Glycidyl methacrylate, 97%, stab. with 100ppm 4-methoxyphenol, Thermo Scientific Chemicals
Thermo Scientific Chemicals
Glycidyl methacrylate, 97%, stab. with 100ppm 4-methoxyphenol, Thermo Scientific Chemicals
製品番号(カタログ番号) L11133.18
または、製品番号L11133-18
価格(JPY)/ Each
-
見積もりを依頼する
数量:
50 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS106-91-2
IUPAC Name(oxiran-2-yl)methyl 2-methylprop-2-enoate
Molecular FormulaC7H10O3
InChI KeyVOZRXNHHFUQHIL-UHFFFAOYNA-N
SMILESCC(=C)C(=O)OCC1CO1
さらに表示
Appearance (Color)Clear colorless to pale yellow
Assay (GC)≥96.0%
Solution Test(10% v/v in diethyl ether) : Clear (UK sourced material only)
Solution Test(10% v/v in methanol) : Clear (UK sourced material only)
Stabilizer4-Methoxyphenol
さらに表示
Glycidyl methacrylate is commonly used as a monomer for the preparation of epoxy resins. It is also used to provide epoxy functionalization to polyolefins and other acrylate resins. Further, it is also useful as an epoxy resin additive for paint coating formulations and adhesive applications.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Glycidyl methacrylate is commonly used as a monomer for the preparation of epoxy resins. It is also used to provide epoxy functionalization to polyolefins and other acrylate resins. Further, it is also useful as an epoxy resin additive for paint coating formulations and adhesive applications.

Solubility
Miscible with benzene, alcohol and ether. Slightly miscible with water.

Notes
Light sensitive. Store in a cool place. Incompatible with strong oxidizing agents, strong acids and strong bases and peroxides.
RUO – Research Use Only

General References:

  1. Carrasco-Correa, E. J.; Ramis-Ramos, G.; Herrero-Martinez, J. M. Evaluation of 2,3-epoxypropyl groups and functionalization yield in glycidyl methacrylate monoliths using gas chromatography. J. Chromatogr. A 2015, 1379, 100-105.
  2. Takahashi, K.; Korolev, K.; Tsuji, K.; Oyaizu, K.; Nishide, H.; Bryuzgin, E.; Navrotskiy, A.; Novakov, I. Facile grafting-onto-preparation of block copolymers of TEMPO and glycidyl methacrylates on an oxide substrate as an electrode-active layer. Polymer 2015, 68, 310-314.