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Journal articles on the topic 'Diglycidyl ether of bisphenol-A'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

GRUMETTO, LUCIA, ORIELLA GENNARI, DOMENICO MONTESANO, et al. "Determination of Five Bisphenols in Commercial Milk Samples by Liquid Chromatography Coupled to Fluorescence Detection." Journal of Food Protection 76, no. 9 (2013): 1590–96. http://dx.doi.org/10.4315/0362-028x.jfp-13-054.

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The presence of five bisphenols, i.e., bisphenol F, bisphenol A, bisphenol B, bisphenol F diglycidyl ether, and bisphenol A diglycidyl ether, was monitored in commercial milk packed in plastic bottles marketed in Italy. The new validated method includes a solid-phase extraction procedure followed by liquid chromatography with fluorescence detection. All positive results were confirmed by liquid chromatography–tandem mass spectrometry analysis. The limits of detection and quantification and the recovery percentages indicated that the method is suitable for detecting bisphenols in milk at concen

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2

Jordáková, I., J. Dobiáš, M. Voldřich, and J. Postka. "Determination of bisphenol A, bisphenol F, bisphenol A diglycidyl ether and bisphenol F diglycidyl ether migrated from food cans using Gas Chromatography-Mass Spectrometry." Czech Journal of Food Sciences 21, No. 3 (2011): 85–90. http://dx.doi.org/10.17221/3481-cjfs.

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Varnishes used for the inner coatings of food cans are mostly based on epoxy resins or vinylic organosols. The epoxy resins are produced from bisphenol A and bisphenol F and they also contain BADGE or BFDGE as stabilising components. A simple method for the quantitative determination of bisphenol A (BPA), bisphenol F (BPF), bisphenol A diglycidyl ether (BADGE), and bisphenol F diglycidyl ether (BFDGE) migrated from food packaging materials was optimised. The can sample was extracted with acetonitrile or with food simulants (distilled water, 3% acetic acid and 10% ethanol) and the extract obtai

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3

Poustka, J., L. Dunovská, J. Hajšlová, K. Holadová, and I. Poustková. "Determination and occurrence of bisphenol A, bisphenol A diglycidyl ether, and bisphenol F diglycidyl ether, including their derivatives, in canned foodstuffs’ from the Czech retail market." Czech Journal of Food Sciences 25, No. 4 (2008): 221–29. http://dx.doi.org/10.17221/689-cjfs.

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A several-year survey (2000–2006) documents a continuing occurrence of bisphenol A (BPA), bisphenol A diglycidyl ether (BADGE), and bisphenol F diglycidyl ether (BFDGE), including their derivatives, migrating from packaging into food. A wide range of bisphenols levels (from traces up to hundreds µg/kg) in canned foodstuffs available at the Czech retail market was found. An analytical procedure suitable for routine monitoring of bisphenols in various matrices was validated. Crude extracts (obtained by dichloromethane extraction in ultrasonic bath) were purified by gel permeation chromatography

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4

Poustková, I., J. Dobiáš, J. Poustka, and M. Voldřich. "Investigation of bisphenol a diglycidyl ether, bisphenol f diglycidyl ether and their hydroxy and chlorohydroxy derivatives stability in water-based food simulants." Czech Journal of Food Sciences 22, SI - Chem. Reactions in Foods V (2004): S272—S275. http://dx.doi.org/10.17221/10679-cjfs.

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Varnishes used as the inner coatings of food cans are often based on epoxy resins or vinylic organosols. The epoxy resins can be produced from bisphenol A (BPA) and bisphenol F (BPF) and they also contain bisphenol A diglycidyl ether (BADGE) of bisphenol F diglycidyl ether (BFDGE) as stabilising components. These compounds may break down during storage and also by influence of food simulants. The stability of BADGE and BFDGE was studied using reverse-phase gradient high performance liquid chromatography (RP-HPLC) with fluorescence detection (FLD). Four experiments were compared: (i) BPA soluti

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5

Poustková, Ivana, Jaroslav Dobiáš, Ingrid Steiner, Jan Poustka, and Michal Voldřich. "Stability of bisphenol A diglycidyl ether and bisphenol F diglycidyl ether in water-based food simulants." European Food Research and Technology 219, no. 5 (2004): 534–39. http://dx.doi.org/10.1007/s00217-004-0995-1.

