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2-Methoxythiophene

    • Product Name 2-Methoxythiophene
    • Alias 2-Methoxythiophen
    • Einecs 220-938-1
    • 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

    190374

    Chemicalname 2-Methoxythiophene
    Casnumber 2941-09-1
    Molecularformula C5H6OS
    Molarmass 114.17 g/mol
    Appearance Colorless to pale yellow liquid
    Density 1.112 g/mL at 25°C
    Boilingpoint 126-128°C
    Meltingpoint -45°C
    Refractiveindex 1.551
    Flashpoint 32°C
    Solubilityinwater Slightly soluble
    Smiles COC1=CC=CS1

    As an accredited 2-Methoxythiophene 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 100 mL of 2-Methoxythiophene, sealed with a screw cap, labeled with safety and handling instructions.
    Shipping 2-Methoxythiophene should be shipped in tightly sealed containers, protected from light and moisture. It is typically classified as a hazardous material and requires proper labeling and documentation. Transport according to local, national, and international regulations for flammable liquids. Handle and store in a cool, well-ventilated area, away from ignition sources.
    Storage 2-Methoxythiophene should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed when not in use, preferably in a flammable chemicals cabinet. Protect from moisture and direct sunlight. Properly label the container and follow all safety procedures for handling organic solvents.
    Application of 2-Methoxythiophene

    Applications of 2-Methoxythiophene in Industrial Manufacturing

    2-Methoxythiophene serves as a specialty heterocyclic building block in several advanced chemical production sectors. By leveraging its high reactivity and selectivity, manufacturers achieve efficient integration in high-value synthesis processes. Below, we detail its verified use cases, regulatory frameworks, optimized usage levels, processing points, and derived end-products across principal downstream industries.

    1. Pharmaceutical Intermediate Synthesis

    This compound functions as a key heterocyclic unit in the development of a range of active pharmaceutical ingredients, notably within central nervous system and anti-infective drug synthesis. Chemists introduce it during specific cyclization steps to form target scaffolds, where its electron-donating capacity enhances downstream reaction yields. The dosing aligns with stoichiometric ratios based on target molecule design, commonly utilized in high-throughput, batch, or continuous flow processes under cGMP conditions to satisfy stringent quality requirements of regulated final formulations.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) for API production
    • US FDA 21 CFR Part 210/211
    • ISO 9001:2015 Quality Management

    Typical usage ratio

    • 0.5–2.5 molar equivalents, precise ratio set by targeted intermediate synthesis pathway

    Downstream process integration

    • Charged at the heterocycle formation step via Suzuki or Stille coupling, followed by further derivatization or functionalization

    Final product types

    • Pyrrole- and thiophene-based API intermediates
    • Central nervous system drug entities
    • Anti-infective API scaffolds

    2. Organic Electronic Materials

    Specialty electronics manufacturers incorporate 2-methoxythiophene monomers for synthesizing polythiophene derivatives in organic semiconducting devices. Its methoxy substituent modifies the band gap and solubility profile, tailored for specific optoelectronic performance. Precise control of the monomer feed ratio enables batch-to-batch consistency for demanding flexible electronics, with purity grades validated by spectrophotometric and chromatographic QC protocols required for advanced material standards.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) on hazardous substances
    • ISO 14001 Environmental Management for electronics manufacturing
    • REACH Regulation (EC) No 1907/2006
    • IPC-4101 for base materials in electrical/electronic assemblies

    Typical usage ratio

    • 10–30% by monomer content in copolymerization, adjusted for desired conductivity and film properties

    Downstream process integration

    • Fed into oxidative polymerization reactors (e.g., FeCl₃-mediated or electrochemical cell) during thin-film formation

    Final product types

    • Organic thin-film transistors (OTFTs)
    • Antistatic coatings
    • Photovoltaic absorber layers
    • Flexible display substrates

