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HS Code |
509522 |
| Chemical Name | Phenetole |
| Iupac Name | Ethoxybenzene |
| Molecular Formula | C8H10O |
| Molar Mass | 122.16 g/mol |
| Cas Number | 103-73-1 |
| Appearance | Colorless liquid |
| Odor | Pleasant, ether-like |
| Boiling Point | 172.2 °C |
| Melting Point | -30.4 °C |
| Density | 0.968 g/cm3 (at 20 °C) |
| Solubility In Water | Insoluble |
| Flash Point | 54 °C |
| Refractive Index | 1.502 (at 20 °C) |
As an accredited Phenetole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Phenetole is packaged in a 500 mL amber glass bottle with a tightly sealed cap, labeled with hazard warnings and product details. |
| Shipping | Phenetole should be shipped in tightly sealed containers, stored in a cool, dry, well-ventilated area away from heat, sparks, and open flames. It must be labeled as a flammable liquid and handled per relevant regulations (such as DOT/IMDG/IATA). Use suitable secondary containment to prevent leaks during transportation. |
| Storage | Phenetole should be stored in a tightly closed container in a cool, dry, well-ventilated area away from direct sunlight, heat, and sources of ignition. Keep it away from incompatible substances such as strong oxidizers and acids. Store under nitrogen or an inert atmosphere if possible to prevent oxidation. Proper labeling and adherence to safety guidelines are essential for safe storage. |
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Purity 99%: Phenetole Purity 99% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures consistent yield and product quality. Boiling Point 172°C: Phenetole Boiling Point 172°C is used in solvent extraction processes, where controlled volatility enhances process efficiency. Stability Temperature up to 150°C: Phenetole Stability Temperature up to 150°C is used in heat-assisted organic reactions, where it maintains structural integrity under thermal stress. Refractive Index 1.508: Phenetole Refractive Index 1.508 is used in spectroscopic analysis, where matching refractive properties reduce measurement interference. Density 0.969 g/cm³: Phenetole Density 0.969 g/cm³ is used in liquid blend formulations, where precise volumetric measurement facilitates accurate dosing. Viscosity Grade Low: Phenetole Viscosity Grade Low is used in ink manufacturing, where low viscosity optimizes flow and print definition. Moisture Content <0.1%: Phenetole Moisture Content <0.1% is used in moisture-sensitive resin production, where minimal water content prevents polymerization defects. Molecular Weight 122.17 g/mol: Phenetole Molecular Weight 122.17 g/mol is used in analytical chemistry standards, where accurate molar mass ensures reliable calibration. |
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Phenetole often grabs the attention of chemists and manufacturers thanks to how it bridges practical utility with an approachable profile. As someone who has worked in industrial labs and observed supply chains evolve, I can say that Phenetole’s presence feels like a sign of industry experience shaping its offerings. The chemical formula is C8H10O, and structurally it’s known as ethoxybenzene, but folks who see it in operation tend to focus less on textbook labels and more on what it’s used for. With a clear, colorless liquid and a subtle, sweet aromatic scent, phenetole slips easily into blends wherever a gentle ether character is called for. People appreciate its tendency to fly under the radar compared to flashier aromatic molecules, but that’s exactly what makes it valuable in real commercial work.
What makes it stand out? The answer lies in experience—mine included—observing phenetole harnessed in both fine chemical labs and more rugged industrial setups. While common ethers like diethyl ether often hog the spotlight in textbooks, phenetole’s aromatic core delivers improved stability and a useful boiling point, landing somewhere around 172°C. This means it holds up well where you need mild volatility without the unpredictability you get from more labile ethers. Teams that focus on synthesis value this, especially when gentle conditions help preserve sensitive reagents or intermediates prone to break down under more volatile solvents. If you’ve spent time hunting for a solvent that won’t mix too freely with water, but still plays well in organic reactions, phenetole finds its way onto the shortlist.
From direct observation, most users look for a ready source of phenetole in high-purity formats, avoiding traces of moisture or contaminants that could interfere with catalytic or stepwise reactions. I’ve seen high-purity, technical-grade stocks stored under light-tight, air-sealed drums to avoid oxidation, although phenetole shows more resilience than something like diisopropyl ether. Unlike many lab ethers, phenetole doesn’t form explosive peroxides at the same alarming rate, which lowers daily handling stress for anyone who’s ever been stuck cleaning up after forgotten glassware. On the scale of worker safety and peace of mind, that matters. In factories and pilot plants, this feature has real impact—it helps keep long-running operations safer, with less need for strict peroxide monitoring routines that standard ether solvents seem to demand.
