Anhui Liwei Chemical Co., Limited
Products

Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]-


    • Product Name Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]-
    • Alias ALPS
    • Einecs 420-320-4
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
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    Specifications

    HS Code

    913305

    Chemicalname Phenol, 4-[[4-(2-Propen-1-yloxy)phenyl]sulfonyl]-
    Molecularformula C15H14O4S
    Molecularweight 290.34 g/mol
    Casnumber 108318-04-7
    Appearance Solid (typically off-white to light yellow powder)
    Boilingpoint Decomposes before boiling
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C=CCOc1ccc(cc1)S(=O)(=O)c2ccc(O)cc2
    Inchi InChI=1S/C15H14O4S/c1-2-10-19-13-6-4-12(5-7-13)20(17,18)15-9-11(16)3-8-14(15)8/h2,4-9,16H,1,10H2
    Storageconditions Store in a cool, dry, well-ventilated place, away from incompatible substances

    As an accredited Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams net quantity, screw cap sealed, labeled with chemical name, hazard warnings, and supplier information for safety.
    Shipping **Shipping Description:** Phenol,4-[[4-(2-Propen-1-yloxy)phenyl]sulfonyl]- should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Ensure compliance with local, national, and international regulations, including proper labeling and hazardous material documentation if required. Recommended transport temperature: ambient or as specified by the manufacturer’s safety data sheet (SDS).
    Storage Store **Phenol, 4-[[4-(2-Propen-1-yloxy)phenyl]sulfonyl]-** in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of heat, ignition, and incompatible materials such as strong oxidizers or acids. Protect it from light and moisture. Use secondary containment for spills and consult the safety data sheet for specific precautions and recommended storage temperature.
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    Certification & Compliance
    More Introduction

    Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]-: Our Experience with Production, Quality, and Application

    A Glimpse Into Manufacturing Precision

    In the chemical industry, real understanding of a compound grows out of hands-on experience. Our journey with Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]- began in response to a clear call from advanced material science sectors and specialty polymer developers who face specific performance demands. Over the years in production, we've watched this compound become a staple whenever formulators require persistent thermal and oxidative stability alongside the unique reactivity brought by the allyloxy group and the aromatic sulfonyl linkage.

    We learned early that synthesis for this compound hinges on proper control at every stage. Phenol-based chemistries are notoriously prone to side-reactions. We dedicated significant resources to developing a process that controls temperature, reaction time, and catalytic environment, minimizing by-product generation and enhancing overall yield. Our reactors, equipped for rapid heat transfer and precise stirring, make it possible to maintain both purity and batch-to-batch consistency—real, measurable advantages for downstream users requiring performance repeatability.

    Quality Parameters that Matter in the Real World

    Lab-scale synthesis rarely reflects the grind of industrial production. In our facility, every lot of Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]- passes through chromatography and high-resolution spectroscopic measurements, confirming absence of unsaturated byproducts and minimizing unreacted intermediates. Customers in specialized thermoset resin production, especially those developing new high-performance matrix materials for electronics or aerospace, often point to the contamination sensitivity of their systems. We focus on purity—not just as a number but as a driver for successful curing, consistent mechanical properties, and avoidance of downstream gel formation.

    Certain applications push these requirements even harder. Take advanced photoresist chemistry. Here, trace impurities from precursor or process side-reactions could throw off the entire photolithographic pattern. We developed ultra-fine filtration processes, using both activated carbon and proprietary adsorbents, to guarantee the highest performance. These steps, combined with strict storage in light- and moisture-controlled environments, shape our reputation among the most demanding customers.

    What Sets Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]- Apart?

    Our team frequently hears this question from researchers and purchasers comparing available sulfonylated phenol derivatives. Many products exist, but not all start with a focus on end-use realities. Some competitors use batch syntheses that leave behind tars and oligomer residues, especially if reaction controls slip or recycling of solvents isn’t clean. Over years of plant operation, we've identified points where deviation of a single degree shifts the molecular weight distribution and alters reactivity.

