|
HS Code |
881845 |
| Productname | 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone |
| Molecularformula | C17H22O5 |
| Molecularweight | 306.36 g/mol |
| Casnumber | Unavailable |
| Appearance | Light yellow liquid or crystalline solid |
| Solubility | Soluble in organic solvents like ethanol, DMSO, and chloroform |
| Purity | Typically ≥98% (can vary by supplier) |
| Storagetemperature | 2-8°C (cool, dry place) |
| Smiles | CCOC(=O)COC1=CC=C(C=C1)OC(C)=CC=C(C)C(=O)C |
| Iupacname | 1-[2-(ethoxycarbonylmethoxy)-4-(3-methyl-2-butenyloxy)]ethanone |
As an accredited 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 50 grams, sealed with a screw cap, labeled with chemical name, CAS number, and hazard warnings. |
| Shipping | The chemical `2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone` is shipped in tightly sealed, inert containers to prevent contamination and degradation. It is transported under ambient conditions, compliant with relevant chemical safety regulations, and accompanied by a Safety Data Sheet (SDS) for proper handling during transit and storage. |
| Storage | 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone should be stored in a tightly sealed container, away from light, heat, and moisture. Keep it in a cool, dry, and well-ventilated area, preferably under an inert atmosphere such as nitrogen. Store away from incompatible substances such as oxidizing agents and acids. Clearly label the container and ensure proper chemical safety protocols are followed. |
Applications of 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone in Industrial Manufacturing2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone supports multiple high-value industrial applications. The following sections outline real-world downstream sectors using this raw material, with details on compliance, formulation ratios, processing steps, and the resulting end products. 1. UV-Curable Coatings for Electronic ComponentsThis compound enters UV-curable coating systems as a photoinitiator for printed circuit boards, connectors, capacitors, and surface-mount devices. Its absorption profile supports rapid curing under LED and mercury lamps. Engineering teams select this initiator for high-speed production lines where fine pitch, minimal migration, and stable photoactivity are critical to performance and downstream reliability testing. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. UV-Initiated Adhesives for Medical Device AssemblyThe molecule functions as a photoinitiator in UV-cured adhesives for disposable and reusable medical devices, such as blood filters, syringe bodies, and dialysis panels. Device manufacturers select this ingredient to balance adhesive cure speed and mechanical strength while maintaining low residual extractables, which supports biocompatibility testing and sterilization resistance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. High-Performance Optical Fiber CoatingsFiber optic manufacturers use this compound in UV-cure primary coatings to protect the glass core during drawing and cabling. The photoinitiator determines curing speed, modulus, and yellowing stability in thin coatings exposed to high-energy lamps. Precision in initiator loading assures performance under extended thermal aging and damp heat cycles, which affect transmission loss and mechanical integrity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Inkjet Printing Ink FormulationsThis substance acts as a photoinitiator in UV-cure inkjet inks, enabling rapid dot fixation on packaging films, labels, and industrial substrates. Ink manufacturers exploit the compound’s fast surface curing and stable reactivity profile, which helps meet regulatory limits on leachables and odor while maximizing machine throughput in high-speed digital presses. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. UV Protective Varnishes for Automotive InteriorsAutomotive OEMs and their tier suppliers deploy this initiator in UV-cured varnishes, enhancing surface hardness and gloss retention of dashboards, instrument panels, and decorative trims. The ingredient supports rapid line speeds and high crosslink density, critical for achieving weather resistance, chemical durability, and scuff resistance in interior applications subject to sunlight and VOC standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone 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
Flexible payment, competitive price, premium service - Inquire now!
Our team has spent years refining the process to synthesize 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone. This isn’t just one of those bench-scale molecules. Every stage, from selecting raw aromatic compounds to choosing the right alkylation conditions, draws from decades of lab experience and accumulated insight on how to minimize side-products and hit purity consistently above 99%. We have run the reactors in batches large and small, from R&D glassware all the way to jacketed steel vessels. At each stage, we watched for resin formation, monitored yield loss, and tuned the distillation to separate the end-product from closely related byproducts. Our process is no longer a lab curiosity—it meets the volume, reproducibility, and cleanliness standards that researchers and technologists demand on a daily basis.
