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Methyl Furan-3-Carboxylate

    • Product Name Methyl Furan-3-Carboxylate
    • Alias 3-Methoxycarbonylfuran
    • Einecs 248-202-1
    • 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
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    VTB
    Specifications

    HS Code

    912583

    Iupac Name Methyl furan-3-carboxylate
    Molecular Formula C6H6O3
    Molar Mass 126.11 g/mol
    Cas Number 1664-44-0
    Appearance Colorless to pale yellow liquid
    Boiling Point 196-197°C
    Density 1.172 g/cm³
    Smiles COC(=O)C1=COC=C1
    Inchi InChI=1S/C6H6O3/c1-9-6(7)5-2-3-8-4-5/h2-4H,1H3
    Refractive Index 1.496
    Solubility In Water Slightly soluble

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

    Packing & Storage
    Packing A 25g amber glass bottle with screw cap, clearly labeled "Methyl Furan-3-Carboxylate," displaying hazard symbols and product details.
    Shipping Methyl Furan-3-Carboxylate is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be transported as a chemical product, following applicable regulatory guidelines for hazardous materials. Proper labeling and documentation are required. Store in a cool, dry place and handle with appropriate protective equipment during transit.
    Storage Store methyl furan-3-carboxylate in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers. Ensure the storage area is equipped to contain spills and is clearly labeled. Follow all standard safety and regulatory guidelines for handling and storing hazardous chemicals.
    Application of Methyl Furan-3-Carboxylate

    Applications of Methyl Furan-3-Carboxylate in Industrial Manufacturing

    Methyl Furan-3-Carboxylate serves as a high-purity intermediate in multiple chemical segments. As the direct manufacturer, we support bulk customization for precise synthetic needs across specialized downstream industries. Below, we outline its major industrial application scenarios with specification details.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    In pharmaceutical synthesis, Methyl Furan-3-Carboxylate acts as a crucial building block for manufacturing certain antiviral agents and heterocyclic drug APIs. Production sites value its consistent assay and impurity control, using it in nucleophilic substitution or esterification stages. Manufacturers monitor trace solvent and byproduct content to comply with strict regulatory requirements, especially during the synthesis of derivatives like furan-based antitubercular agents.

    Industry compliance standards

    • ICH Q7 GMP guidelines
    • United States Pharmacopeia (USP) monograph references for related intermediates
    • European Pharmacopoeia purity standards for residual solvents
    • China Pharmacopoeia 2020 for chemical raw materials used in pharma

    Typical usage ratio

    • Ranges from 5% to 25% by molar ratio, adjusted according to multi-step synthesis efficiency and target compound requirements

    Downstream process integration

    • Introduced during key esterification or condensation steps before side-chain modification; inline HPLC tracks conversion
    • Heated in batch reactors under inert atmosphere, with subsequent distillation to isolate intermediates

    Final product types

    • Intermediate stages of furan-based antivirals
    • Precursors to heterocyclic antitubercular drugs
    • API components requiring furan ring structures

    2. Agrochemical Synthesis for Fungicides and Pesticide Intermediates

    The compound is widely applied in synthesizing agrochemical actives, specifically as a precursor in manufacturing fungicide and insecticide agrochemicals that utilize oxygenated heterocycles. It supports selectivity in downstream coupling reactions, especially for pyrrole and furan systems, and its assay consistency enables reproducible yields in pilot and full-scale batch production targeting regulatory registration batches.

    Industry compliance standards

    • FAO/WHO Technical Specifications for Pesticides
    • ISO 9001:2015 QMS for agro-intermediate production
    • European Union Regulation (EC) No 1107/2009 for plant protection product intermediates
    • REACH registration for imported chemical intermediates

    Typical usage ratio

    • Utilized at 15%–45% of charge depending on the total molecular rearrangement and desired agrochemical concentration

    Downstream process integration

    • Dosed directly into reactors during synthesis of furan-linked acyl chlorides or amidation reactions
    • Employed in intermediate crystallization and solvent swapping stages to ensure purity

    Final product types

    • Key intermediates for fungicidal active ingredients
    • Pesticidal raw materials with heterocyclic backbones
    • Formulated agrochemical concentrate bases

    3. Flavor and Fragrance Industry: Synthesis of Aroma Chemicals

    Chemical processors incorporate Methyl Furan-3-Carboxylate as a specialty intermediate in aroma chemical manufacture, especially for fruity and nutty fragrance components. Certified food-grade batches follow rigorous migration and residual solvent testing due to use in formulations for food and beverage, oral care, and personal care industries. Individual producers fine-tune concentration to maintain olfactory thresholds relevant to finished fragrance standards.

