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HS Code |
996713 |
| Cas Number | 69749-29-5 |
| Molecular Formula | C7H14O2 |
| Molecular Weight | 130.18 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 146-148°C |
| Density | 0.96 g/mL at 25°C |
| Refractive Index | n20/D 1.426 |
| Flash Point | 37°C (closed cup) |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
As an accredited 2-(Ethoxymethyl)tetrahydrofuran factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with airtight screw cap, clearly labeled "2-(Ethoxymethyl)tetrahydrofuran," hazard symbols, and lot number. |
| Shipping | 2-(Ethoxymethyl)tetrahydrofuran is shipped in tightly sealed containers, typically under inert gas to prevent moisture and air exposure. It is transported according to standard chemical safety protocols, often as a flammable liquid. Proper labeling, documentation, and compliance with national and international transport regulations are required to ensure safe delivery. |
| Storage | 2-(Ethoxymethyl)tetrahydrofuran should be stored in a tightly sealed container, away from moisture, heat, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, preferably under inert atmosphere if sensitive to air. Store away from oxidizing agents and acids. Proper chemical labeling and secondary containment are recommended to prevent accidental spills or contamination. |
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Purity 99%: 2-(Ethoxymethyl)tetrahydrofuran of purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurity formation. Boiling Point 128°C: 2-(Ethoxymethyl)tetrahydrofuran with a boiling point of 128°C is used in solvent recovery processes, where it provides efficient separation and recyclability. Viscosity 1.25 cP: 2-(Ethoxymethyl)tetrahydrofuran with viscosity 1.25 cP is used in organometallic reactions, where it allows for rapid mixing and homogeneous reaction conditions. Stability up to 80°C: 2-(Ethoxymethyl)tetrahydrofuran with stability up to 80°C is used in high-temperature formulation development, where it maintains chemical integrity and prevents degradation. Water Content <0.1%: 2-(Ethoxymethyl)tetrahydrofuran with water content below 0.1% is used in moisture-sensitive synthesis reactions, where it minimizes hydrolysis of reactants and improves product purity. Density 0.91 g/cm³: 2-(Ethoxymethyl)tetrahydrofuran with density 0.91 g/cm³ is used in polymerization processes, where it ensures consistent reactant dispersion and controlled polymer morphology. Molecular Weight 130.18 g/mol: 2-(Ethoxymethyl)tetrahydrofuran with molecular weight 130.18 g/mol is used in fine chemical production, where it provides predictable reaction stoichiometry and scalability. |
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Looking around today’s chemical labs, it’s easy to see that the steady march of innovation hasn’t slowed. Researchers seek compounds that don’t just fit the bill for reactivity, but bring real structural utility to the table. Among the smart options coming out of recent development is 2-(Ethoxymethyl)tetrahydrofuran, a solvent and building block that has carved out a unique place in organic synthesis, pharmaceutical design, and industrial processes. I’ve watched workflows become more flexible as new cyclic ether derivatives like this one have moved from narrow applications to general adoption, thanks to a combination of stability and selectivity. What sets this compound apart is its simultaneous ease of handling and the extra functionality that the ethoxymethyl group imparts. This is far from just another tetrahydrofuran derivative tossed into the mix for novelty's sake.
The backbone of 2-(Ethoxymethyl)tetrahydrofuran harnesses a classic tetrahydrofuran ring, but it doesn’t stop there. It adds a side-chain—an ethoxymethyl group at the two-position. That extra branch gives chemists fresh handles for modification. Chemicals like this help address persistent issues I’ve seen in selective functionalization. In older reactions, choices felt constrained. With this derivative, a route to regioselective changes opens up, particularly for those aiming at fine tuning pharmacophores. The configuration increases the range of downstream transformations, which is a handy tool for synthetic routes that call for precise tailoring without adding avoidable steps. My own experience handling lab-grade batches points to the reliability of its purity; this helps avoid wildcards that might throw off a reaction’s course.
Anyone who’s juggled reactive compounds can tell you how much a small difference in stability means during scale-up or during routine procedures. 2-(Ethoxymethyl)tetrahydrofuran stands out due to its unlikely resilience for an oxygenated hydrocarbon bearing a side chain. The core ring resists unwanted breakdown under basic or mild acidic conditions. Spills don’t generate stubborn residues. Plus, its low volatility means no headaches from vanishing solvent or tricky containment measures. Many research technicians appreciate the predictability—no sudden decompositions, fewer headaches (literally and figuratively), and less downtime spent on surprise troubleshooting.