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6

Cabado, Ana G., Susana Aldea, Corina Porro, et al. "Migration of BADGE (bisphenol A diglycidyl-ether) and BFDGE (bisphenol F diglycidyl-ether) in canned seafood." Food and Chemical Toxicology 46, no. 5 (2008): 1674–80. http://dx.doi.org/10.1016/j.fct.2008.01.006.

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7

Crathorne, B., C. P. Palmer, and J. A. Stanley. "High-performance liquid chromatographie determination of bisphenol a diglycidyl ether and bisphenol F diglycidyl ether in water." Journal of Chromatography A 360 (January 1986): 266–70. http://dx.doi.org/10.1016/s0021-9673(00)91673-x.

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8

Gallart-Ayala, H., E. Moyano, and M. T. Galceran. "Multiple-stage mass spectrometry analysis of bisphenol A diglycidyl ether, bisphenol F diglycidyl ether and their derivatives." Rapid Communications in Mass Spectrometry 24, no. 23 (2010): 3469–77. http://dx.doi.org/10.1002/rcm.4801.

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9

Berger, Urs, and Michael Oehme. "Identification of Derivatives of Bisphenol A Diglycidyl Ether and Novolac Glycidyl Ether in Can Coatings by Liquid Chromatography/Ion Trap Mass Spectrometry." Journal of AOAC INTERNATIONAL 83, no. 6 (2000): 1367–76. http://dx.doi.org/10.1093/jaoac/83.6.1367.

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Abstract A reversed-phase liquid chromatographic method combined with fluorescence and multiple mass spectrometric detection in series is presented for the separation and structure elucidation of bisphenol A diglycidyl ether (BADGE) and novolac glycidyl ether (NOGE) derivatives. Atmospheric pressure chemical ionization in the positive ion mode and collision induced fragmentation in the ion trap allowed identification of BADGE- and NOGE-related compounds originating from reactions of the glycidyl ethers with bisphenols, solvents, and chain stoppers. Two extracts from food-can coatings were inve

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10

Nikafshar, Saeid, Omid Zabihi, Susan Hamidi, et al. "A renewable bio-based epoxy resin with improved mechanical performance that can compete with DGEBA." RSC Advances 7, no. 14 (2017): 8694–701. http://dx.doi.org/10.1039/c6ra27283e.

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11

Mat??jka, L., P. Chabanne, L. Tighzert, and J. P. Pascault. "Cationic polymerization of diglycidyl ether of bisphenol A." Journal of Polymer Science Part A: Polymer Chemistry 32, no. 8 (1994): 1447–58. http://dx.doi.org/10.1002/pola.1994.080320806.

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12

Hutson, D. H. "Bisphenol A Diglycidyl Ether as a Potential Metabolic Source of Bisphenol A." Environmental Health Perspectives 106, no. 10 (1998): A473. http://dx.doi.org/10.2307/3434076.

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13

Lee Hia, Iee, Eng-Seng Chan, Siang-Piao Chai, and Pooria Pasbakhsh. "A novel repeated self-healing epoxy composite with alginate multicore microcapsules." Journal of Materials Chemistry A 6, no. 18 (2018): 8470–78. http://dx.doi.org/10.1039/c8ta01783b.

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14

Paseiro Losada, P., J. Simal Lozano, S. Paz Abuin, P. Lopez Mahia, and J. Simal Gandara. "Kinetics of the hydrolysis of bisphenol F diglycidyl ether in water-based food simulants. Comparison with bisphenol A diglycidyl ether." Journal of Agricultural and Food Chemistry 40, no. 5 (1992): 868–72. http://dx.doi.org/10.1021/jf00017a034.

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15

Ramilo, Graciela, Iago Valverde, Jorge Lago, Juan M. Vieites, and Ana G. Cabado. "Cytotoxic effects of BADGE (bisphenol A diglycidyl ether) and BFDGE (bisphenol F diglycidyl ether) on Caco-2 cells in vitro." Archives of Toxicology 80, no. 11 (2006): 748–55. http://dx.doi.org/10.1007/s00204-006-0121-1.

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16

Lintschinger, J., and Walfried Rauter. "Simultaneous determination of bisphenol A-diglycidyl ether, bisphenol F-diglycidyl ether and their hydrolysis and chlorohydroxy derivatives in canned foods." European Food Research and Technology 211, no. 3 (2000): 211–17. http://dx.doi.org/10.1007/s002170050026.

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17

Acocella, M. R., C. Esposito Corcione, A. Giuri, M. Maggio, A. Maffezzoli, and G. Guerra. "Graphene oxide as a catalyst for ring opening reactions in amine crosslinking of epoxy resins." RSC Advances 6, no. 28 (2016): 23858–65. http://dx.doi.org/10.1039/c6ra00485g.