    Industry compliance standards

    • FEMA GRAS listing for structurally related furan derivatives
    • IFRA Standards for fragrance material purity
    • EU Regulation No 1334/2008 for food flavoring substances
    • Codex Alimentarius provisions for food additives and processing aids

    Typical usage ratio

    • Ranges from 0.1% to 3% weight/weight in reaction mixtures depending on the target aroma profile and batch output

    Downstream process integration

    • Reacted at controlled temperatures with alcohols or aldehydes for ester or lactone production, followed by distillation or extraction
    • Subjected to food-grade QC analyses (GC-MS, impurity screening) before formulation into commercial bases

    Final product types

    • Specialty ester aroma chemicals with furan rings
    • Formulated flavor compounds for beverages and confections
    • Custom fragrance bases for toiletries

    4. Advanced Polymer & Resin Modifiers

    Polymer manufacturers utilize Methyl Furan-3-Carboxylate in specialty engineering plastics and resin production where heterocyclic structures enhance UV stability or chemical resistance. The chemical is directly involved in polycondensation or copolymerization steps to tailor mechanical and thermal properties, especially for applications in electronics encapsulation, industrial coatings, and adhesive systems where performance traces back to furanic modifiers.

    Industry compliance standards

    • ISO 14001:2015 for environmental controls in resin production
    • RoHS Directive 2011/65/EU for electronic and electrical applications
    • UL 94 standards for flame retardancy of polymers
    • ASTM D638 for assessment of mechanical properties in plastics

    Typical usage ratio

    • Added at 0.5% to 10% of total monomer feedstock by mass, based on product mechanical specifications

    Downstream process integration

    • Metered into continuous or batch reactors with primary monomers; participates in esterification or transesterification stages
    • Processed through post-polymerization purification to remove unreacted residues

    Final product types

    • Modified polyester resins for composites and laminates
    • UV-resistant plastic compounds for electronics housing
    • Heat-stable adhesives and coating resins

    5. Fine Chemical Synthesis for Specialty Esters

    Producers of fine chemicals rely on Methyl Furan-3-Carboxylate as a starting material for a range of tailor-made esters and amides designed for high value-added end uses, including specialty solvents and additives. Laboratories and commercial facilities synthesize derivatives using both batch and continuous flow processes, with precise control of temperature, pH, and reaction time to ensure high yield and selectivity for downstream product differentiation.

    Industry compliance standards

    • ISO 9001-certified synthesis processes
    • National or regional chemical safety and registration standards (e.g., TSCA for the US)
    • SEFA (Scientific Equipment and Furniture Association) for laboratory-grade chemicals
    • REACH compliance for commercial manufacturing in the EU

    Typical usage ratio

    • Used at 8%–35% of the reactive mixture, variable by desired end-product function and line throughput

    Downstream process integration

    • Charged at the first or second reactor stage for transesterification or amidation reactions, monitored for conversion rate via GC analysis
    • Purified through distillation and crystallization for fine chemical grade specification

    Final product types

    • Custom ester and amide specialty chemicals
    • High-value solvent intermediates
    • Chemical additives for coatings and inks
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    Certification & Compliance
    More Introduction

    Introducing Methyl Furan-3-Carboxylate: A Thoughtful Perspective

    It’s rare to come across a chemical with as much versatility and reliability as Methyl Furan-3-Carboxylate. Its appearance betrays little about the punch it packs in fields ranging from pharmaceuticals to materials science. The first time I heard about this compound, I was sitting in the back of a lecture hall. The professor didn’t hype it up, but those who work with it tend to stick with it for a reason. Too many chemicals on the market write checks their specs can’t cash, either lacking in stability or proving tough to incorporate into formulas consistently. Methyl Furan-3-Carboxylate usually rises above these pitfalls.

    What Makes This Compound Worth Talking About

    This organic molecule carries a distinct furan ring structure, unlike the usual benzene derivatives. It strolls down a unique path, offering its methyl carboxylate group at the third position—so the result isn’t just another bland ester. You get a substance with a slight, lingering aroma and clear performance in synthesis. Its structural nuance isn’t a minor twist; this difference shapes how the compound reacts and integrates with other building blocks, which is why it keeps showing up in research labs and pilot plants worldwide.

