Anhui Liwei Chemical Co., Limited
Products

4-(6-Methacryloyloxyhexyloxy)Phenol


    • Product Name 4-(6-Methacryloyloxyhexyloxy)Phenol
    • Alias 4-(6-(Methacryloyloxy)hexyloxy)phenol
    • Einecs 412-300-0
    • 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

    167924

    Product Name 4-(6-Methacryloyloxyhexyloxy)Phenol
    Cas Number 133405-04-2
    Molecular Formula C16H22O4
    Molecular Weight 278.35 g/mol
    Appearance White to off-white solid
    Melting Point 56-60°C
    Purity Typically >98%
    Boiling Point No data available
    Solubility Soluble in organic solvents (e.g., DCM, ethanol)
    Storage Conditions Store at -20°C, protected from light and moisture

    As an accredited 4-(6-Methacryloyloxyhexyloxy)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25 g amber glass bottle with a secure screw cap, labeled “4-(6-Methacryloyloxyhexyloxy)Phenol”, displaying safety and handling information.
    Shipping **Shipping Description:** 4-(6-Methacryloyloxyhexyloxy)phenol is shipped in sealed, airtight containers, protected from light and moisture. It is packed according to standard chemical safety protocols, with clear labeling and documentation. Transport follows regulations for non-hazardous chemicals, ensuring avoidance of extreme temperatures and physical damage during transit.
    Storage 4-(6-Methacryloyloxyhexyloxy)Phenol should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to heat, oxidizing agents, and direct sunlight. Store at recommended temperature conditions—preferably below 25°C—and label the container clearly. Follow all safety guidelines for handling chemicals to prevent unwanted reactions or degradation.
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    Tel: +8615380400285

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    Certification & Compliance
    More Introduction

    4-(6-Methacryloyloxyhexyloxy)Phenol: A Deep Dive From the Manufacturing Floor

    Introducing a Key Specialty Monomer from Our Reactors

    Bringing 4-(6-Methacryloyloxyhexyloxy)phenol to life means working through the kind of careful chemistry and practical engineering only those close to production truly understand. We see firsthand what distinguishes this specialty monomer and why resin developers, polymer chemists, and advanced materials labs keep coming back for this unique building block. Its performance in cutting-edge polymer systems hinges on the way we manage purity and consistency at every batch.

    Model, Structure, and What That Really Means for Chemists

    The product carries a streamlined molecular backbone—phenol substituted through a six-carbon flexible spacer with a methacrylate group. This particular structure blends two worlds: the rigidity and interaction potential of a hydroxylated aromatic ring, and the reactivity of a methacrylate ready for radical polymerization. Practically, that’s the difference between a monomer that joins any old resin and one that expands what crosslinking chemists can do.

    We’ve set up the model designation—commonly “6-MHP” on our site—based on the six-carbon length in the oxyalkyl linker. In trials, we found that shorter linkers reduce flexibility in the final polymer chain, pinching mechanical properties and sometimes upsetting solubility in common solvent systems. Go too long with the chain, and intermolecular anchoring weakens. After extensive internal screening, we fixed on the hexyl chain as the actual sweet spot: enough length for mobility, enough control for rigidity.

    Specifications: The Kind of Detail Only a Manufacturer Notices

    Our technical staff obsesses over residual solvent content, precise assay, moisture uptake, and whether free radical inhibitors reach the right level for stable shelf life. Not all producers hit the same degree of purity. Trace byproducts from etherification and methacrylation can be nearly impossible for resellers to notice, but polymer builders feel them—clouding UV-cure resins, stalling network formation in adhesives, or leading to persistent odor in finished photopolymers.

    Each produced batch passes a rigorous panel: GC-MS to shore up single-digit ppm on residual unreacted starting material. Water content regularly sits near Karl Fischer values below 0.05%. The viscosity, always measured at a set temperature, serves as an indirect proof of batch homogeneity and successful elimination of higher molecular weight side products. Our consistency translates into real-world confidence for downstream curing, particularly where medical polymer, optical coatings, or electronics encapsulants are sensitive to minute contamination.

    Usage: Beyond Simple Monomer Chemistry

    We see most users targeting the co-polymerization of 4-(6-Methacryloyloxyhexyloxy)phenol in UV-curable resins and advanced adhesives. The methacryloyl group creates plenty of free radicals under UV or thermal initiation. That’s a simple theoretical benefit, but what we’ve watched on the production side tells us more. Customers consistently report higher glass transition temperatures by swapping in this phenolic monomer, noting improved resistance against hot/cold cycling—vital in electronic conformal coatings and advanced screen-printing pastes.

