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HS Code |
584051 |
| Productname | Methyl 2-Benzylacrylate |
| Casnumber | 17639-93-9 |
| Molecularformula | C11H12O2 |
| Molecularweight | 176.21 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 296 °C |
| Density | 1.085 g/cm3 |
| Refractiveindex | 1.541 |
| Flashpoint | 137 °C |
| Solubility | Insoluble in water; soluble in organic solvents |
| Smiles | COC(=O)C(=C)CC1=CC=CC=C1 |
As an accredited Methyl 2-Benzylacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Methyl 2-Benzylacrylate is packaged in a 100g amber glass bottle, with a secure screw-cap and clear hazard labeling. |
| Shipping | Methyl 2-Benzylacrylate should be shipped in tightly sealed containers, protected from light, heat, and moisture. It must be transported in accordance with appropriate chemical safety regulations, clearly labeled, and packaged to prevent leakage. Suitable cushioning and secondary containment are recommended to minimize risk during transit. Consult SDS for additional handling instructions. |
| Storage | Methyl 2-Benzylacrylate should be stored in a tightly sealed container, away from light, heat, and sources of ignition. Store it in a cool, dry, and well-ventilated area, segregated from oxidizing agents, strong acids, and bases. Proper labeling and secondary containment are recommended to prevent leaks and spills. Ensure storage complies with local regulations and safety guidelines. |
Applications of Methyl 2-Benzylacrylate in Industrial ManufacturingAs a direct manufacturer of Methyl 2-Benzylacrylate, we serve customers across advanced polymer synthesis, specialty coatings, and chemical synthesis sectors. Our raw material integrates into mature industrial value chains with precise functional roles, specific dosage requirements, and compliance demands throughout downstream formulation and finishing processes. 1. Acrylic Impact Modifier Intermediates for Engineering PlasticsPolymer compounders use Methyl 2-Benzylacrylate as a reactive monomer to produce specialized acrylic copolymers that improve impact strength in engineering plastics. This application addresses the requirements of automotive, appliance, and electronics manufacturers seeking high-performance materials with controlled flexibility and toughness. End users rely on the product’s unique molecular structure to introduce pendant benzyl groups, optimizing compatibility within multiphase acrylic blends while ensuring stability during high-temperature molding and extrusion processes. Industry compliance standards
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2. Radiation-Curable Coating Oligomers for Printing and PackagingUV-cured formulation producers incorporate Methyl 2-Benzylacrylate to design oligomers with improved film-forming properties and chemical resistance for printing inks and overprint varnishes. The molecular structure’s benzyl group enhances pigment dispersion and controls surface migration, vital for high-speed commercial printing lines on plastics and coated papers. Continuous process monitoring ensures migration limits remain within regulatory thresholds for food packaging and labelling. Industry compliance standards
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3. Synthesis of Specialty Crosslinking Agents in Adhesive ManufacturingHigh-performance adhesive manufacturers select Methyl 2-Benzylacrylate for the copolymerization step when producing crosslinking agents demanded in solvent-free and hot-melt adhesive systems. The pendant aryl group enables increased crosslink density, enhancing adhesion to dissimilar substrates such as metal and engineered composite panels. This monomer supports the development of products requiring long open times and heat resistance after curing. Industry compliance standards
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4. Synthesis Intermediate for Fragrance and Flavor ChemicalsChemical synthesis companies leverage Methyl 2-Benzylacrylate as a key intermediate in the multi-step production of fragrance ingredients and food flavor esters. It serves as a precursor for functionalized aromatic compounds used in personal care formulations and flavoring agents. Native reactivity of the unsaturated ester supports diverse organic transformations, enabling customization of aroma longevity and flavor profile. Industry compliance standards
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Methyl 2-Benzylacrylate stands as one of our most technically rewarding products, reflecting years spent refining both synthesis and purification methods at the production scale. Our teams worked with precision to answer the growing interest coming from specialty polymers, custom monomer applications, advanced adhesive systems, and even the fine chemicals sector developing next-generation materials. This compound, recognized by its clear to pale yellow appearance and subtle, characteristic odor, bridges reactivity and selectivity in a way that classical acrylates never fully achieved.
