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4-Iodotoluene

    • Product Name 4-Iodotoluene
    • Alias p-Iodotoluene
    • Einecs 210-967-7
    • 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
    VTB
    Specifications

    HS Code

    512922

    Cas Number 624-31-7
    Molecular Formula C7H7I
    Molar Mass 218.04 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 52-55 °C
    Boiling Point 210-212 °C
    Density 1.67 g/cm³
    Solubility In Water Insoluble
    Refractive Index 1.632
    Flash Point 91 °C
    Purity Typically ≥98%
    Synonyms p-Iodotoluene, 1-Iodo-4-methylbenzene

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

    Packing & Storage
    Packing 4-Iodotoluene, 25g, is packaged in an amber glass bottle with a screw cap and detailed white printed labeling for safety.
    Shipping 4-Iodotoluene is shipped in tightly sealed containers to prevent leakage and contamination. It should be stored and transported in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling and handling according to hazardous material regulations are required, ensuring safety and compliance during shipping.
    Storage 4-Iodotoluene should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing agents. Avoid exposure to moisture and open flames. Store it in a chemical storage cabinet designated for hazardous materials, clearly labeled, and keep away from sources of ignition to prevent any safety hazards.
    Application of 4-Iodotoluene

    Applications of 4-Iodotoluene in Industrial Manufacturing

    4-Iodotoluene serves as a valuable intermediate in the synthesis of numerous advanced chemical products. Our manufacturing processes consistently deliver high-purity 4-Iodotoluene in large volumes to support specialized downstream sectors. Below, we highlight four principal industrial applications, each characterized by distinct processing use, regulatory obligations, dosage principles, and resulting end products.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Antihypertensive Compounds

    Pharmaceutical companies integrate 4-Iodotoluene in multi-step syntheses for manufacturing key intermediates of antihypertensive medications. The aryl iodide functional group offers high reactivity in palladium-catalyzed C–C bond formation, particularly in Suzuki or Sonogashira cross-coupling reactions, ensuring precisely controlled step-growth polymerization in the production of advanced drug molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Annex 8 (Intermediate Handling & Traceability)
    • USP <659> Packaging and Storage Requirements
    • 21 CFR Part 210/211 (FDA GMP for finished pharmaceuticals)

    Typical usage ratio

    • 0.4–1.2 molar equivalents relative to the coupling reagent; adjustment depends on process yield and desired target molecule structure; stoichiometry tightly managed by online HPLC analytics

    Downstream process integration

    • Introduced during the aryl coupling stage in high-pressure reactors, following primary amine protection and preceding hydrolysis/deprotection steps; purity tracked via NMR and GC-MS to prevent side-product formation

    Final product types

    • Amlodipine besylate (antihypertensive API)
    • Losartan intermediates
    • Azilsartan medoxomil derivatives
    • Other sartan-structure bulk APIs

    2. Advanced Agrochemical Synthesis (Herbicide Intermediate Chains)

    Agrochemical manufacturers employ 4-Iodotoluene as a core building block for assembling specific benzyl ring systems in modern herbicides. Through controlled electrophilic substitution and palladium-catalyzed reactions, they access high-purity, selectively substituted toluene derivatives essential for the synthesis of selective pre-emergent and post-emergent herbicidal active ingredients.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 (Agrochemical Manufacturing)
    • REACH Registration (EU Reg. EC No 1907/2006)
    • China GB/T 1603—International Agrochemical Product Quality

    Typical usage ratio

    • 8%–15% by weight based on batch scale; variation according to target herbicide’s side chain structure; loading rate defined by LCMS-controlled reaction monitoring

    Downstream process integration

    • Charged as the aryl iodide source at the functionalization phase after pre-milling solvents; involved in key Pd- or Cu-catalyzed coupling stages, with solvent and pH optimization for yield maximization

    Final product types

    • Selective pre-emergent herbicides (e.g., substituted benzyl-ureas)
    • Post-emergent weed control agents
    • N-phenylacetamide herbicides
    • Herbicidal synergists

    3. Liquid Crystal Intermediate for Display Technologies

    Producers of liquid crystal materials leverage the distinctive reactivity of 4-Iodotoluene during the alkylation and cyclization steps needed to prepare complex aryl-based mesogens. Integrating this intermediate enables precise structural modifications critical for optimizing electro-optical response characteristics in high-performance display panels and smart device screens.

