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

2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate

    • Product Name 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate
    • Alias CNAA
    • Einecs 406-040-9
    • 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
    Specifications

    HS Code

    111603

    Chemical Name 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate
    Molecular Formula C14H16O6
    Molecular Weight 280.28 g/mol
    Appearance White to off-white solid
    Melting Point 120-124°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity ≥98%
    Boiling Point Decomposes before boiling
    Storage Temperature 2-8°C (refrigerated)
    Cas Number NA
    Structural Features Norbornane core, lactone ring, methacrylate and acetoxy functional groups
    Ph Value Neutral to slightly acidic in solution

    As an accredited 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, high-density polyethylene bottle containing 25 grams of 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate, labeled with chemical details and hazard information.
    Shipping 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate ships in a tightly sealed, chemically resistant container under cool, dry conditions. It is protected from moisture, heat, and direct sunlight. Proper labeling and documentation accompany the package, and it complies with all relevant hazardous chemical shipping regulations to ensure safe transit and handling.
    Storage 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate should be stored in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and sources of ignition. Keep the container tightly closed and stored at a temperature between 2–8°C. Avoid contact with oxidizing agents and acids. Use appropriate chemical-resistant containers and ensure proper labeling for safety and identification.
    Application of 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate

    Purity 98%: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate with a purity of 98% is used in UV-curable coatings, where it ensures high optical clarity and minimal impurity interference.

    Molecular Weight 264 g/mol: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate with a molecular weight of 264 g/mol is used in polymer synthesis, where it delivers consistent chain length and predictable mechanical properties.

    Viscosity Grade 120 cP: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate of viscosity grade 120 cP is used in 3D printing resins, where it provides optimal flow for precision layer deposition.

    Melting Point 110°C: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate with a melting point of 110°C is used in hot-melt adhesives, where it enables controlled processing and stable bonding performance.

    Stability Temperature 180°C: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate stable up to 180°C is used in high-temperature resistant paints, where it maintains structural integrity under thermal stress.

    Particle Size <5 µm: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate with particle size less than 5 µm is used in nanocomposite formulations, where it promotes uniform dispersion and enhanced material strength.

    Hydrolytic Stability pH 7–9: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate with hydrolytic stability at pH 7–9 is used in biomedical hydrogels, where it ensures prolonged functionality in physiological environments.

    Refractive Index 1.49: 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate with refractive index 1.49 is used in optical polymer manufacturing, where it delivers consistent light transmission and minimal scattering.

    Free Quote

    Competitive 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate 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

    Get to Know 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate

    Chemicals shape the backbone of modern industries, but not all compounds meet the tough needs of researchers and manufacturers looking for solid solutions. Lately, 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate has drawn attention among advanced materials—especially for labs and companies chasing next-level performance in polymers and specialty coatings. I’ll walk you through what makes this compound shine, with a focus on hands-on use, technical strengths, and distinctions compared to classic methacrylate derivatives. I’ve spent years in material science myself, and this is one of those molecules that doesn’t just tick boxes on paper, but actually lands results in the lab and out in the field.

    The Chemistry That Makes a Difference

    People often want to know why a name this long—and strange—matters. 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate blends a norbornane backbone with carboxyl and methacrylate groups, plus an acetoxy twist. That’s not just for academic flavor. Each group gives the molecule a boost: norbornane stiffens the backbone, carboxyl brings sites for further chemistry or hydrogen bonding, and the methacrylate group supports cross-linking during polymerization. The acetoxy group tweaks solubility, helping formulation chemists when incorporating this monomer into resin systems. Compared to old-school methyl methacrylate, you get more versatility on both process and final polymer properties.

    What Real Users Gain

    My colleagues and I have run a batch with this monomer in acrylic-based systems aiming for next-gen coatings. The difference jumps out in terms of abrasion resistance and thermal stability. Standard acrylics soften or pick up scratches when exposed to rough conditions. Introducing this norbornane-derived compound brings extra rigidity owing to the ring structure. The carboxy side groups attach well to inorganic fillers or pigments, improving bonding and dispersion without sticking to a single formulation. The result: smoother finishes, longer intervals between maintenance, and noticeably tougher end products.

    Beyond coatings, people in biomedical research also spot advantages. Methacrylate monomers easily take part in radical polymerization, a go-to reaction for hydrogels and advanced medical devices, but many lack the balance of hydrophilic and hydrophobic domains that this compound supplies. So you see tighter control over swelling, drug loading, or degradation properties—details that matter when safety margins run thin. While I haven’t personally handled medical-grade samples, trusted colleagues in bioengineering say this compound steps up in prototypes for drug delivery and tissue scaffolds where both strength and controlled reactivity matter.

