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HS Code |
749252 |
| Product Name | 1,3-Diadamantyl Monomethacrylate |
| Cas Number | 2091524-43-6 |
| Molecular Formula | C23H34O2 |
| Molecular Weight | 342.51 g/mol |
| Purity | Typically ≥98% |
| Appearance | White to off-white solid |
| Melting Point | 65-75°C |
| Boiling Point | Decomposes before boiling |
| Density | 1.08 g/cm³ (approximate) |
| Solubility | Soluble in common organic solvents |
| Storage Condition | Store at 2-8°C, protected from light and moisture |
As an accredited 1,3-Diadamantyl Monomethacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 1,3-Diadamantyl Monomethacrylate is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 1,3-Diadamantyl Monomethacrylate is typically shipped in tightly sealed containers, protected from light, moisture, and sources of ignition. Packaged according to chemical safety regulations, it is transported with appropriate hazard labeling. The shipment includes safety documentation, and temperature control may be required to prevent product degradation or polymerization during transit. |
| Storage | 1,3-Diadamantyl Monomethacrylate should be stored in a cool, dry, well-ventilated area away from heat, sparks, open flames, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from oxidizing agents, acids, and bases. Use appropriate personal protective equipment when handling. Ensure containers are clearly labeled and comply with all local, state, and federal storage regulations. |
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Purity 99%: 1,3-Diadamantyl Monomethacrylate with purity 99% is used in high-performance polymer formulations, where it delivers enhanced mechanical strength and chemical resistance. Viscosity 180 cP: 1,3-Diadamantyl Monomethacrylate with viscosity 180 cP is used in UV-curable coatings, where it ensures uniform film formation and smooth surface finish. Melting Point 148°C: 1,3-Diadamantyl Monomethacrylate with a melting point of 148°C is used in thermally stable adhesives, where it provides superior heat resistance and long-term durability. Molecular Weight 334.53 g/mol: 1,3-Diadamantyl Monomethacrylate with molecular weight 334.53 g/mol is used in advanced dental resins, where it contributes to enhanced biocompatibility and low polymerization shrinkage. Stability Temperature 200°C: 1,3-Diadamantyl Monomethacrylate with a stability temperature of 200°C is used in high-temperature-resistant elastomers, where it maintains flexibility and performance under thermal stress. Particle Size ≤ 5 μm: 1,3-Diadamantyl Monomethacrylate with particle size ≤ 5 μm is used in nanocomposite materials, where it promotes superior dispersion and uniformity. Refractive Index 1.56: 1,3-Diadamantyl Monomethacrylate with refractive index 1.56 is used in optical polymers, where it achieves improved light transmittance and clarity. Monomer Conversion ≥ 98%: 1,3-Diadamantyl Monomethacrylate with monomer conversion ≥ 98% is used in precision 3D printing resins, where it provides high-resolution output and minimized residual monomers. |
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Chemistry keeps pushing boundaries, and 1,3-Diadamantyl Monomethacrylate represents an exciting step forward in the world of specialty monomers. Built around the iconic adamantane scaffold, this compound blends structural integrity with the modern touch of a methacrylate group. Curiosity brought me to its bench a few years ago, mostly driven by frustration with brittle networks in advanced coatings and dental materials. Once dug in, it’s hard to ignore how a small change in molecular design plants new possibilities where brittle’s the old rule.
Plenty of monomers compensate for flexibility, but few offer the rigid yet elegant structure derived from the adamantane core found in 1,3-Diadamantyl Monomethacrylate. Talking shop with other chemists, I learned that adding bulk at the right places in a molecule can knock out a lot of pesky issues in polymer architecture—especially in fields where mechanical strength and durability just can’t be compromised.
This monomer, with its pendant adamantane at the 1 and 3 positions, avoids the slumping under heat that hits lesser methacrylates. Even after repeated stress, I’ve seen polymers hold their shape and gloss, standing up to scratches and harsh cleaning agents. The molecular geometry keeps the chains apart just enough to reduce brittleness without sacrificing a good, hard finish. Instead of chasing toughness with endless blends or tedious crosslinkers, this single molecule helps lay a robust foundation.
