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HS Code |
472508 |
| Cas Number | 488-15-3 |
| Iupac Name | 1,2-di(furan-2-yl)-2-hydroxyethanone |
| Molecular Formula | C10H8O4 |
| Molar Mass | 192.17 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 141-143 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.36 g/cm³ (approximate) |
| Pubchem Cid | 10226 |
As an accredited 2,2'-Furoin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram sample of 2,2'-Furoin is packaged in an amber glass bottle with a screw cap and safety label. |
| Shipping | 2,2'-Furoin is typically shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. The packaging complies with safety regulations for laboratory chemicals. During transit, it is protected from extreme temperatures and physical damage. Appropriate hazard labeling and documentation accompany the shipment to ensure safe and compliant handling throughout delivery. |
| Storage | 2,2'-Furoin should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, protected from direct sunlight. Ensure proper labeling and handle with care to avoid inhalation or skin contact. Store at room temperature and follow all relevant chemical safety guidelines. |
Applications of 2,2'-Furoin in Industrial Manufacturing2,2'-Furoin, as produced in our facilities with strict process control, serves a series of distinct functions in specialized downstream industrial sectors. The following application scenarios outline how this intermediate enables targeted formulation, meets sector-specific regulations, and integrates into critical stages of manufacturing workflows. This section details the practical standards, incorporation ratios, placement in established processes, and finished goods relevant to each sector we supply. 1. Pharmaceutical Intermediates for API SynthesisPharmaceutical manufacturers employ 2,2'-Furoin as a building block in multi-step synthesis routes, especially for certain furan-derivative APIs where carbonyl coupling is required. Its defined purity supports batch consistency and regulatory documentation during cGMP operations, especially for advanced intermediates in heterocyclic drug development. Industry compliance standards
Typical usage ratio
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2. Organic Electronic Materials ProductionIn the organic electronics sector, 2,2'-Furoin acts as a functionalized precursor for developing π-conjugated molecular frameworks. It enables tailored furan-based materials with advanced electron mobility and thermal properties, which are vital in organic semiconductors and optoelectronic layers. Its performance consistency is critical for reproducible device manufacturing. Industry compliance standards
Typical usage ratio
Downstream process integration
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3. Fine Chemical Synthesis for Agrochemical ActivesProducers of fine agrochemicals rely on 2,2'-Furoin to introduce furan rings into novel pesticide or herbicide scaffolds. Its well-defined structure guarantees predictable stepwise synthesis, which is necessary for the high purity demanded in downstream agrochemical active substances. Industry compliance standards
Typical usage ratio
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4. Specialty Polymer Additive ManufactureManufacturers process 2,2'-Furoin within advanced polymer additive synthesis to enhance flexibility, thermal control, or UV stability in final engineering polymers. Its bifunctional structure allows for cross-linking chemistry, contributing to the tailored mechanical properties required in high-performance resins. Industry compliance standards
Typical usage ratio
Downstream process integration
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Competitive 2,2'-Furoin prices that fit your budget—flexible terms and customized quotes for every order.
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At our facility, every batch of 2,2'-Furoin passes through a carefully managed synthesis and purification process. This isn't just about delivering a product by its chemical formula—C10H8O4—it’s about meeting the real-world needs of the chemists, engineers, and formulation specialists who rely on tightly controlled quality. We’ve run countless lots through our reactors, refining conditions over the years to keep impurities at bay and batch-to-batch variability in check.
2,2'-Furoin, also known as 1,2-Di(2-furyl)-2-hydroxyethanone, stands out among aromatic hydroxy ketones because of its unique furan core structure. This brings a blend of chemical stability and reactivity prized by those who convert intermediates into high-value pharmaceuticals, advanced materials, or complex specialty chemicals. Unlike its close cousin benzoin, where two benzene rings encase the central hydroxyketone, the furan rings in furoin give the molecule added solubility in polar organic solvents, and the oxygen heterocycles bring subtle but important differences in how it participates in condensation, polymerization, or further functionalization.
Our experience with 2,2'-Furoin dates back to when small-batch runs in glassware served only a handful of customers looking for grams to test a reaction route. Scaling up production meant addressing safety and purity challenges specific to furan compounds. Each run involves controlled temperature ramping and continuous monitoring to avoid side reactions that could generate colored byproducts or impact downstream performance. The difference between a clear, off-white crystalline solid and a faintly tinted material reveals a lot about reaction control—something we’ve learned matters for both analytical reproducibility and large-volume needs.
Applications for 2,2'-Furoin often demand reproducible melting points, high HPLC purity, and consistent particle size. We typically supply material at a minimum of 98% purity, with the most demanding customers calling for 99%+ verified by both HPLC and NMR. While some laboratories can tolerate a few percent of furaldehyde or unreacted acetoin, pilot plant and production sites push us for tighter controls. Our experienced team works directly with chemists at customer sites, comparing chromatograms and spectra and troubleshooting issues ranging from solubility to crystallization.
