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1,4-Diiodo-2-Fluorobenzene

    • Product Name 1,4-Diiodo-2-Fluorobenzene
    • Alias 1,4-Diiodo-2-fluorobenzene
    • Einecs 629-032-9
    • 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
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    Specifications

    HS Code

    955841

    Chemicalname 1,4-Diiodo-2-Fluorobenzene
    Molecularformula C6H3F I2
    Molecularweight 381.90 g/mol
    Casnumber 57389-44-9
    Appearance White to off-white solid
    Meltingpoint 69-72°C
    Density 2.70 g/cm3 (approximate)
    Solubility Insoluble in water
    Smiles C1=C(C=C(C=C1I)I)F
    Inchi InChI=1S/C6H3FI2/c7-5-2-1-4(8)3-6(5)9
    Pubchemcid 24890801
    Ecnumber none

    As an accredited 1,4-Diiodo-2-Fluorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle with a tightly sealed cap, labeled "1,4-Diiodo-2-Fluorobenzene, CAS 55947-46-1, 5g."
    Shipping 1,4-Diiodo-2-Fluorobenzene is shipped in tightly sealed containers, protected from light and moisture, under standard chemical transportation regulations. It is labeled as hazardous, requiring handling by trained personnel and compliance with local, national, and international shipping guidelines for chemicals. Ensure temperature stability and avoid exposure to extreme conditions during transit.
    Storage Store 1,4-Diiodo-2-Fluorobenzene in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the container clearly labeled and avoid exposure to moisture. Ensure storage in accordance with local, state, and federal regulations, and utilize secondary containment to prevent accidental release or contamination.
    Application of 1,4-Diiodo-2-Fluorobenzene

    Applications of 1,4-Diiodo-2-Fluorobenzene in Industrial Manufacturing

    1,4-Diiodo-2-Fluorobenzene serves as a key halogenated aromatic intermediate in specialty chemical production. The raw material offers targeted reactivity for advanced synthesis in pharmaceutical, electronic, agrochemical, and material science sectors. We ensure technical support and application consultation to help optimize downstream usage according to project needs and regulatory demands.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Many pharmaceutical manufacturers apply 1,4-diiodo-2-fluorobenzene as a core intermediate in the multi-step synthesis of complex aromatic drug molecules, where regioselective halogenation is critical for compound specificity. The compound typically acts in Suzuki or Ullmann coupling steps for attaching aromatic or heterocyclic groups, particularly in oncology, antiviral, and CNS drug programs. Precise control of halide positioning and purity is essential due to tight regulatory mandates and requirements for bioactive molecule synthesis.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF Monograph Standards for related APIs
    • EDQM CEP requirements for pharmaceutical intermediates
    • FDA 21 CFR Part 211 (if used at US sites)

    Typical usage ratio

    • Ranges from 5% to 20% molar ratio of total reactants in target coupling steps; adjusted based on API molecular design and yield optimization

    Downstream process integration

    • Dosed during intermediate or late-stage aromatic substitution reactions
    • Pre-dissolution in high-purity solvents to minimize trace organoiodine impurities
    • Lot certification and full traceability required prior to batch approval

    Final product types

    • Cancer treatment actives (e.g., kinase inhibitors)
    • Antiviral agents
    • Neuropsychiatric small molecules
    • API key building blocks

    2. Liquid Crystal Display (LCD) Material Manufacturing

    Engineers in the electronics sector incorporate this halogenated benzene as a building block for the synthesis of advanced aromatic compounds used in high-performance liquid crystal materials. The dual iodine and fluorine substituents provide unique dielectric and optical behaviors desired in next-generation TFT-LCD display alignment and switching layers. High-purity batches, with precise control of halide content, are needed for reliable color consistency and stability.

