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Ethyl 2-Thiophenecarboxylate

    • Product Name Ethyl 2-Thiophenecarboxylate
    • Alias Ethyl thiophene-2-carboxylate
    • Einecs 221-875-7
    • 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

    417122

    Chemical Name Ethyl 2-Thiophenecarboxylate
    Cas Number 614-99-3
    Molecular Formula C7H8O2S
    Molecular Weight 156.20
    Appearance Colorless to pale yellow liquid
    Boiling Point 106-107°C (17 mmHg)
    Melting Point -21°C
    Density 1.181 g/cm3 at 25°C
    Refractive Index 1.541-1.543
    Flash Point 98°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles CCOC(=O)C1=CC=CS1
    Inchi InChI=1S/C7H8O2S/c1-2-9-7(8)6-4-3-5-10-6/h3-5H,2H2,1H3
    Storage Temperature Store at room temperature

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

    Packing & Storage
    Packing Ethyl 2-Thiophenecarboxylate, 100g, sealed in an amber glass bottle with a secure cap and chemical hazard labeling for safety.
    Shipping Ethyl 2-Thiophenecarboxylate is shipped in tightly sealed containers to prevent leakage and contamination. It must be stored and transported in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials. Compliant with chemical shipping regulations, proper labeling and documentation accompany each shipment for safe handling.
    Storage Ethyl 2-Thiophenecarboxylate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Proper labeling and secondary containment are recommended to prevent leaks. Personal protective equipment should be used when handling to avoid exposure to vapors or spills.
    Application of Ethyl 2-Thiophenecarboxylate

    Applications of Ethyl 2-Thiophenecarboxylate in Industrial Manufacturing

    Ethyl 2-Thiophenecarboxylate serves as a specialized intermediate in several advanced chemical and pharmaceutical manufacturing fields. As a direct manufacturer, we support downstream partners across targeted segments by supplying high-purity grades produced under stringent quality systems. Below, we outline key industrial application tracks with detailed compliance, integration, and end-product perspectives for each sector.

    1. Agrochemical Synthesis: Herbicide and Insecticide Intermediate

    Major agrochemical companies utilize Ethyl 2-Thiophenecarboxylate as a building block for active compounds in both herbicide and insecticide development. During multi-step synthesis, it functions as a core scaffold, providing specific heterocyclic moieties required for biological activity. Its use enables the scalable manufacture of key actives employed in crop protection formulas designed for regulated markets.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System)
    • REACH Regulation (EC No 1907/2006) for agricultural intermediates in Europe
    • EPA TSCA Inventory compliance for US agrochemical supply
    • National Pesticide Standard (GB) for China’s regulated market

    Typical usage ratio

    • 5–14% mass fraction in intermediate-stage batch synthesis; precise ratio determined by target molecule and process optimization studies
    • Adjustment occurs mainly in routes generating thiophene-based actives with varied substitution patterns

    Downstream process integration

    • Introduced at step two or three during core structure assembly (via Friedel-Crafts-type acylation, coupling, or cyclization)
    • Subjected to subsequent functionalization to install side chains or halogen atoms before final product crystallization
    • Used in reaction tanks with controlled temperature and inert atmosphere to prevent unwanted by-products
    • Monitored by HPLC or GC for conversion efficiency and residual monitoring

    Final product types

    • Sulfur-containing herbicide active ingredients (e.g., thiophene analogs of sulfonylureas)
    • Insecticidal agents targeting soil pests in cereal and rice systems
    • Pre-formulated wettable powders or emulsion concentrates incorporating finished actives
    • Bulk active ingredient shipments for downstream formulation into branded crop protection products

    2. Pharmaceutical API Intermediate: Synthesis of Thiophene-Containing Drugs

    Active pharmaceutical ingredient (API) manufacturers employ Ethyl 2-Thiophenecarboxylate when assembling thiophene-substituted heterocycles, a common motif in anti-inflammatory, anti-infective, and neurological agents. It enables targeted C-2 functionalization, often through ester hydrolysis, amidation, or further derivatization stages under cGMP conditions, ensuring purity and traceability for pharmaceutical-grade production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.), United States Pharmacopoeia (USP) monographs for key finished drugs
    • Drug Master File (DMF) registration for regulated markets
    • Audit trails for raw material batch traceability and impurity profiling

    Typical usage ratio

    • 6–18% molar ratio, depending on batch scale and molecular complexity
    • Up to 100–200 g per kg of final API in multi-step syntheses, specific to compound route

