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University of Minnesota • Department of Chemistry


Triclosan News Stories


Photochemical Conversion of Triclosan to 2,8-DCDD
J. Photochem. Photobiol. A. 2003, 158/1 63-66.(Link to Journal)

Photochemical conversion of triclosan to 2,8-dichlorodibenzo-p-dioxin in aqueous solution
Douglas E. Latch,1 Jennifer L. Packer,2 William A. Arnold,2 and Kristopher McNeill1

1Department of Chemistry, University of Minnesota, 2Department of Civil Engineering, University of Minnesota


Abstract
The direct photolysis of triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol), an antimicrobial additive commonly detected in surface waters, is studied. It is found that 2,8-dichlorodibenzo-p-dioxin (2,8-DCDD) is produced in both buffered and natural (Mississippi River) water with yields ranging from 1 to 12% under a variety of conditions. This result indicates that triclosan is likely converted to 2,8-DCDD in sunlight-irradiated surface waters.
News Links
Science NetLinks (AAAS) (Cached)
BBC News (Cached)
CBC News (Cached)
The Alchemist (Cached)
St. Paul Pioneer Press (Cached)
Minneapolis Star Tribune/AP (Cached)
UPI (Cached)
The Hindu Times (Cached)
Neue Zürcher Zeitung, Switzerland

Science Update
(AAAS Radio Show,6/4/03) (Cached)
WPVI-ABC Philadelphia, Television News

Minnesota Public Radio, All Things Considered

Environmental Science and Technology (From the Spring 2002 ACS Meeting)
©2006 Kristopher McNeill