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3-(Trifluoromethoxy)Iodobenzene

    • Product Name 3-(Trifluoromethoxy)Iodobenzene
    • Alias 3-Iodo-1-(trifluoromethoxy)benzene
    • Einecs 617-205-4
    • 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
    VTB
    Specifications

    HS Code

    848152

    Name 3-(Trifluoromethoxy)Iodobenzene
    Synonyms m-(Trifluoromethoxy)iodobenzene
    Cas Number 827-78-7
    Molecular Formula C7H4F3IO
    Molecular Weight 288.01 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 91-93 °C at 15 mmHg
    Density 1.78 g/cm³ at 25 °C
    Purity Typically ≥98%
    Smiles COC(F)(F)(F)c1cccc(I)c1

    As an accredited 3-(Trifluoromethoxy)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 containing 10 grams of 3-(Trifluoromethoxy)iodobenzene, with tamper-evident cap and chemical hazard label affixed.
    Shipping 3-(Trifluoromethoxy)iodobenzene is shipped in tightly sealed containers under cool, dry conditions, protected from light and moisture. As a hazardous material, it is classified for ground or air transport with appropriate labeling and documentation, following regulations for organic halide chemicals to ensure safe, compliant delivery.
    Storage 3-(Trifluoromethoxy)iodobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing or reducing agents. Protect from moisture and direct sunlight. Store under inert gas (such as nitrogen) if recommended, and keep away from heat and open flames.
    Application of 3-(Trifluoromethoxy)Iodobenzene

    Applications of 3-(Trifluoromethoxy)Iodobenzene in Industrial Manufacturing

    3-(Trifluoromethoxy)Iodobenzene occupies an essential role as an advanced building block in fine chemical synthesis, agrochemical intermediates, pharmaceutical development, specialty polymer modification, and advanced material research. Our manufacturing expertise allows integration into varied industrial pipelines with control over purity, trace residues, and reproducibility. Below, we detail the main sector-specific applications and related technical requirements we regularly support for downstream partners.

    1. Pharmaceutical Active Ingredient Synthesis

    This compound serves as a strategic halogenated intermediate during the synthesis of novel small-molecule drug candidates. It enables the introduction of both trifluoromethoxy and iodo functional groups into advanced intermediates for targeted substances, especially for oncology and central nervous system agents. QC control around trace metal content and consistent batch reactivity remains critical for customer process validation. Integration usually occurs at the heterocycle functionalization or arylation stages.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF & European Pharmacopoeia standards on impurity control
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • Chinese Pharmacopoeia Residual Solvents & Metals sections

    Typical usage ratio

    • Applied at 0.2–1.5 molar equivalents versus limiting reagent depending on the stage of intermediate assembly; adjusted for route-specific yield and contamination risk.

    Downstream process integration

    • Charged during aryl halide palladium-catalyzed cross-coupling or nucleophilic aromatic substitution reactions as part of Phase 2 or 3 API route development.

    Final product types

    • Small-molecule target cancer therapies
    • Central nervous system drug candidates
    • Anti-infective preclinical compounds
    • Patent-protected heterocyclic structures

    2. Agrochemical Intermediate Manufacturing

    Downstream agrochemical formulators incorporate this iodoarene when producing functionalized herbicides and fungicides. It acts as an aryl donor for cross-coupling reactions that generate novel active ingredients with enhanced metabolic stability and bioavailability. High batch consistency and low residual iodide are significant for fit-for-use evaluation. The step is typically situated after linker installation or as an advanced intermediate modification.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Agricultural Pesticides (JMPS)
    • ISO 9001:2015 Quality Management for agro intermediates
    • REACH (EC) No 1907/2006 pre-registration if imported into or used in Europe
    • Chinese National Standards for Agricultural Chemicals (GB/T)

    Typical usage ratio

    • Applied at 1.0–1.3 equivalents in coupling protocols, based on bioactive moiety complexity and efficiency of subsequent purification steps.

    Downstream process integration

    • Utilized in Ullmann-type or Suzuki-Miyaura coupling after initial core assembly; featured in late-stage derivatization to introduce electron-withdrawing groups.

