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Methyl 3-Methoxythiophene-2-Carboxylate

    • Product Name Methyl 3-Methoxythiophene-2-Carboxylate
    • Alias Methyl 3-methoxy-2-thiophenecarboxylate
    • Einecs EINECS 695-835-7
    • 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
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    Specifications

    HS Code

    114712

    Chemicalname Methyl 3-Methoxythiophene-2-Carboxylate
    Casnumber 123304-59-6
    Molecularformula C7H8O3S
    Molecularweight 172.20
    Appearance Light yellow to brownish liquid
    Boilingpoint 94-96°C at 15 mmHg
    Purity Typically ≥ 97%
    Density 1.27 g/cm³ (approximate)
    Solubility Soluble in organic solvents like DMSO and methanol
    Smiles COC1=CSC(=C1)C(=O)OC
    Refractiveindex 1.550-1.560

    As an accredited Methyl 3-Methoxythiophene-2-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25g amber glass bottle with a secure screw cap, featuring hazard labeling and product identification details.
    Shipping Methyl 3-Methoxythiophene-2-Carboxylate is typically shipped in sealed, chemically resistant containers to ensure stability and prevent contamination. It should be packed in compliance with local and international regulations, stored at room temperature, and protected from light and moisture. Appropriate labeling and documentation accompany all chemical shipments for safe handling and transport.
    Storage Methyl 3-Methoxythiophene-2-Carboxylate should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. Keep the container tightly closed when not in use. Store in a chemical-resistant, clearly labeled container, and ensure the storage area is equipped for spill containment and complies with all relevant safety regulations.
    Application of Methyl 3-Methoxythiophene-2-Carboxylate

    Applications of Methyl 3-Methoxythiophene-2-Carboxylate in Industrial Manufacturing

    Methyl 3-Methoxythiophene-2-Carboxylate supports advanced synthesis in multiple chemical sectors. As a specialized intermediate, it unlocks access to demanding downstream products through defined quality, reactivity, and regulatory fit. Below, we detail its application in major industry channels, focusing on genuine production flows, governed standards, actual process integration, and finished product classes recognized across established markets.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient (API) Synthesis

    Methyl 3-Methoxythiophene-2-Carboxylate enables the construction of complex heterocyclic scaffolds in API development, especially within cardiovascular and anti-inflammatory drug classes. Medicinal chemistry groups exploit its methoxy and carboxyl moieties for selective functional group transformations, typically via Suzuki, Buchwald, or nucleophilic substitutions. Strict compliance with pharmaceutical production protocols dictates raw material validation, including impurity profiling, batch traceability, and solvent residue controls throughout the workflow. Downstream steps often involve coupling with boronic acids or amines, leading to beta-substituted thiophene cores in small molecule drug candidates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • WHO GMP for APIs
    • USP/NF for residual solvents (USP <467>)
    • EDQM CEP scheme for European generic APIs

    Typical usage ratio

    • 10%–25% of key heterocycle module load, adjusted per target molecule synthesis pathway and step yield optimization

    Downstream process integration

    • Feed into thienopyridine synthesis for cardiovascular candidates
    • Direct use in combinatorial chemistry platforms
    • Precursor in cyclization and aromatic substitution reactions
    • Component for ester hydrolysis or amidation steps

    Final product types

    • Bulk pharmaceutical active substances
    • Advanced pharmaceutical intermediates
    • Custom small molecule APIs for clinical trials
    • Reference compounds for analytical pharmacopeia methods

    2. Agrochemical Synthesis – Herbicide and Fungicide Intermediates

    This thiophene ester facilitates the synthesis of biologically active agrochemical molecules, particularly within selective herbicide and systemic fungicide categories. Its robust stability under standard process conditions allows integration into alkylation and acylation reactions to install complex side chains, essential for binding target enzyme sites in crops. The regulatory environment requires adherence to residue limits, toxicology data submission, and validated trace impurity analysis for supplied intermediates. Manufacturers leverage continuous flow reactors or batchwise systems for the scalable production of targeted agrochemical backbones.

