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HS Code |
928181 |
| Product Name | 2-(Trifluoromethoxy)Benzamide |
| Cas Number | 20630-57-1 |
| Molecular Formula | C8H6F3NO2 |
| Molecular Weight | 205.13 |
| Appearance | White to off-white solid |
| Melting Point | 107-110 °C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.45 g/cm³ (estimated) |
| Smiles | C1=CC=C(C(=C1)C(=O)N)OC(F)(F)F |
| Inchi | InChI=1S/C8H6F3NO2/c9-8(10,11)14-6-4-2-1-3-5(6)7(13)12/h1-4H,(H2,12,13) |
| Storage Temperature | Room temperature |
| Synonyms | o-(Trifluoromethoxy)benzamide |
As an accredited 2-(Trifluoromethoxy)Benzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g sample of 2-(Trifluoromethoxy)Benzamide is supplied in a tightly-sealed amber glass bottle with hazard labeling. |
| Shipping | 2-(Trifluoromethoxy)Benzamide is typically shipped in secure, airtight containers to prevent leakage and contamination. The package is clearly labeled with hazard and handling information, and it is transported in compliance with chemical safety and regulatory guidelines. Temperature and moisture control may be applied as necessary during transit. |
| Storage | Store 2-(Trifluoromethoxy)benzamide in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials such as strong oxidizers. Keep the storage temperature preferably at room temperature. Ensure containers are properly labeled, and minimize exposure to moisture. Follow all chemical safety guidelines and local regulations for hazardous chemicals. |
Applications of 2-(Trifluoromethoxy)Benzamide in Industrial Manufacturing2-(Trifluoromethoxy)Benzamide finds utility in key industrial segments where advanced aromatic and fluorine-containing intermediates are required. Our manufacturing expertise supports consistent supply to formulators and end users in pharmaceutical, agrochemical, specialty polymer, and materials science sectors. 1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) SynthesisThis compound features prominently in exclusive synthesis routes for fluorinated APIs. One major application is as a building block in the assembly of heteroaromatic drugs that require high metabolic and chemical stability. API manufacturers use it during the early-stage amidation step or as a coupling partner for constructing core scaffolds. Its purity and batch consistency support regulatory submissions and validation processes, including GMP protocols for late-phase intermediates. End use includes small molecule APIs targeting CNS and oncology markets. Industry compliance standards
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2. Advanced Agrochemical Intermediate for Herbicide and Fungicide SynthesisMajor crop science formulators use this compound as an intermediate in the production of next-generation herbicides and fungicides featuring trifluoromethoxy-substituted aromatic rings. These fluorinated structures improve environmental stability, rain-fastness, and bioavailability of end-use actives. Manufacturers employ the compound during acylation or amide-coupling phases in multi-step synthesis campaigns. Dossiers for these actives require traceable sourcing and documented impurity profiles for pre- and post-registration quality audits. Industry compliance standards
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3. High-Performance Polymer Modifier in Specialty Polymers and CoatingsProducers of specialty polymers and performance coatings incorporate this aromatic amide to impart fluorine-derived effects such as chemical and UV resistance. It serves as a co-monomer or end-group modifier in architectural coatings, electronic encapsulants, and membrane materials. Integration at the polymerization or compounding stage enables fine-tuning of mechanical flexibility, dielectric resistance, and hydrophobicity. Process consistency is critical to maintain homogeneity and reproducible end-use properties for technically demanding applications. Industry compliance standards
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4. Specialty Material Precursor for Advanced Chemical Research and DevelopmentR&D groups in materials science and analytical laboratories require this compound as a precursor for synthesizing advanced reference materials or functional compound libraries. It supports custom molecule design for sensor applications, fluorinated probes, and ligands in catalysis. As a manufacturer, we ensure full documentation, batch traceability, and impurity profiling to meet the strict requirements of accredited research or pilot-scale innovation. Flexible supply from gram to kilogram quantities supports iterative screening and project scaling. Industry compliance standards
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Over years of direct involvement in the manufacture of aromatic amide compounds, we have watched the landscape grow more specialized, with demands shifting from general building blocks to finely tuned molecules that offer concrete utility in both R&D and commercial synthesis. 2-(Trifluoromethoxy)Benzamide sits in the niche where precision meets reliability; this chemical demonstrates unique properties stemming from its trifluoromethoxy substitution, favoring it for specific synthetic requirements.
As a chemical manufacturer, our approach to producing 2-(Trifluoromethoxy)Benzamide emphasizes consistency and traceable quality. Each batch comes with precisely controlled purity, maintaining levels routinely above 98%. TLC and HPLC chromatograms tell us whether by-products or unreacted starting materials linger in the final product, and we calibrate equipment routinely to guarantee accuracy. Trace metal contamination, once a concern for some pharmaceutical and agricultural chemists, has dropped to below threshold detection in our recent productions after upgrading filtration processes.
When working with an aromatic amide decorated with a trifluoromethoxy group at the ortho position, you see pronounced thermal stability and substantial hydrophobic character. The melting range, which spreads comfortably between 115°C and 120°C in our experience, stays tight and repeats across every lot. Infrared spectroscopy gives a clear fingerprint, with the amide carbonyl and the OCF3 stretching bands standing out, which helps in cross-verifying the product you receive.
