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3,5-Dichloroiodobenzene

    • Product Name 3,5-Dichloroiodobenzene
    • Alias 3,5-Dichloro-1-iodobenzene
    • Einecs 252-137-3
    • 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

    202892

    Chemical Name 3,5-Dichloroiodobenzene
    Molecular Formula C6H3Cl2I
    Molecular Weight 272.90 g/mol
    Cas Number 626-00-6
    Appearance White to off-white solid
    Melting Point 84-86 °C
    Boiling Point 282-284 °C
    Density 2.13 g/cm3
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Smiles C1=C(C=C(C=C1Cl)I)Cl
    Inchi InChI=1S/C6H3Cl2I/c7-4-1-6(9)3-5(8)2-4/h1-3H

    As an accredited 3,5-Dichloroiodobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3,5-Dichloroiodobenzene, sealed with a screw cap, labeled with hazard and identification information.
    Shipping 3,5-Dichloroiodobenzene is shipped in tightly sealed containers, protected from light and moisture. The packaging complies with international regulations for hazardous chemicals, including proper labeling and documentation. During transport, it is handled as a potentially hazardous material and should be kept away from heat, flames, and incompatible substances to ensure safe delivery.
    Storage 3,5-Dichloroiodobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight. Keep it segregated from incompatible substances such as strong oxidizers, reducing agents, and strong bases. Ensure the storage area is equipped to contain spills and is compliant with local chemical storage regulations. Store at room temperature.
    Application of 3,5-Dichloroiodobenzene

    Applications of 3,5-Dichloroiodobenzene in Industrial Manufacturing

    3,5-Dichloroiodobenzene serves as an advanced halogenated aromatic intermediate that plays a crucial role in several downstream industries. The following application scenarios detail how manufacturers integrate this raw material into production chains, specifying sector standards, precise formulation guidance, process stages, and resulting end-use products. All scenarios focus on proven industrial-scale applications, grounded in proprietary experience as an original chemical manufacturer supplying global B2B customers.

    1. Agrochemical Active Ingredient Synthesis

    Leading agrochemical companies utilize 3,5-dichloroiodobenzene as a key intermediate for building certain chlorinated pesticide molecules through Suzuki, Ullmann, and related cross-coupling reactions. Its controlled reactivity enables reliable introduction of multiple halogen groups during the core assembly of pre-emergent and post-emergent herbicide actives, especially where selective aromatic substitution is necessary to achieve target biological activity and environmental stability. Downstream manufacturers commonly cite its purity and consistency for minimizing by-products during scale-up.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management System for suppliers
    • REACH Annex XVII requirements for hazardous substances
    • EU Regulation (EC) No 1107/2009 – Plant Protection Products

    Typical usage ratio

    • 5–12% w/w in the primary coupling step, adjusted by target molecule structure and desired conversion yield during batch synthesis

    Downstream process integration

    • Charged in the initial step of catalytic halogen exchange/coupling with boronic acids or amines for the construction of bioactive aromatic structures in multi-step herbicide or insecticide production

    Final product types

    • Pre-emergent herbicide actives
    • Selective insecticidal formulations
    • Fungicidal intermediates for crop protection
    • Active ingredient masterbatches for seed treatments

    2. Pharmaceutical Intermediate for API Building Blocks

    Pharmaceutical manufacturers incorporate 3,5-dichloroiodobenzene during the synthesis of advanced aromatic scaffolds required for non-steroidal anti-inflammatory drugs, certain antihypertensives, and other small-molecule medicines. Key process engineers leverage its halogen atom configuration for constructing essential API ring systems, enhancing both functional group compatibility and further downstream derivatization. Owing to strict source traceability demanded by regulators, origin and batch consistency of this compound are audited and certified at cGMP-compliant facilities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) drug substance requirements
    • USP General Chapter <232> Elemental Impurities
    • FDA 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • 2–7% m/m relative to the primary reaction substrate in process steps for building functionalized aromatic halosubstrates as API precursors; ratio determined by target API complexity and desired product throughput

    Downstream process integration

    • Fed into early- or mid-stage coupling, substitution, or halogen exchange stages of API intermediate assembly—especially for critical ring-closure or functional group introduction prior to purification and final conversion

    Final product types

    • Pharmaceutical intermediates for antihypertensives
    • Advanced starting materials for anti-inflammatory drugs
    • Intermediate compounds for oncology APIs
    • Building blocks for CNS (central nervous system) therapies