    Downstream process integration

    • Conversion to carboxylic acid via saponification prior to amide coupling or acylation steps
    • Incorporated in closed reactor systems under GMP validation to avoid contamination
    • Utilized during early structure-building blocks assembly, sometimes followed by halogenation or metal-catalyzed modification
    • Process monitored for residual solvents and by-products in line with pharmacopeial requirements

    Final product types

    • API intermediates for NSAIDs with thiophene substitution
    • Precursors to antiepileptic or anxiolytic active compounds
    • Intermediates for antifungal or antibacterial drugs based on thiophene-ring chemistry
    • Final APIs packed according to pharmacopeial standards, destined for formulation into tablets, capsules, and sterile injectables

    3. Scent and Fragrance Manufacturing: Thiophene-Based Aroma Compounds

    Specialty fragrance compounders utilize Ethyl 2-Thiophenecarboxylate in synthesizing sulfur-enriched scent molecules. Its unique aromatic note, characteristic of roasted, nutty, or earthy nuances, makes it a valued starting material for additives in fine fragrance, flavoring essence, and perfumery intermediates. Controlled reaction with aldehydes, ketones, or reduction agents tailors its olfactory properties while meeting safety and purity criteria for indirect food use and personal care.

    Industry compliance standards

    • IFRA Code of Practice for fragrance safety assessment
    • Food Chemical Codex and FEMA GRAS status for flavor ingredients
    • EU Regulation 1223/2009 on cosmetic products for fragrance ingredient traceability
    • ISO 9235:2013 for aroma chemical manufacturing

    Typical usage ratio

    • 0.5–4% in batch blending systems for aroma synthesis; concentration set by target note profile and matrix compatibility
    • Less than 1% in direct flavor compositions for regulatory compliance

    Downstream process integration

    • Subjected to catalytic reduction, alkylation, or acylation to modify fragrance intensity and volatility
    • Blended post-processing into fragrance bases or compositions for personal care and household goods
    • Analytical QA/QC for residual solvents and off-notes using GC-MS and organoleptic panels
    • Identity and purity confirmed per industry safety requirements before bulk dispatch

    Final product types

    • Sulfur-rich aroma chemicals for high-end perfumes
    • Flavor-enhancing agents in processed food (as per food safety approval)
    • Fragrance bases for soaps, detergents, and personal wash products
    • Intermediate scent notes blended into custom olfactory profiles for specialty applications

    4. Specialty Polymer Synthesis: Conductive Thiophene Polymers

    Polymer manufacturers integrate Ethyl 2-Thiophenecarboxylate into the synthesis of polythiophene materials, targeting the growing market for advanced conductive polymers and organic electronic components. Its unique substitution pattern acts as a handle for controlled polymerization, providing tunable electrical properties and improved film formation in thin-film devices and printed electronics. The process demands stringent raw material purity and precise stoichiometric control to enable consistent conductivity and processability in the final polymer matrix.

    Industry compliance standards

    • ISO 14001:2015 for environmental management during polymer production
    • RoHS Directive (2011/65/EU) limiting hazardous substances in electrical/electronic products
    • ASTM D991-89 for polymer electrical resistance measurement
    • Quality system audits aligned with customer electronics sector requirements (IATF 16949 when automotive use)

    Typical usage ratio

    • 2–7% monomer basis in thiophene-based copolymer batch processes; precise content designed by conductivity targets and application field
    • The ratio adjusted by end-use in OLED, OPV, or antistatic coatings

    Downstream process integration

    • Used as monomer or comonomer in oxidative polymerization processes catalyzed by iron(III) salts (e.g., FeCl3)
    • Blended with co-monomers to achieve specific polymer architectures with targeted electrochemical profiles
    • Quality tested for residual monomer and conductivity in finished films or extrudates
    • Materials cast or printed in controlled environments to prevent dust or ionic contamination

    Final product types

    • Polythiophene conductive polymers for antistatic films, ESD packaging, or printed circuits
    • Organic thin-film transistors (OTFTs) and OLED substrates
    • Transparent conductive coatings for touchscreens and flexible electronic devices
    • Specialty polymer blends for research and prototyping in advanced materials labs

    5. Fine Chemical Building Block for Dye and Pigment Precursors

    Producers of specialty colorants employ Ethyl 2-Thiophenecarboxylate in synthesizing key heterocyclic intermediates, particularly for sulfur-containing dyes and pigments required by textile, leather, and ink industries. Its reactivity allows controlled introduction into multi-stage colorant syntheses, supporting chromophore building and specific shade adjustments under regulated conditions for stability and application durability in demanding end-use environments.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substances in textile dyes
    • EN 71-3:2019 safety standard for heavy metals in colorants for toys
    • ISO 9001:2015 certified QC for colorant batch uniformity
    • REACH compliance for EU market pigment shipments

