14228-73-0

Basic information

• Product Name: 1,4-Bis((2,3-epoxypropoxy)methyl)cyclohexane
• Synonyms: 2,2’-[1,4-cyclohexanediylbis(methyleneoxymethylene)]bis-oxiran;2,2’-[1,4-cyclohexanediylbis(methyleneoxymethylene)]bis-Oxirane;1,4-CYCLOHEXANEDIMETHANOL DIGLYCIDYL ETHER;DIGLYCIDYL ETHER OF 1,4-CYCLOHEXANEDIMETHANOL;1,4-bis[(2,3-epoxypropoxy)methyl]cyclohexane;1,4-CYCLOHEXANEDIMETHANOL DIGLYCIDYL ETH ER, TECH., MIXTURE OF CIS AND TRANS;Oxirane, 2,2-1,4-cyclohexanediylbis(methyleneoxymethylene)bis-;1,4-cyclohexanedimethanol diglycidyl ether, mixture of cis and trans
• CAS NO: 14228-73-0
• Molecular Formula: C14H24O4
• Molecular Weight: 256.34
• EINECS: 238-098-4
• Product Categories: Epoxide Monomers;Monomers;Polymer Science
• Mol File: 14228-73-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 154-160°C
• Flash Point: >230 °F
• Appearance: /
• Density: 1.1 g/mL at 25 °C(lit.)
• Vapor Density: >1 (vs air)
• Vapor Pressure: 11.4 mm Hg ( 25 °C)
• Refractive Index: n20/D 1.481(lit.)
• Storage Temp.: Refrigerator, under inert atmosphere
• Solubility: Chloroform (Slightly), Methanol (Slightly)
• Water Solubility: 3.741g/L at 20℃
• CAS DataBase Reference: 1,4-Bis((2,3-epoxypropoxy)methyl)cyclohexane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Bis((2,3-epoxypropoxy)methyl)cyclohexane(14228-73-0)
• EPA Substance Registry System: 1,4-Bis((2,3-epoxypropoxy)methyl)cyclohexane(14228-73-0)

Safety Data

• Hazard Codes: Xn
• Statements: 43
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 14228-73-0(Hazardous Substances Data)

Usage

Uses

1,4-Cyclohexanedimethanol Diglycidyl Ether is used in method for preparing high-strength and high-hardness epoxy modified MS sealant.

InChI:InChI=1/C8H16O2.C6H10O3/c9-5-7-1-2-8(6-10)4-3-7;1(5-3-8-5)7-2-6-4-9-6/h7-10H,1-6H2;5-6H,1-4H2

Upstream product

• 5592-70-1 1,4-bis[(2-propenyloxy)methyl]cyclohexane 

Relevant articles and documents

METHOD FOR PRODUCING EPOXY COMPOUND BY OXIDATION

The present invention provides a method for producing an epoxy compound by oxidation using hydrogen peroxide, in which the generation of oxygen due to the decomposition of hydrogen peroxide can be suppressed in the system, and which does not require complicated post-treatment, is excellent in reactivity, and allows the reaction to be performed in a SUS vessel. The present invention relates to a method for producing an epoxy compound, the method comprising reacting an olefin compound with hydrogen peroxide in the presence of a nitrile compound and a silicate. The silicate is preferably at least one selected from sodium silicate and potassium silicate.