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2-Iodoisopropylbenzene

    • Product Name 2-Iodoisopropylbenzene
    • Alias 2-Iodo-1-methyl-1-phenyl-ethane
    • Einecs 220-975-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    790762

    Chemical Name 2-Iodoisopropylbenzene
    Cas Number 3430-37-1
    Molecular Formula C9H11I
    Molecular Weight 246.09 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 240-242 °C
    Melting Point Unknown
    Density 1.636 g/cm³
    Refractive Index 1.619
    Flash Point 109 °C
    Pubchem Cid 2785598
    Smiles CC(C)C1=CC=CC=C1I
    Inchi InChI=1S/C9H11I/c1-7(2)8-5-3-4-6-9(8)10/h3-7H,1-2H3
    Synonyms 2-Iodo-1-methylethylbenzene
    Storage Temperature Store at 2-8 °C

    As an accredited 2-Iodoisopropylbenzene 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 25g of 2-Iodoisopropylbenzene, sealed with a screw cap, labeled with hazard symbols and product details.
    Shipping 2-Iodoisopropylbenzene is shipped in tightly sealed, chemical-resistant containers, compliant with international regulations for hazardous materials. The package is labeled with hazard information and handled by certified carriers to ensure safety. Temperature and light exposure are controlled, and shipping documentation includes safety data sheets for proper handling upon receipt.
    Storage **2-Iodoisopropylbenzene** should be stored in a cool, dry, and well-ventilated area away from heat, open flames, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from strong oxidizing agents, acids, and bases. Use suitable glass or compatible chemical-resistant containers. Proper labeling and secure storage to prevent leaks or accidental exposure are essential.
    Application of 2-Iodoisopropylbenzene

    Applications of 2-Iodoisopropylbenzene in Industrial Manufacturing

    As a direct manufacturer of fine aromatic intermediates, we supply 2-Iodoisopropylbenzene for established industrial segments where high-purity halogenated aromatics are essential to downstream production workflows. The following applications detail actual B2B end uses, regulatory frameworks, and integration into customer manufacturing lines.

    1. Pharmaceutical Intermediate Synthesis (API Side-Chain Introduction)

    Process chemists use 2-Iodoisopropylbenzene as a building block for constructing isopropyl-substituted aromatic scaffolds employed in active pharmaceutical ingredient (API) synthesis. Its iodine functionality enables regioselective metalation or cross-coupling, supporting efficient side-chain modifications in cGMP-compliant manufacturing where traceability and impurity control are critical. Demand for this intermediate arises from clinical-stage small molecule R&D up to full-scale commercial API campaigns, generally under tightly regulated process control protocols.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • U.S. FDA 21 CFR Part 211
    • European Pharmacopoeia (Ph. Eur.), relevant monographs for APIs
    • Quality control per USP <1058> Analytical Instrument Qualification

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to the core aromatic scaffold; adjusted based on route selection and target yield optimization

    Downstream process integration

    • Introduced during early to mid-stage synthesis across Suzuki-Miyaura or Ullmann-type couplings, following anhydrous charging protocols in high-pressure reactors

    Final product types

    • API drug substances containing isopropyl-phenyl motifs (e.g., cardiovascular agents, CNS actives)
    • Regulatory starting materials (RSM) and advanced intermediates for pharmaceutical contract manufacturing

    2. Agrochemical Synthesis (Herbicide Intermediate)

    Commercial agrochemical producers incorporate 2-Iodoisopropylbenzene in multi-step syntheses to introduce bulky aromatic side chains required for selective herbicide molecules. The compound’s halogenated aromatic structure facilitates electrophilic aromatic substitution, providing controlled substitution patterns unique to crop protection actives. Downstream reactors utilize it during early-stage building block assembly, with rigorous monitoring of residual iodine and by-products to meet pesticide regulatory cut-offs.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 and ISO 14001:2015 for chemical batch traceability
    • REACH (EU Regulation No 1907/2006) substance registration (if shipped to EEA)
    • China GB 20811-2022 technical requirements for pesticide production

