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3,5-Bis(Trifluoromethyl)Iodobenzene

    • Product Name 3,5-Bis(Trifluoromethyl)Iodobenzene
    • Alias 1-Iodo-3,5-bis(trifluoromethyl)benzene
    • Einecs 238-242-6
    • 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

    418571

    Productname 3,5-Bis(Trifluoromethyl)Iodobenzene
    Casnumber 328-81-2
    Molecularformula C8H3F6I
    Molecularweight 355.01 g/mol
    Appearance White to off-white solid
    Meltingpoint 41-44°C
    Boilingpoint None (decomposes)
    Density 1.93 g/cm³
    Purity Typically ≥98%
    Synonyms 1-Iodo-3,5-bis(trifluoromethyl)benzene
    Smiles FC(F)(F)c1cc(I)cc(C(F)(F)F)c1
    Solubility Soluble in organic solvents such as dichloromethane, acetone
    Storageconditions Store at 2-8°C, protected from light and moisture
    Ecnumber 206-399-7

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

    Packing & Storage
    Packing Amber glass bottle, 25 grams, tamper-evident sealed, chemical-resistant cap, labeled with hazard pictograms, supplier, purity, and safety information.
    Shipping 3,5-Bis(Trifluoromethyl)Iodobenzene is shipped in tightly sealed containers, protected from light, heat, and moisture. It is classified as a hazardous chemical, possibly requiring UN identification and compliance with international and local transport regulations. Proper labeling, documentation, and handling instructions are included to ensure safety during transit.
    Storage 3,5-Bis(Trifluoromethyl)Iodobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat, ignition sources, and incompatible materials such as strong oxidizers. Protect from light and moisture. Use appropriate chemical storage cabinets and ensure containers are clearly labeled. Handle with suitable protective equipment to prevent contact and inhalation.
    Application of 3,5-Bis(Trifluoromethyl)Iodobenzene

    Applications of 3,5-Bis(Trifluoromethyl)Iodobenzene in Industrial Manufacturing

    3,5-Bis(Trifluoromethyl)Iodobenzene serves as a key intermediate in advanced chemical synthesis, enabling precise molecular modification in high-value downstream markets. Our manufacturing consistently achieves controlled purity, which critical industries depend on for formulation stability and end-product performance. Below we outline real-world applications across multiple sectors, detailing industry-specific standards, usage ratios, integration points, and the actual products that benefit from this compound.

    1. Pharmaceutical Active Ingredient Synthesis

    High-performance halogenated aromatics like this compound provide essential building blocks for matrix elaboration in targeted pharmaceutical APIs, especially in the design of fluorinated heterocyclic and anti-viral agents. Our material ensures controlled substitution patterns required for process route customization, supporting end-use compliance and batch reproducibility.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monograph 2.2.24
    • US FDA 21 CFR Part 210/211 GMP for pharmaceuticals
    • Chinese Pharmacopoeia standards for fluorinated intermediates

    Typical usage ratio

    • 0.8–2.5 molar equivalents per API synthesis step, adjusted based on target substitution architecture, batch process volume, and desired fluorination density

    Downstream process integration

    • Added during palladium-catalyzed cross-coupling or halogen exchange, typically in the late-stage functionalization phase after core heterocycle assembly; direct charge into reactor vessel after initial substrate activation

    Final product types

    • Fluorinated kinase inhibitors (oncology agents)
    • Anti-influenza novel nucleoside analogues
    • High-barrier anti-viral therapeutics
    • Active pharmaceutical ingredient (API) precursor libraries

    2. Advanced Agrochemical Ingredient Manufacturing

    Specialized trifluoromethylated iodobenzenes enable effective scaffold modification in crop protection molecule synthesis, especially within next-generation herbicide and fungicide programs. Direct halogen introduction at aromatic sites enhances metabolic stability and increases crop selectivity margins for downstream agro-industrial users.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Technical Material and Formulations
    • ISO 17025 Laboratory Accreditation for pesticide synthesis
    • GB 20810-2006 (China) Maximum Residue Levels for crop protection chemicals
    • REACH Regulation (EC) No 1907/2006 for agro-intermediate registration