    Industry compliance standards

    • IEC 62321 for hazardous substances test (RoHS compliance)
    • ISO 9001:2015 Quality Management for material traceability
    • JEITA Guidelines for display materials
    • REACH Regulation (EC) No 1907/2006 compliance for EU

    Typical usage ratio

    • 1% - 8% weight ratio in custom liquid crystal synthesis, depending on required birefringence and viscosity in final blend formulas

    Downstream process integration

    • Enters aromatic coupling and cyclization processes for precursor compounds
    • Incorporated into LC batching lines immediately after purification to avoid cross-contamination
    • Storage and handling under inert atmosphere to reduce halogen loss

    Final product types

    • Twisted nematic and in-plane-switching liquid crystal formulations
    • Color filter materials for high-contrast LCD modules
    • Driver IC encapsulants with improved electrical properties
    • Optical alignment films for thin display panels

    3. Agrochemical Active Ingredient Manufacturing

    1,4-Diiodo-2-Fluorobenzene is used by agrochemical formulators as a targeted precursor in the synthesis of specific halogenated aromatic moieties found in several classes of advanced herbicides and insecticides. Reliable introduction of both iodine and fluorine substituents enhances biological activity, improves molecular stability, and modifies hydrophobicity as required within regulatory and safety constraints typical for crop protection actives.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for agricultural chemicals
    • ISO 17025 Certification for laboratory QC
    • EU Regulation (EC) No 1107/2009 for crop protection product safety
    • China GB 2763-2021 for maximum residue limits

    Typical usage ratio

    • 2% to 10% in key synthesis steps as per targeted molecule’s route; ratio set by required yield and desired halogenation pattern

    Downstream process integration

    • Added during initial and secondary aromatic coupling stages
    • Requires inline halide monitoring to ensure regulatory compliance
    • Used in closed reactor systems to control volatilization and personnel exposure

    Final product types

    • Selective pre-and post-emergence herbicides
    • Pyrazole-based insecticides
    • Fungicidal aromatic intermediates
    • Auxin-mimicking plant growth regulators

    4. Organic Light-Emitting Diode (OLED) Material Synthesis

    Specialty material producers utilize this compound as a functionalized building block for synthesizing conjugated aromatic monomers, tailored for use in the emissive layers of OLED panels. Its controlled halogenation profile allows downstream manufacturers to precisely manipulate electron-withdrawing effects, facilitating improved charge mobility and extended luminance in consumer electronic displays. Purity, consistency, and proven low-metal contamination are essential for commercial OLED manufacture.

    Industry compliance standards

    • ISO 14001 Environmental Management for specialty material sites
    • RoHS and WEEE directives for restricted materials use
    • EICC/GeSI supply chain requirements for consumer electronics
    • Customer-specific cleanroom QC protocols

    Typical usage ratio

    • Between 1% and 12% in core-yield-limited synthetic steps; final ratio tuned to emission spectrum requirements for display application

    Downstream process integration

    • Fed into Suzuki-Miyaura couplings for functionalized aryl structure formation
    • Employed in nitrogen- and oxygen-exclusion environments to prevent degradation
    • Batch QC includes trace halide residue and molar purity authentication

    Final product types

    • Blue, green, and red OLED emitters
    • Electron-transport layers for display tiles
    • High-brightness luminescent conjugated polymers
    • Wearable flexible screen components

    5. Advanced Polymer and Specialty Resin Synthesis

    Chemical producers select 1,4-diiodo-2-fluorobenzene for chain-functionalization during step-growth polymerization of advanced resins and copolymers. Its ability to precisely position both iodine and fluorine atoms enhances desired physicochemical attributes, such as weatherability, dielectric strength, flame resistance, and hydrophobicity. Manufacturers rely on quality-controlled intermediates to develop high-performance polymers for demanding electronic, auto, and coating applications.

