Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Ethyl 3-Benzoylacrylate

    • Product Name Ethyl 3-Benzoylacrylate
    • Alias Ethyl 3-benzoylpropenoate
    • Einecs EINECS 246-302-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    677197

    Product Name Ethyl 3-Benzoylacrylate
    Cas Number 22029-76-1
    Molecular Formula C12H12O3
    Molecular Weight 204.22
    Appearance White to off-white powder
    Boiling Point 375.4°C at 760 mmHg
    Melting Point 63-65°C
    Density 1.17 g/cm3
    Solubility Slightly soluble in water, soluble in organic solvents
    Refractive Index 1.560
    Smiles CCOC(=O)C=C(C1=CC=CC=C1)C=O
    Storage Conditions Store in a cool, dry place, keep container tightly closed
    Purity Typically ≥98%
    Flash Point 180.5°C
    Synonyms Ethyl benzoyl acrylate

    As an accredited Ethyl 3-Benzoylacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle, 100g, with a screw cap. Label displays "Ethyl 3-Benzoylacrylate," CAS number, hazard symbols, and lot number.
    Shipping Ethyl 3-Benzoylacrylate is shipped in tightly sealed containers, protected from light and moisture. Transport follows all applicable regulations for hazardous chemicals, with appropriate labeling and documentation. It is typically shipped at ambient temperature unless specified otherwise, ensuring safety and integrity during transit. Handle with gloves and protective gear upon receipt.
    Storage Ethyl 3-Benzoylacrylate should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Store at room temperature, ideally between 15–25°C. Ensure proper labeling and maintain chemical inventory protocols for safety and traceability.
    Application of Ethyl 3-Benzoylacrylate

    Applications of Ethyl 3-Benzoylacrylate in Industrial Manufacturing

    Ethyl 3-Benzoylacrylate serves as a critical intermediate in several chemical manufacturing sectors. As the primary producer, we observe its strategic value in pharmaceuticals, agrochemicals, specialty coatings, fragrance synthesis, and advanced polymer development. The following scenarios detail the material’s downstream roles, integration protocols, quality system expectations, and typical finished products.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use this raw material in the synthesis of active compounds for anti-inflammatory and anti-cancer therapies. It enters multi-step batch reactions, facilitating Knoevenagel condensations and Michael Addition routes. The high-purity grade aligns with stringent impurity thresholds. Downstream users integrate the material post-column chromatography, ensuring controlled conversion to targeted molecular scaffolds. The material supports scale-up from pilot to commercial volumes, requiring reliable analytical scrutiny at every stage. Final APIs may undergo full cGMP batch record review.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) residual solvent and impurity limits
    • EU GMP Volume 4, Part II for chemical APIs
    • FDA 21 CFR Parts 210/211 – API manufacturing controls

    Typical usage ratio

    • Usually 5–15% of total reactants by mass, with precise ratio adjusted to substrate stoichiometry and reaction kinetics

    Downstream process integration

    • Charged after solvent pre-conditioning in reaction vessels
    • Subjected to controlled temperature and inert atmosphere synthesis
    • Excess reagent removal by rotary evaporation before crystallization

    Final product types

    • Pharmaceutical active intermediates for kinase inhibitor synthesis
    • Lead compounds for preclinical oncology projects
    • Specialty pharmaceutical building blocks

    2. Agrochemical Active Ingredient Synthesis

    R&D and production facilities in the crop protection sector employ this compound to develop selective herbicidal agents. During process chemistry, it acts as a Michael acceptor, enabling synthesis of acrylate-functionalized agrochemicals. Process engineers monitor reaction selectivity and byproduct formation, ensuring alignment with environmental and personal safety regulations. Purification steps rely on phase separation and preparative chromatography before downstream formulation. Application intent dictates the scale and quality needs, directly impacting agrochemical registration workflows.

    Industry compliance standards

    • REACH registration (EC 1907/2006) for chemical intermediates
    • OECD Guidelines for Testing of Chemicals, Section 1
    • ISO 9001:2015 quality management
    • Globally Harmonized System (GHS) labeling/transport

    Typical usage ratio

    • Varies from 3–10% in synthesis batches, tuned to precursor chain length and reactivity of partner molecules

    Downstream process integration

    • Introduced at controlled-phase transition points for acrylation steps
    • Inline HPLC used to verify conversion rates before product isolation
    • Integrated in continuous or batch reactor configurations

    Final product types

    • Pre-emergent herbicide intermediates
    • Acrylate-based insect growth regulator synthons
    • Active herbicidal compounds for registered crop protection packages

