Neopentyl glycol diglycidyl ether

Neopentyl glycol diglycidyl ether

Names
IUPAC name 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane
Other names Neopentyl glycol diglycidyl ether; 1,3-Bis(2,3-epoxypropoxy)-2,2-dimethylpropane; 2,2'-((2,2-Dimethyl-1,3-propanediyl)bis(oxymethylene))bis(oxirane); CCRIS 2640; Diglycidyl ether of neopentyl gylcol; EINECS 241-536-7; Heloxy WC68; UNII-9288EM7AOW; Oxirane, 2,2'-((2,2-dimethyl-1,3-propanediyl)bis(oxymethylene))bis-; Propane, 1,3-bis(2,3-epoxypropoxy)-2,2-dimethyl-
Identifiers
CAS Number	17557-23-2
3D model (JSmol)	Interactive image
ChEMBL	ChEMBL1587512
ChemSpider	26599
ECHA InfoCard	100.037.745
EC Number	241-536-7
PubChem CID	28594
CompTox Dashboard (EPA)	DTXSID8025707
InChI InChI=1S/C11H20O4/c1-11(2,7-12-3-9-5-14-9)8-13-4-10-6-15-10/h9-10H,3-8H2,1-2H3 Key: KUAUJXBLDYVELT-UHFFFAOYSA-N
SMILES CC(C)(COCC1CO1)COCC2CO2
Properties
Chemical formula	C11H20O4
Molar mass	216.275 g/mol
Hazards
GHS labelling:[1]
Pictograms
Signal word	Warning
Hazard statements	H315, H317
Precautionary statements	P261, P264, P272, P280, P302+P352, P321, P332+P313, P333+P313, P362, P363, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Neopentyl glycol diglycidyl ether (NPGDGE) is an organic chemical in the glycidyl ether family. It is aliphatic and a colorless liquid. It has the formula C₁₁H₂₀O₄ and the CAS registry number of 17557-23-2.^[2] It has two oxirane groups per molecule.^[3] Its principle use is in modifying epoxy resins.^[4]

It is REACH registered.^[5] The IUPAC name is 2-[[2,2-dimethyl-3-(oxiran-2-ylmethoxy)propoxy]methyl]oxirane.^[6]

Neopentyl glycol and epichlorohydrin are reacted in the presence of a Lewis acid catalyst to form a halohydrin. This is followed by washing with sodium hydroxide in dehydrochlorination step. This forms Neopentyl glycol diglycidyl ether.^[7] 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.

A key use is modifying the viscosity and properties of epoxy resins. As an Epoxy modifier it is classed as an epoxy reactive diluent.^[8] which may then be formulated into CASE applications: Coatings,^[9] Adhesives,^[10] Sealants and Elastomers and composite materials. These uses include cationic polymerization reactions.^[11][12] The use of the diluent does effect mechanical properties and microstructure of epoxy resins.^[13][14] It is also used to synthesize other molecules.^[15][16][17]

NPGDGE toxicity is fairly well understood.^[18] It is classed as a skin irritant and skin sensitizer.^[19][20]

• Epoxide
• Glycidol

• 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).

• Hexion difunctional epoxy diluents Archived 2022-01-27 at the Wayback Machine
• Denacol epoxy diluent range
• Aalchem NPGDGE
• Cargill Reactive diluents