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1,2-Difluoro-4-Iodobenzene

    • Product Name 1,2-Difluoro-4-Iodobenzene
    • Alias 1,2-Difluoro-4-iodobenzene
    • Einecs 841-832-0
    • 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

    663454

    Name 1,2-Difluoro-4-iodobenzene
    Cas Number 41014-56-6
    Molecular Formula C6H3F2I
    Molecular Weight 239.99 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 66-68 °C at 18 mmHg
    Density 2.02 g/cm³ at 25 °C
    Refractive Index 1.569
    Solubility Insoluble in water; soluble in organic solvents
    Synonyms 4-Iodo-1,2-difluorobenzene
    Smiles Fc1cc(I)ccc1F
    Inchi InChI=1S/C6H3F2I/c7-4-1-2-6(9)5(8)3-4/h1-3H

    As an accredited 1,2-Difluoro-4-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 with a secure screw cap, labeled "1,2-Difluoro-4-Iodobenzene, 25 g." Includes hazard symbols and handling precautions.
    Shipping 1,2-Difluoro-4-iodobenzene should be shipped in tightly sealed containers, protected from light and moisture. Ensure it is labeled according to hazardous material regulations. Handle with care to prevent spills. Transport according to local, national, or international regulations, typically as a hazardous chemical, with appropriate documentation and safety measures in place.
    Storage 1,2-Difluoro-4-iodobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight. Keep it away from incompatible substances such as strong oxidizing agents. Store under inert gas if recommended by the manufacturer to prevent moisture or air exposure. Ensure proper labeling and limit access to trained personnel only.
    Application of 1,2-Difluoro-4-Iodobenzene

    Applications of 1,2-Difluoro-4-Iodobenzene in Industrial Manufacturing

    As a direct manufacturer of 1,2-Difluoro-4-Iodobenzene, we serve specialized industrial sectors requiring organofluorine intermediates. Our material integrates into several advanced production lines, supporting synthesis processes in pharmaceuticals, agrochemicals, liquid crystal displays, and specialty polymers. The following application sections reflect real downstream integrations, detailing compliance, ratio, processing, and end-product specificity.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical API producers use this fluorinated benzene derivative to construct building blocks for kinase inhibitors, antiviral agents, and neuroactive compounds. Manufacturers select this intermediate for targeted substitution reactions, particularly Suzuki-Miyaura and Buchwald-Hartwig couplings, enabling the introduction of functionalized fluorinated motifs into complex heterocycles or aromatic frameworks. Its high purity and precise halogen-fluorine arrangement provide reproducible yields in scale-up.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4: GMP Guidelines
    • 21 CFR Part 211: US FDA Pharmaceutical CGMP
    • Enterprise-specific DMF (Drug Master File) registration requirements

    Typical usage ratio

    • 0.15–0.35 molar equivalents per reaction batch, optimized according to target molecule structure and desired site-specific substitution

    Downstream process integration

    • Reacts during aryl-aryl or aryl-amine coupling stage
    • Enters as a limiting reagent in late-stage synthesis under inert, anhydrous conditions
    • QC confirms halide release and fluorine position retention for metrological analysis

    Final product types

    • Pharmaceutical intermediates for kinase inhibitor compounds
    • Advanced precursors for CNS (central nervous system) APIs
    • Functionalized scaffolds for oncology R&D pipelines

    2. Agrochemical Active Ingredient Manufacturing

    Downstream agrochemical makers incorporate this compound in multi-step syntheses of fluorinated herbicide and fungicide actives. The halogenated benzene core delivers unique binding characteristics, often improving pesticidal selectivity and environmental persistence. Its reactivity in nucleophilic aromatic substitution enables precise introduction of additional agro-functional groups in line with regulatory thresholds for persistence and metabolite formation.

    Industry compliance standards

    • ISO 9001:2015 certified manufacturing for crop protection agents
    • FAO/WHO Specifications for Pesticides
    • REACH Regulation (EC) No 1907/2006
    • Guidance from US EPA for registration of new actives (40 CFR Part 158)

    Typical usage ratio

    • 0.12–0.28 mole per mole of active, set by formulation pathway and yield optimization

    Downstream process integration

    • Initiates substitution during the formation of nitro- or amine-functional crop protection agents
    • Processed post-nitration, prior to sulfonylation step
    • QC for halide residue and fluoride content follows local environmental guidelines

    Final product types

    • Systemic fluorinated herbicide actives
    • Seed treatment agents with selective mode of action
    • Fluoroaryl fungicides for fruit and vegetable crops