    Typical usage ratio

    • 0.5–2.0 eq. per key halogenation reaction; typically 1.2 eq. for selective trifluoromethyl introduction, adjusted based on substrate reactivity and target active

    Downstream process integration

    • Charged during Suzuki or Buchwald coupling to assemble final active ingredient, used as halogen donor in the later stages of agrochemical synthesis route

    Final product types

    • Selective herbicide molecules (e.g. HPPD inhibitors)
    • Fluorinated pyrazole fungicides
    • Insecticidal actives with aromatic halogenation
    • Crop-protection active ingredient concentrates

    3. High-Purity OLED Intermediate Synthesis

    Materials for organic electronic manufacturing require precisely structured aromatic intermediates to achieve device reliability and luminance standards. This fluorinated iodobenzene offers backbone stabilization in OLED light-emitting material synthesis, contributing to molecular rigidity and charge transport characteristics in the final emitting layer compounds.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronics chemicals
    • IEC 61249-2-21:2017 Halogen content in electrical materials
    • ISO 9001:2015 Quality Management Systems for electronics chemical supply
    • IECQ QC 080000 for Hazardous Substance Process Management

    Typical usage ratio

    • 0.2–1.0 eq. per key coupling reaction in light-emitting layer intermediate formation; ratio depends on targeted molecular motif and required degree of fluorination for final device application

    Downstream process integration

    • Introduced in the late-stage organometallic cross-coupling during synthesis of emitter precursors; direct charge after catalyst and ligand addition to minimize side reactions

    Final product types

    • Blue and green OLED emitter intermediates
    • Charge-transport layer additives for OLED displays
    • Organic electroluminescent paste precursors
    • Flexible display material feedstocks

    4. Specialty Liquid Crystal Monomer Production

    Downstream liquid crystal manufacturers employ fluorinated aromatic monomers to attain desired birefringence and dielectric properties for next-generation display panels. Incorporating the iodobenzene moiety at controlled ratios enhances rotational viscosity and thermal stability for temperature-stable liquid crystal mixtures.

    Industry compliance standards

    • IEC 61249-2-21 Halogenated aromatic compound restrictions
    • ISO/TS 16949:2009 (for automotive-grade LC production)
    • JEITA Standard ED-5002A for LC display chemicals
    • REACH requirements for monomeric intermediates

    Typical usage ratio

    • 0.1–0.7 eq. depending on the target mesogen’s molar mass and desired ratio of trifluoromethyl units in the overall mixture; precise formulations tuned by phase transition analysis

    Downstream process integration

    • Added in the aromatic substitution stage when forming the rigid core structure; usually introduced post-initial mesogen backbone assembly for final property adjustment

    Final product types

    • Twisted nematic (TN) LC monomers
    • Fast-switching liquid crystal additives
    • High-temperature LC mixtures for automotive panels
    • LC intermediates for advanced tablet and smartphone displays

    5. Fluorinated Polymer Additive Synthesis

    Polymer manufacturers utilize halogenated benzene intermediates to modulate surface energy, hydrophobicity, and dielectric parameters of fluorinated copolymer additives. This raw material integrates into side-chain functionalization protocols, delivering targeted performance in specialty coatings and engineered plastic formulations.

    Industry compliance standards

    • ISO 14001 Environmental Management for polymer synthesis plants
    • UL 94 Flammability ratings for plastic additives
    • ASTM D638 Standard for tensile properties of plastic resin
    • REACH Annex XVII for chemical safety in sold polymers

    Typical usage ratio

    • 0.3–1.2 wt% relative to total batch, customized by end-use hydrophobicity and surface tension targets in the finished resin or coating

    Downstream process integration

    • Injected during the side-chain introduction phase or as part of the copolymerization catalyst feed for reactive extrusion or batch emulsion polymerization