    3. UV-Curable Coating Formulations

    Specialty coating and ink producers incorporate this compound to formulate UV-curable systems for plastic, wood, and metal surface protection. Resin chemists value its reactivity in synthesizing functionalized acrylic oligomers. Exact integration depends on gloss, adhesion, and curing speed demands. Dispersion and stability require pre-mixing under nitrogen. The material participates in oligomer backbone modification before UV initiator blending and thin-film application. End products undergo strict in-line QA for residual monomer and photo-curing completeness prior to shipment.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for coatings
    • ASTM D7767 for UV Coating Cure Quality
    • RoHS Directive (2015/863/EU) for electronic finishes
    • ISO 9001:2015 in production quality assurance

    Typical usage ratio

    • Typically 2–6% as a co-monomer in UV-curable acrylate blends, adjusted for viscosity and hardness targets

    Downstream process integration

    • Incorporated during initial oligomer synthesis and diluted after functionalization
    • Pre-filtered before UV initiator addition to minimize haze and particle contamination
    • Roll-to-roll or sheet-fed coating lines use continuous dosing pumps

    Final product types

    • Protective coatings for touchscreen panels
    • UV-cured varnishes for engineered wood floors
    • Specialized inkjet receptive layers for high-speed printing

    4. Fine Fragrance Intermediates

    Fragrance compound manufacturers utilize this raw material as a structure-defining intermediate for complex aroma chemicals. The substance undergoes condensation and cyclization with various aldehydes, expanding the palette of musky or floral notes for perfumery. Quality assurance teams implement rigorous GC-MS fingerprinting to ensure olfactory purity in finished isolates. As a manufacturer, we address requirements for contamination-free, food-grade compliant handling, supporting both IFRA-aligned safety and product performance. The downstream blending process dictates exact batch dilution and incorporation.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards for aroma chemicals
    • ISO 9235:2013 for classification and labelling
    • IFRA/IOFI Labelling Manual for composition compliance
    • REACH Annex XIV restrictions for import/export

    Typical usage ratio

    • Ranges between 1–4% in intermediate synthesis; final inclusion in aroma profiles depends on volatility and intensity targets

    Downstream process integration

    • Combined in multi-stage aroma compound synthesis post-primary alcohol distillation
    • Processed in inertized vessels to prevent oxidative degradation
    • Traceable via batch GC-MS retention indexing

    Final product types

    • Fine fragrance ingredients for eau de parfum bases
    • Fragrance isolates in luxury detergents
    • Signature notes for skin-contact personal care products

    5. Advanced Polymer Functionalization

    Polymer R&D facilities integrate this specialty acrylate for targeted molecular weight adjustment and crosslink density control. The material enables syntheses of high-gloss, abrasion-resistant polymers for electronics and automotive markets. Lab teams implement rigid stoichiometric calculations to tune flexibility, refractive index, and thermal resistance. Downstream, technicians blend the material in reactor vessels under controlled heat and vacuum, integrating it before or after initiator addition depending on desired polymer morphology. Final materials undergo profile testing for solvent resistance and clarity according to end-user applications.

    Industry compliance standards

    • ISO 10993-5 for polymer biocompatibility (electronics casings)
    • ASTM D638 for polymer tensile properties
    • RoHS Directive (2015/863/EU) for restricted substances
    • IEC 61249-2-21 for halogen-free polymers

    Typical usage ratio

    • Ranges from 0.5–3% in copolymerization charges, tuned per final mechanical and optical targets

    Downstream process integration

    • Fed into reactor after primary monomer pre-polymerization
    • Monitored via in-process FTIR for conversion tracking
    • Incorporated into both continuous and batch polymerization

    Final product types

    • High-durability smartphone housings
    • Precision optical films for LCD screens
    • Specialty elastomers for automotive interiors
    Free Quote

    Competitive Ethyl 3-Benzoylacrylate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Ethyl 3-Benzoylacrylate: An Inside Look from the Production Floor

    Daily Work with Ethyl 3-Benzoylacrylate

    Ethyl 3-Benzoylacrylate doesn’t show up on mainstream news feeds or gather consumer awareness like some specialty chemicals. Its value grows out of steady work, not marketing trends or enthusiasm. From the view of our chemical plant, this compound stands as a quiet workhorse across pharmaceutical, agrochemical, and materials labs. The care we put into crafting each batch connects directly to the reliability of downstream products.

