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3,4-Dichloroiodobenzene

    • Product Name 3,4-Dichloroiodobenzene
    • Alias 3,4-Dichloro-1-iodobenzene
    • Einecs 839-325-7
    • 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

    201303

    Chemical Name 3,4-Dichloroiodobenzene
    Cas Number 22962-60-7
    Molecular Formula C6H3Cl2I
    Molecular Weight 272.90
    Appearance White to off-white solid
    Melting Point 61-64 °C
    Density 2.03 g/cm³
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Synonyms 1,2-Dichloro-4-iodobenzene
    Smiles Clc1ccc(I)c(Cl)c1
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 3,4-Dichloroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 3,4-Dichloroiodobenzene (25g) is a sealed amber glass bottle with a secure screw cap, labeled with hazard warnings.
    Shipping 3,4-Dichloroiodobenzene is shipped in tightly sealed, chemical-resistant containers, compliant with hazardous materials regulations. It should be packed securely to prevent leaks or breakage, labeled according to international and local transport guidelines, and handled with care due to its potential health and environmental hazards. Store in a cool, dry place during transit.
    Storage 3,4-Dichloroiodobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, moisture, and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and bases. Clearly label containers and store them in a designated chemical storage cabinet, following all relevant safety regulations and handling protocols.
    Application of 3,4-Dichloroiodobenzene

    Applications of 3,4-Dichloroiodobenzene in Industrial Manufacturing

    As a specialized manufacturer, we supply 3,4-Dichloroiodobenzene for diverse industrial sectors that require controlled halogenation chemistry, high selectivity in aromatic compound synthesis, and consistent quality for downstream production. Below, we detail verified, high-impact application scenarios with technical insights relevant to process engineers, formulation chemists, regulatory managers, and industrial procurement professionals.

    1. Agrochemical Intermediate Synthesis

    Agrochemical manufacturers source 3,4-Dichloroiodobenzene primarily for its function as a halogenated aromatic intermediate in the synthesis of selective herbicides and fungicides, where the molecular scaffold with dual chloro and iodo substituents enables targeted ligation and downstream functionalization. Operations integrate this compound into advanced cross-coupling reactions, such as Suzuki or Buchwald-Hartwig amination, widening the spectrum of active ingredient structures for crop protection formulations while maintaining regulatory compliance on impurity profiles and residuals.

    Industry compliance standards

    • ISO 9001:2015 certified quality management for agrochemical synthesis
    • REACH Regulation (EC) No 1907/2006 substance registration
    • EPA 40 CFR Part 169 (US) for technical-grade pesticide intermediates
    • China GB 4839 pesticide product specification

    Typical usage ratio

    • 0.5–2.5 molar equivalents relative to coupling partners depending on the target molecule; laboratories and pilot plants often start at 1.1 equivalents to offset incomplete conversion and manage yield optimization

    Downstream process integration

    • Enters as the key aryl halide substrate in palladium-catalyzed coupling reactors; pre-formulated with specific ligands and bases for selectivity control
    • Captured at the crude purification stage before final crystallization and technical-grade QA release

    Final product types

    • Triazole fungicide technical concentrates
    • Selective herbicide actives for cereal and broadleaf weed control
    • Phenoxy-carboxylic acid derivative intermediates used in post-emergence crop protection blends

    2. Pharmaceutical Building Block Production

    Specialty pharmaceutical synthesis operations utilize the compound as a core halogen source for constructing advanced aromatic rings during the manufacturing of drug intermediates, especially where site-specific direct arylation or halide exchange is required for API development. Its controlled reactivity facilitates high-purity coupling, minimizing contamination risk for later GMP stages and supporting clean process validation for regulatory filings. Integration focuses on pathway flexibility, particularly in anti-infective and anticancer research pipelines demanding precise synthetic routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • USP–NF compendial reference for impurities management
    • 21 CFR Part 211 (cGMP) for finished pharmaceuticals
    • EU EudraLex Volume 4: GMP Guidelines

