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HS Code |
187911 |
| Chemical Name | 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione |
| Molecular Formula | C11H6F3NO2 |
| Molecular Weight | 241.17 g/mol |
| Cas Number | 131038-08-7 |
| Appearance | Off-white to pale yellow solid |
| Melting Point | 95-100°C |
| Purity | Typically ≥ 98% |
| Solubility | Soluble in common organic solvents (e.g., DMSO, DMF, acetone) |
| Synonyms | 3-(Trifluoromethyl)phenylmaleimide |
| Smiles | O=C1C=CC(=O)N1C2=CC=CC(=C2)C(F)(F)F |
| Inchi | InChI=1S/C11H6F3NO2/c12-11(13,14)8-3-1-2-7(6-8)15-9-4-5-10(16)17-9/h1-6H |
| Storage Condition | Store at room temperature, keep container tightly closed |
As an accredited 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle, sealed with a screw cap, and clearly labeled with the compound name and purity. |
| Shipping | **Shipping Description:** 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled as a potentially hazardous chemical, following all applicable regulations for transport. Appropriate labeling and documentation ensure safe delivery via ground or air under standard chemical shipping guidelines. |
| Storage | Store 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione in a tightly sealed container, in a cool, dry, well-ventilated area, away from direct sunlight, moisture, and incompatible materials such as strong oxidizers or acids. Use proper labeling and secondary containment. Handle with appropriate personal protective equipment, including gloves and eye protection, and follow standard laboratory safety procedures. |
Applications of 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione in Industrial Manufacturing1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione serves as a critical intermediate in multiple high-value industrial supply chains. Manufacturers select this compound for its fluorinated aromatic structure, which supports stable performance in advanced materials, agrochemicals, pharmaceuticals, and specialty electronics. Every downstream application features unique quality compliance, dosing, and processing requirements to match stringent end-use standards. 1. Pharmaceutical Intermediate for Novel Drug SynthesisPharmaceutical companies leverage this raw material as a key intermediate in the synthesis of targeted therapies, particularly oncology and CNS candidate molecules. Its trifluoromethyl group introduces improved metabolic stability, supporting synthetic steps in complex molecule construction. Manufacturers incorporate this building block at controlled stages during multi-step reactions with stringent QA oversight and full traceability in cGMP-compliant environments. Industry compliance standards
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2. Building Block for High-Performance Agrochemical Active IngredientsCrop protection manufacturers use this compound to install a fluorinated aromatic moiety in new-generation herbicides and insecticides. The unique structure boosts the metabolic persistence and field efficacy of agrochemical actives. Its integration takes place under ISO regulatory control, with attention to residual profile and environmental safety at each synthesis phase. Industry compliance standards
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3. Functional Monomer Precursor for Specialty Polyimide MaterialsAdvanced materials suppliers rely on this raw material to introduce electron-withdrawing groups during the synthesis of high thermal resistance polyimide polymers. The compound participates in condensation polymerization to enable enhanced dielectric and mechanical properties in end-use films and devices. All production follows strict materials standards to support electronic and aerospace sector requirements. Industry compliance standards
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4. Intermediate for Fluorinated Organic Pigment ManufactureThe pigment industry employs this intermediate to synthesize high-purity organic colorants with enhanced UV and chemical resistance. The product enables the production of specialty pigments for demanding automotive, industrial coating, and plastics applications. Manufacturers stringently control incorporation to meet CI (Colour Index) registration and global regulatory thresholds for pigment purity and stability. Industry compliance standards
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At our manufacturing site, 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione regularly moves from pilot reactors to full-scale production tanks, making its presence felt from plant to lab. Chemists sometimes refer to it as a trifluoromethyl phthalimide derivative, but for operators who run the day-to-day, this compound has simply become an essential tool in the advancement of specialty organics. Its CAS number carries weight in the industry, but more impressive is the way experienced chemists have embraced its unique properties, calling on its strengths in both pharmaceutical and agricultural chemistry.
In production, it appears as a solid white to off-white crystalline powder, with a distinct, slightly sharp odor that speaks to its aromatic core and the fluorine elements built into its ring system. The molecular integrity holds up under scrutiny, confirmed by every NMR, mass spec, and GC trace we run from batch to batch. We avoid any compounding agents or fillers—that’s not our style. Purity levels hold above 98% for every commercial lot we ship out, since our team quickly learned that trace contamination in this class of chemicals leads to trouble downstream. Stability over time remains high, as we’ve seen in stress tests; it resists hydrolysis better than many related maleimide analogues, making it a more reliable partner for complex coupling reactions in medicinal chemistry labs.
