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HS Code |
334741 |
| Productname | 2-Fluoro-5-(Trifluoromethyl)Benzamide |
| Casnumber | 886763-15-5 |
| Molecularformula | C8H5F4NO |
| Molecularweight | 207.13 |
| Appearance | White to off-white solid |
| Purity | ≥98% |
| Meltingpoint | 90-93°C |
| Solubility | Slightly soluble in DMSO, methanol |
| Smiles | C1=CC(=C(C(=C1)C(=O)N)F)C(F)(F)F |
| Inchi | InChI=1S/C8H5F4NO/c9-6-3-2-5(8(10,11)12)4(1-6)7(13)14/h1-3H,(H2,13,14) |
| Synonyms | 2-Fluoro-5-trifluoromethylbenzamide |
| Storageconditions | Store at room temperature, tightly closed |
As an accredited 2-Fluoro-5-(Trifluoromethyl)Benzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10g package features a sealed amber glass bottle with a tight cap, labeled with 2-Fluoro-5-(Trifluoromethyl)Benzamide and safety information. |
| Shipping | The chemical **2-Fluoro-5-(Trifluoromethyl)Benzamide** is shipped in tightly sealed containers, protected from moisture and incompatible substances. It is handled in compliance with all applicable regulations, including proper labeling and documentation. Typically, transportation is arranged via road, air, or sea, adhering to chemical safety protocols and temperature control if required. |
| Storage | Store 2-Fluoro-5-(trifluoromethyl)benzamide in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture. Use appropriate chemical-resistant containers and label clearly. Avoid exposure to direct sunlight and store at recommended temperatures, typically at or below room temperature for stability. |
Applications of 2-Fluoro-5-(Trifluoromethyl)Benzamide in Industrial Manufacturing2-Fluoro-5-(Trifluoromethyl)Benzamide serves as a key intermediate in several specialized chemical manufacturing processes. As an original producer, we deliver material with high purity for direct use in regulated and audited production lines. Its chemical properties support critical reactions in advanced agrochemical synthesis, active pharmaceutical ingredient development, high-performance specialty polymers, and liquid crystal compound manufacture. 1. Agrochemical Intermediate SynthesisThis compound functions as a pivotal intermediate in the synthesis of selective herbicides and fungicides, particularly for active molecules featuring fluoroaromatic backbones. Agrochemical formulators integrate this material during the core transformation stage, leveraging its functional groups to construct target actives with necessary environmental persistence and bioactivity profiles. Batch records and full traceability form part of all commercial transactions into the agricultural chemical sector. Industry compliance standards
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2. Pharmaceutical Intermediate for Active Ingredient ProductionWithin the pharmaceutical sector, 2-Fluoro-5-(Trifluoromethyl)Benzamide is widely adopted as a designated building block for synthesizing APIs targeting CNS, anti-inflammatory, or oncology applications. GMP-certified manufacturers value its compatibility in late-stage functionalization and precision fluorine incorporation. Each delivery includes comprehensive quality documentation and impurity profiles in accordance with current pharmacopoeial requirements. Industry compliance standards
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3. High-Performance Specialty Polymer ManufacturingPolymer manufacturers employ 2-Fluoro-5-(Trifluoromethyl)Benzamide as a monomer precursor in developing functional specialty resins. Its unique fluorinated aromatic structure enables the synthesis of polymers with high thermal stability, chemical resistance, and dielectric properties. Strict quality verification supports safe handling and reproducibility in controlled industrial environments. Industry compliance standards
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4. Liquid Crystal Compound SynthesisManufacturers of advanced display materials select 2-Fluoro-5-(Trifluoromethyl)Benzamide as a functional group donor in liquid crystal compound libraries. The presence of multiple fluorinated substituents imparts improved molecular orientation and stability for high-definition and high-contrast displays. Strict documentation accompanies each lot to support documentation for global device compliance and market release. Industry compliance standards
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Every batch of 2-Fluoro-5-(Trifluoromethyl)Benzamide we produce represents a culmination of years of experience and accumulated knowledge in fine chemical synthesis. Those who work with benzamide derivatives can appreciate the subtle chemical behaviors that minor structural changes introduce. In this compound, a single fluorine bonds with the aromatic ring in the ortho position, and a trifluoromethyl group anchors itself at the meta position. The amide group at the para position stabilizes the entire molecule and imparts useful physical and chemical properties.
In our own work, this molecular structure immediately strikes us not just for its syntactic elegance, but for the performance improvements and reliability it offers during downstream applications. The fluorine and trifluoromethyl groups have a pronounced electron-withdrawing effect. This translates to enhanced stability against metabolic degradation and environmental breakdown when compared to non-fluorinated benzamides. Customers who have switched from regular 5-methyl or non-fluorinated analogs have remarked on cleaner reaction profiles, sharper yields, and fewer problem by-products—facts confirmed by analyses across multiple labs.