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18

Zago, Erika, Eric Dubreucq, Jérôme Lecomte та ін. "Synthesis of bio-based epoxy monomers from natural allyl- and vinyl phenols and the estimation of their affinity to the estrogen receptor α by molecular docking". New Journal of Chemistry 40, № 9 (2016): 7701–10. http://dx.doi.org/10.1039/c6nj00782a.

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19

Rosu, D., F. Mustata, N. Tudorachi, V. E. Musteata, L. Rosu, and C. D. Varganici. "Novel bio-based flexible epoxy resin from diglycidyl ether of bisphenol A cured with castor oil maleate." RSC Advances 5, no. 57 (2015): 45679–87. http://dx.doi.org/10.1039/c5ra05610a.

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20

El Gersifi, K., G. Durand, and G. Tersac. "Solvolysis of bisphenol A diglycidyl ether/anhydride model networks." Polymer Degradation and Stability 91, no. 4 (2006): 690–702. http://dx.doi.org/10.1016/j.polymdegradstab.2005.05.021.

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21

Szymoniak, Paulina, Xintong Qu, Mozhdeh Abbasi, et al. "Spatial inhomogeneity, interfaces and complex vitrification kinetics in a network forming nanocomposite." Soft Matter 17, no. 10 (2021): 2775–90. http://dx.doi.org/10.1039/d0sm01992e.

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A detailed calorimetric study on an epoxy-based nanocomposite system was performed employing bisphenol A diglycidyl ether cured with diethylenetriamine as the polymer matrix and a taurine-modified MgAL layered double hydroxide as the nanofiller.

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22

Ba, Longhan, Qi Zou, Xiaocun Tan, Jiangpeng Song, Jue Cheng, and Junying Zhang. "Structure, morphology and properties of epoxy networks with dangling chains cured by anhydride." RSC Advances 6, no. 94 (2016): 91875–81. http://dx.doi.org/10.1039/c6ra16418h.

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A series of epoxy networks containing side aliphatic dangling chains were prepared by the curing reaction of bisphenol F diglycidyl ether (DGEBF), the monofunctional epoxy (including n-butyl, dodecyl, cetyl) and the anhydride.

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23

Lane, Rachael F., Craig D. Adams, Stephen J. Randtke, and Ray E. Carter. "Chlorination and chloramination of bisphenol A, bisphenol F, and bisphenol A diglycidyl ether in drinking water." Water Research 79 (August 2015): 68–78. http://dx.doi.org/10.1016/j.watres.2015.04.014.

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24

Tarnacka, Magdalena, Michał Mierzwa, Ewa Kamińska, Kamil Kamiński, and Marian Paluch. "High-pressure experiments as a novel perspective to study the molecular dynamics of glass-forming materials confined at the nanoscale." Nanoscale 12, no. 19 (2020): 10600–10608. http://dx.doi.org/10.1039/d0nr02255a.

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We report the pioneering high-pressure dielectric studies on the dynamics of a model van der Waals glass-forming liquid bisphenol-A diglycidyl ether infiltrated into anodic aluminum oxide templates of the mean pore sizes, d = 150 and d = 18 nm.

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25

Summerfield, W., A. Goodson, and I. Cooper. "Survey of Bisphenol A diglycidyl ether (BADGE) in canned foods." Food Additives and Contaminants 15, no. 7 (1998): 818–30. http://dx.doi.org/10.1080/02652039809374716.

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26

Mat?jka, L., K. Du?ek, P. Chabanne, and J. P. Pascault. "Cationic polymerization of diglycidyl ether of Bisphenol A. II. theory." Journal of Polymer Science Part A: Polymer Chemistry 35, no. 4 (1997): 651–63. http://dx.doi.org/10.1002/(sici)1099-0518(199703)35:4<651::aid-pola7>3.0.co;2-s.

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27

Tcharkhtchi, A., L. Audouin, and J. Verdu. "Chemiluminescence of diglycidyl ether of bisphenol A — Norbornene anhydride networks." Journal of Bioluminescence and Chemiluminescence 8, no. 6 (1993): 315–23. http://dx.doi.org/10.1002/bio.1170080605.

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28

Kim, Haechan, Jungsoo Kim, and Donghyun Kim. "Enhancement of Gel Strength of Itaconic Acid-Based Superabsorbent Polymer Composites Using Oxidized Starch." Polymers 13, no. 17 (2021): 2859. http://dx.doi.org/10.3390/polym13172859.