    3. Liquid Crystal Material Formulation

    Producers of liquid crystal display (LCD) materials utilize this intermediate for the design of high-anisotropy fluorinated aryl components. It is introduced in the early stages of the synthesis of biphenyl-based and phenylcyclohexane-based liquid crystals. Its electronegative profile enhances dielectric anisotropy and thermal stability, directly influencing the response speed and color rendering of end-user panels.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for display chemicals
    • TÜV Rheinland standards for display material safety assessment
    • IEC 62474: Requirements for the Content of Substances in LCDs
    • Chinese GB/T 26572–2011: Restriction of hazardous substances

    Typical usage ratio

    • 3%–7% by weight in making tailored fluorinated aryl unit stocks, adjusted for viscosity and phase transition targets

    Downstream process integration

    • Introduced into etherification or nucleophilic aromatic substitution stage to introduce difluorinated ring units
    • Blended with polycyanobiphenyls for high-purity LCD batch production
    • Monitored for iodo residue removal to ensure no ion contamination reaches final LC mixture

    Final product types

    • Twisted nematic (TN) liquid crystals
    • Active-matrix liquid crystals for TFT panels
    • High-performance color filter LC material blends

    4. Specialty Fluoropolymer Monomer Synthesis

    Chemical synthesis operations utilize this compound to prepare monomers for engineering fluoropolymers used in electronics, membranes, and high-performance coatings. Chemists form carbon-fluorine bonds via cross-coupling or nucleophilic aromatic substitution, achieving tailored monomer units that impart chemical resistance and dielectric benefits to finished polymers. QC teams track metal catalyst residues and halogen balance to maintain reproducibility through scale-up.

    Industry compliance standards

    • ASTM D1974: Standard Practice for Analysis of Polymeric Materials
    • ISO 9001:2015 for industrial polymer manufacture
    • UL 94: Flammability standards for polymeric components
    • Restriction of Perfluorooctanoic Acid (PFOA) per EU Regulation (EU) 2019/1021 for certain final formulations

    Typical usage ratio

    • 0.09–0.22 mole per mole of target monomeric fluorobenzene, with ratio chosen for downstream copolymerization efficiency and required fluorine incorporation

    Downstream process integration

    • Introduced during monomer synthesis, prior to transition-metal-catalyzed cross-coupling
    • Monomer purified before addition to bulk copolymerization reactor
    • ICP-MS and GC-MS verification to confirm halogen purity in final monomer stock

    Final product types

    • Fluorinated polyarylenes for high-frequency components
    • Membrane resins for fuel cells
    • Coatings with elevated chemical and UV resistance for electronics casings

    5. OLED and Organic Semiconductor Synthesis

    Electronics material developers employ 1,2-difluorinated aryl precursors in organic light-emitting diode (OLED) and organic photovoltaic (OPV) device component synthesis. The unique substitution pattern supports the formation of electron-deficient cores, facilitating improved charge transport layers. Material enters custom aryl coupling reactions for host, emitter, and charge transport moieties.

    Industry compliance standards

    • IPC-4101: Specification for Base Materials for Printed Boards
    • REACH compliance for imported or manufactured intermediates in the EU
    • RoHS/EN 62321 for halogen content in electronics
    • Corporate internal QC protocols for trace-level metal and halogen byproducts

    Typical usage ratio

    • 1.8–3.6% by weight of small molecule batch, ratio specified for charge mobility and film uniformity

    Downstream process integration

    • Added in aryl-aryl coupling steps to form the electron-transport layers
    • Processed under anhydrous, O2-free environment for maximum yield
    • Material batch traced back through LC-MS profile for batch release

    Final product types

    • OLED emitter and host layers for displays and lighting
    • OPV active layer donor/acceptor molecules
    • Semiconducting films in thin-film transistors (TFTs)
    Free Quote

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    Certification & Compliance
    More Introduction

    1,2-Difluoro-4-Iodobenzene: Reliable Building Block for Advanced Synthesis

    Working with 1,2-Difluoro-4-Iodobenzene Every Day

    Producing 1,2-difluoro-4-iodobenzene isn’t something a chemical manufacturer starts by cutting corners. As someone deeply invested in aromatic halogen chemistry, I see our team choose each raw material for its reliability. Each batch focuses on purity because we’ve learned through countless reactions that even minor impurities can cause bottleneck problems during coupling or functionalization. We don’t just watch numbers from quality control reports. Our operators smell for byproducts, check off-white tints against pure reference samples, and compare actual yield against strict batch records. Model names or catalog numbers matter much less in the plant than the simple fact of lot consistency, measured in GC trace and in how smoothly customers run Suzuki-Miyaura or Hartwig-Buchwald couplings with the material we ship.

