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4-(Trifluoromethyl)Pyridine

    • Product Name 4-(Trifluoromethyl)Pyridine
    • Alias 4-(Trifluoromethyl)pyridine
    • Einecs 221-136-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    451117

    Chemical Name 4-(Trifluoromethyl)Pyridine
    Cas Number 2224-89-5
    Molecular Formula C6H4F3N
    Molecular Weight 147.10 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 145-146 °C
    Melting Point -27 °C
    Density 1.299 g/cm3
    Refractive Index 1.416
    Purity Typically ≥98%
    Flash Point 47 °C
    Solubility Slightly soluble in water, soluble in organic solvents

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

    Packing & Storage
    Packing A 100 mL amber glass bottle with a screw cap, labeled "4-(Trifluoromethyl)Pyridine," includes hazard warnings and handling instructions.
    Shipping 4-(Trifluoromethyl)pyridine is shipped in tightly sealed, chemical-resistant containers, clearly labeled according to hazardous material regulations. The packaging ensures protection against moisture, sunlight, and physical damage. During transit, it is handled as a hazardous chemical, requiring appropriate documentation and compliant shipping methods to ensure safety for handlers and the environment.
    Storage 4-(Trifluoromethyl)pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep it away from heat, sparks, open flames, and incompatible substances such as strong oxidizing agents. Use secondary containment to minimize spillage risks. Ensure storage in accordance with local chemical regulations and guidelines.
    Application of 4-(Trifluoromethyl)Pyridine

    Applications of 4-(Trifluoromethyl)Pyridine in Industrial Manufacturing

    4-(Trifluoromethyl)Pyridine is a highly specialized heterocyclic intermediate that enables downstream synthesis in pharmaceuticals, agrochemicals, advanced polymers, and specialty electronic materials. Our manufacturing facility supplies this compound to leading industry players relying on consistent quality and traceability.

    1. Pharmaceutical API Intermediates

    Pharmaceutical manufacturers use 4-(Trifluoromethyl)Pyridine as a key building block for the development of new-generation active pharmaceutical ingredients, including kinase inhibitors and central nervous system agents. The trifluoromethyl group introduces metabolic stability and enhances bioavailability in multiple drug candidates. Our facility delivers high-purity product that integrates directly into multi-step synthetic routes, typically through nucleophilic aromatic substitution or palladium-catalyzed coupling, serving both pilot and commercial-scale API production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP/NF monograph requirements for impurities and residual solvents
    • EU GMP Part II standards for intermediates handling
    • REACH Registration for pharmaceutical intermediate use in Europe

    Typical usage ratio

    • Mol ratio varies 0.85–1.2:1 vs. the next reactant in final API pathway
    • Adjusted based on desired yield and impurity thresholds in pilot and validation runs
    • Batch scale: 10–100 kg per campaign, adjusted for process step reactivity
    • Process adjustment on molar input based on API crude isolation yield

    Downstream process integration

    • Fed into the initial condensation or nucleophilic substitution step
    • Participates in palladium-catalyzed coupling or bromination steps
    • Integrated pre-final step for API core structure formation
    • Quality controlled by HPLC/GC and residual solvent analysis post-purification

    Final product types

    • Small molecule kinase inhibitors
    • Central nervous system pharmaceuticals
    • Experimental anti-infective agents
    • Advanced cardiovascular drug candidates

    2. Agrochemical Synthesis

    Downstream agrochemical manufacturers select 4-(Trifluoromethyl)Pyridine as a core intermediate in the development of modern crop protection products such as herbicides and specialty insecticides. The electron-deficient pyridine ring, combined with fluorine incorporation, improves activity and persistence. Our product supports process routes involving aryloxypyridine synthesis and Suzuki–Miyaura cross-coupling reactions, fitting agrochemical plants' multistage production lines.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • China GB/T 1606-2019 for pesticide intermediate quality
    • ISO 9001:2015 quality management for chemical plants
    • OECD Principles of Good Laboratory Practice for product development

    Typical usage ratio

    • Applied at 0.9–1.1 equivalent in cyclization or cross-coupling steps
    • Plant campaigns: 50–300 kg/production batch, depending on target pesticide output
    • Proportion fine-tuned based on active ingredient loading in final formulation
    • Scaled for continuous or batch synthesis according to downstream capacity