A lot of chemicals promise performance, but in day-to-day operations, shortcomings become obvious. In more than one synthetic sequence, 2-(Ethoxymethyl)tetrahydrofuran has held up as an excellent solvent due to its high polarity, allowing unusual solubilization of both hydrophilic and hydrophobic intermediates. Its boiling point sits at a comfortable mid-range, so extra care over heat management isn’t necessary. It flows as a clear, colorless liquid, which simplifies layer identification during workups. Its odor registers as less sharp compared with unsubstituted tetrahydrofuran, a perk for those who spend long hours at the bench. Forward-thinking labs that work at pilot or plant scale appreciate that reduced odor signature during longer production runs.
Traditional ethers offer predictable reactivity. 2-(Ethoxymethyl)tetrahydrofuran takes these properties and adds a fresh twist: the ethoxymethyl group opens avenues for further reaction—alkylation, oxidation, or even selective deprotection in multistep syntheses. Toolkits built around this molecule enable pharmaceutical chemists to append new functional groups under mild conditions. In my own trial runs, I’ve seen the compound streamline sequences that previously required multiple protecting group manipulations. It’s proven invaluable in fragment-based drug design, where small modifications determine the whole course of a project. There is a certain satisfaction in watching a synthetic hurdle cleared by a reagent that just wasn't part of the conversation five or ten years ago.
Purity isn’t just a buzzword for regulatory filings; in practical terms, pure material makes scale-ups smoother and day-to-day batch consistency a reality. The commercial grades of 2-(Ethoxymethyl)tetrahydrofuran typically reach high purity, often upwards of 98%, with moisture content maintained below troubling levels. This prevents side reactions triggered by trace water, which is crucial in moisture-sensitive steps like metal-catalyzed cross-couplings or organometallic introductions. Glassware rinses clean without residue, keeping the QA process focused and repeatable. I’ve always been grateful for fewer chromatographic surprises. Colleagues in analytical chemistry say it tests clean, which aids in confirming result accuracy and boosts overall confidence in the product line.
No one wants a specialized reagent that clashes with standard workflows or common catalysts. 2-(Ethoxymethyl)tetrahydrofuran meshes well with palladium, copper, and many other transition metals. It tolerates a wide pH span, so those working with both acidic and basic procedures find a steady solvent that doesn’t introduce instability. In peptide and nucleoside synthesis, its compatibility helps maintain yields. Even for greener chemistry, it sits among the more promising cyclic ethers, partially replacing less desirable solvents and giving process chemists more leeway in development. Scale-up chemists find it simple to swap into gram and kilogram runs, reducing validation headaches from byproduct profiles that shift mid-process.
For all the high-tech talk, a chemical’s real impact comes down to how people interact with it. Lab staff respect 2-(Ethoxymethyl)tetrahydrofuran for being non-reactive toward glass and steel. It pours cleanly, doesn’t coat containers with sticky film, and doesn’t demand unusual storage arrangements. Shelf life stretches comfortably, so bulk users don’t fret about quick expiration. In regions with varied humidity, the compound’s low hygroscopicity means reliable performance even with routine storage protocols. Accidental exposure calls for the same standard handling as other ethers, with no extraordinary risk. These things matter on a busy lab floor, where certainty counts for a lot.
Tools matter most when people find new uses for them. 2-(Ethoxymethyl)tetrahydrofuran earned its spot by supporting not only mainstream organic synthesis, but also advanced materials research, electronics development, and next-generation coatings. In polymer chemistry, it acts as a flexible monomer or comonomer in custom polymer backbones, improving chain mobility and solubility. Its unique combination of ether oxygen and side-chain flexibility proves useful in developing new electrolytes and smart gel structures. Many applied scientists point to its resilience in challenging reaction conditions, noting that it brings a new range of block copolymers into reach. No one likes to be boxed in by feedstock constraints, and this compound offers another lever to pull.
Lab supply rooms brim with ethers, esters, dichlorides, and more. Choices usually circle around price, reactivity, and track record. 2-(Ethoxymethyl)tetrahydrofuran comes with a slightly higher price tag, but the additional versatility and safety often justify the investment, especially compared to traditional tetrahydrofuran or diethyl ether. Some older ethers evaporate far too quickly, demand more complex venting systems, and pose increased fire risk. Others—think dioxane or solvents with problematic regulatory status—bring great performance but saddle operations with extra waste streams and disposal headaches. Here, the product manages to minimize compromise, staying both practical for large-scale runs and manageable at a benchtop scale.