    Industry compliance standards

    • IEC 62321 (Requirements for Hazardous Substance Testing in Electronic Components)
    • JEITA EIAJ-RCR-0102A (Electronic Chemicals Control)
    • ISO 14001 (Environmental Management in Electronics)
    • RoHS Directive 2011/65/EU Compliance

    Typical usage ratio

    • 10–28% by molecular proportion depending on the target mesogen design; proportion established by final LC-phase performance and reactivity matching to downstream cores

    Downstream process integration

    • Added during the Friedel–Crafts or cyclization step post-halogen exchange; subsequent purification via column chromatography required for electronic grade applications

    Final product types

    • Biphenyl-based liquid crystal intermediates
    • Single-component nematic mesogens for smart displays
    • Multiphotonic alignment films for thin-film transistors (TFT-LCD panels)
    • Touchscreen optical retardation plates

    4. Dye and Pigment Intermediate for Performance Coatings

    Specialty pigment and dye manufacturers incorporate 4-Iodotoluene to produce functionalized aromatic compounds used in making premium coatings. The material undergoes regioselective substitution and oxidative coupling, granting chemists precision control over chromophore extension and pigment architecture for high-durability, color-stable coatings in automotive, electronic, or industrial finish applications.

    Industry compliance standards

    • EU Regulation (EC) No 1272/2008 (CLP) on Classification, Labelling and Packaging
    • American Society for Testing and Materials (ASTM D4302: Pigment Quality)
    • ISO 9001:2015 (Specialty Dye Manufacturing)
    • China GB/T 21866-2015 (Industrial Pigment Safety Standard)

    Typical usage ratio

    • 7–17% by weight relative to total chromogen charge; precise proportion determined by depth of target color and fastness requirements; pigmentary systems may require pilot batches for optimization

    Downstream process integration

    • Introduced at colorant core-building stage after base diazotization; iodotoluene derivatives functionalized via cross-coupling, then subjected to oxidative cyclization and filtration

    Final product types

    • High-performance automotive paints
    • Printing ink pigments (electronic, textile, packaging inks)
    • Architectural coatings
    • Plastic coloration masterbatches
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    Certification & Compliance
    More Introduction

    4-Iodotoluene: Manufacturing Strength, Real-World Reliability

    Our Journey with 4-Iodotoluene

    The story of 4-iodotoluene for our team starts right in the reaction vessels where methylation and iodination meet precise process control. We do not see it as just another entry on a catalog. 4-iodotoluene has a character all its own: a crystalline compound, off-white in its purest state, with methyl and iodine hanging together on one aromatic ring. Forming this simple molecule requires patient attention to temperature, raw input cleanliness, and a steady hand on the batch protocol. Each step adds up—quality shows in the final grains or flakes.

    Chemists ask us about our model. We offer 4-iodotoluene with CAS number 624-31-7 in batches graded for laboratory synthesis as well as production-scale lots. Our output maintains high purity—confirmed at each lot through HPLC and GC, plus halogen content assessment by titration. The final result? A low level of residual toluene and near-total conversion of starting material. In effect, this approach avoids headaches for downstream users handling scale-ups or method transfer.

    Building Confidence in the Lab and Plant

    Across our factory floor, yield remains only part of the equation. We inspect not just the target molecule in the drum, but also impurities that create problems later during scale-up or purification. By removing trace iodide and organic by-products at an early stage, we put control in the hands of chemists and engineers.

    Many clients trying to move from pilot to commercial scale tell us: variations in by-products cost hours in chromatography and purification. We manage the main impurities—unreacted toluene, side-chain-iodinated regioisomers, and polyhalogenated aromatics—by optimizing reaction kinetics and using repeated crystallization where necessary. This isn’t about chasing statistical claims, but about making sure the person weighing a scoop from our drum each week gets repeatable, tangible results.

    How 4-Iodotoluene Fits into Real Synthesis Pathways

    All over the world, 4-iodotoluene shows up in workups, retrosyntheses, and process flowcharts. It often pulls double duty: acting as a coupling partner in cross-coupling reactions while also serving as a building block for more elaborate pharmaceutical or agricultural molecules. The p-iodo substituent activates the aromatic ring, giving credible yields in both Suzuki-Miyaura and Sonogashira couplings.

    Synthetic teams tell us they pick 4-iodotoluene because of that iodine atom sitting at the para-position—it leaves more room for substitution, and reactions run cleaner. Compared to ortho-iodotoluene or other halogenated tolidenes, our product leads to higher conversion because steric hindrance is lower on the 4-position. That means larger groups go on where the methyl group sits, while the iodine activates the ring without blocking access for bulky ligands or transition metal catalysts.