    Downstream process integration

    • Introduced during early-stage intermediate coupling reactions
    • Used in Grignard or organolithium addition for arylated analogs
    • Purified by distillation or extraction prior to main chain extension
    • Integrated with catalyst and ligand systems for selectivity control

    Final product types

    • Pyridine-based selective herbicides
    • Trifluoromethylated insecticides for broad-acre crops
    • Advanced fungicide intermediates
    • Seed treatment actives with fluorinated scaffolds

    3. Electronic Specialty Chemicals

    Manufacturers in the electronics sector utilize 4-(Trifluoromethyl)Pyridine in the synthesis of specialty materials for electronic displays and organic semiconductors. The fluorinated pyridine structure imparts unique dielectric and electron mobility properties, supporting the formulation of advanced liquid crystal compounds and organic field-effect transistor materials. Processing involves precision cross-coupling and functionalization stages, where chemical purity robustly supports downstream performance requirements.

    Industry compliance standards

    • IEC 61249-2-21 (Requirements for base materials in printed electronics)
    • RoHS Directive (Restriction of Hazardous Substances)
    • REACH SVHC assessment for specialty electronic chemicals
    • ISO 14001:2015 for environmental management during manufacture

    Typical usage ratio

    • 0.05–0.2 molar fraction in functional monomer blends
    • Integrated 5–12% by weight in special liquid crystal mixtures
    • Exact charge tailored for desired polarity and charge mobility in OECTs
    • Multi-stage processes: total annual consumption 300–2000 kg per production cycle

    Downstream process integration

    • Introduced during monomer synthesis for further functionalization
    • Used in final polymerization or molecular alignment steps
    • Blending and purification under nitrogen to prevent side reactions
    • Stringent QC by NMR and elemental analysis to verify structure

    Final product types

    • Organic light-emitting diode (OLED) display materials
    • Liquid crystal compounds for advanced display technologies
    • Organic semiconductors for thin-film transistors
    • Printable electronics with tailored dielectric properties

    4. High-Performance Polymer Synthesis

    Production facilities manufacturing advanced engineering polymers use 4-(Trifluoromethyl)Pyridine to introduce fluorinated aromatic moieties in custom polymers. This approach enhances thermal and chemical resistance, vital for specialty coatings and membrane production. During synthesis, the pyridine ring acts as a reactive functional handle, allowing step-growth or chain polymerization with co-monomers under controlled conditions.

    Industry compliance standards

    • ISO 9001:2015 for quality management in polymer production
    • ASTM D3368 for elemental analysis of specialty polymers
    • EU Regulation (EU) No 10/2011 for plastic materials intended for food contact
    • UL 94 Flammability Standard for polymeric materials

    Typical usage ratio

    • 2–10% by mole relative to aromatic comonomer for targeted fluorine content
    • Weight-by-weight composition: 1–5% in specialty coatings or films
    • Adjusted based on required hydrophobicity and end-use specification
    • Process scale: 20–200 kg/batch for membrane and coating lines

    Downstream process integration

    • Introduced after initial precursor polymerization or polycondensation step
    • Blending with specific monomers for tailored architecture
    • Purification through precipitation prior to extrusion or casting
    • Processed under inert atmosphere to ensure end-group fidelity

    Final product types

    • Fluorinated barrier membranes
    • Chemical resistant coatings for aerospace and electronics
    • Thermally stable films for fuel cell applications
    • Specialty fibers and laminates with high performance attributes
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    Certification & Compliance
    More Introduction

    4-(Trifluoromethyl)Pyridine: Factory Perspective on a Key Organic Building Block

    The Chemical Behind Countless Possibilities

    On our production floor, 4-(Trifluoromethyl)Pyridine gets the attention of our most meticulous chemists. The molecule, known to veteran organic chemists as 4-CF3-pyridine, shows up as a sharply defined colorless liquid, sometimes appearing faintly yellow when produced in bulk. As a manufacturer, we value its distinct smell and easily measurable density as signs of good batch quality, making identification fast and straightforward throughout production.

