| Identification | Back Directory | [Name]
Cresyl glycidyl ether | [CAS]
26447-14-3 | [Synonyms]
ARALDITE M
ARALDITE 507
ARALDITE 506
ARALDITE 502
Zinc01703516
ARALDITE 6005
cresylglycideether
tolylglycidylether
ARALDITE(R) CY 212
cresolglycidalether
cresolglycidylether
cresyl glycidyl ether
Glycidyl cresyl ether
FORMERLY ARALDITE(R) M
glycidolandderivatives
ARALDITE M HARDENER 964
glycidylmethylphenylether
2,3-epoxypropyltolylether
[(tolyloxy)methyl]oxirane
ARALDITE M ACCELERATOR 960
ARALDITE(R) 506 EPOXY RESIN
ARALDITE(R) HARDENER HY 964
1,2-epoxy-3-(tolyloxy)-propan
1,2-Epoxy-3-(tolyloxy)propane
[(methylphenoxy)methyl]oxirane
((methylphenoxy)methyl)-oxiran
[(methylphenoxy)methyl]-oxiran
oxirane((methylphenoxy)methyl)-
Propane, 1,2-epoxy-3-(tolyloxy)-
cresylglycidylether(mixedisomers)
Glycidyl-(tolyl)-ether, isomer mixture
[(Tolyloxy)methyl]oxiran (all isomers) | [EINECS(EC#)]
247-711-4 | [Molecular Formula]
C10H12O2 | [MDL Number]
MFCD00130544 | [MOL File]
26447-14-3.mol | [Molecular Weight]
164.2 |
| Chemical Properties | Back Directory | [Appearance]
colourless liquid | [density ]
1.14 | [Stability:]
Stable. Incompatible with strong acids, bases and oxidizing agents. May attack some types of plastic. Combustible. | [Water Solubility ]
<=0.1 g/100 mL at 21 ºC | [InChI]
InChI=1S/C10H12O2/c1-8-2-4-9(5-3-8)11-6-10-7-12-10/h2-5,10H,6-7H2,1H3 | [Contact allergens]
It is a reactive diluent added in epoxy resins Bisphenol A type. | [InChIKey]
CUFXMPWHOWYNSO-UHFFFAOYSA-N | [SMILES]
O(CC1OC1)C1=CC=C(C)C=C1 | [EPA Substance Registry System]
Oxirane, [(methylphenoxy)methyl]-(26447-14-3) |
| Hazard Information | Back Directory | [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. | [Description]
Cresyl glycidyl ether is a reactive diluent added in
epoxy res ins of the Bisphenol A type.
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