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2-Iodothioanisole

    • Product Name 2-Iodothioanisole
    • Alias Methyl 2-iodophenyl sulfide
    • Einecs 230-785-7
    • 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

    758222

    Chemical Name 2-Iodothioanisole
    Cas Number 604-85-1
    Molecular Formula C7H7IS
    Molecular Weight 250.10
    Appearance Pale yellow to brown liquid
    Boiling Point 267-269°C
    Density 1.826 g/cm3
    Refractive Index 1.675
    Purity Typically >= 98%

    As an accredited 2-Iodothioanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Iodothioanisole, 25g, is supplied in a sealed amber glass bottle with a secure screw cap, labeled with safety and identification information.
    Shipping 2-Iodothioanisole is shipped in accordance with hazardous chemical regulations. It is packaged in tightly sealed containers, clearly labeled, and protected from light and moisture. Transport is typically via ground or air freight, following all applicable safety guidelines, including proper documentation and compatibility requirements to prevent leaks or reactions during transit.
    Storage 2-Iodothioanisole should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area away from incompatible materials such as oxidizing agents and strong acids. Store under an inert atmosphere if possible to prevent degradation. Ensure appropriate labeling and limit access to trained personnel. Handle in accordance with standard laboratory safety procedures.
    Application of 2-Iodothioanisole

    Applications of 2-Iodothioanisole in Industrial Manufacturing

    2-Iodothioanisole serves as a key intermediate in advanced chemical synthesis, supporting critical sectors such as pharmaceuticals, agricultural chemicals, and material science. Our manufacturing expertise enables direct integration into downstream processes, meeting the demands of specialized applications and aligning with current industry standards for quality, traceability, and regulatory compliance.

    1. Pharmaceutical Intermediate for Thieno[2,3-d]pyrimidine Derivatives

    The pharmaceutical sector employs this compound predominantly in the custom synthesis of thieno[2,3-d]pyrimidine scaffolds, vital for research and development of new drug candidates targeting kinases or anti-inflammatory pathways. Formulation chemists use it as an iodinated starting material in Suzuki-Miyaura or Stille coupling reactions, incorporated at the early stage to introduce thioether functionality and precise iodine labeling. Dosage and reaction scale depend on desired yield and purity profile, directly influencing the synthetic route of investigational active pharmaceutical ingredients (APIs).

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • Ph. Eur. monographs for intermediate documentation
    • US FDA cGMP (21 CFR Parts 210/211) for pharmaceutical raw materials
    • ISO 9001:2015 for quality management in synthesis facilities

    Typical usage ratio

    • 0.8–1.2 equivalents in coupling reactions per desired molar quantity of the core heterocycle; adjusted based on conversion efficiency and target yield for each batch synthesis.

    Downstream process integration

    • Added as a halide source in the initial heterocycle functionalization step before cyclization and purification; subsequent steps use columns for product isolation and HPLC for quality control.

    Final product types

    • New chemical entity (NCE) intermediates for oncology and immunology drug pipelines
    • Reference standards for medicinal chemistry research
    • Lead scaffolds for small-molecule drug development

    2. Advanced Agrochemical Synthesis – Sulfur Analog Herbicide Intermediates

    Producers of advanced agrochemicals apply this material in the synthesis of sulfur-substituted aromatic building blocks, integral to selective herbicide discovery and upscaling. It supplies a protected thioanisole moiety, entering as a precursor for site-directed iodination and downstream thiolation steps, which support structure-activity optimization in active ingredient pipelines. Formulators must calibrate input quantities precisely to regulate substitution pattern and facilitate subsequent desulfurization or coupling reactions.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Plant Protection Products
    • REACH (EC) No 1907/2006 for European chemical registration
    • ISO 9001 in agrochemical intermediate quality control
    • OECD Guidelines for the Testing of Chemicals (as relevant for environmental safety assessments)

    Typical usage ratio

    • 10–15% by mass relative to total aromatic feedstock; the ratio varies by target structure and is determined via analytical quantification at bench and pilot scales.

