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HS Code |
158157 |
| Cas Number | 614-07-1 |
| Molecular Formula | C7H8O2 |
| Molecular Weight | 124.14 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Caramel-like, sweet |
| Boiling Point | 190-193°C |
| Melting Point | -13°C |
| Density | 1.08 g/cm³ at 20°C |
| Refractive Index | 1.537 |
| Flash Point | 85°C (185°F) |
| Solubility In Water | Slightly soluble |
| Vapor Pressure | 0.2 mmHg at 20°C |
| Purity | Typically ≥98% |
| Synonyms | 5-Ethylfurfural, 2-Furancarboxaldehyde, 5-ethyl- |
| Un Number | 2810 |
As an accredited 5-Ethyl-2-Furaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Brown glass bottle containing 100 mL of 5-Ethyl-2-Furaldehyde, tightly sealed, labeled with hazard warnings and chemical identification. |
| Shipping | 5-Ethyl-2-Furaldehyde should be shipped in tightly sealed containers, protected from light and moisture. Handle with care, following safety regulations for flammable liquids. Transport must comply with local and international regulations, including appropriate hazard labeling and documentation to ensure safe delivery and spill prevention during transit. |
| Storage | 5-Ethyl-2-Furaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Keep it away from strong oxidizing agents and sources of ignition. Store at room temperature, protected from direct sunlight, and avoid moisture. Clearly label the container and follow all relevant chemical safety regulations. |
Applications of 5-Ethyl-2-Furaldehyde in Industrial ManufacturingAs a direct manufacturer of 5-Ethyl-2-Furaldehyde, we supply this high-purity specialty aldehyde to end users across multiple industrial sectors. Its unique chemical profile supports efficient downstream production of aroma chemicals, pharmaceutical intermediates, resin modifiers, and fine chemical ingredients, each governed by specific industry standards and processing protocols. Below, we detail real-world downstream application scenarios, including precise compliance, integration, and end use requirements from major manufacturing partners and regulators. 1. Flavor and Fragrance Ingredient Formulation5-Ethyl-2-Furaldehyde is a key aldehydic note in the compounding of high-impact flavor bases and specialty fragrance accords. Its furan core and ethyl substituent deliver a distinctive nutty-grain character required in premium flavor/aromatic ingredients for food, beverage, and perfumery. Downstream manufacturers use tight formulation controls to align with international food safety and fragrance material regulations. Industry compliance standards
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2. Pharmaceutical Intermediate SynthesisThis material serves as a pivotal intermediate in the multi-step synthesis of certain heterocyclic and furan-based pharmaceutical compounds—including active pharmaceutical ingredients (APIs) and advanced intermediates. Process control and material traceability are enforced in compliance with regional and international pharmacopeias to ensure active ingredient quality and batch reproducibility. Industry compliance standards
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3. Polyester and Phenolic Resin Modification5-Ethyl-2-Furaldehyde finds critical use as a reactive chain-branching or crosslinking agent in the production of high-performance polyesters and phenolic resins, where its furan ring structure enhances thermal stability, mechanical strength, and chemical resistance. Resin formulators in coatings, adhesives, and composites rely on this additive to fine-tune rheology and end-use durability, under rigorous materials certification protocols. Industry compliance standards
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4. Fine Chemical Synthesis: Agrochemical Building BlocksThis specialty aldehyde acts as a selective synthon in the production of various agrochemical intermediates, especially in constructing furan-based herbicide and fungicide scaffolds. Agrochemical formulators apply precise reaction monitoring and satisfy sector-specific product stewardship guidelines throughout the multi-stage synthesis and scale-up processes. Industry compliance standards
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5. Specialty Chemical Intermediates in Electronic Material ManufacturingDownstream electronic materials manufacturers specify 5-Ethyl-2-Furaldehyde for its role in synthesizing furan-derived specialty chemicals applied in photoresist additives, conductor pastes, and dielectric polymers. Batch and continuous processes require strict input purity control and documentation per electronics quality protocols to ensure consistent material performance and traceability. Industry compliance standards
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From a chemist’s perspective on the factory floor, 5-Ethyl-2-Furaldehyde doesn’t just fill a slot on a product listing; it brings specific advantages into processes that require precise, stable, and character-driven aldehyde chemistry. Over the years, demand has grown for this compound both as a flavor precursor and as a building block in specialized syntheses. Decades of hands-on production experience reveal what sets it apart, especially when compared to more common furfural derivatives.
At the bench and in downstream applications, the presence of a five-membered furan ring attached to a two-position aldehyde—and further, the ethyl substituent at position 5—represents a structural advantage. It changes the way the molecule reacts, influences volatility, and unlocks new organoleptic profiles as well as industrial performance. Looking beyond text-book descriptions, the actual physical handling of 5-Ethyl-2-Furaldehyde in our plant reflects the care required, the unique aroma signature, and the consistency buyers seek.
