• 1. Polymerization of a biscalix[5]arene derivative
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• 2. Update and critical reanalysis of IUPAC benchmark propagation rate coefficient data
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• 3. In-plane oriented highly ordered lamellar structure formation of poly(N-dodecylacrylamide) induced by humid annealing
  Yuki Hashimoto,Takuma Sato,Ryosuke Goto,Yuki Nagao,Masaya Mitsuishi,Shusaku Nagano,Jun Matsui RSC Adv. 2017 7 6631
• 4. Molecular motion in solid amorphous polymers. The dielectric relaxation of a poly-nonyl methacrylate and poly-n-lauryl methacrylate as a function of frequency, temperature and applied pressure
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• 5. Study of the RAFT homopolymerization and copolymerization of N-[3-(dimethylamino)propyl]methacrylamide hydrochloride and evaluation of the cytotoxicity of the resulting homo- and copolymers
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• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty alcohol esters
• Solvents and Organic Chemicals Organic Compounds Acids/Esters

Lauryl Methacrylate (CAS No. 142-90-5): Applications and Recent Advances in Chemical Biology

Lauryl Methacrylate, chemically known by its CAS number 142-90-5, is a versatile monomer widely utilized in the field of polymer chemistry and material science. This compound, derived from methacrylic acid and dodecanol, exhibits unique properties that make it invaluable in the development of advanced materials, particularly in biomedical applications. The increasing interest in Lauryl Methacrylate stems from its ability to form polymers with desirable mechanical and chemical characteristics, which are essential for modern pharmaceutical and biotechnological innovations.

The molecular structure of Lauryl Methacrylate consists of a methacrylic acid group attached to a lauryl (dodecyl) chain. This configuration imparts both reactivity and solubility advantages, making it an ideal candidate for various synthetic processes. The methacrylic acid functional group allows for easy polymerization via radical initiation, while the long hydrocarbon chain enhances hydrophobic interactions, which is particularly useful in designing hydrogels and amphiphilic polymers.

In recent years, significant research has focused on the applications of Lauryl Methacrylate in drug delivery systems. Its ability to form cross-linked networks provides a controlled environment for encapsulating therapeutic agents, ensuring sustained release profiles. For instance, studies have demonstrated its efficacy in creating micelles and nanoparticles that can target specific cells or tissues. These advancements are particularly relevant in oncology, where targeted drug delivery can minimize side effects and improve patient outcomes.

Moreover, the field of tissue engineering has seen remarkable progress with the use of Lauryl Methacrylate-based hydrogels. These hydrogels mimic the extracellular matrix (ECM) of biological tissues, providing a scaffold for cell growth and differentiation. Recent research has highlighted the potential of these materials in regenerating damaged tissues, such as skin and cartilage. The biocompatibility and tunable mechanical properties of Lauryl Methacrylate-derived hydrogels make them promising candidates for clinical translation.

The polymerization process of Lauryl Methacrylate is also being explored for creating smart materials that respond to external stimuli. For example, photo-crosslinkable polymers derived from this monomer can be designed to change their properties upon exposure to light. This feature is particularly useful in developing responsive drug delivery systems where stimuli such as UV light can trigger the release of therapeutic agents. Such innovations are at the forefront of chemical biology research, offering new avenues for treating complex diseases.

Economic considerations also play a crucial role in the adoption of Lauryl Methacrylate. Its relatively low cost compared to other methacrylic acid derivatives makes it an attractive option for industrial-scale applications. Additionally, its high reactivity ensures efficient synthesis processes, reducing production time and costs. These factors contribute to its widespread use in both academic research and commercial product development.

The environmental impact of using Lauryl Methacrylate is another area of growing interest. Efforts are underway to develop sustainable polymerization methods that minimize waste and energy consumption. Green chemistry principles are being integrated into the synthesis of these materials, ensuring that their production aligns with environmental regulations and sustainability goals. Such initiatives not only enhance the ecological footprint but also improve the overall safety profile of products derived from this compound.

In conclusion, Lauryl Methacrylate (CAS No. 142-90-5) remains a cornerstone material in modern chemistry and biology due to its multifunctional properties and broad range of applications. From drug delivery systems to tissue engineering scaffolds, its versatility continues to drive innovation across multiple scientific disciplines. As research progresses, we can expect even more groundbreaking applications that will further solidify its importance in advancing human health and technological development.

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