2,2'-Furoin has earned a steady place in organic synthesis as an acyloin condensation product useful for constructing heterocyclic frameworks and as a critical building block for specialty resins. End users reach out each year with new projects: designing ligands for asymmetric catalysis, exploring polymer precursors, or incorporating furan content into organic electronics.
Unlike commodity chemicals, furoin’s market size isn’t defined by price wars, but by reliability and fitness-for-use. We’ve supported teams working on furan-based macrocycles, who required low residual solvents—especially limiting trace water and alcohols—to avoid interfering with catalyst systems. Researchers working in dye chemistry focus on color metrics and request samples for spectral testing before scaling up. Even small deviations in impurity profiles can show up in these specialized applications, so we invest heavily in both analytical capacity and feedback loops between production and QA.
Whether a customer asks for a 25 kg drum or a single 100-gram jar, our job is to think through how each process step—from crystallization to drying to packaging—can influence the final product. For furoin, trace metallic impurities can influence downstream reactions, making the source and quality of catalysts a constant topic of interest in our process engineering meetings. On each batch, tracking residuals like acids and volatiles is not just a box to tick, but a necessity that supports high-yield syntheses in pharmaceutical and research labs.
Solid-state purity and the way the crystals form can impact handling and dosing accuracy. Early on, we noticed that slow cooling could yield larger, more manageable crystals, while fast quench leads to finer, less flowable powder. Feedback from production chemists has helped us fine-tune crystallization profiles to reduce static and sticking, which in turn supports easy transfer and reliable weighing—an overlooked challenge until you see a technician fighting with persistent clumps. We rely on this practical, problem-solving approach rather than automated controls alone.
Documented specifications like melting point range and residue on ignition tell one part of the story. The other part comes from real-world testing, such as solubility trials in DMSO, acetonitrile, and other process solvents. We check particle size distribution because it affects packing in preparation vessels and influences how quickly the furoin dissolves during charge-in. Analytical standards have drifted over time—not because industry wants weaker material, but because each new application demands tighter, cleaner, and more traceable inputs.
Recent inquiries have centered on trace metal analysis and more rigorous identification by LC-MS and NMR. For some projects, furoin must meet food-grade standards, free from specific allergens or banned solvents—a separate and more demanding production line. We respond by maintaining full traceability on our raw materials and capturing full batch histories, down to which reactor produced each lot. This hands-on approach to record-keeping earns trust from those navigating regulatory audits or qualification for clinical supply chains.
More than once, customers ask us, “Why choose 2,2'-Furoin over benzoin, or over simple furan derivatives?” That comes down to the interplay between structure and reactivity. The twin furan rings set furoin apart, giving distinct electronic and steric environments. This can influence the reaction kinetics in downstream uses—furan rings participate more readily in cross-coupling reactions, and the oxygens can stabilize intermediates differently compared to benzene analogues.
Pairing furoin with traditional cross-linkers often results in materials with better thermal properties or increased flexibility, thanks to the inherent reactivity at the alpha position of the furan. Where benzoin’s aromaticity gives it a certain inertness, furoin remains accessible for functionalization, especially in applications seeking more environmentally friendly or biodegradable outcomes. In some synthesis streams, attempts to swap in benzoin end in lower yields or persistent side-products, proving that not all acyloin structures fit every task.
Each year, we field requests for documentation about environmental profile—questions like whether our furoin meets ISO or regional sustainability standards, or if our process generates non-recyclable waste. We designed our process to minimize organic solvent usage, recapture furfural byproducts, and return usable water to the plant. Feedback from multinational partners drove changes to our waste stream controls, which now track volatile organics and solvent discharge at each production stage.
Feedback from users on furoin’s environmental persistence keeps us alert to routes for greener synthesis. Chemists working in green chemistry ask for data like acute aquatic toxicity or biodegradable packaging options. While furoin’s furan rings make it more biodegradable than many aromatic compounds, safety practices like closed transfers and strict PPE in our plant support the highest standards for worker and community health.
Controlling quality for 2,2'-Furoin means balancing analytical rigor with production feasibility. We put every lot through GC, HPLC, and NMR testing, with titrations on moisture content and checks for residual process solvents. Field feedback taught us not to rely solely on specification sheets. Material with perfect numbers can behave unpredictably if storage conditions drift or shipment delays push up moisture pickup, so we include customer stability trials in our QC review.
Besides analytical tests, we run process suitability checks—dissolving samples in typical formulation solvents, stress-testing samples at elevated humidity, and monitoring color change under UV exposure. These real-life tests can uncover small material changes that go unnoticed by instruments; chemists have caught subtle yellowing or a faint odor shift indicating a byproduct or oxidation. Tuning our drying cycles and storage protocols reduces these risks, especially for customers scaling up to hundred-kilogram lots.
