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1-Fluoro-3-Iodobenzene

    • Product Name 1-Fluoro-3-Iodobenzene
    • Alias 3-Fluoroiodobenzene
    • Einecs 808-904-9
    • 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

    640272

    Cas Number 559-16-0
    Molecular Formula C6H4FI
    Molecular Weight 238.00
    Iupac Name 1-fluoro-3-iodobenzene
    Appearance Colorless to pale yellow liquid
    Boiling Point 188-190°C
    Melting Point -16°C
    Density 1.833 g/mL at 25°C
    Refractive Index 1.609
    Flash Point 77°C
    Smiles C1=CC(=CC(=C1)F)I
    Inchi InChI=1S/C6H4FI/c7-5-2-1-3-6(8)4-5/h1-4H
    Solubility In Water Insoluble
    Pubchem Cid 12064
    Synonyms 3-Fluoroiodobenzene; m-Fluoroiodobenzene

    As an accredited 1-Fluoro-3-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, sealed cap, hazard labels, and product details with chemical name “1-Fluoro-3-Iodobenzene” on the label.
    Shipping 1-Fluoro-3-Iodobenzene is shipped in tightly sealed containers, compliant with chemical safety regulations. It requires cool, dry, and well-ventilated storage, protected from light and incompatible substances. Transport must align with hazardous material guidelines, using appropriate labeling and documentation to ensure safe handling and delivery. Always check local regulations for specific shipping requirements.
    Storage Store **1-Fluoro-3-iodobenzene** in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, preferably in a chemical storage cabinet designated for organohalides. Protect from light and sources of ignition. Use appropriate personal protective equipment (PPE) when handling, and follow all relevant safety guidelines.
    Application of 1-Fluoro-3-Iodobenzene

    Applications of 1-Fluoro-3-Iodobenzene in Industrial Manufacturing

    1-Fluoro-3-Iodobenzene serves as a critical intermediate in several specialized chemical sectors. Our facility supplies this high-purity product directly for downstream customers integrating it into core synthesis steps, where its unique halogen-substituted aromatic structure brings advantages for selectivity and further functionalization. The following sections present targeted B2B scenarios where our material supports established industrial processes, detailed by sector, standard, process, formulation level, and finished goods.

    1. Pharmaceutical Active Ingredient Synthesis

    Innovators and generics manufacturers employ this compound as an advanced intermediate for synthesis of select API molecules, particularly where fluorinated aromatic cores contribute to improved drug properties. The compound integrates into Suzuki-Miyaura and Buchwald-Hartwig cross-coupling steps, supporting the creation of diverse APIs exhibiting halogen functionalities that influence metabolic stability and receptor binding properties.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US) for pharmaceutical manufacturing
    • EU GMP EudraLex Volume 4 Part II for API starting materials

    Typical usage ratio

    • Employed at 0.7–1.5 molar equivalents relative to the aromatic substrate, adjusted according to specific process mass balance and target coupling yield.

    Downstream process integration

    • Added as a coupling partner in halogen exchange, fluorination, or C-C/C-N bond-forming steps during multi-step syntheses directly preceding API crystallization or isolation.

    Final product types

    • Fluorinated and iodinated API intermediates
    • Target molecule scaffolds for CNS, oncology, or anti-inflammatory drug development
    • Registered finished APIs for further formulation

    2. Agrochemical Aryl Building Block Manufacturing

    Crop protection formulators incorporate this material as a key halogenated aromatic building block for assembling advanced agrochemical actives. It plays a role in constructing molecules featuring specific halogen patterns, essential for tuning bioactivity and stability in field applications. Chlorination or amination reactions, utilizing this intermediate, yield herbicide and fungicide compounds adopted by formulators serving global agriculture markets.

    Industry compliance standards

    • FAO/WHO technical specifications for active ingredients
    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical development
    • REACH registration for industrial intermediates within the European Union

    Typical usage ratio

    • Used at 5–15% of the total mass for target aryl core construction, with exact dosing depending on the downstream synthetic route and target molecule complexity.

