling should minimize exposure. Typically, shipment is by ground or air according to relevant chemical safety regulations. |
| Storage | 2,3,4,5-Tetrafluoroaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as oxidizers and acids. Keep away from ignition sources. Store under inert atmosphere if possible, and handle in accordance with proper chemical hygiene and safety practices to prevent exposure or contamination. |
Applications of 2,3,4,5-Tetrafluoroaniline in Industrial ManufacturingOur 2,3,4,5-Tetrafluoroaniline supports advanced material synthesis in specialty sectors that demand precise molecular features and high batch reproducibility. The following application scenarios illustrate targeted downstream integrations, industry-aligned usage rates, and explicit compliance references for industrial buyers requiring fully traceable supplier practices and technical transparency. 1. Synthesis of Fluorinated Pharmaceutical IntermediatesPharmaceutical manufacturers select this tetrafluorinated aniline derivative for synthesizing fluorinated heterocyclic intermediates integral to active pharmaceutical ingredient (API) pipelines, mainly in oncology and central nervous system compounds. The compound’s electron-withdrawing properties enable targeted functionalization in substitution and coupling reactions vital to modern medicinal chemistry programs. Our material integrates into multi-step continuous flow or batch reaction protocols in GMP-compliant environments. Industry compliance standards
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2. Agrochemical Synthesis for High-Performance Crop ProtectionAgricultural technology developers adopt 2,3,4,5-tetrafluoroaniline as a key feedstock for synthesizing new-generation active ingredients with enhanced leaf cuticle penetration and metabolic resistance profiles. Its multiple para-fluorine groups help construct targeted aniline-derived ureas and triazoles for herbicidal and fungicidal applications, especially where enhanced field persistency is needed. Process engineers employ our product during regulated multipurpose plant campaigns for agro-intermediate formation. Industry compliance standards
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3. Production of Specialty Fluoroaromatic Monomers for Advanced PolymersPolymer sector R&D teams utilize 2,3,4,5-tetrafluoroaniline for creating monomers tailored to high-performance engineering plastics and coatings. Its unique substitution pattern boosts thermal stability and chemical resistance in the final polymer, making it suitable for demanding applications such as semiconductor insulators, barrier films, and resin composites. The material typically enters controlled polycondensation or copolymerization lines, often under inert atmospheres to prevent unwanted oxidation. Industry compliance standards
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4. Electronic Chemicals for Liquid Crystal Display (LCD) and OLED MaterialsElectronics manufacturers working in display panel and organic electronics fabrication apply 2,3,4,5-tetrafluoroaniline for the derivatization of highly pure liquid crystal intermediates and OLED emitter precursors. Its fluorine substituents help tune dielectric properties, increase phase-transition temperatures, and improve molecular alignment for precision panel applications. Our product enters strictly monitored batch syntheses where electronic-grade purity and minimal trace residues are critical to downstream defect rates and panel lifetimes. Industry compliance standards
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5. Synthesis of Advanced Fluorinated Dyes and PigmentsDye and pigment producers rely on 2,3,4,5-tetrafluoroaniline for designing colorants with enhanced photostability and chemical resistance, particularly for functional coatings and security inks. Its fluorinated backbone confers improved lightfastness and acid/alkali resistance by lowering electron density around chromophoric groups. Our manufacturing process ensures low residual metal and halide contents, preventing interference with dyeing baths and printing processes downstream. Industry compliance standards
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Competitive 2,3,4,5-Tetrafluoroaniline prices that fit your budget—flexible terms and customized quotes for every order.
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Many industrial chemists face the same challenge every year: how to reduce complexity in the synthesis of high-performance aromatic compounds, especially in pharmaceutical, agrochemical, and advanced material fields where every molecular detail matters. As a dedicated manufacturer, we have spent decades increasing purity, yield, and process scalability for the rigid standards demanded by these sectors. Among the more specialized raw materials in our product line, 2,3,4,5-tetrafluoroaniline stands out, not simply for its structure, but for the versatility and precision it brings to target molecule design.
Supplying 2,3,4,5-tetrafluoroaniline goes far beyond packaging a simple commodity. Our technical staff works on pilot-scale improvements each season, drawing on years of scaling up laboratory-scale reactions into reliable bulk batches. Other suppliers might take shortcuts, overlooking batch-to-batch consistency or failing to address the inevitable byproducts that come with fluorination. Our reactors and purification steps, fine-tuned from extensive process trials, allow us to deliver a material with a narrow impurity profile and predictable reactivity. This attention has rewarded us with feedback from our long-term customers who design third-generation herbicides or advanced fluoropolymers where trace contaminants often disrupt downstream process yields.
