Cresyl glycidyl ether
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)
MSDS
- Language:English Provider:1,2-Epoxy-3-(tolyloxy)propane
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.
Cresyl glycidyl ether Supplier
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- 021-69185552 13701777608
- kangtuochem@163.com
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- +86-0519-82038123,18951201333
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- 021-69106960 13701823733
- 13701823733@163.com
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- 021-33516722 13701817765
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- 021-69992220 13701886816
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Cresyl glycidyl ether (26447-14-3)Related Product Information
- C8E3
- Resin epoxy
- Methanol
- Methylparaben
- Acetonitrile
- Allyl glycidyl ether
- 1,2-EPOXYTETRADECANE
- DIGLYCIDYL ETHER
- Dimethyl ether
- BISPHENOL A DIGLYCIDYL ETHER RESIN
- METHYLSTYRENE
- 1,2,3-PROPANETRIOL GLYCIDYL ETHER
- Ethylene glycol diglycidyl ether
- 2-Ethylhexyl glycidyl ether
- Basic Violet 1
- Ethylbenzene
- ETHYLENE OXIDE
- Propane