There’s no shortage of phthalimide derivatives, but the trifluoromethyl phenotype stands out once you begin working with it. The electron-withdrawing strength from the CF3 group changes the reactivity. After years of close observation, our analytical chemists find this compound achieves higher selectivity in Diels–Alder and nucleophilic aromatic substitution than standard N-phenyl or alkyl-maleimides. The presence of the trifluoromethyl ring tames unwanted side-products, meaning that on the production trestles, reaction yields often land far ahead of competing intermediates. We’ve seen pharmaceutical researchers drastically reduce steps in their syntheses, all by shifting to our material when looking to introduce a trifluoromethylated aromatics motif.
Some products in this arena bring inconsistency—one batch may dissolve cleanly, another leaves residue. Our compound, with no added solvents or stabilizers, maintains solid solubility in common polar aprotic solvents: DMF, DMSO, and acetonitrile. At our facility, each batch is dried and milled under nitrogen to minimize water uptake, so researchers never need to rerun their work over moisture issues. We don’t just do this to chase specs; it’s how crude intermediates become reliable building blocks, not lab headaches.
Over the last decade, applications for 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione have grown far beyond theoretical chemistry seminars. In our experience, pharmaceutical API groups push this molecule forward in the search for new antifungal and anticancer scaffolds. The trifluoromethyl group’s lipophilicity and metabolic resistance add value to molecules seeking better drug-like properties. We’ve supplied this compound for targeted kinase inhibitor projects, where it acts as a masked, stable Michael acceptor, giving new structure–activity relationships a starting point that does not degrade rapidly in basic or aqueous environments.
Outside of healthcare, agrochemical innovators use the same core structure for new plant growth regulators and pest control agents. The molecule delivers activity at lower dosages, helped by the electron-deficient ring. Our agricultural partners often note that compared to o-tolyl or p-chlorophenyl analogues, the trifluoromethyl version avoids rapid decomposition in field conditions, with less photolysis or volatilization during spraying. Their feedback tells a clearer story than any technical spec: crops stay protected, rates drop, and environmental profile improves.
We’ve handled dozens of similar aromatic maleimides, and only a few earn a permanent place on our annual production run list. The decision mostly comes down to performance across the plant and feedback from end-users. Compounds with bulky halogen groups or thio analogues frequently cause clogging or excess fines during crystallization; the trifluoromethyl version flows well, moves smoothly during packaging, and rarely generates static or dust, keeping both line workers and product clean. This isn’t something most datasheets ever mention, but our plant engineers mark it as a top strength for workplace safety and throughput.
From raw material supply chains to final shipment, we know every input. Fluorinated aromatics sometimes raise sustainable sourcing questions, but we track our starting trifluoromethyl aniline right back to established European and Asian fluorine specialists. Each lot meets thresholds for residual solvents, heavy metals, and halide byproducts—compliance means less trouble across the board, for our workers and our customers. Material handling, storage, and process safety never take a back seat in our shop, given how quickly residue or static build-up can turn a promising batch into a failed lot.
People working the night shift will tell you that certain chemicals telegraph their condition—bad batches leave awkward clumps, stick to bin edges, or pick up moisture. Any batch of 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione that comes off-spec gets held back for internal analysis. We make a point to keep the drying and packaging rooms at controlled temperature and humidity. After some trial and error, we found regular paper bags pick up traces of the compounds in the liner—so everything now ships in four-layer LDPE and foil laminate drums.
Unlike some related crystalline heterocycles that develop yellowing after weeks on warehouse shelves, 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione retains its color, signaling consistent purity and freedom from self-coupling or oxidation. Each time we’ve deployed a new filter cake or drying step, we benchmark not just routine melting points but also shelf stability and ease of use for synthesis groups. Operators at client sites confirm, sometimes within hours, that powders weighing out from our drums respond predictably during subsequent reactions.
Year after year, logistics tends to separate serious manufacturers from fly-by-night resellers. We see the effect of poor packing on arrival every time new customers bring us competitive samples—powder caked at the bottom, stuck chunks, strange discoloration, even unsealed liners. Our regular clients expect four-layer, oxygen- and moisture-resistant packing. Producers who cut corners here invite shelf-life problems and batch failures. As seasons change, we monitor drum seals and use inert gas packing on sensitive lots headed overseas. US and EU clients also value clearly labeled drums for compliance tracking and regulatory handoffs. Supply chain disruptions have become more frequent, and our stock policy ensures clients can rely on year-round availability with consistent lot sizes, which a trader or virtual broker rarely matches.
