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1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole

    • Product Name 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole
    • Alias 3,5-Bis(trifluoromethyl)phenylpyrrole
    • Einecs 694-042-7
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    936439

    Iupac Name 1-[3,5-bis(trifluoromethyl)phenyl]pyrrole
    Molecular Formula C12H7F6N
    Molecular Weight 293.18 g/mol
    Cas Number 872840-88-9
    Appearance White to off-white solid
    Melting Point 48-51 °C
    Solubility Soluble in organic solvents such as DMSO and dichloromethane
    Pubchem Id 18083123
    Smiles C1=CC=CN1C2=CC(C(F)(F)F)=CC(C(F)(F)F)=C2
    Inchi InChI=1S/C12H7F6N/c13-11(14,15)8-5-7(1-3-19-9-8)6-10(16,17)12(18)4-2-8/h1-6H,9H
    Synonyms 3,5-Bis(trifluoromethyl)-N-pyrrolylbenzene

    As an accredited 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, labeled “1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole.” Secure screw cap, tamper-evident seal, hazard warnings included.
    Shipping **Shipping Description:** 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole is shipped in sealed, chemical-resistant containers under ambient conditions. The package is labeled in accordance with local and international chemical transport regulations. Appropriate safety datasheets are included. Protect from moisture, heat, and direct sunlight during transit. Handle with gloves and avoid rough handling to prevent container damage.
    Storage Store **1-[3,5-bis(trifluoromethyl)phenyl]pyrrole** in a tightly sealed container at room temperature, in a cool, dry, and well-ventilated area away from direct sunlight, heat, and sources of ignition. Keep away from incompatible materials such as strong oxidizing agents. Use appropriate personal protective equipment when handling, and store under an inert atmosphere if stability data require it.
    Application of 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole

    Applications of 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole in Industrial Manufacturing

    Our 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole is manufactured to meet the demands of advanced chemical synthesis in several specialty downstream sectors. The following application scenarios reflect the actual industrial deployment of this raw material, emphasizing genuine processes, regulatory requirements, operational dosage ranges, and the final product portfolios produced by our customers worldwide.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers incorporate this pyrrole derivative as a core intermediate during the construction of fluorinated heterocyclic scaffolds required for targeted small molecule APIs. Its electronic properties facilitate site-selective transformations under established GMP synthetic workflows, supporting the preparation of regulatory-compliant production batches for generic and patented therapies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (APIs)
    • US FDA 21 CFR 210/211 (Finished Pharmaceuticals)
    • Relevant monographs from Ph. Eur. and USP (for APIs produced using pyrrole intermediates)

    Typical usage ratio

    • 0.7–1.3 molar equivalents per target heterocycle moiety, dependent on the required substitution pattern and reactivity profile

    Downstream process integration

    • Introduced at the heterocycle formation or fluorination stage, prior to purification and crystallization of intermediate or API

    Final product types

    • Oncology and CNS drug intermediates
    • Final formulated APIs for oral or parenteral delivery
    • Regulatory submission batches for NDA/ANDA filings

    2. Specialty Agrochemical Synthesis

    Agrochemical manufacturers integrate this fluorinated pyrrole unit in the multi-step synthesis of new-generation crop protection agents. Its high fluorine content improves metabolic stability and soil mobility profiles in patented herbicides and fungicides, with strict adherence to agrochemical synthesis standards and field safety evaluations.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical development
    • FAO/WHO Guidelines for Pesticide Residues
    • REACH Registration and Notification (EU Agrochemicals)
    • ISO 17025 for Quality Control Laboratories

    Typical usage ratio

    • 3–7 wt% in the coupling reaction for target fluorinated active compounds, adjusted based on molecular substitution complexity and yield targets

    Downstream process integration

    • Enters during the late-stage coupling or fluorination step prior to formulation into technical concentrate

    Final product types

    • Pre-emergent herbicide intermediates
    • Systemic fungicidal active ingredients
    • Registered technical grade crop protection agents

    3. Advanced Organic Electronic Materials

    Producers of organic electronic components employ this compound as a building block in synthesizing semiconducting polymers used for OFETs (organic field-effect transistors) and OLED (organic light-emitting diode) devices. The dual trifluoromethyl substitution optimizes dielectric and charge-transport properties, essential for achieving reproducible electronic performance under ISO and RoHS regimes.