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Herein, core-superabsorbent polymer (CSAP) composites are prepared from oxidized starch (OS) via aqueous solution copolymerization using ammonium persulfate as the initiator, and 1,6-hexanediol diacrylate as the inner-crosslinker. The surface-crosslinking process is performed using various surface-crosslinkers, including bisphenol A diglycidyl ether (BADGE), poly(ethylene glycol) diglycidyl ether (PEGDGE), ethylene glycol diglycidyl ether (EGDGE), and diglycidyl ether (DGE). The structures of the CSAP composites and their surface-crosslinked SAPs (SSAPs) are characterized using Fourier transfo

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29

Sue, H. J., P. M. Puckett, J. L. Bertram, L. L. Walker, and E. I. Garcia-Meitin. "Structure and property relationships in model diglycidyl ether of bisphenol-a and diglycidyl ether of tetramethyl bisphenol-a epoxy systems. I. Mechanical property characterizations." Journal of Polymer Science Part B: Polymer Physics 37, no. 16 (1999): 2137–49. http://dx.doi.org/10.1002/(sici)1099-0488(19990815)37:16<2137::aid-polb16>3.0.co;2-i.

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30

Tong, Yongfen, Hailong Lyu, Yuzhong Xu, et al. "All-solid-state interpenetrating network polymer electrolytes for long cycle life of lithium metal batteries." Journal of Materials Chemistry A 6, no. 30 (2018): 14847–55. http://dx.doi.org/10.1039/c8ta03062f.

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All-solid-state interpenetrating network polymer electrolytes (INSPEs) were fabricated by a simultaneous reaction of 3-armed poly(ethylene glycol) methyl ether methacrylate-co-glycidyl methacrylate and bisphenol A diglycidyl ether (BPDE) with polyether diamine (ED2003) in the presence of LiTFSI, exhibiting high ionic conductivities at room temperature and remarkable stability towards lithium metal.

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31

Wang, Tianyu, and Cong Zeng. "Study of Cement-Based Superhydrophobic Composite Coating: New Option for Water Drainage Pipeline Rehabilitation." Materials 13, no. 21 (2020): 5004. http://dx.doi.org/10.3390/ma13215004.

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A great number of urban underground concrete water drainage systems in China are facing challenges of corrosion, blockage, and leakage. This could result in engineering accidents such as urban inland inundation, pipeline collapse, leakage, and blockage. The common contributing factors for pipeline leakage and blockage are the porous structures and the perishable surfaces of concrete pipes. To address these issues, we synthesized superhydrophobic coating materials such as SiO2 aerosol, bisphenol A diglycidyl ether (DGEBA), and N-β-aminoethyl-γ-aminopropyltrimethoxysilane (AEAPTS). Our superhydr

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32

Malburet, Samuel, Chiara Di Mauro, Camilla Noè, Alice Mija, Marco Sangermano, and Alain Graillot. "Sustainable access to fully biobased epoxidized vegetable oil thermoset materials prepared by thermal or UV-cationic processes." RSC Advances 10, no. 68 (2020): 41954–66. http://dx.doi.org/10.1039/d0ra07682a.

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Beyond the need to find a non-toxic alternative to DiGlycidyl Ether of Bisphenol-A (DGEBA), the serious subject of non-epichlorohydrin epoxy resins production remains a crucial challenge that must be solved for the next epoxy resin generations.

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33

Chen, Qiao, and Fang Ke Shao. "Proton Exchange Membranes Based on POSS." Advanced Materials Research 953-954 (June 2014): 985–88. http://dx.doi.org/10.4028/www.scientific.net/amr.953-954.985.

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Two kinds of proton exchange membranes (PEMs) containing POSS are designed and prepared, one is sulfonated poly (ether ether ketone) (SPEEK)/bisphenol S diglycidyl ether (DEBS)/POSS hybrids with the semi-interpenetrating polymer networks (IPNs) structure and the other is sulfonated polyimides (SPI)/POSS hybrids with cross-link structure. IPNs should be more contributed to improve the proton conductivities of PEMs than cross-link structure.

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34

Ekincioglu, Ozgur, M. Hulusi Ozkul, Yoshihiko Ohama, Silvia Patachia, and Georgeta Moise. "Effect of Epoxy Resin Addition on the Moisture Sensitivity of Macro Defect Free Polymer-Cement Composites." Key Engineering Materials 466 (January 2011): 65–72. http://dx.doi.org/10.4028/www.scientific.net/kem.466.65.