    Typical usage ratio

    • 5–10 wt% of target batch charge, tailored to reaction conversion efficiency and downstream purification constraints

    Downstream process integration

    • Charged in batch or semi-batch reactors during Grignard or Friedel–Crafts alkylation to form aryl herbicide precursors

    Final product types

    • Precursor intermediates for isopropyl-phenyl herbicides and related crop protection agents
    • Technical grade herbicide actives for formulation into EC, SC, and WG products

    3. Liquid Crystal Material Manufacturing (Display Technology Grade)

    Specialty electronics manufacturers use this halogenated aromatic as a precursor in synthesizing specific biphenyl and terphenyl derivatives for liquid crystal display (LCD) applications. Its high purity minimizes ionic and particulate contaminants, crucial for maintaining electro-optical consistency in thin-film displays. The intermediate enters the production pipeline in custom syntheses, following purification and QA screening matching stringent electronics-grade specifications.

    Industry compliance standards

    • IEC 61340-5-1 Electrostatics (cleanroom handling for electronics)
    • RoHS Directive (EU 2011/65/EU) hazardous substance limits
    • ISO 9001:2015 QMS for electronic material manufacturing
    • SEMATECH Guidelines for organic LCD intermediates

    Typical usage ratio

    • 0.5–2.5 wt% relative to target liquid crystal precursor recipe; modified based on molecular structure requirements for phase behavior

    Downstream process integration

    • Integrated during initial monomer formation for custom functionalized biphenyls, before coupling and distillation refinement stages

    Final product types

    • High-performance liquid crystal compounds for TFT-LCD and OLED displays
    • Material blends for advanced display substrates in tablet, monitor, and television panels

    4. Fragrance Intermediate Synthesis (Aromatic Isopropyl Key)

    Selective perfumery ingredient manufacturers employ this compound as a halogen source for molecular frameworks found in specialty musks and aromatic notes. It enters the aromatic substitution stage, bringing controlled isopropyl positioning for batch consistency. Formulators use robust QA to minimize off-aroma and guarantee alignment with IFRA safety profiles and purity standards required for consumer product safety audits.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards and Guidelines
    • ISO 9235 for aroma chemical source verification
    • REACH Annex XVII (restricting hazardous substances)
    • GMP for Cosmetic Ingredients (EFfCI GMP Guide, ISO 22716)

    Typical usage ratio

    • 0.2–1.0 wt% of total formula in the intermediate synthetic step; fine-tuned to target aroma concentration and purity constraints

    Downstream process integration

    • Added to initial aromatic alkylation stage in closed-glass reactors, preceding distillation and crystallization for desired olfactory attributes

    Final product types

    • Musky and woody fragrance intermediates for fine fragrance, air care, and personal care market segments
    • Aromatic base notes for use in compound fragrance libraries
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    Certification & Compliance
    More Introduction

    Introducing 2-Iodoisopropylbenzene: A Reliable Intermediate for Specialized Synthesis

    Deep Roots in Organic Chemistry Manufacturing

    2-Iodoisopropylbenzene, sometimes recognized by the chemical formula C9H11I, has served as a valuable intermediate for those working with complex organic molecules. In this facility, years of handling halogenated alkylbenzenes have illuminated the distinct performance and reactivity this compound delivers. As direct manufacturers, our experience does not rely on the recycled narratives of traders or distributors; we know the subtleties involved in controlling quality and consistency, batch after batch. We have engaged with chemists seeking reliable building blocks and have witnessed the challenges presented when intermediates lack predictable behavior—this material solves real laboratory obstacles, not just theoretical ones.