    Typical usage ratio

    • 0.8–1.3 molar equivalents in one-pot halogen exchange and direct arylation stages; selection based on impurity control specifications and reagent cost management

    Downstream process integration

    • Charged as the halogenated aromatic partner during medicinal chemistry scale-up and kilo-lab validation batches
    • Integrated with in situ catalyst systems for process flexibility and minimized timeline to final intermediate isolation

    Final product types

    • Pyridine-based pharmaceutical intermediates
    • Specialty benzene ring API precursors for oncology and CNS drug discovery
    • Small molecule chemical libraries for high-throughput screening

    3. Electronic Materials and Liquid Crystal Monomer Manufacturing

    Producers of high-performance electronic chemicals and liquid crystal monomers rely on the unique halogenation pattern of this compound to synthesize anisotropic aromatic compounds as precursors for advanced liquid crystal displays and OLED device layers. Its predictable reactivity during nucleophilic aromatic substitution and site-selective coupling ensures batch consistency, meeting the tight tolerances imposed by electronic-grade purity requirements and supporting end-use material innovation in optoelectronics manufacturing.

    Industry compliance standards

    • IEC 62474 for material composition reporting in electronics manufacturing
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances
    • JEITA EM-3601 standards for electronic chemical purity and QC
    • IPC-1752A Declarable Substance List protocols (for supplier management)

    Typical usage ratio

    • Up to 5% by molar proportion in custom monomer synthesis; adjusted based on chain length and optical performance goals of the downstream display product

    Downstream process integration

    • Reacted directly in aryl halide exchange and polycondensation stages of liquid crystal monomer assembly
    • Employed in initial functionalization before further side-chain elaboration steps

    Final product types

    • Liquid crystal monomers for TFT-LCD display panels
    • Specialty electronic intermediates for OLED light-emitting compounds
    • High-purity aromatic precursors for advanced electronic resins and dielectrics

    4. Dye and Pigment Intermediate Manufacturing

    Colorant and pigment industries incorporate 3,4-Dichloroiodobenzene in aromatic amine and azo dye intermediate production. The dual halogen function is key for controlled diazotization and cross-coupling processes, yielding pre-colored intermediates with improved colorfastness and chromatic selectivity for high-end inks, plastics, and textile pigments. Compliance with environmental and worker safety directives is essential due to regulatory oversight on halogenated aromatic processing.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for finished pigment safety in textiles)
    • EU REACH Annex XVII (restriction of certain aromatic amines)
    • ZDHC Manufacturing Restricted Substances List (MRSL 3.0)
    • ISO 9001:2015 (for pigment and dye intermediate production)

    Typical usage ratio

    • 1.0–1.5 equivalents in substitution and diazotization reactions; tuned to achieve the desired depth of color and target yield based on pigment application segment

    Downstream process integration

    • Introduced at the heterocyclic ring formation step during aromatic amine synthesis
    • Employed in closed-system high-pressure reactors to maximize coupling efficiency and minimize halogenated byproduct formation

    Final product types

    • High-strength diazo pigment intermediates
    • Chloro- and iodo-substituted dye precursors for plastics and specialty coatings
    • Color-stable inks for electronic imaging and textile printing
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    Certification & Compliance
    More Introduction

    3,4-Dichloroiodobenzene: Expertise From the Manufacturer’s Bench

    A Proven Intermediate for Demanding Synthesis

    In the chemistry world, intermediates play a bigger role than many people might realize. They shape both the pace and outcome of specialty and bulk chemical creation. At our manufacturing site, 3,4-dichloroiodobenzene, known in the lab by its CAS number 16178-47-9, stands as a pillar in halogenated aromatic chemistry. Our teams don’t see it as just another material – we’ve watched it change the approach of both experienced and upcoming chemists across pharmaceutical and materials science projects.

    We manufacture 3,4-dichloroiodobenzene as a solid, with a typical purity exceeding 98%. Every lot comes with a light off-white to pale yellow crystalline appearance, which our colleagues confirm by eye at every packing stage. This visual checkpoint is often backed up by NMR and GC analysis, conducted right in our onsite QC labs. Through years of refining these processes, the chemical’s melting range stays reliably between 58°C and 62°C, handled in sealed drums and double-lined fiber cartons depending on end-user bulk requirements. That way, we avoid the dusting and loss issues that sometimes come up with strong halogenated aromatics, especially in coastal climates.