Manufacturing 5-Ethyl-2-Furaldehyde starts with pure, carefully selected raw materials. Purity levels consistently exceed 98%, as even tiny impurities disrupt specialty uses, particularly in fragrance and fine chemical synthesis. Strict in-house controls allow us to achieve a clear pale-yellow liquid, with a boiling point that typically falls higher than standard furfural, owing to its ethyl substitution. End-users in perfumery or advanced chemical production recognize the importance of both purity and reproducible physical properties batch after batch.
Unlike simpler aldehydes, 5-Ethyl-2-Furaldehyde demands a careful balance during condensation and isolation. Our plant relies on close temperature monitoring, inert gas protection, and immediate stabilization after synthesis. These measures result in material that carries the distinctive sweet, nutty, and slightly caramelized note that formulators chase—without the off-odors and instability seen with less rigorously produced material. From firsthand experience running tens of metric tons per season, inconsistencies in raw furans or an uncontrolled reaction easily mar final quality, which is why we reject any compromise in feed or equipment maintenance.
Work in the lab and production shows 5-Ethyl-2-Furaldehyde doesn’t just act as a stand-in for related compounds. In flavor and fragrance, it imparts depth and complexity unmatched by furfural or 2-furaldehyde. One drop adds a warm, subtle bread or nutty finish in bakery or confectionery flavors, which cannot be matched by more basic furan derivatives. Perfumers report it brings unusual roundness to gourmand and tobacco notes, its profile surviving even after blending with intense animalic or woody bases. Culinary chemists who test it appreciate the way it holds up under thermal processing, unlike many aldehydes that devolve into bitterness.
Customers in advanced chemistry have taught us how the ethyl group acts as a handle for further transformation. Synthetic routes need control at every step, so a mistake with upstream quality creates headaches down the road. Chemists favor our grades for their clean chromatographic and NMR profiles; we receive direct feedback from partners describing fewer purification steps and higher downstream yields. These details grow from years of technical dialogue and follow-up, not just sending a sample and moving on.
Working directly with 5-Ethyl-2-Furaldehyde reveals much about its nature compared to toluene- or methane-derived aldehydes or even to close cousin 2-furaldehyde. The ethyl group shifts the volatility, lowering the risk of accidental vapor loss during dosing, and also lends more resistance to oxidation than aldehydes lacking this substitution. Our storage tests and long-term shipments show batches remain stable through seasonal temperature changes, provided they stay in tightly sealed nitrogen-blanketed containers.
Many first-time users approach it expecting the same handling quirks as furfural. In practice, the slightly higher boiling point means less aggressive vapor management tools are needed, which saves time and effort on the production line. It doesn’t stain equipment as easily, and fewer circumstances trigger rapid exothermic behavior, so process safety margins are wider.
Over the years, we’ve also recorded feedback from large-scale flavor houses. They report that 5-Ethyl-2-Furaldehyde delivers more consistent performance in baked-good and alcoholic beverage matrices, partly because of this better thermal resistance and reduced volatility. Perfume manufacturers state that their bases maintain more consistent headspace over time, critical for both mass-market and luxury fragrance formulations. The molecular tweak of adding ethyl at the five-position brings both new creative options and valuable process improvements.
Running a chemical factory that produces 5-Ethyl-2-Furaldehyde means more than ferreting out yields. Production hinges on not only synthesizing the core molecule but also controlling byproducts that can quickly spoil downstream value. Aldehydes rank among the most reactive organic groups—moisture, careless temperature spikes, or even the wrong joint material can result in failed batches. Laboring hands-on with the reaction means checking every cooling bath, monitoring distillation rates, and swapping out seals before the slightest yellowish haze or odd odor develops.
By focusing on process optimization over decades, our team cuts out unreacted furan and ensures unwanted acid contaminants never appear in finished lots. We also enforce closed-system transfers within production rooms. Staff training and rigorous SOPs reflect the hazards of aldehyde production; any leaks spell downtime and risk for both plant workers and the outside environment. This responsibility and drive to minimize loss or contamination brings long-term reliability; partners depend on this stability as much as on the chemical itself.
5-Ethyl-2-Furaldehyde continues to win favor in application labs that move from bench to pilot scale. Our partners in research emphasize the molecule’s potential in developing higher-value flavor and fragrance intermediates. Trials replacing standard furfural in bakery, nut, and brown-note flavors consistently report smoother profiles and more appealing finished goods. The ethyl substitution introduces warm, almost buttery undertones without the harsh top notes that sometimes mar comparable furan derivatives. This isn’t theory; we receive direct feedback from developers conducting double-blind taste panels and GC-MS-based aroma tracing.
Process chemists working on advanced syntheses for medical or agrochemical starters note that the ethyl group’s presence at the five-position enables regioselective reactions not possible with unsubstituted furaldehyde. These synthetic advantages have real impact—less time spent on protection/deprotection schemes and cleaner isolation of late-stage intermediates. The stories come through after months of method trials and dozens of kilogram-scale runs, often as follow-up discussions on how to adjust reactivity for the next molecule in the pipeline.
