Bis-GMA

Bis-GMA
Names
	Preferred IUPAC name Propane-2,2-diylbis[4,1-phenyleneoxy(2-hydroxypropane-3,1-diyl)] bis(2-methylprop-2-enoate)
	Other names Bowen monomer; Silux; Delton; NuvaSeal; Retroplast
Identifiers
CAS Number	1565-94-2 ;
3D model (JSmol)	Interactive image;
ChemSpider	14549;
ECHA InfoCard	100.014.880
EC Number	216-367-7;
PubChem CID	15284;
UNII	454I75YXY0 ;
CompTox Dashboard (EPA)	DTXSID7044841 ;
	InChI InChI=1S/C29H36O8/c1-19(2)27(32)36-17-23(30)15-34-25-11-7-21(8-12-25)29(5,6)22-9-13-26(14-10-22)35-16-24(31)18-37-28(33)20(3)4/h7-14,23-24,30-31H,1,3,15-18H2,2,4-6H3 Key: AMFGWXWBFGVCKG-UHFFFAOYSA-N;
	SMILES CC(=C)C(=O)OCC(COC1=CC=C(C=C1)C(C)(C)C2=CC=C(C=C2)OCC(COC(=O)C(=C)C)O)O;
Properties
Chemical formula	C29H36O8
Molar mass	512.599 g·mol−1
Appearance	colorless oil
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H315, H317, H318, H319
Precautionary statements	P261, P264, P272, P280, P302+P352, P305+P351+P338, P310, P321, P332+P313, P333+P313, P337+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

Bis-GMA (bisphenol A-glycidyl methacrylate) is a resin commonly used in dental composite, dental sealants. and dental cement. It is the diester derived from methacrylic acid and the bisphenol A diglycidyl ether. Bearing two polymerizable groups, it is prone to form a crosslinked polymer that is used in dental restorations. For dental work, highly viscous bis-GMA is mixed with aluminosilicate particles, crushed quartz and other related acrylates; changes to component ratios lead to different physical properties in the end product. Bis-GMA was incorporated into composite dental resins in 1962 by Rafael Bowen. Until matrix development work in the early 2000s, bis-GMA and related methacrylate monomers were the only options for organic matrix composition.