    Unlike standard hydroxyethyl or hydroxypropyl methacrylates, which set the lower floor for crosslink density and chemical resistance, the phenol core in our monomer brings in extra hydrogen-bonding potential. We’ve found that users form denser networks with fewer mobile segments. That matters as soon as you want tougher, scratch-resistant, or more dimensionally stable polymers but want to avoid introducing toxic crosslinkers or losing processability.

    Dental researchers, for instance, pull our product into new adhesive formulas set to last through hundreds of brushing and chewing cycles. On the electronics side, it shows up in encapsulants and coatings, quietly protecting circuit assemblies against flux residues, moisture, and environmental drift. These aren’t theoretical performance boosts. Over the years, direct line tests and client feedback have shown us: parts built with this monomer resist solvent pickup, keep their clarity even under extended high-intensity UV, and hold up against punishing cycling during device assembly.

    Biomedical engineering groups, especially, appreciate the dual profile: a hard, glassy thermoset backbone, but one carrying pendant hydroxyl groups. That extra functionality opens the door for post-polymer modification—surface grafting, enzyme attachment, or secondary crosslinking routes. We’ve worked with coatings specialists using it to anchor antibody fragments or oligonucleotide chains for biosensor applications. This isn’t just a story about one reaction; the practical chemistry makes a difference on the factory floor in both usability and new product design.

    Comparison to Other Monomers: Nuances That Matter in Real Production

    Off-the-shelf monomers often boil down to a handful of basics—hydroxyethyl, hydroxypropyl, methyl, t-butyl analogs. Every manufacturer that’s invested time into pilot-scale testing learns just how finicky polymer properties can get when only short-chain or non-aromatic additives are present. We’ve run direct A/B cures: using hydroxyethyl methacrylate under standard photoinitiated crosslinking, then swapping in 4-(6-Methacryloyloxyhexyloxy)phenol at an equal ratio. The cured films aren’t alike. Phenolic inclusion routinely boosts Tg by 10–20 °C, slows down hydrolytic breakdown, and gives a glassier, more robust optical finish.

    In production, consistency often comes down to how well a supplier manages side reactions and controls molecular weights. Generic monomers from high-volume plants sometimes contain oligomers or badly emulsified side fractions, pushing up haze and color. We tackle that with extra purification cycles—working closely between synthesis and quality control so that polymer chemists don’t have to worry about foul odors, off-colors, or erratic cure behaviors.

    A number of buyers arrive after struggling with shrinkage-related cracking or incomplete cure fronts in multilayer films. Standard methacrylates lack the aromatic-ether bridge this monomer provides; without it, hot spots in UV systems or areas shielded from initiator don’t cure fully. Our product’s backbone—and the carefully selected hexyl spacer—add flexibility and extend the working time under ambient conditions, without losing rigidity in the cured resin.

    Challenges On and Off the Reactor

    Running the etherification and methacrylation steps that build 4-(6-Methacryloyloxyhexyloxy)phenol is demanding. We work under strict inert-gas purging. Trace oxygen can poison free radical inhibitors; a failed seal leads to runaway polymerization at the wrong stage. Raw material selection, especially for phenol precursors and alkylating agents, shapes both the reaction yield and byproduct profile. Our engineering team tunes the reactor conditions to minimize fouling—critical for reducing reactor shut-down days and maintaining long-term, predictable output.

    Each time we scale from pilot plant to industrial batches, we confront new thermal management demands. Exotherms from the methacrylate group addition ramp up temperatures quickly—without proper temperature tracking and staged reagent addition, you risk out-of-spec product or hazardous conditions. Reworking off-spec product isn’t always possible. We opt to scrap and restart over risking doubts about purity or inhibitor level.

    Customers also ask us about storage and handling. The risk of premature polymerization, particularly during summer shipments or extended storage, has pushed us to invest in extra refrigerated warehousing and moisture-protected packaging. Pre-shipment testing includes not just standard chemical analysis but also stress-testing for thermal stability and cure inhibition.