    Specifications Shaped by Experience

    Users in pharmaceutical and OLED research think in terms of end results, and as manufacturers, we’ve adopted this mindset. We keep the water content low, less than 0.2%, because excess moisture encourages hydrolysis and destabilizes organometallic intermediates. We target iodine content with narrow HPLC and NMR acceptance ranges, usually above 99.5%, so the aromatic ring supports both bench-scale experimentation and plant-scale production. Every time customers request custom bulk packaging, such as Schlenk bottles or ampoules for air-free handling, we coordinate directly to keep the product stable all the way to their reactor.

    Why 1,2-Difluoro-4-Iodobenzene Finds a Unique Spot in Research Pipelines

    We don’t manufacture intermediates by checking boxes, and 1,2-difluoro-4-iodobenzene keeps proving its value in real-world applications. Medicinal chemists return to this core because it brings two orthogonal handles to play: the fluorines and the iodine. Fluorine atoms are tough—once incorporated, they influence bioactivity and stability through strong C–F bonds. The iodine opens up site-selective cross-coupling. So if a client needs to introduce an aryl or alkynyl group at the para site, it’s straightforward using palladium catalysts. Over the years, more screening libraries build on this dual functionality, especially as fluorinated motifs become a constant demand in anti-cancer and CNS drug leads.

    Applications Beyond the Lab Scale

    Looking at the last two years, we saw a marked uptick in orders from agrochemical development teams and display materials R&D. They aren’t only looking for niche reactivity. In those sectors, the extra cost of high-purity iodoarenes is justified by measurable gains in product performance. Electronic-grade OLED and LCD materials require strong electron-withdrawing groups for performance. The difluorinated ring supports more aggressive conditions for follow-up chemistry without breaking down, and the iodine position allows precise functional group installation.

    On the process chemistry side, researchers tell us that scaling up transformation is easier when they can count on the aromatic ring’s integrity. Fluorine and iodine together allow stepwise transformation—activate one, leave the other untouched. In contrast, trifluorinated or non-halogenated aromatics often demand more protecting group maneuvers, higher catalyst loadings, or longer purification steps that can introduce inefficiencies. These small details matter in a multi-ton campaign, and we hear feedback from teams that switching intermediates can add weeks of troubleshooting and process optimization.

    Practical Differences from Other Halogenated Benzenes

    Experience tells us that not all halogenated aromatics react the same way. We’ve loaded reactors with 4-iodoanisole, 1,2,4-trifluorobenzene, and countless other building blocks. What stands out each time is the fine balance offered by the difluoro-iodo pattern. For example, compared to 4-iodobenzotrifluoride, the 1,2-difluoro-4-iodo variant provides a site-specific balance—its ortho fluorines influence reactivity at the para iodine differently, allowing more predictable selectivity in metal-catalyzed reactions. Milestones in our own plant runs back this up: we’ve hit better isolated yields and sharper melting point consistency because this arrangement avoids overactivation, which sometimes makes trifluorinated rings more prone to byproduct formation.

    Clients have tried to substitute with non-fluorinated iodobenzenes but end up revisiting their process due to solubility issues or lower compatibility with newer catalytic systems. Today’s catalysts and ligands, especially in cross-coupling fields, respond favorably to subtle electronic tuning. Every major journal in organic synthesis now features difluoroaryl scaffolds because they balance processability and property enhancement.

    Quality Control Tied Directly to Customer Outcomes

    A raw material like this puts our quality assurance process on the front line. We don’t accept “pretty close” on certificate of analysis reporting. Process chemists show us that even a slight deviation in halogen pattern or GC purity can derail a synthesis hundreds of liters down the line. To stay accountable, every lot draws a fingerprint NMR and GC trace before it ships out. We keep samples of each batch in inert storage for traceability. Research teams sometimes come back months later with an impurity they spotted, and we always pull up retained samples to trace the origin. This approach means we get ahead of issues and give project managers confidence, knowing decisions on their end rest on solid ground.

    Handling and Storage: Lessons from the Factory Floor

    Some compounds demand more care during handling, and 1,2-difluoro-4-iodobenzene isn’t any different. We watch for hydrolysis, so we keep it under dry nitrogen. Experience taught us the wrong lid seal or casual exposure to humid air can turn a shipment into a headache for a client. That’s why we use air-tight, moisture-resistant packaging straight from the final purification. Our plant layout includes designated storage with temperature and humidity monitoring. No matter what literature says, we base our procedures on real world experience—every so often, an accidental exposure to light or air signals a potential for trace byproducts, prompting us to tweak shades, light covers, or moisture scavengers in storage.

