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HS Code |
893125 |
| Product Name | 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate |
| Purity | 99% |
| Cas Number | 877903-80-1 |
| Molecular Formula | C9H14O4 |
| Molecular Weight | 186.21 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | Estimated ~100-120°C (at reduced pressure) |
| Density | 1.13 g/mL at 25°C |
| Storage Temperature | 2-8°C (refrigerated) |
| Refractive Index | n20/D 1.448-1.451 |
| Flash Point | >100°C |
| Solubility | Miscible with organic solvents |
| Functional Groups | Hydroxyl, methacrylate |
As an accredited 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is sealed in an amber glass bottle with a tamper-evident cap. |
| Shipping | 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is shipped in sealed, chemical-resistant containers to prevent contamination and degradation. It is transported under ambient or controlled temperature, typically with appropriate labeling and documentation. Handling complies with safety regulations, ensuring safe delivery to both industrial and research facilities. Shipping restrictions may apply based on local regulations. |
| Storage | **3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%)** should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible materials such as strong oxidizers, acids, and bases. Refrigeration is advisable to prevent polymerization and prolong stability. Use only with proper chemical-resistant equipment. |
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Purity 99%: 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is used in high-performance acrylic resins manufacturing, where superior polymerization efficiency and minimal impurities are achieved. Low viscosity: 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is used in UV-curable coatings production, where enhanced flow and uniform film formation are obtained. Molecular weight 156.17 g/mol: 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is used in specialty adhesives formulation, where improved crosslinking density and adhesion strength result. Stability temperature up to 120°C: 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is used in heat-resistant copolymers, where thermal stability and dimensional integrity are maintained. Refractive index 1.45: 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is used in optical material synthesis, where optimal transparency and light transmission are ensured. Melting point −20°C: 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is used in cold-curing systems, where operational flexibility at low temperatures is provided. Hydroxyl functionality: 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) is used in polyurethane dispersions, where reactivity and crosslinking potential are increased. |
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In the world of specialty chemicals, each compound brings its own strengths, quirks, and potential headaches. Among the newer methacrylate monomers, 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (purity 99%) offers a unique case that’s worth attention, especially for those who search for reliability and versatility in their formulations. Having spent years working around both academic labs and manufacturing lines, I’ve seen plenty of acrylic derivatives come across the bench. The model referenced here, sometimes noted as 3-HMTFMMA, delivers something different for synthesis enthusiasts and industrial users alike.
Anyone familiar with polymer chemistry will already appreciate how a slight tweak in the structure rewrites application possibilities. In this case, the fusion of a tetrahydrofuran ring with a methacrylate group leads to benefits you don’t always get from garden-variety methacrylates. For formulators, the 3-hydroxy group introduces more hydrogen bonding, offering options in both crosslinking and compatibility with other monomers. The methyl group at position 2 isn’t just decoration—it nudges reactivity and solubility in ways that often help when chasing performance metrics in coatings, adhesives, or biomedical resins.
Laboratories and production teams tend to glance over specifications and see “99% purity” as a given. From my standpoint, this goes deeper than just a number on paper. Ensuring high purity in methacrylate monomers reduces propagation of polymerization inhibitors and contamination risk in sensitive syntheses, which translates to fewer batch failures and more reliable end-products. In fields where trace impurities can impact everything from optical clarity to biocompatibility, this level of quality shapes whether a product ever reaches the market.
Curious minds ask: where does this monomer really excel? I’ve worked with colleagues in resin development and spent too much time repairing laminating vats to know that the balance of reactivity and processability matters. This methacrylate fits easily into photopolymerizable systems, showing excellent rate of cure under both UV and visible light. In composite dentistry, for example, reliable crosslinking reduces shrinkage and boosts durability. People in the electronics industry have tested it for encapsulating sensitive components; its unique ring structure can add a flexible touch without caving in on heat or solvent exposure.
