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1-(4-Trifluoromethylphenyl)Imidazole

    • Product Name 1-(4-Trifluoromethylphenyl)Imidazole
    • Alias 4-(Trifluoromethyl)phenylimidazole
    • Einecs 249-360-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    VTB
    Specifications

    HS Code

    915238

    Chemical Name 1-(4-Trifluoromethylphenyl)Imidazole
    Cas Number 3077-78-1
    Molecular Formula C10H7F3N2
    Molecular Weight 212.17
    Appearance White to off-white solid
    Melting Point 76-78 °C
    Boiling Point 317.7 °C at 760 mmHg
    Density 1.33 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles FC(F)(F)c1ccc(n2cncc2)cc1
    Inchi InChI=1S/C10H7F3N2/c11-10(12,13)8-1-3-9(4-2-8)15-6-5-14-7-15/h1-7H
    Purity Typically ≥98%

    As an accredited 1-(4-Trifluoromethylphenyl)Imidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 1-(4-Trifluoromethylphenyl)imidazole, labeled with safety, hazard, and product information.
    Shipping The chemical **1-(4-Trifluoromethylphenyl)Imidazole** is shipped in tightly sealed containers to prevent moisture and contamination. Packaging complies with international regulations for chemical transport. The product is typically dispatched under ambient conditions, with clear labeling of hazard information and safety instructions. Shipping documentation accompanies each package for traceability and regulatory compliance.
    Storage Store 1-(4-Trifluoromethylphenyl)imidazole in a cool, dry, and well-ventilated area, away from sources of ignition or heat. Keep the container tightly closed and protected from moisture, direct sunlight, and incompatible substances such as strong oxidizing agents. Use suitable, chemically resistant containers and ensure that the storage area is clearly labeled and equipped with appropriate spill containment measures.
    Application of 1-(4-Trifluoromethylphenyl)Imidazole

    Applications of 1-(4-Trifluoromethylphenyl)Imidazole in Industrial Manufacturing

    1-(4-Trifluoromethylphenyl)Imidazole serves as a key intermediate in chemical synthesis across several complex downstream markets. As a direct manufacturer, we collaborate with global clients requiring stringent quality standards and engineered formulations for advanced industrial uses. Detailed below are actual industrial applications, integration points, and regulatory frameworks tailored to each segment.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antifungal Agents

    Pharmaceutical companies utilize this material for the targeted synthesis of azole-class antifungal compounds, such as the precursor stage for triazole and imidazole APIs. It enters at the critical heterocycle formation or halogenation step to impart the trifluoromethyl moiety, which enhances the pharmacokinetic profile of the drug molecule. Quality assurance involves rigorous impurity profiling and batch-to-batch analysis under GMP controls. Production scales from pilot to commercial involve multi-stage purification and real-time release testing to meet global regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP-NF Monograph requirements (where applicable)
    • EudraLex Vol. 4 – EU Guidelines for GMP
    • FDA 21 CFR Parts 210/211

    Typical usage ratio

    • 10–25 mol% relative to the total batch size, adjusted based on target molecule molar mass and downstream yield requirements

    Downstream process integration

    • Added at the heterocycle assembly or substitution stage in API synthetic route
    • Serves as the building block for trifluoromethyl-imidazole core structures
    • Use in in-line continuous reaction or closed batch reactors
    • Follows in-process monitoring for purity and residual solvent control

    Final product types

    • Voriconazole
    • Fluconazole intermediates
    • Other triazole antifungal API substances
    • Generic pharmaceuticals for systemic or topical antifungal therapy

    2. Synthesis of Agrochemical Fungicides

    Agrochemical manufacturers rely on this compound as a crucial intermediate for synthesis of next-generation triazole fungicides. The molecule's electronic profile supports selective crop protection active components with improved environmental stability and bioavailability. Formulation processes demand tight process control to limit residual precursor and meet international residue limits in finished agrochemicals.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EU Regulation (EC) No 1107/2009
    • US EPA Pesticide Registration (FIFRA)
    • ISO 9001 quality management (for technical material production)

    Typical usage ratio

    • 5–15 mol% in the intermediate stage of technical-grade fungicide synthesis; adjusted based on required active ingredient content and conversion rates

    Downstream process integration

    • Charged during the alkylation or coupling step to introduce trifluoromethylphenyl structure
    • Often processed in high-shear or emulsion reactors for technical concentrate preparation
    • Careful control of exothermicity and by-product formation during scale-up
    • Subsequent purification and solvent exchange prior to formulation blending

