|
HS Code |
506219 |
| Chemical Name | 2,2-Bis-[4-(Methacryloyloxydiethoxy)-Phenyl]-Propane |
| Common Name | Ethoxylated Bisphenol A Dimethacrylate |
| Cas Number | 41637-38-1 |
| Molecular Formula | C29H38O8 |
| Molecular Weight | 514.61 g/mol |
| Appearance | Clear to pale yellow liquid |
| Density | 1.12 g/cm³ (approximate) |
| Boiling Point | Decomposes before boiling |
| Flash Point | > 110°C (closed cup, approximate) |
| Viscosity | 400-600 mPa·s at 25°C |
| Solubility | Insoluble in water; soluble in organic solvents |
| Refractive Index | 1.520 - 1.535 at 20°C |
| Function | Crosslinking monomer in polymer and resin formulations |
| Odor | Faint, characteristic odor |
| Storage Conditions | Store in a cool, dry, and well-ventilated place away from light and heat |
As an accredited 2,2-Bis-[4-(Methacryloyloxydiethoxy)-Phenyl]-Propane = Ethoxylated -4-Bisphenol A Dimethacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Opaque, high-density polyethylene (HDPE) bottle, screw cap sealed, 500g label: "2,2-Bis-[4-(Methacryloyloxydiethoxy)-Phenyl]-Propane, for research use only." |
| Shipping | 2,2-Bis-[4-(Methacryloyloxydiethoxy)-Phenyl]-Propane (Ethoxylated 4-Bisphenol A Dimethacrylate) should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Classified as a chemical substance, it may require labeling for hazardous materials. Transport in accordance with local, national, and international regulations, ensuring temperature control and spill containment as required. |
| Storage | 2,2-Bis-[4-(Methacryloyloxydiethoxy)-Phenyl]-Propane (Ethoxylated Bisphenol A Dimethacrylate) should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sunlight, ignition sources, and incompatible materials such as strong oxidizing agents. Refrigeration may be recommended to prevent polymerization. Avoid moisture and direct heat to maintain chemical stability and ensure safe handling. |
Competitive 2,2-Bis-[4-(Methacryloyloxydiethoxy)-Phenyl]-Propane = Ethoxylated -4-Bisphenol A Dimethacrylate prices that fit your budget—flexible terms and customized quotes for every order.
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As a chemical manufacturer with decades of experience pouring, blending, and purifying specialty acrylate and methacrylate monomers, the push for new monomer structures has never slowed. Customers in advanced composites, dental, and 3D printing circles want to see more out of their resins. They expect strength, toughness, and different surface properties. They also expect lower toxicity and easier processing. Among the products our R&D team has brought forward, 2,2-Bis-[4-(Methacryloyloxydiethoxy)-Phenyl]-Propane, commonly called Ethoxylated-4-Bisphenol A Dimethacrylate, has gotten real attention.
Traditional Bisphenol-A dimethacrylate, well known as Bis-GMA’s cousin, sets the baseline for mechanical strength and versatility in a variety of formulations. Chemists often struggle with balancing viscosity, reactivity, and stress build-up. By inserting ethoxylate spacers between the aromatic rings and the methacrylate groups, manufacturers achieve a more flexible chain. This chemical modification allows for a lower viscosity without sacrificing strength or crosslink density. That ethoxy bridge makes the polymer network both tougher and more compatible with many fillers and co-monomers used in today’s applications.
In our own process, we have worked to produce this specialty monomer in high purity—aiming for extremely low residual monomers and color. This improves UV curing performance and minimizes the risk of yellowing over time. Each batch undergoes multiple stages of distillation and fine filtration before reaching our customers.
Ask anyone who has worked with neat Bis-GMA and they recall the challenge: an unyielding, honey-like material that barely moves in winter. Our ethoxylated dimethacrylate completely turns that story around. Flow improves, mixing times drop, and formulating with fillers or pigments gets easier—all this comes with minimal shrinkage during cure.
Operators on the factory floor have shared feedback with us. Adjusting mixer speeds or preheating tanks used to be daily rituals. Now, batching and pouring this monomer requires far less preparation even when ambient temperatures fluctuate. Shelf life extends because the extra ethoxy groups provide stability against slow polymerization. There is less tackiness during handling before cure, too, which matters in automated dosing systems.
