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2(5H)-Furanone

    • Product Name 2(5H)-Furanone
    • Alias gamma-Crotonolactone
    • Einecs 207-086-1
    • 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

    270150

    Chemical Name 2(5H)-Furanone
    Molecular Formula C4H4O2
    Molar Mass 84.07 g/mol
    Cas Number 497-23-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 84-85 °C (18 mmHg)
    Melting Point 4 °C
    Density 1.163 g/cm3 at 20 °C
    Solubility In Water Miscible
    Smiles O=C1CC=CO1

    As an accredited 2(5H)-Furanone 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 100g of 2(5H)-Furanone, sealed with a screw cap and labeled with hazard and handling information.
    Shipping 2(5H)-Furanone is shipped in tightly sealed containers under cool, dry conditions, away from heat and ignition sources. Proper chemical labeling, protective packaging, and compliance with national and international transport regulations (such as DOT, IATA, IMDG) are ensured. It is typically shipped as a hazardous material due to its chemical properties.
    Storage 2(5H)-Furanone 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 oxidizing agents. Protect it from moisture and direct sunlight. Proper labeling and secure shelving are important to prevent leaks, spills, or accidental exposure. Store in accordance with local regulations and chemical safety guidelines.
    Application of 2(5H)-Furanone

    Applications of 2(5H)-Furanone in Industrial Manufacturing

    As a direct manufacturer of 2(5H)-Furanone, we supply this intermediate-grade chemical for targeted industrial applications where precision in formulation and compliance with global standards are critical. Our customers incorporate 2(5H)-Furanone into their processes for specialty syntheses in the pharmaceutical, agrochemical, fine chemicals, polymer, and flavor & fragrance sectors. Below we outline the main validated use cases with their technical requirements and regulatory frameworks.

    1. Pharmaceutical Intermediate Synthesis

    2(5H)-Furanone serves as a reactive intermediate in the synthesis of various active pharmaceutical ingredients (APIs), particularly in heterocyclic compound scaffolds for anti-infective and anticancer medicines. Reaction efficiency, purity control, and residual solvent management remain top priorities in GMP-regulated API manufacturing. Our customers typically introduce 2(5H)-Furanone during key cyclization or condensation steps, enabling efficient ring construction and high-yield transformations.

    Industry compliance standards

    • ICH Q7 GMP for active pharmaceutical ingredients
    • European Pharmacopoeia (Ph. Eur.) guidelines for impurities and residual solvents
    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals)
    • Chinese Pharmacopoeia (ChP) for process intermediates

    Typical usage ratio

    • 5% to 25% of molar equivalents in target step, adjusted by API design and yield targets

    Downstream process integration

    • Employed at the cyclization/coupling step in heterocycle assembly
    • Added as a charge to jacketed glass-lined or stainless reactors under nitrogen purge
    • Followed by work-up, isolation, and downstream purification processes

    Final product types

    • Cephalosporin antibiotic intermediates
    • Fluoroquinolone precursors
    • Anti-tumor drug API precursors
    • Intermediate stock for contract synthesis

    2. Agrochemical Synthesis

    Major agrochemical manufacturers utilize 2(5H)-Furanone for crafting biologically active lactone structures, which are key building blocks in the synthesis of plant growth regulators and insect pheromone analogues. The chemical’s reactivity profile allows controlled, high-selectivity coupling and ring-modification steps vital for pesticide actives. Industry protocols require careful solvent recovery and impurity profiling within the process chain.