Walk into a lab focused on dental composites or high-tech adhesives and you’ll find researchers leaning on the predictable curing of 1,3-Diadamantyl Monomethacrylate. Its polymerization behavior overcomes the high shrinkage and stress cracking that follows more flexible analogues. The methacrylate group acts as a familiar reactive handle, letting chemists combine it seamlessly with other acrylates, and the adamantane locks everything in place.
It’s tempting to skim past structure when talking chemistry, but experience tells me that details make all the difference. The molecular formula features the signature adamantyl rings bonded to a methacrylate functional group, which works in many of the same free radical systems as other common monomers. Where 1,3-Diadamantyl Monomethacrylate stands out is in its balance—offering the heat resistance and chemical stability of a high molecular weight monomer, yet remaining surprisingly manageable in standard lab workflows.
I remember grinding my gears over viscosity issues in UV-curable resins. Too thick and the mix won’t flow; too thin and the final polymer won’t hold up. This monomer walks the line between the two. Its molecular weight and steric hindrance keep the mixtures smooth, without giving up on the kind of dense crosslinking that improves mechanical properties. Once cured, the adamantane framework delivers a level of hardness that’s hard to match with linear or branched alkyl methacrylates.
While it doesn’t dissolve in every solvent out there, it fares better than bulkier analogues thanks to the spacing of its functional groups. This modest solubility helps during processing, especially in composite mixing or thin-film applications. I learned firsthand that heating gently gets it into solution without breakdown, a contrast to some more sensitive specialty monomers that can lose their edge under the same conditions.
Working in dental material R&D, I saw the battle between strong yet brittle resins and those too soft for real-world use. 1,3-Diadamantyl Monomethacrylate lands in a sweet spot. During polymerization, its bulky side groups reduce the overall shrinkage strain. Fillings and sealants made with it set hard and maintain margins, resisting micro-leakage far better than those relying exclusively on standard methyl methacrylate. Dentists and materials scientists both look for reliability, and experience tells me that adding a touch of adamantane widens the safety margin.
Electronics makers, always fishing for the next stable encapsulant, also benefit. High-performance polymers with adamantane cores keep their form under heat and UV stress, essential for circuit board coatings and LED encapsulation. I remember a project where alternative methacrylates started fogging and yellowing after weather chamber testing. Swapping to 1,3-Diadamantyl Monomethacrylate held off discoloration and kept electrical properties in check long after others failed.
In advanced optics, refractive index and resistance to scratching often pull in opposite directions. Adamantane-based monomers bring both closer together, letting opticians grind lighter, tougher lenses. Personal experience in watchmaking restoration has brought me face to face with scratched and dulled crystals. Lenses and covers with this monomer just last longer.
Methyl methacrylate (MMA) and ethyl methacrylate remain giants, forming the backbone of everything from acrylic glass to nail kits. Their small, linear structures don’t offer much resistance to heat or chemical attack. Polymers from these monomers can craze, crack, or yellow, demanding frequent replacement or touch-up. Old MMA-based bath surrounds and phone cases tell that story well.
Switching to larger, bulkier monomers like iso-bornyl methacrylate brings improvement in hardness and UV resistance, but often at the expense of easy processing and flexibility. Taking the leap to adamantyl substitution at the 1,3-positions raises the bar for thermal and oxidative stability without clogging up formulations or making everything unwieldy. From personal experience mixing up batches, 1,3-Diadamantyl Monomethacrylate delivers a consistency that makes it a go-to ingredient in high-end applications.
Compared to bis-GMA, a heavyweight in dental composites, 1,3-Diadamantyl Monomethacrylate’s simpler structure gives a clearer curing profile and less risk of free residual monomer, which can boost biocompatibility. Watching cure times shrink without the need for aggressive thermal cycling saves effort both at the bench and on the production floor.
Modern chemistry can’t afford to ignore the health and environmental impact of its products. Handling 1,3-Diadamantyl Monomethacrylate requires the usual lab sense—good ventilation, gloves, and eye protection—but years of seeing results suggests it's less volatile than common monomers. Lower volatility translates to fewer complaints of headaches or skin sensitivity, though nothing substitutes for careful personal protective equipment.
Less vapor means better air quality in workspaces, something I’ve come to value after years in labs heavy with acrylic fumes. The stability of adamantane derivatives generally leads to improved resistance against degradation, which can help cut down on the frequency of polymer breakdown and microplastic generation in the environment. Reducing replacement rates for industrial and consumer goods is an overlooked, practical way to reduce waste.