Over time, our direct relationships with researchers have shaped how we refine and upgrade this product. We frequently get early feedback from new R&D projects, which informs our purification and QA process. One project in oncology research relied on quick turnaround and ultra-low moisture content—the result of working closely with these groups led us to modify our final drying procedures, introducing in-line Karl Fischer titration checks to ensure results keep pace with stricter analytical standards.
Academic groups and biotech startups with smaller needs often voice concerns about minimum order quantities. We work directly with these teams to package material in multiple size options, all without repacking or transfer steps that would increase contamination risk. It's this type of practical, application-driven collaboration that separates experienced, invested producers from generic suppliers who rarely see the product outside of a spreadsheet or invoice.
We set out to build a material that allows for reproducible results. In the maleimide field, variation in melting point, trace metal residues, or color often signals a lack of process control upstream. Custom derivatives like the trifluoromethyl version seem more prone to drop in quality among traders or resellers trying to chase quick profit margins; batch reprocessing or untracked recycles provoke inconsistency. Our routine QA picks up micro-impurities from off-spec starting material that slip through in loosely managed operations. We resolve these issues with full traceability, so the same high-purity material goes to every client.
Feedback from contract research groups tells us that lesser quality batches (especially those sourced without documentation) present wider melting point ranges and more NMR ghosts than what they receive from us. The full spectrum of analytical data goes with every shipment, so chemists know exactly what sits in their flask, down to the tenth of a percent. We don’t substitute grades or alter specifications based on client size or order frequency; the consistency comes from repeatable, transparent method development—not reactive tinkering on the fly.
Manufacturing organofluorine compounds in today’s climate entails not just technical precision but environmental responsibility. Disposing of halogenated waste, handling spent solvents, and maintaining safe workspaces for local teams—these issues remain central to how we design and scale up every process. Over the last few years, support for closed-loop solvent recovery systems has grown, driven by both regulation and direct benefit to our bottom line. Waste handling protocols match the continually evolving standards set by local agencies and industry consortia.
Certifications for REACH compliance and regular internal audits underpin every run. We stay ahead of changing global standards, whether they're for workplace safety, green chemistry priorities, or new restrictions on certain process reagents. Internally, our team monitors not just product specs but carbon footprint and safety metrics, sharing regular updates with our stakeholders on how raw material planning and process investments contribute to safer, more sustainable outcomes.
Clients are often surprised at the depth of routine inspections and in-house documentation that follow this product through our facility. Each stage gets signed off by actual operators, not filed away by distant auditors. It’s common for visiting partners or customers to walk our labs and watch new batches run through mill, dryer, bagging, and QA in close succession. Trust develops when people see that product quality is no abstraction; it’s built from real work, real oversight, and a continuous drive to improve each part of the chain.
Through years of production, we’ve come to believe that integrity in manufacturing is a lived reality, not a value statement or slogan. Each batch that leaves our facility has already proven reliability, not by hitting a minimum spec but by making life easier for the chemists who work with these building blocks day in and day out. That relationship between informed manufacturing and customer experience keeps us committed to continuous learning and proper investment in every new project.
The scope for 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione remains dynamic. As downstream users in life science and advanced materials push into new territory, requests for higher purity, lower metal content, or new analytical certainties drive ongoing upgrades at our site. Recent collaborations with bioconjugation researchers exploring targeted payload delivery needed material prepared under stricter cross-contamination protocols; adjustments to our workflow delivered better reproducibility and cleaner synthetic results.
In the field of electronic materials, trialists discovered that the unique pairing of stability, minimal side reactions, and electron-withdrawing profile allowed for the design of next-generation polymer backbones and charge transport layers. These advances did not arise from reference work alone—they surfaced from ongoing dialogue around how the product behaves on the bench, in the pilot plant, and ultimately, in the marketplace where performance translates into business outcomes.
The story of 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione from the manufacturer’s floor underscores the difference made by experience, practical investment, and attention to real-world conditions. Our teams draw lessons from every shipment, each feedback call, and all the late-night adjustments made to hit shipping windows and purity targets. While pure technical data remains important, more critical is the connection with end-users—the give-and-take that lets good materials become great through direct, responsive manufacturing.
Our path forward continues to rely on building a community of trust, accountability, and practical improvement. Knowing that clients succeed using our material in critical research and real-world applications serves as ongoing motivation. 1-(3-Trifluoromethyl-Phenyl)-Pyrrole-2,5-Dione stands as more than a product of chemical synthesis; it functions as a benchmark of collaboration, technical skill, and the kind of attention to detail only a seasoned manufacturer can provide.