    Downstream process integration

    • Dosage occurs during the initial feed of aromatic iodination stage, followed by sulfur functionalization, purification, and formulation into technical concentrate for further derivatization or blending.

    Final product types

    • Intermediates for ether/thioether herbicides (e.g., precursor compounds for HPPD-inhibitor discovery)
    • Analytical standards for residue and environmental traceability
    • Agrochemical research samples for pre-commercial field trials

    3. Organic Electronic Material Precursor

    Developers in the field of organic electronics utilize this molecule in the construction of sulfur-containing conjugated systems for optoelectronic devices and specialty polymers. It enters as a controlled monomer for thiophene polymerization, providing specifically iodinated thiol groups that enable site-selective coupling. This material supports the fine-tuning of electronic properties, crucial for the design of organic semiconductors and advanced thin-film transistors.

    Industry compliance standards

    • IEC 60747 for semiconductor device performance criteria
    • ISO 9001 for electronic material traceability and process documentation
    • RoHS Directive (2011/65/EU) for hazardous substance control
    • Conflict Minerals Due Diligence (per customer supply chain requirements)

    Typical usage ratio

    • 0.5–2.0 wt% as a functionalized monomer relative to total polymer batch; adjusted for required conjugation density and film uniformity.

    Downstream process integration

    • Charged into the polymerization reactor during the thiophene linkage stage, followed by copolymerization and casting or spin-coating onto substrates for device fabrication.

    Final product types

    • Precursor polymers for organic field-effect transistors (OFETs)
    • Functional additives in high-refractive index resins
    • Precision coatings for organic light-emitting diodes (OLEDs)

    4. Building Block for Specialty Dye and Pigment Synthesis

    Manufacturers in the colorant sector use this raw material for synthesizing sulfur- and iodine-containing aromatic dyes, particularly for high-value niche applications such as analytical stains, fluorescence markers, and specialty color formulations. Its unique structure contributes controlled substitution patterns, supporting spectral tuning and enhanced photostability in final colorant products. Batch input levels reflect structural requirements and conversion rates during coupling or cross-coupling reactions.

    Industry compliance standards

    • EN 71-3:2019 for dye and pigment safety in toys and consumer goods
    • ISO 9001/14001 for quality and environmental management of dye manufacturing
    • OEKO-TEX® Standard 100 for textile application safety (if used in apparel dyes)
    • REACH Annex XVII compliance for use in European Union regulated colorants

    Typical usage ratio

    • 3–8 mol% relative to total aromatic base in laboratory or pilot-scale dye synthesis; scaled according to molecular design and efficiency of functionalization.

    Downstream process integration

    • Introduced in coupling or diazotization steps for site-specific iodination, followed by purification and formulation into either crystalline or concentrated liquid dye formats.

    Final product types

    • Analytical chromatography stains
    • Fluorescent probes for life science kits
    • Specialty pigment dispersions for high-value plastics or coatings
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    Certification & Compliance
    More Introduction

    Introducing 2-Iodothioanisole: A Core Reagent Built on Practical Manufacturing Expertise

    A Substance Rooted in Careful Synthesis

    Producing 2-iodothioanisole relies on knowledge built from handling aromatic sulfur compounds every day. Over the years, we have refined the process to bring forward a material whose value shows in its consistency, clarity, and reliability, attributes that serve chemists scaling up from bench to plant. The path to this quality starts long before packaging and shipping—years of hands-on work with iodoaromatic intermediates have shaped the approach. By adapting protocols to the realities of industrial chemistry, we mitigate the risk of unwanted side reactions and minimize byproducts, saving time down the line for customers who know the true cost of time in chemical manufacturing.

    This compound, identified in various texts as 2-iodothioanisole or 1-iodo-2-methylsulfanylbenzene, anchors its appeal in the combination of sulfur and iodine directly on a benzene ring. The nature of each batch comes from precisely monitored iodination under sulfur conditions. Each product lot matches our internal benchmarks for purity and trace metals—not just because we are required to do so, but because we have run enough reactions ourselves to know how trace contaminants change downstream chemistry. Thin-layer chromatography, NMR, and GC trace every step. As volumes rise, so does our attention to safety and environmental questions tied to iodine and sulfur byproducts.