    Industry compliance standards

    • ISO 9001 quality management for agrochemical production
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • REACH registration for new agrochemical intermediates in Europe
    • China Pesticide Registration (ICAMA)

    Typical usage ratio

    • 3% to 18% by process batch mass; varies with target structure complexity and area of application

    Downstream process integration

    • Added post-initial fermentation or intermediate isolation for synthetic modification
    • Reacted in batch or continuous systems under tightly controlled temperature and pH
    • Feeds into downstream purification and crystallization units

    Final product types

    • Insect attractant active compounds
    • Lactonic herbicide precursors
    • Plant growth regulator intermediates
    • Pheromone-based pest control actives

    3. Fine Chemicals and Specialty Additives

    In advanced fine chemical manufacturing, 2(5H)-Furanone plays an important role as a monomer precursor and reactive modifier in the creation of high-performance specialty additives. Customers use it to introduce furan-based ring systems where controlled reactivity and select functionalization are key. Applications range from corrosion inhibitor synthesis to photoinitiator intermediates for specialty polymers, demanding strict traceability and quality documentation under ISO frameworks.

    Industry compliance standards

    • ISO 9001 for chemical production and QMS traceability
    • Responsible Care® Management Systems
    • Local chemical safety regulations (e.g., TSCA for US)
    • Specific contractual QC protocols as per end-user requirements

    Typical usage ratio

    • 2% to 12% in additive formulation weight; adjusted for target molecule properties, molecular weight, and performance profile

    Downstream process integration

    • Introduced in stirred-tank reactors for targeted condensation or functionalization reactions
    • Fed into closed systems to limit volatilization and control humidity
    • Integrated with liquid dosing modules in automated blending apparatus

    Final product types

    • Corrosion inhibitor additive intermediates
    • Specialty plasticizer precursors
    • Photoinitiator building blocks
    • Custom-designed fine chemicals

    4. Polymerization Initiators and Functional Monomers

    Manufacturers of advanced polymer materials use 2(5H)-Furanone as both a functional comonomer and an initiator for controlled polymerization processes, especially in the production of specialty polyesters, degradable copolymers, and biomedical hydrogels. Reactivity and stability integration into polymer backbones allow for tunable mechanical and degradation profiles as demanded in regulated end-use sectors, including packaging and medical device components.

    Industry compliance standards

    • EN ISO 13485 for medical device polymer manufacturing
    • FDA 21 CFR 177.1630 for indirect food contact polymers
    • EU Regulation No 10/2011 on plastic materials in contact with food
    • ISO 9001 for general polymer production

    Typical usage ratio

    • 0.5% to 10% of total monomer feed; optimized for targeted copolymer ratio and end-use performance

    Downstream process integration

    • Dosed as part of the monomer blend prior to polymerization reaction initiation (ring-opening or free radical)
    • Controlled addition to batch/autoclave reactors, with in-line viscosity and conversion monitoring
    • Residual monitoring via GC for release certification

    Final product types

    • Biodegradable polyester copolymers
    • Functionalized hydrogel precursors
    • Specialty medical-grade materials
    • Performance resin building blocks for coatings

    5. Flavors and Fragrances Manufacturing

    Within the flavors and fragrances sector, specialists use food-grade 2(5H)-Furanone (when produced to FSSC 22000 or equivalent) for creation of creamy, caramel, and fruity notes in natural-identical aroma compounds. The compound undergoes further derivatization and blending in controlled batch reactors. Manufacturers strictly observe flavor purity, allergen labeling, and residual solvent controls in accordance with global food ingredient codes.

    Industry compliance standards

    • FEMA GRAS listing for flavor materials
    • EU Regulation (EC) No 1334/2008 on flavorings
    • US FDA 21 CFR 172.515 for flavoring agents
    • ISO 22000 or FSSC 22000 food safety system certification

    Typical usage ratio

    • 0.01% to 0.5% in concentrated flavor bases; subject to local flavor profiles and regulatory maximums

    Downstream process integration

    • Dosed into batch reactors for esterification or lactone formation
    • Blended with carrier solvents during aroma compound finishing
    • Quality verified by GC-MS and sensory panel evaluation

    Final product types

    • Creamy caramel flavor bases
    • Natural-identical fruit aroma compounds
    • Bakery and confectionery flavor emulsions
    • Dairy and beverage fragrance enhancers
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    Certification & Compliance
    More Introduction

    Introducing 2(5H)-Furanone: Versatility and Precision in Chemical Manufacturing

    What Sets 2(5H)-Furanone Apart?