    Industry compliance standards

    • FAO/WHO JMPR technical guidelines
    • OECD Good Laboratory Practice (GLP) for residue studies
    • ISO 9001:2015 Quality Management for chemical intermediates
    • REACH registration for Europe (substance-specific tonnage band)

    Typical usage ratio

    • 5%–20% of reaction mixture, determined by target molecular scaffold and process selectivity

    Downstream process integration

    • Stepwise construction of thiophene-derived herbicide cores via cross-coupling
    • Intermediate in synthesis of triazole- and pyridine-based fungicides
    • Feedstock for selective chain extension using Grignard or Friedel-Crafts conditions
    • Introduction point for ethylation or amination in final compound assembly

    Final product types

    • Selective pre- and post-emergence herbicides
    • Curative systemic fungicide formulas
    • Agrochemical active ingredients for formulation houses
    • Technical concentrates for end-user dilution

    3. Electronic Chemicals – Organic Semiconductor Material Precursor

    The compound’s electron-rich thiophene ring and methoxy functionality provide a tunable platform for synthesizing conjugated oligomers and polymers used in organic field-effect transistors (OFETs), organic photovoltaics (OPV), and light-emitting diodes (OLEDs). Integration into downstream processes revolves around solution-phase coupling polymerizations, with exacting standards for metal catalyst residue, low ionic contamination, and color index. Electronic-grade quality systems mandate lot traceability and routine specification verification, ensuring that downstream device performance meets customer reliability standards.

    Industry compliance standards

    • IEC 60747-1 for semiconductor devices
    • RoHS (Restriction of Hazardous Substances) for electronics
    • Cleanroom ISO 14644-1 standards for synthesis and handling
    • Internal electronic chemical material QC test regime

    Typical usage ratio

    • 15%–30% by monomer feed weight, based on the molecular design of the target organic semiconductor and polymerization protocol

    Downstream process integration

    • Monomer input for Stille or Suzuki polycondensation
    • Functionalization via direct arylation polymerization (DArP)
    • Precursor to low band-gap copolymers for OPV
    • Incorporation into vacuum-vapor deposition feedstock

    Final product types

    • P-type and ambipolar OFET devices
    • Photoactive layers for organic solar panels
    • Emission layers in flexible display OLED production
    • Organic thin film transistor (OTFT) modules

    4. Fine Chemical Intermediate for Fragrance and Flavor Synthesis

    Methyl 3-Methoxythiophene-2-Carboxylate serves as a specialty building block in the production of heteroaromatic aldehydes, ketones, and alcohols for high-value fragrance accords and food-safe flavorings. Sulfur-containing molecules play a critical role in reproducing natural gourmand, roasted, or savory notes. Downstream flavor and fragrance manufacturing utilizes catalytic hydrogenation, oxidation, and chain extension, with precise GC-MS monitoring for flavor/odor purity. Adherence to international food and fragrance safety regulations is compulsory, including controls for allergens and restricted substances.

    Industry compliance standards

    • IFRA Code of Practice (International Fragrance Association)
    • FEMA GRAS status review for food flavorings
    • EU Regulation (EC) No 1334/2008 on flavorings
    • ISO 22000 Food Safety Management, where food-grade applies

    Typical usage ratio

    • 1%–10% of synthesis charge, adjusting for downstream transformation yield and olfactory strength targets

    Downstream process integration

    • Catalytic reduction to methylthiophenyl alcohols for top-note enhancement
    • Oxidative conversion to aldehydes in savory and roasted flavors
    • Substrate in asymmetric synthesis for chiral fragrance molecules
    • Precursor steps leading to pyrazine and thiazole derivatives

    Final product types

    • Food-compatible savory and roast flavor formulations
    • Perfumery middle-note heterocycles
    • Aroma chemical ingredients for F&F blending houses
    • Specialty chemical additives in gourmet and bakery product lines
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    Certification & Compliance
    More Introduction

    Methyl 3-Methoxythiophene-2-Carboxylate

    Developing high-quality heterocyclic compounds has always grounded our work on the production floor and in the laboratory. Methyl 3-Methoxythiophene-2-Carboxylate stands out for both its chemistry and the way teams rely on its dependable structure during challenging syntheses. We began producing this compound after listening to researchers in pharmaceuticals and materials development. Requests came from chemists who needed a reliable methoxy-substituted thiophene carboxylate to build more complex molecules quickly, without constant concerns about inconsistencies or quality lapses.

    Structure, Purity, and Production Approach

    Our batches display a clean profile—top-end gas chromatography reveals little in the way of side products. We’ve learned this clean separation relies less on brute force and more on consistent handling of precursors and carefully maintained reaction temperatures. The molecule itself, 3-methoxy substitution on thiophene’s ring alongside the ester group at position 2, opens paths for selective functionalizations. This is what many medicinal chemists value: the methoxy group blocks unwanted reactions along the ring while the ester steps easily into transformations like amidations or reductions.

    Specifications have been set through regular feedback. High-purity requirements saw us refining our solvent recovery systems and switched us from bulk drying to more tightly controlled vacuum ovens. Our typical product reaches well above 98% purity via HPLC. No batch leaves our plant unless both our lab and an external lab confirm that result. Beyond purity, our own experience taught us to watch for water content. Too much can ruin later steps in a customer’s sequence. Routine Karl Fischer titration keeps this in check, and our drums hold down moisture pickup during storage or shipment.