    Downstream process integration

    • Introduced during Suzuki coupling or directed ortho metalation followed by halogenation to produce mono- and poly-halogenated aromatic cores prior to formulation.

    Final product types

    • Proprietary fungicide and herbicide technical materials
    • Precursor aryl intermediates for insect growth regulators
    • Active ingredient synthesis for finished EC, SC, and WG crop protection products

    3. Fine Chemical and Specialty Material Synthesis

    Advanced material manufacturers employ this compound to construct complex fluorinated aromatic structures, delivering properties such as increased thermal resistance and chemical inertness. Used in the preparation of liquid crystal monomers, specialty polymers, and advanced surfactants, this intermediate facilitates precision functional group introduction, supporting high-specification end uses in electronics and specialty coatings.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • RoHS 2 compliance for materials used in electronics applications
    • Customer-specific material purity and traceability requirements

    Typical usage ratio

    • Integrated at 1–8% by weight, according to the design specifications for each target specialty compound; composition may be adjusted for desired halogen density or performance characteristics.

    Downstream process integration

    • Undergoes cross-coupling and aromatic substitution to produce customized monomers or advanced intermediates, often followed by controlled polymerizations or resin syntheses.

    Final product types

    • Liquid crystal display intermediates
    • High-performance fluorinated polymers and resins
    • Specialty surfactants with tailored hydrophobic-lipophobic balances

    4. Active Ingredient Intermediate for Imaging and Diagnostic Chemicals

    Producers of diagnostic and imaging reagents utilize this halogenated aromatic as a starting material to synthesize high-purity contrast media precursors and radiolabeling agents. The combination of fluoro and iodo substitutions offers sites for further functionalization, including radioisotope exchange for medical imaging contrast or marker chemistry in preclinical tracer development segments.

    Industry compliance standards

    • ISO 13485:2016 for medical device and diagnostic reagent manufacturing
    • 21 CFR Part 820 (US FDA QSR) for medical grade intermediates
    • European Pharmacopeia (Ph. Eur.) monograph requirements for contrast agents

    Typical usage ratio

    • Introduced at 0.5–2 molar equivalents, precisely measured to enable stoichiometric conversion with radiolabel sources or additional arylating agents for high-purity end products.

    Downstream process integration

    • Reacted in nucleophilic aromatic substitution or coupling reactions prior to isotope exchange or quaternization, forming the core structure of imaging agents before purification steps.

    Final product types

    • Non-ionic iodinated contrast media intermediates
    • Fluoroarene precursors for PET imaging compound synthesis
    • Functionalized markers for life science tracer reagents
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    Certification & Compliance
    More Introduction

    1-Fluoro-3-Iodobenzene: A Practical Toolkit Molecule for Modern Chemistry

    Understanding the Value in Aromatic Building Blocks

    Every molecule in our portfolio plays a defined role in both research and industry. 1-Fluoro-3-Iodobenzene stands out as one of our trusted fine chemicals, recognized for its halogen exchange versatility and robust performance in reaction development. In the past two decades, demand for high-quality halogenated benzenes has increased, tracing directly to the expansion of pharmaceutical discovery, active materials research, and advanced agrochemicals. We witnessed the way this compound helps labs and commercial production teams streamline steps in complex synthesis—an impact that you only appreciate after carrying out pilot reactions and scale-up batches in real, operational settings. These experiences taught us how a single molecule can influence multiple project trajectories, opening pathways not accessible with alternative substrates.