    Working in fine chemical manufacturing for over a decade, I have seen firsthand how one compound can fundamentally change the performance and outcome of a process. 2(5H)-Furanone appears deceptively simple, yet offers a unique lactone scaffold with a reactive double bond that makes it remarkably useful across several downstream applications. In the lab and the plant, people often ask what makes it different from other furanones or lactones found in the market. The answer comes down to its structure and the way it interacts during synthesis or modification reactions.

    From the synthetic bench to pilot plant scale, 2(5H)-Furanone stands out due to its balance of stability and reactivity. A five-membered unsaturated lactone can serve as a backbone for many other molecules. Cyclic esters like this one give process chemists a chance to design targeted transformations, using its conjugated system to attach substituents or carry out ring-opening reactions. Furanone-based synthons play central roles in pharmaceuticals and agrochemicals, contributing significantly to both industries’ innovation.

    Understanding 2(5H)-Furanone: Model, Specifications, and Characteristics

    We produce 2(5H)-Furanone to a high purity — typically upwards of 99 percent. Its molecular formula is C4H4O2, offering a concise structure that minimizes byproduct formation in many synthesis routes. Our product is a colorless to pale yellow liquid at standard conditions, with a boiling point around 210°C. Specific gravity rests close to 1.15, and it provides a piercingly sweet, hay-like odor, which chemists recognize almost instantly once the bottle is open.

    Our internal QC protocols screen for isomeric impurities and trace contaminants that could hinder downstream applications. Careful distillation and stringent controls keep our furanone pure and reliable for both research and commercial-scale demands. Chemists choose our 2(5H)-Furanone because it delivers consistent analytical profiles, minimizing surprises during analytical testing or reaction scale-up.

    Linking Structure to Performance

    The value of 2(5H)-Furanone goes well beyond its basic appearance or chemical formula on a paper. This molecule contains an α,β-unsaturated carbonyl, which gives plenty of flexibility. In solid-state or solution processes, Michael addition and nucleophilic attack proceed cleanly, which allows researchers to quickly build out more complex intermediates. The way the double bond is placed next to the lactone ring increases its potential reactivity without introducing excessive instability.

    Every batch we run highlights this balance. Whether synthesizing a fragrance precursor or functionalizing agrochemical scaffolds, identical conditions applied to a well-prepared 2(5H)-Furanone nearly always lead to high-yield transformations. Unlike some isomeric forms, such as 3(2H)-furanone, which has altered reactivity due to the position of its carbonyl and double bond, this compound acts predictably in standard organic synthesis, which saves both time and budget.

    Industry Adoption: Practical Applications

    2(5H)-Furanone has become a keystone intermediate in pharmaceutical R&D. Medicinal chemists pursue this molecule for library generation and as a building block for drugs targeting infectious and chronic diseases. Sulfonamides, macrolide analogues, and certain antiviral agents often draw on its ability to introduce unsaturation in fully functionalized rings. Biologically active natural products that originated in plants and marine organisms very often feature the furanone core, so access to a consistent industrial supply opens up a wide spectrum of synthetic possibilities.

    Agrochemicals require high-purity intermediates just like the drug industry. Our product helps synthesize herbicidal and insecticidal scaffolds, sometimes directly anchoring key substituent groups that impart selectivity and potency to the final active ingredient. As an additive, the lactone structure contributes to controlled-release formulations or modulates volatility for foliar-applied chemicals.

    While other lactones get used in polymer chemistry, we have noticed 2(5H)-Furanone providing clear benefits in certain specialty plastics and biodegradable films. Polymer scientists value the conjugated system’s ability to not only enhance polymerization but also tailor-degradation profiles in eco-sensitive materials. The predictable reactivity and purity of our product simplifies QA in scale-up and meets the specifications global brands look for in a sustainable supply chain.