    Final product types

    • Propiconazole
    • Epoxiconazole and similar triazole crop protection agents
    • Technical-grade fungicide concentrates
    • Crop protection finished products (suspension concentrates, emulsifiable concentrates, wettable powders)

    3. Advanced Electronic and Photoinitiator Material Production

    Companies operating in electronics and specialty coating sectors employ this raw material as a functional monomer or intermediate for photoinitiator compounds. The unique electron-withdrawing properties of the trifluoromethyl group enhance efficiency and stability of UV-curable systems and microelectronic coatings, supporting optimal photochemical properties necessary for high-speed device manufacturing.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for hazardous substances
    • REACH Regulation (EC) No 1907/2006
    • IPC/JEDEC J-STD-033 for handling, packaging, shipping of moisture-sensitive devices (relevant for electronics sector)
    • Internal customer-specific QC and certification protocols

    Typical usage ratio

    • 0.1–3 wt% in photoinitiator blends; concentration depends on resin compatibility and targeted cure speed

    Downstream process integration

    • Introduced during the synthesis of UV-absorber or photoinitiator functional groups in resin formulations
    • Directly involved in microemulsion or solution polymerization processes
    • Processed in inert-atmosphere reactors to avoid side reactions
    • Downstream blending with electronic-grade acrylate or epoxy monomers before application

    Final product types

    • Photoinitiators for UV-LED applications
    • Printed circuit board (PCB) photoresists
    • High-purity microelectronics encapsulants
    • UV-cured adhesives and coatings for optical components

    4. Synthesis of Specialty Polymer Additives

    Polymer manufacturers incorporate this intermediate during the synthesis of additives that improve thermal stability and resistance of engineering plastics and advanced polymer films. Its chemical structure is particularly valuable in modifying flame retardancy and barrier properties without compromising color stability or polymer transparency in demanding industrial applications.

    Industry compliance standards

    • UL 94 flammability standards for plastics
    • REACH SVHC compliance for polymer additives
    • ASTM D256 and D638 for mechanical and tensile property verification
    • ISO 9001 system for specialty additive production

    Typical usage ratio

    • 0.5–2.5 wt% in polymer masterbatch formulations; fine-tuned based on targeted flame retardancy, migration, and final application requirements

    Downstream process integration

    • Dosed into polymerization reactors during the additive pre-polymer stage
    • May be co-extruded in masterbatch or directly compounded during pelletizing step
    • Quality control includes melt-flow and compatibility testing
    • Dispersed into resin matrix ahead of extrusion, molding, or film-casting processes

    Final product types

    • Flame-retardant polycarbonate and polyamide compounds
    • Barrier layers in multilayer packaging films
    • High-impact plastic cases for consumer electronics
    • Technical-grade cable insulation and automotive plastics
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    Certification & Compliance
    More Introduction

    Introducing 1-(4-Trifluoromethylphenyl)Imidazole: From Our Reactors to Your Workflow

    From Synthesis to Application: A Practical Take on 1-(4-Trifluoromethylphenyl)Imidazole

    At our chemical plant, manufacturing 1-(4-Trifluoromethylphenyl)Imidazole feels like working directly with the pulse of innovative process chemistry. Our team has spent real hours in production halls, not just pushing buttons or following flowsheets but refining each step in the sequence to reach consistently pure outcomes. From the day we began scaling up this compound, the handling of the trifluoromethyl group—both robust and demanding—in our reactors led us down a route where control over moisture, temperature, and by-product management became more than just checkpoints. Every batch in our reactors reflects fine-tuned parameter controls and hands-on troubleshooting, not just a checklist processed by automation.

    Specifications: What Sets Our 1-(4-Trifluoromethylphenyl)Imidazole Apart

    This compound—the imidazole ring bearing a para-trifluoromethylphenyl group—delivers a unique electronic character shaped by both components. The trifluoromethylphenyl group delivers pronounced electron-withdrawing effects, changing the reactivity profile compared to parent imidazole or phenyl imidazoles without fluorines. Handling the right ratios, ensuring that water doesn’t sneak into the reaction mix, and keeping unwanted side reactions at bay all come from experience. The white to off-white crystalline product coming off our lines is the output of procedural discipline, not mere chance. Analytical confirmation comes through HPLC, GC-MS, and other pharmacopeia-aligned techniques we apply batch after batch. Such consistency isn't the result of remote procurement or boardroom management—it’s the work of technicians who recognize the subtle color shifts at the endpoint or who know the faint, distinctive odor when the reaction is nearing completion.

