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Cresyl glycidyl ether

CAS No. 26447-14-3
Chemical Name: Cresyl glycidyl ether
Synonyms: ARALDITE M;ARALDITE 507;ARALDITE 506;ARALDITE 502;Zinc01703516;ARALDITE 6005;cresylglycideether;tolylglycidylether;ARALDITE(R) CY 212;cresolglycidylether
CBNumber: CB9192083
Molecular Formula: C10H12O2
Formula Weight: 164.2
MOL File: 26447-14-3.mol
Cresyl glycidyl ether Property
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: Oxirane, [(methylphenoxy)methyl]-(26447-14-3)
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)

Cresyl glycidyl ether Chemical Properties,Usage,Production

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.
Cresyl glycidyl ether Preparation Products And Raw materials
Raw materials
Preparation Products
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26447-14-3(Cresyl glycidyl ether)Related Search:
C8E3 Resin epoxy Methanol Methylparaben Diethyl ether CRESYL VIOLET 2-NITRO-4-METHYLSULFONYLTOLUENE Epoxy Resins 1,2,3-PROPANETRIOL GLYCIDYL ETHER Ethylene glycol diglycidyl ether Propane METHYLSTYRENE EPOXY Acetonitrile Allyl glycidyl ether 1,2-EPOXYTETRADECANE DIGLYCIDYL ETHER Dimethyl ether
((methylphenoxy)methyl)-oxiran [(methylphenoxy)methyl]-oxiran 1,2-epoxy-3-(tolyloxy)-propan 2,3-epoxypropyltolylether cresolglycidalether cresolglycidylether cresylglycideether cresylglycidylether(mixedisomers) glycidolandderivatives glycidylmethylphenylether oxirane((methylphenoxy)methyl)- tolylglycidylether Microscopy Reagents Embedding Media cresyl glycidyl ether FORMERLY ARALDITE(R) M ARALDITE(R) CY 212 ARALDITE(R) 506 EPOXY RESIN ARALDITE(R) HARDENER HY 964 ARALDITE M HARDENER 964 ARALDITE M ACCELERATOR 960 ARALDITE M ARALDITE 6005 ARALDITE 507 ARALDITE 506 ARALDITE 502 [(methylphenoxy)methyl]oxirane 1,2-Epoxy-3-(tolyloxy)propane Analytical Reagents Analytical Chromatography Product Catalog 26447-14-3 [(tolyloxy)methyl]oxirane Glycidyl cresyl ether Glycidyl-(tolyl)-ether, isomer mixture [(Tolyloxy)methyl]oxiran (all isomers) Propane, 1,2-epoxy-3-(tolyloxy)- Zinc01703516
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