    Model and Physical Features

    The primary model we prepare for the open market sits at a purity level greater than 99%, a benchmark our reactors and distillation columns hit regularly thanks to automated feedback systems and vigilant staff. Moisture-sensitive checks, gas chromatography, and NMR give us the confidence to stamp each drum with our logo. From a handling perspective, despite the volatility of the trifluoromethyl group, our final product stores safely in steel or lined drums as long as they stay sealed.

    Its molecular formula, C6H4F3N, forms the basis of discussion with project partners. The trifluoromethyl group, set at the fourth position on the pyridine ring, is what chemical engineers look for during quality audits and structure confirmation. This electron-withdrawing group distinguishes the compound’s reactivity; that’s why requests for alternatives from seasoned chemists rarely surface unless a process absolutely demands a different substitution pattern.

    What Sets This Molecule Apart

    Years of batch production remind us that not all pyridines perform the same in the hands of a process chemist. The CF3 group, attached by direct fluorination or halogen exchange in our reactors, adds a sturdy steric hindrance and shifts the electron density around the aromatic ring. Compared to pyridine itself or other alkyl- or halogen-substituted pyridines, this variant behaves very differently in directed ortho-metalation and cross-coupling reactions. Its use seldom results in unwanted side product formation, a headache for anyone running scale-up reactions downstream.

    Countless times, we’ve discussed with pharmaceutical teams how 4-(Trifluoromethyl)Pyridine lets drug candidates pass metabolic screens that would trip up non-fluorinated analogues. The trifluoromethyl group resists oxidation and survives under harsh biological and process conditions. As a result, inclusion of this motif helps medicinal chemists boost their compound’s in vivo stability. In agrochemical synthesis, the story unfolds similarly – pest control agents demand precisely this resistance to breakdown, and our process lines have adjusted to offer large-scale, consistent production.

    Application and Technical Uses

    Many customers arrive at our gates searching for a reagent with robust performance in nucleophilic aromatic substitution (SNAr), cross-coupling, and functional group transformations. From our experience, 4-(Trifluoromethyl)Pyridine fills this role as predictably as any workhorse in the plant. We watch hundreds of kilos leave our warehouse each quarter, bound for teams building block libraries for drug discovery.

    During scale-up trials, chemists in our pilot plant have found that this compound handles well under both batch and continuous flow conditions. In some syntheses, such as the Suzuki–Miyaura or Buchwald–Hartwig couplings, the electron-withdrawing CF3 not only accelerates desired couplings but also cuts down on competing side reactions. We’ve collaborated with researchers switching from 2- or 3-substituted trifluoromethylpyridines who note the drastic difference in regioselectivity and yield when moving to our 4-substituted variant.

    Outside pharmaceuticals, polymer researchers order this pyridine for incorporating fluorinated backbones into specialty plastics and coatings. The CF3 group locks in hydrophobicity, thermal stability, and chemical resistance, properties driving next-generation material innovation. We watched a customer develop fluorinated polyvinylidene fluoride (PVDF) blends, noting that monomeric impurities dissolve quickly away thanks to the clean nature of our product. Electronic manufacturers rely on 4-(Trifluoromethyl)Pyridine as well; this pyridine’s stability in strong acids and bases sets it apart from less robust heterocycles.

    Quality Comparison and Production Consistency

    Compared to commercial stocks offered by trading firms, our 4-(Trifluoromethyl)Pyridine comes with traceable records from synthesis to delivery. Batch records remain open for customer audits, showing environmental controls, yield variances, and analytical runs every step of the way. Some batches endure more stringent endotoxin and elemental impurity checks for regular customers sending our reagent straight into GMP validated routes. We rely on in-house expertise to spot early signs of batch drift, saving downstream clients from compounding purity issues.

    From hands-on experience, batches from third-party traders often exhibit minor yet persistent impurities—dimers, halide precursors, or heavy-metal residues. In our own processing, the closed-loop reactors and specialized catalyst beds put a hard stop to these risks, supporting steady yields and consistent physical characteristics. The product leaves our warehouse ready for direct use in process development without requiring further distillation or laborious purification steps that eat up profit margins and delay timelines.