    Why Chemists Favour 3,4-Dichloroiodobenzene

    Most buyers come looking for this molecule because of its dual reactivity. The two chlorine atoms at the 3 and 4 positions offer just the right blend of electron-withdrawing effects and steric profile. The iodine, positioned para to the nearest chlorine, brings the advantage of high reactivity in transition-metal-catalyzed coupling reactions. Our customers leverage this in Suzuki, Heck, and Sonogashira couplings, using it to introduce both small and bulky nucleophiles onto aromatic systems.

    Pharmaceutical synthesis benefits the most directly. Research chemists turn to this compound when they need to introduce difficult substituents onto benzene rings, especially during late-stage development of kinase inhibitors and anti-infective leads. Because the substrate handles well at larger scales, process chemists scale up operations without redesigning for each batch—that saves months in development time and keeps project costs from ballooning.

    Another side of the story comes from materials scientists. They work with 3,4-dichloroiodobenzene to build up functionalized polymers, liquid crystals, and soon-to-be electronics applications. In printed electronics especially, the difference between consistent and uneven batch quality changes performance at the device level. Our focus on not just purity, but also on isomeric control, comes directly from feedback received from these users.

    Comparison: 3,4-Dichloroiodobenzene and Its Relatives

    We hear from new customers every season: How does 3,4-dichloroiodobenzene compare to simple di-chlorobenzenes or its bromo- and fluoro- derivatives? Experience in our team dates back to when halogenated aromatics came mainly through much less selective routes, so we’ve seen how product choice impacts the entire downstream process.

    In standard dichlorobenzenes, you only get the activating effect of the chlorines, which restricts the scope of later-stage coupling. Adding an iodine atom not only opens up the aromatic ring for cross-coupling, it also increases selectivity for both palladium and copper catalyzed steps. The bromo analog—3,4-dichlorobromobenzene—offers similar reactivity, but the iodine delivers higher yields and milder conditions under the same protocols. This reduces the formation of stubborn byproducts that can spoil high-purity synthesis, especially under push for sub-ppm halide residues in pharmaceutical actives.

    On the flip side, switching the position of the iodine from the 3 or 4 to the 2 or 5 position on the benzene ring results in reduced selectivity. Side reactions can climb, along with complicated mixtures requiring labor-intensive chromatography. Many process chemists come to us after struggling with those isomers; we’ve worked with them to transition operations seamlessly and achieve faster phase changes in their synthetic plans.

    Process Hazards and Real-World Handling

    Not all halogenated benzenes behave the same way on the shop floor. Unlike polychlorinated compounds, 3,4-dichloroiodobenzene doesn’t present the same volatility risk, but it can still trigger allergic reactions and respiratory discomfort if not handled with basic PPE. Our operators use powered air respirators and layered gloves not out of protocol, but based on first-hand lessons learned during pilot runs in the past. This practical experience has also prompted us to design powder transfer systems that limit open handling. We’re reminded every year by the operators: keeping handling simple and predictable minimises both dust generation and material waste.

    Storage and shelf stability also matter. As a moderate halogenated aromatic, this material stores well below 30°C in sealed vessels away from sunlight. We tested bags against drums over five years of inventory; metal drums with an interior lining remained most reliable, keeping moisture and light away and preventing trace decomposition. Our chemical remains unchanged for up to two years under normal warehouse conditions, with regular retesting intervals.

    Disposal gets special attention. We support customers in managing residual powders. Waste streams containing 3,4-dichloroiodobenzene pass through licensed incineration contractors. The practical advice from our EHS team: avoid washing any residual into drains, as this prevents organohalide buildup in public wastewater networks.