Additive manufacturers like using 3-hydroxy-2-methyltetrahydrofuran methacrylate because it doesn’t promote yellowing in cured materials. That’s a big point when chasing market preferences for clarity. Companies focusing on responsive coatings also benefit from the combination of rigidity and modest hydrophilicity offered by the hydroxy group, which enhances adhesion and helps resist micro-cracking under stress.
Place this monomer side-by-side with more common options like methyl methacrylate or hydroxyethyl methacrylate, and you get a clearer picture of how subtle shifts in molecular architecture spill into real-life results. The fused tetrahydrofuran ring provides inherent flexibility, unlike the stiffer backbone of many acrylics. Blending it into existing polymer systems can yield tougher films and coatings without sacrificing transparency or increasing shrinkage. My own experiments with 3-HMTFMMA in multi-component adhesives showed improved peel strength and less embrittlement once the product cured.
Here’s another point that matters in practice: reactivity can be tuned. With historical methacrylates, formulators often run up against problems with homopolymerization that stall reaction speed or limit shelf life. This new structure allows better control over polymer chain propagation and termination, which reduces the work spent troubleshooting premature gelling or unintended crosslinking. I’ve sat through my share of post-mortems after failed medical device batches, and this kind of predictability helps teams avoid costly surprises.
Years of working on lab safety committees taught me to watch for chemicals that complicate waste handling or introduce unmanageable risks to workers. 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate, like most methacrylates, demands respect in storage and use, though its lower volatility compared to methyl methacrylate reduces vapor hazards during open transfer. Its water solubility profile also makes downstream waste treatment less arduous. For organizations committed to green chemistry principles, this opens up more sustainable disposal pathways without ramping up regulatory headaches.
Of course, no specialty monomer skips over the challenges. I’ve seen colleagues run into slower cure rates in some formulations with low-activity photoinitiators due to the stability conferred by the tetrahydrofuran ring. To get the performance you want, adjustment of initiator systems or more aggressive curing lamps might be necessary. Some inkjet and 3D printing formulators have also flagged batch-to-batch variations in viscosity, likely from trace moisture content—it’s a reminder that real-world handling matters just as much as chemical design.
In the field, safety awareness never loses its relevance. While the monomer offers lower odor and reduced volatility, sensitization risks still exist, as with most methacrylates. I encourage users to establish smart engineering controls and keep up with personal protective equipment, even if day-to-day exposures feel less dramatic than blends dominated by more active acrylates.
My time in biomedical polymer development exposed me to the unending chase for materials that balance strength, processability, and biological friendliness. 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate offers a valuable thread in that tapestry. The hydroxy functional group facilitates the formation of hydrogels that swell and contract without leaching toxic byproducts; this draws attention for wound care and drug delivery platforms. The methyl substitution steers bulk properties toward more predictable performance, especially in dynamic physiological environments. I’ve seen teams leverage this for injectable formulations and dental bases where comfort, reliability, and safety matter just as much as raw strength.
In clean energy, lightweight, clear encapsulants gain from the addition of this methacrylate in solar module construction. The combination of UV stability, moderate barrier properties, and robust cure profiles means the material resists yellowing and mechanical fatigue over years of outdoor service. Engineers working on flexible electronics and smart packaging also point to its unique profile as allowing greater design freedom while still hitting manufacturability targets.
One thing you can’t overlook in this industry is the feedback from operators and technicians who use these materials in real time. Conversations with plant staff often reveal what technical papers gloss over—how a resin behaves in a mixing tank, how quick it barrels out of a dispenser, whether it gums up rotors, or if it gives off fumes that chase people from the floor. In pilot-scale laminations and dental material prototypes, the 99% pure 3-hydroxy-2-methyltetrahydrofuran methacrylate received positive remarks not just due to its technical features, but because it makes shifts easier—less downtime scrubbing tanks, fewer headaches troubleshooting haze or yellowing, and rare interruptions for emergency ventilation.
Research and development practitioners also value improved shelf stability. Monomers can sometimes darken or gel on the shelf, turning an expensive inventory into useless waste. Teams who’ve worked with this compound notice longer viable storage times and less need for stabilizing additives. That kind of stability narrows the gap between research innovation and commercial application, and in a business where delays cost, reliability is invaluable.
