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4-Chloro-2-Iodotoluene

    • Product Name 4-Chloro-2-Iodotoluene
    • Alias 2-Iodo-4-chlorotoluene
    • Einecs 841-732-5
    • 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

    550838

    Productname 4-Chloro-2-Iodotoluene
    Casnumber 57311-89-2
    Molecularformula C7H6ClI
    Molecularweight 252.48
    Appearance Colorless to pale yellow liquid
    Boilingpoint 255-257 °C
    Density 1.81 g/cm3
    Refractiveindex 1.630
    Flashpoint 107 °C
    Solubility Insoluble in water
    Purity Typically ≥97%
    Storagetemperature Store at 2-8°C
    Synonyms 2-Iodo-4-chlorotoluene

    As an accredited 4-Chloro-2-Iodotoluene 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 4-Chloro-2-Iodotoluene, sealed with a screw cap, labeled with safety and chemical information.
    Shipping 4-Chloro-2-Iodotoluene is shipped in tightly sealed containers, typically made of glass or compatible plastic, and cushioned to prevent breakage. It is transported as a hazardous material, following appropriate regulations for chemicals. The package includes safety labeling and documentation, ensuring compliance with local, national, and international transport standards.
    Storage 4-Chloro-2-iodotoluene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of heat, ignition, and direct sunlight. Keep it separate from strong oxidizing agents and incompatible materials. Store under inert atmosphere if sensitive to moisture or air. Always follow relevant safety guidelines and label containers clearly.
    Application of 4-Chloro-2-Iodotoluene

    Applications of 4-Chloro-2-Iodotoluene in Industrial Manufacturing

    As a manufacturer of high-purity 4-Chloro-2-Iodotoluene, we supply this intermediate to leading industrial sectors with well-defined synthesis routes. The following application scenarios describe how our material supports specialized downstream manufacturing in advanced chemical processes.

    1. Agrochemical Active Ingredient Synthesis

    Agrochemical formulators utilize 4-Chloro-2-Iodotoluene as a key halogenated aromatic intermediate for custom herbicide and fungicide molecule development, specifically where selective activity or controlled environmental stability relies on unique halide substitution. The compound serves as a core building block in Suzuki coupling reactions and other palladium-catalyzed conversions, introducing high substrate reactivity for target agrochemical backbone construction. Downstream formulators precisely adjust input volumes of this raw material based on the final molecular architecture desired, resin load, and reaction yield targets. This integration supports the manufacture of differentiated crop protection actives meeting stringent purity and safety profiles required by global regulatory frameworks.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC 1907/2006) Substance Registration and Safety Data
    • ISO 9001:2015 Quality Management Systems
    • OECD Guideline 5: Chemical Identity and Characterization

    Typical usage ratio

    • 0.5%–5% by weight relative to the total synthetic batch, adjusted depending on targeted agrochemical compound structure and coupling efficiency; optimization may incorporate process yield monitoring and intermediate purity analysis.

    Downstream process integration

    • Introduced at the halogenation and cross-coupling stage for C–C bond formation; dissolved in organic solvents (e.g., DMF, toluene) and reacted under controlled temperatures with metal catalysts and base.

    Final product types

    • Systemic herbicides with heteroaryl substitution
    • Triazole or strobilurin fungicides
    • Pre-emergent soil treatment actives

    2. Pharmaceutical Intermediate Production

    Pharmaceutical API manufacturers incorporate 4-Chloro-2-Iodotoluene into synthetic schemes demanding precise control of halogen positioning, where its dual halogen motif enables efficient step-growth for advanced intermediates. It participates in process-scale Grignard and lithium-halogen exchange reactions, supporting the synthesis of halogenated iodobenzenes, which ultimately yield non-steroidal anti-inflammatory drugs or oncology agents. Quality assurance teams monitor incoming batches for trace-level impurity profiles and lot traceability required by international pharmacopoeial standards prior to use in regulated synthesis suites.

    Industry compliance standards

    • ICH Q7A: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Monographs (where applicable to downstream intermediates)
    • 21 CFR Part 211 Current GMP in Pharmaceutical Manufacturing
    • European Pharmacopoeia standards for raw material impurities

    Typical usage ratio

    • 0.3%–2.5% of total batch mass, calculated by intermediate yield data and desired molecular transformation; increased for multi-stage or high-value molecule synthesis with strict controls at each stage.

    Downstream process integration

    • Charged into protected vessel reactors at the halogen-exchange or organometallic coupling step; handled under nitrogen or argon streams to suppress moisture and preserve iodinated structure, prior to acid/base work-up and crystallization.

