Avobenzone (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Avobenzone" in French language version.

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dguv.de

gestis.dguv.de

  • Entrée « Avobenzone » dans la base de données de produits chimiques GESTIS de la IFA (organisme allemand responsable de la sécurité et de la santé au travail) (allemand, anglais), accès le 14 juin 2020 (JavaScript nécessaire)

doi.org

dx.doi.org

  • « A Blocked Diketo Form of Avobenzone: Photostability, Photosensitizing Properties and Triplet Quenching by a Triazine-derived UVB-filter », Photochemistry and Photobiology, vol. 85, no 1,‎ january–february 2009, p. 178–184 (PMID 18673327, DOI 10.1111/j.1751-1097.2008.00414.x)
  • « Influence Of Substituent On UV Absorption And Keto–Enol Tautomerism Equilibrium Of Dibenzoylmethane Derivatives », Spectrochim Acta a Mol Biomol Spectrosc., vol. 96,‎ , p. 815–819 (PMID 22925908, DOI 10.1016/j.saa.2012.07.109, Bibcode 2012AcSpA..96..815Z)
  • « Sunscreens with an absorption maximum of > or =360 nm provide optimal protection against UVA1-induced expression of matrix metalloproteinase-1, interleukin-1, and interleukin-6 in human dermal fibroblasts », Photochem Photobiol Sci, vol. 5, no 3,‎ , p. 275–282 (PMID 16520862, DOI 10.1039/b516702g)
  • « Photostabilization of Butyl methoxydibenzoylmethane (Avobenzone) and Ethylhexyl methoxycinnamate by Bis-ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb S), a new UV broadband filter », Photochemistry and Photobiology, vol. 74, no 3,‎ , p. 401–406 (ISSN 0031-8655, PMID 11594052, DOI 10.1562/0031-8655(2001)074<0401:POBMAA>2.0.CO;2)
  • « Changes in ultraviolet absorption of sunscreens after ultraviolet irradiation », Journal of Investigative Dermatology, vol. 113, no 4,‎ , p. 547–553 (PMID 10504439, DOI 10.1046/j.1523-1747.1999.00721.x, lire en ligne)
  • « A new long-chain UV absorber derived from 4-tert-butyl-4'-methoxydibenzoylmethane: absorbance stability under solar irradiation », Journal of Cosmetic Science, vol. 56, no 2,‎ mar–apr 2005, p. 135–148 (PMID 15870853, DOI 10.1562/2004-03-09-ra-106)
  • « Design of a photostabilizer having built-in antioxidant functionality and its utility in obtaining broad-spectrum sunscreen formulations », Photochemistry and Photobiology, vol. 82, no 3,‎ may–jun 2006, p. 823–828 (PMID 16492073, DOI 10.1562/2005-07-15-RA-612)
  • « Influence of hydroxypropyl-beta-cyclodextrin on photo-induced free radical production by the sunscreen agent, butyl-methoxydibenzoylmethane », Journal of Pharmacy and Pharmacology, vol. 54, no 11,‎ , p. 1553–1558 (PMID 12495559, DOI 10.1211/002235702207)
  • « Influence of hydroxypropyl-β-cyclodextrin on transdermal penetration and photostability of avobenzone », European Journal of Pharmaceutics and Biopharmaceutics, vol. 69, no 2,‎ , p. 605–612 (PMID 18226883, DOI 10.1016/j.ejpb.2007.12.015)
  • Warwick L. Morison, M.D., « Photosensitivity », The New England Journal of Medicine, vol. 350, no 11,‎ , p. 1111–1117 (PMID 15014184, DOI 10.1056/NEJMcp022558)
  • « The effects of manganese doping on UVA absorption and free radical generation of micronised titanium dioxide and its consequences for the photostability of UVA absorbing organic sunscreen components », Photochem Photobiol Sci, vol. 3, no 7,‎ , p. 648–652 (PMID 15238999, DOI 10.1039/b403697b)
  • Zhang G, Lu J, Sabat M et Fraser, CL, « Polymorphism and Reversible Mechanochromic Luminescence for Solid-State Difluoroboron Avobenzone », Journal of the American Chemical Society, vol. 132, no 7,‎ , p. 2160–2162 (PMID 20108897, DOI 10.1021/ja9097719, lire en ligne)
  • Wang, Bavcon Kralj, Košmrlj et Yao, « Stability and removal of selected avobenzone's chlorination products », Chemosphere, vol. 182,‎ , p. 238–244 (PMID 28500968, DOI 10.1016/j.chemosphere.2017.04.125, Bibcode 2017Chmsp.182..238W)
  • Trebše, Polyakova, Baranova et Kralj, « Transformation of avobenzone in conditions of aquatic chlorination and UV-irradiation », Water Research, vol. 101,‎ , p. 95–102 (PMID 27258620, DOI 10.1016/j.watres.2016.05.067)