Switching from classic Bis-GMA dimethacrylate to the ethoxylated variant brings a clear set of practical changes. For one, formulators gain flexibility over the resin’s viscosity. Eliminating the need for large percentages of reactive diluents like TEGDMA can reduce both shrinkage and leaching risk. Our experience in pilot projects for dental materials has shown as much as a 60% drop in final viscosity with equivalent crosslinking capability. This allows formulators to cut back on low-molecular-weight monomers, which have been flagged for potential health and regulatory reasons in several international markets.
Reaction kinetics also see improvement. Cure times speed up, both thermally and under UV lamps. In continuous production processes or additive manufacturing, those split seconds matter. The difference becomes even more obvious in thick-section parts or filled systems—light and heat travel further and more evenly through ethoxylated resin, lowering the risk for uncured spots and warpage.
Mechanical properties follow suit. Impact strength and elongation improve, while stiffness and compressive strength remain closely aligned with legacy resins. These gains have led several of our customers in electronics and printed circuit board fields to move toward ethoxylated dimethacrylates where small finishes and controlled expansion rates have a direct influence on device lifetimes.
We supply this monomer to different sectors because it performs reliably when the demands change. Dental laboratories choose it to improve polishability and lower the risk of microcracking in restoratives and cements. Dental composites formulated with it achieve more natural-looking luster and require less finishing chairside. The lower monomer mobility after cure keeps color stable for years, as proven in our weathering chambers and by independent test labs.
Composites engineers working in automotive or sports equipment have a different set of priorities: thermal resistance, dimensional consistency, and compatibility with glass or carbon fibers. With the ethoxylated dimethacrylate backbone, resins wet out fibers more completely, especially in dense layups. Shrink stress and dimpling around inserts drops significantly. Real feedback from composites lines shows that parts pull from molds cleaner and show reduced void counts compared to unmodified resins. The same holds true for digital light processing (DLP) and stereolithography (SLA) printing resins. Detailed parts print sharper, and support removal is easier because the cured structure resists brittleness.
In electronics, the dielectric performance receives a notable benefit. Traditional monomers run into problems above certain field strengths, leading to arcing or premature aging. The ethoxylate modification disrupts charge transport pathways, so insulating performance endures for longer periods. Boards and encapsulants finished with this chemistry withstand temperature cycling without cracks, as our own reliability data from customer returns demonstrates.
Making this product demands more than a recipe. Specialty glass reactors and precise temperature control keep side products at bay. We have learned that even slight off-ratio addition of ethylene oxide, or impurities in starting Bisphenol A, show up as color or high-molecular weight residues in the finish. Early on, we invested in improved distillation and storage for ethylene oxide and protected our process lines against cross-contamination from standard acrylates.
We know real production happens at scale, and the difference between gram vials and tonne lots can be dramatic. To ensure batch-to-batch consistency, our QC team runs gel permeation chromatography and spectroscopic purity tests on every shipment. Any sign of high-molecular-weight tailing or oligomers triggers an internal review. We believe rigorous process checks directly cut customer downtime and rejected lots.
Early batches of ethoxylated-4-BPA dimethacrylate weren’t perfect. We saw haze in UV-cured samples and inconsistent color in thick pours. By learning from those flaws, and adopting a two-stage purification, we delivered the colorless, low-odor product now sent out daily. Customers come back and request the same batch every time, which tells us the spec matters more to them than a certificate of analysis could ever promise.
Recent years have made it obvious that customers want more information on health and environmental effects for each material in their supply chain. We have addressed this head-on. Our process limits free Bisphenol A and residual diethyl ether. Low volatility and lower skin absorption rates compared to conventional monomers offer added safety for operators. Routine lab testing measures hazardous impurities at concentrations well below international guidelines.
Producing lower-toxicity monomers does not guarantee user safety alone. We promote open discussion with downstream formulators, sharing our most current testing data and listening as they run their own situational assessments. Practical experience from customers who run 24-7 dental resin printing, or who use the monomer for thin electronics encapsulation, guides adjustments in our on-site safety training.
Waste streams are easier to manage, too. Reduced unreacted monomer content means spent cleaning wipes or filter pads test clean faster. We run a closed-loop solvent recovery system. This both saves cost and reduces landfill.