    Final product types

    • Antifouling fluorinated paints
    • Low-friction engineering plastics
    • Dielectric polymer films
    • Stain-resistant surface coating additives
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 3,5-Bis(Trifluoromethyl)Iodobenzene: Precision Chemistry for Advanced Needs

    Our Perspective as Chemical Manufacturers

    Every time we open a reactor for another batch of 3,5-Bis(Trifluoromethyl)Iodobenzene (CAS 328-32-7), we come back to the same conclusion—this molecule rarely leaves a chemist’s bench unremarked. Our team handles the process from raw material sourcing, through precision halogen exchange, right down to the purity check and final dry-off. We’re not brokers passing products through; our staff sweat over each kilogram, aware that trace contaminants or inconsistent quality will throw off entire syntheses further down the line. In our lab journals, no two lots ever look exactly the same, but the best ones share one trait: reproducibility.

    Product Profile & Chemistry that Matters

    3,5-Bis(Trifluoromethyl)Iodobenzene stands out with its chemical formula of C8H3F6I and a molecular weight of 355.01 g/mol. Years ago, shifting from conventional iodobenzene derivatives to this bis(trifluoromethyl) analog opened a new chapter in our product line. High selectivity in coupling reactions, robustness under demanding conditions, and a reliably sharp melting point became essential demands from research and scale-up customers. Through consistently tight process control—including vacuum purifications and repetitive analysis by GC and NMR—our manufacturing line achieves a product purity fitting the more stringent applications in medicinal chemistry, agrochemical research, and electronics.

    Why Trifluoromethylation Changes the Game

    Traditional iodobenzenes underperform where stability, reactivity, and functional group tolerance become bottlenecks. Replacement by 3,5-bis(trifluoromethyl) substituents delivers more than higher electronegativity. The perfluoroalkyl groups not only add steric protection—important in cross-coupling—but also stabilize the aryl iodide against side reactions like oxidation and dehalogenation. In our hands, the shelf stability alone reduces off-spec returns and improves reliability, especially for customers pushing Pd- or Cu-catalyzed reactions to the limit.

    The wet and dry rooms at our plant see several aromatic iodides, but this one, with its two CF3 groups at the meta positions, delivers a different level of performance. We’ve watched researchers adopt it for Suzuki-Miyaura, Sonogashira, and Buchwald-Hartwig reactions where competing products—plain iodobenzene or even para-substituted versions—fell short due to instability or limited substrate scope. Order logs often spike near grant application deadlines, a strong signal that innovation begins with reliable sourcing.

    Physical Characteristics and Batch Integrity

    Take a look at the crystalline material on the bench: colorless, fine, and free-flowing, with a melting point typically in the 56–58 °C range. The odor is negligible, a welcome property for lab staff. We monitor the products under ambient and inert atmosphere for any sign of decomposition, always watching for batch-to-batch consistency. Over time, we’ve fine-tuned the drying process to deliver crystals that pack tightly and do not absorb moisture—even in humid regions. This isn’t a happy accident. Getting a homogenous product requires real effort at each distillation and recrystallization step.

    Every drum, from our smallest research-scale jars to the high-volume lots destined for process chemistry partners, ships with a certificate linked to actual QC data—not a generic template. Some customers have shared stories of using material from other suppliers that arrived clumpy, discolored, or containing persistent traces of byproducts. By talking directly with chemists in academic and industrial labs, we closed these gaps. Our technical team remains on-hand to clarify batch records and share analytical spectra so anyone down the pipeline can cross-check purity and identity without delay.

    What Sets Our 3,5-Bis(Trifluoromethyl)Iodobenzene Apart

    The advantage begins upstream. Starting with high-purity 3,5-bis(trifluoromethyl)aniline as the building block, we run carefully controlled diazotization and Sandmeyer processes to minimize overreaction or contamination from side products. Precursor screening and reagents are never chosen by price alone; we’ve rejected batches that technically retained “spec” but yielded less robust final products. Our analytic lab doesn’t just sample end materials. We check intermediates throughout the batch to flag issues as early as possible, reducing waste and avoiding rework that would otherwise slip into the final drum. FTIR, NMR, and GC are run more often than required, giving us real confidence when product documentation states a 99-per-cent minimum purity standard—backed by actual retention times and peak integrations.

