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3-Chloro-4-Iodotoluene

    • Product Name 3-Chloro-4-Iodotoluene
    • Alias 3-Chloro-4-iodo-1-methylbenzene
    • Einecs 877-367-0
    • 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
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    Specifications

    HS Code

    163706

    Iupac Name 1-Chloro-2-iodo-4-methylbenzene
    Molecular Formula C7H6ClI
    Molecular Weight 252.48 g/mol
    Cas Number 57311-87-2
    Appearance Colorless to pale yellow liquid
    Boiling Point 258-260°C
    Density 1.78 g/cm³
    Purity Typically ≥98%
    Smiles Cc1ccc(I)c(Cl)c1
    Solubility Insoluble in water, soluble in organic solvents

    As an accredited 3-Chloro-4-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 3-Chloro-4-Iodotoluene, sealed with a tamper-evident cap and labeled with hazard warnings.
    Shipping 3-Chloro-4-Iodotoluene is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be handled as a hazardous material, protected from direct sunlight, moisture, and incompatible substances. Shipping follows all relevant local and international regulations, including labeling and documentation requirements for transport of potentially hazardous chemicals.
    Storage Store 3-Chloro-4-Iodotoluene in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Keep away from direct sunlight and moisture. Ensure proper labeling, and handle under an inert atmosphere if possible. Use personal protective equipment when handling to prevent contact and inhalation.
    Application of 3-Chloro-4-Iodotoluene

    Applications of 3-Chloro-4-Iodotoluene in Industrial Manufacturing

    3-Chloro-4-Iodotoluene sees focused adoption by leading chemical synthesis and pharmaceutical intermediates producers due to its favorable halogenated aromatic structure. As the manufacturer, we supply this key building block to select downstream sectors where its unique reactivity and substitution pattern prove essential for high-purity end products meeting international quality and safety standards.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Major pharmaceutical companies incorporate this compound in multi-step routes to non-steroidal anti-inflammatory drugs, antitumor agents, and selective receptor modulators. It functions as a halogenated aromatic precursor for Suzuki couplings and nitration reactions, where tight control over impurity profiles is critical for regulatory registration and commercial launch.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia, General Notices
    • Chinese Pharmacopoeia (ChP) API synthesis guidance

    Typical usage ratio

    • Commonly 0.7–1.5 w/w equivalents versus coupled substrate, modulated by target molecule and reaction yield optimization.

    Downstream process integration

    • Charged directly to halogen-exchange, Grignard or palladium-catalyzed coupling reactors as initial aromatic block for subsequent functionalization and ring substitutions.

    Final product types

    • API intermediates for anti-inflammatory medication series
    • Pyridine-based receptor antagonists (key in CNS drugs)
    • Halogenated aromatic compounds for oncology research

    2. Agrochemical Intermediate Production

    Leading agrochemical companies utilize this compound during production of high-performance herbicide and fungicide intermediates, where dual halogenation enhances bioactivity and selectivity on target crops. The strict residue and impurity profile requirements mean compliance with multiple regional standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management for Agrochemicals
    • China GB 2763-2023 (Maximum Residue Limits for Pesticides in Food)
    • REACH Regulation (EC) No 1907/2006

    Typical usage ratio

    • Ranges from 1.0–2.2 molar equivalents depending on crop-protection molecule pathway and reaction sequence scaling.

    Downstream process integration

    • Added to halogenation and methylation steps in early or mid-stage batch reactors as the defining structural element for cyclic and acyclic herbicide intermediates.

    Final product types

    • Intermediate substrates for triazole and pyridine-based fungicides
    • Precursors for phenoxy herbicides
    • Small-scale R&D reference standards for crop-protection innovation

    3. Specialty Dye and Pigment Intermediate Manufacturing

    Producers targeting high-value specialty dyes—including photoresist and display panel colorants—deploy this compound because the chlorine and iodine positions drive selective chromophore extension, controlling shifting and intensity of absorption spectra. Strict colorant purity and heavy metal content standards require traceable raw material inputs.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile and Dye Safety)
    • EN 71-3:2019 (Safety of Toys – Migration of Certain Elements)
    • Regulation (EC) No 1223/2009 (Cosmetic Products Directive, where applicable)
    • RoHS 2 (EU 2011/65/EU – Restriction of Hazardous Substances)

    Typical usage ratio

    • Supplied at 0.5–1.3 molar equivalents based on chromogenic core structure and target pigment hue adjustment. Adjusted by color depth and stability requirements.