    Why the Structure Matters in Downstream Use

    For our customers in pharma and specialty chemistry, the differences brought by adding a trifluoromethyl group onto the phenyl ring are not trivial. This group shrugs off metabolic degradation in many biological systems, giving rise to molecules that last longer or behave differently in target pathways. In the lab, differences show up clearly in NMR, IR, and reaction conditions required downstream. The imidazole ring, widely found in essential pharmaceuticals and enzyme inhibitors, combines with the altered electron density created by the CF3-phenyl group to open up routes not accessible with basic imidazoles or methylphenyl imidazoles.

    Our Manufacturing Difference: Full-Process Control

    Every kilogram of 1-(4-Trifluoromethylphenyl)Imidazole we ship stems from reaction protocols that have been optimized and lived with on our own site. We aren’t buying intermediates from faraway plants; we have set up the full process, from raw material assessment through reductions, condensations, and purifications, all the way to staged drying and precise packaging. Troubleshooting happens in real time—our teams have responded to subtle upsets in pressure, achieved reproducible yields, and re-engineered crystal separation to avoid fines and dusting. These details matter beyond purity: they impact recovery, packing, and the confidence of every user at the bench.

    Specifications That Spring from Real Experience

    Years of production have taught us more than any data sheet possibly could. Product melting points, solubility in various solvents, and shelf stability aren’t generic numbers picked from literature—they’re based on our own day-to-day handling. We track each shipment lot over six months or more, checking for caking, discoloration, or other changes. We know from direct testing which solvents really keep the product mobile and which don’t, and how moisture affects the crystalline texture over time. Each package has its own identification and record trail, but what truly matters is that behind those records stands a team with an eye for real-world product behavior—not just box checking.

    Practical Uses in Medicinal and Material Chemistry

    We hear from researchers who use our 1-(4-Trifluoromethylphenyl)Imidazole in kinase inhibitor scaffolds, anti-infective screens, and as key intermediates in agrochemical research. The fluorinated aromatic system enables target molecules to achieve bioactivity with increased selectivity, while the imidazole ring offers access to a familiar, reliably functional handle for further transformations. We see product going into both microwave-assisted syntheses, where reproducible melting point and phase behavior directly impacts yields, as well as classical solution-phase chemistry. The difference compared to non-fluorinated analogs often shows up dramatically in biological response or binding studies, a fact reported time and again by clients across Asia, the US, and Europe. The product isn’t just a stepping stone—it shapes discovery in ways other aromatic imidazoles or simple imidazoles cannot.

    Differences that Matter: The Role of the Trifluoromethylphenyl Group

    The CF3 group isn’t decorative; it changes every key property. We noticed early on that our 1-(4-Trifluoromethylphenyl)Imidazole resists oxidation better than non-fluorinated phenyl imidazoles under similar conditions. In scale-up settings, its low moisture uptake compared to some other substituted imidazoles keeps caking and bridging low in our shipping drums. Customers share that these differences matter, especially in reactions sensitive to trace water or requiring strict stoichiometric control. Our production team recognizes that under reducing or basic conditions, there’s less by-product and better main compound clean-up compared to benzyl or methyl-imidazole analogs. These are facts read off reactor performance logs, not generic claims.

    Consistency in Every Lot: From Reaction Onset to Final Loading

    Each run begins with careful validation of reagents. Our plant managers have adjusted input criteria for every raw material source based on real-life inconsistencies we’ve met. Even minor differences in trifluoromethylbenzaldehyde grade or imidazole feedstock can show up downstream, so our procurement and QC teams maintain rigorous cross-checks. Our reactors, fitted with real-time temperature and pressure alarms, are adjusted to match seasonal changes in ambient humidity or cooling water temperature. These adjustments, learned from years of handling the process, preserve yield, cut waste, and secure a consistent product package. Problems get solved right where they arise—on the production floor by people who have seen the process trouble-spots and who remember past solutions that actually worked.

    Handling, Safety, and Practical Convenience

    Our staff work with 1-(4-Trifluoromethylphenyl)Imidazole daily, so we know what the compound demands in terms of respect for safety. The product, supplied as a dry solid, can generate nuisance dust if mishandled—a detail our operators take seriously, using local fume extraction and ensuring work surfaces are kept clear. Storage away from open moisture ensures the crystals remain free-flowing and ready for weighing, with no need for heavy re-drying or sieves on the user end. We developed improvements in product packaging—multi-layer liners, continuous humidity monitoring, and efficient sealing—to help customers skip tedious pre-use handling.