    Industry compliance standards

    • RoHS Directive (EU and international electronics production)
    • ISO 9001:2015 Quality Management Systems
    • IEC 62341 (OLED Performance and Safety Testing)
    • ITU-T Recommendation L.1000 for eco-design of electronic devices

    Typical usage ratio

    • 15–22 mol% as a co-monomer in the polymerization feed, depending on target bandgap and mobility specifications

    Downstream process integration

    • Fed into the monomer mixture for Suzuki or Stille polymerization prior to solution processing of device layers

    Final product types

    • High-mobility OFET arrays
    • Display-grade OLED emissive layers
    • Printed organic photovoltaic modules

    4. High-Performance Coating Additives

    Coatings manufacturers select this pyrrole structure as a specialty additive in the development of fluorinated polymer resins for industrial anti-corrosion and weather-resistant coatings. Its chemical stability enables applications subject to severe chemical or environmental stress, with formulation under strict regulatory compliance for workplace and environmental safety.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • GHS/CLP for Classification, Labeling & Packaging of Substances
    • ASTM D5201 Standard for Chemical-Resistant Coating Systems
    • ISO 12944 for Protective Paint Systems

    Typical usage ratio

    • 0.8–2.3 wt% within the total resin solids, optimized through accelerated weathering and corrosion resistance tests for each end-use formulation

    Downstream process integration

    • Dispersed in pre-polymer mixture before crosslinking, then included as a functional comonomer during resin synthesis

    Final product types

    • Chemical tank lining coatings
    • Automotive and aerospace exterior coatings
    • Architectural anti-graffiti finishes

    5. Analytical Reference Standards Production

    Analytical laboratories and reagent manufacturers use this pyrrole derivative as a structurally defined reference compound for LC-MS and NMR method validation. Its unique fluorinated aromatic profile enables calibration and qualitative analysis of complex sample matrices, conforming to global analytical reagent standards.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for reference material producers)
    • ISO/IEC 17025:2017 (Testing and calibration laboratories)
    • USP General Chapter <11> (Reference Standards)
    • Good Laboratory Practice (GLP) Guidance Documents

    Typical usage ratio

    • Specified as a primary or secondary reference at 0.1–1 mg/mL for LC-MS calibration, with concentration adjusted per analytical sensitivity requirements

    Downstream process integration

    • Prepared as a certified solution or solid standard, supplied to analytical laboratories for batch validation and quality control

    Final product types

    • Certified reference material vials
    • Calibration mixes for mass spectrometry
    • Analytical method validation kits

    6. Specialty Fluorinated Ligand Synthesis for Catalysis

    Chemical manufacturers employ this compound in the preparation of fluorinated ligand scaffolds, which serve as key components in metal-catalyzed cross-coupling and C–H activation platforms. Its electronic effects influence catalyst selectivity and life cycle, supporting scale-up trials in fine chemical and process chemistry sectors with strict batch traceability requirements.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Good Manufacturing Practice for Fine Chemicals (voluntary standards)
    • Compliance with Responsible Care® chemical management
    • Documentation per global chemical inventory requirements (e.g., TSCA, REACH)

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to metal precursor, optimized per catalyst loading and performance requirements

    Downstream process integration

    • Reacted with phosphine or nitrogen ligating agents to provide customized fluorinated ligand structures, introduced in situ in catalyst screening and process development

    Final product types

    • Pd, Ni, or Cu ligated catalyst complexes
    • Specialty catalyst kits for organic synthesis
    • Catalysis screening libraries for process optimization
    Free Quote

    Competitive 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole – Built on Experience, Trusted in Application

    Proudly Made by the Manufacturer: Our Journey with 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole

    Decades of work in fluorinated aromatics have taught us that every molecular tweak brings out a world of difference in performance and reliability. Producing 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole starts not with a catalog entry, but deep in the benchwork—optimizing reaction conditions, refining purification, and committing to raw material purity because anything less leads to unpredictable batches and wasteful downstream headaches. We take this synthesis seriously, and can track every run from reactor to finished vial.

    Over countless pilot lots and scale-ups, we found that the double trifluoromethyl groups at the 3 and 5 positions on the phenyl ring are anything but cosmetic. They push electron density, shift the reactivity profile, stand up to oxidative stress, and change the way this compound partners in coupling reactions. In the pyrrole scaffold, those fluorinated arms amplify stability without locking down the core functionalities chemists rely on. We watch the sharp NMR signatures light up at each stage, reminding us why this molecule stands apart.

    Some customers only care about seeing “high purity” or “meets specification” on a label. We live in the world behind that phrase, refining work-ups, repeatedly filtering, drying under stringent conditions, checking for trace water and byproducts that could sideline a run in a hurry. Tight melting point ranges and consistently clean chromatograms are the norm, because anything drifting from target purity simply gets rejected and reworked. Having control from the very beginning—chemical selection, apparatus maintenance, solvent handling—builds reliability you can test in every gram.

