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HS Code |
664942 |
| Product Name | Cyclopentyl Methyl Ether |
| Chemical Formula | C6H12O |
| Cas Number | 5614-37-9 |
| Molar Mass | 100.16 g/mol |
| Purity | ≥99.9% |
| Appearance | Colorless liquid |
| Boiling Point | 106-107 °C |
| Melting Point | -80 °C |
| Density | 0.862 g/mL at 25 °C |
| Refractive Index | 1.414 at 20 °C |
| Flash Point | 18 °C (closed cup) |
| Solubility In Water | Slightly soluble |
| Vapor Pressure | 30 mmHg at 25 °C |
As an accredited Cyclopentyl Methyl Ether (≥99.9%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1L amber glass bottle with secure cap, labeled "Cyclopentyl Methyl Ether (≥99.9%)", hazard warnings, and lot number for traceability. |
| Shipping | Cyclopentyl Methyl Ether (≥99.9%) is shipped in tightly sealed, chemical-resistant containers to prevent leaks and evaporation. It is transported as a flammable liquid under regulated conditions, avoiding heat, sparks, and open flames. Packaging complies with hazardous material standards, including appropriate labeling, documentation, and handling procedures for safe delivery. |
| Storage | Cyclopentyl Methyl Ether (≥99.9%) should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizers. Keep the container tightly closed and properly labeled. Protect from moisture and direct sunlight. Use approved safety containers and ground all equipment when transferring to avoid static discharge. Store under inert atmosphere if possible. |
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Purity: Cyclopentyl Methyl Ether (≥99.9%) with ultra-high purity is used in pharmaceutical synthesis, where it ensures minimal impurity incorporation and high product yield. Low Water Content: Cyclopentyl Methyl Ether (≥99.9%) featuring low water content is used in moisture-sensitive Grignard reactions, where it prevents hydrolysis and degradation of reactants. Boiling Point: Cyclopentyl Methyl Ether (≥99.9%) with a boiling point of 106°C is used in process-scale extractions, where it enables efficient solvent recovery by distillation. Chemical Stability: Cyclopentyl Methyl Ether (≥99.9%) with superior chemical stability is used in organometallic catalysis, where it minimizes side reactions and maintains catalyst activity. Low Peroxide Formation: Cyclopentyl Methyl Ether (≥99.9%) with low peroxide formation is used in storage and handling of sensitive reagents, where it reduces the risk of hazardous decomposition. Solubility: Cyclopentyl Methyl Ether (≥99.9%) with high solubility for lipophilic compounds is used in drug formulation, where it enhances dissolution and bioavailability. Flash Point: Cyclopentyl Methyl Ether (≥99.9%) with a flash point of 13°C is used in closed-system chemical processing, where it optimizes safety and fire control measures. Density: Cyclopentyl Methyl Ether (≥99.9%) with a density of 0.86 g/cm³ is used in phase separation protocols, where it enables efficient liquid-liquid extraction. Inertness: Cyclopentyl Methyl Ether (≥99.9%) with demonstrated inertness is used in lithium battery electrolyte research, where it prevents adverse chemical interactions. Low Residue: Cyclopentyl Methyl Ether (≥99.9%) with low evaporation residue is used in semiconductor cleaning, where it avoids surface contamination and maintains substrate purity. |
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Cyclopentyl Methyl Ether, often shortened to CPME, doesn’t stand out in conversation the way "acetone" or "ethanol" might. But for chemists and folks in the lab, its role can steal the show. The model on the market marked at ≥99.9% purity creates a different playing field—one where less interference and more precise results become possible. Years working in both start-up and academic labs taught me that that final percentage point can matter more than you expect. CPME blends safety, performance, and versatility, which explains why many researchers and manufacturers pick it up for both routine and demanding projects. Its CAS number is 5614-37-9, and its molecular formula reads C6H12O, giving a molecular weight of 100.16 g/mol.
Chemical reactions rarely go as planned if you mix in unwanted guests. Even tiny traces of water, peroxides, or leftover synthesis byproducts can bend your data, cut into yields, or fill up your waste stream with surprises. CPME at ≥99.9% purity draws a line in the sand: you know what you’re working with, and you’re not forced to guess what’s hiding in the bottle. People with time logged in medicinal chemistry, materials science, or process scale-up see the difference between 99.0% and 99.9%. They notice shorter purification steps, fewer side reactions, and less need to filter or dry solvents before use. If your protocol depends on anhydrous or low-residue conditions, CPME’s high purity can mean fewer headaches and re-dos.
Diethyl ether and tetrahydrofuran (THF) have been the default solvents for a long time. CPME grew in popularity for a few simple reasons. I still remember the first time I saw a bottle in the lab and wondered if it could really match the classics. The differences show up fast when you get your hands dirty: CPME’s lower tendency to form peroxides gives it a safety edge. Old-school ethers seem harmless until a bottle sits too long and crystals start to form—nobody wants to handle an explosive hazard. CPME doesn’t fix every safety issue, but it reduces this particular risk.