    Final product types

    • Trifluoromethoxy-substituted fungicides
    • Herbicide candidates with increased bioactivity
    • Pre-formulated agrochemical concentrates
    • Stabilized pesticide precursors

    3. Fluorinated Polymer Additive and Modification

    Chemical engineers and formulators select this compound as a reactive additive for introducing fluorinated aromatic functionality into specialty high-performance polymers. This yields polymers and copolymers with improved hydrophobicity, chemical inertness, and dielectric properties for demanding environments. Control of additive concentration and reaction completeness determines product reproducibility. This step normally takes place during backbone functionalization by crosslinking, or as a monomer modifier in free-radical or step-growth polymerizations.

    Industry compliance standards

    • ASTM D882 Standard Test Method for Tensile Properties of Thin Plastic Sheeting
    • ISO 9001:2015 for specialty polymer manufacturing
    • RoHS (EU Directive 2011/65/EU) for electrical and electronic applications
    • UL 94 Flammability for plastics, when relevant

    Typical usage ratio

    • Blended at 0.1–2.0 wt% in the polymer feed or as determined by desired end-use property change, molecular weight aims, and compounding method.

    Downstream process integration

    • Added in the prepolymerization stage or during extrusion compounding with compatibilizer for electronic coating and specialty film applications.

    Final product types

    • High-frequency electronic insulator films
    • Fluorinated engineering resins
    • Low-permeability packaging
    • Thermoplastic blends with heat and solvent resistance

    4. Advanced Materials R&D and OLED Intermediate Synthesis

    Research teams utilize this compound in the synthesis of novel aryl fluorides for next-generation organic light-emitting diode (OLED) emitters and advanced electronic materials. The trifluoromethoxy and iodo functionalities allow specific substitution patterns critical for tuning charge transport, photoluminescence, and thermal stability in display and lighting technologies. Manufacturers benefit by targeting ultra-pure input, low trace impurity, and consistent isotopic purity during scale-up. The compound enters late in the molecule construction to introduce selective fluorination and aryl iodide linkages.

    Industry compliance standards

    • IEC 62341-5-1 OLED Display Safety
    • ISO 14644 Cleanroom Standards for contaminant control in R&D
    • RoHS (EU Directive 2011/65/EU) for electronic and display chemicals
    • Company-internal QC protocols for photophysical material reproducibility

    Typical usage ratio

    • Dosed at 0.2–2.0 equivalents in the key arylation or fluorination steps, based on molecular design and luminescence requirement optimization.

    Downstream process integration

    • Charged in the final or penultimate synthetic step for OLED small molecule or polymeric emitter development, prior to purification and device fabrication.

    Final product types

    • Blue and green OLED emitters
    • Organic semiconducting layers
    • Specialty photonic films
    • Custom fluorinated arene labs hits for further material evaluation
    Free Quote

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    Certification & Compliance
    More Introduction

    3-(Trifluoromethoxy)Iodobenzene: A Reliable Fluorinated Intermediate Direct from Our Factory

    What We Bring to Chemists: Consistency and Control in Advanced Intermediates

    Sourcing high-value intermediates often means balancing purity, responsiveness, and real-world process expertise. We have built our business on synthesizing building blocks for demanding customers, and 3-(Trifluoromethoxy)Iodobenzene demonstrates what direct-from-manufacturer relationships provide to innovative labs and industry projects. As the team that actually puts the chemistry into motion, we know how important each batch is, whether it’s destined for pharmaceutical research, material science, or agrochemical development. The 3-(Trifluoromethoxy)Iodobenzene we supply under model number 3TFMOB-I directly reflects our approach: strict process oversight, routine QA audits, and the flexibility to deliver what research or scale-up needs call for.

    Product Profile: 3TFMOB-I, Manufactured with Control from Start to Finish

    The core feature of this compound—its trifluoromethoxy group—gives more than just a difference in reactivity or stability versus simpler halogenated benzenes. For many years, we have worked to tighten our synthesis so customers don’t deal with troublesome byproducts, heavy metal carryover, or color contamination. Our process builds the molecule through controlled substitution, protecting functional group integrity and hitting a purity target that doesn’t just show up in the certificate of analysis, it’s proven by real test reactions in-house and by the feedback from repeat research partners. What separates our material is a predictable ratio of isomers, minimal moisture load, and the ability to customize impurity profiles if a customer needs it for sensitive organic transformations.

    Why the Trifluoromethoxy Moiety Matters in Organic Synthesis

    There are plenty of substituted iodobenzenes out there, but the trifluoromethoxy group changes everything from lipophilicity to oxidative stability. Medicinal chemistry teams report longer in vivo half-lives and higher metabolic resistance with these fluorine-rich aryl building blocks. Our partners in crop protection and advanced materials point to the improved hydrophobic character and electron-donating nature, creating new handles for tuning reactivity in their creative syntheses. When quality control asks what makes our 3TFMOB-I worth specifying on a synthetic route, our engineers point out real gas chromatography and NMR data that track down even trace halogen byproducts—the kind of fouling agents that can disrupt downstream reactions.

