1607-23-4

Usage

Uses

Used in Polymer and Resin Production:
1,2-epoxy-3-(propenyloxy)propane is used as a monomer for its ability to undergo polymerization and crosslinking reactions, which is essential in the manufacturing of various polymers and resins. Its reactivity contributes to the formation of stable and versatile materials with a range of applications.
Used in Adhesives:
1,2-epoxy-3-(propenyloxy)propane is used as a component in adhesive formulations due to its capacity to form strong bonds through crosslinking, making it suitable for various industrial applications where durable adhesion is required.
Used in Coatings:
In the coatings industry, 1,2-epoxy-3-(propenyloxy)propane is used to enhance the properties of coatings, such as durability, chemical resistance, and adhesion to various substrates. Its reactivity allows for the creation of coatings with improved performance characteristics.
Used in Composite Materials:
1,2-epoxy-3-(propenyloxy)propane is utilized in the production of composite materials to improve their structural integrity and performance. Its role in crosslinking reactions aids in the development of composites with enhanced mechanical properties and resistance to environmental factors.

InChI:InChI=1/C6H10O2/c1-2-3-7-4-6-5-8-6/h2-3,6H,4-5H2,1H3/b3-2+

Upstream product

• 106-92-3 Allyl glycidyl ether 
• 998-30-1 Triethoxysilane 
• 3277-26-7 1,1,3,3-Tetramethyldisiloxane 

Relevant academic research and scientific papers

Hydrosilylation of Allyl Ethers in the Presence of Platinum(II) Immobilized on Polymethylene Sulfide

The reactions of allyl ethyl, allyl butyl, allyl glycidyl, allyl benzyl, and allyl phenyl ethers with 1,1,3,3-tetra-methyldisiloxane in the presence of platinum(II) immobilized on polymethylene sulfide have been studied.

Hydrosilylation of Allyl Ethers in the Presence of Supported Sulfur-Containing Platinum(II) Complexes

Hydrosilylation of allyl ethyl, allyl butyl, allyl glycidyl, allyl benzyl, and allyl phenyl ethers by 1,1,3,3-tetramethyldisiloxane in the presence of supported sulfur-containing platinum(II) complexes with the general formula [{SiO2}O2S/

DEHYDROGENATIVE SILYLATION, HYDROSILYLATION AND CROSSLINKING USING PYRIDINEDIIMINE COBALT CARBOXYLATE CATALYSTS

A process for producing a silylated product comprises reacting a mixture comprising (a) an unsaturated compound containing at least one unsaturated functional group, (b) a silyl hydride containing at least one silylhydride functional group, and (c) a catalyst, optionally in the presence of a solvent, to produce a dehydrogenative silylated product, a hydrosilylated product, or a combination of a dehydrogenative silylated product and a hydrosilylated product, wherein the catalyst is chosen from a pyridine diimine cobalt dicarboxylate complex or a cobalt carboxylate compound, and the process is conducted without pre-activating the catalyst via a reducing agent and/or without an initiator or promoter compound. The present catalysts have been found to be active in the presence of the silyl hydride employed in the silylation reaction.

Hydrosilylation of allyl glycidyl ether with triethoxysilane

Hydrosilylation of allyl glycidyl ether with triethoxysilane in presence of Speier's catalyst leads to triethoxy(3-glycidoxypropyl)silane and triethoxy(2-glycidoxy-1-methylethyl)silane and is accompanied by isomerization of allyl glycidyl ether and cleavage of the oxirane ring and the ether bond. An effect of admixtures in allyl glycidyl ether on the process is revealed. Some other hydrosilylation catalysts and additives to Speier's catalyst are studied.