|
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 | 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. |
Applications of 1,4-Diiodo-2-Fluorobenzene in Industrial Manufacturing1,4-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) SynthesisMany 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
Typical usage ratio
Downstream process integration
Final product types
2. Liquid Crystal Display (LCD) Material ManufacturingEngineers 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
Typical usage ratio
Downstream process integration
Final product types
3. Agrochemical Active Ingredient Manufacturing1,4-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
Typical usage ratio
Downstream process integration
Final product types
4. Organic Light-Emitting Diode (OLED) Material SynthesisSpecialty 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
Typical usage ratio
Downstream process integration
Final product types
5. Advanced Polymer and Specialty Resin SynthesisChemical 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
Typical usage ratio
Downstream process integration
Final product types
6. Specialty Dye and Pigment Raw MaterialDye 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
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 1,4-Diiodo-2-Fluorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.