Few compounds stir as much direct feedback from bench chemists as 2-(Trifluoromethoxy)Benzamide. Those engaged in medicinal chemistry turn to it in the early development of central nervous system agents, seeking electron-withdrawing substitution patterns that shift metabolism, solubility, and receptor affinity in measurable ways. In late-stage functionalization, the molecule allows for derivatization on the benzamide backbone while preserving the trifluoromethoxy handle, granting medicinal scientists a controlled experiment in how subtle modifications influence pharmacodynamics.
Outside the pharmaceutical field, material scientists have picked up on its use. The same features that empower medicinal breakthroughs – electron-withdrawing effects and stability – play out in high-performance coating research. Polymers designed for specialty films borrow inspiration from trifluoromethoxy systems, and our product supports those early proof-of-concept studies, minimizing the batch-to-batch variability that would otherwise delay timelines.
A close comparison between 2-(Trifluoromethoxy)Benzamide and simpler benzamide cousins illustrates how adding a trifluoromethoxy group shifts a molecule’s characteristics. Ordinary benzamides, lacking electron-withdrawing and steric effects, enter reactions more readily with electrophilic agents but suffer from decreased selectivity when it comes to certain aromatic substitutions. As manufacturers, we measure these differences in both yield and purity when scaling up alkylation or acylation reactions.
On the other hand, introducing just a trifluoromethyl group without the oxygen component, as in 2-(Trifluoromethyl)Benzamide, often results in altered metabolic stability and changes in aromatic ring reactivity. The extra oxygen in the trifluoromethoxy group gives unique resonance and inductive effects, making the compound less susceptible to unwanted hydrolysis and shifting basicity in a predictable way – characteristics that chemists value when working under strongly acidic or basic conditions.
Many clients used to face issues with the solubility of unsubstituted benzamides in non-polar solvents, especially in multi-step synthesis involving organic extractions or chromatographic separations. Our 2-(Trifluoromethoxy)Benzamide displays markedly improved solubility in halogenated solvents and certain ethers, which streamlines purification and formulation stages.
Cost and supply issues have driven several rounds of process development over the years. Original syntheses relied on niche starting materials or older transition-metal catalysts that generated significant metal waste. Through years of direct process review and troubleshooting, we moved towards routes that favor high atom economy and low-waste streams, making use of modern fluorination techniques and reusable catalytic cycles. Newer steps have trimmed down the number of solvent washes and improved the ease of isolation by targeted crystallization instead of non-selective precipitation.
Our technical team implements real-time analytical feedback during each step, allowing fast interventions if a temperature spike or pH drift arises. This minimizes batch failures and lets us share reliable timelines with our customers. Chemists in the lab benefit because every drum or bottle matches what they saw in earlier batches; pilot-scale consistency scales upward because of these controls at the manufacturing floor.
We have heard from partnering research groups who struggled with inconsistent yields or shifting chromatograms while sourcing similar compounds from general distributors. One common thread was the presence of co-eluting fluorinated by-products or incomplete amide formation. By narrowing the process window and expanding our traceability for every issued batch, we help chemists eliminate a major source of error in discovery campaigns. Purity isn’t just marketing for us: it directly impacts assay performance, toxicology profiles, and reproducibility in scale-up.
Another practical benefit surfaces in spectroscopic analysis. Graduate students and R&D teams often look for sharp, reliable signals with minimal baseline noise. Our product’s NMR and mass spec data regularly show resolved peaks, letting users skip long purification steps and accelerate structure verification, synthesis validation, and SAR exploration.
Decades in chemical manufacturing bring home the importance of safe materials handling, for both workers and users downstream. 2-(Trifluoromethoxy)Benzamide, like other fluorinated benzamides, requires specific care in storage and transfer. We design packaging to minimize air and moisture ingress, using lined barrels and sealed vials that get tested at the warehouse before shipment.
Worker protection at the plant relies on robust local exhaust and dust containment, since aromatic amides can become irritants at high concentrations. Our safety protocols run routine air sampling and spot training – not just paperwork but hands-on practice with protective equipment, so that incidents stay rare. Outbound shipments follow international chemical transport rules, so researchers and process engineers receive reliable, intact material at their door.
Fluorinated organics also raise environmental questions, particularly in terms of downstream degradation and disposal. Onsite waste treatment centers have moved toward closed-loop capture for fluorine-containing residues. By controlling process waste at the source, and partnering with recyclers for chemical by-products, we believe stewardship links directly to long-term business stability. We continue to monitor advances in green chemistry, exploring options for further process intensification and reduction of solvent use.
Beyond filling orders, we regularly field calls from chemists troubleshooting their reactions. Some find that switching amide variants can change solubility in screening assays; others want to swap out trifluoromethoxy starting points in their parallel synthesis run. We help decipher where the subtle properties of our product actually matter. During route scouting and optimization, knowing exactly how a batch behaves—how quickly it dissolves, whether it precipitates in cold solvent, or how its reactivity shifts with pH—can decide the success of the entire project.