    Supporting Developments in Green Chemistry

    Our commitment to responsible manufacturing drives us to constantly refine the way we make, package, and ship this product. By switching to more atom-economic routes, we dropped our use of heavy metals in iodination steps by nearly 90% over the last decade. Where older synthesis relied on multi-stage halogen exchange and strong acid waste, we now operate a more direct oxidative coupling system developed by our senior R&D chemist. Fewer steps, less hazardous waste, higher yields—these aren’t just academic targets, but practical improvements that customers see in cost, environmental reporting, and product performance.

    Sometimes we see pushback: new regulations or client audits push for documentation at a level not common in the past. We meet these requirements by integrating real-time QC records and sample tracking in every batch. Our digital tracking means customers can see full chain-of-custody, dating back to raw iodine and precursor shipments. Several times, this has resolved questions during ISO and GMP audits, ensuring downstream suppliers can defend their own certifications based on our traceable documentation.

    Shipping and Packaging: Quality Outlasts the Distance

    Shipping halogenated aromatics looks simple on paper, but international buyers face unpredictable delays and temperature swings. Our shipping crew once tracked an air freight batch that sat in desert heat for twenty-one days due to a paperwork hold. That batch arrived with unchanged assay and visual purity—precisely because of our two-layer moisture barrier and inert gas blanket built into the drums. This wasn’t a lucky break, but a direct result of years of direct customer feedback and accelerated aging tests. Repackaging errors on the client side also get attention: We open our process to third-party inspection, supporting customers who need to subdivide for research, by either training their teams or offering in-country repackaging based on volume.

    Bulk buyers sometimes struggle to balance price and purity, especially when imported material shows up with trace brown oils or off-odors. In these cases, we work with clients not just as a supplier, but as a technical partner, sharing in-house reference chromatograms or even running confirmatory tests side by side. That partnership approach shortens the learning curve for both researchers and purchasing managers who deal less often with halogenated aromatic substances.

    Challenges in Scaling: A View From the Production Floor

    Scaling production for 3,4-dichloroiodobenzene looks predictable, but even small changes in batch size or input quality shift yields or waste production. During scale-up trials, we noticed subtle colour shifts in the crude stages depending on the source of dichlorobenzene feedstock or catalyst batch. Process stability came from direct real-world monitoring rather than relying solely on literature predictions. Only after multiple campaigns did we standardize both our purification route and our drying protocols. Moisture levels below 0.15% proved critical for both storage stability and downstream reactivity—regardless of outside humidity swings.

    Customers sometimes request custom volumes, which might sound like a routine job. From the factory’s perspective, switching from one ton per run to a pilot-lot of ten kilograms changes everything: the creation of fresh working solutions, realigning the crystallizer, and recalibrating filtration units. That’s why clear communication ahead of time matters most. Regular calls with client chemists help us avoid retooling errors, ultimately saving everyone valuable time in the development window.

    Case Studies: 3,4-Dichloroiodobenzene in Action

    Over the years, we’ve supported clients moving from bench-scale research up to full manufacturing of specialty APIs. In one project, a partner in Europe transitioned from in-house iodination of dichlorobenzene to using our finished 3,4-dichloroiodobenzene. Time constraints and inconsistent quality from rotary-evaporator operation had stunted their pilot lots for six months. After switching, they reported a sustained increase in coupling yields and were able to move to regulatory filing with both a cleaner impurity profile and faster production turnaround. Real feedback: production runs jumped from 65% to 90% isolated yield for a key intermediate.

    Another example: A startup in the OLED materials sector required kilogram-scale batches with a strict maximum allowable metallic residue. This project demanded more than standard lot-to-lot consistency—they supplied us with their own desired NMR control for byproduct baseline. After several pilot runs, mutual learning led us to fine-tune our purification, which gave them a product that improved film-forming characteristics in their electronic device fabrication.

    Problems don’t always come from the factory: one set of clients found that imported lots of 3,4-dichloroiodobenzene included trace copper, which played havoc with their catalyst system. By tracing the supply chain back, our chemists identified the contamination was introduced through the packaging process, not synthesis. We responded by shifting to inert liner material and verifying cleanliness of all equipment after maintenance.