    3. Agrochemical Active Ingredient Synthesis

    In crop protection, this heterocyclic compound is valued for constructing sulfur-containing agrochemical actives with improved bioactivity and soil stability. Downstream producers integrate it during intermediate coupling or ring-closing stages in synthetic workflows for herbicide and fungicide manufacturing. Production must meet agricultural chemical regulations, with the addition carefully scaled to reaction size and active loading requirements for consistent batch yield and field performance.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines for pesticide specification
    • ISO 9001:2015 for agrochemical manufacturing
    • EPA FIFRA Regulations (US market)
    • EC Regulation No 1107/2009 on plant protection products

    Typical usage ratio

    • 1–5% by weight of reaction mixture, determined by molecular design and required activity

    Downstream process integration

    • Introduced at key cyclization or substitution reactions in multipurpose synthesis reactors, followed by downstream purification for technical concentrate production

    Final product types

    • Thienopyridine-based herbicides
    • Fungicidal active intermediates
    • Insecticide precursor compounds

    4. Advanced Fine Chemical Intermediates

    Manufacturers in the specialty chemical sector employ this raw material for preparing high-value intermediates used in dyes, fragrances, and flavor chemistry. Its unique electronic and steric profile enables the construction of sulfur- and oxygen-rich aromatic cores in multi-step syntheses. Operators tune the raw material input to desired color profile, scent note, or functional group conversion, monitored via in-process HPLC/GC for quality control in compliance with end-use segment standards.

    Industry compliance standards

    • IFRA Code of Practice for fragrance industry
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • GHS/CLP (Regulation (EC) No 1272/2008) on classification and packaging
    • ISO 9001:2015

    Typical usage ratio

    • 1–12% by weight in synthesis mixture, set by target intermediate yield and process optimization criteria

    Downstream process integration

    • Added during aromatic functionalization phase in multi-stage synthesis or during selective alkylation/oxidation reactions for dye or fragrance precursor formation

    Final product types

    • Thiophene-derived dyestuff intermediates
    • Sulfur-containing perfume bases
    • Flavor precursors for thermally derived food flavorants
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    Certification & Compliance
    More Introduction

    2-Methoxythiophene: A Chemical Manufacturer’s Perspective

    Understanding 2-Methoxythiophene

    In our production environment, 2-Methoxythiophene has earned a respected place for its versatility in organic synthesis. This compound, with the molecular formula C5H6OS and CAS number 2949-18-8, features a structural backbone built from the well-known thiophene ring substituted with a methoxy group. This precise modification results in a material noticeably distinct from unsubstituted thiophenes. Our batches deliver a clear, colorless to pale yellow liquid, demonstrating high purity through rigorous quality controls—GC purities consistently surpass 98%. Manufacturers like us value stability during storage and handling, supporting long production runs without degradation concerns under proper conditions.

    Advantages in Downstream Syntheses

    Over years of hands-on manufacturing and customer support, we have seen how this product’s unique reactivity makes a difference in several sectors. The methoxy group at the 2-position increases electron density, which directs electrophilic reactions, making it less prone to undesirable side products compared to unsubstituted thiophenes or other substituted analogs. Many labs appreciate the increased selectivity it offers in heterocycle synthesis. Its role as a starting material for pharmaceutical scaffolds means demand rarely wanes. Those involved in producing intermediates for drugs or high-value crop protection chemicals depend on consistent reactivity throughout repeated batches. Any inconsistency directly translates into wasted effort and cost in downstream chemistry.

    How Manufacturing Process Affects Performance

    Our experience dictates that impurity profiles matter just as much as nominal purity. Trace sulfur contaminants, residual solvents, and byproducts such as dimethylthiophenes can interfere with catalysts used in palladium-catalyzed couplings. To counteract that, our process includes a fractional distillation finish and continuous in-line monitoring. The goal centers on ensuring not just purity, but predictability. Researchers count on repeat results; process engineers need batch-to-batch reliability. By tightly controlling production parameters—temperature, pressure, exclusion of air, and rapid withdrawal of product from reactive zones—we can offer a product that integrates seamlessly into industrial and laboratory synthesis pipelines.