    The specifics matter. We see methyl furan-3-carboxylate regularly weighing in at a molecular mass of 126.1 g/mol, and its chemical formula, C6H6O3, keeps it straightforward and predictable in computations. Quality samples arrive as a pale, oily liquid, and you won’t find the same volatility in competitor esters. Purity levels often top 98 percent in the best supplies, laying to rest many common headaches about side-reactions or inconsistent yields in bench work.

    Putting It to Work

    Chemists reach for this compound during the creation of heterocyclic drugs, flavors, and specialty polymers. Some of the earliest days of my own career involved endless trial runs with different intermediates. Furan-based esters broke open doors that stayed locked with more conventional aromatics. The furan ring resists degradation, and that methyl carboxylate group lends itself to functionalization in a way that speeds up synthetic routes.

    Many fine chemicals used today—especially those in research and molecule discovery—lean heavily on intermediates of this kind. Making antiviral agents? The methyl group at the third spot offers anchor points that lead to more selective, less hazardous synthetic paths. Aromatic esters that lack this furan skeleton usually don’t provide the same selectivity. During polymer design, additives or linkers derived from methyl furan-3-carboxylate offer increased flexibility and reactivity, resulting in materials better equipped for next-generation electronics or coatings.

    Differences that Stand Out from the Crowd

    Comparing it with similar esters, the first thing that jumps out is the reactivity balance. Many standard methyl benzoates or pyrrole carboxylates present nice stability but fall short in controlled synthesis—they either react too slowly or too unpredictably once you push temperatures or introduce catalysts. Methyl furan-3-carboxylate achieves a real sweet spot, holding up under the heat and showing manageable reaction kinetics. In industrial terms, that translates to fewer ruined batches and less downtime for retooling setups.

    This isn’t just about better yields; it’s also about safer working conditions. In pharmaceutical synthesis, for example, you sometimes deal with esters prone to forming explosive peroxides or unpleasant by-products. The furan ring offers less risk on this front, and established literature supports its lower side-product profile. Anyone who’s struggled with recurring purification headaches will appreciate what this means for streamlined lab work and less waste.

    I’ve seen colleagues compare processing methyl furan-3-carboxylate to working with plain methyl esters, expecting similar issues. They quickly notice fewer issues with hydrolytic degradation—a boon in climates with high humidity or in scaled-up aqueous processes. These practical strengths aren’t just theoretical, either: research from the European Journal of Organic Chemistry highlights how furan-based intermediates like this ester demonstrate superior selectivity and lower impurity formation compared to simpler ring systems.

    Meeting the Demands of Modern Chemistry

    As the pharmaceutical landscape leans toward greener, more sustainable synthesis routes, chemical tools like methyl furan-3-carboxylate seem more vital than ever. There’s a clear push toward step economy and atom efficiency. Many legacy intermediates just can’t keep up, requiring hazardous catalysts or creating extra separation steps. This methylated furan carboxylate presents clear opportunities for one-pot processes. The furan ring itself often survives conditions that rip apart benzene-based systems.

    It’s not just about performance in a vacuum. Regulations on chemical safety and environment stewardship tighten year after year. While some esters demand special handling or leave persistent organic pollutants behind, methyl furan-3-carboxylate fares better during breakdown. The parent furan structure degrades more fully and naturally—an advantage for both large-scale industry and small research outfits aiming for less impact.

    Supply Chain and Availability

    Even the best chemicals don’t help much if sourcing turns into a logistical maze. Methyl furan-3-carboxylate benefits from streamlined routes of production, often stemming from biomass-based furan sources. That means suppliers aren’t so reliant on petrochemicals, which can fluctuate in price or availability. Over the past decade, bio-derived furans have carved out a steady, robust pipeline. This has kept market prices comparatively stable, especially as global interest in renewable feedstocks grows.

    During strained periods in raw materials supply—as we’ve all witnessed in recent years—products that come from alternative routes carry a lot of value. Process chemists, customers, and financial planners share this perspective. Methyl furan-3-carboxylate gives them more consistent access while sidestepping some of the volatility facing other specialty esters.

    Working With It in the Lab and Plant

    Ease of handling makes a huge difference when you’re managing dozens of reactions per day. Methyl furan-3-carboxylate’s liquid state, coupled with its moderate boiling point, keeps transfer and measurement straightforward. Unlike more volatile esters, it doesn’t demand elaborate low-temperature storage. Once, in a poorly insulated research shed, we kept samples stable even without chilled storage, and performance stayed solid over weeks. That’s not something you can expect from all functionalized esters.

