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Page 1
Amended final report on the safety assessment of ethyl methacrylate.
Cosmetic Ingredient Review Expert panel. Cosmetic Ingredient Review Expert panel. Int J Toxicol. 2002;21 Suppl 1:63-79. doi: 10.1080/10915810290096397. Int J Toxicol. 2002. PMID: 12042061 Review.
Information from several clinical registries of sensitization reactions to various agents reported that Ethyl Methacrylate is a sensitizer, but not a potent one. Because Ethyl Methacrylate monomer is short-lived in the normal course of using artificial finger …
Information from several clinical registries of sensitization reactions to various agents reported that Ethyl Methacrylate is a sensitizer, …
Butyl methacrylate monomer and ethyl methacrylate monomer--frequency of reaction.
Maibach H, Hjorth N, Fregert S, Menghini C, Bandman HJ, Malten K, Pirillä V, Magnusson B, Cronin E, Calnan C, Wilkinson D, Marzulli F. Maibach H, et al. Contact Dermatitis. 1978 Feb;4(1):60. doi: 10.1111/j.1600-0536.1978.tb03731.x. Contact Dermatitis. 1978. PMID: 657794 No abstract available.
Size Control and Biological Properties of PAMAM-Cored Multiarm Block Copolymers.
Yu B, Sun Y, Xiao P, Li C, Yuan K, Zhang L, Jiang X, Wu W. Yu B, et al. ACS Appl Bio Mater. 2023 Jun 19;6(6):2426-2434. doi: 10.1021/acsabm.3c00236. Epub 2023 May 31. ACS Appl Bio Mater. 2023. PMID: 37259528
The multiarm copolymers were synthesized by the ring-opening polymerization of N-carboxyanhydride of the l-glutamic acid-5-tert-butylester [Glu(OtBu)-NCA] monomer with the amine-terminated PAMAM as the initiator, followed by the synthesis of the poly(carboxybetaine) (PCB) block v …
The multiarm copolymers were synthesized by the ring-opening polymerization of N-carboxyanhydride of the l-glutamic acid-5-tert-butylester [ …
Neurotoxicity of ethyl methacrylate in rats.
Abou-Donia MB, Abdel-Rahman AA, Kishk AM, Walker D, Markwiese BJ, Acheson SK, Reagan KE, Swartzwelder S, Jensen KF. Abou-Donia MB, et al. J Toxicol Environ Health A. 2000 Jan 28;59(2):97-118. doi: 10.1080/009841000157005. J Toxicol Environ Health A. 2000. PMID: 10653438
Heterocyclic methacrylates for clinical applications. I. Mechanical properties.
Patel MP, Braden M. Patel MP, et al. Biomaterials. 1991 Sep;12(7):645-8. doi: 10.1016/0142-9612(91)90110-v. Biomaterials. 1991. PMID: 1742407
The homopolymers gave Young's moduli in the range 1.38-2.19 GN/m2, i.e. lower than poly(methyl methacrylate). The moduli of poly(ethyl methacrylate)/monomer systems are theoretically predictable from the moduli of the homopolymers involved. ...
The homopolymers gave Young's moduli in the range 1.38-2.19 GN/m2, i.e. lower than poly(methyl methacrylate). The moduli of poly(ethyl …
Concurrent self-regulated autonomous synthesis and functionalization of pH-responsive giant vesicles by a chemical pH oscillator.
Poros-Tarcali E, Perez-Mercader J. Poros-Tarcali E, et al. Soft Matter. 2021 Apr 21;17(15):4011-4018. doi: 10.1039/d1sm00150g. Soft Matter. 2021. PMID: 33666638
The semibatch BrO3--SO32- pH oscillator serves as the radical source for the in situ polymerization of the pH-responsive 2-(diisopropylamino)-ethyl methacrylate monomer on poly(ethylene-glycol)-macroCTA chain and generates an amphiphilic block copolymer. ...
The semibatch BrO3--SO32- pH oscillator serves as the radical source for the in situ polymerization of the pH-responsive 2-(diisopropylamino …
21 results