1607-23-4

Basic information

• Product Name: 1,2-epoxy-3-(propenyloxy)propane
• Synonyms: 1,2-epoxy-3-(propenyloxy)propane;Oxirane, (1-propenyloxy)methyl-;Einecs 216-530-2
• CAS NO: 1607-23-4
• Molecular Formula: C₆H₁₀O₂
• Molecular Weight: 114.1424
• EINECS: 216-530-2
• Mol File: 1607-23-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 143.1°Cat760mmHg
• Flash Point: 39.6°C
• Appearance: /
• Density: 0.993g/cm³
• Vapor Pressure: 6.82mmHg at 25°C
• Refractive Index: 1.456
• CAS DataBase Reference: 1,2-epoxy-3-(propenyloxy)propane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-epoxy-3-(propenyloxy)propane(1607-23-4)
• EPA Substance Registry System: 1,2-epoxy-3-(propenyloxy)propane(1607-23-4)

Safety Data

• Hazardous Substances Data: 1607-23-4(Hazardous Substances Data)

Usage

General Description

1,2-epoxy-3-(propenyloxy)propane, also known as glycidyl allyl ether, is a chemical compound with the molecular formula C6H10O2. It is a colorless liquid with a pungent odor, and it is commonly used as a monomer in the production of polymers, resins, and other industrial chemicals. Glycidyl allyl ether is highly reactive and can undergo polymerization and crosslinking reactions, making it valuable in the manufacturing of adhesives, coatings, and composite materials. However, it is also considered a hazardous chemical, as exposure to high concentrations can cause irritation to the skin, eyes, and respiratory system, and it is classified as a potential carcinogen. Therefore, proper handling and safety precautions are necessary when working with this compound.

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 
• 3277-26-7 1,1,3,3-Tetramethyldisiloxane 
• 998-30-1 Triethoxysilane 

Relevant articles and documents

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.

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.