    The viscosity and solvency characteristics help with blending into multistep reactions. If a reagent keeps gumming up equipment or requires constant rehomogenization, productivity grinds to a halt. Methyl furan-3-carboxylate flows well, mixes easily, and shows good solubility in most common organic solvents. Think of sessions spent trying to coax reluctant ingredients into solution—this ester usually spares you that struggle, allowing for seamless integration even in automated reactor systems.

    Looking to the Future: Why It Matters

    Anyone writing off methyl furan-3-carboxylate as just another niche reagent misses the wider context. This compound stands at the intersection of reliable bulk production and high-end synthetic performance. That’s no small feat. Demands in life sciences show no sign of slowing. New treatments, agrochemicals, and advanced materials increasingly require intermediates that don’t just ‘get the job done’ but also simplify downstream processes, minimize waste, and enable next-generation chemistry.

    In polymer science, new sustainable materials keep grabbing headlines. The durability and tunability of furan-based linkers help bring about biobased plastics and resins. The methyl group at the carboxylate position locks in performance benefits, setting the stage for custom-tailored materials that remain affordable and competitive against older, less green alternatives. You find more research pointing to this route each year, especially from university consortia focused on ‘future-proof’ material development.

    Some might ask if newer or more exotic methyl esters deserve the spotlight. The truth is, those alternatives often lack the decades of data and practical feedback supporting methyl furan-3-carboxylate. It’s easier now to trace safety records, long-term stability studies, and published application notes from reputable sources. For project leads weighing regulatory risk or batch-to-batch consistency, established documentation makes all the difference. In my experience, the value of proven reliability never goes out of style, especially under strict QA requirements.

    Possible Challenges and Room for Improvement

    No product comes without shortcomings, and methyl furan-3-carboxylate isn’t immune. Sometimes, the furan ring’s partial reactivity works against you in oxidation reactions or under harsh acidic conditions. Labs must keep a sharp eye on protocol, as overzealous processing can chop up the ring and introduce unexpected side products. That said, this issue highlights why ongoing education and careful planning stay crucial in chemical work.

    Supply chain disruptions do remain a background concern, given shifting regulations and feedstock changes. Even as bio-based furan sources solidify supply, pricing and region-dependent factors could alter the landscape. Staying engaged with multiple suppliers pays off, and industry groups could do more to push for greater transparency in production standards. Traceability and tight quality benchmarks offer a buffer against bad batches.

    Safety protocols for handling still call for vigilance. Though milder than many alternatives, methyl furan-3-carboxylate has a vapor profile that nudges chemists toward well-ventilated environments or local exhaust extraction. Responsible training, periodic lab audits, and up-to-date MSDS reviews can stave off trouble. Many of us learned old-school habits the hard way—it makes sense to pair the strengths of trusted chemicals with respect for potential risks.

    Potential Solutions for Better Performance and Access

    Driving further improvement in methyl furan-3-carboxylate availability and performance benefits the entire sector. Consortium-driven synthesis methods—like route optimization based on greener catalysts—cut both waste and costs. Sharing open-source data on reaction yields and impurity profiles could reduce trial-and-error in customer labs and shortens the learning curve for new users.

    Investment in post-processing automation stands out. Chemists relying on hand-batch separation lose precious time and risk exposure. Automated purification and distillation, paired with real-time monitoring, could keep purity above 99 percent across the board and slice human error out of the equation.

    On the sourcing front, standardizing feedstock origins and ramping up third-party verification would help labs trust their supply. Pushes toward ISO standards in specialty chemicals are already gaining traction. Bringing methyl furan-3-carboxylate sourcing under a similarly rigorous system strengthens the field and brings peace of mind from bench chemistry to pilot scale.

    Summary: Why It Catches Attention

    With dozens of methyl esters competing for a spot in modern laboratories, methyl furan-3-carboxylate has built a reputation rooted in practical strengths and adaptability. The furan ring ensures stability in demanding reactions, while the methyl carboxylate group provides unique entry points for synthesis. It stands up to both strict quality controls in pharma and the shifting requirements of cutting-edge materials research.

    From early bench-scale curiosity to established industrial reagent, methyl furan-3-carboxylate doesn’t just keep pace—it earns respect with real-world results. Researchers and industrial chemists know they’re not just buying a bottle but gaining a reliable partner in pursuit of invention and discovery. New advances in materials and medicines keep pushing boundaries, but the classics—backed by practical experience and modern improvements—deserve their spot in the toolkit.

    That’s why this compound keeps showing up in forward-thinking labs, bridging the gap between tradition and tomorrow’s possibilities. For those lucky enough to have worked with it, there’s a lot to recommend to the next generation of chemists, designers, and builders shaping the world from the atomic level up.