    3. Specialty Chemical Synthesis for Liquid Crystal Materials

    Producers in the advanced materials sector employ 3,5-dichloroiodobenzene as a high-purity ingredient for constructing biphenyl and terphenyl core units in liquid crystal mixture formulations. Its defined halogenation profile ensures precision in molecular alignment and electro-optical characteristics, which are critical for the performance of display-grade liquid crystals. Stringent quality control and upstream documentation accompany every batch to support downstream compliance audits and ensure defect-free integration.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for hazardous substances in electronics manufacturing)
    • ISO 9001:2015 certified supply chain traceability programs
    • REACH Regulation (EC No 1907/2006) for chemical safety and usage documentation
    • IEC 61249-2-21:2018 Material standards for display technologies

    Typical usage ratio

    • 3–8% by molarity as a coupling component in core liquid crystal intermediate synthesis; ratio subject to mixture composition and targeted electro-optical phase performance

    Downstream process integration

    • Introduced during the formation of rigid-core molecular structures via palladium-catalyzed cross-coupling with other aromatic monomers; the resulting intermediates further processed into nematic or smectic liquid crystal blends

    Final product types

    • Liquid crystal intermediates for LCD screens
    • Active matrix displays for consumer electronics
    • Industrial display panels
    • Flexible display component mixtures

    4. Fine Chemical Intermediate for Dye and Pigment Manufacture

    Colorant and specialty dye manufacturers leverage 3,5-dichloroiodobenzene to build halogenated aromatic backbones required for high-performance pigments and specialty dyes. Its integration supports synthesis routes demanding oxidative stability and precise colorimetric control, especially in the creation of azo and phthalocyanine derivatives. Strict adherence to dye regulatory and material safety legislation ensures safe downstream use in text iles, plastics, and coatings destined for regulated markets.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile chemical safety)
    • REACH Annex XIV and XVII (restrictions on hazardous azo dyes)
    • ISO 12402-7:2020 (pigment quality and purity)
    • Global Organic Textile Standard (GOTS) for inputs where applicable

    Typical usage ratio

    • 4–10% by weight in aromatic coupling reactions, adjusted by pigment chromophore structure and color intensity needed for final dispersion properties

    Downstream process integration

    • Charged into early-stage aromatic substitution/coupling during the core chromogen assembly; post-synthesis, intermediates are finished through cyclization, sulfonation, or metallation steps for targeted hues

    Final product types

    • High-performance textile dyes
    • Plastic and polymer-bound pigments
    • Special effect colorants for coatings
    • Industrial ink intermediates
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    Certification & Compliance
    More Introduction

    Digging Deeper into 3,5-Dichloroiodobenzene: A Manufacturer’s Perspective

    Background and Product Overview

    3,5-Dichloroiodobenzene has shaped the way we approach halogenated aromatic intermediates in chemical manufacturing. Our experience, rooted in hands-on synthesis and scale-up, highlights how subtle changes in molecular architecture can set the stage for a broader range of chemical transformations. From the outset, working directly with 3,5-dichloroiodobenzene brought both opportunities and challenges not readily apparent to outsiders. Producing this compound in-house streamlined our control over every step, offering pure and reliable output for demanding end uses.

    The model we produce, C6H3Cl2I, is synthesized under tightly monitored conditions. Over years of production batches, we learned the importance of maintaining exact chlorine and iodine ratios—small shifts tend to cascade into off-spec material or unwanted byproducts. Our methods, developed through extensive benchwork and continuous feedback from our technical team, focus on consistent crystallinity, high purity, and predictable reactivity. Handling 3,5-dichloroiodobenzene at scale exposed issues with temperature management and halide recovery—solving those puzzles improved not only output, but also the safety and environmental footprint across our facility.

    The Why—And What Sets It Apart

    We chose to specialize in this compound because of its unique electronic and steric properties. The positioning of the chlorine atoms on the benzene ring, coupled with the heavier iodine substituent, shifts reactivity in ways that differ from its cousins like 2,4-dichloroiodobenzene or the lighter halogen analogues. Our customers in agrochemical and pharmaceutical intermediate fields need a platform that accepts a diverse set of coupling reactions. 3,5-Dichloroiodobenzene responds sharply to processes like Suzuki-Miyaura and Ullmann coupling. Our experience has shown that integrating a purer, reliably sourced starting material slashes the number of side products and simplifies purification downstream—issues we attack at the root through meticulous quality controls.

    Over time, the market has flooded with lower-grade material—often from batch processes that prioritize yield over selectivity. Mass spectroscopy and HPLC records in our own QA lab show clear differences in minor impurity levels compared to random commercial lots. Even minor contaminants drag down reactions, especially for drug synthesis where regulatory filings demand full impurity profiles. We work hard to keep batches within a narrow impurity range, mainly to reduce troubleshooting for our customers, but also because our own process yields improve over repeated cycles when less waste builds up in the lines.