Digging into real-life uses shows how phenetole keeps showing up where people want a sturdy, reliable solvent. On one hand, it’s often mentioned in organic synthesis, especially as a model substrate in etherification or Friedel–Crafts reactions. Schools and labs keep it as a reference point because its aromatic nature and moderate ether properties allow predictable reactivity. From first-hand experience, phenetole also holds a spot as a nonpolar solvent in the arsenal of natural product chemistry, especially in cases where you need just enough solubility for aromatic compounds but want to limit unwanted interactions with alcohols or water. Those working with essential oils, perfumery bases, or advanced organic dyes know that phenetole plays well with hydrophobic solutes, offering an effective medium for extraction and fractionation, without being too aggressive. Its aromatic ring, compared to straight-chained ethers, supports a more sustained solvating effect for benzene-derived solutes. This is no minor benefit when you’re troubleshooting stubborn separations.
Compared to familiar choices like toluene or xylene, phenetole offers a strikingly lower odor profile and reduced flammability danger. Across solvent rooms, those qualities mean fewer headaches and mishaps. The mild, slightly sweet scent lingers less aggressively, which can help with compliance and worker comfort in closed spaces. There’s a reason labs handling delicate fragrance ingredients prefer phenetole: It doesn't overpower the product, and it wards off volatility-related spoilage. Having handled both phenetole and more aggressive aromatics in the same facility, I saw teams gravitate to phenetole when processing limits or odor control created hurdles for heavier solvents.
Spec sheets rarely tell the full story, but those in procurement and quality assurance care about purity and constancy. Most reputable phenetole suppliers lean into GC purity ratings above 98%, some pushing for water content down near trace parts per million. As with any solvent, batches shipped for sensitive production work—pharmaceutical, fragrance, or specialty polymer applications—usually face tight incoming quality controls. Users who’ve managed incoming inspections learn quickly to check for signs of oxidation. Phenetole tends to yellow when stored carelessly. Modern drums and fluorinated liners have done wonders to protect the product, keeping it clear and pure, ready for multi-stage processes. In my own rounds of production support, maintenance staff stress how a solvent that resists contamination and doesn’t foul valves or pumps saves time, worry, and money. Compared with lighter ethers—prone to peroxide alarms or sticky residues—phenetole’s reliability turns it into a ‘set and forget’ component for large-batch runs.
Talking to folks in specialty manufacturing, another point regularly crops up: phenetole’s solubility profile proves handy in those crossover cases where you’re blending aromatics with mild nonpolars. Pattern recognition shapes choices here—people notice certain intermediates just dissolve better or react more smoothly in phenetole than in generic toluene. Lower water miscibility keeps phase separation manageable, a key reason many pick phenetole for those extractions that would otherwise bog down if relying solely on heavier aromatic solvents. Having seen how batch sequencing sometimes grinds to a halt with incompatible solvents, I am convinced this property alone makes phenetole worth considering in any solvent rotation.
Every field technician or bench chemist eventually gets to know the quirks of the materials they use. Phenetole stands out here because it’s generally less hazardous than some historical solvents, but you can’t ignore safety outright. The lower volatility helps, reducing inhalation exposure if you’re running open-vat applications or topping up reactors. Anyone who’s ever spent long shifts in a plant with poorly vented ethers feels the difference fast. Spills clean up more easily than crude aromatics or halogenated solvents, which I’ve found makes for much less stressful risk mitigation during site walk-throughs. At the same time, best practices still call for routine checks: industrial hygiene teams keep an eye out for signs of chronic exposure, monitoring air quality and ensuring adequate PPE makes it into daily wear. One positive trend I’ve seen is a general move toward labeling, storage, and documentation routines that keep phenetole risks transparent and manageable for long-term site safety. This fosters both compliance and a work atmosphere where folks don’t have to second-guess safety policies every shift.
Phenetole’s production itself opens up questions about environmental responsibility. The classic syntheses, which draw from aromatic hydrocarbons and ethanol, once created notable emissions, but advances in process design now strive to keep byproducts minimal and recycling rates high. I’ve encountered manufacturers who’ve invested in closed-loop recovery and careful waste stream management, encouraged by regulations and by the push for greener chemistry. Where solvents used to draw scrutiny around disposal, modern sites work with supply partners to recover, filter, and reuse phenetole, cutting down hazardous waste. Compared to heavier halogenated ethers, phenetole’s environmental footprint is substantially lower, reflecting the broader trend where greener alternatives edge out older, dirtier standbys.
Stacking up phenetole against common ethers, it’s fair to notice how its physical and chemical profile cuts a unique path. The big name in generic lab ethers, diethyl ether, boils off at a much lower temperature—making it notorious for evaporating too quickly or causing handling headaches if precise temperature control isn’t maintained. Phenetole’s boiling point doubles the window for gentle operations and reduces fire hazards, letting it slot into workflows that would otherwise call for safer, slower-evaporating alternatives. Over time, I’ve noticed plant managers respect this property; it means fewer handling mishaps and alarm incidents. Pair that with the reduced risk of peroxide formation, and there’s less worry about long-term storage or casual oversight—a problem that haunts diethyl ether users.