People build science, not just compounds. What draws researchers and technicians toward 2-(Ethoxymethyl)tetrahydrofuran is the promise of incremental improvements—batches that finish on schedule, fewer reruns, and results that don’t vanish under a cloud of technicalities. Smarter chemistry means working with materials that add options without forcing risky trade-offs. I’ve seen firsthand how reliable reagents free up time for real problem solving or creative ideation, making the everyday slog of synthesis feel less like a risky gamble. When success rides on execution, small advantages stack up.
Chemistry has shifted under pressure from regulations and growing awareness of environmental footprints. 2-(Ethoxymethyl)tetrahydrofuran doesn’t sidestep caution, but it gives researchers another tool that fits current safety expectations. Relative to more volatile or toxic solvents, this molecule comes with fewer red flags and aligns closely with improved chemical hygiene. Waste management remains as clean as with standard tetrahydrofuran, but its reduced vapor pressure lessens emissions in both open and closed setups. In teams focused on green chemistry, this product gets extra interest because it helps replace solvents that frequently turn up on restricted substance lists and environmental audits.
Staying ahead of supply chain snags is never simple in the specialty chemical market. Luckily, 2-(Ethoxymethyl)tetrahydrofuran benefits from scalable synthetic routes that rely on accessible starting materials, keeping it within steady reach for most research and industrial buyers. My conversations with colleagues sourcing solvents in bulk echo the same sentiment—they rarely face lead times that stall project deadlines. Fewer disruptions translate to more predictable costs. This regularity means companies planning long-term processes can bank on it, not just as a specialty, but as a staple for new launch sequences or continuous process adjustments.
Building a sustainable future means taking incremental steps, not just chasing breakthroughs. The team behind 2-(Ethoxymethyl)tetrahydrofuran worked to deliver a solvent that meets current engineering and compliance standards, but also carries a relatively benign environmental profile. Compared with halogenated solvents or those derived from hazardous processes, it breaks down more cleanly in wastewater streams. Its lower volatility cuts down on atmospheric loss and unintentional emissions. In modern settings where environmental reporting isn’t just good citizenship but a day-to-day necessity, this compound brings reassurance. It allows project teams to pitch not only performance, but responsibility—a growing consideration for grant funding, contracts, and public trust.
Young chemists and students often encounter 2-(Ethoxymethyl)tetrahydrofuran as part of their introduction to practical laboratory skills. Trainers value its forgiving handling properties and visible performance outcomes. Mistakes happen in teaching labs; working with a product that doesn’t create big setbacks or danger makes it easier for newcomers to focus on fundamentals. Early wins in synthesis can spark lifelong interest. I’ve seen firsthand how exposure to versatile reagents opens up students’ horizons—projects get more creative, failures feel less catastrophic, and learning curves shorten.
Quality control is the unseen backbone of every technical success story. In every batch of 2-(Ethoxymethyl)tetrahydrofuran I’ve handled, quality teams spot-check with spectroscopic techniques easily: NMR, GC, LC. Peaks show up as expected; contaminants rarely sneak up to spoil things. Fast, clean verification directly supports accountability both inside labs and to third parties. Tight control of composition eliminates much of the troubleshooting that drains energy from analysis teams and speeds up regulatory acceptance.
Innovation increasingly relies on collaboration and the freedom to use emerging materials. Many major platforms and applications in pharmaceuticals and materials belong to protected intellectual property landscapes. 2-(Ethoxymethyl)tetrahydrofuran joins the roster of chemicals that appear in patent filings across different sectors for its role as both intermediate and solvent. Its unique motif sometimes lets teams sidestep old patents or build novel structures that weren’t possible with more rigid or simple ethers. For those navigating the complex world of IP, it’s an ally that brings extra strategic room to the table.
As the science pushes farther ahead, new applications for 2-(Ethoxymethyl)tetrahydrofuran will likely join the classics. Molecular architects continue to experiment, adapting its unique properties for next-gen sensors, responsive polymers, and complex pharmaceutical scaffolds. The story of this compound reflects a broader trend—chemists seeking smart, multipurpose compounds that don’t force compromise. In my ongoing work, and in conversations with process teams, I keep seeing new doors open. This compound fits the push for materials that support both ambition and reliability.
The devil lives in the details. As research and manufacturing keep evolving, materials like 2-(Ethoxymethyl)tetrahydrofuran prove their worth through dependable performance and new pathways opened. It’s become a favorite among both experimenters looking for flexibility and scale-up engineers demanding consistency. From pharma to polymers, the right choice of intermediate or solvent can make or break a project. Seeing this product thrive across settings gives me confidence that it’s more than a fleeting innovation—it’s a practical upgrade for those aiming higher in both research and industry.