• Source: Diglycidyl resorcinol ether

Diglycidyl resorcinol ether, also called Resorcinol diglycidyl ether (RDGE) is a liquid aromatic organic chemical compound and chemically a glycidyl ether.
The formula is C12H14O4 and the CAS Registry Number 101-90-6. It is one of a number of glycidyl ethers available commercially that are used to reduce the viscosity of epoxy resins. These are then further used in coatings, sealants, adhesives and elastomers. It has the CAS Registry Number 101-90-6. It has the IUPAC name 2-[[3-(oxiran-2-ylmethoxy)phenoxy]methyl]oxirane and is registered on TSCA (Toxic Substances Control Act of 1976) as Oxirane, 2,2'-[1,3-phenylenebis(oxymethylene)]bis-. It is REACH registered and on EINECS.




Synonyms


1,3-Bis(2,3-epoxypropoxy)benzene
1,3-Diglycidyloxybenzene
2,2'-(1,3-Phenylenebis(oxymethylene))bisoxirane
Araldite ERE 1359
Diglycidyl ether of resorcinol
m-Bis(2,3-epoxypropoxy)benzene
meta-Bis(glycidyloxy)benzene
Oxirane, 2,2'-(1,3-phenylenebis(oxymethylene))bis-
RDGE
Resorcinol bis(2,3-epoxypropyl)ether
Resorcinol diglycidyl ether




Synthesis


Resorcinol and epichlorohydrin are reacted in the presence of a base and not a Lewis acid catalyst as normal with glycidyl ethers. A halohydrin is formed. This is followed by washing with sodium hydroxide in dehydrochlorination step. This forms Resorcinol diglycidyl ether. The waste products are water and sodium chloride and excess caustic soda. One of the quality control tests would involve measuring the Epoxy value by determination of the epoxy equivalent weight.




Uses


The material has two oxirane groups and is thus used mainly in epoxy resins systems as a reactive diluent and modifier. It has found use as an additive for bonding resin systems and also as a modifier for phenolic resins Despite the toxicity it generally gives excellent properties and so there are military applications. The use of the diluent does effect mechanical properties and microstructure of epoxy resins. However, this diluent is one of the best for not reducing properties too much.




Toxicology


It is classed as IARC group 2B by the International Agency for Research on Cancer. The toxicology has been studied for a long time and is fairly well understood.




See also


Epoxide
Glycidol




References






Further reading


Epoxy resin technology. Paul F. Bruins, Polytechnic Institute of Brooklyn. New York: Interscience Publishers. 1968. ISBN 0-470-11390-1. OCLC 182890.{{cite book}}: CS1 maint: others (link)
Flick, Ernest W. (1993). Epoxy resins, curing agents, compounds, and modifiers : an industrial guide. Park Ridge, NJ. ISBN 978-0-8155-1708-5. OCLC 915134542.{{cite book}}: CS1 maint: location missing publisher (link)
Lee, Henry (1967). Handbook of epoxy resins. Kris Neville ([2nd, expanded work] ed.). New York: McGraw-Hill. ISBN 0-07-036997-6. OCLC 311631322.
"Dow Epoxy Resins" (PDF).




External Websites


Parchem RDGE
Technical Data Sheet
Safety Data Sheet

Kata Kunci Pencarian:

• Diglycidyl resorcinol ether
• Bisphenol A diglycidyl ether
• Diglycidyl ether
• 1,4-Butanediol diglycidyl ether
• Neopentyl glycol diglycidyl ether
• 1,6-Hexanediol diglycidyl ether
• Allyl glycidyl ether
• 1,4-Cyclohexanedimethanol diglycidyl ether
• C12–C14 alcohol glycidyl ether
• Diethylene glycol diglycidyl ether