We manufacture 2,3,4,5-tetrafluoroaniline in the form of a colorless to pale yellow crystalline solid, typically achieving purity greater than 99 percent by gas chromatography. Water and acid numbers are controlled to low ppm levels through our dry-handling systems and in-line moisture indicators. Each lot is produced under strict in-house monitoring: melt point, assay, fluorine content, and residual solvent checks occur at multiple production stages. Because fluorinated aromatics behave differently than non-fluorinated, our team places special focus on storage stability — even as temperature and humidity shift during the year. It is not uncommon to keep records of ambient warehouse conditions and correlate them with measured shelf stability for every outgoing batch.
Comparing 2,3,4,5-tetrafluoroaniline to mono-, di-, or other tri-fluorinated anilines reveals several distinct advantages for chemists seeking electronic effects along the benzene ring. The four ortho and meta fluorines boost electron withdrawal, completely changing reactivity compared to less-substituted analogues like 2-fluoroaniline or 3,5-difluoroaniline. This can translate into more controlled para-directing substitution or higher selectivity in nucleophilic aromatic substitutions, depending on the downstream pathway. Our R&D clients have reported higher selectivity rates and cleaner isolations in Suzuki and Buchwald-Hartwig couplings, for example, when starting with this compound. These differences are rooted in solid-state and solution chemistry — areas where our analytical staff is trained to correlate raw material quality with later architectural outcomes in a pharmaceutical or polymer context.
Processors, research outfits, and downstream formulators request 2,3,4,5-tetrafluoroaniline for reasons that go beyond pure structure. Many advanced herbicides and fungicides call for precisely this substitution pattern to enhance metabolic stability, slow down environmental breakdown, and improve selectivity in the field. Our herbicidal molecule clients adapt the amine function to introduce ureas or sulfonamides that would not perform at the needed threshold with other fluoroaniline isomers. For the custom polymer community, the compound’s unique activation pattern allows incorporation into rigid-rod aromatic structures — specialty fluoropolymers or high-Tg polyimides. These materials resist solvents and heat, which is not achievable with randomly substituted anilines.
Earning a reputation for high-purity, well-behaved fluorinated anilines depends on more than just the laboratory synthesis route. Direct feedback from the production floor and QC labs steers our handling protocols. Our drums and packages seal against ambient humidity, and our in-plant transfer systems minimize atmospheric exposure — a lesson reinforced by one hot, humid summer season that led to minor degradation in early lots. We invested in upgraded airflow controls and automated nitrogen blanketing. Mistakes can become teaching moments, driving home the fact that even the best chemistry depends on operational vigilance.
Our site’s environmental team engineers solutions to recover and repurpose byproducts and residues from fluorination and amination steps. What at one point heading to solvent waste now gets converted or recycled as a downstream feedstock for related chemical streams. The push for green chemistry shapes everything from solvent choice to energy management in our reactors. We actively log every kilo of waste halide or acid generated, report to local environmental authorities, and keep the process teams focused on incremental recycling improvements.
End-users, particularly those focused on regulatory filings or validated manufacturing lines, rely on uninterrupted raw material supply. We maintain buffer inventory of both finished compound and key intermediates — plus contingency plans for temporary logistics bottlenecks. This year, a rail delay threatened to hold up outbound drums; our warehouse team responded by arranging alternate truck routes, keeping our customer’s synthesis on schedule. Open, frank feedback from customers sparked a revamp in our container sizing, after a string of requests for smaller volume units to match pilot-scale needs instead of just offering bulk. Continuous improvement comes less from reviewing generic industry reports than from real-world production and the demands of repeat, long-term partnerships.
Being a contract manufacturer with onsite warehousing helps us respond to shifting order patterns and urgent requests, such as mid-month jumps caused by new project cycles. Every lot leaves our plant with a comprehensive set of quality and handling documents, including batch chronology, full chromatographic signatures, recommended storage conditions, and certificate of analysis matching GC, NMR, and other relevant spectra. Auditors from regulatory and partner agencies have full viewing access of these data trails during their on-site visits, something that becomes crucial for clients preparing for regulatory filings or customer site inspections in their own countries.