    Most biopharma and crop science research groups we serve rely on the reproducibility that comes from clean halogenated intermediates. Commercial teams building libraries of new molecules cite the need for consistency—minor batch-to-batch changes in content or physical state, which most buyers don’t notice, can ruin a medicinal chemistry campaign. We commit know-how and patience to minimize that risk, batch after batch.

    Our Experience: Addressing Common Pain Points

    Chemicals such as 4-iodotoluene cause familiar headaches in the wrong hands. Left unchecked, even slight contamination by heavy metals, acidic residues, or residual solvents can poison a catalyst or skew a kinetic study. From our earliest product launches, we learned to direct attention where it matters: that means watching each input—a base here, a solvent there—with the same focus as we place on the finished molecule.

    Teams honest about data always appreciate a precise spec, but they trust most what they see after a few batches. Our customers ask straightforward questions: how does it handle in a drybox? Does it clump in storage? What’s the off-gassing profile? We designed our process and packaging to answer those unspoken needs. Our drums carry clear labeling for traceability; moisture protection and tamperproofing help protect quality. We ship each batch with a full COA covering halide assay, melting range, and main impurity content.

    We often hear from formulators: not all iodotoluenes are created equal. Sourcing 4-iodotoluene from trading channels sometimes brings brown or yellowish batches with odd odors, or sticky messes that don’t weigh correctly. That usually means shortcuts during synthesis or poor purification. We believe these shortcuts save no one time. Instead, we double down on filtration, multi-step recrystallization, and real scrutiny at the blending stage. It’s routine to discard batches that underperform, rather than risking a downstream process failure.

    Differentiating 4-Iodotoluene from Others in the Aromatic Family

    In practice, 4-iodotoluene’s niche comes from its para-substitution pattern. Its main relatives—2-iodotoluene, 3-iodotoluene, and multi-iodinated toluenes—bring their own quirks to the lab bench. Compared with ortho- and meta-isomers, the para compound runs cleaner under cross-coupling, with fewer by-products and less isomerization. The methyl group sitting directly opposite the iodine on the ring means less steric shield, so reactions that stall or give poor regioselectivity using the meta or ortho isomers tend to succeed with our product.

    For those scaling to kilo or ton lots, higher melting ranges, tighter particle size, and reliable downstream filtration make a difference to yield calculations. From our experience, 4-iodotoluene consistently crystallizes in a uniform form, easing drying and storage. We learned to control the process to prevent formation of agglomerates or amorphous powder, ensuring smoother transfer into reactors and easier dissolution.

    We avoid excess focus on technical jargon and instead speak directly to outcome: batches stay easier to filter, ship, and weigh. Years of feedback taught us to work on the frontlines of product handling—no one wants to fight with lumpy stock or blocked filters. That’s not merely convenience; it determines the success of multi-step syntheses, where recovery percentage and purity at every transition matter.

    Broader Uses, Lower Risks

    4-iodotoluene repeatedly finds use beyond routine research. It supports contract manufacturing pipelines making custom substrates, small molecule drugs, agricultural actives, and advanced intermediates for new functional materials. Its role in photoinitiators, specialty pigments, and even certain types of OLED display precursors is confirmed by the orders coming in across industries.

    We learn much from our most innovative partners. Some have developed radical pathways—catalytic transformations that create new classes of compounds for diagnostics, imaging, or flavor enhancement. Each pathway places unique demands on the 4-iodotoluene supply. Sometimes it’s lower residual water for organometallic work, or the need for tight control over color and odor for sensitive analytical applications. We fit these needs by adjusting cut points and offering additional downstream drying or purification on request; not as extras, but as part of building trust over many cycles.

    Handling and storage rank high among persistent questions. Years dealing with shipping and warehousing taught us that inconsistent packaging or exposure to light and air triggers degradation or caking. Our facilities invest in lined steel drums with inert liners, designed around container sizes that match typical consumption rates. This avoids repeated decanting, which often introduces ambient moisture or contamination. Cautious suppliers spot-check for peroxide formation and halogen loss as standard practice; we do the same, because we’ve seen what happens when these checks get skipped.

    Trust Earned by Results, Not Promises

    In synthesis chemistry, execution matters more than packaging or sales lines. Chemists and procurement partners rarely forgive poor reproducibility. With 4-iodotoluene, mistakes show fast—a flawed batch means missed yields and longer filtration times. We design our processes so these problems won’t crop up. Our customers prefer results over words. Repeat orders and direct feedback show whether a manufacturer delivers substance, not just claims.

