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Regioselective Synthesis of a Branched Isomer of Nonylphenol, 4-(3′,6′-Dimethyl-3′-heptyl)phenol, and Determination of its Important Environmental Properties

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dc.contributor.author Lalah, Joseph O
dc.contributor.author Schramm, Karl-Werner
dc.contributor.author Lenoir, Dieter
dc.contributor.author Henkelmann, Bernhard
dc.contributor.author Hertkorn, Norbert
dc.contributor.author Kettrup, Antonius
dc.contributor.author Günther, Klaus
dc.date.accessioned 2015-06-02T12:49:09Z
dc.date.available 2015-06-02T12:49:09Z
dc.date.issued 2001
dc.identifier.citation Chemistry - A European Journal Volume 7, Issue 22, pages 4790–4795, November 19, 2001 en_US
dc.identifier.uri http://onlinelibrary.wiley.com/doi/10.1002/1521-3765%2820011119%297:22%3C4790::AID-CHEM4790%3E3.0.CO;2-L/full
dc.identifier.uri http://hdl.handle.net/123456789/1257
dc.description.abstract A method for the synthesis of a pure nonylphenol isomer, 4-(3′,6′-dimethyl-3′-heptyl)phenol, by Friedel–Crafts reaction between anisole and 3-bromo-3,6-dimethylheptane that gives a 47.3 % overall yield is reported. The reactions were followed by GC-MS, and the chemical structures are in agreement with the NMR and IR spectra. The log Kow value for this compound, its water solubility, vapor pressure, and Henry's Law constant were also determined. These physicochemical properties were required for prediction of the compound's behavior in aquatic ecosystems. en_US
dc.language.iso en en_US
dc.subject Environmental chemistry en_US
dc.subject Friedel–Crafts alkylation en_US
dc.subject Nonylphenol isomer en_US
dc.subject Synthesis design en_US
dc.title Regioselective Synthesis of a Branched Isomer of Nonylphenol, 4-(3′,6′-Dimethyl-3′-heptyl)phenol, and Determination of its Important Environmental Properties en_US
dc.type Article en_US


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