    The core difference lies in molecular design. The 2-propen-1-yloxy (allyloxy) substituent, directly attached to the phenolic ring, opens the door to crosslinking possibilities that are either impossible or unpredictable with simple methyl, ethyl, or propoxy groups. In polymer matrices, it behaves as a site for controlled polymerization, leading to networks with higher thermal and chemical resistance. In contrast, using more conventional phenol derivatives lacking this substituent often results in softer, less durable polymers prone to creep or oxidative degeneration.

    Another detail: the para-sulfonyl linkage on the second aromatic ring does more than increase hydrophilicity. Based on both in-house and customer feedback, this group significantly modulates compatibility with sulfonated resins and ion exchange media, providing better miscibility and stable morphology during processing. Attempts to recreate similar properties by blending with simple sulfonated monomers often introduce phase separation or uncontrolled precipitation, which we never see with properly processed 4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl] derivatives.

    Meeting Application Demands Beyond the Standard

    Electronics manufacturers have shown us how much the performance envelope can shift with minor structural tweaks. For example, circuit board producers prefer this compound because the balance of rigidity and processability proves essential in high-frequency PCB prepregs. During lamination, structures built from this phenol derivative demonstrate greater glass transition temperatures and a much lower coefficient of thermal expansion, which cuts down risk of microcracking and solder joint failure over repeated thermal cycling. Competing alternatives often rely on heavier halogenated phenols—substances that pose issues both in production toxicity and long-term environmental impact.

    Epoxy formulation chemists in coatings and adhesives look for both reactivity and final bond robustness. Here, the combination of the aromatic backbone with reactive allyl functionality allows for tougher, crack-resistant films and encapsulants. Water absorption levels drop when compared to traditional phenolic resins, and the best results come from using our product in formulations that endure both high humidity and aggressive chemical splash. This trait is especially valued in semiconductor underfills and chip encapsulation, where micro-leakage can spell disaster within months if the resin foundation isn't up to standard.

    One of the more recent trends steers toward sustainable, lower-toxicity alternatives in high-value plastics and composite manufacturing. Many large producers hope to cut out free formaldehyde, orthophthalates, and other regulated additives from their processes altogether. While this shift creates technical problems—particularly for those depending on established cure chemistries—Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]- offers a viable route to crosslinked networks without such compounds. Our in-house trials, corroborated by customer data, confirm that using this phenol bridges the divide between necessary performance and new health/environmental standards.

    Technical Insights from Years on the Line

    No amount of marketing can substitute for operational experience. Over the years, our technicians have observed that the synthesis and downstream use of this compound reward consistency above all else. Temperature excursions, even slight, during sulfonylation or allyl etherification immediately show up in the end product’s melting range and solubility. Attention to minute details—like preventing atmospheric moisture ingress or controlling the cool-down rate—can mean the difference between prime product and unusable off-spec material.

    Every week, batches undergo extensive physical property testing—HPLC, GC-MS, FTIR, and hot-stage microscopy. These tests spot minor deviations early, and lessons learned over hundreds of campaigns feed directly into our manufacturing SOPs. We’ve eliminated common pain points: browning from oxidative side-reactions, slow cures from incomplete functionalization, and particulate contamination from reactor scale-up. Instead, we offer a compound that real-world customers say performs right out of the drum, not just in academic literature.

    Supporting Scale and Customization

    Polymer chemists tell us their biggest hurdles aren’t always about the molecule itself, but about getting material at the quantity and quality level required in prototyping, piloting, and full production. We run both kilogram-scale campaign setups for R&D as well as multi-ton programs when products cross the adoption barrier. Logistics teams invest heavily in maintaining product integrity—every drum and tote ships under argon, and we maintain storage at controlled temperature and humidity to sidestep age-related degradation.

    Researchers sometimes need a slight modification—an adjustment in the degree of substitution, or a tailored particle size distribution for unique dispersion needs. Technicians and engineers on our floor have delivered custom syntheses, whether tweaking reaction stoichiometries or providing expert advice on compatibility with resin partners. We work closely with customers, not only to supply a molecule, but to ensure the entire process from order to delivery fits within their workflow—whether that means smaller packing for university benches or larger consignment volumes for composite panel lines.