Disposal of monomer and polymer waste always demands caution. Consult with local authorities for best practices, since even robust materials can leave a mark if mishandled. I have seen research exploring the possibility of reclaiming or recycling adamantane-based polymers, but this frontier still needs more development. Continued advances in green chemistry may soon make reprocessing a real option, especially as regulatory pressure rises.
Anyone who’s worked with higher performance materials knows the push for longer service life and improved user experience never rests. Adamantane’s rigid cage structure transforms the behavior of plastics, shifting properties toward higher glass transition temperatures and lower water absorption. My time in specialty coatings taught me that these subtle shifts dramatically reduce maintenance cycles in everything from automobile finishes to marine applications.
Adamantane derivatives catch on where other monomers lag behind—lasting through temperature swings, relentless UV exposure, and chemical spills. Maintenance teams spend less time patching and swapping damaged sections, and end-users see improved product reliability. Over the years, I’ve watched costs fall not just from longer part life but also from lower downtime across whole systems.
Adoption often trails behind innovation, partly because tried-and-true methods die hard. Yet the strong momentum behind 1,3-Diadamantyl Monomethacrylate reflects a growing trust in its performance. Industry reports show a steady interest in monomers that drive material evolution in medical, optical, and electronics manufacturing, as reporting in journals and conferences becomes more frequent.
No specialty monomer solves every problem. For all its stability and hardness, 1,3-Diadamantyl Monomethacrylate lacks the flexibility of smaller alkyl-based methacrylates. That means materials made with it sometimes call for clever blending or the addition of plasticizers when a balance of hardness and elasticity is needed.
My experience with 3D printing resins showed that high adamantane content improved edge definition and layer adhesion, but could make parts too rigid for prototype hinges. Engineers working on flexible gadgets or wearable displays look elsewhere or engineer in enough flexibility through the polymer matrix. Guiding users toward the right formulations speeds learning and keeps costly trial-and-error to a minimum.
Access and cost present another limit. Specialty reagents like 1,3-Diadamantyl Monomethacrylate don’t appear as shelf standards in most general-purpose labs. Synthesis takes more effort than for mass-market monomers, and pricing reflects that. This keeps its use focused on high-value products rather than bulk packaging or disposable goods. Continued innovations in synthetic routes, perhaps by route optimization or using greener feeds, could cut costs and widen availability.
Challenges in materials science rarely last forever. My own journey in polymer labs taught me that today’s limitations often lead tomorrow’s breakthroughs. Chemists keep tinkering with more efficient methods for making adamantane derivatives and exploring how small tweaks to the molecular structure can cut costs and boost versatility.
Collaboration between research groups and manufacturers shows promise for scaling up production. Bringing high-performance building blocks like 1,3-Diadamantyl Monomethacrylate into mainstream use means integrating them into established workflows without slowing down throughput or overhauling equipment. Investments in process safety and green chemistry could make these advanced monomers less expensive and more sustainable.
On the regulatory front, the focus on long-term safety and environmental sustainability grows each year. Transparent reporting and continuing toxicology research support responsible product development. In my early career, information on new monomers felt scattered or incomplete, but industry best practices and open communication now provide a better foundation to judge safety.
Innovation in materials science stands out most when it solves both today’s and tomorrow’s problems. From years behind a lab bench and in field trials, I have seen that 1,3-Diadamantyl Monomethacrylate answers many of the calls for better stability, processing reliability, and durability. Combining the classic adamantane rigidity with a reactive methacrylate handle allows users in a range of industries—dental, optical, microelectronics—to create products that last longer while maintaining high performance under demanding conditions.
Pushing toward wider use will need both continued investment in research and honest feedback from those actually using these materials in the field. Involving end-users in development means fewer surprises and products that do exactly what the job demands. Sharing my own lessons learned encourages more open dialogue, which often ignites the next leap ahead. 1,3-Diadamantyl Monomethacrylate doesn’t close the story; instead, it opens the door to a far broader palette for designers and engineers hungry for materials that won’t let them down. New frontiers in materials demand tough, innovative building blocks—this monomer steps confidently onto that stage.