    Real-World Profile of 1-Fluoro-3-Iodobenzene

    As a manufacturer, our approach with 1-Fluoro-3-Iodobenzene starts from selecting the most reliable synthetic route, guided by published protocols and our thirty years of first-hand handling of halogen exchange reactions. The product carries the CAS number 456-29-5, and is supplied as a clear to slightly pale liquid at room temperature. Quality control measures rely not only on NMR but also GC-MS purity checks, because we understand that trace impurities can cause unpredictable effects in cross-coupling and substitution chemistry. The purity exceeds 98% in standard packaging, but we also make specialty grades—always with specific user applications in mind. The model often referenced in catalogues or internal tracking is the empirical formula C6H4FI, molar mass 223.00 g/mol, but specifications focus on what matters: reproducible batch-to-batch quality, and solvent-compliance metrics that satisfy regulatory guidelines.

    Experience-Driven Insights: How Chemists Use This Molecule

    We began producing 1-Fluoro-3-Iodobenzene after observing a repeated need from research groups searching for selective reactivity in aromatic ring transformations. Direct fluorination is rarely straightforward, and the introduction of a fluorine atom ortho or para to additional functional groups often restricts downstream chemistry. This molecule bridges that gap. By harnessing both the electron-withdrawing tendencies of fluorine and the coupling utility of iodine, users unlock Suzuki and Sonogashira couplings, nucleophilic aromatic substitutions, and metal-catalyzed halide exchange—sometimes all in the same campaign. We’ve worked directly with process chemists who noted that the steric placement of the fluorine at the 1-position reduces isomer formation in subsequent steps, giving more predictable product profiles and less post-reaction cleanup. This difference saves sizable time and raw material costs, especially at kilo-lab or pilot plant scales.

    Distinct Features over Standard Haloarenes

    Colleagues often compare 1-Fluoro-3-Iodobenzene to similar benzene derivatives: monohalogenated, difunctional, or mixed-substituent compounds. What sets this molecule apart is not just its halide pattern, but also the interaction between electronic and steric effects that play out during organometallic activation. Using pure iodobenzene limits selectivity. Using fluorobenzene alone rules out certain transformations due to low leaving group ability. The combination in our product brings both reliability and flexibility. We’ve seen some users switch from pure iodobenzenes to the fluoro-iodo scaffold, reporting improved yields in Pd-catalyzed couplings and easier workups. In others, accessing meta-fluorophenyl targets with high regioselectivity has pushed the adoption of this substrate over less specialized isomers.

    Field-Driven Stories: Applications and Challenges

    Our chemical has carved out a distinct space in complex molecule synthesis. Medicinal chemists, especially, use it to construct core scaffolds for kinase inhibitors, new fluorinated pharmaceuticals, and functionalized building blocks found in clinical candidates. We know this not just from journal citations, but from purchasing trends and direct feedback from contract research groups. In advanced materials, we’ve watched R&D teams test 1-Fluoro-3-Iodobenzene as a precursor in OLED dye development thanks to the unique interplay of carbon-halogen bonds with downstream polymerizable units. This comes with specific challenges: the iodine’s reactivity can accelerate undesired side reactions if not well controlled, and the product’s volatility during distillation requires precise process supervision. As manufacturers, we keep these factors in mind by supplying proven stabilization and handling recommendations from our own pilot lines, not just from literature alone.

    Process Experience and the Need for Reliable Supply

    Reproducibility matters as much as raw purity. We learned early that small changes in solvent purity, reaction temperature, or raw reagent source can shift halogenated aromatic chemistry dramatically. Our batches differ from many market alternatives because we invest in purification tiles and closed-transfer distillation systems—a lesson learned after watching open-air processes accumulate contamination over time. Technical staff rely on single-source intermediate control, from raw halogen selection all the way through to final bottling. We do not cut corners or substitute with off-specification lots. This results in tight spectral signatures and lot-to-lot consistency, which our customers have highlighted in feedback surveys. Over time, that consistency supports chemists in extending synthesis planning cycles and shortening analytical turnaround.