    Handling and Packaging from Factory Line to End User

    Years in the field have shown us the dangers of “good enough” packaging. Methyl 3-Methoxythiophene-2-Carboxylate comes in tightly sealed HDPE drums designed for chemical compatibility and handled in climate-stabilized loading bays. Because we run our own logistics, we have clear traceability from our synthesis tank to your bench—a crucial part of maintaining batch uniformity and handling customer returns or queries. Mistakes with containment or atmospheric exposure can quickly run up costs for everyone involved, so we’ve kept package sizes flexible and compliant with typical lab use. This approach keeps the supply chain more agile, something our clients repeatedly say shortens their development cycles and lowers waste.

    Why This Compound Matters in Synthesis

    Thiophene derivatives gained their reputation in pharmaceuticals, crop science, and polymer research for good reason. A key use for Methyl 3-Methoxythiophene-2-Carboxylate revolves around the ease of transforming the methyl ester group—alkaline or enzymatic hydrolysis delivers the free acid, and the methoxy group holds firm under common conditions. This reliable protection allows for more robust synthetic planning. For researchers scaling hits to multi-gram or kilogram quantities, unpredictability at this stage leads to loss of both material and time. Even in academic collaborations, we hear “no more worries about batch-to-batch jumping or unexplained side peaks.”

    Polymer scientists value the compound for conjugated system building blocks. They modify the position-3 methoxy group to introduce electron-donating effects or enhance solubility, and they keep the carboxylate for anchoring onto carrier substrates. The selectivity achievable in downstream chemistry gave several industry consortia the flexibility needed during new material discovery. Our own process R&D team worked with external partners on fullerene analogs where this compound’s predictable reactivity allowed for higher yields in critical coupling reactions.

    Comparison With Related Thiophenes

    We have manufactured various thiophene carboxylates and watched their performance across customer fields. Compared to straight Methyl Thiophene-2-Carboxylate, the 3-methoxy variant provides extra electronic bias on the ring, reducing overreaction and minimizing problems with regioisomer formation. This is a subtle but critical advantage in multistep API synthesis and optoelectronic material construction, where some routes fail due to minor isomer impurities. Chemists needing an unobstructed reactive site often prefer the parent ester but sacrifice ease in subsequent deprotection. Adding the methoxy in position 3 gets both selectivity and downstream versatility.

    Some labs turn to nitro- or cyano-substituted thiophenes, seeking greater electron-withdrawing effects. Experience says these tend to boost reactivity but at the cost of stability—moisture and air degrade the material and can lead to shelf-life headaches. Methyl 3-Methoxythiophene-2-Carboxylate instead maintains its molecular integrity through standard environmental swings, proven through six-month comparative testing in our own warehouse. The molecule stays workable longer, letting customers stretch project timelines without rush orders from us or red tape around storage requirements.

    Regulatory Position, Trace Elements, and Process Residues

    Compliance officers and project leads often ask about residual catalyst or process-derived metal content. Almost every batch we release falls within the lowest tolerable limits for palladium, copper, and iron, confirmed using ICP-MS. Judicious catalyst filtration and solvent switches keep trace contamination in check. That extends to the use of class 2 residual solvents—the methylation step avoids common problem agents, supporting those working under global regulatory filings or pursuing cGMP directions. Many new clients report that their own analytical teams find these levels satisfactory with no extra cleanup. We list our known process aids for customers’ documentation needs, providing auditability down to the individual reagent barrel.

    From a regulatory standpoint, this ester fits into established global chemical frameworks. Our compliance statements cover REACH pre-registration, and we cooperate with those looking to file under TSCA or similar. Our technical support can provide batch history, spillage track record, and process updates for any site audit or project review.

    Challenges with Process Scale-Up

    While small lab runs seem straightforward, scale introduces its own complications. In the early years, we learned how quickly a slightly off-ratio methylation step introduced hard-to-remove byproducts—especially at the 10 kg scale. Inconsistent heating also played havoc with our yields and impurity profiles. Regular investment in jacketed reactors and mass-flow controllers fixed much of that unpredictability. Mixing times and feed rates were mapped out in close detail. Some of our older team members recall plenty of late-night troubleshooting as we transitioned from glassware to stainless steel reactors.