    Downstream process integration

    • Fed into azo coupling, oxidative cyclization or bromination reactors as a halogenated precursor to fine tune final dye molecular properties.

    Final product types

    • Specialty red and violet organic pigments for display panels
    • Dyes for high-end textile printing
    • Chromophore-modified intermediates for inkjet and security printing ink

    4. Advanced Material and Liquid Crystal Monomer Synthesis

    In the field of electronic materials, manufacturers integrate this compound into production of monomer precursors for liquid crystal displays (LCD) and organic electronic device layers. The electronic effect of dual halogens promotes precise molecular alignment needed for advanced optical performance. Usage is governed by stringent purity, trace metals, and environmental compliance frameworks.

    Industry compliance standards

    • ISO 9001:2015 and IATF 16949 (automotive/electronics QMS)
    • IEC 61249-2-21 (halogen-free materials for electronic assemblies)
    • RoHS 2 (EU 2011/65/EU – Hazardous Substance Restrictions)
    • REACH Regulation (EC) No 1907/2006, Annex XIV/XVII compliance

    Typical usage ratio

    • Added at 0.3–0.9 molar equivalents to backbone monomer streams, calibrated for electronic anisotropy and alignment properties.

    Downstream process integration

    • Dosed as a core functional monomer in fluorination, condensation or phenylation batch steps, enabling structural precursors for final polymerization of display-grade films.

    Final product types

    • Monomer intermediates for nematic and chiral-nematic liquid crystal mixtures
    • Functionalized aromatic compounds for OLED electroluminescent layers
    • Specialty polymers for display and photovoltaic modules
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    Certification & Compliance
    More Introduction

    3-Chloro-4-Iodotoluene: Precision in Aromatic Synthesis

    Manufacturing Expertise, Tested at Every Batch

    Synthetic chemistry asks for reliability and proof with each order. 3-Chloro-4-iodotoluene sits among those intermediates where small process errors show up quickly. Our approach begins with iodine and chlorination reactions that we have improved batch by batch over years. We tune reaction times, source high-purity toluene, and work with analytical confirmation at each step. Over dozens of pilot and commercial campaigns, strict control of moisture, handling of iodine byproducts, pressure management, and reflux conditions shape the product. Anyone who has struggled with sticky residues during halogenation knows that minor slips overshoot impurity specs fast. Every facility run faces the same demands—consistency over ton-lot orders, tight compliance with reach and other regulatory thresholds, and nimble response when custom volumes or tailored specs come through.

    Product Identity and Model Confidence

    3-Chloro-4-iodotoluene, CAS number 56341-41-4, appears on the bench as a pale to light brown crystalline solid. The compound's formula, C7H6ClI, keeps the molecular weight manageable for downstream reactions. We track every kilo from raw material receipt to final packaging. Analytical support, mostly by GC and NMR, ensures that the halogen positions never shift from target—para-iodo and meta-chloro on the toluene core. This matters not only for catalog reference but for reactivity in follow-on couplings, where misplaced halogens break yields or lead to persistent side products.

    Our team avoids revising specifications unless clients or regulatory shifts dictate. Assay is minimum 98% by GC, and water content checks below 0.5%. Impurities tend to center on dihalogenated or partially iodinated isomers. Over dozens of scale-ups, we prioritize lot documentation and retain samples to give an audit trail that matches contract manufacturing expectations.

    Handling the Hard Parts: Sourcing, Safety, and Waste Controls

    Sourcing reliable raw materials for 3-chloro-4-iodotoluene poses persistent supply challenges. Iodination reagents, especially over the last decade, have seen price spikes, leaving purchasing departments at the mercy of market swings. We buy direct from global producers, qualifying each source, and stock strategic reserves to hedge risks during transport disruptions or regulatory clampdowns. Shifts in chlorine pricing also hit margins, especially as environmental restrictions rise on chlorinated solvents and byproducts.