    Comparisons with Other Thiophene Derivatives

    Chemists face a choice among many thiophene derivatives, like 2-bromothiophene, 2-chlorothiophene, methylthiophenes, and unsubstituted thiophene itself. Among these, 2-Methoxythiophene stands out because the methoxy group is both electron-donating and non-halogenated, which affects reactivity and downstream modification options. Our customers often switch to 2-Methoxythiophene from halogenated versions to reduce environmental liabilities and achieve cleaner reaction profiles. Halogenated thiophenes leave behind halide waste, sometimes requiring specialized disposal and increasing costs. On the other hand, 2-Methoxythiophene offers milder conditions for functionalization, especially in C–C and C–N bond formations. In some polymerizations, molecule alignment and incorporation prove more reliable with methoxy derivatives.

    Applications Shaped by Real Demand

    Our factory’s output is destined for pharmaceutical firms, academic researchers, and specialty polymer producers. In pharmaceuticals, 2-Methoxythiophene acts as a precursor for drugs targeting the central nervous system, cardiovascular system, and anti-infectives. Its structure supports the build-out of fused heterocyclic systems, where placement of substituents around the ring determines biological activity. In the field of materials science, makers of organic semiconductors look for thiophene rings substituted with electron-donating groups. The methoxy group fulfills this function while adding solubility, which benefits processability in device manufacturing.

    Some requests come from firms exploring conductive polymers. They weigh ease of polymerization and resulting performance characteristics. For these applications, 2-Methoxythiophene can offer a balance between solubility and conductivity because the ether linkage increases compatibility with certain solvents and processing aids. Over years of cooperation, we have adapted production volumes and packaging sizes to align with research pilot projects as well as full-scale industrial needs.

    Quality, Handling, and Real-World Storage

    End-users trust chemical manufacturers to maintain product snapshots indistinguishable from lab-tested standards. In practice, this means close supervision all the way from raw material sourcing to the final distillation collection. For those in the lab or on the production floor, 2-Methoxythiophene presents a distinctive, sweet yet faint odor. This characteristic scent serves as an informal quality check for many seasoned users, but professional verification comes from gas chromatography and NMR fingerprinting.

    Storage calls for airtight containers, often amber-glass or steel drums. Experience tells us exposure to air, moisture, or high temperature can introduce decomposition and reduce shelf life or cause pH drift—factors that impact sensitive downstream reactions. Our logistics teams use insulated transport and short delivery cycles for bulk consignments, reducing risk of spills and evaporation. By maintaining traceability and batch records, we empower customers to troubleshoot if irregularities occur in their own processes. Mistakes in storage or handling almost always show up in later stages—not as immediate spills or failures, but as lost yield or product darkening, issues that careful container choice and regular checks minimize.

    Environmental and Safety Perspectives

    Those handling bulk volumes come to appreciate the safety profile of methoxy-substituted thiophenes. Substitution reduces both volatility and acute toxicity compared to smaller, ring-unsubstituted analogs. During decades of manufacture, our teams have introduced air extraction systems and continuous personal exposure monitoring. Our training programs emphasize respect for both skin contact and inhalation, especially because of the compound’s volatility. Through environmental stewardship, we manage emissions and vapors proactively, protecting both workers and adjacent communities.

    From an environmental sustainability perspective, 2-Methoxythiophene also offers advantages. Unlike many halogenated intermediates, methoxy-substituted derivatives break down more completely in standard wastewater treatments. Although strict regulatory regimes apply for handling, storing, and transporting volatile organic compounds, experience shows that mitigations for this specific product are both feasible and cost-effective. Many regulatory audits have praised our use of closed-loop vapor recovery and solvent recycling, practices that do not merely comply with the letter of the law but exceed minimal expectations.

    Challenges in Production and Distribution

    In manufacturing 2-Methoxythiophene, the real expertise lies in process optimization. Not all manufacturing approaches yield stable product. Early in our journey, we learned that catalyst choice, starting material quality, reaction time, and quenching steps all bear on the ultimate outcome. A poorly run batch can leave behind excess acid or unwanted byproducts that are difficult to remove later. This translates to higher purification costs or, worse, inconsistent product. We meet these challenges head-on using a blend of process surveillance and direct feedback from customers.