The molecule consists of a methyl ester on the acrylate framework, with a benzyl group at the 2-position. This brings significant differences from methyl acrylate or ethyl acrylate, both in terms of physical properties and reactivity patterns in polymerization, nucleophilic additions, and modification chemistry. Over the years, chemists and engineers have sought building blocks that offered more than just bulk commodity performance. Through direct experience in production, our process ensures batch-to-batch consistency, which supports demanding customer protocols, especially in materials and coatings where uniformity becomes essential for reproducible performance.
Our main production line for methyl 2-benzylacrylate utilizes a selective esterification, tailored for low levels of residual acid and minimal formation of side products. The process runs at moderate pressure and temperature, maintaining product integrity across volumes. Typical GC purity exceeds 99.0%, and water content sits below 0.2% by Karl Fischer titration. The product maintains stability in sealed drums for extended periods, and we use nitrogen blanketing throughout the chain to reduce risk of oxidation or polymerization during storage and transport. With our history of serving high-end research and manufacturing, we built quality monitoring directly into the factory floor, meaning each dispatch comes with full batch data records.
Methyl 2-benzylacrylate holds a molecular weight of 190.23 g/mol, with a boiling point near 300°C at ambient pressure. At room temperature, it remains pourable and non-crystalline, supporting a variety of handling methods and compatibility with standard reaction setups. Its solubility covers a range of common organic solvents including toluene, chloroform, ethyl acetate, and dichloromethane, without significant hydrolysis in short-term contact with water. The benzyl group confers steric shielding for the β position, so reactions that might proceed rapidly with unsubstituted methyl acrylate can slow or change selectivity, a fact not lost on the synthetic design communities relying on this structure.
It pays to ask why customers increasingly request methyl 2-benzylacrylate rather than settle for more typical acrylate esters. The answer often comes from the need for well-defined polymer architectures. In our own trials with radical and anionic polymerization techniques, the presence of the benzyl group at the 2-position not only shifts polymer growth processes but can lead to narrower molecular weight distributions and reduced transfer reactions, depending on conditions. Researchers leveraging living polymerization chemistries have published cases using this monomer as an active block in multi-segment copolymers, seeking improved thermal and mechanical properties. Our sample program for academic groups helped uncover structure-property relationships that might otherwise have gone overlooked in routine bulk acrylate usage.
In adhesives and coatings, methyl 2-benzylacrylate appears in formulations targeting improved glass transition temperatures and enhanced adhesion to nonpolar substrates. The steric and electronic impact of the benzyl unit resists rapid UV degradation in comparison to methyl acrylate, a fact we traced across long-term weathering studies conducted both in the lab and outdoors in real application environments. Several partners building specialty tapes and sealant systems reported sharper cure profiles and reduced odor after processing, which traced back to the lower volatility and unique surface-active characteristics of this compound.
Beyond large-volume manufacturing, this compound supports the medicinal and agrochemical spaces. Medicinal chemists value its reactivity in Michael addition and conjugate coupling steps when searching for lead analogs with distinct hydrogen bond acceptor and donor profiles. In our own collaboration projects, methyl 2-benzylacrylate was found to outperform methyl acrylate and ethyl acrylate in reactions requiring selective alkylation, especially in crowded target molecules. The result: faster routes to novel chemotypes and improved conversion rates across a range of solvent systems. In crop protection, fine chemical groups designing new herbicide candidates looked at this monomer for selective ring closures, noting that the increased steric bulk prevents overalkylation in later synthesis steps.