    Halogenated toluenes never leave a plant unnoticed due to waste concerns. In-process containment runs beyond regular fume extraction. Each halogenation step includes scrubber units tuned for iodine vapors, tertiary containment for spills, and routine audits on emission points. Waste water from the process meets or exceeds local discharge standards after secondary treatment, and all solid residues go for approved incineration through licensed handlers. Only a plant operator faced with recrystallization gone awry or a misplaced drum can describe the aftermath, but we design our workflows to catch those mistakes early.

    Real-World Use — Built for Organic Synthesis

    3-Chloro-4-iodotoluene rarely ends up as a finished product on a shelf. Instead, it acts as a central intermediate, especially in pharmaceutical and agrochemical syntheses. Medicinal chemists use this molecule to introduce the iodo group at the para-position of a benzene, which opens up cross-coupling reactions—Suzuki, Sonogashira, and Buchwald–Hartwig among the leading ones. The attached chloro improves later functionalization flexibility. This makes the molecule a strong option for creating diverse scaffolds when other regioisomeric halotoluenes fall short.

    In recent years, the demand profile shifted from bulk commodity sales to custom volumes for project-specific molecules. Research groups demand tighter specs on trace metal content or smaller lots, whereas production campaigns in active ingredient manufacture focus on purity and reproducibility across metric tons. We run both drum-scale and flask-scale orders from a single purified tank, with matched certificates of analysis tied to individual batches.

    Many chemists comment on the clean reaction profiles 3-chloro-4-iodotoluene delivers compared to simple iodotoluenes. The chloro substituent directs subsequent metalation or amination steps at preferred sites, removing much of the guesswork from pilot campaigns. It's this specificity—realized during decades of trial, analytic method development, and constant tweaks in crystallization steps—that brings our repeat customers.

    Comparing with Other Halogenated Toluenes

    We handle a suite of halogenated toluenes day in and out: 4-iodotoluene, 3-chlorotoluene, 2-chloro-4-iodotoluene among them. The distinctive signature of 3-chloro-4-iodotoluene begins with its substitution pattern. Adding a chloro group at the meta-position delivers steric and electronic effects that standard iodotoluenes lack. Cross-coupling partners often show higher selectivity and milder reaction conditions using this compound, saving time and reducing byproduct formation downstream.

    Some clients ask for 4-chloro-2-iodotoluene or 2-chloro-4-iodotoluene for their own projects. Based on our in-house data, the relative reactivity and ease of handling with the 3-chloro-4-iodo isomer outpace those closer to the ortho-position. We have tested the stability of these compounds under standard storage—dark, sealed, below 30°C. Compared with other isomers, 3-chloro-4-iodotoluene holds its color and crystalline texture longer, resists caking, and maintains assay without additional stabilizers.

    Focusing on Traceability, Regulatory Support, and Reproducibility

    Large-scale chemical plants earn their keep through transparency and repeat performance. Each campaign for 3-chloro-4-iodotoluene comes with a full manufacturing record, shelf-life data, and compliance information for labeling and transport according to GHS, CLP, and various customs regimes.

    In an age of customer audits, the pressure isn’t only about running reactors at spec—it’s about documentation that anticipates every likely regulatory request, be it for trace iodine, dioxins, or nitrosamine byproducts. Our analytical packages cover not just basic purity, but also heavy metal screening, low-level impurity spikes after long-term stability, and even special requests for residual solvents. Auditors and long-term clients value the habit of batch-to-batch fingerprinting archived for years beyond product delivery.

    Manufacturing reproducibility comes from staff experience as much as from process chemistry. Our operations team trains on each specialty intermediate annually, troubleshooting minor procedural drift before it cascades. A single off-note in the NMR spectrum sends the batch for extra purification or, if needed, whole-lot rejection—lost time and money, but better than risking a customer’s pilot run.