    Customer Feedback and Process Adaptation

    Every report from a client about product performance gets relayed directly to our process development team. We act on feedback about unexpected behavior—one example being a case last year where a batch used in a pilot medicinal chemistry run gave slightly slower dissolution in DMF. Immediate analysis traced back to a batch that had spent slightly longer in vacuum drying than the norm. Adjustments were made, not only for that batch but for every subsequent one. These real-world improvements and the feedback loop with bench chemists build trust. We test our product by the standards someone at the bench—or in production—actually faces, not by arbitrary specification limits.

    Supporting Latest Research and Industrial Needs

    Synthetic organic chemists care about predictability, not just purity. Our 1-(4-Trifluoromethylphenyl)Imidazole gives repeatable results under both high-throughput screening and bench-scale reaction setups. The compound’s melting range and phase behavior are published from measurements we have made in-house, not simply copied. In recent collaborative work with external researchers, we tracked how our product’s stability affects longer storage in automated sample stores, helping users plan batch syntheses over extended campaigns. This kind of support grew out of years spent benchmarking storage conditions and testing packaging stability, responding to what clients experience, not what theory assumes.

    Technical Support: Chemical Know-how, Not Scripted Responses

    People buying specialty chemicals want more than correspondence or robotic FAQs. Our technical support team functions as an extension of our production group; we answer questions based on what we’ve tried and seen in our own reactors, not just what’s printed in public literature. Difficulties with co-crystallization, odd color changes, or filtration quirks are handled with input from people who have solved real-world problems. Chemists on the floor can run split-lot reactivity tests rapidly, giving users direct answers rooted in our decade-plus of process and handling experience. We don’t defer to outside contractors or pass customers through call centers; we’ve seen how our substance behaves, and we share those specifics willingly.

    Scale, Sustainability, and Future Adaptations

    As production volumes for 1-(4-Trifluoromethylphenyl)Imidazole have grown, so has our ability to adapt sustainability measures. Solvent recovery at our plant now reaches high recapture rates; spent mother liquors are treated and re-used. Energy management during the exothermic stages of synthesis led us to retrofit chillers and improve process efficiency. Waste minimization didn’t come from regulations, but from engineering changes that made daily life easier for operators and lowered energy bills. These measures benefit both our team and our customers, who increasingly ask about greener processes beyond just product purity.

    Lessons Learned and Ongoing Developments

    Scaling up and maintaining production of 1-(4-Trifluoromethylphenyl)Imidazole taught us that chemistry doesn’t run smoothly by default. Differences in each batch have to be hunted down and understood. Early trials taught us to expect occasional runaway dissolutions or unexpected minor by-products, especially during startup production campaigns. SOPs written after batch failures or short yields mean little if they aren’t rooted in how real reactors behave and what operators have experienced. Every improvement and shortcut we’ve made came from this place of learning and relentless incremental change.

    Why Expertise Matters for End Users

    Ordering specialty chemicals directly from the manufacturer—especially one with integrated process control—brings advantages beyond purity numbers and on-time shipment. The dialogue enabled by a close connection to those who actually make your material means users receive contextual advice, fast answers, and a clarity that doesn’t show up from trading schemes or catalog sellers. We view our clients’ results as a direct reflection of our daily work. When a customer’s late-stage process struggles, the solution often traces back to an actual production parameter or learning from our side—knowledge we openly share because we understand the pressures, challenges, and stakes inherent in high-value synthesis and research.

    Trust Built on Practical Transparency

    We don’t hide our methods or short-circuit information sharing. If a batch runs slightly off in physical form or spectral purity, we alert customers in advance and share test data promptly. If a rare out-of-trend impurity appears, it triggers not just a retest but a collaborative investigation. Most of our long-term customers arrived through recommendations from other chemists who saw our openness as a real asset. We have built a reputation not just on reliable deliveries but on being a technical partner, ready to dig in and solve problems side by side.

    Summary of Material Value: More than Specification

    The value of our 1-(4-Trifluoromethylphenyl)Imidazole comes from compounded experience, not commoditization. Every insight, improvement, and adjustment is the result of people who know what each reactor, dryer, and packaging line actually requires. Over the years, by staying directly involved in the full process—from raw material choice, through reaction, work-up, purification, to final delivery—we’ve refined a product that continues to unlock new research potential and stand the test of real-world laboratory and industrial use. Rather than trading on reputation alone, we anchor our service and quality in years of genuine, hands-on experience with every lot shipped and every challenge faced together with researchers around the world.