    Specifications and Confidence

    Years of fielding questions about reducing volatility or boosting reactivity have taught us the real concerns faced in research, scale-up, and full production. That’s why we deliver 2-iodothioanisole with tight purity standards—minimum 98% on GC for nearly every batch, visualized by consistent color and odor. This matters because even small amounts of off-spec byproducts can hinder the copper-catalyzed coupling and cross-coupling steps that form the backbone of organosulfur synthesis.

    Our product reaches chemists as an oil or, in cooler climates, as pale-yellow, crystallizing puddles. Each bottle carries a label produced in-house—no generic rebranding, always tracked back to the reactor and work-up shift that put it there. The model number matches our production records, never rearranged to fit a catalog page. Real results depend on trust, and trust shows up in traceability.

    Practical Uses: Beyond the Lab Bench

    We recognize that 2-iodothioanisole has built its reputation not in the theoretical but among chemists scaling up reactions who demand materials that respond predictably when added to a pot reactor, Schlenk line, or pilot scale batch. Entry-level books might call it a “building block for C–S coupling,” but in practice its role expands as a versatile aryl halide. Teams working in pharmaceuticals, materials science, and agrochemical discovery have used it for introducing methylthio groups with fidelity not always available from cheaper halogenated anisoles.

    Put to work, the product faces rigorous Suzuki, Sonogashira, or Buchwald-Hartwig coupling protocols. Early on, we found that controlled water content and freedom from oxygenated degradation byproducts define whether a batch works at lab scale or creates headaches during scale-up, so our units ship under dry, argon-flushed conditions with caps rated for real-world lab use—not cost-cutting alternatives.

    Clients rely on our material in development of heteroaromatic scaffolds, peptidomimetics, and as a pivot in constructing ligands for transition metal catalysis. The iodine group in the ortho position offers activation energy that cannot be easily mimicked with lighter halogens, and the methylthio moiety acts as a handle for directing selectivity. Customers working in exploratory synthesis, fragment coupling, and even OLED materials have highlighted the difference a well-prepared batch makes to their timelines.

    Key Distinctions: What Sets 2-Iodothioanisole Apart?

    Experience in scaling up halogenated thioanisoles has shown a pattern: the combination of molecular weight, position of the iodine atom, and cleanliness of the methylthio side chain shift reaction outcomes more than abstract purity ratings would suggest. 2-Iodothioanisole stands out thanks to the ortho relationship—a critical factor in the way palladium, copper, or nickel catalysts approach the ring. Trials with meta- and para-derivatives often end with lower catalyst turnover and increased side reactions. Our customers, whose questions often arise after failed attempts at using less expensive, differently substituted thioanisoles, return to this compound not for a promise on paper, but because it bypasses issues in the field: consistent melting and boiling points, narrow impurity profiles, and minimal catalyst deactivation.

    Working close to reactors and analytical labs, our chemists spent years learning how small fluctuations in iodine content or trace oxidation byproducts can change reaction routes. We focus on thorough, batch-level impurity screening that picks up where basic GC measures leave off, using in-house spectrometers to catch low levels of DMSO, methylsulfinyl, and iodobenzene impurities. There’s no shortcut here; results show up only when the supply chain tracks every drum from the start.

    From Batch to Bottle: Foundation of Reliable Sourcing

    Sourcing starting materials for 2-iodothioanisole is no small feat. We vet suppliers of methylthio precursors and iodine, running side-by-side pilot batches before approving even a single drum for production. A single shipment of off-spec iodobenzene, for example, can derail weeks of production. Our incoming raw materials program includes regular visits and chemical auditing. Finished lots are documented and stored under an inert atmosphere, with sample retention for backtracking.