    Handling and Storage Considerations

    Day-to-day, our operations avoid open handling. 4-(Trifluoromethyl)Pyridine can volatilize and give off an acrid odor if left uncapped, something our warehouse team knows well from early experiences with hand-filled sample bottles. We stick to sealed transfer lines and inert gas blankets, lessons learned from costly evaporation losses during the early years. Frequent inventory cycles and real-time environmental monitoring keep moisture at bay and maintain batch quality, especially during warmer months when bulk drums might otherwise sweat.

    No one working with this compound forgets the hazards of skin contact – a feature echoed across pyridine derivatives. Proper barrier gloves, fume hoods with local exhaust, and quick cleanup supplies surround each loading bay. Customer teams touring our site often remark on the contrast between our containment routines and those commonly seen in small-scale or trading operations, reminding us that the upfront investment pays back through happy, repeat customers confident about the quality they source.

    Addressing Common Issues and Market Expectations

    Many companies get tripped up in meeting regulatory registrations for new chemical entities, especially for molecules with the CF3 tag. Our compliance and analytical teams spend significant resources navigating registration requirements—REACH, TSCA, and other global notification schemes. We regularly update our dossiers, guided by evolving restrictions on fluorinated compounds, to ensure ongoing supply flows smoothly across borders.

    Clients occasionally request low-residual solvent variants or pressing needs for ultra-low heavy metal batches. Instead of pushing these questions back, our technical team works shoulder-to-shoulder with development chemists to custom-tailor purification runs or adjust column designs. Our chemists understand that small molecules like 4-(Trifluoromethyl)Pyridine sit at inflection points in process chemistry, where even parts-per-million impurities ripple through the next five or six synthetic steps. Small decisions made at the factory translate directly to the bottom line across a customer’s R&D budget.

    From a factory bench viewpoint, the biggest pain point tends to be supply chain delays during peak demand. Since 4-(Trifluoromethyl)Pyridine feeds into high-value end products, a shortfall on our line means ripple effects through pharma and agrochemical output for clients on tight deadlines. To head off such bottlenecks, we lock in year-round raw material contracts and maintain serviceable spare equipment on site. A culture of continuous improvement, shaped by regular audits and customer feedback, underpins the reliability clients now expect from every outgoing drum.

    Supporting Evolving Innovation

    Feedback loops between our technical support staff and development chemists speed up real-world application development. A recent case involved a customer developing kinase inhibitors, who needed fresh insight on protecting groups compatible with the trifluoromethyl motif. Our group, working from a position of hands-on process experience, recommended a new deprotection strategy, cutting two steps from their workflow and saving weeks of optimization.

    Years spent refining reaction conditions have taught us where the boundaries sit for this compound: parts of the process benefit from gentle oxygen exclusion, and careful monitoring for side products like trifluoromethylaniline ensures peace of mind for synthesis managers. Troubleshooting crystallization issues during formulation, we highlighted how changes in solvent grade or storage conditions impact the purification of sensitive downstream intermediates. Bringing together knowledge from both early research and late-stage scale-up, the product improves steadily, reinforcing its status as a cornerstone in the chemist’s toolkit.

    Global and Environmental Concerns

    Responsible stewardship demands foresight. Over recent years, environmental scrutiny over fluorinated compounds has grown. While 4-(Trifluoromethyl)Pyridine isn’t flagged as a high-priority persistent pollutant, we still follow strict guidelines covering effluent handling and solvent recycling. Our in-house waste treatment facility neutralizes pyridine residues before discharge, capturing organofluorine species and sending the majority of process waste for high-temperature incineration. Customers sourcing our material often note their auditors’ comfort with our documented, enforceable controls.

    Reducing the environmental impact of syntheses that use this chemical involves more than safe waste handling. By concentrating on yield optimization and byproduct minimization, our chemists help keep the management of fluorinated waste within industry norms. Partnerships with academic researchers and technology innovators occasionally produce new, greener catalysts or alternative reaction pathways, which we assess in pilot runs before shifting them into full-blown production.

    Customers from outside the region deal with transportation risks linked to hazardous goods. Our logistics and regulatory team walks them through paperwork and training, aiming for full transparency about the transit and storage risks. Shared long-term partnerships mean quicker responses to customs queries and less risk of accidental detainment at docks.

