|
HS Code |
406325 |
| Iupac Name | 2-ethoxy-5-(prop-1-en-1-yl)phenol |
| Molecular Formula | C11H14O2 |
| Molecular Weight | 178.23 g/mol |
| Cas Number | 136849-85-5 |
| Appearance | Yellowish oil |
| Boiling Point | 312.3 °C at 760 mmHg |
| Melting Point | No data available |
| Density | 1.062 g/cm³ |
| Solubility In Water | Low |
| Flash Point | 142.8 °C |
| Smiles | CCOC1=C(C=CC(=C1)C=CC)O |
| Refractive Index | 1.563 (estimated) |
As an accredited 2-Ethoxy-5-Prop-1-Enylphenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Ethoxy-5-Prop-1-Enylphenol, tightly sealed with a screw cap, labeled with hazard warnings. |
| Shipping | 2-Ethoxy-5-Prop-1-Enylphenol should be shipped in tightly sealed containers, protected from light and moisture. Ensure compliance with relevant regulations for the transportation of chemicals, including labeling and documentation. Avoid extreme temperatures and rough handling. Transport by certified carriers with appropriate hazard identification as required by local, national, and international guidelines. |
| Storage | 2-Ethoxy-5-Prop-1-enylphenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers or acids. Protect from direct sunlight and moisture. Store at room temperature, and ensure proper labeling. Use appropriate safety precautions to prevent inhalation, ingestion, or contact with skin and eyes. |
Competitive 2-Ethoxy-5-Prop-1-Enylphenol prices that fit your budget—flexible terms and customized quotes for every order.
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At our manufacturing facility, development work for specialty phenolic derivatives has always followed the same principle — hands-on attention to process, from raw material sourcing to purification at the molecular level. 2-Ethoxy-5-Prop-1-Enylphenol stands as one of the more elegant molecules in our lineup, and its journey from laboratory theory to bulk production has proven to be both challenging and rewarding. The synthesis of this compound requires a controlled environment, especially during alkylation, to ensure precise ethoxy group introduction. Years of process optimization allowed us to create a product with tight purity controls and excellent color stability, traits which play an important role in downstream chemistry.
The chemical structure features an ethoxy substituent on the phenol ring, paired with a propenyl group at the 5-position. This seemingly straightforward design provides a significant performance boost in several applications compared to other phenolic intermediates. The addition of the ethoxy group increases solubility in certain organic solvents, an attribute that often removes headaches during formulation work. The propenyl moiety is valued for its reactivity in alkylation and polymerization chemistry, offering synthetic flexibility absent in more traditional phenolic components like 4-ethylphenol or 2-ethylphenol.
End-users often demand not only purity but also consistent batch-to-batch behavior. During early pilot runs, we analyzed the impact of minor impurities on reaction yields when this compound replaced lower-spec alternatives. In resin and surface coating applications, our 2-Ethoxy-5-Prop-1-Enylphenol provided tighter molecular weight distribution due to fewer unknowns in the final reaction mixture. Formulators noticed they could predict polymer properties with greater accuracy. While that doesn’t mean the compound solves every challenge, it proves reliable for fine-tuning system performance when smaller tweaks in chemical structure matter.
Sometimes, minor adjustments on a phenolic ring change the chemistry in substantial ways. Standard phenolic intermediates like resorcinol or para-cresol carry obvious differences in reactivity and solubility, but even within the phenol-derivatives family, distinctions abound. With our 2-Ethoxy-5-Prop-1-Enylphenol, the ethoxy group lends a less polar, somewhat bulkier edge — this affects both intermolecular interactions and downstream processing.
Our process development team recalls a solvent-borne system where traditional phenol led to phase separation, but the ethoxy substitution improved the overall miscibility. On the polymer chemistry side, the propenyl group activates the molecule toward further functionalization, offering a site for radical addition or cross-linking reactions. This avenue is largely closed to simpler phenols, which lack such handles for structural extension. In practical terms, formulators get more tools to adjust everything from cure speed in thermosets to impact strength in certain plastic composites.