    We’ve found it pays off for customers needing reliability over months, not just weeks. Some labs design projects that take months for final cure, stress testing, and validation. They need to trust that each kilogram from us will match both the physical specs and the shelf stability posted on our documents. That reliability comes from lived production experience, ongoing feedback with polymer development teams, and a commitment to maintaining communication between QC, shipping, and technical support.

    Why Demand Persists in a Competitive Market

    Chemists choose 4-(6-Methacryloyloxyhexyloxy)phenol for tangible, seen-in-the-field reasons. It handles the balance between rigidity and flexibility non-aromatic methacrylates just can’t. Customers reporting failures from cheaper monomers—cracking, yellowing, or incomplete cure—return to materials made with a phenolic anchor and recognize improved outcomes.

    Some try to replace it with more basic monomers out of cost pressure, but they turn back after long-term reliability testing highlights subpar results. Performance in UV-curable systems for fiber-optic connectors, high-resistance dental composites, and optically clear coatings comes up again and again in feedback. This specialty choice rarely dominates the lowest-cost bracket, yet users facing demanding environmental, thermal, or processing conditions do not accept cut corners.

    R&D investment on our side targets not just polymer property improvement, but the day-to-day operational headaches for formulators and manufacturing lines. Stable viscosity, reliable reactivity, and well-controlled side product profiles matter more to chemists than vague product specs listed in a spreadsheet.

    Solutions Leaving the Pilot Plant—How Collaboration Drives Real Results

    Years of fielding technical queries and troubleshooting alongside users has shaped the way we support this monomer. We’ve run multi-week sample testing for research teams needing single-digit ppm impurity cutoffs. Collaborations with adhesive and coating developers led us to manual tweaks in inhibitor loading and fill size based on seasonal shipment cycles.

    Not every application follows a recipe. Polymer scientists will mix in new UV initiators, change solvent blends, or introduce new co-monomers. The reliable response from our quality teams comes from knowing firsthand how the material behaves under UV, thermal, or dual-cure systems. Over time, this approach pushes incremental improvements: more resilient packaging, tighter analytical screening, faster sample turnarounds.

    We don’t see our job as filling a catalog slot. The ability to keep production lines running with minimal surprises is part of what separates our approach. Documented test results, direct communication about any batch anomalies, and an open line with the chemists actually using the product bring efficiency and trust. Supply chain interruptions—like raw material shortages or logistical delays—spike anxiety for industrial users. Our strategy links real-time inventory tracking and prior notification so customers aren’t left exposed mid-project.

    Looking Toward the Future With an Eye on Real-World Demands

    Materials science is always moving. Formulators ask for higher performance out of less material, want to cut VOC emissions, and need functionality their old recipes can’t offer. 4-(6-Methacryloyloxyhexyloxy)phenol fits the niche for labs and manufacturers ready to add complexity and performance to polymers—but that only works if the supply chain and technical support keep pace.

    Sustainability pressure grows as regulations evolve. We aren’t waiting for new laws to rethink solvents, byproduct handling, or emissions from our plants. Investment into waste minimization, solvent reuse, and safer chemical intermediates leads to better product and less headache for environmentally sensitive clients. That proactive approach gives major customers confidence their choices will keep them ahead of compliance or customer demands.

    Fielding requests for greener, safer, and even higher-purity variants continues—especially from medical device and electronics developers. We coordinate with purchasing, R&D, and regulatory teams to prioritize batch changes or trace impurity cutoff targets. Sometimes customers request full traceability of raw materials or extra documentation; we provide what’s needed, drawing from records and continuous production improvements across our facility.

    The Result: More Than Just a Chemical, a Platform for Innovation

    Bringing a specialty monomer to scale and consistently outperforming mainline commodity products doesn’t happen from isolated R&D or sporadic attention to detail. It is an ongoing collaboration—between the engineers on the reactor floor, the lab personnel screening impurities, the shipping staff managing storage, and the chemists pushing boundaries in their development labs.

    Every kilogram of 4-(6-Methacryloyloxyhexyloxy)phenol leaving our site carries the weight of practical experience and deep understanding of the chemistry’s demands in production and real-world application. By focusing on what makes this compound special—the aromatic backbone, the carefully chosen linker, the tight purity—users in fields as diverse as electronics, dental science, coatings, and biomedical engineering get tools they trust. Our commitment, borne out of years on the manufacturing line, ensures that this isn’t simply another ingredient, but an enabler for next-generation materials.