    Working With the Research Community

    Our technical staff don’t stop at answering emails. They serve as sounding boards for research questions—sometimes challenging us to find better ways of making a familiar molecule, sometimes pushing our QC team to test for new impurities. High school chemistry students arrive every year for summer internships, learning directly how theoretical chemistry meets hands-on manufacturing. We invite visiting professors and process engineers from time to time to walk the line, examine impurities, and suggest improvements. This openness isn’t just for show—it’s grown our in-house expertise and helped us adapt to an industry that moves quickly.

    We openly share case data and analytical methods. At conferences, our teams present real findings, not just marketing slides. Recent collaborations have brought together process engineers, toxicologists, and regulatory specialists, with the goal of refining worker safety procedures and suggesting ways to make even greener halogenations. By engaging with the research community, we both shape and respond to emerging best practices.

    Traceability and Customer Support

    Some buyers need only bulk commodity material, but others rely on documentation that covers each handling step. We offer batch-level traceability and issue up-to-date Certificates of Analysis with every order. Our internal database goes past the usual lot records, tracking all test results, operator logs, and storage conditions dating back five years. This information becomes crucial during pharmaceutical validation or international regulatory reviews.

    Beyond paperwork, we know that customer support defines a successful relationship. Our experienced chemists can walk through analytical data, troubleshoot suspected contamination, and assist with validation re-testing. For research customers who need to modify the product’s packaging or break down bulk drums, we offer guidance and short-turnaround sampling without rigid bureaucracy. Many long-term partnerships grew out of solving a specific technical problem, not just a simple purchase order.

    Reducing the Carbon Impact

    Global regulations continue to emphasise environmental responsibility. In our plant, we invest not just in compliance, but in reducing the overall environmental burden. Captured emissions from halogenation steps undergo multi-stage scrubbing to avoid atmospheric and wastewater release. By pioneering direct recovery and reuse of solvents within the plant, we consistently lower the carbon footprint for every ton made.

    Supply-chain looping—recycling off-grade materials into non-critical internal applications—keeps wastage low and strengthens our purchasing leverage. Every year we review new green chemistry advances, looking for practical upgrades. Some initiatives, like switching to renewable energy to power reaction vessels, take longer to implement, but the work continues with clear real-world benchmarks.

    Market Trends and Outlook

    Demand for 3,4-dichloroiodobenzene continues to shift as new applications arise in pharmaceuticals, agricultural research, and high-end polymers. Pharmaceutical demand spikes when a new candidate enters clinical development, only to wane if a project fails. Materials science, on the other hand, has brought steady new inquiries for higher-purity, low-residue material. We also notice movement from smaller, niche chemical development firms seeking to escape inconsistent spot markets—and looking for reliability in scheduling and technical support.

    We’ve seen the occasional concern about supply stability during geopolitical turmoil or pandemic-related shipping shutdowns. Here, direct production capability and deep stocks of raw materials have helped us weather uncertainty and keep delivering, whereas brokers have sometimes struggled to secure enough inventory. Customers who rely on continuity for validated production see value in direct lines to the manufacturer's team.

    Listening to Feedback

    Direct customer feedback improves not only technical delivery but also strengthens trust. From packaging tweaks to changes in purity thresholds, much of our product evolution reflects what our partners need on the ground. Some have asked for improved labeling or smaller pack sizes for pilot work; others want documentation to meet evolving regulatory regimes. We take this feedback seriously and integrate changes quickly wherever they make a meaningful difference for safe handling or efficient processing.

    The Manufacturer’s Perspective

    Having produced 3,4-dichloroiodobenzene for over a decade, our team has built significant operational know-how. The product is not just a line-item in a catalogue—it represents years of learning about what makes a difference for chemists in the field. From precise management of crystallization variables, to the lessons our operators have learned about handling powder safely, everything shapes the consistency that our customers rely on.

    Other companies might sell the same chemical, but only direct manufacturing brings the insight and agility to respond when something unexpected happens. We remain committed to direct, informed technical support, clear documentation, and practical problem-solving for every buyer and user who works with this versatile building block.