Sometimes, we see requests to customize packing, integrate documented chain-of-custody, or split lots for blinded studies. Because we control production at each stage, we can implement these requests quickly, reducing the usual inertia that plagues many larger chemical conglomerates relying on long supply chains or outsourcing. The result for the buyer is shorter project lead times and consistent, reproducible results.
Research teams report several concrete successes drawing upon the unique aspects of 2-(Trifluoromethoxy)Benzamide. One pharmaceutical group shared how they achieved increased selectivity during aromatic bromination, exploiting the electron-withdrawing effect of the ortho trifluoromethoxy group. In library synthesis for structure-activity relationship work, chemists found substitution patterns around the amide allowed for new hydrogen bonding interactions, only possible when the group held steady on the ring.
Another area of growth comes from agrochemical discovery. Some crop-protection leads start with diverse benzamide scaffolds and move towards fluorinated variants seeking improved metabolic stability and environmental persistence. Better shelf-life and field performance stem directly from the enhanced stability that our product delivers. We watch as customers document extended trial periods, confident that the parent compound won’t degrade before field efficacy is measured.
In materials science, users adding our compound into specialty resins mention improved chemical resistance and weathering in formulated coatings. Solubility gains compared to non-fluorinated relatives enable easier blending and application, speeding development time across product lines aimed at electronics, medical devices, or outdoor surfaces.
Our perspective is different from that of a reseller or bulk trader. Each year, we invest in process upgrades not just to cut costs, but to address acute pain points that our customers tell us about. Wild swings in purity or variable crystalline habit once complicated scale-up for both API and specialty chemical producers. Focusing on traceable, consistent output solves these challenges head-on. Each batch starts with validated raw materials, sourced from longstanding suppliers, and passes through checkpoints designed by our technical team, not outsourced to third parties with less care for final utility.
Some users have asked, “How do you keep impurities so low, given the complexity of the synthesis?” It takes not just upgraded reactors or fume management, but a production philosophy that expects problems and builds in solutions: in-process checks, careful workup, and detailed documentation that chemistry teams can review. If a deviation ever appears, feedback loops send information directly from the end user to our quality control teams in real-time, and corrective actions roll out before new lots ship.
Many downstream applications now have their own tight regulatory controls, and we maintain documentation and batch records accessible for customer audits. Scientists operating under GMP or ISO constraints can review analytical data packages and chain of identity records for every lot shipped. This transparency is a product of our experience: after decades in synthesis and supply, we understand firsthand that trust in a substance forms the bedrock of safe and effective research.
Working with 2-(Trifluoromethoxy)Benzamide offers both advantages and some boundaries. On the plus side, teams value the predictability it brings to multi-step synthesis workflows. The chemical’s robustness under a range of conditions lets researchers push the envelope in reaction development or formulation studies, especially where challenging conditions or strong reagents are concerned. Its well-defined solubility profile in both polar and non-polar media shortens time spent optimizing extraction or workup procedures.
This doesn’t mean flawless performance in every circumstance. Some groups report that the trifluoromethoxy group can resist further functionalization, especially under nucleophilic aromatic substitution pathways. Extra planning is needed if subsequent modifications to the ortho position are desired; we recommend access to route design input for chemists seeking additional substitutions.
Another aspect worth noting: cost. Synthesizing high-purity, trifluoromethoxy-substituted aromatics draws upon specialty intermediates and exacting process control, resulting in higher unit pricing than generic benzamides. For projects in early-stage screening, this can restrict volume, but for later-stage optimization or commercial use, the performance benefits more than balance the extra investment.
Ongoing dialogue with academic and industrial users shapes every update we make. Researchers in organic synthesis flag opportunities for new derivatives, asking for altered ring substitution, chain extension, or isotopically labelled analogs. Our R&D team experiments internally, looking for scalable routes that keep purity and performance as high as with our founding product. The next generation of 2-(Trifluoromethoxy)benzamides may feature additional groups for specialty pharmacology or novel material science targets.
As we talk to partners working on emerging therapeutic classes, or pioneering new specialty polymers, we hear about the parameters that matter most: solubility in complex mixtures; stability during long, multi-step reactions; freedom from confounding side products. We aren’t a middleman: these stories feed directly into our process development meetings and shape what comes out of the next reactor run.
2-(Trifluoromethoxy)Benzamide isn’t just another entry on a catalog. Behind every bottle or drum stands a story of process refinement, constant learning, and hands-on troubleshooting. By producing this compound in-house, rather than through a chain of intermediaries, we stay connected to the sharp end of chemical innovation, where each modification can set a research program forward or backward by months.
This attention to detail, paired with openness to customer insight, guides our approach to both production and service. Chemistry remains a science of practical results: reliable reagents, repeatable results, and fewer setbacks in the lab or on the plant floor. For those seeking a partner with a real track record in advanced fluorinated aromatic synthesis, our experience manufacturing 2-(Trifluoromethoxy)Benzamide stands ready to support the pace and complexity of tomorrow’s discoveries.