dsm.com

eurekalert.org

fda.gov

hallstar.com

harvard.edu

ui.adsabs.harvard.edu

issn.org

portal.issn.org

makingcosmetics.com

nature.com

nih.gov

ncbi.nlm.nih.gov

  • « A Blocked Diketo Form of Avobenzone: Photostability, Photosensitizing Properties and Triplet Quenching by a Triazine-derived UVB-filter », Photochemistry and Photobiology, vol. 85, no 1,‎ january–february 2009, p. 178–184 (PMID 18673327, DOI 10.1111/j.1751-1097.2008.00414.x)
  • « Influence Of Substituent On UV Absorption And Keto–Enol Tautomerism Equilibrium Of Dibenzoylmethane Derivatives », Spectrochim Acta a Mol Biomol Spectrosc., vol. 96,‎ , p. 815–819 (PMID 22925908, DOI 10.1016/j.saa.2012.07.109, Bibcode 2012AcSpA..96..815Z)
  • « Sunscreens with an absorption maximum of > or =360 nm provide optimal protection against UVA1-induced expression of matrix metalloproteinase-1, interleukin-1, and interleukin-6 in human dermal fibroblasts », Photochem Photobiol Sci, vol. 5, no 3,‎ , p. 275–282 (PMID 16520862, DOI 10.1039/b516702g)
  • « Photostabilization of Butyl methoxydibenzoylmethane (Avobenzone) and Ethylhexyl methoxycinnamate by Bis-ethylhexyloxyphenol methoxyphenyl triazine (Tinosorb S), a new UV broadband filter », Photochemistry and Photobiology, vol. 74, no 3,‎ , p. 401–406 (ISSN 0031-8655, PMID 11594052, DOI 10.1562/0031-8655(2001)074<0401:POBMAA>2.0.CO;2)
  • « Changes in ultraviolet absorption of sunscreens after ultraviolet irradiation », Journal of Investigative Dermatology, vol. 113, no 4,‎ , p. 547–553 (PMID 10504439, DOI 10.1046/j.1523-1747.1999.00721.x, lire en ligne)
  • « A new long-chain UV absorber derived from 4-tert-butyl-4'-methoxydibenzoylmethane: absorbance stability under solar irradiation », Journal of Cosmetic Science, vol. 56, no 2,‎ mar–apr 2005, p. 135–148 (PMID 15870853, DOI 10.1562/2004-03-09-ra-106)
  • « Design of a photostabilizer having built-in antioxidant functionality and its utility in obtaining broad-spectrum sunscreen formulations », Photochemistry and Photobiology, vol. 82, no 3,‎ may–jun 2006, p. 823–828 (PMID 16492073, DOI 10.1562/2005-07-15-RA-612)
  • « Influence of hydroxypropyl-beta-cyclodextrin on photo-induced free radical production by the sunscreen agent, butyl-methoxydibenzoylmethane », Journal of Pharmacy and Pharmacology, vol. 54, no 11,‎ , p. 1553–1558 (PMID 12495559, DOI 10.1211/002235702207)
  • « Influence of hydroxypropyl-β-cyclodextrin on transdermal penetration and photostability of avobenzone », European Journal of Pharmaceutics and Biopharmaceutics, vol. 69, no 2,‎ , p. 605–612 (PMID 18226883, DOI 10.1016/j.ejpb.2007.12.015)
  • Warwick L. Morison, M.D., « Photosensitivity », The New England Journal of Medicine, vol. 350, no 11,‎ , p. 1111–1117 (PMID 15014184, DOI 10.1056/NEJMcp022558)
  • « The effects of manganese doping on UVA absorption and free radical generation of micronised titanium dioxide and its consequences for the photostability of UVA absorbing organic sunscreen components », Photochem Photobiol Sci, vol. 3, no 7,‎ , p. 648–652 (PMID 15238999, DOI 10.1039/b403697b)
  • Zhang G, Lu J, Sabat M et Fraser, CL, « Polymorphism and Reversible Mechanochromic Luminescence for Solid-State Difluoroboron Avobenzone », Journal of the American Chemical Society, vol. 132, no 7,‎ , p. 2160–2162 (PMID 20108897, DOI 10.1021/ja9097719, lire en ligne)
  • Wang, Bavcon Kralj, Košmrlj et Yao, « Stability and removal of selected avobenzone's chlorination products », Chemosphere, vol. 182,‎ , p. 238–244 (PMID 28500968, DOI 10.1016/j.chemosphere.2017.04.125, Bibcode 2017Chmsp.182..238W)
  • Trebše, Polyakova, Baranova et Kralj, « Transformation of avobenzone in conditions of aquatic chlorination and UV-irradiation », Water Research, vol. 101,‎ , p. 95–102 (PMID 27258620, DOI 10.1016/j.watres.2016.05.067)

qmul.ac.uk

chem.qmul.ac.uk

semanticscholar.org

  • Zhang G, Lu J, Sabat M et Fraser, CL, « Polymorphism and Reversible Mechanochromic Luminescence for Solid-State Difluoroboron Avobenzone », Journal of the American Chemical Society, vol. 132, no 7,‎ , p. 2160–2162 (PMID 20108897, DOI 10.1021/ja9097719, lire en ligne)

web.archive.org