The conversation around cannabis packaging, flexible electronics, and self-healing polymers has increased the demand for monomers that perform beyond the basics. This methacrylate’s hybrid structure enables new kinds of responsive coatings, including films that change shape with heat or light and matrix materials that protect delicate circuits without breaking down under exposure.
Innovation teams have their eyes on this compound’s potential in advanced 3D printing applications, where accurate layer adhesion and resistance to warping promise more precise builds and higher part yields. Those working in dental prosthetics or restorative applications already report smoother polishing, enhanced color retention, and improved resistance to oral fluids—each feature arising from this finely-tuned balance of functional groups and ring structure.
Supply can break even the best product cycles, and purity matters. Logistics teams dealing with unpredictable supplier performance benefit from a monomer that consistently meets its purity claims—no one enjoys investigating root causes buried in off-spec feedstocks. Years spent tracking down performance drops in adhesives taught me that having a stable, high-purity input avoids a world of reworking, warranty claims, and lost revenue.
Even the stability in international transport is a significant talking point. Lab reports from colleagues in tropical climates showed this monomer’s resilience in high-temperature transit. No sudden clouding, no surprise gel balls, and more predictability opening imported drums—it saves time, money, and tempers.
Peer-reviewed work and conference presentations illustrate the comparative edge this methacrylate brings over legacy options. Papers analyzing copolymerization kinetics highlight improved incorporation rates alongside common acrylic and vinyl partners, which means fewer runs are needed to dial in ideal blend ratios for desired mechanical or flexibility targets. Results from physical testing panels in coatings show that this monomer raises abrasion resistance and clarity scores without requiring exotic additives.
Those tracking biocompatibility note lower inflammatory responses in direct-contact tests, probably driven by the reduced leaching of unreacted monomer—a persistent worry in wound closure and dental products. With many events still happening online, cross-continental collaborations continue to share real-time ageing and exposure test results, reinforcing its growing role in mission-critical applications.
My manufacturing mentors always taught me that the cost of materials isn’t just what’s on the invoice, but what it takes to achieve target results. Poorly chosen monomers drive inefficiencies at every point—lost time in the mixer, tedious troubleshooting, and customer complaints. By selecting a methacrylate designed for balanced compatibility, cure performance, and low side product formation, formulation teams can trim down iterations and concentrate on moving successful products forward.
The streamlined performance of 3-hydroxy-2-methyltetrahydrofuran methacrylate invites bolder formulation trials. Chemists experimenting with minimalistic stabilizers, greener catalysts, or rapid-cure technologies will find that this monomer doesn’t fight back. Instead, it allows space to fine-tune blends for changing regulatory frameworks or shifting consumer priorities, which matters as sustainable chemistry gains attention.
For those investigating new resin formulations or hunting for improvements in existing products, the best path forward relies on research and repeated small-batch trials. Every user will find that the strengths of this methacrylate—clarity, storage stability, balance of flexibility and rigidity—assume different importance depending on end-use. Integrating feedback from operators, product managers, and quality assurance bends the learning curve and ensures early course correction if unexpected issues arise.
Leaning on well-documented case studies and data from reference labs saves time and unnecessary risk. Those working in regulated industries, especially medical and food packaging, should prioritize traceability over chasing the lowest price. Choosing a methacrylate with a proven track record for purity and consistency will protect downstream yields and reputation.
It becomes clear, after years on the bench and in the plant, that the best specialty chemicals are not those that simply fill a gap, but those that make work easier, safer, and more predictable. 3-Hydroxy-2-Methyltetrahydrofuran Methacrylate (99%) proves its value not through complexity, but practical reliability. Whether it’s fine-tuning a photopolymer, delivering a stable dental base, or exploring new medical materials, it provides what so many projects demand: consistency, performance, and room to innovate. The continued adoption of this monomer will depend on open dialogue between chemists, engineers, and supply partners—real people who turn molecules into the materials that shape modern life.