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1-Iado-4-(Trifluoromethoxy)Benzene

    • Product Name 1-Iado-4-(Trifluoromethoxy)Benzene
    • Alias 4-(Trifluoromethoxy)phenyl iodide
    • Einecs 629-278-6
    • 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

    407409

    Product Name 1-Iodo-4-(Trifluoromethoxy)Benzene
    Cas Number 873-56-1
    Molecular Formula C7H4F3IO
    Molecular Weight 288.01 g/mol
    Appearance White to off-white solid
    Melting Point 42-44 °C
    Density 1.97 g/cm³
    Purity Typically ≥ 98%
    Smiles C1=CC(=CC=C1I)OC(F)(F)F
    Inchi InChI=1S/C7H4F3IO/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4H
    Solubility Insoluble in water, soluble in organic solvents
    Storage Condition Store at room temperature, in dry conditions
    Synonyms 4-Iodophenyl trifluoromethyl ether

    As an accredited 1-Iado-4-(Trifluoromethoxy)Benzene 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 25 grams of 1-Iodo-4-(trifluoromethoxy)benzene, tightly sealed with a tamper-evident cap and hazard labeling.
    Shipping 1-Iodo-4-(Trifluoromethoxy)benzene is shipped in tightly sealed containers to prevent moisture and contamination. It is classified as a hazardous material and is transported according to international regulations for chemicals, typically by ground or air with appropriate labeling and documentation. Personal protective equipment is recommended when handling upon receipt.
    Storage **1-Iodo-4-(trifluoromethoxy)benzene** should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong bases and strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use chemical-resistant containers, and store in a designated area for hazardous chemicals, following all applicable safety and regulatory guidelines.
    Application of 1-Iado-4-(Trifluoromethoxy)Benzene

    Applications of 1-Iodo-4-(Trifluoromethoxy)Benzene in Industrial Manufacturing

    1-Iodo-4-(Trifluoromethoxy)Benzene supports advanced synthesis in several high-value chemical sectors. As a direct manufacturer, we serve formulators who require strict reproducibility, high purity, and precise feedstock performance in complex organic transformations. The following scenarios highlight how industrial users incorporate this compound at scale, observing sector-specific quality, process, and compliance parameters.

    1. Active Pharmaceutical Ingredient Synthesis

    Pharmaceutical process chemists employ this compound as an intermediate for the preparation of fluorinated aromatic scaffolds in targeted drug molecules. Its incorporation provides a unique combination of halogen and electron-withdrawing trifluoromethoxy functionality, enabling efficient subsequent palladium-catalyzed coupling reactions for complex molecule assembly. Customers require documented batch traceability, impurity profiles, and full regulatory support during scale-up from pilot to commercial API production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF Monograph requirements for related organic solvents/reagents
    • European Pharmacopoeia (Ph. Eur.) General Chapter 5.10 on residual solvents (where relevant to process)
    • FDA and EMA inspection readiness (site and documentation standards depend on customer regulatory pathway)

    Typical usage ratio

    • Mol ratios range from 1.05:1 to 1.5:1 versus primary aryl substrate, adjusted to maximize yield while controlling halide by-products
    • Excess reagent purged in aqueous work-up; detailed stoichiometry determined by each synthesis protocol

    Downstream process integration

    • Fed into Suzuki, Sonogashira, and Buchwald–Hartwig cross-coupling steps for aryl/alkyl/aminated API intermediate synthesis
    • Pre-dissolved in anhydrous organic solvent (e.g., DMF, DMSO, or toluene) for homogeneous catalyst compatibility
    • QC monitoring of tracer iodine impurities and trifluoromethoxy retention throughout process

    Final product types

    • Late-stage fluorinated API candidates (oncology, CNS, antiviral agents)
    • Regulatory filing batches (both preclinical and GMP clinical)
    • Chiral resolved fluorinated drug intermediates
    • Custom fluorinated small molecule building blocks

    2. Agrochemical Intermediate Production

    Plant protection and crop science companies utilize this compound in the multi-step assembly of herbicidal and fungicidal actives. Its distinct substituents offer sites for controlled downstream functionalization, including ether, amine, and organometallic transformations. Operations require segregation to avoid cross-contamination, environmental controls for waste capture, and documentation to meet stewardship and environmental protection obligations during synthesis.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for fine chemical synthesis
    • REACH registration for European supply chain integration
    • Globally Harmonized System (GHS) labeling and MSDS management
    • National agrochemical manufacturing codes (China, India, EU member state according to export jurisdiction)

    Typical usage ratio

    • 1.20:1 to 1.3:1 molar equivalents versus alkylation/amidation reactant, with emphasis on full conversion and minimal waste
    • Variations dictated by targeted molecule (e.g., fungicidal ether or herbicidal amine)