Our process for 2-Fluoro-5-(Trifluoromethyl)Benzamide does not rely on a single-step conversion. Through years on the production line and in the development lab, we have reached a protocol that maintains strict control over fluorination and substitution levels. Starting with high-purity substituted benzenes, we use a controlled introduction of fluorine reagents under low temperature and moderate pressure. This avoids undesired side reactions that would complicate purification. We know the results: a crystalline, off-white solid with high assay rates and reliably tight melting point ranges.
Quality monitoring during every step reduces the risk of contamination by process-related impurities. Our crystallization and washing stages serve to eliminate residual starting materials and intermediate by-products, something critical to those in research and process development who require reproducible results. We rely on direct NMR, HPLC, and GC testing for every lot—not as a formality, but as the only sure way to guarantee identity and purity batch after batch.
Having produced thousands of kilograms of this compound, we’ve become intimately familiar with its performance. 2-Fluoro-5-(Trifluoromethyl)Benzamide forms stable, free-flowing crystals that store well under normal ambient conditions. The low hygroscopicity means it doesn’t clump or degrade over time—a key concern for those planning to use it in large scale or store for months. Melting point remains consistent, above 150°C in nearly every batch, pointing to stable polymorphism and practical utility in high-temperature reaction protocols.
Its solubility profile stands out for those chemists developing new molecules: it dissolves freely in most polar organic solvents but resists aqueous breakdown. This property streamlines isolations and extractions, minimizing solvent usage and lowering overall production costs for our customers. Chemical reactivity, especially in condensation and substitution reactions, remains sharp, and the trifluoromethyl and fluorine groups improve the molecule’s profile in both chemical and biological screenings.
Our compound has moved through the hands of pharmaceutical researchers, agricultural chemists, and material scientists. In drug discovery labs, 2-Fluoro-5-(Trifluoromethyl)Benzamide serves as a building block for synthesis of kinase inhibitors, antibacterial scaffolds, or diagnostic imaging agents. The unique combination of halogen substituents confers a level of metabolic resistance highly sought after in candidate molecules. Once, a customer in Germany reported how their new lead compound resisted P450-mediated oxidation far more robustly than matched controls. Over time, we have seen a shift in project pipelines toward more fluorinated scaffolds, and this molecule supports those evolving needs.
In agricultural chemistry, its functionalized structure offers avenues for creating advanced crop protection agents. Here again, environmental breakdown rates matter. Field trials have demonstrated that fluorinated benzamides display extended half-lives and favorable degradation profiles, which can help farmers achieve lower application rates and fewer chemical inputs over a season. Though we always urge responsible stewardship and assessment of environmental persistence, the data from multi-year studies supports the inclusion of such building blocks in modern agrochemical design.
For the specialty materials sector, 2-Fluoro-5-(Trifluoromethyl)Benzamide plays a role in creating advanced polymers or high-performance coatings. The compound’s electron-withdrawing groups increase chemical resistance and thermal stability in final formulations, and the molecular geometry can impart desired orientation and packing within engineered films. Our partners in flexible electronics have provided feedback about improved layering and adhesion characteristics when integrating aromatic fluorinated amides.
Experience shows that even a minor change in functional groups can cascade through every subsequent application. 2-Fluoro-5-(Trifluoromethyl)Benzamide holds an advantage over simple benzamide not only because of its altered electron distribution but also due to its enhanced physicochemical properties. Non-fluorinated versions show a much higher rate of hydrolysis during stress testing and produce more polar by-products in analytical screens. Substituting alternative halogens—such as chlorine or bromine—creates shifts in melting point, solubility, and reactivity that chemists have struggled with at scale.
Unlike 2-chloro analogs, this fluorinated derivative offers balanced lipophilicity and metabolic stability. Our customers note that it bridges the gap between highly lipophilic, poorly soluble halogenated benzamides and more polar, water-soluble ones that fail to penetrate target membranes. More importantly, from a synthesis perspective, the predictable reactivity under established coupling conditions means fewer failed batches and a shorter route from lab bench to kilogram production.
We consistently hear about better downstream control—higher selectivity, fewer off-target effects in bioassays, and improved retention during chromatographic work. In the case of trifluoromethyl-substituted analogs lacking the ortho fluorine, physical handling issues and inconsistent assay results have crept in. Adding the ortho fluorine seems to strike a performance sweet spot. Peer-reviewed papers have documented these same trends, and our QA data only reinforces what end-users have already observed in their own labs.
As chemical manufacturers, we do not just respond to regulatory standards—we anticipate them. Our protocol for handling and producing 2-Fluoro-5-(Trifluoromethyl)Benzamide adheres to both REACH and GHS guidelines. Closed-loop containment, fume hood collection, and robust PPE policies mean production staff avoid unnecessary exposure throughout the process. We handle all residues and off-gas inline, neutralizing as needed before waste leaves the building.