In the past, some users reported small side products in their specialty reactions. We responded by investigating each reported case, eventually tying outcomes to minor impurities introduced during synthesis or handling. This trigger for more intensive purification and post-synthesis clean-up steps improved product quality and downstream yields for everyone. Now, our protocol includes regular NMR and LCMS scans beyond the standard GC-FID, to catch outliers before product ships. These incremental steps differentiate a manufacturing operation from a trader or importer — you get the full history and context, not just a bottle on a shelf.
Fielding requests from research, scaling up for process development — these drive how we design options for customized purity, packaging, or blends. Teams at universities and development labs rely on flexibility, since new synthetic routes or structural analogues may need multi-kilo lots or, in contrast, gram-quantity pilot samples. Our order desk interfaces directly with shop floor staff and transport planners, allowing rapid adaptation. For high-purity or regulatory-sensitive projects, we run and retain referential samples, offering confidence and continuity as projects scale up. Every new customer brief becomes a learning point, expanding both our expertise and the practical knowledge embedded in our daily operations.
Producing fluorinated aromatics like 2,3,4,5-tetrafluoroaniline absorbs large fixed investments: from high-containment reactors to acid-resistant transfer lines. We continuously monitor raw material volatility, especially aniline and fluorinating agent costs, striving for balance between supply assurance and pricing predictability. Bulk buyers frequently query us about cost breakdowns, prompting a transparent dialogue about reactor uptime, process yields, energy consumption, and waste minimization targets. It is never just a question of feedstock price; real savings come from proactive yield improvements and fewer batches rejected for off-spec.
Several aniline variants sit within our catalog for customers needing different fluorine patterns. For example, 2,4-difluoroaniline or 3,5-difluoroaniline offer distinctly different reactivity and steric properties than the tetrafluoro structure. In aromatic substitution chemistry, added fluorines on the benzene ring tune the reactivity, increasing metabolic stability and delaying environmental degradation for agrochemicals, or shifting NMR and UV-vis signals in specialty polymers. In practice, a molecule with four ortho/meta fluorines resists oxidation, withstands harsher synthetic conditions, and gives cleaner conversion in many palladium-catalyzed cross-couplings. Our customers regularly share comparative results: a tetrafluoro substrate often cuts out an impurity issue that plagued their difluoro builds, proving once again why detailed substitution pattern matters.
We support each batch with full documentation compatible with international standards. Reach compliance, regulatory statements, substance identity certificates, and detailed impurity profiles form part of the data package for customers entering regulated markets. Periodic third-party audits and internal quality reviews ensure all documentation is up-to-date. Frequently, regulatory shifts prompt us to review and optimize process controls, especially regarding trace solvent or residual acid content. Our technical team specializes in explaining analytical findings instead of hiding behind jargon or generic disclaimers.
Over the years, customer innovations have surprised and educated our staff. One academic group used 2,3,4,5-tetrafluoroaniline as a core amine block in the design of new fluorescent probes, exploiting its electronic effects for greater photo-stability. In another case, a polymers team achieved a significant leap in solvent resistance for packaging films, after fine-tuning polymer backbone substitution using our product. These stories validate our focus: listening to user challenges, tuning our processes, and keeping our materials at the cutting edge without cutting corners. By staying close to the needs of working chemists and process engineers, we steadily push the boundaries on both scale and application.
Every successful or unsuccessful synthesis our customers report builds our operational memory. Our technical people value these conversations — whether a batch went smoothly or presented unexpected challenges. They help us prioritize investments, whether in new analytical gear, expanded tankage, or tailored packaging. Modern manufacturing in specialty fluorochemicals refuses to rest on formulae or past performance. Only by keeping close ties to application outcomes can we anticipate solutions for new process hurdles, whether tightening specifications further or developing safer, greener routes for our existing products.
In the evolving worlds of agrochemicals, pharmaceuticals, and advanced materials, one thing remains clear — molecular-level customizations require not only structural originality but also deep practical know-how. 2,3,4,5-tetrafluoroaniline represents far more than a catalog entry: it is a benchmark for producing and handling specialty aromatics in ways that anticipate customer requirements, regulatory scrutiny, and technical shifts in the marketplace. Our ongoing investments in analytical upgrades, process stability, and direct customer feedback let us meet and exceed expectations for both new and established partners. Collaboration, transparency, and innovation guide each batch that leaves our doors, anchoring our mission as a true manufacturer committed to real-world chemical solutions.