    Product Overview: Detailed Characteristics and Real-World Advantages

    Our 2-iodo derivative emerges as a colorless to pale yellow liquid, boasting high purity as evidenced by modern chromatographic and spectroscopic analysis. The heavy iodine atom appended to the isopropylbenzene ring transforms the molecule’s reactivity profile. Through routine monitoring of melting points, NMR spectra, and impurity levels, we ensure structural integrity and high selectivity in downstream synthesis.

    Careful control of synthesis parameters, including reaction temperature, stoichiometry of iodine sources, and exclusion of unwanted side-products, leads to a clean, reliable product. We often hear from returning clients who have tested materials from other sources, noting lower yields, unpleasant odors, or erratic performance. Rigorous purification on our production line eliminates these frustrations. In a market where trace byproducts can compromise crucial steps such as metal-halogen exchange or cross-coupling, consistency is not just an ideal—it's a necessity.

    Suitability for Key Synthetic Routes

    Chemical research never stands still, and more labs have been turning to 2-iodo aromatic compounds due to their unique position in facilitating efficient cross-coupling reactions. Our 2-Iodoisopropylbenzene particularly finds regular demand in Suzuki-Miyaura, Heck, and Sonogashira couplings. The iodo group brings clear benefits over its bromo or chloro analogues, notably in their reactivity under milder conditions and greater compatibility with sensitive substrates.

    Researchers have shared feedback on improved yields, minimized side reactions, and consistent product formation using our material as a coupling partner, especially during the construction of more hindered or electron-rich frameworks. Applications span from agrochemical building blocks to pharmaceutical intermediates, reflecting its utility in more than just classic synthesis. The isopropyl group at the ortho position manifests improved solubility in organic phases and sometimes alters regioselectivity—qualities that can make or break a project.

    Direct Experience with Emerging Applications

    Over the last decade, requests have shifted as new challenges in organic synthesis arise. Our technical teams are often involved beyond simple supplying. Synthetic chemists have approached us with questions about functional compatibility; for example, what side chains might survive a given Pd-catalyzed transformation or how best to store halobenzenes for long-term purity.

    We have tracked the material’s adoption in scale-up environments, from initial milligram experiments to multi-kilogram pilot runs. The low volatility, combined with high chemical stability under inert conditions, comes from the robust aromatic system married to the bulky isopropyl group. Chemists value this stability when scaling procedures—exposure to air and slight temperature fluctuations do not rapidly degrade the product or generate off-odors, unlike more fragile aryl halides.

    On several occasions, clients pivoted to 2-Iodoisopropylbenzene after facing reproducibility issues with 2-bromo- or 2-chloro- derivatives. Not every substitution seems trivial; the iodine atom’s larger size and stronger carbon-iodine bond dramatically shift the compound’s engagement with catalysts and nucleophiles. As manufacturers, we can trace these compound-specific nuances directly to the synthesis table, often working through process development ourselves to answer customer technical queries in real-time.

    Comparisons and Notable Differences from Other Halogenated Derivatives

    Much has been written about the comparative merits of iodo-, bromo-, and chloro- isopropylbenzenes. Our practical perspective shows where the differences become significant. Bromides and chlorides, while less costly on the raw material front, generally show lower reactivity in key cross-coupling protocols. End-users report longer reaction times, need for higher temperatures, and increased chances of decomposition—none of which make for a stress-free day in the laboratory.

    The iodine analog, on the other hand, shortens reaction times. Its greater leaving group ability in transition-metal catalysis is tangible in anyone’s hands, not a detail only seen in reviews or textbooks. After troubleshooting many customers’ coupling reactions, switching to our iodo derivative often corrects low conversions or byproduct issues, especially for highly hindered sites. The isopropyl group further shields the aromatic ring; in competing Friedel-Crafts conditions, this results in greater selectivity and less polymerization—which those who handle reactors daily recognize as a maintenance and safety advantage.