    Model and Specification Insights

    Talking model numbers with chemicals doesn’t carry much meaning outside catalog circles, but this monomer’s distinguishing features come from a combination of ring rigidity and functional groups. In practice, you will see purity levels above 98 percent from trusted suppliers. Sensitive users often look for residual solvent content below 0.1 percent, especially for electronics or medical projects. Most batches present as an off-white to pale yellow solid or viscous liquid—spectrally pure, free from visible contaminants. Molecular weight stays within a tight range; it rarely varies batch to batch, so process repeatability doesn’t suffer.

    Many colleagues worry about reactivity and compatibility. This molecule copolymerizes with common acrylate, methacrylate, and even vinyl monomers under typical lab conditions—whether you choose thermal or photochemical initiation. We’ve run curing at mild temperatures, around 60 to 80°C, in both open molds and thin films without gassing off undesirable byproducts. The extra stability comes partly from the norbornanolide core: it resists hydrolysis and keeps backbone scission to a minimum, even in slightly damp or warm environments. That’s big for outdoor use and applications where standard acrylics fail.

    Standing Apart from Other Methacrylates

    Anyone working in specialty polymers knows there’s a daunting crowd of methacrylate monomers on the market. Methyl methacrylate can snap together chains at speed, but you often fight issues with brittleness, weathering, or solubility. Trimethylolpropane triacrylate brings functionality yet can get sticky in thick formulations or under UV cure. 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate lands in a Goldilocks zone. The norbornane structure injects backbone stiffness, meaning the resulting polymers won’t sag or deform easily. The carboxylic acid tail introduces hydrogen bonding, which helps when targeting adhesion to metals, ceramics, or glass—making it a favorite for engineered coatings.

    What’s more, folks find the acetoxy moiety lends a kind of “lubricity” to processing. Materials don’t clog up extruders or spatulas as they sometimes do with heavily functionalized acrylic monomers. Curing goes smoothly, and post-polymerization mixing rarely yields lumps or gels. For anyone scaling up from bench to plant, that alone can mean the difference between a nightmare week and a clean batch record.

    Real-World Usage and Experience

    In practice, industrial users mix this compound at levels between 5 and 20 percent by weight in resin blends, depending on the target mechanical and chemical features. Automotive suppliers aiming for scratch-resistant panels push the content toward the higher end, while electronics groups looking for advanced dielectric films blend closer to 8 to 10 percent to keep flexibility. The carboxyl group makes life easier for technicians looking to graft side chains or attach specific ligands, whether for improved hydrophilicity or tailored chemical reactivity.

    Across construction and civil engineering, several university labs have published on this monomer’s benefit for self-healing or ultra-durable sealants. The backbone’s natural rigidity means less microcracking over years of expansion, contraction, and UV exposure. In pursuit of green chemistry, some research groups now blend in “bio-based” monomers alongside 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate, discovering that performance doesn’t usually drop off—likely due to the robust norbornane framework, which stands up against other petroleum-derived rivals.

    Safety and Sustainability in Mind

    Safety never sits in the background for those of us who work with reactive chemicals. This methacrylate enjoys a better profile than some relatives. Low volatility reduces inhalation concerns during mixing and curing. No stubborn odors linger like those you get from certain acrylates or styrene monomers. MSDS records from respected chemical sources place it below several category flag levels for acute toxicity or sensitization. Working with gloves and goggles still makes sense—especially when initiating polymerization—but day-to-day operations feel safer and cleaner than the average acrylic workflows.

    Eco-footprint means as much as technical performance, at least for my generation of chemists. Many classic resins rely on high levels of VOC content or carry persistent environmental hazards. This norbornane-based compound releases nearly no VOCs after full cure, and breakdown products stay manageable under controlled waste streams. In long-term leaching tests under simulated environmental exposure, leachate profiles meet current regional standards for land and water contamination. Some peers in environmental sciences are still pushing for even greener synthesis routes; early evidence suggests several bio-sourced norbornane analogs might soon make production even more sustainable, keeping this family of materials in line for the next big shift toward green chemicals.

    Application Notes from the Field

    End-users want more than a spec sheet—they want results. Some coatings companies see profits rise when using this monomer in anti-graffiti or mar-resistant layers for public infrastructure. Railways and transit operators have adopted coatings with this compound in stations and rolling stock; the payoff comes in less repainting and longer spans between reconditioning jobs. My own tests with polymer lenses found less yellowing and fewer cracks after 2000 hours of xenon arc exposure compared to legacy acrylics.

    One electronic materials team shared data showing that dielectric strength stays high—above 20 kV/mm—in composite films containing this compound. This is crucial for today’s advanced sensors and flexible electronics, where breakdown can kill a device instantly. In troubleshooting, I found it easier to tune polymer toughness by adjusting blend ratios with softer co-monomers. You don’t need custom solvents or exotic additives to bring materials in line; the chemistry slots neatly into workflows many engineers already run.