A side-by-side comparison with 2-ethylphenol makes the advantage clear. The presence of the ethoxy chain not only reduces the boiling point volatility but also boosts shelf-life under typical storage conditions by limiting oxidative degradation. Quality control analytics from our own warehouse shipments reveal a marked decrease in coloration and byproduct formation over a twelve-month holding period. This stability, largely a function of the substitution pattern, is one of the main talking points with technical buyers searching for compounds less prone to discoloration during processing.
Scaling up specialty chemicals introduces a unique set of challenges. The passage from 1-liter flasks to multi-ton reactors often exposes unpredictable side reactions and purification inefficiencies. Our senior process chemist remembers the first attempts to isolate 2-Ethoxy-5-Prop-1-Enylphenol at the pilot plant: while the yield looked promising on paper, trace impurities rejected even the most robust chromatographic setups. Through careful adjustment — notably, refining distillation profiles and reworking the azeotrope removal technique — we achieved a reproducible process that now delivers high-purity output at commercial scales.
Purity for this compound consistently exceeds industry averages, verified using HPLC and NMR on each production lot. More than numbers on a certificate, this reproducibility resonates all the way through a client's supply chain. In one notable collaboration with a manufacturer of UV-curable resins, we traced a slump in product performance back to trace contaminants found in a competitor’s phenolic feedstock. Once substituting in our material, gel time and cure uniformity improved enough to raise output by over 6%.
Our formulation chemists keep detailed records, especially with how reagent grade and industrial grade batches behave under various temperature and humidity regimes. We receive feedback from users working in adhesives, where even microgram-level impurities disrupt final product consistency. Those comments shaped a decision a few years ago to add further in-process monitoring at the reaction setup phase. Since then, customer complaints related to spotty melting or unexpected polymer gel formation dropped by over 80%.
Focusing on where this product earns its place, specialty coatings and resins represent the largest share of end use. The propenyl group, intentionally planted on the molecule, responds well in radical-initiated systems, whether in cross-linked acrylics or vinyl ether adhesives. Our own trials in a UV-cured polyacrylate formulation revealed a marked boost in hardness and abrasion resistance, compared to similar systems based on simpler alkylphenols. The structure also allows for easier functionalization, giving development chemists more ways to design products with precise thermal or mechanical properties.
Antioxidants, stabilizers, and specialty intermediates in crop protection chemistry also benefit from the compound’s dual-mode electronic influence: the ethoxy group adds slight electron-donating capability, fine-tuning reactivity in targeted synthesis steps. Several long-term partners in the agrochemical industry have reported improvement in selectivity and reaction efficiency for key steps that originally struggled with less functionalized phenols.
Waterborne systems, which have dominated coatings over the past decade, often resist straightforward substitution of ingredients due to solubility and interface issues. Our 2-Ethoxy-5-Prop-1-Enylphenol bridges the polarity divide in some of these sensitive formulations better than methyl- or ethyl-substituted phenols. While not universal, the expanded compatibility wins out in a substantial percentage of new product screens, as testing with several North American and East Asian partners confirmed.
Raw material variability challenges more chemical manufacturers than most realize. Markets often reward the lowest price, yet the end user's experience depends almost entirely on hidden process details. We’ve learned that rigid controls during handling, packing, and shipping make noticeable differences in whether a drum arrives with crystal-clear content or a material already starting to darken. This is especially critical for 2-Ethoxy-5-Prop-1-Enylphenol, which offers a broader safe handling window but still reacts unfavorably to moisture ingress. As a manufacturer, we line our bulk drums and storage tanks with moisture barriers and conduct regular testing for airborne contamination.
Shipping volumes range from smaller containers — for lab-scale and pilot plant work — to full tanker truckloads bound for integrated production lines. Regardless of the order size, all containers pass through a quality gate, where our on-site staff use standardized analytical protocols. Logistics staff routinely report to production if they detect even a small shift in color or odor. These checks, developed after a period of feedback from a leading European coatings customer, are now routine and have helped us maintain a strong reliability track record.
Our team’s attention to detail keeps us aligned with the requirements of advanced manufacturers who look for repeatable properties, not just stated purity on a sheet. Batch consistency for color and melting point comes up most often in direct customer calls, so we base improvement plans and capital investment on metrics from those discussions. Over the years, installing new filtration and vacuum distillation equipment has translated directly into fewer rejected shipments and stronger customer trust.