    Consistent quality matters here more than anywhere because a small impurity ripples through every reaction that follows. In our daily routine, specialists in our synthesis workshops weigh out raw materials with robust repeatability, prepare clean reactors, adjust vacuum lines, and monitor temperature profiles by hand as well as through instrument monitoring. Over repeated syntheses, we’ve learned that controlling temperature rise during condensation protects yield and purity better than chasing numbers alone. Not every procedure guideline can account for humidity shifts or idiosyncrasies of a new solvent lot, so our operators adapt with the kind of intuition that only long exposure brings.

    Product that leaves our hands carries an identity, not just a label. Batches of Ethyl 3-Benzoylacrylate pass internal checkpoints, from thin-layer chromatography to spectral fingerprinting with NMR and IR, and we carry out Karl Fischer titrations to monitor water content despite specification paperwork that rarely mentions those last lines. We recognize the significance of preventing even small traces of byproducts such as benzoic acid or acrylate oligomers; labs that source from us know they can scale their reactions without the persistent chemical “background noise” that creeps in from careless synthesis or packed warehouse trading.

    Model Types, Real-World Specificity, and Batch-to-Batch Discussion

    The “model” of Ethyl 3-Benzoylacrylate doesn't follow widget logic or SKU-driven thinking. We don’t stamp out endless identical units from a mold. Variability grows from source material lots, reaction scale, and purification cycles. Our main batch sizes typically run in the tens of kilograms—enough to serve pilot plant work at an API producer or to keep a fragrance R&D group engaged for weeks. Some clients return to us year after year, requesting the same secondary specifications: lower aldehyde residuals, higher UV purity at 254 nm, or an extended melting point range for specialty analysis.

    Unlike simple esters or bulk acrylates, Ethyl 3-Benzoylacrylate requires extra attention during isolation. The molecule’s structure features both an activated benzoyl group and a conjugated alkene, so minor tweaks in crystallization can result in subtle changes in color, scent, or handling performance in the next stage of synthesis. For a company planning to develop an active pharmaceutical ingredient, small physical changes predict downstream difficulties—so we record and track physical appearance, crystal habit, and solubility checks in ethanol or acetonitrile with every lot.

    As a result, every order we ship reflects choices we made about fermentation-derived benzoic acid quality, the quality of ethanol we procure, the phase separation method at intermediate purification steps, and the drying curve we selected for a given season. These aren’t abstract decisions made by corporate committees; they’re choices made by our frontline technicians, lab staff, and synthesis teams through repeat interaction with real product.

    Where Ethyl 3-Benzoylacrylate Goes: Downstream Uses

    Chemistry is full of behind-the-scenes contributors, and Ethyl 3-Benzoylacrylate stands as one of them. For pharmaceutical teams, this compound assists in building more complex scaffolds—often forming the basis for substituted cinnamic acid derivatives, or serving as a coupling partner in nucleophilic addition ladders. The ethyl ester group proves easier to remove by standard basic hydrolysis, so downstream transformations can happen with a lighter reagent load than bulkier protecting groups require. The benzoyl motif, retained through well-chosen reactions, carries through to final active ingredients or high-value intermediates for novel drugs, agrochemicals, and materials.

    We’ve seen research groups incorporate our Ethyl 3-Benzoylacrylate in cycloaddition studies, in photochemical reaction development, and as a template for fluorophore synthesis. It takes only minor adjustments to solvent or temperature to allow this starting material to feed directly into organic electronics prototypes, or as a precursor to flavor ingredients with defined UV–Vis absorption. Our in-house technical liaisons keep notes on which solvent blends help researchers avoid emulsion phases or drop extraneous byproducts early in a route—a level of feedback made possible by direct conversations with project leads and hands-on review of our own purification endpoints.

    In the agricultural sector, it finds use as a bridge intermediate on the path toward herbicide or fungicide active ingredients, where substitution on the benzoyl ring sets up further diversification for structure–activity studies. Fragrance chemists chase particular aroma profiles using this ester scaffold, since post-synthetic transformations of the benzoyl or acrylate backbone lead to ketones, aldehydes, or more elaborate esters with “green” or floral notes.

    In materials and coatings, Ethyl 3-Benzoylacrylate provides a conjugation platform. Tuning electronic properties by functionalizing the aromatic ring gives materials scientists another lever for controlling polymer backbone reactivity or enhancing cross-link density. We’ve watched as some manufacturing partners use this compound to prepare photo-reactive resins, placing it in a growing lineup of specialty acrylates optimized for light-curing applications.