    Downstream process integration

    • introduced after base aromatic skeleton formation, during formation of advanced intermediates
    • utilized in nucleophilic substitution and palladium-catalyzed coupling routes
    • online analytics confirm completion before subsequent derivatization

    Final product types

    • Proprietary pre-emergent herbicide intermediates
    • Broad-acre antifungal crop active ingredients (technical grade)
    • Fluorinated agrochemical research compounds for field trial batches
    • Custom intermediates for third-party crop protection contract manufacturing

    3. Electronic Material Synthesis

    Organic electronics manufacturers adopt this compound for custom synthesis of specialty fluorinated monomers and advanced intermediates in the design of liquid crystal and OLED material systems. The electron-withdrawing groups strengthen thermal stability and tune electro-optical properties. Strict exclusion of metallic and ionic contaminants is mandatory, while documentation for purity profiles and trace element analysis supports the high-reliability applications targeted by downstream customers.

    Industry compliance standards

    • IPC-6012 and IPC-4101 (for relevance to PCB substrate compatibility and purity)
    • RoHS and REACH (pollutant-free and environmental hazard restrictions)
    • Internal customer-facing QC protocols for organic electronic intermediates
    • Documentation for trace metals (ICP-MS, ion chromatography according to customer methods)

    Typical usage ratio

    • 0.8–1.1:1 versus main aromatic core material, typically optimized for conversion efficiency and minimized excess
    • Detailed in joint development agreements; adjusted for direct material cost and post-synthetic purification

    Downstream process integration

    • introduced at late-stage functionalization (electron-transport or hole-transport layer building blocks)
    • applied in stepwise, anhydrous batch processes with in-line spectroscopic verification
    • active transfer under nitrogen to cleanroom-compliant packaging

    Final product types

    • High-performance liquid crystalline monomers (for display applications)
    • OLED aromatic intermediates and conductive polymer blocks
    • Semiconductor-grade organic fine chemicals
    • Specialty resins for high-voltage and electro-optic devices

    4. Advanced Dye and Pigment Manufacturing

    Producers of specialty fluorinated dyes use this compound as a halogenated building block in the design of high-durability pigments and functional colorants. It allows stepwise incorporation into extended aromatic or heterocyclic frameworks, imparting solvent resistance and improved photostability for demanding industrial, textile, and imaging applications. Raw material traceability, batch blending homogenization, and heavy-metal control form the core compliance requirements in this industry segment.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for dyes in the textile supply chain)
    • ISO 9001/14001 for production and environmental management (dye/pigment manufacture)
    • Contact allergen and impurity screening (customer-specific analytical protocols)
    • Compliance with EU REACH Annex XVII for dyes and pigments

    Typical usage ratio

    • 0.7:1 to 1:1 compared to parent aromatic structures, depending on final chromophore structure and desired fluorine loading
    • Ratio set to balance reaction cost versus desired performance attributes

    Downstream process integration

    • Stagewise introduced after initial chromophore skeleton formation, in step with other halogen or sulfonation steps
    • Monitored by HPLC/LC-MS for complete incorporation and purification efficiency
    • Dissolved in controlled solvent blend for color consistency and particle fineness

    Final product types

    • UV-resistant textile dyes (polyester and nylon application)
    • Solvent-stable printing inks for electronics and specialized packaging
    • High-durability imaging pigments for industrial coatings
    • Photoactive dye intermediates for research and development
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    Certification & Compliance
    More Introduction

    1-Iodo-4-(Trifluoromethoxy)Benzene: A Reliable Specialty Building Block for Modern Synthesis

    A Practical Choice in Advanced Organic Synthesis

    Working every day in the field of chemical manufacturing means focusing on reliability and consistency for every batch that leaves the plant. For synthetic chemists looking for a versatile aryl iodide, 1-Iodo-4-(Trifluoromethoxy)Benzene offers a robust solution that supports diverse research and commercial projects. We produce it with a clear eye toward quality and reproducibility, aiming to deliver a material that gives dependable results from lab development through to scale-up.

    Simplifying Cross-Coupling Chemistry

    Much of the demand for this chemical comes from its proven usefulness in palladium-catalyzed cross-coupling reactions. Suzuki, Sonogashira, and Buchwald–Hartwig couplings all benefit from the high reactivity and ease of handling that this compound brings. The trifluoromethoxy group draws interest due to its strong electron-withdrawing properties, which impact reactivity and allow chemists to fine-tune the properties of target molecules, especially in pharmaceutical and agrochemical projects. We focus on batch consistency because we have seen how small impurities can derail an entire research effort, particularly when working with demanding synthetic protocols. Our customers in medicinal chemistry regularly tell us that they choose this compound to access novel fluorinated scaffolds—the trifluoromethoxy group is valued for conferring greater metabolic stability and increased bioactivity.

