Search
Element Search
Structure Search
Thermo Scientific Chemicals
Allyl glycidyl ether, 97%
CAS: 106-92-3 | C6H10O2 | 114.144 g/mol
Have Questions?
Change view
Catalog number L11634.22
also known as L11634-22
Price (USD)
37.65
Special offer
Online exclusive
Ends: 28-Dec-2026
44.60Save 6.95
Each
Quantity:
100 g
Price (USD)
37.65
Special offer
Online exclusive
Ends: 28-Dec-2026
44.60Save 6.95
Each
Chemical Identifiers
CAS106-92-3
IUPAC Name2-[(prop-2-en-1-yloxy)methyl]oxirane
Molecular FormulaC6H10O2
InChI KeyLSWYGACWGAICNM-UHFFFAOYNA-N
SMILESC=CCOCC1CO1
View more
Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless
Assay (GC)≥96.0%
Identification (FTIR)Conforms
Refractive Index1.4325-1.4365 @ 20?C
FormLiquid
Allyl glycidyl ether is useful in hydrosilylation, including the H2PtCl6·xH2O (cat. no. 206083) catalyzed hydrosilylation of siloxanes to epoxysiloxanes.
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
Allyl glycidyl ether is useful in hydrosilylation, including the H2PtCl6·xH2O (cat. no. 206083) catalyzed hydrosilylation of siloxanes to epoxysiloxanes.
Solubility
Soluble in water (140 g/L at 20°C).
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
Allyl glycidyl ether is useful in hydrosilylation, including the H2PtCl6·xH2O (cat. no. 206083) catalyzed hydrosilylation of siloxanes to epoxysiloxanes.
Solubility
Soluble in water (140 g/L at 20°C).
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Hye-Lim Shim.; Seshachalam Udayakumar.; Jeong-In Yu.; Il Kim.; Dae-Won Park. Synthesis of cyclic carbonate from allyl glycidyl ether and carbon dioxide using ionic liquid-functionalized amorphous silica. Catalysis Today. 2009, 148 (3-4), 350-354.
- Dae-Won Park.; Na-Young Mun.; Kyung-Hoon Kim.; Il Kim.; Sang-Wook Park. Addition of carbon dioxide to allyl glycidyl ether using ionic liquids catalysts. Catalysis Today. 2006, 115 (1-4), 130-133.