    No Substitute for Manufacturer Control: Product Differences that Matter

    Ethyl 3-Benzoylacrylate stands out from generic acrylates and esters with its dual reactivity. Most traders lump it in with basic cinnamic acid ethyl esters or methyl acrylates, but those cutting corners overlook major functional contrasts. The benzoyl group is more than decorative—its electron-withdrawing power and steric footprint alter reactivity throughout any synthetic sequence. That means a missed purification step, or excessive heat during synthesis, can introduce side products that hamper yield for R&D chemists or cause headaches during scale-up.

    Since we control our starting points all the way back to crude benzoic acid, our staff can spot changes in color, scent, or crystal habit before batch records go final or QC signatures appear on a shipment. By contrast, traders swapping product in sealed bags or relying on drop-shipment from warehouse inventory may not catch these variations in time to alert an end user. Over the years, several customers have told us how even low-percentage off-spec batches from a previous source halted their pilot plant for days when an impurity caused a surprise exotherm—or gummed up lines with high-melting byproducts.

    We insist on full traceability not because it’s a buzzword for compliance but because we remember what happens when poorly documented material hits a technical bottleneck. In our shop, we keep spectral archives on each lot and maintain background checks on all major solvents and additives. If a researcher or process chemist needs to know residual aldehyde values, or whether our ethyl 3-benzoylacrylate matches a custom melting point range, we send that supporting data by next business day. Our close connection to manufacturing means tailored reruns are possible; some pharmaceutical clients have unique impurity thresholds we address by modifying purification steps, not by swapping out product from a catalog.

    Process Insights: What We See that End Users Can’t

    Standing inside the plant in the early morning, the reality of chemical manufacturing diverges from what spreadsheets or material data sheets suggest. Each reactor load runs differently as seasons change. Summer production brings higher water content in feeds, so drying times stretch. Winter means slower solvent separation. Not every batch will crystallize with textbook color or drop out at the same temperature range. For Ethyl 3-Benzoylacrylate, tracking these “minor” variances makes the difference between routine shipment and a lot requiring extra attention. Personnel watch distillation heads for drifts that indicate premature thermal rearrangement—something that matters with this sensitive conjugated molecule. By tracking actual solvent evaporation rates, rather than relying solely on pressure and temperature charts, we minimize the formation of coloring impurities that downstream labs dislike.

    From our end, adjustments in filtration, phase separation, and column chromatography allow us to pull through a cleaner product. Analytical teams flag water sensitivity in batches that show even trace cloudiness after overnight storage. Now and then a customer sends back feedstock solubility data, flagging up issues we wouldn’t catch except through years of collaborative supply. With so much riding on multi-step reactions in drug development or specialty materials, we treat each feedback point as an opportunity to fine-tune the next batch.

    Product packaging never operates on autopilot, either. Packed-out material undergoes internal visual QC just before sealing. Each drum or bag receives additional labeling to flag storage temperature and desiccant requirements. These procedural steps can seem repetitive to newer technicians, but those who’ve responded to shipment complaints involving hydrolysis or caking after an ocean crossing treat these final precautions as non-negotiable.

    Working at the manufacturing level teaches us that collaboration between chemical producers and downstream labs shortens project cycles. Every time we supply suggestions about optimal solvent mixes, or solventless isolation approaches, we see customers enter scale-up phase faster and with less waste. It takes time to gain trust, but the knowledge we share flows both directions: our process operators collect stories from the field, and many improvements to our manufacturing routine grew out of direct researcher and technician feedback.

    Supporting Research and Problem Solving with Reliable Substance Integrity

    Startups and established research labs alike face stringent development timelines. Reactions must proceed smoothly, yields must hold, and analytical teams press for clear data, fast. Ethyl 3-Benzoylacrylate, produced with care at the manufacturer’s level, helps streamline these efforts. End users can approach multi-step synthesis with lower risk, since they aren’t fighting contamination or inconsistency from input materials. Early discovery and scale-up often run on tight budgets and tighter project windows; stopping to verify structure or track an unknown impurity hampers project flow.

    We back up Ethyl 3-Benzoylacrylate shipments with full QC tracing, offering spectral and chromatographic support whenever a customer hits an uncertainty. Our technical liaisons readily discuss the nitty-gritty: which solvent preps reduce side reactions, whether minor modifications in heating ramps can improve batch quality, and how purification changes can shift downstream reactivity. Internal notes, collected across hundreds of lots, give us leverage in troubleshooting real issues. In one case, tweaking the recrystallization temperature by just five degrees reduced formation of a yellow side product, a result not found in standard data sheets, but shared from resolved field problems.