    Production Methods: What Knowledge Teaches

    Traditional chlorination and iodination sequences rarely offer clean selectivity. Early in our production history, we saw inconsistent yields when relying on sequential halogenation, especially during scale-up from glassware to pilot reactors. Chlorine atom placement proved tricky—orthogonal approaches led to complex mixtures if not carefully tuned. Drawing on year-to-year process learning, our team uses finely controlled solvent selection, temperature ramps, and staged reagent addition. Equipment upgrades, such as jacketed reactors with fine temp control and in-line monitoring systems, answer directly to the practical hurdles we’ve faced.

    Each batch tells its own story. Some days, trace moisture in the system shifts reactivity; at other times, starting stock purity subtly influences the final outcome. Chemically, the benzene ring’s electron-withdrawing groups change behavior with scale. Our on-floor technicians track these patterns, head-off potential runaway reactions, and adjust parameters to keep purity and yield on target. These tweaks aren’t theoretical—they’re responses to concrete production hiccups that impact not only immediate output, but longer-term reactor life and safety.

    Real Needs in Application: Listening to Customers

    Our partners in pharmaceutical R&D demand high-purity inputs to keep their syntheses predictable, but their pain points go deeper than advertised assay values. In our own runs and joint projects, inconsistency in 3,5-dichloroiodobenzene led to variable bioactive compound yields and unexpected chromatographic peaks. For an agrochemical client, downstream hydrodehalogenation runs consistently failed with some off-grade lots. Through collaborative troubleshooting, we traced the problem back to nonuniform halogen placement or trace over-chlorination. Small things matter when milligram-scale R&D must scale up to multi-ton purchases.

    Our close-up view proved that end-users rely on regular, direct dialogue with us, the manufacturer—not just for product data, but for operational advice. We get calls about solubility differences when switching suppliers, and questions on how our product compares in cross-coupling performance. We credit our technical support team’s field work, testing samples in real application environments, for keeping the gap between theory and practice as small as possible. Their work feeding data and feedback into our manufacturing protocols led to material that responds as users want—batch after batch.

    What Distinguishes 3,5-Dichloroiodobenzene from Other Halogenated Benzenes

    Other versions of halogenated benzenes—4-chloroiodobenzene, 2,4-dichloroiodobenzene, or 1,3-dichlorobenzene—carry different reactivity signatures. It seems basic on paper, but in synthetic chemistry, these differences can make or break a project. The 3,5 orientation of the chlorine atoms leaves open ortho and para positions, impacting both regioselectivity and steric hindrance in nucleophilic aromatic substitution. From our hands-on results, nucleophilic reactions run cleaner with this configuration, minimizing byproducts common in more congested isomers.

    Our technical staff ran numerous head-to-head reaction studies with analogous halobenzoid systems. The 3,5-dichloro substitution pattern resists unwanted side reactions sparked by electron density differences, granting a bit more leeway for less controlled reaction conditions. Pharmaceutical route scouting teams appreciate the improved reliability, especially for sensitive palladium-catalyzed couplings. We noticed, too, that downstream crystallization or filtration proceeds with fewer blockages and fouling episodes—a practical edge when running kilo-scale processes.

    Quality Assurance: It’s Personal

    Nothing replaces the confidence gained from running one’s own synthesis batches. Real accountability happens on the factory floor, not in spreadsheets. Our QA department samples material at multiple stages—raw feedstock, intermediate, final packed product. GC-MS, NMR, and classical titration methods back up each certificate, but the real testament is in hassle-free performance for the end user. We track every feedback call, every batch deviation, and adjust our process controls accordingly.

    Our audits with regulatory agencies push us to hold even tighter specifications, especially on residual solvents and heavy metals. Repeat buyers know they’ll get material that doesn’t introduce hidden variables into their production. That reputation matters more than flash marketing, and it springs from the care put into material handling, process design, and experienced eyes watching each stage.

    Role in the Supply Chain: Relationships Matter

    We serve both global, high-volume formulators and small specialty research houses. Many of these relationships run for years, cemented on a foundation of consistent batch behaviors and open technical communication. Our position as a direct manufacturer sharpens attention to supply reliability—tracking precursor markets, adjusting order timing for reagents, investing in local utility upgrades to keep the plant running no matter the season.

    Some customers approach us after struggling with off-branded imports or third-party amalgamators whose lots vary unpredictably. Our response centers on shipment tracking, live batch traceability, and documented change management in process tweaks. The feedback loop—talking directly to process chemists at our clients’ sites—anchors product refinement as well as delivery reliability. We’ve learned it’s not enough to just offer a specification sheet; customers look for an extra layer of trust built on shared problem-solving. Our plant tours and open audits build confidence and allow for ongoing improvement on both sides.