    Why Customers Switch to Our Product

    Competing compounds exist, and we regularly welcome users switching from standard bisphenol or simple monomer alternatives. The difference, they report, typically boils down to reduced batch rejects, improved processability, and better long-term durability in the field. A major adhesives manufacturer attributed a 30 percent drop in line fallout to switching to this product, largely because of greater batch stability during mixing and a higher degree of functional group incorporation. These small but critical details matter at every step, from mixing tank to finished product performance years later.

    A manufacturer of high-frequency antennas managed to eliminate both early delamination and yellowing, a problem they traced back to residual impurities in their previous monomer source. By switching to our cleaner, more consistent product, they were able to meet demanding telecom OEM reliability standards—which, in turn, brought new contracts and market expansion. These achievements do not happen by accident, but result from control at every layer of production.

    Regulatory and Safety Focus

    As regulatory frameworks shift globally, the demand for compounds with lower volatility and toxicity levels continues to grow. Unlike many halogenated alternatives, this phenol derivative provides a route to compliance with strict European and domestic restrictions on hazardous substances in electronics, coatings, and industrial resins. Our process avoids high-risk reagents and maintains occupational exposure below accepted thresholds—an advantage we see resonating with safety managers in downstream firms. We maintain transparent, comprehensive documentation for every batch, reflecting our commitment to both user well-being and responsible industry practice.

    Customers often ask about the waste byproducts in our process. Through continual overhaul of our solvent recovery and purification loops, we’ve driven down both hazardous waste and product loss. That’s a benefit for us and for end users, who increasingly seek to minimize upstream Scope 3 emissions. This focus on operational sustainability keeps us at the front of adoption by manufacturers looking to green their value chain.

    Limitations and Problem Solving

    It’s important to note this compound isn’t a miracle solution for every application. In very high-alkaline environments, the allyloxy group can suffer degradation, slowing cure or reducing molecular weight in the final polymer. Our technical group is open about these cases. For certain waterborne systems, additional stabilizers or processing aids might be required to keep product performance at its peak—customers benefit from prompt, hands-on support in formulating around such issues.

    Working directly with formulators means troubleshooting challenges in real time. Last year, we supported a partner launching a new UV-cured acrylic. They encountered haze and low crosslink density during scale-up. Our team identified minor oxygen traces during their blending stage as the culprit—an issue not caught at lab scale, but devastating in five-ton lots. Tightening seal integrity and minor changes to their process brought yields back into specification. Lessons like these reflect the kind of collaborative relationship you can only achieve by working day-to-day with chemical users, not through distant, transactional distribution.

    Looking Ahead: Future Directions from Our Perspective

    Demand for high-performance, functionally specialized phenol derivatives continues to climb as end-user industries embrace both higher operating temperatures and greener processes. As material requirements grow more demanding in telecommunications, energy storage, and construction composites, we are investing in reactor capacity, analytical infrastructure, and collaborative R&D. These steps ensure reliable access and continual improvement for all partners who depend on real-world material performance and true chemical transparency.

    Innovation rarely comes from isolated benchwork. We see success emerging from continual dialogue—pilot lines sending early feedback, formulation chemists outlining the next roadblock, engineers requesting new product forms or more stringent controls. That’s how our plant has grown its capabilities and why we count on ongoing customer engagement to shape our future suite of phenol-based specialty products.

    Conclusion: Value in Experience, Not Just the Molecule

    Phenol,4-[[4-(2-Propen-1-Yloxy)Phenyl]Sulfonyl]- stands out not as a commodity, but as a compound shaped by experience. Close control from raw material sourcing to finished product shipment ensures the high quality that leading manufacturers require. As users raise the bar on product consistency, safety, and environmental impact, we remain committed to matching industry demands with practical knowledge and direct problem-solving. Through decades of innovation and real-world production, we’ve come to understand that achieving these standards is rarely about marketing language or datasheet promises—it comes from discipline, open partnership, and an unwavering focus on each customer’s real applications.