    This substance isn’t meant for standardized, one-size-fits-all manufacturing. It attracts customers looking to build on a core scaffold, tweak structure–activity relationships, or pursue novel reaction sequences. Differentiating by provenance has value in every area where product quality impacts bench work. In the agrochemical sector, optimization projects for new fungicides stem from small changes made possible by reliable starting materials. Feedback loops between our synthesis teams and agricultural research clients keep unnecessary project errors at bay, so field testing can advance without supply chain delays.

    The same holds for those developing advanced dyes, OLED backbones, or specialty coatings. Here, unpredictable solubilities or byproduct formation could set a research team back for months if starting ester material varies widely. From our vantage point, minor lot-to-lot adjustments sometimes carry through to final application performance—a point we raise frequently in conversations with product developers searching for suppliers who take quality seriously.

    Transparency, Traceability, and Commitment to Real-World Outcomes

    Industrial chemistry has long been shaped by pressure from regulators, environmental agencies, and conscientious R&D teams. We openly support transparent supply chains for fine chemicals such as Ethyl 3-Benzoylacrylate not because of external compulsion, but because we’ve seen too many projects derailed by poor communication between traders, resellers, and actual producers. By documenting batch source data and collecting feedback from every major sectors—pharma, agriculture, R&D—we stand accountable to both project outcomes and safety expectations.

    Batch summaries detailing impurity profiles, trace element checks, and extended spectral data leave our facility with each order. Instead of relying on templated lab reports, we build final QC summaries from actual production runs. Common customer requests for data include GC impurity cutoffs, HPLC purity at target wavelengths, or water content checks for direct-use batches. If a requesting team has a specific need—perhaps an exact melting point or guaranteed absence of a certain side-product—our team addresses this directly in the lab, isolated from the generic “MSDS” copy-paste approach many distributors take.

    Clients who run discovery trials for new drugs test our materials within days of receipt. Feedback arrives with urgency and clear description: spectral drift after storage, a slight yellowing on heating, or solubility mismatch. We track outcomes with a focus on practical results, not just meeting statistical quality lines. In our view, an open-door approach to problem reporting, and internal willingness to rerun extra purification cycles as needed, makes us a reliable link in countless project chains.

    If environmental rules or customer needs shift, as they have over the last several years, our production team explores greener alternatives in solvents or tries improved energy efficiency in batch heating. In more than one instance, our team has cut solvent waste through process rebalancing at customer request, supporting eco-focused projects with hard changes rather than paperwork promises.

    Why Manufacturer-Involvement Beats Trading: Stories from the Plant

    Knowledge born from making Ethyl 3-Benzoylacrylate daily offers a view unavailable to traders or secondary suppliers. Direct handling tells our team how even slight increases in ambient plant humidity result in noticeable product differences. Technicians see changes occur in real time—particle size, color gradation, residual odor. We’ve had cases where a single off-characteristic batch, flagged on color by our night-shift team, led to a root-cause trace on an upstream benzoic acid lot, saving a client downstream from a failed synthesis run.

    This kind of connection between production and user marks a sharp distinction from distribution networks that treat each chemical as just another inventory item. If a client needs a batch rerun for adjusted purity or a minimum amount of a specific isomer, we can recalibrate directly through the next batch, communicate expected timelines, and share updated sample results. In our experience, the “manufacture-to-order” approach of direct synthesis allows better fit to client project timelines than the generic inventory-from-stock model.

    We maintain technical backup not out of obligation, but borne from a continuous stream of compound-specific questions and requests—insights that shape how we plan future runs, and improve consistency for users who depend on our materials not once, but week after week, and project after project.

    A Final Word on Value and Next Steps

    Ethyl 3-Benzoylacrylate presents clear differences from lower-tier acrylates, esters, or repackaged fine chemicals. It cannot be commoditized without serious risk to downstream reliability. Structural features mean laboratory and industrial R&D cannot substitute it out of their synthetic plans without sacrificing yield or purity. The direct manufacturer approach brings traceability, technical feedback, and flexible customization into a complex, demanding field.

    As detailed through this window into our daily practice, each kilogram grown, purified, packed, labeled, and shipped reflects accumulated experience by our technicians and process specialists. We field and act on direct feedback, not generic trend data, so each customer’s investment turns into progress, not troubleshooting delays or rework cycles. For any group looking to move research, new product pipelines, or process engineering forward with Ethyl 3-Benzoylacrylate as a foundation, collaborative engagement with an experienced manufacturer remains not just preferred, but essential.