Years of hands-on production show us that not every acetophenone derivative behaves the same way. You might expect structural similarity to mean physical and chemical profiles line up—yet, this particular molecule defies that easy assumption. Classic acetophenones often carry bulky or electron-donating groups; most lack the dual substitution on the aryl ring and the ester functionality on a side chain. This dual substitution brings a noticeable shift in melting point and solubility. The molecule flows as a slightly viscous liquid at room temperature, which remains stable in sealed glass at ambient conditions for well over a year. In the early days, we worried about hydrolysis from atmospheric moisture, but practical bench storage has disproved those concerns.
During oxidative or UV-driven transformations, the molecule demonstrates a resilience against unwanted side-reactions common in more reactive acetophenones. In practice, that means fewer colored byproducts and a cleaner solution for downstream chemistry. The 3-methyl-2-butenyloxy group lends flexibility in photoinitiator synthesis, and the ethoxycarbonylmethoxy arm creates additional routes for further derivatization—important advantages for chemists who do more than follow recipes.
Our experience shipping to resin, polymer, and specialty chemical firms shapes how we view this product. Customers who’ve handled other common acetophenone derivatives speak up about handling quirks: either poor stability, unexpected crystallization, or troublesome volatility. Here, the product manages a favorable compromise. The liquid form pours easily, and dosing remains accurate without grappling with static buildup or losses to container walls. Daily routines involve drawing from a drum or bulk package and dispensing into pilot-scale kettles, with yields matching batch records week in, week out. Cleanup is manageable—our operators have never logged any odorous residues that linger and cause headaches.
In photopolymer development, this acetophenone structure takes on a core role. Formulators want a balance of absorption and reactivity in the UV range, and modifications on the aromatic ring shift the spectrum to suit cationic or free-radical curing. Chemists working with this product describe sharper cure profiles and improved depth penetration, especially when pushed in thick or pigmented films. The reactivity against both acrylates and vinyl ethers stands out for those building new monomer platforms. That kind of performance doesn’t fall out of thin air. It comes from tuning substitution on both sides of the aromatic core—something lesser acetophenones can’t match because they lack structure to support those shifts.
Moving into fine chemical intermediates, our product supports direct conversion to surface modifiers, UV stabilizers, and grafted copolymers. Downstream, we watch it pick up utility in materials for optical coatings and functional urethanes. Over years, one thing holds true: practitioners want less fuss and more predictability, whether they’re working at bench scale or running a continuous reactor. In the projects we’ve supplied, our molecule’s shelf stability and consistent reactivity save them troubleshooting steps. They build experimental plans on fewer variables and scale ups land closer to expectation.
Running a chemical plant means more than just making a molecule; it’s about controlling variables on the floor every day. Process development focused on batches with sharp endpoints, high conversion, and low impurity carryover. Over time, operators learned what signals a clean endpoint—clear visual clues show as the color shifts and viscosity drops. Our internal labs run GC and NMR checks for each batch and flag any drift in isomer ratio or unwanted residue. Bottles that don’t meet the minimum standards don’t end up shipped—period.
Once, a scale-up trial drew attention to an impurity cluster that standard silica gel could not resolve. We isolated the trouble, traced it to a late-stage side reaction under higher agitation, and re-tuned the mixer to avoid introducing oxygen at that point. Purity jumped two percent and the yield stabilized. That kind of hands-on trouble-shooting sets the ground rules for offering a product worthy of continuous industrial use. Customers recognize this—returning for batch after batch because their own recipes don’t have to change every time a new drum arrives.
We log every batch, note every deviation, and keep a file of every real-world troubleshooting event. Field engineers working at customer sites call for advice and find a team that understands not just the chemistry, but the reality of plant-floor operations. That, in daily life, means less wasted material, more consistent processing, and fewer hours lost to variability.
Collaborating with industrial partners sheds light on what end-users care about. Resin and ink formulators told us about their struggles with viscosity drift. Our product holds a steady profile across a reasonable temperature range and stays pourable down to temperatures that force competitive acetophenones to seize up. During hot weather shipping, it resists premature reactivity while many lower-mass analogs risk degradation or color shift. UV curable coatings producers, especially those tackling thick-layer applications or three-dimensional projects, report better cure uniformity at lower photoinitiator loadings—a cost and quality advantage.
As a building block, this acetophenone derivative brings more than a single synthetic pathway. Its unique backbone allows further etherification, transesterification, or addition to various monomers. Industrial labs who need a longer reach for innovation find better yield in processes that start with a well-built foundation. Polymer engineers cite compatibility with new-generation bio-based co-monomers, opening experimental paths that weren’t practical with earlier acetophenones.