    Typical usage ratio

    • 1–8% of total mass in multi-step colorant synthesis lines, depending on desired depth and stability of color
    • Fine-tuned by shade intensity required for target application

    Downstream process integration

    • Combined with aromatic amine, diazonium, or sulfonic acid units in colorant-building stages
    • Subjected to controlled oxidation, condensation, or metal complexation steps
    • Quality checked for unreacted monomer and colorfastness in textile and print tests
    • Batches packed under inert atmosphere to protect dye substance stability

    Final product types

    • Heterocyclic dyes for high-washfast textiles
    • Sulfur-containing organic pigments for industrial inkjet formulations
    • Color concentrates for automotive or industrial coatings
    • Specialty colorant intermediates for electronics or security marking
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    Certification & Compliance
    More Introduction

    Ethyl 2-Thiophenecarboxylate: A Reliable Building Block in Organic Synthesis

    From Chemical Manufacturer’s Floor to Industrial Innovation

    Ethyl 2-thiophenecarboxylate, offered as our Model: E2TC123, comes through years of hands-on experience and steady investment in reliable chemical process control. In our plant, raw materials come in straight from inspected sources, because consistency starts at the loading dock long before the reactor charges line up. Over the course of many batches, optimization doesn’t just mean adjusting output—it means handling fluctuations in feedstock quality and minor variations in temperature profiles. Our crew works with continuous feedback from every stage, translating to a finished product that doesn’t carry a vendor’s batch-to-batch headache.

    In synthetic chemistry, Ethyl 2-thiophenecarboxylate stands as a backbone for a significant range of applications. Its molecular formula, C7H8O2S, implies a versatile arrangement: the fused thiophene ring and the ethyl carboxylate moiety offer a springboard for transformations. Our team—chemists and operators through years of collaboration—focuses heavily on purity and trace impurity analytics. We tune specifications to meet a GC area percent greater than 99.3% as measured on equipment routinely checked by external calibration standards. Our material comes as a clear, almost colorless to pale yellow liquid, with particular attention paid to moisture content, since reactions in pharmaceuticals and advanced materials can go sideways even with ppm-level water content.

    How It Is Made: Precision Over Routine

    Many commercial syntheses of ethyl 2-thiophenecarboxylate start with the acylation of thiophene. On our floor, we saw enough blocked reactors and out-of-spec distillations years ago to know that timing and heat distribution matter more than textbook diagrams ever let on. We set up jacketed columns and batch reactors, invest in real-time temperature mapping, and modify distillation profiles based on in-process analytics rather than just a fixed recipe. A lot of our downtime never ends up in a data sheet—but it means the bottle of product you receive looks, smells, and performs the same way every time, whether you’re running a pilot batch or a commercial campaign.

    As a responsible manufacturer, we don’t use recycled solvents or unqualified raw intermediates for this product. Our process-specific specs have a knock-on effect: smoother chromatography, fewer active impurities, and tighter control over sulfur content, which our downstream customers in pharmaceutical R&D particularly appreciate.

    Applications: More Than a Single-End Use

    Lab stories pile up over the years. In agrochemical development, our ethyl 2-thiophenecarboxylate gets used as a functionalized aromatic precursor, helping teams build novel herbicidal scaffolds that strike a balance between efficacy and low field persistence. Over in pharmaceutical synthesis, smaller labs and large process teams alike work this raw material into heterocyclic cores for lead candidate molecules, always aiming for maximum synthetic yield with minimum purification headaches.

    These advantages don’t come just from being another ring-shaped building block. The ester group on the thiophene confers predictable reactivity in substitutions, metal-catalyzed couplings, and hydrolytic steps. This means chemists can avoid convoluted protecting group strategies or repeated reworks. In consumer electronics and specialty polymer sectors, certain research operations take advantage of the clean sulfur heterocycle to produce organic semiconductors with higher stability or altered electron mobility.

    End uses evolve. Fifteen years ago, we saw this compound mostly shipped into the pharmaceutical world. Today, battery innovators, performance coatings developers, and even fragrance formulators have turned to this material’s blend of stability with selective functional reactivity. In every field, trace odor, low volatility, and modest boiling point help ensure cleaner process flows, fewer unplanned emissions, and easier containment.