    We believe reliability flows from experience—years troubleshooting minor impurities, adapting to new reaction setups, solving bottlenecks one flask at a time. Early on, we learned that a standard product does not serve everyone. Some want tighter specs for advanced couplings; some just need reliable kilogram lots for market-mature processes. We match our approach to those needs, giving real choices in purity, particle size, and presentation—no generic, one-size-fits-all philosophy. Each week of production brings new challenges and lessons, constantly shaping the way we work.

    Listening and Learning from the Field

    It’s easy to talk specs and make guarantees from the produce side, but lasting partnerships build on open lines of communication. Engineers, lab techs, and project managers reach out with problems ranging from bottlenecks in purification and crystallization to trickier issues like unexpected discoloration or trace metal contamination. We respond by reviewing logs, running extra analyses when needed, and investigating root causes at both lab and plant scale. This approach helped refine not just our own SOPs, but also supported team members at the receiving end who troubleshoot the next synthetic step.

    Some who use 4-iodotoluene in bulk find surprises—a slight jar-to-jar variation that shows up in HPLC or GC, batches that seem drier or wetter depending on how long they sit. Having spent time in the trenches running kilo-scale syntheses, we advise customers on real-world storage tips: keeping stock in sealed, dry containers, dosing under inert gas when possible, and minimizing exposure to humidity. Our operations teams maintain regular checks for water activity, odor, and off-color development as an ongoing measure.

    Beyond chemical analysis, we learn the most from hands-on experience, such as opening containers after months of storage and seeing how the crystals behave. Running comparison trials on site and on customer factories gives us an edge in refining both our purification and logistics workflows. No amount of upfront spec work replaces a steady loop of feedback, troubleshooting, and putting new lessons into the next batch.

    Cleaner Chemistry, Less Waste

    Sourcing 4-iodotoluene from direct manufacturers means gaining not just a consistent supply, but often a cleaner process downstream. Having long worked with contract manufacturers facing increasingly strict environmental standards, we shifted much of our own plant toward minimizing halogenated waste, reducing solvent residues, and closing loops for spent iodine. Each metric ton recycled means less landfill and improved sustainability for those buying from us.

    Chemists in pharma and specialty chemicals have little tolerance for uncontrolled variables. We adapted by offering options for low-water, low-residual solvent product, and investing in post-synthesis waste reduction. The pressure to go greener led us to switch cleaning solvents, recapture iodine, and use higher-efficiency dryers that cut down on both emissions and utility demands.

    Direct collaboration with end users drives practical improvements: batch traceability, smaller lot options, and detailed impurity profiling. These aren’t afterthoughts. After many years and thousands of shipments, we found that fine-tuning in response to customer feedback gives much higher returns than chasing only the cheapest cost base.

    Pushing the Limits of Quality

    Quality isn’t a line on a certificate—it’s a discipline that runs from raw input to the final drum. We sample every material coming into the plant, double-check every critical control point, and run comparison studies on retention, melting point, and impurity content. There’s little room for error when a single off-batch can halt multi-million-dollar synthesis campaigns.

    Direct feedback loops from users encourage us to keep raising the bar. Labs using our 4-iodotoluene for palladium-catalyzed cross-couplings push for more certification on trace metals. Custom manufacturing clients expect every delivery to pour, weigh, and dissolve the same each time. We answer by continually reviewing and improving process control and expanding analytical checks.

    Skills honed in the daily grind—the way a material flows during transfer, the subtle change in crystal sheen that signals possible contamination—define real quality standards. These skills develop over many seasons, much trial and error, and a strong regard for both chemistry and the people running it.

    Setting Standards for 4-Iodotoluene: Our Ongoing Mission

    Our commitment to 4-iodotoluene is bound tightly with our experience walking both the plant floor and the lab bench. We don’t see production as a finished project, but as an ongoing mission shaped by the evolving standards of those who use what we make. Every adjustment we make—whether to solvents, drying protocols, packing, or purity targets—follows from real-world results and a willingness to learn from mistakes.

    What separates a capable producer from a routine supplier is the willingness to adapt—sometimes fast—to shifting project demands, developing regulatory expectations, and feedback from the sharp end of industry. We welcome those tough conversations, because each challenge makes us better partners and sharper manufacturers.

    Through collaboration and discipline, we strive to keep raising the benchmark for 4-iodotoluene—not just by tightening specifications, but by building a feedback-driven relationship with those relying on our expertise batch to batch, year after year.