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Macro-defect-free (MDF) cements are cement-polymer composites and were developed by Birchall et al. three decades ago. The composites are produced by mixing small amounts of polymer and water with cement. However, they have a different production method than that of cement pastes, which was inspired by rubber production. Mixtures of cement, polymer and water are processed by using a two-roll mill. The composites are known with their high flexural strengths. Unfortunately, there are not any known commercial products using MDF cements because of their poor durability under moisture. In this stud

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35

Chandran, Sarath, F. Antolasic, K. J. Eichhorn, Robert A. Shanks, and S. Thomas. "Stereochemistry and miscibility of epoxy resin–poly(trimethylene terephthalate) blends." RSC Adv. 4, no. 48 (2014): 25420–29. http://dx.doi.org/10.1039/c4ra01429d.

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Stereochemistry is proposed to contribute to the miscibility of poly(trimethylene terephthalate) (PTT) and bisphenol-A diglycidyl ether (BADGE), since molecular conformation is one of the determinants of the close packing ability and hence the interactions of such a system.

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36

Barral, L., J. Cano, J. López, et al. "Cure kinetics of amine-cured diglycidyl ether of bisphenol." Thermochimica Acta 344, no. 1-2 (2000): 127–36. http://dx.doi.org/10.1016/s0040-6031(99)00335-4.

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37

Tian, Qiao, Yan Chao Yuan, Min Zhi Rong, and Ming Qiu Zhang. "Synthesis and Characterization of a Novel Epoxy with Improved Processability." Advanced Materials Research 47-50 (June 2008): 290–93. http://dx.doi.org/10.4028/www.scientific.net/amr.47-50.290.

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For purposes of developing a novel epoxy with low viscosity and high activity, N,N-diglycidyl-furfurlamine (DGFA) was successfully synthesized through a two-step reaction between 2-furfurylamine and epichlorohydrin involving ring-opening and ring-closure mechanisms. The product structure was verified by FTIR, 1H-NMR, 13C-NMR and elemental analysis, respectively. Its viscosity was found to be 0.02 Pa·s at 25oC. To understand its curing behavior, exothermic habit of the model mixture of DGFA and the curing agent methylhexahydrophthalic anhydride (MHHPA) at stoichiometric ratio of epoxy ring/anhy

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38

Wang, Lei, Jingchuan Xue, and Kurunthachalam Kannan. "Widespread Occurrence and Accumulation of Bisphenol A Diglycidyl Ether (BADGE), Bisphenol F Diglycidyl Ether (BFDGE) and Their Derivatives in Human Blood and Adipose Fat." Environmental Science & Technology 49, no. 5 (2015): 3150–57. http://dx.doi.org/10.1021/acs.est.5b00096.

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39

Chen, Qiao, Fang Ke Shao, and Gang Wu. "Ternary Hybrid Proton Exchange Membranes Based on POSS." Advanced Materials Research 550-553 (July 2012): 493–96. http://dx.doi.org/10.4028/www.scientific.net/amr.550-553.493.

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The sulfonated poly(ether ether ketone) (SPEEK)/bisphenol S diglycidyl ether (DEBS)/POSS ternary hybrids is designed and prepared to incorporate POSS into SPEEK to form a new cross-linked proton exchange membrane (PEM). Compared with the SPEEK, the ternary hybrids possesses lower water uptake (WU) and linear expansion (LE), but higher proton conductivity. The proton conductivity of SPEEK/DEBS/POSS can reach to 1.1×10-1 S/cm.

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40

Lin, Qin-Bao, Long-Fei Cai, Shao-Jing Wu, Zhi-Nan Chen, and Zhi-Wei Wang. "Migration of Bisphenol A and Bisphenol A Diglycidyl-ether from Can Coatings into Food Simulants." Asian Journal of Chemistry 27, no. 8 (2015): 3013–18. http://dx.doi.org/10.14233/ajchem.2015.18790.

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41

Pham, Quoc-Thai, Jung-Mu Hsu, Jing-Pin Pan, Tsung-Hsiung Wang, and Chorng-Shyan Chern. "Non-isothermal degradation of bisphenol A diglycidyl ether diacrylate-based polymers." Thermochimica Acta 573 (December 2013): 10–17. http://dx.doi.org/10.1016/j.tca.2013.08.013.