    Differentiate in a Crowded Market

    Among the range of pyridines, the 4-(Trifluoromethyl) variant draws the repeat business and long-term contracts. While other substituted pyridines circulate widely, their chemical and physical quirks rarely line up with the strict needs of pharmaceutical R&D or specialty polymer synthesis. We find some clients arrive with experience using cheaper halogenated pyridines, drawn in by their upfront cost savings. After their first run with our trifluoromethyl compound, they see the differences as side reaction rates drop, downstream purification gets easier, and final product reproducibility beats their initial expectations.

    Fluorine chemistry presents non-trivial hazards and technical challenges, often requiring investments in special handling equipment and advanced analytical techniques. Our plant’s history with sustained, high-volume trifluoromethyl chemistry gave us a head start over generalist chemical manufacturers. By mastering the subtle art of controlling reagent stoichiometry and strictly isolating water-reactive intermediates, the process pushes the boundaries of both safety and scale. These advantages surface directly in the quality difference between material made by specialists versus importers or jobbing traders.

    Our regular clients know to request certificates of analysis and batch-specific spectral data, usually delivered electronically along with their shipment. Having real spectra in hand—proton and fluorine NMR, GC-MS, water content, and assay results—means process changes or new applications can launch without weeks lost to internal re-testing. That accessibility shortens timelines and builds confidence between the bench and the factory floor.

    Challenges and Solutions from a Manufacturer’s Viewpoint

    Pandemic-induced supply disruptions a few years ago pressed us to rethink raw material sourcing. With the global fluctuation in fluorine and pyridine precursor availability, our plant switched to dual-source procurement and grew on-site storage so lines could run through periods of upstream uncertainty. It became clear that communication with logistics partners and real-time inventory tracking—not just in the plant, but across the broader supply chain—made the difference between smooth delivery and empty customer shelves.

    Genuine factory expertise translates to problem-solving agility. Equipment failures, process upsets, and unplanned regulatory audits hit every experienced manufacturer eventually. Our learning: robust process controls, frequent preventive maintenance, and a culture of visible corrective action ensure continuity and reduce unplanned downtime. By openly sharing lessons learned from each near-miss or process deviation, staff awareness improves and risks shrink.

    For clients ramping up production at their own sites, we regularly consult on tank storage, transfer systems, and personal protective equipment suited to this compound’s volatility and potential health hazards. Years of in-house use, including accidental exposures and rapid remediation drills, have shaped our protocols. Our training tips get passed to downstream handlers along with the product, shrinking injury rates and boosting regulatory compliance.

    Driving Progress Through Partnership

    Real progress in specialty chemical manufacturing springs from close connections between supplier and user. Long-term relationships with R&D chemists and production engineers ensure that feedback isn’t lost in translation. From batch consistency checks to development of new derivatives, user insights shape the next iteration of our 4-(Trifluoromethyl)Pyridine. We welcome pilot batch modifications and experimental runs with customer process teams present on site—the kind of flexible, transparent operation not often seen at trading firms or multinationals focused on bulk commodities.

    Every year, requests surface for novel fluorinated heterocycles as customers look to expand or fine-tune their product portfolios. With our in-house expertise honed on 4-(Trifluoromethyl)Pyridine, we offer design input and scale-up experience so that new candidates reach production targets quickly. This collaborative approach translates directly into faster regulatory clearances, less rework, and ultimately, quicker market launches.

    The Role of Trust in a Specialized Portfolio

    Our credibility rests on consistent delivery, technical depth, and real-world knowledge. Customers repeatedly cite the transparency and detailed technical support offered—attributes forged through years troubleshooting side reactions and navigating supply chain challenges side by side with users. This stands in contrast to the more transactional approach common among intermediaries, who often lack the tools or the institutional memory to solve deep-rooted process issues.

    Each feedback loop, product tweak, and logistics improvement ties back to the unique properties of 4-(Trifluoromethyl)Pyridine. The product has grown from a simple reagent to a linchpin across the projects that drive industry forward. If you walk our plant, the attention paid to this one molecule mirrors the attention we give to every bottle, drum, and tanker rolling out the gate, bound for the next round of innovation across chemistry, materials, and life sciences worldwide.