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Brown Note: Difference between revisions

Rescuing 1 sources and tagging 0 as dead.) #IABot (v2.0.8.7
(Rescuing 1 sources and tagging 0 as dead.) #IABot (v2.0.8)
(Rescuing 1 sources and tagging 0 as dead.) #IABot (v2.0.8.7)
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So butyl isocyanide is, well, something to experience. I've never had the pleasure, and will take pains not to. I can do no better than to quote the 1937 observations of one of the first groups to figure out how to prepare this noble reagent in quantity:
«''Butyl isocyanide proved to be so disagreeable to manipulate that none of its physical constants except boiling point were determined. Even when a hood with an extra forced draft was used, the odor pervaded the laboratory and adjoining rooms, deadening the sense of smell and producing in the operator, and in others, severe headaches and nausea which usually persisted for several days.''»}}
*** Or [https://web.archive.org/web/20151127001542/http://blogs.sciencemag.org/pipeline/archives/2012/05/15/things_i_wont_work_with_selenophenol this]:
{{quote|The chemical literature has numerous examples of people who are at a loss for words when it comes to describing its smell, but their attempts are eloquent all the same. A few years ago, Gaussling at the Lamentations on Chemistry blog referred to it as “''The biggest stinker I have run across... Imagine 6 skunks wrapped in rubber innertubes and the whole thing is set ablaze. That might approach the metaphysical stench of this material.''”
«''The odor of diphenyl diselenide is extremely disagreeable but is not nearly so bad as that of selenophenol. [...] The odor of selenophenol is very penetrating, and is nauseating beyond description.''» }}
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