    From a handling standpoint, we also see that iodine behaves more favorably than bromine or chlorine at the bench. Less volatility means less inhalation risk, and less aggressive corrosion on glassware or metal parts. This matters for technicians responsible for machinery through multiple synthesis runs—expenses and delays vanish down the line due to reduced cleaning and repair needs.

    Specifications That Matter in Practice

    Our product typically registers a purity of not less than 98% by GC and HPLC. Minor impurities, chiefly unreacted starting isopropylbenzene or mixed halogen products, are pushed below detectable thresholds via repeated fractional distillation, augmented by silica filtration. Each drum passes spectroscopic confirmation; the iodine signature is unmistakable in the NMR, and we archive reference spectra for every lot.

    Moisture content stays consistently below 0.1%, confirmed by Karl Fischer titration, which speaks to the rigor of our drying and sealing processes. This matters for those conducting moisture-sensitive reactions—trace water can quench reactive organometallics and bring costly surprises. The density, viscosity, and refractive index remain steady, helping with dosing accuracy in automated synthesis units, especially in continuous flow labs.

    The odor profile stands largely neutral—chemists working in confined fume hoods remark favorably compared to sharply pungent or acrid halides. We invest in robust packaging: fluorinated polyethylene containers prevent leaching and breakdown, allowing for shelf-lives beyond a year under recommended storage conditions. Customers who receive off-spec material from casual distributors often share stories of contamination and breakdown; our records illustrate a steady performance curve, even for archived products retained for years.

    Practical Handling, Storage, and Safety Reflections

    Working inside our own facility, direct interaction with 2-Iodoisopropylbenzene through all stages—from crude synthesis to container filling—has refined our protocols. The lower volatility compared to other iodobenzenes keeps handling straightforward. Standard nitrile or neoprene gloves, basic eye protection, and chemical-resistant aprons offer ample protection. Even so, this is a compound best respected by trained hands, given the heavy-atom nature of iodine-containing molecules.

    We instruct our shipping and storage teams to maintain drum integrity by exclusion of ambient light and strict temperature controls. After several cycles of storage at room and sub-zero temperatures, our in-house tests register no visible polymer formation or iodide leaching, issues that have dogged previous generations of less stable aryl iodides. Maintenance of dry, oxygen-low conditions brings out the full benefit of our purification steps.

    Waste disposal and environmental impact have been scrutinized closely. Our waste stream analyses confirm manageable volumes, and we neutralize spent iodide content with established reducing protocols before release for further treatment. Our familiarity with the EPA and related domestic standards means we prioritize clear documentation and traceability, giving confidence up the supply chain, especially for customers pursuing audited green chemistry credentials.

    Overcoming Industry Challenges with Manufacturing Insights

    Being at the source, we have witnessed recurring problems faced by clients who rely on intermediaries for supply. Fluctuating material quality often stems from inconsistent upstream processes—either impurity drift in raw iodine stocks, variable reaction conditions, or absence of thorough purification. We have smoothed these inefficiencies by direct investment in real-time process analytics and batch record systems. This drives measurable reductions in batch-to-batch variability, keeping client production on track.

    After several years supplying high-throughput pharmaceutical and fine chemical partners, we've adapted our own large-scale reactors for increased throughput without sacrificing purity. Inline sampling and feedback controls prevent overheating, runaway reactions, and trace impurity creep—problem areas that, left unchecked, have led to failed productions elsewhere. Clients have reported seeing overruns evaporate by switching to a producer with direct process understanding and rapid resolution capacity.

    One central challenge comes from the volatility in iodine feedstock pricing. Rather than hiding behind supply contracts, we openly discuss raw material trends with bulk buyers and offer production forecasts to stabilize budgets over the year. Our production planning teams monitor global trends in halogen supply, adjusting inventory in advance when spikes appear likely. Customers have expressed trust in our transparency, especially through difficult market stretches or raw material bottlenecks—a benefit unattainable from disconnected traders.