    What Sets Ours Apart: Beyond Just Purity

    Many folks equate purity with quality. Our lab technician who has worked across multiple product lines will tell you: for ethyl 2-thiophenecarboxylate, purity is just one slice. We emphasize lot-to-lot stability. Some plants cut corners on final drying or use packaging with lingering olfactory contamination—our team figured out better glass lining and pre-flushing procedures after we saw a spike in customer rejections years back. We keep peroxide-forming residues near lab-detectable limits, and monitor storage for decomposition, which can creep in unnoticed if bottles sit too long in direct sun or exposed to air. The color consistency and sulfurous aroma both tell you something about underlying stability and trace contaminants.

    We learned the hard way not to treat shipping and sealing protocols as afterthoughts. Bottling lines run under inert gas. Every outgoing batch undergoes headspace analysis and is checked for major airborne volatiles to keep long-haul customers from opening a bottle to find the product has shifted.

    It’s not just quality for the sake of QC paperwork. If you come from a plant making liquid crystals for displays, the faintest byproduct can ruin whole kilograms of high-value intermediate. Customers in catalyst development told us about spectral impurities wrecking reproducibility in organometallic screens. More than once, we’ve run parallel samples to dial in autoclave protocols for partners scaling up, absorbing the cost so the learning doesn’t travel both ways.

    Comparisons: Why This Compound Over Alternatives?

    Chemists always ask about alternatives—could you just use methyl 2-thiophenecarboxylate, or even switch to pyridine-based esters? The answer, tested over multiple years and dozens of customers, hinges on both reactivity and workup. Ethyl esters offer a manageable tradeoff: not as volatile as methyl, not as bulky as propyl or isopropyl, striking a sweet spot for reaction times and recovery yields without creating byproducts stuck in purification columns.

    Some developers compare thiophene esters to benzene derivatives, but thiophenes introduce sulfur into the molecule pool, opening doors for downstream cyclizations, oxidation, and C-H activation steps that benzene can’t match without significant extra process steps or metal reagents. Our crew has tested the hydrolysis rates of ethyl esters versus methyl esters under both acid and base catalysis, finding consistently that ethyl groups facilitate both controllability and moderate processing temperatures. Overheating to force methyl group removal increases risks of side reactions and darkened reaction mixtures.

    We field requests from material scientists looking for esters with increased conjugation, but cost and shelf stability swing the balance back to ethyl 2-thiophenecarboxylate for many scale-up projects. For every case where customers want the next exotic heterocycle, a few tried-and-true materials provide real value because new process issues often outweigh any hypothetical gains.

    Our Commitment: Sustainable and Transparent

    Regulatory compliance does not happen in a vacuum because our product lands in applications tied to health and safety, so we build documentation on traceability and batch records from day one. We cut down on waste streams through solvent recovery and smart venting design, reducing both local emissions and overall carbon impact across every batch. Partners running LEED-certified or ISO 14001 factories repeatedly ask about lifecycle data—our supply chain analytics document sourcing, process energy, and disposal pathways. Sustainability is a running conversation, not a one-time certification.

    Long-term process security for customers drives a lot of our planning. We keep stocks of critical raw materials above projected run rates to cushion against logistics delays or sudden regulatory shifts. Our site operations planners regularly review weak links in the supply chain, and our QC team is trained not just in analytical technicalities but in recognizing trends before they snowball into product issues.

    Addressing Common Challenges: Stability and Safety in Use

    Over the last few decades, we faced repeated stability challenges, especially for customers running reactions under aggressive conditions. Ethyl 2-thiophenecarboxylate, like other esters, can hydrolyze with excessive moisture or high temperature. We took lessons from early returns—tightened drum liners, switched to more robust seals, taught users about refrigerated storage, and revamped our documentation to include in-plant best practices that actually came from user labs, not just the regulatory manuals.

    Shipping didn’t always run smoothly. Fluctuating warehouse temperatures on the road once wiped out whole lots. Our logistics team now audits transport partners for temperature swings and humidity control, particularly during hot summer months or for overseas freight. It took several years to see the bite-size operational changes actually feed back into fewer complaints. This isn’t just theory—each procedural tweak gets tracked from the warehouse to field deployment.

    We advise avoidance of extended exposure to strong acids or bases near handling equipment, because the ester can degrade unnoticed, especially at larger scale where thermal management gets tricky. Residual decomposition products can foul expensive downstream tools. We adjusted our batch turnover targets to improve shelf life with less risk of end-use degradation.

    User Feedback and Product Advancement

    Direct customer reviews and plant trials shaped many of our process advances. For example, some early users reported difficulty in scaling up two-step reactions because intermediate crystallization yielded inconsistent lots. In response, we worked with them to tweak filtration regimes and minimize unknown residues. The end result: fewer failed syntheses and less wasted time and materials.