    Final product types

    • Pyridine-based CNS active drug intermediates
    • Halogenated APIs for targeted cancer therapeutics
    • Sulfonamide pharmaceutical building blocks

    3. Electronic and OLED Material Precursors

    In the advanced electronics sector, 4-Chloro-2-Iodotoluene provides designers with a functionalized aromatic building block for the creation of high-purity conjugated compounds needed in organic light-emitting diode (OLED) device fabrication. Material scientists value the precise substitution pattern for its influence on molecular orbital alignment and charge mobility in custom emitter molecules. Downstream users dose the compound into controlled coupling processes, accommodating the required purity levels and performing batch QC by HPLC and GC–MS to confirm absence of trace contaminants that would disrupt device performance.

    Industry compliance standards

    • IEC 62321: Hazardous Substance Testing for Electronic Materials
    • RoHS Directive (2011/65/EU) for restricted substances
    • ISO 14001:2015 Environmental Management for Electronic Chemical Processes
    • Internal OEM specifications for OLED raw material purity

    Typical usage ratio

    • 1%–4% by mass, depending on the final molecular weight of the OLED precursor and device layer requirements; rate set according to stoichiometric balance in subsequent coupling reactions and device yield feedback.

    Downstream process integration

    • Dosed at the initial aromatic substitution or Suzuki–Miyaura coupling step; batch-mixed under controlled temperature and inert conditions, followed by multi-stage purification and solvent exchange prior to film deposition.

    Final product types

    • Blue, green, and red OLED emitter molecules
    • Organic semiconductors for display backplanes
    • Functional oligomers and polymers for display applications

    4. Dye and Pigment Intermediate Manufacturing

    4-Chloro-2-Iodotoluene serves as a specialty raw material in the dyestuff industry, where its unique dual-halide structure allows precise introduction into azo, anthraquinone, and heterocyclic dye intermediates. Technicians adjust the charge-in weight to balance chromophore intensity against solubility requirements, leveraging its reactivity in nucleophilic aromatic substitution and halogen-metal exchange reactions. Downstream users reference lab-scale conversion data to ensure consistent color fastness attributes in the final pigment dispersions, especially for applications in high-value textiles and printed circuit inks.

    Industry compliance standards

    • REACH (EC 1907/2006) for chemical substance safety
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substance List) for textile chemicals
    • ISO 105-A02:2019 Color Fastness to Washing Standards
    • Chinese Standards GB 38507-2020 for Industrial Dyes

    Typical usage ratio

    • 0.8%–3% by synthetic batch, with actual percentage fine-tuned based on targeted pigment loading and desired color strength; higher inputs are reserved for deep-shade or high-density dispersion production runs.

    Downstream process integration

    • Reactive charge-in at the nucleophilic aromatic substitution, coupling, or halogen–metal exchange stage; integration followed by sequential filtration, drying, and sometimes sulfonation prior to pigment dispersion and formulation.

    Final product types

    • Textile dye intermediates for synthetic fibers
    • High-performance printing inks for electronics
    • Specialty colorants for industrial coatings
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    Certification & Compliance
    More Introduction

    4-Chloro-2-Iodotoluene: Connections Between Innovation, Purity, and Value

    Understanding 4-Chloro-2-Iodotoluene as a Building Block

    From decades of hands-on work at the reactor, I have seen the demand shift for halogenated toluenes such as 4-Chloro-2-Iodotoluene in the research bench and the production-scale plant alike. This compound has helped power progress in pharmaceutical synthesis, crop science, and various specialty organic applications. Our day-to-day efforts keep one core principle in sight—consistency in quality and honest communication about how this substance performs compared to similar aryl halides.

    4-Chloro-2-Iodotoluene, with its iodine and chlorine atoms arranged on the toluene ring, gives chemists more freedom during coupling reactions. The selective placement of these groups opens doors for regioselective Suzuki and Sonogashira couplings, enabling easier connectivity between complex fragments. Researchers frequently turn to this molecule when looking to build up advanced, functional organic structures, especially when the activation and reactivity patterns offered by chlorine and iodine are both required on a single frame.

    The model we prepare features a purity level refined well beyond 98%. Each batch leaves our doors with a trace water content, heavy metal trace levels, and residual solvent presence all documented and contained within extremely tight control. You can spot differences by NMR and HPLC every time. Anyone who's spent hours in the lab can appreciate the time and frustration saved by receiving product with consistency across lots—no unexplained peaks, no weird baseline noise. Our pride comes from sending out material that does what the chemist expects, letting project timelines move forward without hitch.

