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HS Code |
697388 |
| Chemical Name | 4-Amino-2,5-Difluorobenzotrifluoride |
| Cas Number | 183239-99-4 |
| Molecular Formula | C7H4F3N |
| Molecular Weight | 175.11 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 57-62°C |
| Density | 1.49 g/cm³ (estimated) |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Synonyms | 4-Amino-2,5-difluoro-1-(trifluoromethyl)benzene |
| Inchi | InChI=1S/C7H4F5N/c8-4-2-5(9)7(13)3-1-6(4)12-10/h1-3H,13H2 |
| Smiles | C1=CC(=C(C=C1N)F)C(F)(F)F |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
As an accredited 4-Amino-2,5-Difluorobenzotrifluoride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Amino-2,5-Difluorobenzotrifluoride is packaged in a 25g sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 4-Amino-2,5-Difluorobenzotrifluoride should be shipped in tightly sealed, chemical-resistant containers. It must be clearly labeled and transported according to local, national, and international regulations for hazardous chemicals. During shipping, protect from moisture, physical damage, and sources of ignition, and ensure compatibility with adjacent shipments to prevent adverse chemical reactions. |
| Storage | 4-Amino-2,5-Difluorobenzotrifluoride should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Ensure containers are clearly labeled and stored in accordance with relevant chemical safety regulations and guidelines to prevent unauthorized access or accidental release. |
Applications of 4-Amino-2,5-Difluorobenzotrifluoride in Industrial Manufacturing4-Amino-2,5-Difluorobenzotrifluoride is an established specialty intermediate across several advanced manufacturing sectors. Our production expertise ensures precise specifications and consistent quality for the demanding needs of industrial formulating and processing environments. See below for key application scenarios—each representing a major downstream market, complete with practical formulation, processing, and regulatory details directly relevant to ongoing B2B manufacturing projects. 1. High-Performance Agrochemical Active Ingredient SynthesisThis compound plays a pivotal role as a core building block during the synthesis of difluoro-substituted phenylurea and phenylcarbamate herbicide actives. Its electronic and steric properties enable targeted crop protection molecule design, supporting finely controlled selectivity and degradation profiles demanded in regulated agrochemical markets. Industry compliance standards
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2. Pharmaceutical Intermediate in Fluorinated Drug Compound SynthesisThis molecule is commonly utilized as a fluorinated aromatic amine source during the synthesis of active pharmaceutical ingredients (APIs) that target receptor modulation and metabolic pathway inhibition, especially for oncology and CNS drug candidates. Its unique substitution pattern enables medicinal chemists to precisely modulate lipophilicity, bioavailability, and metabolic resistance. Industry compliance standards
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3. Electronic Materials Precursor for Display and PCB ChemistryThis aromatic amine frequently serves as a functional group donor for advanced fluorinated monomers in the production of specialty polyimides and polyaryl materials targeting flat panel display films and high-frequency printed circuit boards. Its tailored electron-withdrawing properties promote dielectric stability, chemical inertness, and environmental reliability required in consumer and industrial electronics. Industry compliance standards
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4. Specialty Fluorinated Coating and Resin ModifierThis compound finds application in the modification of coating resins and specialty polymers to confer fluorinated surface properties, such as enhanced weather resistance, low surface energy, and chemical inertness. Coating formulators use its incorporation to boost lifespan and performance of protective paint systems and industrial floorings. Industry compliance standards
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At our manufacturing site, 4-Amino-2,5-Difluorobenzotrifluoride stands out among specialty fluorinated aromatics. Over the years, as we’ve refined its production, we’ve come to appreciate its combination of stability and reactivity—a balance that many synthetic chemists value. The chemical structure might look straightforward on paper, yet it offers performance that plays a crucial role in advanced chemistry.
This chemical, also known by the model code AFDFBT, carries a CAS number that laboratory teams recognize right away: 883589-95-9. Its hallmark lies in the difluoro substitution pattern paired with a benzotrifluoride backbone, combined with a para-amino group. We typically deliver it as an off-white crystalline solid, purity exceeding 98% by HPLC, with moisture well under 0.2%—removing any ambiguity for process engineers. The melting point sits in line with what researchers expect in similar trifluoromethylated substrates.