Producing methyl 2-benzylacrylate for demanding use means more than just securing starting materials and monitoring reaction vessels. Early in development, we encountered bottlenecks linked to by-product removal and batch uniformity. Rather than implement generic off-the-shelf methods, our engineers designed a hybrid purification step for excess alcohol, unreacted acid, and trace benzyl chloride elimination. Analytical chemistry guides every run, using both HPLC and GC-MS for impurity profiling and forensics. Our customers regularly request custom finished purity specifications or blended grades, which our operations team fulfills through close communication. We run campaigns based on customer preference—some prefer bulk intermediate solutions, others need chromatographically purified, isolated neat monomer for analytical work. This flexibility is possible because every stage runs on in-house engineering and not on toll-manufacturing frameworks, giving us tighter oversight and real-time process improvement.
Addressing concerns about contaminants like heavy metals, residual initiators, and color bodies, we adopted additional in-process QA. Lab insights lead to real investment on the plant floor. Years ago, a major customer flagged an isomeric contaminant after scaling their pilot line. We refined our protocol to minimize thermal rearrangements during heating, added peroxide scavengers, and provided analytical breakdowns on request. These refinements mean that our methyl 2-benzylacrylate now shows high repeatability and transparency, especially valued by regulatory-driven sectors.
As a manufacturer, it can be tempting to treat acrylate esters as interchangeable. Direct experience disproves this regularity very quickly. Many commodity acrylate users expect methyl acrylate, ethyl acrylate, or even butyl acrylate to deliver in a pinch, yet this often results in troubleshooting and batch rework. The benzyl group in methyl 2-benzylacrylate isn’t just a minor structural tweak: the aromatic ring changes electron density across the double bond, modulates both reactivity towards radicals and nucleophiles, and prevents runaway side reactions in finely tuned catalyst systems. Makers of optical polymers, for instance, reported less yellowing and crisper refractive indices after switching from conventional acrylates to this more specialized grade.
Physical handling also reflects the underlying chemistry. Standard acrylate esters can suffer from volatility and off-gassing, requiring higher-grade fume extraction in large applications, especially during hot-melt or UV-curable manufacturing. Because of its higher molecular mass and lower vapor pressure, methyl 2-benzylacrylate enables longer pot life under ambient conditions and less loss to evaporation or odor nuisance. We have observed this difference not only in the lab but on facility floors where solvent cost and odor control matter. In some regions, strict air emissions laws have prompted customers to shift away from lower molecular weight acrylates; methyl 2-benzylacrylate answers those restrictions without sacrificing formula flexibility.
From a reactivity standpoint, methyl 2-benzylacrylate resists uncontrolled chain transfer, making it a choice for specialty copolymers, fine chemical intermediates, and functionalized polymers. In our internal comparative polymerizations, the product supports higher conversion rates in anionic and radical conditions, especially when paired with tailored initiators or catalysts designed for aromatic monomers. Selectivity proves superior, as unwanted side reactions fall sharply compared to plain methyl acrylate or ethyl acrylate, resulting in purer, more consistent output.
Seasoned chemists and process engineers ask about handling, storage, and downstream utility before selecting a new monomer. Our warehouse teams adopt double-sealed drums and nitrogen protection down the entire supply chain. Customers in Southeast Asia once reported local humidity spikes causing premature polymerization. After reviewing these events, we adopted new drum head technologies and detailed anti-static and desiccant guidelines. These adjustments minimized returns and reduced downtime on customer lines. For groups running continuous reactors or pilot-scale production, our technical team supplies handling protocols gleaned from our own experience—whether it’s drum heating or managing returnable containers.
Our conversations with customers highlighted the diversity of end-use. Analytical teams at consumer product companies probe trace impurities, especially where downstream uses or regulatory filings require full compositional disclosure. We respond with transparency—providing full certificates with each shipment, including GC, NMR, and infrared data. No two industrial settings are exactly alike: some partners operate semi-manual lines in regions with unpredictable climates, while others manage ultra-high-throughput synthesis. By approaching every use case as unique, we offer production planning insights, after-sales support, and, if necessary, technical troubleshooting, all informed by our years manufacturing this chemical.
We recognize the cross-disciplinary role methyl 2-benzylacrylate plays. Small-scale research sites working on organic electronics care about minute impurities and batch aging, so we devised monitoring protocols to track product freshness and contaminant migration. Larger polymer manufacturers ask for periodic large-scale deliveries and robust technical follow-up. Developing long-term business ties means listening to site-specific challenges and collecting feedback for continuous improvement.