    From Raw Materials to Purified Output: Real-World Process Details

    Production lines for this compound demand reliable feedstocks and a sharp eye on every reaction. Chlorotoluene and iodobenzene starting materials contribute unique handling quirks, and there’s little room for short cuts when you start scaling. On the shop floor, the balance between cost efficiency, safety, and minimizing process impurities informs every loop. Using iodination strategies that serve both yield and purity, and working in close contact with solvent recovery operations, we produce at a scale that covers both R&D and commercial needs without pausing for batch-to-batch troubleshooting.

    Some competitors on the market aim to cut corners on crystal washing or purification, but these savings bring hidden problems. Side-iodination, over-chlorination, and para-related impurities creep in and resist purification with standard crystallization. In our tanks, we build in redundancy: careful stoichiometry, temperature hold periods, and staged solvent systems keep the impurity profile tight. Our team puts each batch under analytical scrutiny, including GC-MS, high-resolution NMR, and elemental analysis before any kilogram goes to packaging.

    It is not only about reducing microimpurities for show—catalyst poisons in pharmaceutical intermediates have real costs. Plant chemists know how resource-intensive late-stage purifications can be, especially when a run is jeopardized by a misbehaving aryl halide input. By minimizing varied impurity profiles, we preempt headaches that ripple far beyond the price per kilogram paid at the start.

    Key Applications: Driving Innovation in Organic Synthesis

    The dual halogen arrangement in 4-Chloro-2-Iodotoluene serves as a flexible launching pad in many breakthrough syntheses. In drug discovery teams, those developing novel kinase inhibitors or advanced fragment-based lead compounds depend on aryl systems that can take a wide set of downstream transformations. Our product spends its life not on shelves, but in the hands of process chemists who rely on both the reactivity and the robust performance profile it brings.

    Pesticide research groups regularly reach for this intermediate when they need substitution versatility and exceptional control over byproducts. We’ve participated in custom partnerships with groups pushing the boundaries of aryl-heterocycle formation, who have documented that even trace levels of side-chain halogen swapping or incomplete iodination in the raw material can lower final yields and introduce unacceptable regulatory risk. Constant monitoring and feedback cycles with these customers have led to progressive improvements not always visible on a typical certificate of analysis but clear in bench-to-plant reproducibility.

    In cross-coupling chemistry, especially where a site must be differentiated between chlorine and iodine for stepwise functionalization, this intermediate proves its worth on a regular basis. The higher reactivity of the aryl iodide towards palladium-catalyzed reactions allows selective functionalization without excessive forcing conditions—saving on both time and catalyst loading. Having spent hours running these reactions ourselves, we can say certainty in the feedstock beats a speculative reagent order, every time.

    Differences from Related Aryl Halides—Real Performance, Not Just Specifications

    Choosing between related products such as 2-Chloro-4-Iodotoluene, 4-Chloro-2-Tolylboronic acid, or dihalogenated xylenes often comes down to subtle points in reactivity and impurity manifestation. Chemical catalogs can affirm broad similarity in structural formula or degree of halogenation, but actual lab results tell a much richer story. For 4-Chloro-2-Iodotoluene, the relative positions of halogens govern the electron density across the aromatic ring, making certain couplings easier to control and less prone to wandering regioisomer formation compared to many ortho/para alternatives.

    Practical differences emerge under real-world use conditions. When working with more symmetrical dihalotoluenes, or those with both halogens in meta positions, controlling regioselective cross-coupling or halogen-metal exchange becomes much more difficult, requiring additional protective group steps or less scalable conditions. Our product gives a balance between robust stability in storage—helped by the methyl substituent’s lowering of volatility and chemical sensitivity—and desirable high reactivity in the most common C–C bond forming reactions. That means a lessened need for extra reaction optimization or side-product clean up, translating directly to fewer column runs and more reliable downstream syntheses.

    Scalability and Real-World Inventory Control

    Transparency about global supply chain disruptions and precursor pricing is a sore subject in this industry. Over the past years, swings in iodine and aromatic base costs have led to volatile pricing and, at times, unreliable lead times from some sources. Our team keeps a direct line to raw material producers, side-steps major intermediaries, and has invested in on-site storage and emergency feedstock capacity, buffering our customers from market shocks that slow R&D cycles.