Boiling point separates CPME from typical ethers. While diethyl ether boils around 35°C and THF at 66°C, CPME feels sturdy at about 106°C. Anyone who’s lost precious product to evaporation during distillation or solvent exchange understands the value. This higher boiling point adds flexibility and reduces loss during reactions above room temperature. It lets you run workups that would chase off lighter ethers, and it stands up to rotary evaporation or vacuum distillation without drama.
Water solubility often frustrates teams who use THF: it mixes well with water, making extraction steps messier and sometimes wasting product. CPME solves some of these problems by being only slightly soluble in water, which keeps organic layers clean and simplifies separations. Many who’ve struggled to dry out THF or worried about water-washed products ending up in the wrong phase find CPME is less finicky, and that means more reliable workflows day after day.
Pharmaceuticals, fine chemicals, and agrochemical manufacturing turn to CPME for both research and scaling up to production. My own experience teaching university lab classes showed me students catch on quickly to its benefits. The moderate polarity makes it useful for a variety of reactions—Grignard, Suzuki, reductions, and the like. It’s more than just a place for molecules to bump into each other. CPME supports sensitive organometallic chemistry because it tends to stay dry and avoids strong coordination with reactive species.
Many researchers explore greener chemistry. CPME, derived from renewable feedstocks, fits better into sustainability goals compared to some petrochemical alternatives. As solvents move up the greenness scale, CPME’s lower toxicity, higher flash point, and favorable biodegradability start to matter. Not every project cares about a few grams of solvent here or there, but scale up to a pilot plant and you’ll see how quickly solvent selection shapes cost and safety profiles.
Storing CPME doesn’t demand a unique playbook, but there are lessons learned from years of handling solvents in facilities both fancy and makeshift. Its higher boiling point slows evaporation, so you lose less to the air during storage or transfer, which cuts waste and exposure. Unlike ethers with a reputation for accidental peroxide formation, CPME holds up longer in storage, which means laboratories that don’t cycle through stock each week have less to worry about. Standard solvent cabinets work well, and most users find it less “smelly” and easier to manage day to day.
No solvent operates risk-free. CPME can still cause irritation, and at high enough concentrations, could pose health risks if handled carelessly. Old habits—wearing gloves, checking fume hoods, minding storage caps—stay important. But compared to ether cousins, CPME brings lower flammability and slower evaporation, both of which ease some safety worries. Reaction failures from old peroxide-laced solvent or mystery water in the extraction step can punish teams with tight budgets or deadlines. CPME, with its stability and lower tendency to form peroxides, marks a step toward safer bench and pilot plant work.
Environmental awareness grows steadily every year. CPME’s profile as a greener solvent comes both from its production and its end-of-life pathway. Released into the air or water, it breaks down faster than many alternatives. Lower toxicity in waste streams and reduced air pollution count as wins for compliance teams and site managers trying to toe the line with new regulations. Over my time talking to industrial chemists, the shift toward such greener solvents feels more grounded in real experience than abstract pledges made in boardrooms.
Some products promise to fix every problem. CPME doesn’t fit that mold, but it does solve several issues in one package. It dissolves a wide range of organic substrates—more than diethyl ether, less than NMP (a far more polar, less user-friendly solvent). In practice, I’ve seen CPME handle everything from nucleophilic substitution to transition metal catalysis. Its stable behavior with strong bases and acids makes it a workhorse in synthetic routes that need resilience.
That said, every tool has limits. CPME’s higher boiling point—great for stable heating—means it demands more energy to remove. Simple vacuum can speed it up, but where ultrafast solvent removal counts, lighter ethers still hold an edge. In chromatography, some columns—especially silica—interact with CPME differently than classical solvents. New users notice this right away, and shifting to CPME might require a tweak in TLC stains or eluent choices.
Peroxide formation causes headaches in any laboratory. CPME forms peroxides far more slowly than ethers like THF or diethyl ether, buying extra safety and shelf life. Instruments that require frequent calibration, like GCs or high-performance preparative systems, operate smoother with less downtime when CPME is the solvent, since purity and low peroxide risk reduce unexpected baseline drift or artifacts.
Lab managers track budgets down to the penny, and CPME often costs more upfront than diethyl ether or THF per liter. But there’s more to the bottom line than sticker price. Think about the labor hours reclaimed from fewer purification runs, less solvent loss to evaporation, and reduced hazardous waste processing. Factoring in the bigger picture, CPME wins back some costs through reliability and safety.
Handling CPME brings little surprises, and my own shifts in research labs saw fewer accidents or headaches moving toward it. Older ethers have a knack for leaking out of seals or gaskets because of their volatility. CPME’s weightier vapor reduces laboratory odors, solvent chase-outs, and cross-reactions. Flammability drops too, lowering insurance rates and fire risk when stored in reasonable quantities.
Long-term, CPME’s environmental advantages become clearer. Switching major synthetic steps from chlorinated solvents to CPME means fewer regulatory forms to file, less need for scrubbing or burning waste, and better worker safety records. Analysts and process chemists develop a deeper appreciation for those gains after a few years’ worth of progress reports and safety meetings.