There’s no substitute for seeing the subtle differences in reactivity, aroma, and processability caused by a single ethyl group on a furan ring. 5-Ethyl-2-Furaldehyde illustrates this principle better than most widely used aldehydes. For a production chemist, the benefits begin at the reactor—yield improvements, easier separation, and less fouling—before extending to supply-chain and formulation stages. For a flavor chemist, the naturally occurring nuances that this molecule imparts outshine both furfural and more heavily substituted analogues, offering complexity without the need for masking agents.
These advantages multiply in real-world use. In beverage flavoring, the aldehyde persists during heat treatment and over shelf life, keeping intended notes true even six months after bottling. In fragrance, basic stability under light means brand owners enjoy longer shelf-life and retail appeal. Across the board, both internal testing and customer-provided analyses show that thermal stability, resistance to hydrolysis, and reduced unwanted side-product formation offer a step up from simpler analogues.
Manufacturing and handling any aromatic aldehyde brings environmental challenges. While some in the industry cut corners with open systems, we moved to closed-loop recovery and neutralization years ago. Waste streams are closely managed; spent solvents undergo in-plant recovery, minimizing what leaves for off-site disposal. Our production teams monitor stack and drain samples, with licensed third-party labs providing periodic air and water testing.
Many of our partners require assurance of compliance with regulatory standards in different regions. 5-Ethyl-2-Furaldehyde sits in a complex landscape. Depending on the intended application, it can fall under food additive, fragrance, or specialty chemical oversight. Across each batch, we maintain traceability—every lot documented from entry of raw material and process modification to the final drum. Feedback from auditors and regulatory officers in multiple markets guides the ongoing refinement of our process and paperwork systems.
In response to growing global concern for worker safety, both physical and administrative safeguards remain central. On-site air monitoring, targeted aldehyde detection badges, and hands-on safety training all contribute to lower exposures and fewer lost-time incidents. These practices took years to implement, based on both mandatory and hard-won lessons. Customers, in turn, recognize the difference in stability profiles and the trace-level impurity control that comes from better operator protection and stricter containment.
Supplying a specialty aldehyde like 5-Ethyl-2-Furaldehyde goes beyond logistics. Customers rely on real-time technical support—troubleshooting aroma interactions, answering shelf-life questions, and recommending optimal storage conditions. Over time, these conversations shape improvements in both our chemical and service quality. For instance, clients formulating new blends in alcohol-based products needed help adjusting to the slightly higher boiling point and lower vapor pressure of this aldehyde. Standard protocols written for furfural didn’t solve the sticking points, so our chemists provided direct support and on-site advice to streamline adjustments.
Years of feedback from flavorists and fragrance developers speed up turnaround for batch testing. Our lab replicates common downstream conditions—thermal cycling, UV exposure, formulation with common co-ingredients—and provides data supporting customer QA or regulatory submissions. In one case, a European flavor house found rapid solution to repeated haze formation in a new dessert concentrate after receiving both technical advice and a revised documentation package from our team. It’s this hands-on, rapid-response problem solving that keeps the relationship between chemical manufacturer and end-user dynamic.
Despite its established value, 5-Ethyl-2-Furaldehyde continues to inspire R&D. Both internal teams and partners keep probing for new uses—be it as a precursor for high-performance polymers, components in climate-adaptive flavors, or as a scaffold for catalytic transformation. Successful adoption comes on the back of close collaboration, not one-way transfer. Site visits, joint lab work, and shared pilot trials remain essential.
Because feedstock, market, and regulatory pressures never stand still, ongoing process improvement remains non-negotiable. Recent upgrades include enhanced in-line monitoring for byproduct suppression, reconfigured vent capture to further narrow emissions, and upgraded tank linings to resist mild acidification. Customer-facing improvements keep pace, from digitized lot tracking to expanded shelf-life studies, all reflecting the demands of a more transparent and tightly regulated marketplace. For us, the question is never whether to adapt, but how—driven by chemical reality, external requirements, and above all, feedback from those who use our product.
For all its technical nuances, the real value of 5-Ethyl-2-Furaldehyde lies in the tangible difference it brings to both the lab and the production hall. Our direct experience in making and improving this chemical confirmed long ago that not all aldehydes are created equal. Performance in application, reliability under diverse storage and shipping conditions, and flexibility in synthesis tie back to small but critical tweaks like the ethyl group at position five.
What matters most isn’t a checklist of properties, but the proven, lived-through results on aroma recovery, process safety, and downstream synthesis—outcomes that our teams see play out every working day. Continued application feedback, regulatory dialogue, and commitment to safe and precise manufacturing give shape to the evolving future of 5-Ethyl-2-Furaldehyde, securing its role in high-value, high-integrity chemical production for years to come.