We have sent samples to large university research centers and certified labs. Adhesion, scratch resistance, and yellowing resistance under xenon lamp tests have been run on multiple cured forms of the monomer. In every review, ethoxylated dimethacrylate produced better results against traditional, non-ethoxylated analogues. In dental, water uptake and solubility numbers show real advantage, making it a strong contender where mouth erosion and temperature cycling are unavoidable.
Tensile strength and fracture tests confirm the cured resin offers higher elongation at break, with similar compressive modulus to Bis-GMA-based blends. Even in high-humidity storage, batch stability persists for over a year without measurable polymerization or darkening. Some third parties have used it as a direct replacement in dental adhesives and confirmed lower leaching of methacrylic acid or BPA, a growing concern in child and senior dental products.
Anyone mixing their own resins for dental or industrial composites eventually faces the problem of clumping, sedimentation, or filler-monomer phase separation. The ethoxylated backbone structure acts as a built-in modifier for many micro- and nano-filler types. Silica, aluminum oxide, or functionalized fibers stay suspended longer. During our own test runs, pigment pastes knead out more evenly—and post-cure colors show higher gloss without hazing.
Cure synergy matters, too. Several common photoinitiator systems—both acyl phosphine oxides and benzoin ethers—trigger cure more efficiently in our ethoxylated formula than standard resin blends. A side benefit: less photoinitiator is required, which reduces cost and further cuts down on low molecular weight residues. Some users have switched to lower-energy lamps or reduced UV exposure cycles and still hit target hardness and conversion.
Transparency about limits matters. Ethoxylated dimethacrylate improves performance, but for some ultra-low-shrinkage applications or where solvent resistance must equal that of special high-Tg oligomers, further modification or co-blending remains necessary. Painstaking pilot trials have shown that using our product about 80% as the main crosslinker with ultra-toughened urethane dimethacrylates or silicon-modified acrylates achieves results similar to the newest commercial dental crowns and fillings.
Temperature extremes—not just on the lab bench but out in real-world factories—can affect mixture homogeneity. We have responded by offering guidance on matching photoinitiator and inhibitor types, advising our customers not to exceed safe storage windows. For large composite molds, controlling exotherm through filler ratios remains the best way to harness the increased reactivity that ethoxylation brings.
We are working with universities on ways to recycle and reuse process water and minimize waste. These projects aim to lower the environmental impact of all monomer manufacturing, a dialogue that involves not only manufacturers like us but also recyclers and end users. So far, closed-loop approaches and higher-purity output have cut our scrap rates and supported new ISO certifications for our production lines.
As more countries put up chemical registration walls and impose lower acceptable exposure levels for monomers, finding ways to responsibly supply advanced materials grows in importance. Direct customers, from foreign dental labs to composite component makers, tell us their customers read labels and track ingredient origins. By selecting ethoxylated-4-Bisphenol A dimethacrylate, we help these companies earn certifications and minimize red-flag components identified in new FCM (Food Contact Materials), REACH, or Prop 65 guidelines.
Our teams take regular part in regulatory updates and product stewardship circles. We know that the rules never stand still. Transparency about our process, and responding quickly with reformulations as needed, allows us and our customers to plan years ahead. It hasn’t escaped anyone’s notice that global trends continue driving toward lower exposure and more material origin verification.
Dialogues with customers remain the clearest path to product improvements. Engineers, dentists, and manufacturing line supervisors write to share technical reports, challenge results, or request further testing. We have incorporated suggestions, from changing inhibitor levels to extending certified shelf-life. Many have shifted entire product lines to leverage the low viscosity and enhanced compatibility of ethoxylated dimethacrylate. Some have even pooled resources with us to jointly test new photoinitiators or secondary crosslinkers that expand the monomer’s application range.
Our outlook remains ambitious. New catalyst systems and polymerization technologies drive us to continuously evaluate the limits of ethoxylated-4-Bisphenol A dimethacrylate. Our research staff have filed design improvements on the monomer core, shifting ethylene oxide chain length and substitutions to target special needs—especially for medical and optoelectronic markets. This collaboration between production, application R&D, and customer partnerships keeps us agile and responsive to the changing world of specialty methacrylates.
We see the push for safer, cleaner, and smarter monomers only accelerating. As a manufacturer, the commitment to producing reliable, high-purity, and adaptable products shows in the way our ethoxylated dimethacrylate moves from laboratory to plant to the hands of makers worldwide.