Switching to CPME doesn’t erase every challenge. Compatibility with plastics varies—a few types swell or crack after contact, so metal or glassware stays the safer bet. Reaction kinetics shift slightly compared to THF or diethyl ether, which means some methods need tuning for yield or selectivity. Older practitioners, set in daily routines, sometimes bristle at the learning curve.
Not all reagent suppliers stock the same grade or packaging for CPME, creating frustrations for scale-up or process teams. Logistics managers should double-check source reliability; it pays to work directly with suppliers who guarantee purity at the specification level. More than one synthesis campaign ran into delays waiting on backorders or seeing batches that just didn’t match expectations.
Analytical teams also note unique impurities. Even at ≥99.9% purity, analytical traces might pick up minor byproducts—interpretation depends on how well they know both their instrument and the solvent’s supply chain. Investing time up front to calibrate, discard the first pour from larger drums, and confirm certificate-of-analysis details can prevent headaches down the line.
Out on the lab floor, small changes help teams get more from CPME with fewer headaches. I’ve seen success with a few smart habits. Setting aside a quiet bench for weighing out dry reagents and solvent minimizes water pickup. Scrupulously labeling CPME bottles, marking open dates, and storing them away from strong acids or bases preserves both shelf life and data quality. Training new staff on CPME’s properties and common pitfalls makes a noticeable impact—no one wants to lose a week’s work for want of a quick solvent check.
To streamline procurement, group orders and pick suppliers with traceable batch information and strong after-sales support. Request consistent documentation, including gas chromatography or NMR analysis with every drum or bottle. Seasoned process chemists cross-check this information against published standards, not just supplier marketing. Investing time in sourcing quality up front avoids the cost and risk of troubleshooting inconsistent feeds.
For reactions that lag or stall, teams can tweak conditions around CPME’s unique properties. Slight adjustments in temperature settings or base equivalents can bring yields back in line. Switching up drying agents (molecular sieves instead of sodium/benzophenone) and optimizing quench protocols for its water solubility keeps extractions crisp. Chromatography purification benefits from pilot runs using CPME-based eluent, as thin-layer chromatography can react differently compared to more traditional ethers.
Fire safety shouldn’t get lost in the solvent shuffle. CPME still burns, so proper grounding, spark-proof fans, and secondary containment stay fundamentally important. Learning from nearly two decades working in diverse laboratory settings, no one ever regretted a few extra minutes spent on spill drills, regular chemical hygiene checks, and fume hood airflow monitoring.
Trends push more labs to look past legacy solvents. Regulatory changes, environmental targets, and cost pressures shift habits across the industry. CPME’s reputation grew not just from marketing, but from word of mouth between chemists who sought better results and safer working conditions. Academic publications comparing ether solvent systems turn up more CPME-based protocols each year. Presenters at green chemistry conferences name CPME among their preferred choices for both new synthesis and old standbys.
Major pharmaceutical operations and contract research organizations invest in switched solvent processes. Fine chemical manufacturers report measurable drops in hazardous waste disposal and spill incidents after adopting CPME. Environmental Health and Safety officers at more than one facility now suggest CPME as a preferred solvent, especially for reaction sequences that previously struggled with peroxide-prone ethers. Over time, cleaner supplies and lower waste rates move from side notes to accepted practice.
From the frontlines of research and process development, those tweaks and swaps rarely go backward; once CPME finds a home in method development, teams prefer to keep it there. Several process scale-ups I’ve watched switched to CPME for specific hydrogenation, Suzuki, or nucleophilic substitution reactions. Their project managers praised the drop in column pressure issues and cleaner product profiles. The solvent’s reliability saved time in QC, getting batches out the door that much faster.
If a solvent feels novel to experienced workers, new generations of chemists should learn its strengths and oddities from the start. Undergraduate and graduate programs update curricula to feature CPME alongside traditional reactions. New teaching labs add CPME to the solvent line-up, and instructors pass along practices from their own research. Young researchers who see solvent safety as second nature embrace CPME’s combination of performance and protection. Their early wins build confidence, encourage broader adoption, and chip away at risk for the next group to step up.
By embedding best practices—using CPME where it makes processes safer, greener, and more stable—institutions develop a culture of careful chemical stewardship. That culture roots itself deeper every time a class or research team shares a success story and folds in lessons learned about purity, procurement, and process resilience.
Change in chemistry doesn’t happen overnight. Solvent choices that once seemed minor now sit at the crossroads of cost, safety, and sustainability. From what I’ve seen in labs across several countries, teams who pick CPME at a purity of 99.9% or higher cut down on side reactions, lower exposure to hazardous byproducts, and inch closer to regulatory benchmarks for green chemistry. Over the last decade, its use spread beyond boutique syntheses into larger, more routine operations. Reliable performance and regulatory compliance play as big a role as the chemistry on the page.
As requirements for cleaner, more predictable manufacturing grow, CPME delivers a clear advantage—one rooted in hands-on experience as much as in numbers on a specification sheet. Its performance fits today’s demanding protocols while answering real needs in health, safety, and environmental responsibility. No single solvent fits every team or workflow, but CPME’s footprints in modern labs keep getting deeper. The stories researchers and operators bring—less downtime, fewer lost batches, cleaner workspaces—chart a future where higher standards and better results go hand in hand.