    For those transitioning from gram to multi-kilogram quantities, consistent product quality and reliable shipment timelines make a marked difference. We routinely handle sudden scale-up requests due to project pivots—a new biological target, a promising SAR trend, or an unexpected manufacturing bottleneck. The consistency that comes from in-house control lets us honor volume increases without introducing contamination issues or regulatory surprises that can accompany spot-market purchases. Experience tells us a box with a familiar, trusted supplier’s label means more than a list of purity figures.

    Product Handling, Safety, and Responsible Operations

    Each production run brings a real sense of caution, both for staff and the broader community. Halogenated aromatics often carry handling concerns, so regular air monitoring, dust control, and process validation audits have become daily routine. On the packaging and distribution front, the work goes far beyond ticking boxes on regulatory checklists. Our warehouse and transport partners all receive frequent training and clear communication about the hazard profile, so every container is traceable, accounted for, and packaged to minimize exposure risk throughout its journey.

    Our operations team continually refines protocols to minimize loss and contamination, drawing insights from decades in specialty chemical logistics. We also invest in controlled waste treatment, ensuring reactant residues and mother liquors do not impact local landfill or water quality. Over time, this approach has resulted in cleaner, safer working environments—and ongoing approval from neighboring communities and local authorities. As manufacturers, we see this sense of duty not as a burdensome add-on, but as part of delivering value and upholding trust in our product and our name.

    Partnering with Research, Supporting Commercial Success

    Manufacturers occupy a unique vantage point between fundamental research and commercial delivery. Our ongoing collaborations with academic and industrial partners help chart the future for aryl halide chemistry. Regular cycles of feedback from customers have guided modifications to product specs, batch labeling formats, and delivery practices. That direct dialogue forms the backbone of our continuous improvement program, which has minimized downtime, product rejections, and unplanned regulatory audits.

    Feedback from process development groups has led us to offer detailed documentation packages for each batch, supporting regulatory submissions and intellectual property management. Having technical staff ready to answer detailed queries about impurity sources, residual solvent profiles, or reactivity nuances gives project teams the resources to keep progress high and setbacks low. In our experience, the extra steps taken before shipment—extra drying, repeat analyses after packaging, traceability logging—prevent far more work down the line than they cost up front.

    Commercial customers often must move faster than ever. With tighter regulatory deadlines and patent cliffs looming, they look for a manufacturer who can keep up without cutting corners. Our planning mindset means supply flexibility for both small-lot shipments to research labs and larger container-scale deliveries to industrial plants, with clear documentation to enable smooth transfer across continents and regulatory jurisdictions. We think of ourselves not merely as batch producers of aryl halides, but as partners growing together with our customers’ ambitions.

    Sustainability, Regulatory Evolution, and Long-Term Value

    Environmental initiatives continue to reshape how sensitive organoiodine compounds are produced and regulated. As stricter rules emerge on halogenated waste, solvent use, and process emission, our facility adapts with continuous investment in greener processes. We have piloted advanced filtration and closed-loop solvent systems, leading to lower overall emissions and more cost-effective methods for capturing and reusing both solvents and process byproducts.

    With increased scrutiny from regulatory agencies in North America, Europe, and Asia, documentation standards for all intermediates regularly evolve. We keep technical and regulatory staff trained in the latest requirements, whether on controlled substance lists, batch traceability, or new hazard pictograms. Staying a step ahead of new compliance frameworks allows us to support partners rolling out new product lines or entering stricter markets without delays or costly reformulations.

    Waste minimization has always been more than a buzzword for real manufacturers. Every kilogram saved from waste disposal saves not only fees, but headaches in the long run—lower liability, lower insurance costs, and a stronger reputation with inspectors and neighboring communities. Local and global partners now actively seek suppliers who demonstrate such responsible, forward-thinking management as part of their long-term value chain.

    Closing Thoughts: Why 4-Chloro-2-Iodotoluene Continues to Matter

    Innovation in organic synthesis draws on tools that offer reliability and versatility; 4-Chloro-2-Iodotoluene stands out among these tools for reasons best understood by those who work with it daily. Each stage of its production, testing, and delivery reflects a focus on chemistry, trust, and meaningful human connection. Long-term partnerships form not just around product purity or technical documentation, but through shared goals in sustainability, safety, and commercial progress.

    Our path as manufacturers isn’t just about filling orders. It’s about growing with our partners, refining our approach through careful observation and response, and supporting the industry as both standards and expectations evolve. Every flask, drum, and shipping carton we send out carries the weight of those relationships, always driven by the desire to deliver more than just a reagent, but a solution built on real-world experience, scientific rigor, and commitment.