    Subtle points, such as avoiding over-methylation and keeping the carboxyl group intact, meant adjusting quenching steps and switching base types. The right amount of agitation kept reaction layers homogeneous. Our operators look for visual cues during these steps, picking up on droplet texture and color shifts before moving ahead with workups. This kind of mindfulness contributes to the high yield and low impurity count that returning customers rely on. We share our process improvements with repeat clients, helping them solve their own bottlenecks by passing along what we’ve learned.

    End-Use Customization and Collaboration with Researchers

    End-users each come with their own expectations and constraints. Early conversations with process chemists made it clear that off-the-shelf purity or particle size specifications only go so far. Some teams requested higher surface area for improved dissolution, prompting us to fine-tune our crystallization and post-processing. Others building scale quickly asked for larger pack sizes and tighter fill-level controls to match their GMP protocols.

    Direct communication with users led to additional support services—traceability documents, impurity tracking, and open doors for site audits. By discussing application goals and failure modes, we helped several start-ups and university labs move projects along faster. Whether it’s for Suzuki coupling, peptide modifications, or even niche agricultural actives, Methyl 3-Methoxythiophene-2-Carboxylate adapts well. The flexibility comes not from generic promises but from our repeated iterations and shared experience with those at the bench.

    Sustainability Initiatives and Waste Reduction

    Environmental impact often gets overlooked until costs mount or regulations bite. Our reaction processes have shifted toward greener methylating agents and solvent recovery systems, cutting both waste stream load and material cost. We’ve phased in solvent distill-and-reuse procedures and invested in bulk waste monitoring. No material leaves the site without passing waste minimization tracking. These steps stem not from external pressure alone but from internal reviews where every kilogram recovered means both lower purchasing and lower disposal fees.

    Our facility’s wastewater pre-treatment followed input from on-the-ground operators; the simple act of switching out a fouling-prone neutralization agent saved thousands in annual maintenance. Regular environmental audits helped us catch solvent vapor leaks before they became a problem for neighbors. That kind of vigilance doesn’t show up internally on the balance sheet but keeps regulators and communities at ease, allowing production to continue uninterrupted even as local environmental rules tighten.

    Supporting Innovation: Cutting Red Tape and Enabling Speed

    Competition in specialty chemicals depends as much on speed and transparency as it does on the molecule itself. We’ve heard frustration from innovators who see supply chains bogged down by vague delivery quotes or unclear batch records. Our strategy eliminates these headaches, with thorough batch documentation and transparent stock updates. Feedback flows both ways—when a chemist flags a need for improved reactivity or an impurity not caught by standard tests, our QA and R&D teams re-check both our processes and analytical protocols in real time. We’ve even added temporary extra analytical runs when a customer faced an urgent timeline.

    Partnerships with start-up incubators and university consortia grew out of this mindset. We provide pilot-scale sample lots, and in several cases, adjusted our campaign schedules to match grant timelines. Even subcontracted logistics went through our vetting before making supply chain integrations. As a result, our clients spend less time chasing down information and more time driving projects ahead.

    Looking Forward: Addressing Market and Technical Gaps

    Demand tracks directly with trends in pharmaceuticals, advanced materials, and fine chemistry scale-up. Recent years brought a wave of new applications involving conductive polymers and next-generation agrochemicals. These fields keep demand high, but not without new technical gaps. Customers now ask for greener chemistry compliance, better-defined isomer distributions, and stricter control of trace organics.

    We responded by integrating more inline analytics and process automation. Real-time NMR and batch-to-batch impurity mapping are now standard at critical points of production. We’ve worked with external labs to create reference libraries, helping early-stage developers choose the best derivative without weeks of trial and error. Scale-up feasibility studies are done openly—failures get flagged and corrected, and both results and process notes are made transparent for clients working under full confidentiality.

    Knowledge-sharing means fewer lost batches and a stronger chance for everyone’s project to succeed. Downstream users now gain a clarity about available options, how process changes affect performance, and where further tweaks can save both cost and time.

    Conclusion: The Value of Substance and Proven Experience

    Producing specialty esters like Methyl 3-Methoxythiophene-2-Carboxylate goes beyond blending raw materials. It means overseeing each step from sourcing and precise synthesis to quality confirmation and knowledge-sharing with end-users. Focus on transparency, adaptability, and technical improvement didn’t emerge from marketing goals, but from ongoing conversations with the people working day and night on real projects. Robust, well-characterized supplies allow those teams to pursue innovation without unnecessary setbacks.

    This product’s track record in pharma, materials, and polymer research mirrors both the underlying chemistry and the practical lessons won through years of on-the-ground manufacturing. Every adjustment and every improvement comes after reviewing both process and outcome, never simply to tick off another box but to give real value to the chemists using each shipment. That dedication to detail and continuous improvement remains the core commitment to our partners in science and industry.