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Estrogenicity of Octyl Glucoside Synthesized by Direct Glucosidation as Non-Endocrine Disruptive Surfactant.
Chung, Kyong-Hwan; Kim, Hangun; Park, Young-Kwon; Kim, Byung-Hoon; Kim, Jung-Sik; Jung, Sang-Chul.
Afiliación
  • Chung KH; Department of Environmental Engineering, Sunchon National University, Suncheon 57922, Korea.
  • Kim H; College of Pharmacy, Sunchon National University, Suncheon 57922, Korea.
  • Park YK; School of Environmental Engineering, University of Seoul, Seoul 02504, Korea.
  • Kim BH; Department of Dental Materials, Chosun University, Gwangju 61452, Korea.
  • Kim JS; Department of Materials Science and Engineering, University of Seoul, Seoul 02504, Korea.
  • Jung SC; Department of Environmental Engineering, Sunchon National University, Suncheon 57922, Korea.
J Nanosci Nanotechnol ; 18(2): 1478-1481, 2018 Feb 01.
Article en En | MEDLINE | ID: mdl-29448618
The estrogenicity of octyl glucoside was studied with its preparation method using microporous zeolites. Its estrogenicity was estimated using E-assay method to confirm the possibility as non-endocrine disruptive surfactant. The octyl glucoside was synthesized from D-glucose with 1-octanol by direct glucosidation. The high conversion of D-glucose was obtained on H-FAU zeolite which has a mild acid strength. The conversion and yield were improved with increasing of acid site amount of the zeolite catalysts. The octyl glucopyranoside is more hydrophilic than nonylphenol and has a high wettability. The octyl glucosides represented extremely lower estrogenic cell proliferation compared with nonylphenol.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Nanosci Nanotechnol Año: 2018 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Nanosci Nanotechnol Año: 2018 Tipo del documento: Article