    The Unique Experience from the Manufacturer’s Perspective

    Living inside manufacturing every day, we constantly face real-world challenges that don’t just show up in textbooks or on specs sheets. Take, for example, the trend in market demand cycles. Research institutes drive small batch orders, while global pharmaceutical players request tonnage customization, each with unique requirements for water content, isomer contamination, or even packaging. It is one thing to make a kilogram for a chemistry department; it is something else entirely to maintain safety, yield, and quality for multi-ton bulk shipments.

    Experienced operators handle the distillation columns, solvent recoveries, and reaction containment as procedures that must remain vigilant to the compound’s unique volatility and hygroscopic properties. High-purity streams don’t just appear from a single run; we double check at every step, with on-site gas chromatography and infrared analysis to verify each specification before containers leave the plant. Over years, we found that investment in digital temperature controllers and in-line moisture analyzers paid for itself in fewer rejected shipments and tighter downstream processing for our clients.

    Handling and storage pose their challenges; purity drops if exposed too long to ambient humidity or left unsealed after sampling. We established protocols centered on pre-measured single-use ampoules for R&D and nitrogen-blanketed drums for plant-scale orders, further extending shelf life. In this respect, 2(5H)-Furanone doesn’t behave like heavier, less sensitive lactone cousins. Knowledge gained through daily plant management shapes how we instruct customers on storage, which helps them avoid headaches on their end, especially when preparing delayed portion runs or doing parallel synthesis.

    Comparing 2(5H)-Furanone with Similar Molecules

    Over the years, several alternatives to 2(5H)-Furanone crossed our reactors, such as γ-butyrolactone, δ-valerolactone, and isomeric furanones. All provide their own set of reactivities and side-effect profiles. We noticed that γ-butyrolactone, now tightly controlled in many jurisdictions, cannot match the unsaturation of 2(5H)-Furanone for the introduction of specific double bonds in a target molecule, nor can it support stable enamines or Michael donor-acceptor interactions with quite the same finesse.

    Differences become obvious when running side-by-side trials for certain synthesis sequences. Customers seeking easy hydrolysis and low odorous impact typically shift to more saturated lactones, but those aiming for late-stage functionalization and nucleophile acceptor sites consistently end up choosing 2(5H)-Furanone. Other furanones, such as 3(2H)-furanone, have altered electron distributions, leading to side reactions or less predictable yields under identical reaction settings.

    Some new users approach us after failed scale-ups with substituted cyclic ketones or with lactones that lack the necessary α,β-unsaturation. They encounter problems—low conversion, unexpected hydration, impurity formation, or unpredictable olfactory properties in fragrance work. By recommending a shift to 2(5H)-Furanone, many such bottlenecks dissolve, since the structure enables not only cleaner synthesis but also easier post-reaction separation.

    Supporting Innovation Through Reliable Chemistry

    Demand from companies developing greener technologies continues to grow. We pay attention to sustainability in our manufacturing routes, sourcing feedstocks from renewable origins where feasible and capturing or recycling waste streams. More dynamic companies are now pursuing furanone derivatives prepared using biocatalytic processes or coupling routes that minimize hazardous reagents. Large-scale chemistries rarely adapt at the pace of new lab discoveries, but our technical team monitors developments, aiming for upgrades that foster both safety and environmental stewardship while maintaining or boosting product yield.

    Many established pharmaceutical and agrochemical products on today’s market rely on derivatives formed from this backbone. Some fermentation-based production processes can access similar structures, but the precision, speed, and consistency we provide with a well-controlled synthetic process means supply bottlenecks rarely occur. As an OEM supplier, our objective is to keep the quality parameters fixed, the documentation transparent, and the application possibilities broad, whether our customer base comprises university researchers, multinational conglomerates, or mid-sized formulation firms.

    Enhancing Process Chemistry and Downstream Flexibility

    The greatest value of 2(5H)-Furanone as a starting material comes from its reactivity in the hands of a capable process chemist. Nucleophilic additions introduce diverse functional groups and create possibilities in heterocycle construction. In polymer applications, block copolymerization proceeds smoothly with well-matched comonomers. Formulators appreciate how well it dissolves in common solvents, reducing the need for exotic handling protocols or costly process modifications.