As manufacturing professionals, we must take responsibility for chemical stewardship. Methyl 2-benzylacrylate poses moderate handling risks. Our plant adopted enhanced ventilation and regular monitoring for airborne contaminants, both for operator safety and quality assurance. By managing temperature and oxygen exposure in the storage area, we keep auto-polymerization to a minimum. Deciding to add advanced oxygen scavengers, safer drum linings, and pressure-relief measures stemmed from field reports—not regulatory minimums.
Waste minimization grows more urgent every year as environmental frameworks tighten. We recovered more than 90% of reusable solvents across our lines and invested in new filtration units that enable continuous side-stream purification. These changes arose after studying solvent loss and off-gassing at our own site. Following these improvements, on-site air monitoring showed a clear reduction in VOC emissions. Customers running critical environmental audits often request in-depth safety reviews; we welcome joint audits and site visits so buyers can see risk management in practice.
On the application side, methyl 2-benzylacrylate’s elevated boiling point and low vapor pressure cut occupational exposure compared to its smaller analogs. Most users incorporate straightforward PPE—nitrile gloves, lab coats, and safety goggles—along with local exhaust ventilation at handling points. Our own health and safety advisers contributed advice into packaging choices, spill response planning, and regulatory updates, ensuring consistency in both plant and customer compliance programs.
Staying competitive means more than filling orders. The team reviews feedback from every batch that leaves our facility, with chemists and process engineers troubleshooting, refining, and exploring ways to elevate performance. Whether a customer requests a tighter impurity profile, new packaging formats for lean logistics, or collaborative development projects, our approach favors direct engagement. The result: methods honed to the realities of scale-up chemistry and downstream use rather than assumptions about marketplace averages.
Earlier product generations lagged behind on purity and stability, pushing some customers away in favor of bespoke, smaller-scale alternatives. By investing in technology, process control, and in-house training, output now matches or exceeds expectations held by top R&D groups worldwide. The benefits show up directly at application sites, whether polymer labs, adhesive manufacturers, or specialty synthesis groups. Trust is earned batch by batch, demonstrated in both analytical records and end-use performance.
One lesson stands out: open dialogue with users pays tangible dividends. Several years back, a partner working on nanostructured copolymers needed a blend-grade methyl 2-benzylacrylate with trace stabilizer for UV polymerization. Standard products did not meet their window for gel point control. At their request, the technical team worked through reaction screens, adjusting stabilizer content and altering headspace conditions in packaging until the onsite results matched specification. This level of engagement extends beyond transaction—it reflects mutual investment in successful application.
The gradual shift away from lowest-cost commodity acrylates tells an industry-wide story. Makers of advanced polymers, functional coatings, high-performance adhesives, and specialty materials now rely on unique molecular frameworks to deliver competitive and regulatory advantage. Through daily contact with the realities of large-scale production, we see that methyl 2-benzylacrylate upholds the promise of controlled performance, batch reliability, and application versatility. These attributes are not theoretical; they arise from continuous work in synthesis, purification, packaging, and after-sales support.
As demand for specialty monomers and building blocks increases, production protocols and real-world experience inform every stage of our operation. The partnership that develops between manufacturer and user ensures the compound’s capabilities fully translate to the application environment. Whether for the chemist searching for a new route in medicinal chemistry, an adhesive formulator seeking robust bond strength, or a coatings developer requiring weatherable, UV-resistant films, our methyl 2-benzylacrylate offers real-world advantages forged through persistent investment and close attention to feedback.
Methyl 2-benzylacrylate continues to open new avenues in product design and practical chemical engineering. Success stories often start with a single conversation, technical exchange, or a specific application hurdle. Our record shows that focusing on molecular detail, quality, and direct support equips both our operation and our customers to turn chemical insight into significant advances. Investing in quality at every stage underpins not only today’s product expectations but tomorrow’s industry standards.