    On the packaging floor, environmental factors play a real role. This compound asks for double-sealed containers, lined with non-metallic barriers, to avoid contact reactions that cheaper packaging can trigger. We’ve learned that labeling is more than regulatory formality; chemists working on night shifts or in high-throughput screening need unambiguous, resistant labels that survive multiple glove changes and even chemical splashes.

    End-Use Insights Gleaned from Decades in the Field

    Peering back through customer records, the real shift in this product’s profile started about twenty years ago, as fluorinated aromatic compounds drew greater attention for their properties in complex molecule synthesis. Medicinal chemists streamlining routes to novel pharmaceuticals turn to this aryl iodide for immediate halogen exchange, CF3 introduction, or further functionalization. These applications expose the shortcomings of alternative products: higher byproduct load, less consistent reactivity, or lower tolerance for sensitive functional groups.

    We see it in the agrochemical sector as well. Synthesis pipelines for advanced crop protection products increasingly favor substrates that support aggressive chemistry without caving to side-reactions. Here, every contamination event spells headache in the field. Our process control, by cutting down on unknown impurities, lets customers go straight from small-scale trial runs to process validation—no need to revisit the synthetic route at the last minute due to failed reactions.

    In the materials sector, high-performance polymers and specialty electronics demand raw materials with both electronic resilience and chemical traceability. The two CF3 groups impart a unique blend of hydrophobicity and electron-withdrawing character. This combination enables better performance in liquid crystal display components, OLED intermediates, or specialty fluorinated coatings where lesser aryl halides often fall short. Feedback from industrial partners regularly emphasizes not just product quality but also batch documentation, since downstream audits depend on our certificates being as robust as the product itself.

    Comparisons with Other Halogenated Aromatics

    Chemists balancing reactivity and cost often compare 3,5-bis(trifluoromethyl)iodobenzene against more traditional halobenzenes: iodobenzene, bromobenzene, even pentafluoroiodobenzene. Each serves in cross-coupling or functionalized arene syntheses, yet the selectivity profile, reactivity rate, and stability look significantly different.

    Plain iodobenzene reacts quickly but lacks both the stability and substrate scope offered by bis(trifluoromethyl) derivatives. Brominated analogs are widely available but require higher temperatures, result in lower yields, or suffer more side-reactions in Pd-catalyzed couplings. Substrates like 1,3,5-trifluorobenzene introduce electron-deficiency but miss out on the combination of bulk and reactivity from the iodo and CF3 grouping.

    We’ve run in-house head-to-head trials for pilot customers, demonstrating increased product lifetime on the shelf and in solution when using our product. This is not just an incremental improvement. In batch fermentation or high-value molecule campaigns, the switch to 3,5-bis(trifluoromethyl)iodobenzene can mean the difference between two chemical steps or five, lower yields or reliable product every run. Our technical reports detail not just each result, but which conditions bring out the greatest advantages, based on actual plant and R&D experience.

    Supporting Advanced Synthesis: Real-World Lessons

    We’ve stayed in close touch with users tackling demanding cross-coupling chemistry to learn what really matters. Feedback from process chemists underscores practical points rarely listed in textbooks: reliable solubility in common organic solvents, absence of sticky residues in glassware, and rapid filtration out of aqueous work-ups. The iodo group, positioned in concert with CF3 units, plays a meaningful role in substrate activation—allowing researchers to access intermediates that would otherwise break down or escape.

    Some suppliers have tried shortcutting with variants that substitute only one CF3 (at the 4-position), or offering higher halide content at a discount. These alternatives often result in fouling downstream processes, increased purification costs, or unpredictable outcomes. We made an early decision to commit to rigorous sourcing and full synthetic control, limiting the range of byproducts and impurities to trace levels. Analytical work consistently confirms this, and returning customers often cite lower troubleshooting needs and decreased instrument downtime.