    The Value of Purity in Research and Production Scale

    Quality control sits at the front line of our process. Specifications for 1-Iodo-4-(Trifluoromethoxy)Benzene follow years of internal refinement, based on feedback from dozens of research collaborations and manufacturing contracts. We deliver it in purity levels above 98%, with typical batches reaching 99% by GC. Rigorous monitoring for byproducts, residual solvents, and elemental impurities takes place, using validated analytical methods. Researchers expect consistency; any deviation in starting materials can introduce unnecessary troubleshooting or failed batches. In our experience, controlling moisture content and iodine impurity levels is especially critical, since these can easily impact downstream reaction yields or catalyst life.

    Choosing the Right Halide: A Case for Iodides

    Some projects might consider bromo or chloro analogues. In our manufacturing experience, the iodine derivative often provides higher yields and smoother conversions under mild conditions. The carbon–iodine bond is weaker and more reactive than its bromide or chloride counterparts, allowing couplings to proceed at lower temperatures and with reduced reaction times. This can matter when working with heat- or sensitive functional groups, or when seeking to improve selectivity. While the cost of the iodide is somewhat higher, the downstream benefits in workflow efficiency and product purity frequently justify the choice. By keeping our process lean and controlling key material inputs, we can keep pricing competitive at both research and production scale.

    Handling, Storage, and Packaging: Experience-Driven Details

    Hands-on production teaches many lessons about safe handling and optimized storage conditions. 1-Iodo-4-(Trifluoromethoxy)Benzene arrives as an off-white to pale yellow crystalline solid. Exposure to light and air can slowly degrade it, which is why we recommend storing it tightly sealed in amber bottles and under inert gas whenever possible, especially for long storage periods. In our facilities, we maintain storerooms at cool and dry conditions, which allows for stable long-term inventory without measurable changes in purity. Small-scale researchers often choose glass bottles with sturdy seals, while commercial customers request bulk packaging in lined drums or high-density polyethylene containers to minimize permeation or contamination risks.

    Observations from Manufacturing: Addressing Practical Challenges

    Scaling up aryl iodide production comes with a unique set of hurdles, especially regarding reagent cost, exothermic reactions, and byproduct management. Our teams have dedicated significant process development time to green chemistry approaches in iodination steps, focusing on mild and selective oxidants and minimizing hazardous waste. Managing exothermic reactions at larger scale demands well-calibrated cooling and strict addition rates. With repeated practice, we’ve reached process controls that allow us to confidently offer kilogram-scale lots with reliable reactivity profiles.

    Waste handling and environmental responsibility rank among our primary concerns. The iodine source and fluorinated reagents produce waste streams with stricter disposal requirements, so we’ve invested in on-site reclamation and safe neutralization systems. By minimizing perfluorinated byproducts at the source, we help our customers meet regulatory guidance and lessen downstream treatment loads.

    Applications and Use Cases

    The primary market for 1-Iodo-4-(Trifluoromethoxy)Benzene lies in complex molecule synthesis. Drug discovery professionals look to it as a building block for small-molecule pharmaceuticals, especially where metabolic stability and strong electron-withdrawing effects are required. The trifluoromethoxy motif, less common in generic offerings, grants unique physicochemical properties compared to non-fluorinated analogues. This enables the development of APIs and advanced intermediates with improved selectivity or bioavailability. In crop science, research teams report using this chemical as a gateway to new herbicidal or fungicidal scaffolds showing improved environmental persistence or efficacy.

    Materials scientists and electronic researchers also find value in the compound. The introduction of a strongly electronegative group onto the benzene ring enables the synthesis of organic semiconductors with better charge-transport properties. The product has played a role in the development of liquid crystal materials, organic light-emitting diodes, and advanced polymers. In each of these applications, exacting demands for purity and reproducibility steer these users toward manufacturers capable of consistent, traceable lot histories.

    Differentiation from Other Aryl Iodides

    A customer with experience substituting plain aryl iodides or even those with simple electron-donating/withdrawing groups quickly sees the difference working with the trifluoromethoxy variant. We produce other iodoaromatics, but the intense electron-withdrawing character of the trifluoromethoxy group changes reactivity, aromatic substitution patterns, and physical properties. Its strong influence can push a sluggish coupling to high yield, or permit the formation of previously unstable motifs. With less polar substituents, downstream intermediates may show lower reactivity, and customers often face more laborious purification processes; the trifluoromethoxy ring helps here by leading to higher selectivity and a distinctive analytical fingerprint.