    Every analytical certificate comes from data collected in our QA lab, not farmed out for third-party testing. This means rapid feedback to formula adjustments, correction of unexpected hot-spots, and a hand-in-glove relationship between manufacturing, QC, and process improvement teams. Small-scale producers may find ways to cut these steps, but anyone who has spent days tracing contamination in their own plant realizes these checks prevent disasters. Chemical manufacturing is only as strong as its weakest link, and we refuse to make trade-offs at the expense of client confidence.

    Responsible Production and Environmental Focus

    The methods we use to make 2-iodothioanisole reflect the lessons of years spent monitoring waste streams and effluents. Working with both iodine and sulfur, our team knows what happens when disposal corners are cut or water untreated. Our plant runs tracing of effluent iodine, batch recapture of organic sulfur, and incineration of volatile organoiodides. Instead of pushing dilute washings out the door, we reclaim solvents. We put used iodine back into internal recycling loops when purity allows. This is a far cry from older industry standards, and we do it because community trust and environmental licensing depend on these practices.

    We have fielded enough regulatory audits to know enforcement comes from both the top down and from local communities. Complaints and odors mean costs. By integrating waste tracking into production records, we hold all operators responsible for each drum of wash or off-gas. This attention to detail—beyond simple compliance—pushes us to reduce both emissions and costs. In real-world terms, we spend less on waste disposal, use less make-up solvent, and avoid regulatory headaches others may face down the road.

    The Real Reason for Quality Commitment

    Feedback from customers drives the way we approach both process and product. Too many times, chemists have struggled with unreliable supply or unexplained performance drop-offs. Our entire workflow takes these realities seriously. Running kilogram-scale couplings in a pilot facility, we understand what goes wrong—trace water kills Grignard reactions, and dust introduces hotspots in sealed-tube couplings. For 2-iodothioanisole, careful filtration and air-free packaging change these results.

    Accountability does not stop at the shipping dock; it extends to after-sale support. We respond quickly to questions about handling, analytical profiles, or batch variations, all with knowledge gained on the factory floor. In cases where clients encounter technical challenges, we work through their troubleshooting steps, bringing both practical plant experience and deep familiarity with reaction chemistry.

    We have seen teams waste months because of inconsistent quality from resellers or brokers, and we've welcomed many clients who return after such experiences. Our ability to back trace every bottle to a work-up record keeps labs running smoothly, sparing them the costs of redocking, resynthesizing, or chasing down contamination.

    Handling Challenges with an Eye on Real-World Use

    Chemists are aware of the issues surrounding sulfur and iodine in scale-up environments. While 2-iodothioanisole is a staple in research, its odor, volatility, and stability require robust handling protocols. Our packing crew works in ventilated rooms and always uses compatible PTFE-lined caps, which prevent leaks or unwanted odors even during summer shipments. This additional work sometimes means higher costs, but field experience shows clients save far more by avoiding product loss through permeation or off-gassing.

    We recommend opening containers under an inert atmosphere, not as a box-ticker, but because we’ve seen firsthand how humidity and oxygen degrade aryl thioethers over time. Our plant staff trains institutional buyers and procurement teams on safe, long-term storage. We supply containers in sizes most suited for research or pilot batch—including custom fills—so that nobody faces downtime from splitting or repackaging drums in unsuitable lab environments.

    Our decades spent supporting both academic chemists and commercial process engineers have driven constant improvements in closing the loop between laboratory innovation and plant-scale delivery. Handling questions—such as whether to use inert gas blanketing, or how to split product from one drum to multiple laboratories—reflect not only our product know-how but our willingness to help customers avoid the costly mistakes we’ve learned from.

    Comparisons to Other Aryl Iodides and Thioanisoles

    Manufacturers and end users often compare 2-iodothioanisole to more basic aryl iodides or to mono-, di-, and tri-substituted thioanisoles, expecting similar outcomes. Through experience, our team has seen why small changes at the molecular level have outsized effects on large-scale reactions. For example, iodobenzene may serve similar routes in coupling chemistry, but missing the methylthio at ortho changes selectivity, reactivity, and post-coupling properties. Mixing up structural isomers leads to unexpected byproducts. Para- or meta-locked analogs often show poorer reactivity in palladium catalysis, marking 2-iodothioanisole as unique for high-value C–S or C–C coupling steps.