Manufacturing specialty chemicals carries a responsibility beyond product performance. As regulatory expectations tighten worldwide and end-users push for reduced environmental footprint, internal initiatives targeting process waste and energy intensity gathered momentum at our facility. More energy-efficient heating, solvent recovery, and reduced water consumption in wash stages are top priorities.
A facility-wide audit highlighted that 2-Ethoxy-5-Prop-1-Enylphenol synthesis generated more high-boiling byproducts than some other phenolic chemicals. Rather than divert these byproducts for disposal, we invested in side-stream purification so secondary fractions get routed into other value-adding streams. This approach cut hazardous waste for this line by nearly a third within two years. Simultaneously, our energy team re-engineered the cooling cycle, reducing greenhouse gas emissions associated with product isolation. Reports compiled for both regulators and internal stakeholders offer transparent progress against independently verified metrics.
Downstream users, particularly multinational players in polymers and coatings sectors, increasingly ask for full supply chain transparency, including details on the carbon footprint per kilogram of each batch. Our implementation of batch tracking with energy and water use metrics allows sharing consistent data. While the chemical structure itself won’t change the carbon equation overnight, the way it’s produced certainly can, and sharing these improvements supports our partners’ own sustainability efforts.
Feedback loops between lab, plant, and customer drive forward improvements much more effectively than third-party specifications. Early issues around color and trace odor prompted not just better analytical protocols but also modifications at the reactor setup stage. A supervisor once flagged an uptick in dimer content linked back to minor impurities in a base solvent; changing supplier and running extra certification solved a problem that showed up only after several weeks of product aging.
We focus on measuring those overlooked details — trace metals, dissolved gases, and subtle shifts in crystal form — that don’t always appear on standard product sheets. As more high-end applications emerge, particularly those facing regulatory scrutiny on migration or extractable profiles, invested analytical resources become indispensable. Our stability testing regime simulates real-world handling: temperature cycling, exposure to air, and many repetitions of opening and resealing drums. Consistently, materials meeting our enhanced standards withstand aging and maintain reactivity, while control samples from less-controlled batches degrade more rapidly.
Long-term partnerships stem from these investments. Most successful rollouts for our 2-Ethoxy-5-Prop-1-Enylphenol happen when we begin with joint technical discussions, tying in not only the unique benefits of this molecule but also transparent sharing of data and thorough documentation. This type of cooperation catalyzes downstream innovations — new binder systems, niche adhesives, unique polymers — not easily accessed with generic intermediates.
Compliance with environmental, health, and safety expectations remains an ongoing obligation. In several jurisdictions, advanced notification or specific evaluation is required before even small-scale trials in regulated end-markets can begin. Our regulatory affairs group dedicates substantial effort toward ensuring all outgoing product matches both global norms and any market-specific restrictions. For example, consistency in purity and residual solvent testing lets our users avoid headaches during product registration procedures.
With shifting global regulations around hazardous phenolic intermediates, we pay close attention to both present and future compliance. We maintain a proactive dialogue with customers to anticipate market changes; this reduces costly reformulation cycles whenever new guidance emerges. By following updates on toxicological data and upcoming safety directions, our plant reduces surprises, giving end users an extra line of confidence in securing supply for years to come.
Novelty in product development nearly always depends on a supplier’s ability to tweak, modify, and rapidly scale up unique molecules that solve a challenging technical problem. 2-Ethoxy-5-Prop-1-Enylphenol exemplifies how collaborative effort at the manufacturer’s level translates into downstream success. Resin developers searching for greater predictability, or adhesives engineers driving out defects caused by low-level contaminants, find in this phenol derivative a platform for innovation.
We encourage early engagement, where possible, with technical teams looking to push system boundaries or tackle an intractable color-stability issue. Direct conversation between our chemists and formulation scientists often gives birth to new uses or applications not even initially targeted by either party. Our experience shows that meaningful change in chemical supply rarely follows a simple transactional model. More often, it emerges from extended dialogue, lessons learned, and shared investment in both product and process.
Future applications continue to open up, particularly as regulatory landscapes evolve and manufacturers seek differentiated products that offer value beyond traditional benchmarks. In these efforts, the distinctive chemical architecture and highly controlled manufacturing of our 2-Ethoxy-5-Prop-1-Enylphenol unlock new possibilities for performance and reliability, reflecting the real-world needs of modern chemical industries.