    Feedback from process chemists often touches on this: reactions featuring 1-Iodo-4-(Trifluoromethoxy)Benzene frequently benefit from shorter purification times and better step yields, since the product's volatility and polarity reduce overlapping byproducts. In practice, this means fewer hours lost on column chromatography and more time spent advancing the project itself.

    Customization and Technical Support: Manufacturer Experience Counts

    After years scaling and shipping specialty chemicals, we have seen that each customer brings a slightly different set of needs. Some request larger crystals for improved filtration; others work with microgram-scale automation and want minimal surface contamination. Researchers in academic, biotech, or Fortune 500 settings approach synthesis with distinct tolerances for solvent content or trace element profile. Our direct involvement in every stage of manufacturing allows us to consult with clients, understand where off-the-shelf specifications work, and where custom batches can close project gaps. Experience in quality control also means we can rapidly analyze and troubleshoot, minimizing lost time when issues arise. This kind of practical, engagement-driven support stands in contrast to one-size-fits-all offerings or drop-shipped intermediates; direct manufacturer discussions matter for fast-moving research pipelines.

    Reliability Through Controlled Manufacturing Practices

    Frequently, end users voice concerns about synthetic intermediates sourced indirectly, due to batch-to-batch inconsistency or undisclosed process changes. By managing everything from raw-material procurement through to finished product packaging and shipment, we maintain clear traceability and accountability. Auditable batch records, frequent in-process controls, and open-chain-of-custody records provide reassurance for regulated applications and for efforts requiring precise reaction modeling. Longevity in the manufacturing space gives us firsthand knowledge about the intricacies that make or break a run, especially for difficult steps such as halogen-metal exchange or directed ortho-metalation.

    Recent Trends: Fluorinated Building Blocks Gaining Prominence

    Demand for fluorinated aromatic building blocks has climbed steadily across research sectors. Regulatory changes and intellectual property trends push for new patent space, and trifluoromethoxy-aryl motifs enable both. End users focus on reaching higher metabolic stability, better oral bioavailability, and new binding interactions. From our vantage point, shipment volumes of 1-Iodo-4-(Trifluoromethoxy)Benzene have grown faster than traditional aryl iodides, and inquiries for kilogram-plus quantities are on the rise. We have responded with expanded reactor capacity, new purification train investments, and continual raw material vetting.

    Chemists favor compounds that let them introduce high-value fluorine atoms early in their synthesis, sidestepping the safety and reactivity complications of late-stage fluorination. By starting from a prefunctionalized aromatic, customers speed up both discovery and manufacturing. Success here depends on traceable, thoughtfully manufactured intermediates—experience proves this again and again when clients come back after faster-than-expected scale-up.

    Continuous Process Improvement

    Each year brings updates in both process chemistry and analytical technology. Our development teams regularly explore new, more selective iodination methods, and review options for minimizing hazardous waste. Analysts vet stronger purification and crystallization tools to push impurity levels lower, while supply-chain managers seek stable, globally sourced raw materials. As regulatory landscapes shift, especially around the use and handling of perfluorinated materials, the manufacturing process needs to evolve. Staying ahead of these trends allows us to keep assurances to our customers, whether they operate in regulated pharmaceutical spaces or frontier materials science.

    The Human Factor Behind the Molecule

    It is easy to overlook the effort that goes into making high-quality specialty chemicals, but as a producer, each bottle, drum, or shipment is the end result of dozens of individual decisions—from raw material selection to packaging integrity checks. The team’s experience allows us to recognize developing industry needs, such as more precise control over moisture content, finer particulate thresholds, or less common packaging sizes. Small details, like preventing cross-contamination during grinding, drying, or liquid transfers, matter at customer labs where each gram becomes a valuable experiment. Our communication with clients both informs our own process refinements and prompts improvements that benefit future users as well.

    Meeting the Modern Demands of Science and Industry

    Serving today’s research and production users means listening closely, responding quickly, and delivering materials that keep projects on track. 1-Iodo-4-(Trifluoromethoxy)Benzene stands as both a technical resource and a case study in how thorough manufacturing matters for the end user’s success. Whether optimizing medicinal chemistry leads or refining new functional materials, this specialty building block continues to find new relevance. Our commitment to robust process control, thorough documentation, and deep customer support has grown out of hands-on experience and the direct feedback loop that only real manufacturing can provide.

    Looking Forward: Innovating Together With Our Clients

    Keeping pace with shifting industry needs requires constant attention to both technical excellence and customer priorities. As demand for fluorinated building blocks grows, so too does the complexity of requirements around purity, regulatory compliance, and supply chain resilience. Collaborating directly with researchers and manufacturers keeps our production flexible and alert to new opportunities for innovation. Experience suggests that close partnerships unlock better chemistry—a philosophy that guides every shipment and every batch. Our team looks forward to supporting the next generation of chemical research, one carefully manufactured product at a time.