    Feedback and Practical Solutions for Users

    Customers’ feedback directs our product evolution. Requests for higher-purity grades inspired our introduction of advanced column purification and stricter crude iodine quality thresholds. When several pharmaceutical partners encountered trouble with consistent scale-up yields, our team was able to travel onsite, observe actual bench procedures, and recommend changes to metal-catalyzed preparation and handling steps—yield bumps of up to 20% resulted within months.

    In discussions with educational institutions and research labs, demand for affordable lab quantities met with our internal pilot program that splits production runs for smaller, pre-weighed aliquots. This initiative has reduced cross-contamination and unnecessary waste—a change which would not have occurred had we remained removed from the lab environment.

    One recent collaboration with an agrochemical manufacturer required low-halogen residuals for regulatory approval. We dedicated an entire batch to custom filtration and testing, resulting in a successful batch release for their downstream use—underscoring the advantage of having direct control over the reaction and purification stages.

    Guidance for Successful Applications

    There’s no one-size-fits-all approach for synthetic chemistry. We understand clients often pursue unique targets—no amount of specification sheets can substitute for practical, experience-backed advice. Our process engineers routinely assist with scale-up calculations, reagent compatibility checks, and troubleshooting guidance. This collaboration helps laboratories shift confidently from benchtop to bulk, not just with cleaner data but with confidence in material stability and reactivity.

    For cutting-edge synthesis—whether in medicinal chemistry, advanced materials, or agricultural research—using a cleaner, highly characterized aryl iodide offers a measurable edge. Having navigated these paths ourselves, we know precisely how differences in halide choice can shift the outcome of complex syntheses, impact downstream purification, and affect cost efficiency, even for seasoned project managers.

    Responsibility and Sustainability in Production

    Today’s customers demand more than product quality—they seek out partners who minimize environmental impact and regulatory risk. Our commitment is embedded in day-to-day operations. We use closed-vent reaction vessels, recycle process solvents, and collect residual iodine for recovery. Real-time environmental monitoring checks emissions, and we use best-practice secondary containment for all halogenated waste.

    Working as both producer and steward, we stay on top of the latest developments in chemical handling and sustainability. We continually update safety protocols, train new operators with senior staff oversight, and conduct periodic external audits. This culture of responsibility supports our clients’ own EHS (Environment, Health, and Safety) programs and makes regulatory compliance straightforward during site visits or certification renewals.

    We have developed internal benchmarks for “green chemistry” compatibility. These measure not just solubility or stability but also lifecycle footprint, recyclability of packaging, and fate of side-products. For many customers aiming for low-impact processes, these performance metrics add tangible value—helping achieve both regulatory and marketing advantages in competitive global markets.

    Outlook: The Value of Manufacturer-Level Perspective

    Every molecule tells a story beyond its chemical structure. Here, our direct daily work with 2-Iodoisopropylbenzene has shaped strong practices and inspired us to push boundaries for quality and responsible production. Our hands-on perspective reveals the realities of supply, transformation, and application that distributors or brokers rarely encounter. Laboratory teams partnering with us gain a reliable, tested source of this critical intermediate—supported not just by guarantees but by lived experience, technical guidance, and adaptability to the ever-shifting landscape of modern organic synthesis.

    As research trends move toward ever-more sophisticated cross-coupling schemes, diverse substrate compatibility, and aggressive timelines for product launch, materials like our 2-Iodoisopropylbenzene continue to underpin essential innovation. We invest daily in refining not just the product, but the relationship between manufacturer and chemist, understanding that real progress stems from shared experience, transparency, and a willingness to solve challenges as they arise.

    Whether you are navigating the scale from grams to tons, troubleshooting a difficult reaction, or charting a path toward more sustainable synthesis, our doors and minds remain open. The journey of a single molecule—from batch reactor to finished product—takes far more than blending the right inputs. It requires expertise, care, and an ongoing dialogue with those who shape the world through chemistry.