    Advocating for Data Transparency

    Our philosophy favors radical transparency. Every customer receives access to chromatograms and NMR spectra for every delivered lot. This practice, rare among upstream manufacturers, grew out of conversations with frustrated research teams who had to chase down sample provenance or piece together reaction histories. We also invite technical questions—our manufacturing and analytical chemists respond directly, not through sales intermediaries.

    Material data stays only as good as its real-time traceability. We maintain retrievable, electronic batch records dating back years, in line with updated regulatory and auditing expectations for ‘track and trace’ authenticity. While some competitors lean on reputation, we let our open-door data policy keep everybody honest and aligned.

    Sustainability, Safety, and Continuous Improvement

    Handling organoiodines, especially at scale, demands more than just good practice—it calls for relentless vigilance. From fume extraction around aromatic reagents to triple-checking halide waste management protocols, lessons in process safety have come through decades of improvement. We committed to closed-system transfers when early runs revealed the risk of vapor buildup. Temperature monitoring and pressure release protocols prevent any chance of runaway reactions or off-gassing incidents.

    Our plant continuously reviews and updates solvent recovery, byproduct capture, and thorough end-of-life treatment for all halogen-containing reagents. Environmental responsibility cannot end at the factory door; downstream users face mounting regulatory requirements covering halogenated waste. By sharing best practices in waste minimization and solvent selection, we help users stay ahead of future compliance standards.

    Reliable Supply Chains—Direct from Manufacturer

    Current market tension has strained global supplies for specialty fluorinated aromatics. As true chemical manufacturers—not resellers or repackers—we control both sourcing and final blending. This direct oversight shields our product lines from sudden shocks or speculative pricing swings. Over the years, strong relationships with fluoroaromatic suppliers and halogen specialists have given us resilience—customers count on material arriving as requested, unadulterated and matched to prior lots. No detours, no last-minute substitutions, no surprise delays.

    Constant Dialogue with Our Partners

    We operate as partners with researchers and process teams using our 3,5-bis(trifluoromethyl)iodobenzene. Open feedback loops help us define and troubleshoot challenges—whether it’s solubility in less-common green solvents, or quantifying trace metal contaminants for new regulatory filings. Our facilities can tailor purification steps, documentation style, or packaging to specific project requirements. This isn't a service added on, but an ongoing relationship where we act not just as suppliers, but as team members committed to long-term project success.

    A few years ago, a process chemist requested alternate container closures to minimize exposure in a new cleanroom facility. Within weeks, we modified our packing line, sourced compatible closures, and performed accelerated stability checks under simulated conditions. Similar cases pop up across the workflow, reinforcing the lesson that flexibility improves outcomes for everyone. By refining feedback into our daily operations, we keep our standards both high and responsive.

    Looking Ahead: Expanding Potential

    As demand for advanced building blocks grows, we continue to scale production capacity, reinvest in process automation, and support research into new functionalized derivatives. The chemistry community benefits when industrial partners provide not just high-quality materials, but also a context for application and improvement. Our engineering and technical teams remain alert to shifts in catalyst needs, regulatory frameworks, and emerging technologies requiring specialized aromatic halides.

    In recent years, more customers have diversified into photoredox, nickel-catalyzed, and flow chemistry approaches. Our support does not end at routine batch production—we collaborate on pilot implementations and solvent compatibility, all while maintaining strict controls on residual metals, water, and trace halides. We recognize that no two application environments look identical, so we treat every inquiry not as a transaction, but as a possible avenue for technical progress.

    Conclusion

    Our journey developing and producing 3,5-bis(trifluoromethyl)iodobenzene goes far deeper than producing and shipping a commodity. Every synthesis, batch record, and analytic test reflects decades of learning and a commitment to continuous reliability. By controlling our processes, documenting our chemistry, and staying in dialogue with end users, we make sure each shipment contributes to the advancement of chemistry, not just to a warehouse inventory. If your work demands a halogenated aromatic that keeps pace with demanding research and development ambitions, our team is ready to partner with you—expert to expert, bench to bench.