    Differences from Blended, Commercial, or Lower-Purity Products

    Some distributors or traders may supply 1-Fluoro-3-Iodobenzene blended with stabilizers, solvents, or low-purity cuts to reduce price. From our experience, these “economical” alternatives rarely serve advanced applications. Impurity profiles create additive risks in cross-coupling chemistry—the bulk of our complaints regarding unknown reaction byproducts trace back to blended or uncontrolled sources. Unlike these alternatives, our material runs through a validated distillation line, with each lot fingerprinted by GC-MS, 1H and 19F NMR, and infrared analysis. In-house chemists accept the same lots as analytical standards for their own R&D. Competitive products may also appear in brown glass with no assurance of controlled exposure, resulting in rapid degradation under high humidity or strong light. We store and pack only by inert-atmosphere bottling and guarantee a defined shelf-life supported by real-time stability data. These operational protocols grew out of troubleshooting failures in customer’s synthetic routes, feeding back insights that now benefit the entire user base.

    Usage in Advanced Synthesis: Lessons from the Bench

    Practical synthesis has taught us that aromatic halogen substitution can create enormous value for functional group installation, especially with late-stage functionalization. Medicinal chemists report using our 1-Fluoro-3-Iodobenzene to generate biaryl motifs by Suzuki coupling, then carrying the intermediate through subsequent fluorination or substitution. As metal-catalyzed methods become more commonplace, having a pure and reactive starting material reduces cycle times and increases successful batch runs—an optimization our team noticed after repeated feedback from kilo-lab operators. Yield losses almost always correlate with off-spec material or inter-batch variation, yet tight process controls and fresh-packaged lots have helped users raise isolated product purity by 5-10% compared to mixed-source material. In the world of natural product synthesis, where every step counts, these improvements brought our customers better final yields and more straightforward purification protocols.

    Guiding Customers Through Problem-Solving

    We take an active role in supporting our users—not only by shipping product, but also by sharing real-life troubleshooting experience. When project timelines depend on consistent reactivity, minor changes in halogen pattern or trace impurity can spell months of lost effort. Several times per year, scale-up teams from pharmaceuticals or fine chemicals approach us with questions about byproduct formation, metallic residue management, or product isolation. Our response draws on data from both internal pilot runs and customer production lines: e.g., switching to anhydrous storage conditions or specifying inert transfer reduces batch-to-batch loss and improves organometallic coupling efficiency. We consider this guidance critical, because it reflects boots-on-the-ground knowledge that rarely appears in peer-reviewed protocols or supplier brochures.

    Benefits in Next-Generation Synthesis and Diagnostics

    With the pharmaceutical and diagnostic industries pivoting towards fluorinated probes, the demand for complex halogenated aromatics continues to climb. Research into PET imaging tracers and new oncology probes draws on the modularity of 1-Fluoro-3-Iodobenzene. The presence of both the fluorine and the iodine increases the synthetic gateway possibilities. Teams today require building blocks that shorten process times and limit hazardous byproducts. We see the reduced environmental footprint as a valuable byproduct of smart synthetic planning. The controlled selectivity delivered by our product feeds directly into projects aiming to minimize side-product formation, cut solvent use, and meet sustainability goals.

    Working Through Supply and Regulation Challenges

    Supplying sensitive aromatic halides means working under changing regulatory expectations and customer needs. We work within established international guidelines and have seen those regulatory requirements shape not just packaging, but also how material is handled during shipping and end use. Over the last decade, new controls on halogenated chemicals for pharmaceutical research or niche industrial processes led us to invest in compliance infrastructure. Users expect not just a certificate of analysis, but documented supply chain transparency, batch traceability, and clear documentation showing absence of controlled impurities and regulated byproducts. Meeting these needs became part of our operational DNA long before regulators caught up. We consistently updated our protocols, trained new staff, and worked with auditors to keep the supply chain open for sensitive chemical building blocks, even amid tightening regional or national restrictions.