    University labs supplied feedback on student-scale reactions and safety handling—some of our recommended protocols stem from common missteps among academic groups not used to scaling up. The academic community pushed us to include side-by-side reactivity profiles with structurally related compounds, giving new users clearer guidelines for reaction tuning.

    On several occasions, we opened our facility for customers to observe quality control testing in real time, improving transparency and communication between production, application, and customer service. These exchanges built a two-way trust that influences how we approach process upgrades and transparency in documentation.

    Supply Chain Pressures and Industry Trends

    Global demand for thiophene esters shows no sign of slowing, especially in regions investing in domestic pharmaceutical manufacturing and advanced materials research. Trade tensions, evolving legal landscapes, and wider shifts toward greener chemistry all put pressure on suppliers. Some attempts to short-cut the process show up in the market as material with visible color or off-spec acid residue. We maintain direct relationships with verified raw material producers and regularly audit supplier plants. Regulatory shifts, such as new restrictions on solvent effluent or labeling requirements, prompt us to adapt storage and shipping procedures before compliance deadlines.

    To hedge against future interruptions, our operations group established alternate synthesis routes on a pilot scale, evaluated every few quarters in real production to ensure viable switchover should primary routes hit a snag. We keep a running book of location-based risk analyses—so each order doesn’t depend on a single time zone’s smooth running. Our customers can see the difference in fewer delays and consistent output.

    Some industry disruptors point to bio-derived processes or alternative heterocyclic scaffolds. We monitor pilot trials, look at comparative reactivity, and evaluate long-term logistics. As of this writing, bio-based routes can’t yet match the process safety or yield of established synthesis, but we keep channels open for collaboration and early adoption if the balance changes.

    Working Closely with Downstream Partners

    We do more than push boxes out the door. Our staff visits customer plants, reviews process bottlenecks, and helps troubleshoot field synthesis and storage issues. For some pharmaceutical clients developing active ingredient scale-ups, we offer side-run lots to check for reductive or oxidative byproducts under their specific reaction infrastructure. Our team assists in establishing handling protocols to reduce operator exposure and minimize cumulative trace contamination in high-purity operations—especially critical when working around other sulfur compounds or oxygen-sensitive intermediates.

    Our experience suggests most process failures downstream do not arise from exotic contaminants but predictable variables such as improper solvent choice, storage outside recommended temperature windows, or overlooked moisture ingress. We work with partners to build redundancy into their QC workflows—spot testing at point-of-use rather than relying solely on our outgoing certificate of analysis. This practice dropped joint failure rates noticeably.

    In global projects, translation errors in documentation or local regulatory differences caused problems for customers in the past. We now issue local-language guidelines and maintain a technical support line direct to in-plant chemists who know the product hands-on, not just through paperwork or routine scripts.

    Safety as Day-to-Day Practice

    A lot gets written about safe handling, but best practices sink in where technicians understand everyday habits can save a project. Maintenance teams regularly recheck bulk heads, seals, and spill protection. Supervisors and new hires rotate through practical hazard-prevention training tailored to likely in-plant incidents. Few events ruin a month like a solvent drum breach in a busy work zone, so we don’t just check the box on training—everyone on our floor has handled real-world cleanup.

    Our safety managers systematically investigate near-miss events, even if nothing hit the news or disrupted shipments. The data we gather informs process redesigns and sometimes even instrumentation changes, helping us continually adjust risk assessment. Safety is not just compliance—it's direct operational discipline.

    What Our Insight Means for Customers

    Working directly as a manufacturer, we see how a good batch of ethyl 2-thiophenecarboxylate means more than just neat label copy. It’s about rigorous sourcing, stable processing, honest batch communication, and willingness to iron out end-use problems together with users. Not every competitor wants to answer tough technical questions, but lessons from our plant mean customers get consistent outcomes in the real world—helping them innovate without fighting unreliable reagents.

    We’re invested in what happens downstream; our business succeeds both in tonnage and in the technical success stories from those who trust us with the early stages of their synthesis. Every specification comes from production floor headaches, troubleshooting, and real cooperation with world-class users, from the lab bench to the full-scale factory.

    Looking Forward

    Progress in the world of specialty chemicals depends on steady partnership between supplier and user. As new applications for ethyl 2-thiophenecarboxylate arise—across battery tech, crop science, high-end fragrance, and smart polymers—we continue to invest in process transparency, joint development, and open channels for customer feedback. Our end goal is to keep simplifying R&D and production so users spend more time pushing the envelope, less time debugging a starting material. In a fast-changing chemical landscape, experience makes the difference.