Products

Cresyl Glycidyl Ether

Product Introduction

Cresyl glycidyl ether Basic information

Product Name:	Cresyl glycidyl ether
Synonyms:	((methylphenoxy)methyl)-oxiran;[(methylphenoxy)methyl]-oxiran;1,2-epoxy-3-(tolyloxy)-propan;2,3-epoxypropyltolylether;cresolglycidalether;cresolglycidylether;cresylglycideether;cresylglycidylether(mixedisomers)
CAS:	26447-14-3
MF:	C10H12O2
MW:	164.2
EINECS:	247-711-4
Mol File:	26447-14-3.mol

Cresyl glycidyl ether Chemical Properties

density	1.14
Water Solubility	<=0.1 g/100 mL at 21 ºC
Stability:	Stable. Incompatible with strong acids, bases and oxidizing agents. May attack some types of plastic. Combustible.
EPA Substance Registry System	Cresyl glycidyl ether (26447-14-3)

Safety Information

Hazard Codes	Xn
Risk Statements	61-36/38-43-51/53-62
Safety Statements	53-26-36/37-45-61
RIDADR	UN 3082 9/PG 3
WGK Germany	3
F	21
Hazardous Substances Data	26447-14-3(Hazardous Substances Data)

Provider	Language
1,2-Epoxy-3-(tolyloxy)propane	English

Cresyl glycidyl ether Usage And Synthesis

Description	Cresyl glycidyl ether is a reactive diluent added in epoxy res ins of the Bisphenol A type.
Chemical Properties	colourless liquid
General Description	Colorless liquid. Sinks and mixes with water.
Air & Water Reactions	Oxidizes readily in air to form unstable peroxides that may explode spontaneously [Bretherick, 1979 p.151-154, 164]. Insoluble in water.
Reactivity Profile	A phenol and epoxide. Phenols do not behave as organic alcohols, as one might guess from the presence of a hydroxyl (-OH) group in their structure. Instead, they react as weak organic acids. Phenols and cresols are much weaker as acids than common carboxylic acids (phenol has Ka = 1.3 x 10^[-10]). These materials are incompatible with strong reducing substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat of the reaction may ignite the gas. Heat is also generated by the acid-base reaction between phenols and bases. Such heating may initiate polymerization of the organic compound. Phenols are sulfonated very readily (for example, by concentrated sulfuric acid at room temperature). The reactions generate heat. Phenols are also nitrated very rapidly, even by dilute nitric acid. Epoxides are highly reactive. They polymerize in the presence of catalysts or when heated. These polymerization reactions can be violent. Compounds in this group react with acids, bases, and oxidizing and reducing agents. They react, possibly violently with water in the presence of acid and other catalysts.
Health Hazard	Contact with eyes causes irritation. Contact with skin causes primary irritation and allergic sensitization.
Fire Hazard	Special Hazards of Combustion Products: Wear full body and respiratory protection.
Contact allergens	It is a reactive diluent added in epoxy resins Bisphenol A type.

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