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42

Janerva, Lasse, Ritta Jolanki, Liisa Halmepuro, Heskinen, and Tuula Estlander. "Immediate and delayed allergy to diglycidyl ether bisphenol A epoxy resin." Contact Dermatitis 23, no. 4 (1990): 252. http://dx.doi.org/10.1111/j.1600-0536.1990.tb05048.x.

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43

Jain, Preeti, Veena Choudhary, and I. K. Varma. "Thermal characterization of diglycidyl ether of bisphenol-A/phosphorus containing amines." Journal of Applied Polymer Science 81, no. 2 (2001): 390–95. http://dx.doi.org/10.1002/app.1450.

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44

Liu, Guodong, Xiaoqun Zhu, Bingbing Xu, Xiaochun Qian, Guoqiang Song, and Jun Nie. "Cationic photopolymerization of bisphenol A diglycidyl ether epoxy under 385 nm." Journal of Applied Polymer Science 130, no. 5 (2013): 3698–703. http://dx.doi.org/10.1002/app.39612.

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45

Jost, Sylvie, Laurent Vanbellinghen, Philippe Henderson, and Jacqueline Marchand-Brynaert. "ChemInform Abstract: Reaction of Bisphenol-A Diglycidyl Ether with Substituted Phenols." ChemInform 30, no. 31 (2010): no. http://dx.doi.org/10.1002/chin.199931119.

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46

Kanerva, L., M. Pelttari, R. Jolanki, K. Alanko, T. Estlander, and R. Suhonen. "Occupational contact urticaria from diglycidyl ether of bisphenol A epoxy resin." Allergy 57, no. 12 (2002): 1205–7. http://dx.doi.org/10.1034/j.1398-9995.2002.13118.x.

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47

Cao, Xu-Liang, Guy Dufresne, Genevieve Clement, Stphane Blisle, Andr Robichaud, and Franca Beraldin. "Levels of Bisphenol A Diglycidyl Ether (BADGE) and Bisphenol F Diglycidyl Ether (BFDGE) in Canned Liquid Infant Formula Products in Canada and Dietary Intake Estimates." Journal of AOAC INTERNATIONAL 92, no. 6 (2009): 1780–89. http://dx.doi.org/10.1093/jaoac/92.6.1780.

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Abstract A method based on solid-phase extraction followed by HPLC analysis with fluorescence detection was developed for the determination of bisphenol A diglycidyl ether (BADGE) and bisphenol F diglycidyl ether (BFDGE) in liquid infant formula. In this method, instead of trying to isolate and measure each individual form of the molecules, hydrolysis of BADGE, BFDGE, BADGEH2O, and BFDGEH2O was forced to completion to their stable forms, BADGE2H2O and BFDGE2H2O, before extraction. The method LODs were 2.0 ng/g for BADGE and 3.0 ng/g for BFDGE. Extraction recoveries were 6191 for BADGE, and 558

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48

Szczepańska, Natalia, Paweł Kubica, Błażej Kudłak, Jacek Namieśnik, and Andrzej Wasik. "Stabilities of bisphenol A diglycidyl ether, bisphenol F diglycidyl ether, and their derivatives under controlled conditions analyzed using liquid chromatography coupled with tandem mass spectrometry." Analytical and Bioanalytical Chemistry 411, no. 24 (2019): 6387–98. http://dx.doi.org/10.1007/s00216-019-02016-5.

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49

Kostoryz, E. L., J. D. Eick, A. G. Glaros, et al. "Biocompatibility of Hydroxylated Metabolites of BISGMA and BFDGE." Journal of Dental Research 82, no. 5 (2003): 367–71. http://dx.doi.org/10.1177/154405910308200508.

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Unpolymerized dental monomers can leach out into the oral biophase and are bioavailable for metabolism. We hypothesize that metabolites would be less toxic than parent monomers. We first identified the formation of metabolites from bisphenol F diglycidyl ether (BFDGE) and Bisphenol A glycidyl methacrylate (BISGMA) after their exposure to liver S9 fractions. Then, the metabolites and parent compounds were subjected to in vitro cytotoxicity, mutagenicity, and estrogenicity studies. Bisphenol A bis(2,3-dihydroxypropyl) ether and bisphenol F bis(2,3-dihydroxypropyl) ether were the hydroxylated met

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Sharma, P., V. Choudhary, and A. K. Narula. "Curing kinetics and thermal stability of diglycidyl ether of bisphenol." Journal of Thermal Analysis and Calorimetry 91, no. 1 (2008): 231–36. http://dx.doi.org/10.1007/s10973-006-7749-1.

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