The standard batch size rarely deviates from 10-25 kilograms, though adjustments occur for pipeline projects. We pack it in double-lined polyethylene drums, sealed to preserve the stability that comes from careful control at every stage, from raw material handling to final product isolation.
Years of manufacturing this compound reveal a simple truth: every gram reflects practical lessons. Stray too far from target specifications, and downstream users notice. Several times, we’ve gotten requests for tighter control on isomeric purity or feedback about the presence of minute residual solvents. Because the amino group sits ortho to a fluorine, it’s sensitive to trace acids or oxidants during shipping. Small tweaks in our process—such as adjusting the acid wash step or extending vacuum drying—make a real difference in shelf life.
It’s not just about certificates of analysis. In the real world, high-performance materials go beyond passing a checklist. We routinely hear from clients experimenting with pharmaceutical intermediates or custom agricultural actives who want the batch-to-batch consistency that isn’t possible with off-grade or repacked lots.
Chemists gravitate toward 4-Amino-2,5-Difluorobenzotrifluoride for the bond selectivity that its structure gives. In our facility, we’ve witnessed teams develop multiple synthesis routes for urea, amide, and carbamate linkages on the aromatic core. In pharmaceutical explorations, the two ortho-fluorines slow down metabolic breakdown, so intermediates derived from this compound often show up in screening studies. The trifluoromethyl tail resists hydrolysis, which passes down to the end product—key for stability in challenging biological environments.
Experienced teams working with complex heterocycles mention the ease of further derivatization. The para-amino group behaves predictably in coupling reactions, minimizing side products when making active pharmaceutical ingredients. Even for those venturing into electronic materials, the electronegativity of the difluorobenzotrifluoride ring opens pathways for new OLED or display technology building blocks. We’ve seen partners branch into this territory thanks to the solid data and supply continuity we bring.
Some years back, buyers often substituted simple mono-fluorinated anilines in pilot projects. But after repeated stability tests and complaints about inconsistent reactivity, most now look for the better-performing difluorinated options. 4-Amino-2,5-Difluorobenzotrifluoride demands more careful fluorination and workup at the plant, yet the extra step in synthesis is justified when you see cleaner conversions and less waste downstream—even at the process development stage.
Contrasted with 4-Amino-2,3-Difluorobenzotrifluoride, our product offers improved positional selectivity. The 2,5-substitution pattern changes how electrons distribute in the ring, leading to a slightly higher stability against oxidative degradation in some pharmaceutical applications. Colleagues developing new-generation agrochemicals specifically request this isomer, reporting fewer formulation problems and better field stability.
Non-trifluoromethylated aminodifluorobenzenes fall short in solvent compatibility and tolerance during catalytic cross-coupling runs. We often hear from industrial chemists frustrated by material loss or need for extra purification—feedback that we’ve validated by running parallel tests in our own R&D setup. The trifluoromethyl group in our compound eliminates a lot of the headaches linked to poor solubility in organic media.
Anyone producing this molecule at scale soon learns that the main bottleneck isn’t the initial synthesis; it’s what happens in the purification and packaging steps. Unchecked residual hydrochlorides or byproduct amides ruin entire batches. Early on, our team spent months recalibrating solvent washes and crystallization conditions to reliably achieve the target chemical profile customers need. Now, NMR and GC-MS verification step in before anything goes out the door.
From a practical standpoint, this compound puts a load on gloves and seals, so we source higher-grade process liners. Exposing the material to even trace atmospheric moisture during sampling can shorten its usable lifetime. A week-long storage test at 40°C and 70% relative humidity highlighted degradation paths that now inform our SOP for every container shipped.
Clients at contract research organizations mention the importance of clear labeling and smaller packaging options for multi-project labs. In response, we’ve adapted—offering pre-weighed aliquots with barcoded batch numbers for full traceability. This shift came directly from user feedback and hands-on collaboration between the packing floor and client R&D scientists.
Global interest in selective fluorinated aromatics has surged in recent years. Increased regulatory requirements for environmental persistence and biostability push end-users toward molecules with robust profiles—4-Amino-2,5-Difluorobenzotrifluoride fits this shift. We’ve witnessed surges in demand after regulatory bodies flagged older, less robust ingredients for closer scrutiny.