    Industry compliance standards

    • UL 94 for flammability ratings
    • IEC 60243 for electrical insulating materials
    • ISO 10993 for biocompatibility (for medical device use)
    • REACH SVHC declarations

    Typical usage ratio

    • 0.5% to 5% of total monomer feed; ratios adjusted based on targeted functional group loading and mechanical specifications

    Downstream process integration

    • Introduced during condensation polymerization or as a terminal block capping agent
    • Integrated with precision dosing systems to maintain reproducible halogen distribution
    • Required precursor for functional resin synthesis with post-polymerization purification

    Final product types

    • High-performance epoxy and polyimide resins for electronics
    • Specialty coating binders with enhanced weather resistance
    • Wire insulation polymers with superior dielectric strength
    • Medical device encapsulant plastics

    6. Specialty Dye and Pigment Raw Material

    Dye and pigment manufacturers leverage the unique halogenated structure in this benzene ring for creating high-stability chromophores in specialty colorant lines. Its dual halogen substitution significantly increases resistance to photobleaching and solvent damage, which is critical for demanding printing inks, technical textiles, and plastic coloration. Full traceability and batch consistency underpin compliance with both application performance and environmental standards in regulated markets.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile applications
    • EN 71-3 (Toy Safety) for migration of certain elements
    • ISO 2846 for printing ink standards
    • FDA 21 CFR 176.170 for colorants in food contact plastics

    Typical usage ratio

    • 1% to 6% in the chromophore synthetic stage, ratio finalized by the absorption spectrum and color fastness targets

    Downstream process integration

    • Used in ring-functionalization steps for azo and anthraquinone dye synthesis
    • Integrated under controlled temperature and agitation to ensure optimal hue development
    • Post-reaction purification geared for low residual halogen content

    Final product types

    • Photo-stable printing dyes
    • Textile pigments for technical fabrics
    • High-resistance inkjet colorants
    • Plastic-compatible specialty pigments
    Free Quote

    Competitive 1,4-Diiodo-2-Fluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing 1,4-Diiodo-2-Fluorobenzene: Quality and Consistency in Every Batch

    Real Experience in Chemical Manufacturing

    In our production plant, 1,4-diiodo-2-fluorobenzene has become one of the most reliable building blocks for customers working in pharmaceutical, agrochemical, and specialty material synthesis. Our years of hands-on experience go well beyond listing a CAS number and ticking boxes for purity. The process begins with sourcing quality raw materials, ensuring that every input aligns with stringent control measures. Over the years, many researchers and process developers have come to equate our version of 1,4-diiodo-2-fluorobenzene with repeatable results. That kind of trust doesn’t happen by chance: it grows from steady investments in upgraded reactors, employee training, and a daily commitment to keeping each batch free from unwanted byproducts.

    Specifications That Match Industry Demands

    1,4-Diiodo-2-fluorobenzene (model: 2-Fluoro-p-diiodobenzene) enters as an off-white to pale beige solid with a structure that places both iodine atoms in para positions and a fluorine atom at the ortho location. From our own testing, the melting point sits in the expected range, matching what the literature describes. Consistent batch analysis using NMR and HPLC confirms the low impurity levels customers look for. Chemists developing new intermediates or working on aryl iodide-coupling reactions have pointed to our material’s ability to keep byproduct formation under control—an edge that accelerates complex molecule synthesis.

    Our technicians take each order through a series of purification and drying steps. Too little drying, moisture sneaks in and changes the course of sensitive cross-coupling reactions. Too much heat or aggressive handling, and the product can discolor or form trace byproducts. By leaning on real-world troubleshooting and in-house analytics, we protect the product’s character all the way to sealed drums and high-purity containers.

    Why 1,4-Diiodo-2-Fluorobenzene Matters to Chemists

    The right functionalization opens doors in organic synthesis. In this molecule, the balance between two iodo groups and a single fluorine yields unique reactivity. Many partner products offer only bromine or chlorine variants, which can alter selectivity or reaction temperature requirements. Our experience with this specific compound goes back over a decade, supplying kilo lots and small research-scale batches alike. Academic researchers have sought it for new biaryl synthesis and mechanistic studies, and process chemists have included it in pilot-scale routes to active pharmaceutical ingredients (APIs).