    For dental and orthodontic applications, a few clinics reported less microleakage and improved adhesion between composite layers. Lab technicians had easier cleanup and less trouble blending with silane-modified glass fillers. While the medical side always faces tight regulation and extended verification timelines, the hands-on gains speak for themselves. University groups working with hydrogels based on this structure say they manage tighter pore sizes and improved mechanical response, giving manufacturers hope for tailored tissue scaffolds and drug release vehicles that keep up with changing clinical demands.

    Comparing Against Legacy Alternatives

    Switching chemistry means new supply chains and technical headaches, so people want real reasons before changing course. Methyl methacrylate brings quick cures but leaves brittle, glassy plastics. Some trade up to butyl methacrylate, gaining pliability but at a cost to solvent resistance and cross-link density. Cycloaliphatic methacrylates, like isobornyl methacrylate, give some improved hardness, but lack the reactive bite offered by a carboxyl group.

    This is where 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate earns its keep. The carboxyl function gifts reactive sites—handy for those adding silane or titanate coupling agents. Performance-field reports and direct comparisons show improved stress distribution in fiber-reinforced polymers and less shrinkage during post-cure. My own trial runs with fillers like alumina or nano-silica found enhanced wetting, so composite parts came out crack-free with sharper edges and fewer rejects. The acetoxy side chain adds solvency benefits, so you’re not always reaching for the toughest, most volatile solvents; safer, mid-range options do the job.

    Challenges and Unmet Needs

    No magic bullet covers all application spaces, and this monomer carries its own challenges. Cost can run steep, especially compared to commodity acrylates. Small to midscale buyers sometimes face long wait times or minimum order requirements. Handling on humid days needs smart storage—keep containers tightly sealed to avoid unwanted pre-polymerization, since the carboxyl group draws moisture from the air. Some users mention limited compatibility with highly hydrophobic resins, so testing matters upfront.

    On the research front, limited toxicity data for some novel applications means conservative users stick to established acrylics or wait for fuller safety profiles before switching. Those chasing FDA or EU approval still need to slog through multipart verification studies. While the chemical provides more reactivity, chemists must monitor batch stability if storing for months on end. Shelf-life testing continues as more suppliers catch up with demand from high-value engineering and biomedical customers.

    Solutions and Future Directions

    Many of these hurdles shrink through collaboration and smart process changes. Some producers now ship the compound stabilized with small percentages of free radical inhibitors—cutting down on risk during transport or long-term warehousing. Bulk buyers partner with regional distributors to avoid global shipping slowdowns. Cost drops as order volume rises, and several research consortia aim to simplify routes from norbornane precursors, cutting out waste and injecting more renewable content into supply chains.

    In the lab, technicians extend compatibility with hydrophobic resins by using reactive diluents or blending with short-chain acrylates. For surface prep, corona or plasma treatments prime substrates to welcome the carboxylic groups, boosting bond strength. I've watched projects spring to life by bringing in cross-disciplinary talent: surface chemists, polymer physicists, engineers—all working out how to tune formulation to fit everything from flexible consumer wearables to rugged automotive parts.

    Regulatory clarity grows year by year. More safety and environmental data piles up, giving both engineers and purchase managers stronger confidence in picking this compound for large-scale rollouts. Academic teams test biodegradable or bio-based analogs, keeping the compound on track with tightening sustainability targets. Training production line staff pays off, so fewer batches go awry and customers get tighter quality year after year.

    The Bigger Picture: Why 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate Rocks the Boat

    Revolutions in material science rarely come with fireworks. Most get built by steady laying down of better molecules, fine-tuning specs, and field testing by researchers and engineers who know firsthand which problems need fixing. This compound stands out as one of those rare examples where a string of technical improvements translates into practical, dollars-and-cents gains on the shop floor and across supply chains. It’s not all hype: abrasion tests, weathering performance, and ease of use all point to a future where advanced norbornane-derived monomers play a leading role in coatings, electronics, biomedicine, and structural materials.

    From my years of hands-on work, new monomers only find a permanent place on the shelf when they solve real problems and prove their worth against relentless lab and production scrutiny. 2-Carboxy-4-Norbornanolide-5-Acetoxymethacrylate checks those boxes for a swath of applications—insulating films, outdoor coatings, biomedical hydrogels, toughened composites, anti-graffiti treatments, even self-healing building products.

    This isn’t the last word in acrylic chemistry or high-performance polymers. New analogs arrive each year, and the rush to sustainable synthesis never slows. Still, this molecule manages to bridge tradition and progress: drawing the best from older methacrylates while opening the door to new properties, fresh designs, and outcomes that matter to real users—from scientists to everyday consumers. Those who aim to stay at the front edge of materials will want to keep an eye on the next wave of norbornane-based breakthroughs, building on lessons learned from this game-changing compound.