Supply chain interruptions, raw fluoroarene shortages, and international transport disruptions have all influenced our approach. Direct control over every ingredient, from fluorinating agents to solvents, buffers us against unexpected quality dips in global markets. During the raw materials crunch of the last two years, our operations team ramped up inventory monitoring, shifting to alternative suppliers only after direct onsite audits. Traceability continues from the initial receipt of starting materials down to the last repackaged drum.
Sharing technical data and real-time stability results with our clients pays dividends. Our technical support line often gets direct calls from formulation labs in Europe and North America, asking for advice on downstream processing or troubleshooting odd results. Practical, rapid feedback between the customer bench and our plant directly shapes the way we monitor and improve every production lot.
As a manufacturer, we face rising questions about environmental impact. 4-Amino-2,5-Difluorobenzotrifluoride features a trifluoromethyl ring that resists breakdown, raising legitimate concerns about end-of-life disposal. Over the past decade, our plant has invested in closed-loop solvent recycling and rigorous waste management to minimize environmental exposure. Third-party audits verify that halogenated byproducts do not make it beyond the factory gates.
Collaborations with key downstream users have led to innovations in recovery and reuse. For example, partners in fine chemical production now send back offcuts for reprocessing, lowering cradle-to-grave impact. Safe handling remains a priority—clear hazard labeling and training mean we don’t see lost time or health issues among technical staff.
The broader chemical industry keeps a watchful eye on persistent organofluorines. We stay tuned to emerging global guidelines, ready to implement stricter containment, not only for compliance but for true operational safety. Employees and neighbors expect nothing less.
Modern catalytic and photochemical methods push us to rethink manufacturing approaches. Customers challenge us with requests for greener, more scalable synthesis. Some years ago, production leaned heavily on batch reactions; today, we explore continuous processes and greener solvents. Investing in newer filtration and crystallization equipment not only improves yield but meets requests for “cleaner” certification from audited labs.
Recent process improvement cycles focused on reducing solvent usage during product isolation. By switching to a more selective crystallization protocol, we achieved a 20% reduction in process solvent demand. That does more than save costs; it means less residual solvent in the final product and easier compliance with ICH Q3C guidelines on organic impurities.
Customers repeatedly tell us that smaller but more frequent production runs help them respond to rapidly changing project demands. We have embraced modular scheduling, adapting reactor and drying capacity to support this new way of working without driving up delivery times. The reality is sometimes messy, but the resulting flexibility gives everyone from startup biotechs to established multinationals confidence in our supply.
One of the greatest anchor points in our work is the direct relationship between technical support and the R&D bench of our clients. We field questions not just about our compound’s properties, but about broader synthetic routes. In response, our lab regularly tests the latest palladium-catalyzed cross-coupling or nucleophilic aromatic substitution reactions with our product. These practical trials save time for downstream teams who can build on real lab data, not just theoretical projections.
Several years ago, a major user shared reaction yields using our competitor’s product versus ours. The side-by-side comparison highlighted a marked drop in byproduct formation when they ran with our lot—feedback we passed straight to the plant floor. The result: further tightening on residual halide quality control, an adjustment that drove customer retention.
We treat these exchanges as true partnerships. When a top-five pharma group wanted sub-ppm metal levels, we coordinated with analytical chemists and made process tweaks that filtered into our standard operating procedures. Each call or shared dataset informs a cycle of adaptation grounded in our experience and their project realities.
Constant change is part of chemical manufacturing. Market demands, regulatory shifts, environmental pressure, and technology all push us to adapt. The same spirit of innovation that brought 4-Amino-2,5-Difluorobenzotrifluoride into our catalog years ago now keeps us striving for better process efficiency, tighter specifications, and lower environmental footprint.
No supply chain stays static. Fluctuating raw material purity, evolving quality requirements, new synthetic use cases—each batch is an opportunity to reinforce lessons from the last, whether it means recalibrating equipment, retraining staff, or reaching out for technical exchange.
We see manufacturers like us as stewards of every molecule that leaves the door. That means never losing sight of both technical requirements and real-world applications. Whether making batches for a next-generation medicine or helping a customer troubleshoot in scale-up, we balance rigorous in-plant controls with the flexibility real customers require.
Working this way over years, not months, reveals the true value a manufacturer brings beyond shipping a boxed drum. That value lies in shared technical progress, trust in product quality, and the honest acknowledgment that every process can always improve.