    Long-term demand planning, secured raw materials at negotiated quality grades, and local storage buffer us from upstream hiccups that can throw schedules. When upstream raw materials show volatility, we react by transparently communicating with partner companies, buying consignment stock, or even adjusting transfer windows to keep production and shipment flowing.

    Environmental Responsibility: Beyond Compliance

    Many halogenated aromatic compounds carry the burden of potential toxicity and environmental persistence. Our factory team approaches this challenge not as a box-ticking exercise for compliance, but as a vital area for innovation. From the outset, we invested in closed-loop solvent recovery systems, halide recycle loops, and continuous monitoring of effluent streams. Lessons learned over production cycles prompted us to redesign ventilation, select process-compatible containment materials, and optimize reaction cleanouts for minimal discharge.

    Our plant teams run regular drills on spill control and train incoming operators on the real risks associated with these intermediates. One discovered shortcut in process wastewater handling forced a full line audit and retraining session. That experience cemented a culture where every operator shares responsibility for environmental outcomes. Our partnerships with third-party environmental auditors led to project collaborations—like reusing process brines in local industrial parks—which reduce both footprint and local water stress.

    Addressing Challenges and Pursuing Solutions

    Scaling 3,5-dichloroiodobenzene production brings specific engineering headaches. Sensitive feeds and reaction exotherms often require rapid response to prevent runaway conditions, especially in warm climates. We constantly refine our control logic and automate critical points on the production lines. On several occasions, recalibrating temperature sensors or overhauling valve controls averted incidents that could have spiraled. Our engineering staff logs every incident, feeds lessons learned into future process upgrades, and shares findings with peer teams across locations.

    Another challenge lies in waste minimization. Older processes generated large halogen-containing byproduct streams. We overhauled our workups after consulting with external chemical engineers, introducing phase-separation auxiliaries and more selective crystal-forming solvents. In the past, lost product in the mother liquor or fines escaping in dust cost not just in dollars, but increased hazard in waste streams. Now, in-plant recycling and recovery have become embedded in our daily routines, and we share those methods openly with downstream users.

    We faced logistical bottlenecks during high-demand periods. Batch management and rapid order fulfillment only work with careful planning and skilled warehouse teams. Rather than outsourcing warehousing, integrated inventory systems now allow our floor managers real-time tracking and three-day shipment forecasts. Even during unpredictable global logistics swings, reliable stock against contract commitments remains our benchmark.

    Engagement with End Users: Technical and Human Connections

    No batch leaves the factory until we hear back from the field—literally. Users on the ground, from PhD process chemists to operations managers, offer feedback on flowability, reaction timeline, and residue build-up. We treat this input as fact, not anecdote. Our technical support staff run shadow batches with submitted customer solvents and catalysts, sometimes even renting time on our pilot plant to resolve scale-up hiccups. That hands-on, collaborative pattern has become a hallmark of our approach.

    Engagement won’t end at the boundary of a C-of-A. Troubleshooting requests come in at midnight, during year-end push, or in the middle of regulatory filing cycles. Our chemists don’t just answer emails—they dial in, volunteer in-plant visits, and sometimes send improved samples drawn off our own research lines.

    Continuous Improvement and Looking Forward

    This molecule may not grab headlines, but in our business, its careful production links whole supply chains. Investment in R&D keeps us ahead of market shifts and regulatory tightening. Whether it’s tweaking our purification steps, running pilot reactor studies to boost selectivity, or scouting for greener halogenation approaches, we treat each advance as a new floor, not a ceiling. Our plant engineers meet quarterly with the production and safety teams, hammering out updates to batch protocols, reviewing recent feedback, or launching new improvement projects. Each production campaign builds on the last—habitual introspection and willingness to adjust keep us resilient.

    For growing sectors like specialty agrichemicals, material traceability and reproducibility keep management awake at night. The bar gets raised every year for reliability, responsiveness, and transparency in the chain. Experience tells us that “almost good enough” batches translate into wasted time, money, and reputational risk for both our company and our partners. Maintaining that precision is more than a business goal—it’s a point of professional pride and personal investment for our staff, many of whom have grown their careers inside our own labs and plant floors.

    Concluding Thoughts: Why We Stand Behind Our Product

    At the end of the day, our value doesn’t rest solely in the price or the number stamped on a label. We focus on real-world performance, traceable quality, technical partnership, and commitment to both people and planet. Decades of experience have shaped every gram of 3,5-dichloroiodobenzene we produce. Each hurdle—regulatory, technical, or logistical—has left its mark on our protocols, our teams, and the product in the drum. We hear and value direct voices from the factory floor to the customer’s lab, viewing each as an essential partner in getting this vital intermediate right. Consistency, transparency, resilience, and a collaborative spirit shape our path forward. These values, forged in the act of making, stand behind every shipment that leaves our site.