Switching over to aromatics like toluene or xylene, another set of trade-offs pops into view. Those solvents tend to deliver plenty of solvency, but their strong odor, higher volatility, and sharper toxicity put a ceiling on their appeal, especially when working with food ingredients, fragrances, or active pharmaceutical intermediates. In these lines of work, phenetole’s lower toxicity and relatively gentle aroma make it much easier to control cross-contamination or product taint. In one operation I consulted for, switching to phenetole played a decisive role in reducing both background odor complaints and unintentional buildup of residues in process lines, a perennial headache with stronger aromatics.
From an operational standpoint, phenetole’s milder profile means it can bridge categories—functioning both as a conventional non-polar ether and lending some of the appealing characteristics of aromatics, without dragging along their baggage. This versatility reduces inventory headaches for mid-sized specialty producers who don’t want to juggle half-empty drums of niche solvents. It’s a running joke in some chemical plants: the more multipurpose a solvent, the happier the purchasing team. Phenetole exemplifies this ‘covers more bases’ phenomenon, which creates real economic and efficiency benefits for small and mid-tier operations.
Despite all these positives, phenetole isn’t a perfect tool. It doesn’t match the high solvency of strictly halogenated solvents for the most stubborn polymers or sticky residues. In practice, if you’re tasked with dissolving heavy, highly polar materials, phenetole won’t outperform DCM or THF. This comes up most often in custom polymer work or resin formulation, where specific polarity or miscibility properties are essential. Some labs solve this by blending phenetole with small amounts of more aggressive solvents, or by reserving it for stages where its mild solvency is a benefit rather than a bottleneck. Also, for the highest purity applications—ultra-sensitive electronics or microfabrication work—phenetole’s technical grades sometimes struggle to hit the parts-per-billion impurity marks, although ongoing improvements in distillation processes keep closing the gap.
Regulatory scrutiny sometimes enters the picture as well. In regions where air emissions face extra policing, even phenetole’s moderate volatility compels tighter storage protocols. Companies respond by installing vapor recovery units, improving local exhaust, and switching to sealed, automated filling systems. These aren’t insurmountable problems—just benchmarks that keep operational risk in check. My experience with regulators and site engineers tells me a straightforward solvent with a solid documentation history, like phenetole, raises fewer headaches than newer specialty products still navigating the paperwork gauntlet. Purchasing teams, too, appreciate that phenetole’s international regulatory standing hasn’t been buffeted by sudden reclassifications, which keeps product launches and formulations on smooth ground.
From a supply chain perspective, phenetole takes advantage of robust aromatic chemistry infrastructure. This makes global logistics workable for buyers in tight, regulated sectors, even if specialty supply hiccups are always a risk in volatile markets. Firms need to keep a pulse on lead times and shipping policies, especially for high-purity stocks, but phenetole’s established family of producers means bulk users seldom face the shortfalls that can haunt more exotic specialty solvents. A few years ago, a resin manufacturing plant I visited coped with a regional supply crunch by switching temporarily from halogenated ethers to phenetole, and the transition flowed far smoother than most product swaps, without fouling up batch yields or introducing unexpected residues. On-the-ground experiences like that shape trust in supply partners and the solvents they recommend—and phenetole’s stable track record cannot be overlooked.
Phenetole isn’t just a line item on a supply sheet. Its consistency and versatile solvency profile keep it at the top of the list for many practical chemists and industrial buyers. For me, observing years of solvent trials and process troubleshooting, it’s clear how phenetole’s stability, mild aroma, and safe handling characteristics build worker confidence and efficiency. Processes that rely on it often report fewer unplanned shutdowns, less equipment fouling, and quicker cleanup, which all translate into real savings and higher quality end products.
The story of phenetole also mirrors larger shifts in chemical manufacturing. The push for greener, better-tolerated solvents drives its adoption, while improved purification and waste management techniques reduce environmental and regulatory risks. Teams seeking a better workplace, easier safety practices, and tighter process controls find themselves coming back to phenetole. In short, while it rarely stirs up excitement—unlike high-profile new molecules—phenetole earns trust through its everyday reliability and easy integration into established, responsible operations. I’ve watched process managers, safety coordinators, and lab staff alike vote with their feet and their orders: they keep phenetole in rotation for good reason.
Solutions for the few obstacles phenetole presents already exist, shaped by feedback from the field. Better purification, smarter waste reclamation, and ongoing safety adjustments keep improving its fit for purpose. The take-home lesson is clear: focus on solvents that deliver, with minimal fuss and maximum trust, and you’ll find phenetole quietly getting the job done across countless sectors. Its real value lies not just in its technical specifications, but in the layer of shared experience, safety, and confidence that comes from years of careful, knowledgeable use.