    One thing stands out: iodo-substitution brings higher reactivity, reducing the energy demands in Suzuki and other cross-coupling reactions. The attached fluorine not only changes electronics across the ring, but also impacts how subsequent modifications play out. Most customers report that switching from a diiodo-benzene to the diiodo-2-fluoro derivative increases the chance of getting a cleaner product at mild temperatures. In large-scale runs, that means lower energy bills and less troubleshooting.

    This niche but critical compound also finds a home in some electronics R&D labs. The unique ring system sometimes slips into specialty monomers, which show up later in high-performance polymers or coatings. Industrial users tend to value consistency, so during each run, our personnel stick close to the process, making real-time adjustments if residual moisture or residual acids threaten overall purity.

    Product Differentiation Born from Hands-On Manufacturing

    We have watched other suppliers try to rush production and cut corners by running less rigorous purification or skipping key intermediate checks. The difference becomes clear the moment the product enters a chromatography column or a sensitive coupling reactor: lower-quality batches leave behind stubborn byproduct residues. Operators find themselves spending days cleaning reactors and repeating runs, with lost time and increased solvent use eroding any savings found upfront.

    In scaling up 1,4-diiodo-2-fluorobenzene, our team has tackled all the headaches associated with side-product formation. We use analytic feedback at each weigh-up, not just for the sake of checking a box but to confirm that the next step won’t introduce drift in color or reactivity. We keep fresh glassware and use only compatible linings for all containers, because we have seen how trace leaching from the wrong vessel can throw off sensitive reactions involving this compound. These in-the-trenches lessons show up in the reliability of our product.

    Addressing Common Production Challenges

    Many producers underestimate the impact of minute impurities in halogenated aromatics. Using upstream purification and targeted crystallization techniques, we avoid introducing unwanted halogen exchange products or excess solvents. Some of these byproducts tend to look harmless on paper but have outsized effects during later steps, especially with today’s more sophisticated catalyst systems. Our plant’s analytical team runs iterative tests well before shipping; they spot not just total impurity percentages but also the actual identities—information some labs neglect, bringing hidden risks to end-users.

    Maintaining stability poses another significant challenge for compounds with multiple halogens. Over the years, we have refined packaging and storage protocols, observing reactions to light, temperature, and container linings. Every improvement draws on the expertise of line operators and QC staff, not just management. In one series of shipments to long-distance clients, we noticed slight color development traced back to temperature fluctuations in transit. Adjusting the packaging protection layer eliminated this issue. Through trial, error, and open feedback from our customer base, we now routinely deliver batches that reach users in excellent condition.

    Differences from Other Halogenated Benzenes

    1,4-Diiodo-2-fluorobenzene sits apart from typical diiodobenzenes and other halogenated benzene derivatives. The presence of the fluorine group exerts a surprisingly strong influence on both selectivity and reaction speed in coupling processes. In traditional diiodobenzene, similar methods demand more robust catalysts and higher temperatures. Chemists regularly ask us about switching from dichloro or dibromo analogs, and the pattern emerges: success rates climb, waste generation falls, and the whole process becomes less stressful on equipment.

    In contrast to triiodo or trifluoro compounds, this product keeps the number of reactive sites balanced, allowing for controlled single or double substitutions as desired. The purity benchmarks we keep for this compound consistently reach above 99 percent, measured by a full suite of methods from NMR to GC and LC. The differences play out during scale-up, too—other products can cause troublesome emulsions or persistent halide residues when worked up, especially at the kilo scale. The fine-tuned protocols used in our plant make these issues rare, based on real observed feedback and repeat order data.

    Direct Applications Highlight Value

    Some molecules are purchased for stock or catalog inclusion. 1,4-Diiodo-2-fluorobenzene heads straight to the bench or process suite and gets put to work. Its two iodo groups act as convenient leaving groups in coupling chemistry, whether for Suzuki, Sonogashira, or other palladium-catalyzed pathways. The ortho fluorine changes how nucleophiles attack, leading to products that would take far more effort using other substituents. For instance, in setting up symmetrical diaryls or intersecting a fluorinated ring system with another aromatic, chemists come back with fewer isolated impurities and more dependable yields.