    Raw Material Selection—From Scale-Up to Continuity

    We don’t leave raw material procurement to chance. Our differences show up in how we trace every vendor, qualify each shipment, and even run parallel pilot syntheses when adopting a new solvent or precursor. Supply chain hiccups happen, but our backup plans, local relationships with reagent producers, and robust batch documentation help us recover quickly. If the cost of a single component rises, we eat the loss instead of adjusting product standards downward. Our partners depend on that continuity, especially because switching to even a slightly different grade could jeopardize months of optimization.

    Observing Industry Trends and Responding with R&D

    We don’t manufacture in a vacuum. We track trends in pharmaceutical patent filings, custom synthesis requests, and regulatory updates. Over the past decade, the industry has seen a strong push towards more heavily fluorinated compounds, but the research details point to practical limitations when adding too many fluorines. Our focus on 1,2-difluoro-4-iodobenzene emerged not from theoretical discussions but from hundreds of conversations with chemists looking for pieces that balance reactivity, cost, and environmental safety.

    The move towards green chemistry also shapes our manufacturing route. Early on, we faced tough questions about solvent choice, waste management, and halogen recovery. We looked for non-explosive alternatives to sodium or potassium in the metal exchange steps. Our waste streams pass through on-site halogen scrubbing and recycling. The factory team meets quarterly to review process safety reports, and any near-miss related to batch exotherms or trace halide release becomes a lesson for all operators. Keeping pace with regulatory demand for safer conditions means regular investment in ventilation, monitoring, and personal protective equipment, not just a one-time fix.

    Supporting Innovation Through Customization and Feedback

    We learned long ago that researchers don’t always need the same format. Sometimes a kilogram batch heads out with a stability certificate ready for GMP campaigns, while another client wants a split sample for rapid SAR validation. We accommodate those requests the way only an actual manufacturer can: blending flexibility into scale. Working side-by-side with client development teams, we refine our specs in real time, reporting exact impurity profiles or helping diagnose stuck reactions. Chemists want to know how their material stood up to storage, transportation, and run-to-run variability. We don’t treat these as peripheral concerns—they help us improve batch records, fine-tune purification, and adjust our own internal procedures.

    Collaborative Problem-Solving and Ongoing Challenges

    Not every batch goes perfectly, and manufacturing specialty chemicals means dealing with setbacks openly. One memorable run saw a minor change in starting material supply introduce a faint impurity that showed up only under preparative HPLC at a client’s site. We worked directly with their team to resolve the issue—running reanalysis, sending detailed logs, and extending credit until the corrective campaign finished. Such lessons shape our internal protocols, driving us to new analytical benchmarks and reinforcing the need for ongoing communication.

    Shipping internationally always brings new variables, especially with temperature sensitivity or customs delays. We coordinate not just with logistics partners, but with receiving chemists at each customer site to anticipate and eliminate snags. We’ve seen batches held for inspection and intervened directly to clarify hazardous material status—a level of care only possible by intimately understanding not just the product, but also each destination’s regulatory quirks.

    Environmental Responsibility in Halogen Chemistry

    Fluorinated and iodinated aromatics have a reputation for environmental persistence, and as a manufacturer, we shoulder responsibility for minimizing impact. Our plant features closed-loop halide capture, and we maintain a detailed record of every reagent and byproduct stream leaving the site. We work with local authorities on waste reduction targets and participate in industry-led benchmarking to reduce emissions. As these materials find new uses in crop protection and display technologies, the pressure rises to prove that specialty chemical production can combine performance with stewardship.

    Every time a client asks about life-cycle impact, we provide a transparent breakdown—not only for compliance, but also for our own improvement. We scrutinize energy use in fluorination, haul spent solvents for external treatment, and constantly review our safety data. By tracking benchmarks like recovered halogen fractions, solvent recycling efficiency, and batch carbon footprint, we show our clients and our own employees that manufacturing fluorinated aromatics doesn’t have to mean environmental compromise.

    Final Thoughts Born from Experience

    Sourcing 1,2-difluoro-4-iodobenzene from someone who makes it in-house provides advantages that no trader or distributor can match. Beyond the specification sheet, customers depend on plant-proven reliability, custom support, and continual improvement built into every step—from raw material curation through analytical confirmation. The real value stems from our shared commitment to the results our customers count on, shaped by hands-on experience and a relentless drive to keep process chemistry, material science, and environmental responsibility moving forward together.