Shipping furoin safely and economically wastes less material and keeps our customers’ processes running. Over the years, too many stories of bent drums or leaky bags have prompted us to phase out old-style packagings. Most material leaves our plant in double-lined, chemical-resistant containers designed for stackable, moisture-proof storage. This keeps handling at customer sites straightforward. Customers working with high-purity lots often request smaller, resealable jars to limit air exposure and cross-contamination.
Feedback on transport reliability shapes our choices, too. We keep stock on hand for fast turnaround, and our shipping team checks weather and transit times to avoid supply gaps. These details matter for research and production managers racing against tight deadlines. We also support temperature monitoring for long-haul cargo, an adjustment we made after customer feedback on seasonal transport challenges.
Supporting users means more than sending out a COA or technical datasheet. Our technical team brings hands-on chemical manufacturing experience to trouble-shooting requests, from advising on solvent selection for furoin dissolution to comparing impurity profiles when transitioning between suppliers. We answer the phone, walk through chromatographic data, and help optimize reaction protocols. This personal, experienced support is something our customers value, especially when compounding yields appear to slip or unexpected reactivity arises in scale-up.
Chemists in production facilities have called with concerns about batch color—experience taught us that even slight color shifts can signal new impurity formation, pointing to a subtle shift in process conditions. Over time, we refined both our monitoring and process controls to respond proactively. The aim is not just to fix problems, but to partner with customers as they develop new products that push the boundaries of furoin’s chemistry.
The world of specialty chemicals doesn’t stand still. New uses for 2,2'-Furoin continue to emerge, from advanced resin intermediates to bio-derived polymer building blocks. As patent landscapes and regulatory structures evolve, we monitor changes and invest in process upgrades to meet new requirements. Our participation in industry collaborations and technical societies helps us keep an eye on evolving customer needs and process safety alerts.
A clear trend is the need for ever-lower impurity levels and more reliable supply chains. Customers involved in GMP-regulated production have raised the bar for traceability and documentation. In response, we upgraded batch-control systems and expanded our in-house analytics. As synthetic targets grow more complex, our team tracks requests for custom grades—sometimes ultra-high-purity, sometimes with tailored physical properties—to help innovators bring new therapies and materials to market.
Among acyloin derivatives, 2,2'-Furoin carries its weight by striking a balance between reactivity, processability, and cost. Process chemists pick it over simple furans when a stable hydroxyketone group is needed for follow-on chemistry. Medicinal chemists value its ability to build more complex, functionalized rings. In electronics R&D, the unique electron-rich furan rings offer pathways to new classes of conductive or optically active polymers. We supply pilot-scale material to research teams exploring these applications, sharing our experience navigating the quirks of furan chemistry—like moisture sensitivity and reactivity with strong acids.
Long-term partnerships with R&D teams inform how we tweak production and packaging. Many of today’s custom requirements trace back to one-off requests from research groups that have since set industry standards. The importance of close collaboration and real-time feedback can’t be overstated. Our on-site chemists know the common stumbling blocks—such as batch crystallization failures, variable dissolution rates, or surprise resonance signals in NMR—and we bake those lessons into our processes.
Global supply chains have become less predictable. We put extra effort into qualifying alternate raw material sources, maintaining stock buffers, and coordinating logistics to reduce risk of supply interruption. Our long-term customers appreciate direct access to the production team—eliminating layers of middlemen means faster responses and greater flexibility if something in their supply chain shifts. Control over production timing, batch sizes, and packaging all help address cyclical demand or sudden changes in project timelines.
In response to feedback from process managers, we introduced regular supply updates and rolling forecasts to keep customers informed. This gives them a real sense of how much material they can expect, with transparency about any shifts due to raw material supply or transport. Supply reliability isn’t just about having material on the shelf—it comes from a responsive, knowledgeable manufacturing team that understands and anticipates downstream needs.
At the end of the day, manufacturing 2,2'-Furoin means more than producing to a spec. It means backing up every shipment with the knowledge and support honed over years of hands-on production, collaborative troubleshooting, and adapting processes to fit unique challenges. Whether a project depends on hundred-kilogram lots or just a few specialized vials for a clinical study, we invest in knowing what matters to our customers, tuning both product and support to match.
We believe that our close communication, practical problem-solving, and willingness to adapt—shaped by years of manufacturing and supporting users—make the difference between just supplying a chemical and building trust as a true manufacturing partner. 2,2'-Furoin isn’t just another product in our catalog; it’s a material we stake our reputation on, with every batch sent out backed by experience and a clear understanding of what users in the lab, the pilot plant, and full-scale production actually need.