    Tangible Differences: How the Structure Sets Our Compound Apart

    In practice, chemists notice the dual trifluoromethyl substitution right away. Unlike simpler pyrrole derivatives, the 3,5-bis(trifluoromethyl) aryl ring brings real-world value. In ligand synthesis, this motif can drive selectivity at catalytic centers, tune electron flow in organometallic frameworks, and offer new handles for further functionalization. Medicinal chemistry teams have shown interest for reasons that go beyond academic curiosity: the effectiveness of the trifluoromethyl group in improving metabolic stability, membrane permeability, and even target affinity is well-documented. Adding two of them to a phenyl ring joined to pyrrole on the nitrogen turns an otherwise routine scaffold into a specialized tool.

    The presence of those CF3 groups also transforms the material’s physical profile. Fluorinated aromatics require more nuanced storage, since they can be both more volatile and less polar than their hydrogenated peers. We pay close attention to packaging, using amber glass and airtight seals to guard purity. This means your product arrives ready for reaction, not for troubleshooting. Years on the drying line have shown us that any slight exposure to air or trace acids can cause subtle shifts in appearance or reactivity—so we preemptively test and document these vulnerabilities.

    Some laboratories source “similar” pyrrole derivatives and run into headaches: inconsistency from lot to lot, byproduct signatures clogging sensitive HPLC methods, or small residuals that only show up in stringent downstream screening. Our process minimizes these risks. Doing the synthesis ourselves keeps the process transparent, the workflow reproducible, and the staff accountable. When a customer from a pharmaceutical team calls and asks about a specific impurity profile, we provide details, batch data, and the synthetic path—because we know exactly what went into the flask.

    Real-World Applications and the Value of Trustworthy Quality

    Manufacturing teams and R&D chemists bring us some of their toughest challenges. In collaborative projects focusing on drug discovery, polymer development, or catalysis, we have seen this compound occupy a unique niche. It stands as a bridge between the electronic advantages of pyrrole systems and the beneficial effects of multiple trifluoromethyl groups on pharmacokinetic properties. Computational models predict, but it’s the real reaction flasks—run under tight, reproducible conditions—that tell the real story.

    Many researchers buy basic pyrroles as building blocks and then try to introduce fluorinated groups later in their sequence. They end up with unpredictable yields and troublesome purification steps, because incorporating CF3 groups late in the process can lead to a mess of partially substituted products, leftover reagents, and purification headaches. We provide a robust, pre-assembled 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole so that teams can dramatically shorten route scouting and focus on the next functionalization. The final product from our reactors saves hours, sometimes days, in iterative development cycles.

    For those in material science, we’ve seen this compound slot into specialty polymers, liquid crystals, and advanced surface treatments. Its electron-deficient nature lets formulators fine-tune solubility, hydrophobicity, and light absorption properties. Our own test labs have observed that even slight shifts in starting material purity can drag down device performance, leading to costly time spent on post-synthesis clean-up. By providing high-purity product, fully documented, we help safeguard process reproducibility and scale-up confidence.

    Facts that Shape the Day-to-Day – Our Experience as the Producer

    Routine production never means complacency. Every new lot cycles through extensive quality controls: from incoming raw material verification, to continuous in-process checks, through to final NMR and HPLC analysis. Each step is logged, every operator follows detailed protocols, and inspections happen at every turn. Years spent in manufacturing fluorinated organics have taught us that leniency at any stage translates to trouble down the line—missteps show up in purity, stability, or solubility, and nobody wants surprises at a late stage of their own synthesis.

    Our teams field detailed technical questions about handling and long-term storage. We recommend keeping sealed vials under inert conditions, ideally in low-humidity spaces, since fluorinated aromatics react differently than their non-fluorinated analogs. Chemists working in air-sensitive domains can source product from us with reliable specifications and supporting analytical data. Every batch ships with real spectra, not generic data sheets, because data matters in troubleshooting and method development. Open lines of communication with those using our material in bench or pilot-scale settings lead to regular feedback and incremental process improvements.

    In larger-scale manufacturing, even processes that run smoothly in 1-gram scale can break down in the reactor. Pressure spikes, issues with phase separation, or impurities that sailed under the radar in milligram quantities can torpedo whole runs. Direct experience as the manufacturer allows us to share troubleshooting insights—from solvent selection, to temperature ramp rates, all the way to safe waste handling for halogenated byproducts.

