Glycidyl methyl ether (CAS 930-37-0)
Alternate Names:
1,2-Epoxy-3-methoxypropane
CAS Number:
930-37-0
Purity:
≥ 85%
Molecular Weight:
88.11
Molecular Formula:
C4H8O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Glycidyl methyl ether (GME) is used as a solvent for resins, paints, and coatings. It can interact with proteins, lipids, and carbohydrates, allowing it to act as a surfactant and solubilize various molecules. Scientific research utilizes Glycidyl methyl ether as a solvent for the extraction of proteins and other macromolecules from biological samples. It can also interact with hormones and other signaling molecules. Additionally, it is used as a reactant in organic synthesis.
Glycidyl methyl ether (CAS 930-37-0) References
- Studies on a new class of organogelator containing 2-anthracenecarboxylic acid: influence of gelator and solvent on stereochemistry of the photodimers. | Dawn, A., et al. 2009. Org Biomol Chem. 7: 4378-85. PMID: 19830286
- Azaphosphatranes as structurally tunable organocatalysts for carbonate synthesis from CO2 and epoxides. | Chatelet, B., et al. 2013. J Am Chem Soc. 135: 5348-51. PMID: 23528185
- Propargyl-functional aliphatic polycarbonate obtained from carbon dioxide and glycidyl propargyl ether. | Hilf, J. and Frey, H. 2013. Macromol Rapid Commun. 34: 1395-400. PMID: 23893471
- In-depth analysis of switchable glycerol based polymeric coatings for cell sheet engineering. | Becherer, T., et al. 2015. Acta Biomater. 25: 43-55. PMID: 26143602
- Correlation between the chemical composition of thermoresponsive nanogels and their interaction with the skin barrier. | Giulbudagian, M., et al. 2016. J Control Release. 243: 323-332. PMID: 27793686
- Specific uptake mechanisms of well-tolerated thermoresponsive polyglycerol-based nanogels in antigen-presenting cells of the skin. | Edlich, A., et al. 2017. Eur J Pharm Biopharm. 116: 155-163. PMID: 28027923
- Biocompatibility and characterization of polyglycerol-based thermoresponsive nanogels designed as novel drug-delivery systems and their intracellular localization in keratinocytes. | Gerecke, C., et al. 2017. Nanotoxicology. 11: 267-277. PMID: 28165853
- Poly(glycidyl ether)-Based Monolayers on Gold Surfaces: Control of Grafting Density and Chain Conformation by Grafting Procedure, Surface Anchor, and Molecular Weight. | Heinen, S. and Weinhart, M. 2017. Langmuir. 33: 2076-2086. PMID: 28191961
- Endothelial, smooth muscle and fibroblast cell sheet fabrication from self-assembled thermoresponsive poly(glycidyl ether) brushes. | Stöbener, DD., et al. 2018. Soft Matter. 14: 8333-8343. PMID: 30298896
- Novel Thermosensitive Polyethers Prepared by Anionic Ring-Opening Polymerization of Glycidyl Ether Derivatives | Aoki Sayuri 1, Koide Aya 1, Imabayashi Shin-ichiro 1, Watanabe Masayoshi 1. 2002,. Chemistry Letters. Vol.31, No.11: 1128-1129.
- A Challenging Comonomer Pair: Copolymerization of Ethylene Oxide and Glycidyl Methyl Ether to Thermoresponsive Polyethers | Sophie S. Müller†‡, Christian Moers†‡, and Holger Frey*†. 2014,. Macromolecules. 47, 16,: 5492–5500.
- Unexpected Random Copolymerization of Propylene Oxide with Glycidyl Methyl Ether via Double Metal Cyanide Catalysis: Introducing Polarity in Polypropylene Oxide | Rebecca Matthes, Carolin Bapp, Manfred Wagner, Sirus Zarbakhsh, and Holger Frey*. 2021. Macromolecules., 54, 24,: 11228–11237.
- The thermal degradation of glycidyl methacrylate-methyl methacrylate copolymers | A Piracha, S Zulfiqar - Polymer degradation and stability, 1996 - Elsevier. Issue 1, 1996,. Polymer Degradation and Stability. Volume 51,: Pages 27-34.
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| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Glycidyl methyl ether, 25 ml | sc-486488 | 25 ml | $169.00 |