    Expert Perspective from the Manufacturing Line

    Our plant operators and process chemists work directly with each batch, so we catch changes in viscosity, color, or odor faster than a remote warehouse or purely trading middleman. There’s no disconnect between an order placed and the hands producing it. Our chemists have refined reactor temperature controls and phase separation techniques for this material—improving yields over the years and keeping our operation cleaner than the waste-heavy older methods you sometimes see in less controlled settings. We track every reaction step, maintain detailed batch records, and perform random spot-checking for process drift. This hands-on oversight translates into reliability when customers scale up from gram to multi-kilogram quantities.

    Purity as a Function of Process, Not Just Policy

    Over time, we learned that off-the-shelf purity claims don’t mean much if microscopic contaminants still sabotage a multi-step synthesis. Every order of our 3-(Trifluoromethoxy)Iodobenzene comes off the line with batch-specific spectral analysis attached, not a generic “≥98%” claim. Our in-house purification runs use modern distillation systems and sorbents vetted against real-world synthetic reactions. If a customer flags an impurity that threatened their process, we bring it back into our own validation pipeline to dig up the source—be it a marginal solvent residue, a catalyst trace, or even packaging static. There’s no substitute for this level of vertical integration when complex, patent-sensitive molecules are on the line.

    Use Cases in Medicinal Chemistry and Materials Science

    The main groups using this product work at the forward edge of organic synthesis. Medicinal chemistry teams need intermediates that fit tight SAR programs and deliver reproducible yields in heterocycle formation, cross-coupling, and C–H activation reactions. With the aryl iodide handle and the electron-withdrawing trifluoromethoxy group, researchers step into Suzuki-Miyaura, Negishi, Stille, and Buchwald–Hartwig couplings that standard iodobenzene or trifluoromethoxybenzene simply can’t deliver. The selective reactivity allows for C–C and C–N bond formations under milder conditions. For teams working on new pesticides or specialty polymers, the extra fluorines bring oxidative resistance and moisture stability, forming products that last through field trials or outdoor exposure. Materials scientists tell us they value the fluorinated moiety for boosting hydrophobic coatings and tuning dielectric properties.

    Solving Real Supply Chain Worries: In-House Production, Not Sourcing

    Our factory never depends on resellers or brokers to secure our intermediates. That means if supply chain disruption hits a key precursor, we are the ones who find the workaround. Over the last few years, this made a huge difference for pharma producers who watched prices jump or lead times expand. We control logistics, documentation, and shipping direct from our site, so nobody is left waiting on slow customs delays or ambiguous sourcing. When inventory is low for a key project, customers trust our operations team because we know exactly where our raw materials and finished goods are sitting, and we chop days or weeks off fulfillment by avoiding the third-party shuffle.

    Difference from Standard Iodobenzenes and Other Substituted Benzenes

    It only takes one failed coupling or misstep in late-stage synthesis to realize that not all aryl iodides behave the same. Standard iodobenzene works in basic transformations, but lacks the tuning the trifluoromethoxy group brings to oxidative resistance, electronic effects, and selectivity. Monofluorinated or standard methoxy analogues don’t push biological or materials performance anywhere near as far, especially in endpoints demanding metabolic resistance, soil persistence, or tunable solubility. Handled by a manufacturer like us, these differences mean less time spent troubleshooting unexplained NMR peaks, fewer batches needing expensive repurification, and more projects sticking to aggressive timelines.

    Example: Cross-Coupling Successes and Lessons

    Every month, a different research team calls us to recount where “off-the-shelf” material let them down. In one memorable case, a pharmaceutical client planned a multi-step sequence using commodity 3-(Trifluoromethoxy)Iodobenzene from multiple distributors. Yields drifted unpredictably, some reaction partners dropped out, and impurity load made purification challenging. By contrast, direct supply from our reactors gave them a material profile matching their tightest specifications—moisture under 150 ppm, no observable N-heteroaromatic byproducts, and IR spectra confirming pure assignment of the trifluoromethoxy group. Their process snapped back into control, saving months of lost time. These case studies drive our team to keep pushing purification and batch consistency further, never settling for “good enough” when it means risking a key customer’s IP or product timeline.