    We see the technical results in action: higher throughput, reduced impurity profiles, enhanced shelf life of downstream products, and easier analytical monitoring. For flavors and fragrances, adding the furanone moiety sparks sought-after notes and extends the olfactory footprint of the blend. Case studies sent to us by clients regularly mention a move away from more simplistic esters or overly aggressive oxidants—citing improved reproducibility and environmental compatibility as key drivers.

    Early on, some newcomers struggled with its potential for side reactions, especially in non-inert environments or with certain mineral acids. We now work directly with technical partners to advise on compatible reagents, suggesting minor adjustments to process pH, or adding inert gas blanket steps during open transfers. This type of hands-on support is the kind only a true manufacturer can offer because our engineers and chemists have worked directly with and around the material for years in real plants.

    Quality, Testing, and Analytical Transparency

    Purity and performance drive every batch we dispatch. Across each production cycle, we sample for water content, color, residual solvent, and acid value. Our analytics group double-checks each result against established limits published in pharmacopoeial and industrial chemical monographs. Long-term experience taught us that less scrupulous sourcing can lead to product with faint haze or marginally off-color that changes final formulation properties in sensitive applications such as injectable drugs or clear polymer blends.

    Each certificate of analysis is more than a mere formality; it details actual measurements, with supporting chromatograms and IR spectra available for review. Clients in high-risk sectors ask about traceability, and we keep detailed batch records and raw material logs to provide confidence not just in the product, but in the documentation chain supporting it.

    Challenges and Solutions in Real-World Production

    One of the greatest production challenges revolves around scale. Small bench or kilo-lab runs can tolerate small contamination or yield drops. Commercial lots produced for continuous plant operations, on the other hand, must avoid cumulative byproduct formation which could clog distillation lines or foul condenser surfaces. We continuously invest in cleaning in place systems, automated valve control, and regular staff retraining to keep quality on track without excessive downtime.

    Regulatory concerns, especially regarding solvent choice and waste disposal, have pushed updates in both our internal protocols and external reporting. Some regions demand proof of minimal environmental impact before import is allowed. Our compliance team works alongside production management to anticipate such shifts, aligning supply logistics with up-to-date documentation and responding swiftly to new requirements.

    Customer Success With 2(5H)-Furanone

    Feedback from long-time partners drives our improvements. Laboratories aiming to prepare new lead molecules in anti-infective research describe increased throughput, as the reliable supply lets them run dozens of parallel experiments without interruption or the need for excessive purification. Fragrance developers mention the subtle but lasting effect the furanone skeleton imparts, moving away from older synthetic musk chemistries that increasingly face regulatory restrictions.

    Agrochemical producers operating pilot plants report shorter refinement cycles and fewer batch failures, especially during adjustments to world supply chains or regional regulatory changes. These companies value both the technical support and continuity of supply. Early warning of potential disruptions, coupled with real attention to customized packaging or transport solutions, has helped several avoid costly shutdowns in their own manufacturing schedules.

    Future Developments and Industry Outlook

    The chemical industry faces pressure to move toward greener production and reduce dependency on petroleum sources. We participate in pilot-scale efforts to harness bio-based precursors and streamline our waste management. Market research points to continued growth in demand for lactone intermediates, especially as specialty polymers and innovative pharmaceuticals gain traction worldwide. Our ongoing R&D efforts aim to expand functional group compatibility, improve reactor recycling efficiency, and explore catalyst systems that further curb effluent and energy use.

    2(5H)-Furanone represents more than a simple raw material. It embodies the convergence of practicality, predictability, and creative chemistry. Our decades of production experience, continuous technology upgrades, and commitment to end-user satisfaction set apart what we make from distant, repackaged supplies. We look forward to supporting future discoveries—one batch at a time—by maintaining the reliability and integrity customers have come to expect from direct manufacturers.