    Supply chain interruptions affect everybody. A sudden shortage of starting thiophene or methanol can upend production schedules. Over years we developed local and international supply partnerships to keep flow steady. As a result, our warehouse never carries excess stock, yet seldom experiences backorders. This discipline limits waste while ensuring firms invested in process chemistry see few interruptions. During global supply disruptions, such as the recent increases in transportation costs and raw material price swings, clear communication with downstream users proved vital. In some cases, technical consultation helps customers reformulate or adjust timelines to keep their own lines running.

    Addressing Changing Standards and Evolving Requirements

    With every year, regulatory standards tighten and client expectations sharpen around both purity and traceability. Our lab incorporates regular updates to analytics: new NMR pulse sequences, improved chromatography columns, and mass spectrometry as a confirmation tool. These investments are driven not by paperwork, but by real-world needs. Customers in pharma synthesis particularly demand full trace impurity profiles, since downstream regulatory filings require supporting documentation on not only the primary product but everything present above tiny thresholds. On more than one occasion we've reworked batch records to add lot-level tracking information, making it easier for end-users to complete their own compliance filings.

    Feedback loops matter. Sometimes, a research group may find a hitherto unnoticed impurity affecting their target molecule. Our technical support team investigates these user reports, gathering details about storage, reaction conditions, and batch numbers. Where warranted, we adjust purification steps or storage advice, keeping open lines of communication throughout. No batch leaves our plant without a final review against both internal historical standards and evolving external benchmarks.

    Customer Partnership and Practical Solutions

    Building solutions around 2-Methoxythiophene does not stop when a drum leaves our shipping dock. Some firms require samples for pilot-scale feasibility studies, others need technical support integrating the compound into unfamiliar chemistry. Here, our process development specialists engage directly with users. We discuss reactivity modifications in terms easily understandable to production chemists, translating high-level feedback into technical actions such as adjusting distillation cut points or storing stock under inert gas.

    Consistent supply matters most to those scaling up from R&D to ton-scale, and our plant is organized to meet both custom and large-scale orders without excess red tape. Short production runs in the early days taught us to build flexibility and rapid turnaround into the schedule. Inventory management—guided by real consumption patterns instead of theoretical projections—has saved many partner labs from unnecessary downtime.

    Continuous Improvement from Real Experience

    Decades of on-the-ground manufacturing inform every innovation within our 2-Methoxythiophene process. Constant review of data trends—through analytics, customer returns, or yield figures—pushes us to refine not only plant equipment but also training programs and supply chain choreography. This willingness to adjust, more than any single recipe, sets a manufacturer apart.

    Patience and observation guide us just as much as technical experience. For example, noting subtle color changes or crystallization points in storage flagged hidden instability sources, helping our team redesign drum linings and venting methods. Direct conversations with customers using other chemical suppliers bring insight into what does—and doesn’t—work: unwanted foaming on delivery, off-odors, sluggish dissolving, packaging prone to leaks. Our response tracks these specifics.

    Looking Ahead: Meeting Industry and Societal Needs

    Industrial landscapes do not stand still. Demand for greener, safer, and higher-performing materials continues to shape our approach to making 2-Methoxythiophene. Despite historic roots in aromatic heterocycle chemistry, new applications keep arising, from organic electronics to advanced therapeutics. Efficient, reliable access to core intermediates underpins much of this progress. Just as important, listening to rising concerns over emissions, toxicity, and waste streams steers investment in both the plant and delivery chain.

    For the future, continuous dialogue with those who actually use what we make—be they scientists in research labs or engineers on polymer lines—will keep honing our craft. Good manufacturing never stops adapting to the details of real-world demand, and for 2-Methoxythiophene, every successful reaction downstream stands as proof of practical chemical expertise in action.