    Continuous Evolution – Improving Quality and Solving Problems

    We do not rest on our initial process, even for well-validated products. As fluorinated intermediates become more essential in new chemistries, regulatory and quality expectations rise. Our staff keeps close tabs on evolving analytical methods, refining detection of low-level impurities, and developing new purification workflows. Batch traceability forms a cornerstone of our business, not just as a compliance box to check, but because it shields our downstream partners from avoidable risk.

    Feedback cycles tightly into our manufacturing ethos. We consult colleagues in medicinal chemistry who stress the importance of not just nominal purity but eliminating specific types of contaminants. Even trace halogenated side-products may affect bioassay outcomes or trigger false positives. Our QC teams constantly develop new gradient methods, monitor for unexpected shadow peaks, and keep documentation current and accessible. Analytical transparency makes it possible for product adopters to plan syntheses with real data, not assumptions.

    As we scale up for larger contracts, equipment limitations and throughput demands prompt targeted investments. New drying ovens, improved filtration systems, and solvent recovery apparatus respond to the real-world demands of batch production. Many operational headaches vanish when maintenance logs, parts replacement schedules, and calibration routines are followed consistently—lessons learned from long nights in front of malfunction-prone pumps and ovens.

    Downtime and wasted raw materials cost more than money; they sap staff morale and delay partners' timelines. We have implemented cross-training for both synthesis and QA/QC. Chemists who run the reactions also interpret the spectra, so there is ownership and understanding at every phase. Problems don’t get buried—they drive new trials, fresh approaches to impurity management, and clear communication channels between our labs and customer teams.

    Differences Set by True Manufacturing Expertise

    Some competitors supply 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole by contracting the work to third parties or mixing lots from varied sources. Batch-to-batch variability, unknown stabilizers, or adulterants can sneak in along long supply chains. We manage our own raw materials from the beginning, select suppliers with care, and keep slack out of inventory management. Expired or poorly stored intermediates never enter our production line.

    Direct synthesis under our roofs delivers peace of mind to procurement managers, synthetic chemists, and scale-up teams. Any problems that emerge get addressed rapidly and directly. We are not left calling down a chain of subcontractors—it’s our technical staff on the phone, pulling batch records, reviewing analytical results, and devising corrective action if something strays from spec. Years of customer feedback and real-world troubleshooting form the backbone of our quality assurance system.

    Quality is not a static target but a living process, getting sharper based on what we see, test, and hear from partners. Our control over the synthesis, work-up, and final product release means product that matches the data—stable under defined conditions, free from known contaminants, and delivered with an analytically proven profile.

    Supporting Healthy Innovation: Offering Solutions, Not Just a Product

    As trends shift in medicinal chemistry, new applications for fluorinated pyrrole derivatives emerge every year. This pushes us to innovate both in our synthesis and in the ways we support research teams. We offer detailed support, sharing reaction hints drawn from our years of scale-up experience. Chemists in early-stage discovery appreciate discussions around solvent systems, temperature control, and troubleshooting strategies, since few publications dive into the practical hurdles of working with advanced fluorinated intermediates.

    On the industrial side, production lines face pressure to adapt quickly. Documentation on prior batches, analytical archives, and validated methods cut development time and minimize costly uncertainty. We know from experience that a consistent, traceable supply chain can make or break a high-stakes campaign. Whether synching to Good Manufacturing Practice or fulfilling local compliance requirements, our history as a direct manufacturer lets us adapt to shifting regulatory environments with confidence.

    Problems do not always show up in Day 1 testing. Our approach keeps communication channels open, so teams know they can reach us with questions, concerns, or troubleshooting needs weeks or months down the road. By focusing on reliability and transparency, we build repeatable success—project after project, gram after kilogram.

    Conclusion: Building on Knowledge, Delivering Real Value

    Producing 1-[3,5-Bis(Trifluoromethyl)Phenyl]Pyrrole is an ongoing process of learning, tweaking, and investing—one that only truly experienced manufacturers can maintain at a consistently high level. Those double CF3 groups add more than molecular weight; they introduce tangible differences that ripple through electronic, physical, and functional properties. Each batch reflects years spent mastering the subtleties of fluorinated chemistry—from the first flask to the final, signed-off analytical report. We stand by the product, its performance, and the commitment we bring to each partnership.

    Whether supporting innovation in life sciences, materials chemistry, or advanced catalysis, we bring focus, skill, and accountability to every step of the process. Our promise is simple—supply quality, back it with experience, and keep improving. Trust built on transparency and proven process forms the foundation of our work.