Feedback from downstream users has highlighted the need for batch-to-batch reproducibility and rigorous impurity control. We have seen colleagues elsewhere struggle with “minor” impurities that turn into major headaches when scaling from gram to kilogram. In our own practice, rigorous monitoring—especially for residual halogenated byproducts and heavy metal catalyst traces—keeps levels consistently below detection thresholds. The final material’s purity and chemical fingerprint enable users to qualify it for regulated studies with a minimum of retesting.
Shipping considerations—thermal sensitivity, spill control, and tamper-evident seals—have only increased as customers run larger pilot campaigns and move toward registration batches. Durable, inert packaging and bulk-compatible container options resolve many of these worries. We understand the difference between what a laboratory researcher needs for a few grams and the requirements of a process chemist running a hundred kilos. Each format receives tailored QA oversight and documentation, often incorporating user feedback from the field.
Our approach embodies a cycle of feedback and adjustment. Early batch runs years ago yielded crystals with inconsistent particle size, causing delays on customer process lines. We ran trials to map cooling profiles and solvent ratios, correlating specific crystallization conditions with flowability, dissolution rates, and even pressing behavior. The current product reflects not only those formal studies, but frequent practical input from customers running real-world chemistry on strict timelines.
Routine checks against newly available analytical standards—ranging from trace nitrogen content to sub-ppm halogen balance—offer a window into process drift. All alteration of batch records and process parameters passes through a live review, not just for compliance purposes, but for the genuine improvement it brings. Operators know from experience that issues often show up not in numbers on paper, but in a sudden difficulty during an early-morning filtration or a change in odor or hue noted by eye.
Learning from both near misses and rare batch failures, we have built redundant process checks. Staff rotate through different production lines to keep every operator familiar with new challenges and techniques. Our philosophy remains focused on improving every part of the manufacturing journey, not just the end product.
Rarely does a batch come off the line without some challenge—be it a minor foaming during solvent addition or a hiccup in the cooling controls. We trust our crew’s eyes and hands to spot anomalies early. In one instance, a seasoned technician noticed a slight tackiness in the intermediate cake—an early warning of a solvent ratio issue that, caught quickly, saved an entire batch from downtime and reprocessing. These small daily interventions separate successful, reliable production from the era of “acceptable loss.”
Our understanding of 2-Fluoro-5-(Trifluoromethyl)Benzamide did not emerge overnight. Technicians, chemists, and engineers built up familiarity over years, learning subtle cues that predictive analytics may not always flag. Minor color changes, subtle residue patterns on filter paper, and the scent of the exhaust—these remain as meaningful to us as analytical charts and spectra sent for recordkeeping.
Many customers arrive with technical sheets and synthesis schemes, but genuine breakthroughs appear only after candid feedback about bottlenecks and unexpected hurdles. Only by integrating customer lessons from pilot plant failures, workup changes, and missed project milestones into our manufacturing can we claim to deliver a truly reliable intermediate. Over time, we supply more than just chemical lots: we share process data, analytical trends, and improvement strategies, working alongside partners to resolve scale-up and downstream handling problems.
This cooperative approach lets everyone along the chain make smarter resource decisions. Successful launches into clinical trials or market-ready products often emerge from these deeply shared insights. Our best partnerships thrive when open dialogue replaces purely transactional relationships, and customers feel comfortable disclosing struggles or needs directly. Because we work with their problems, not just their orders, we become a long-term resource and connection to the broader world of fine chemical manufacturing.
Chemistry continues to evolve toward more selective, more persistent, and safer building blocks. In the face of growing resistance to old-line antimicrobials and old-school pesticides, as well as increasing environmental scrutiny, novel fluorinated aromatics such as 2-Fluoro-5-(Trifluoromethyl)Benzamide stand at a critical juncture. Our ongoing work to widen production scales, improve impurity profiles, and extend shelf life reflects both market demand and our own drive for excellence.
We recognize that upcoming regulatory requirements and end-user expectations will place greater emphasis on transparency. Traceability, carbon footprint accounting, and digital records already form part of our regular business practice. Our own challenge now turns on delivering not only a molecule, but a fully mapped, ethically produced, and thoroughly certifiable product.
New applications continue to emerge. As machine learning-driven drug design suggests more halogenated scaffolds, and as material engineers probe the frontiers of durable, functional coatings, each batch of 2-Fluoro-5-(Trifluoromethyl)Benzamide represents a step toward addressing those advances. Drawing on the expertise and flexibility that only real-world production confers, we remain firmly anchored in the day-to-day realities of manufacturing, even as we look forward to next-generation opportunities.
In years spent mastering this class of chemicals, we have learned that a good product means more than a correct structural formula. Customer trust grows in the daily discipline of precise, thoughtful manufacturing, not merely in accreditation or checklists. Open records, candid dialogue about limitations, and a willingness to adapt comprise our most valuable resources. 2-Fluoro-5-(Trifluoromethyl)Benzamide remains more than a name or a model number—it is a dependable tool, refined by shared knowledge and continuous improvement. Our path forward depends on listening, learning, and applying human experience to the complexities of a changing scientific landscape.