    Specification Isn’t Just a Sheet—It’s a Commitment

    The specs on paper—appearance, melting point, GC area percent, and trace element content—all matter, but our team has learned the real authority comes from comparative test reactions. Every large batch gets split, with one portion retained for in-house benchmarking against peer materials. We work up a complete set of HPLC, GC-MS, and NMR data and track how these numbers correspond to outcomes in model phosphorylation, amination, and palladium-catalyzed processes. Some clients with ultra-sensitive endpoints want to see this, and some only care about baseline analytics. Either way, our records hold up under repeat audits and scientific scrutiny.

    Supporting Custom Research Demands

    It’s not uncommon for advanced research groups to press us for slight variations, be it in isotopic labeling, form factor, or packaging environment. Unlike bulk resellers, our process chemists design modifications inline with our batch reactors—so unique intermediates, deuterated analogues, or unusual particle size grades come directly from the same validated process as our standard material. This translates into less risk of cross-contamination and reduced downtime for new route validation. Our ethos relies on the expertise of custom synthesis, as well as clear dialogue between our lab and the customer. By providing this interaction at the factory level, we let research programs shift, pivot, and accelerate without losing sight of core quality standards.

    Safety, Environmental Impact, and Responsible Handling

    Producing specialty fluorinated intermediates comes with safety and environmental responsibilities, and we treat that as part of our job—not a regulatory checkbox. Our team operates closed-loop reactors with robust scrubbing systems for vented byproducts. Every solvent or waste stream gets tracked, neutralized, and, where possible, recycled or destroyed in our own treatment units. Packaging is designed for both chemical separation and resilience in challenging climates, keeping containers intact from our facility to your lab bench. Our plant engineers conduct regular risk assessments and safety reviews, and we incorporate lessons from every batch into protocols for safe transfer, storage, and disposal. We believe that downstream customers benefit when hazardous chemistry is handled upfront, not pushed down the line.

    Direct Collaboration: From Research Bench to Production Scale

    Customers start their journey with tiny research quantities—sometimes just a few grams to validate a new coupling or derivatization. As processes succeed, the order jumps to multi-kilo, or even hundreds of kilos for pilot launch. Because we operate with our own reactors and QA lab, we transition with you—screening for process impurities at each scale, performing shelf-life and storage studies, and tuning the crystallization or isolation procedures as the volume grows. No batch history is ever lost, and you always know who handled your material, not just where it shipped from. Our chemists keep lines open for problem-solving, whether it means running a fresh analytical scan, tweaking purification, or revisiting a process condition based on your latest feedback.

    The Bottom Line: Trust in Real Chemical Manufacturing

    3-(Trifluoromethoxy)Iodobenzene stands as more than just a reagent—it's the product of years of process development, real-time troubleshooting, and collaborative problem-solving between our chemists and yours. Labs working directly with manufacturers build certainty into their synthesis and free up energy to innovate, rather than chase down hidden contamination, supply chain gaps, or vague sourcing. Our day-to-day experience with handling, refining, and scaling advanced building blocks like 3TFMOB-I gives our customers results that go beyond spec sheets. Reliable material means fewer failed syntheses, faster project turnaround, and data you can stand behind in front of auditors, regulators, or peer review. Sourcing from our operation gives you a partner that knows the risks and delivers confidence at every step.

    Ongoing Commitment to Innovation and Transparency

    We never stop improving our process. Each year brings updates to our QA systems, investments in analytical equipment, and deeper partnerships with supply partners for raw fluorine sources. The science drives us—we watch emerging literature and stay in touch with academic groups exploring new uses for trifluoromethoxy-substituted aromatics. We welcome feedback and problem reports, using them as opportunities to refine process steps and raise the bar on purity and performance. Our direct production model enables fast pivoting, whether it's in anticipation of regulatory changes, new synthetic methodologies, or advances in green chemistry.

    Our Perspective Moving Forward

    Long-term relationships in this industry go beyond pricing or delivery time. They’re built on steady performance, honest communication, and a shared investment in getting results where they matter. Every flask, drum, and vial of 3-(Trifluoromethoxy)Iodobenzene we make represents transparent manufacturing, open process dialogue, and a dedication to helping chemists worldwide achieve their goals without supply-side uncertainty. By delivering a fluorinated building block ready for modern synthesis, directly from manufacturer to your lab, we back every innovation with deep process knowledge and a resolve to make the difference between routine and remarkable chemistry.