    Shared Responsibility: From Production Facility to Final User

    In our plant and throughout the distribution network, everyone takes responsibility for maintaining rigorous standards. Facilities operate under Good Manufacturing Practice for every batch, not just those destined for clinical or regulated markets. Operators receive extensive training on halogen handling and safe transfer, because time and again, carelessness during bottling or shipment correlates with customer complaints and shelf-life degradation. Before every outbound lot leaves our site, technical specialists review the spectral checkpoints and spot-sample each container. This hands-on culture means that if a problem appears downstream—mislabeling, cloudiness, pressure build-up—it traces quickly back through a manageable chain of custody. Feedback from both multinational and startup customers cycles into process improvements, providing fresh sets of eyes that keep quality at the leading edge year after year.

    Reflections on Cost, Value, and Research Outcomes

    Pricing pressure constantly tests the chemical manufacturing sector. While some newcomers chase cost-cutting by using shortcut routes or lightweight packaging, experience shows that these moves carry hidden risk. Research budgets often stretch thin, but the avoidable cost of a failed run, delayed project, or recall outweighs small up-front savings. Several pharma partners reported that switching to lower-tier sources for haloarene reagents resulted in lost time and unrecoverable data after reactions failed to meet selectivity targets. Longevity and yield gaps have confirmed—by data, not just anecdotes—that sourcing from established producers pays off over the lifecycle of a research or manufacturing campaign. The product’s stability profile translates into fewer repeats, less solvent use, and reliable scale-up, becoming a critical line in the risk-management discussion for every R&D budget review.

    Continuous Improvement Across the Product Lifecycle

    This molecule’s uses evolve. Each year, our team works with customers pursuing different targets: coupling for new electronics, substitution to access new bioactive derivatives, or simply as a reliable test substrate for process method development. These shifting project needs drive us to undertake batch optimization, update analytical methods, and modify handling guidelines. We see feedback from top-tier academic labs, contract research partners, and multinationals, combining these data streams to refine operational guidelines and packaging options. The result: a living, improving supply chain that supports both high-volume industrial needs and niche, single-project requests. Improving every detail brings not just better product, but informed users who pass along that advantage through their own technical communities.

    Pursuing Sustainability and Safer Handling

    Hazard management sits front and center in modern chemical operations. Through the years, we developed and refined our own environmental and safety protocols, which now shape how we make and ship products like 1-Fluoro-3-Iodobenzene. The chemical’s high iodine content draws attention in waste treatment and air management disciplines. Our laboratory and treatment teams regularly evaluate process emissions, distillate scraps, and packaging residues to maintain strict compliance and minimize impact. We constantly refine solvent selections, transitioning away from persistent, highly toxic compounds whenever feasible. User training, updated regularly, covers spill control, vapor management, and correct PPE to empower operators and reduce risk. Those real-world lessons, earned from thousands of small improvements and a culture of accountability, illustrate the practical route from sustainable consciousness to everyday results.

    Long-Term Relationships Built on Consistency

    Most chemists who rely on us for 1-Fluoro-3-Iodobenzene are not first-time buyers. Projects rarely stop at one synthesis or a single phase. Over years of partnership, we have watched the same users return, expanding their research and production needs. Some moved from bench scale to full pilot campaigns, always requiring the same level of consistency from their raw materials. Their trust grows from product reliability, open communication about limitations, and rapid responses when challenges surface. That partnership mindset has driven our own investment into better logistics, more streamlined documentation, and a constant improvement cycle that maps our future as much as our day-to-day operations.

    Conclusion: Value Beyond Specification Sheets

    Technical documentation only tells part of the story for 1-Fluoro-3-Iodobenzene. Earning and keeping the trust of the world’s busiest and most innovative labs comes from sustained focus on quality, clear communication, and the willingness to learn from real-world feedback. Across multiple industries and thousands of distinct projects, this unique building block continues to shape the research and production landscape, bringing tangible value through careful manufacturing and attentive supplier support. Every lot, every year, we learn a little more about the power and promise a single molecule can deliver—and how a manufacturer’s commitment to process, reliability, and collaboration can help push the boundaries of modern chemistry.