Our regulars from fine chemicals and materials science appreciate that purity brings reproducibility in complex syntheses. By keeping impurities away, our offerings help chemists avoid downstream traps. That sort of reliability simplifies everything from analytics to product registration, allowing researchers to get answers quickly and avoid repeat experiments. The work we put in before the product ships saves time and expense across dozens of projects, something end-users notice in everyday lab life.
Market comparisons show where this product’s design becomes valuable. Simple acetophenones—whether unsubstituted or just alkylated at a single position—fail to deliver on long-shelf life, reactivity in ambient air, or fine-tuned solubility for specialty monomers. The additional functional groups here mean fewer sacrifices in formulation and more latitude for innovation. The product carries a new set of options for those who can’t rely on traditional acetophenones or benzoin ethers, especially in the face of modern requirements for volatility, stability, and environmental compliance.
Consider classic photoinitiators—some dry to crystals or degrade under long storage, while others introduce yellowing or odor. Over years of plant-scale production and customer feedback, our experience with 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone shows none of these issues at typical concentrations and handling protocols. Our logistics partners confirm low loss rates from breakage or unexpected phase changes, saving shipment headaches and ensuring predictable inventory on arrival.
Other products falter in specialty applications where surface adhesion or optical clarity are critical. Our product’s molecular layout brings advantages for coating and curing applications in electronics, medical adhesives, and advanced printing. Researchers working with sensitive polymers and functional films note that this product’s profile meets both technical needs and operational ease.
Technical documentation and analytical support make a clear difference. Whenever a user explores a new chemistry or sets up a new application, technical service holds weight. Drawing from our own in-plant knowledge, we guide customers past routine pitfalls—everything from recommended purge steps in the reactor, to typical shelf lives under real-world conditions.
Every chemical manufacturer contends with increasing scrutiny from agencies and customers worldwide. Regulators ask questions about solvent residues, safe handling, process emissions, and waste disposal. We run our production in line with modern environmental requirements, reducing solvent exposure and closing vented streams wherever feasible. Our product’s low volatility means less emission in transport or use—a practical win for compliance and workplace safety.
Down the line, adhesives or coatings built with this product routinely meet stringent VOC and safety profiles. Working hands-on with our own analytical labs, we tailor support to customers needing detailed trace analyses for REACH, TSCA, or Asian regulatory filings. We tackle those tasks because we know product stewardship isn’t just about paperwork—it’s about making real improvements to daily safety and environmental performance in labs and manufacturing plants.
Everyone along the supply chain, from operator to formulator, benefits from usability improvements. We learned early not to take packaging for granted; handling tests led us to shift from brittle glass to robust polymer drums for bulk deliveries, sparing our customer labs accidental breakage. Product labels don’t just list a name—they track the lot, manufacture date, and outcome of our last QC run, ensuring customers never have to worry about what’s inside the drum.
Feedback loops matter. Our technical managers take customer calls on process glitches and genuine experiments. If a customer’s batch isn’t reacting as expected, our archives of real-plant conditions and troubleshooting make a difference. Field notes document how best to rinse lines, which valves and seals avoid residual hang-ups, and how to tweak mixing or reaction schedules to solve daily problems. You can see the influence each time we ship a new batch—each improvement drawn from dozens of real-world plant trials.
We see chemical manufacturing as an ongoing conversation between what’s possible and what users actually want. Our own R&D is active—finding smoother routes to the final molecule, trimming solvent use, and simplifying work-up for both workers and the environment. End-users in the polymer, coating, and electronics sectors push for greater integration, shorter supply chains, and ever-tighter tolerances.
The driving force lies in practical performance. Chemistry only moves ahead if the underlying building blocks support new ideas. We spend our effort ensuring that this acetophenone derivative meets the needs of modern formulation, scale-up, and innovation. Customers draw on our experience when they need answers, and we keep the cycle moving—each improvement, each fix, made real through operator know-how and technical partnership.
At its core, this product reflects the sum of years in the lab, on the plant floor, and out in customer facilities seeing what works and what doesn’t. The molecule’s unique layout, stability, and adaptability offer advantages you just won’t get from older, simpler acetophenones. Whether you’re developing a next-generation UV ink, tough optical adhesive, or breakthrough polymer blend, 2'-Ethoxycarbonylmethoxy-4'-(3-Methyl-2-Butenyloxy) Acetophenone stands out thanks to the detailed, practical attention paid at every step of its journey from reactor to application.