• 1. Highly efficient synergistic CO2 conversion with epoxide using copper polyhedron-based MOFs with Lewis acid and base sites
  Jiaming Gu,Xiaodong Sun,Xinyao Liu,Yang Yuan,Hongyan Shan,Yunling Liu Inorg. Chem. Front. 2020 7 4517
• 2. Bi-functional heterogeneous iron complexes for catalytic conversion of epoxides to cyclic carbonates and their application in the synthesis of polyurethane
  Shailesh Verma,Mohd. Nazish,Rukhsana I. Kureshy,Noor-ul H. Khan Sustainable Energy Fuels 2018 2 1312
• 3. Inclusion of organic species in exfoliated montmorillonite nanolayers towards hierarchical functional inorganic–organic nanostructures
  Xi Xi Chen,Jia Hui Liu,Alfin Kurniawan,Ke Jin Li,Chun Hui Zhou Soft Matter 2021 17 9819
• 4. Porous polymeric membranes: fabrication techniques and biomedical applications
  Amane Shiohara,Beatriz Prieto-Simon,Nicolas H Voelcker J. Mater. Chem. B 2021 9 2129
• 5. Manipulating the regioselectivity of a Solanum lycopersicum epoxide hydrolase for the enantioconvergent synthesis of enantiopure alkane- and alkene-1,2-diols
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Phenol ethers
• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers
• Solvents and Organic Chemicals Organic Compounds Alcohol/Ether

Comprehensive Overview of 2-(2-Methylphenoxymethyl)oxirane (CAS No. 2210-79-9): Properties, Applications, and Industry Insights

2-(2-Methylphenoxymethyl)oxirane (CAS No. 2210-79-9), also known as 2-Methylphenyl glycidyl ether, is a specialized epoxy compound widely utilized in industrial formulations due to its unique reactivity and versatility. This chemical belongs to the glycidyl ether family, characterized by an oxirane ring (epoxide group) attached to a 2-methylphenoxymethyl moiety. Its molecular structure enables applications ranging from adhesives to advanced material science, aligning with growing demand for high-performance epoxy modifiers and reactive diluents.

In recent years, the compound has gained attention for its role in sustainable material development, particularly in low-VOC coatings and bio-based polymers. Researchers and manufacturers frequently search for CAS 2210-79-9 solubility data, 2-(2-Methylphenoxymethyl)oxirane synthesis methods, and epoxy resin compatibility, reflecting its technical relevance. The compound’s thermosetting properties make it valuable in electronics encapsulation, where thermal stability and mechanical strength are critical.

From a regulatory perspective, 2-(2-Methylphenoxymethyl)oxirane complies with major chemical inventories such as REACH and TSCA, though users should always verify regional guidelines. Analytical studies highlight its hydrolytic stability and reactivity with amines, key factors for formulators optimizing curing kinetics. Industry forums often discuss its use as a viscosity reducer in composite matrices, addressing pain points in fiber-reinforced plastic production.

Emerging trends link this compound to green chemistry initiatives, with patents exploring its derivatization for waterborne epoxy systems. Searches for CAS 2210-79-9 MSDS and safe handling practices remain prevalent, underscoring the need for clear technical documentation. Its molecular weight (178.23 g/mol) and boiling point (265°C) are frequently cited in process design, while its low crystallization tendency enhances storage stability.

Innovative applications include UV-curable inks and 3D printing resins, where the compound’s crosslinking efficiency improves end-product durability. Laboratories evaluating 2-(2-Methylphenoxymethyl)oxirane NMR spectra or HPLC purity methods contribute to quality control protocols. The compound??s compatibility with silicones further expands its utility in high-temperature sealants, meeting aerospace and automotive specifications.

Market analysts note rising demand in Asia-Pacific regions for epoxy-based adhesives, driving interest in CAS 2210-79-9 suppliers and bulk pricing trends. Technical whitepapers emphasize its low volatility compared to aliphatic epoxies, reducing workplace exposure risks. As industries prioritize energy-efficient curing, this compound’s balanced reactivity profile positions it as a viable candidate for next-generation composite materials and electronic packaging solutions.

Future research may explore 2-(2-Methylphenoxymethyl)oxirane derivatives for biodegradable polymers, aligning with circular economy principles. Current literature confirms its hydrophobicity benefits in moisture-resistant coatings, a recurring topic in corrosion protection forums. With stringent emission standards shaping chemical innovation, this compound’s role in environmentally compliant formulations is likely to expand.

• 64777-15-7(Oxirane, 2,2'-[(2-methyl-1,4-phenylene)bis(oxymethylene)]bis-)
• 69557-50-2(3-(2,4,6-trimethylphenoxy)propane-1,2-diol)
• 64425-89-4(Phenol, 2-methyl-, polymer with formaldehyde, oxiranyl methyl ester)
• 4287-29-0(2-(2,5-dimethylphenoxymethyl)oxirane)
• 59-47-2(Mephenesin)
• 62318-38-1(Oxirane, 2,2'-[(4-methyl-1,3-phenylene)bis(oxymethylene)]bis-)
• 17181-49-6(2-Propanol,1,3-bis(2-methylphenoxy)-)
• 52153-44-3(1,2-Propanediol, 3-(2-methylphenoxy)-, (S)-)
• 52153-43-2(1,2-Propanediol, 3-(2-methylphenoxy)-, (R)-)
• 51673-11-1(2-[(2,4,6-trimethylphenoxy)methyl]oxirane)