    Pharmaceutical developers appreciate the speed-up in reaction cycles. With this building block, they cut steps from multi-stage syntheses. That doesn’t just boost metrics on paper—lab teams feel less frustration, equipment longevity improves, and cleaning times fall. We see this feedback across projects from fine chemical development to active ingredient synthesis.

    In the electronic materials sector, researchers have praised the compound’s integration into custom-designed monomers. The resulting specialty polymers exhibit enhanced thermal and chemical resistance due to the combined halogen effects, and the clean substitution patterns mean downstream polymerization goes off without much purification hassle.

    Supporting Responsible Use and Compliance

    As regulatory requirements evolve, we reinforce good stewardship at every step of production and shipping. 1,4-Diiodo-2-fluorobenzene often travels internationally and falls under import and storage controls for halogenated materials. Our compliance team tracks every lot through detailed records, supported by traceable batch data. This isn’t just paperwork for us: keeping full visibility across each drum safeguards both our customers and our own team, making it easier to resolve questions and clear customs without holdups.

    We stay current with chemical control regulations and emerging best practices for worker safety, waste handling, and environmental care. For example, we recycle iodine-rich process streams in-house, minimizing off-site waste transport and reducing environmental risk. Onsite containment, regular employee training, and transparent reporting ensure that safety and environmental metrics improve each year.

    Why Quality Still Wins in the Marketplace

    Manufacturing specialty halogenated benzene compounds in-house illuminates a simple fact: shortcuts in QC or small batch loss of control lead to headaches for everyone in the value chain. We see downstream users recognize the value of a product that arrives consistent, pure, and ready to use. Their reports echo our own QC logs—minimum fuss, high yields, and fast transitions between projects. Each successful run cements loyalty and shapes reputation, both of which carry more weight than advertising.

    We don’t stop at baseline purity. By investing in analytical verification and incorporating customer feedback, we identify issues before they cost time or materials. If a new reaction or innovation calls for tighter tolerances, we aim to provide the support that gets users moving quickly from R&D to pilot scale without revalidating every input.

    Price pressure remains a constant challenge, but our insight is drawn from years on the manufacturing floor: trying to undercut market leaders by delivering lower-grade material saves nothing in the end. Users lose time, reactors end up at risk, and projects stall. By keeping the entire supply chain in-house and staying hands-on with every batch, we maintain a competitive edge built on dependability rather than just price.

    Continuous Improvement Driven by Feedback

    Working directly with research chemists, process engineers, and end-users, our plant often receives specific requests for custom packaging or analysis, and we adjust as needed. If a customer reports a shift in solubility or a change in reactivity tied to a small impurity, our team digs into the root cause and shares solutions. That openness creates a two-way street of knowledge, moving us forward with each production cycle.

    We apply new insights from every complaint, test, and follow-up. Real improvement means moving past routine methods, adopting better drying, storage, or transfer techniques when issues arise. Batch-to-batch reproducibility doesn’t rest on luck; it demands steady focus and willingness to try new tools. Inside our plant, each shift contributes tips and helps set process flags, catching issues before they escape into the marketplace.

    Looking Ahead With Confidence

    1,4-Diiodo-2-fluorobenzene continues to support key advances in synthesis, materials, and scale-up projects worldwide. From our practical experience, quality matters more every year, as innovation speeds up and customers expect fewer interruptions. It isn’t enough to merely meet specs—each drum we ship must accelerate rather than complicate the next stage in a global chain of discovery and application.

    Producing this compound has taught us the value of learning from every run, staying transparent with users, and investing in long-term reliability. That approach doesn’t just help us stand apart; it strengthens trust with each new collaboration. In the crowded world of specialty chemicals, real results come from experience, attention to detail, and a commitment to continuous improvement.