    Quality, Packaging, and Customer Expectations

    3-Chloro-4-iodotoluene requires packaging that balances moisture protection and ease of use without breaking budget expectations. We supply this product sealed in fiber drums or HDPE-lined cans, purged with nitrogen to minimize oxidation. Our largest pharma and agro customers often request special liners, batch splitting, or delivery under inert shipping protocols, especially for storage at remote sites.

    Packaging teams document fill weights, tamper indicators, and each container by lot number. Customers with internal barcoding or special need for data sheets get those bundled with shipments in hard and electronic copy. Shipping follows ADR and UN hazard guidelines, with secondary containment for air or sea bulk. We maintain records for each outgoing batch, so any question about shipment, shelf-life, or storage quality figures can be answered within hours—not days.

    Facing Issues: Supply Chain, Environmental, and Market Pressures

    Volatility in iodine pricing affects the economics of 3-chloro-4-iodotoluene as sharply as any byproduct supply shock. We respond by maintaining strategic stocks, locking valued suppliers into annual contracts, and running quarterly raw material validation analyses. Staff must constantly balance just-in-time demands with warehouse space, absorbing occasional delays to avoid production stoppages.

    Environmental obligations never stay static, either. European regulatory changes around halogenated waste mean our disposal fees trend upward yearly. Over the last five years, we upgraded emission controls and traced every drop of spent solvent or reaction water back to batch-level reporting. Plant leadership signs off on environmental compliance and meets with inspectors as a regular part of business, not as an ad hoc fix.

    Market expectations continue to shift, with end users demanding not only compliance but green chemistry alignment. We run pilot studies to minimize halogenated waste at source, exploring continuous flow and alternative workups to cut byproducts. Much of this comes from direct customer requests, so the driving force for innovation runs both ways.

    Supporting Advanced Synthesis

    Process chemistry teams rely on intermediates like 3-chloro-4-iodotoluene for reliable cross-coupling. Pharmaceutical process engineers and contract manufacturers often bring us directly into custom synthesis discussions, knowing the product acts as both a building block and a bottleneck if purity drops. Over the last decade, many new molecular entities have started their journey with this single compound.

    Many of our customers return not because the product is unique, but because its reliability saves hours and uncertainty at the bench. Each multi-kilo order solves more than a supply need—it closes the lab-to-plant gap that feeds the broader pharmaceutical and crop protection pipeline. Our technical service and site managers maintain one-to-one relationships with client chemists, fielding troubleshooting calls, interpreting HPLC or NMR glitches, or proposing alternate purification methods if downstream bottlenecks crop up. We see our work as part of a broader chain where small improvements add up to better clinical outcomes or field performance years later.

    Research, Development, and Process Improvement

    Like every specialty intermediate, 3-chloro-4-iodotoluene doesn’t escape the march of new process technology. Our R&D group runs annual retrospectives on plant campaigns, identifying steps for yield improvement, waste reduction, or cycle time gain. Over five years we moved from batch crystallization relying on open tanks to enclosed systems with better solvent recovery and in-line drying. We reduce solvent consumption incrementally—fraction by fraction—targeting both environmental gains and cost reductions that hold in the face of raw material spikes.

    Some requests test what the chemistry allows, such as limiting trace palladium or lead content for tighter application specs. In these cases, we partner with clients, run extended pilot purifications, and supply detailed impurity profiles. While the molecule itself remains the same, deeper analysis and batch-by-batch optimization reveal the hidden steps that make the difference at scale.

    Conclusion: What Matters Down the Line

    Every kilo of 3-chloro-4-iodotoluene carries the story of plant engineering, supply negotiation, customer dialogue, and process discipline. For users in industrial laboratories, specialty pharma, or crop science R&D, this compound represents more than a catalog entry—it’s a test case for trust in the broader manufacturing chain. Teams at the plant, from shift operators to chemists, know each missed analytical check or quality slipback shows up in a customer’s campaign, not just in lab records. Our objective goes beyond shipping pure product. We match production runs to customer need, back each batch with full traceability, and learn with every feedback loop. The work never really ends.