    Substituted thioanisoles lacking an iodine atom at the ortho position won’t deliver on reactivity under mild conditions—something important for protecting sensitive downstream chemistry. The choice to use this product over other sulfur- or iodine-bearing arenes comes from seeing how reactivity translates to yields and how product stability simplifies logistics. Downstream, even the odor profile shifts: material made with cleaner methylthio sources avoids the pungency and instability linked to high-sulfur impurity grades.

    Chemical plants using cheaper aryl iodides frequently run into catalyst-binding impurities or spend excess time purifying product away from non-volatile sulfur byproducts. We hear from chemists who choose 2-iodothioanisole for reliability as much as for reactivity. Our team never cuts corners with catalysts or solvents, so the product supports requirements for reproducibility—an asset in any high-throughput screen or analytical workflow as much as in scale-up.

    Supporting Clients Across Sectors

    Large pharmaceutical groups may use 2-iodothioanisole to introduce aryl thioethers in complex small molecules, and university researchers often turn to it to access new ligand families for catalysis. Our history serving both brings a depth of perspective uncommon among traders or catalog suppliers. We have witnessed, in day-to-day operations, how reproducible batches and transparent supply shorten discovery cycles and streamline tech transfer.

    Commitment to technical support has grown from solving real user problems. We draw on bench-top failures and troubleshooting in commercial labs—not from templated service scripts but from hands-on use of the same product. If a team working on OLED chemistry faces crystallization trouble, we suggest melting point manipulation and check the temperature logs on their specific batch. When issues of scale come up, whether in pharmaceuticals, fine chemical R&D, or crop science, our chemists connect processing logic to the reality of supply and use, grounding every suggestion in practice.

    Consistency across sectors matters. If an agrochemical research team budgets a timeline for multi-step synthesis, skipping a week or two on procurement can cost orders of magnitude more than pennies per gram saved. We ensure stocks are managed not just to fill a warehouse but to support year-long planning cycles—driven by the understanding gained from missed deadlines and overtime shifts spent scrambling for inputs.

    Continuous Improvement and Industry Responsibility

    Our journey producing and refining 2-iodothioanisole does not end with each improved batch. Our plant undergoes routine retrofitting to incorporate greener technologies. We monitor solvent recycling rates, minimize energy use during process heating, and implement containment practices that limit releases. We have moved away from wasteful, high-extraction processes common in the past, confident that doing so supports both long-term profitability and environmental stewardship.

    Efficiency comes from learning. Instead of holding to outdated formulas, we tweak runs based on client feedback and evolving industry data. Onsite chemists pilot new ways to recycle mother liquors and recover unreacted iodine, reporting monthly on both yields and process emissions. Just as we expect transparency from our suppliers, we share improvement data with long-term customers looking to model their own procurement cycles and environmental tracking.

    We know that sustainable practice today guarantees access to permits tomorrow. By investing in emissions-cutting technologies and voluntarily reporting to industry round tables, we signal long-term intent to be reliable partners—not just for supply, but for the communities in which we operate.

    A Reliable Partner for Real-World Chemistry

    2-Iodothioanisole is more than just another aromatic fine chemical. Its quality comes from the work put in by the team at every step—raw material vetting, synthesis monitoring, QC, packaging, and after-sales support. Our plant runs on the understanding that innovation and reliability in the specialty chemicals sector come from persistent, hands-on experience. Supply chain confidence, industry trust, and long-term business health grow not from short-term savings or quick sales, but from process integrity.

    We see first-hand how missed analytical details, subpar shipping, or ignored batch variations hurt production lines and research labs. Our commitment to producing 2-iodothioanisole stems from decades of learning in the trenches, where each drum, bottle, and sample carries the pride and diligence that have set us apart in a crowded field. Those who demand depth from their suppliers choose us because we carry the substance and story behind every order—for today’s challenges, and for the ones waiting to be solved tomorrow.