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Bisphenol a glycerolate dimethacrylate bis gma

Manufactured by Merck Group
Sourced in United States

Bisphenol A glycerolate dimethacrylate (bis-GMA) is a chemical compound used as a component in various lab equipment and materials. It is a dimethacrylate monomer derived from bisphenol A and glycerol. The primary function of bis-GMA is to serve as a resin in the formulation of dental composites and other materials used in laboratory settings.

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5 protocols using bisphenol a glycerolate dimethacrylate bis gma

1

Synthesis and Characterization of Antibacterial Monomers

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The chemical structures of the different reactants are shown in Fig. 1. Bisphenol A glycerolate dimethacrylate (bis-GMA), tri(ethyleneglycol) dimethacrylate (TEGDMA), camphorquinone (CQ), and ethyl 4-dimethylamino-benzoate (EDMAB) were purchased from Sigma-Aldrich (St. Louis, MO, USA). QAS antibacterial monomers (MAE-DB and TMH-DB), with the molecular formula shown in Fig. 1, were supplied by Xylmed Biomedical (Xi'an, China). All materials were used as received without further purification.
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2

Composite Material Characterization Protocol

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Bisphenol-A-glycerolate dimethacrylate (bis-GMA), triethylene glycol dimethacrylate (TEGDMA), 2-diurethane dimethacrylate (DUDMA), camphorquinone (CQ), dimethylaminoethyl methacrylate (DMAEMA), DPEPHA, and barium oxide (BaO) were procured from Sigma (Sigma-Aldrich Co., St Louis, MO, USA) and used as received. Barium fluoride (BaF2) was purchased from Sisco Research Laboratories Pvt. Ltd. Maharashtra, India. Zirconia nanoparticles (ZrO2) were purchased from Nano Research Laboratory, Jamshedpur, Jharkhand, India. Institutional Animal Ethics Committee (IAEC; Reg. No. 889/PO/Re/S/05/CPCSEA; January 30, 2018) approved the protocol of the study (Approval No. SVCP/IAEC/PhD/2/02/2020).
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3

Dental Composite Material Synthesis

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Bisphenol A glycerolate dimethacrylate (Bis-GMA), tri (ethylene glycol) dimethacrylate (TEGDMA), camphorquinone (CQ), ethyl-4-dimethylaminobenzoate (4-EDMAB), zinc oxide nanopowder (<100 nm particle size), and urea were purchased from Sigma-Aldrich Co. (St. Louis, MO, USA). Zinc nitrate hexahydrate was purchased from Duksan Chemicals Co. (Ansan, Republic of Korea). Halloysite nanotubes (HNTs) were provided by Saejeon Int’L Inc. (Seoul, Republic of Korea). All materials were used without further purification.
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4

Epoxy Resin-based Nanocomposite Synthesis

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The epoxy resin was bisphenol A type resin (YD-128, Kukdo Chemical, Seoul, Korea). Bisphenol A glycerolate dimethacrylate (BisGMA) as acrylate resin and fumed silica with a particle size of 0.25 µm and specific surface area of 395 m2 g−1 were purchased from Sigma-Aldrich (Sigma-Aldrich Korea, Seoul, Korea). Adipic acid dihydrazide (ADH) as conventional hardener was received from Tokyo Chemical Industry. Irgacure 651 (Ciba Specialty Chemicals, Basel, Switzerland) was used as a photoinitiator. To synthesize the PMMA/PEI core-shell nanoparticle, methyl methacrylate (MMA), branched PEI (Mn = 60,000), and tert-butyl hydroperoxide (TBHP; 70 wt% in H2O) were obtained from Sigma-Aldrich (Sigma-Aldrich Korea, Seoul, Korea).
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5

Dihydrazide-Epoxy Resin Composites

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As stated above, four types of dihydrazide derivatives, including adipic acid dihydrazide (ADH, Tokyo Chemical Industry, Tokyo, Japan), isophthalic dihydrazide (IDH, Tokyo Chemical Industry, Tokyo, Japan), sebacic dihydrazide (SDH, Tokyo Chemical Industry, Tokyo, Japan), and 4-isopropyl-2,5-dioxoimidazolidine-1,3-di(propionohydrazide) (VDH, Ajinomoto Fine-Techno, Kanagawa, Japan), were utilized in this study and demonstrated in Figure 1. The epoxy resin was a bisphenol A-type epoxy resin with an epoxy equivalent weight of 184-190 g/eq (YD-128, Kukdo Chemical, Seoul, Korea). The acrylate resin of bisphenol A glycerolate dimethacrylate (BisGMA) was received from Sigma-Aldrich (St. Louis, MO, USA). The photoinitiator, Irgacure 651, was purchased from Ciba Specialty Chemicals (Basel, Switzerland). Fumed silica with an average diameter of 250 nm was obtained from Sigma-Aldrich (St. Louis, MO, USA).
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