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- Path: sparky!uunet!paladin.american.edu!darwin.sura.net!news.larc.nasa.gov!grissom.larc.nasa.gov!kludge
- From: kludge@grissom.larc.nasa.gov (Scott Dorsey)
- Newsgroups: talk.bizarre
- Subject: Re: how one becomes drunk
- Followup-To: talk.bizarre,sci.med,sci.chem
- Date: 11 Jan 1993 23:41:42 GMT
- Organization: NASA Langley Research Center and Reptile Farm
- Lines: 19
- Message-ID: <1it0jmINNajo@rave.larc.nasa.gov>
- References: <gHw5wB2w165w@cerianthus.pinetree.org> <1inv0mINNons@rave.larc.nasa.gov> <3580@accucx.cc.ruu.nl>
- NNTP-Posting-Host: grissom.larc.nasa.gov
- Keywords: lemur
-
- In article <3580@accucx.cc.ruu.nl> verhaar@accucx.cc.ruu.nl (Henk Verhaar) writes:
- >Watch it :) introducing chlorine groups or unsaturations 'next' to the
- >hydroxy-group makes the compound reactive - an electrophile. While this
- >doesn't mean reactive as in readily attacks other chemicals, this does mean
- >not inert towards e.g. biomolecules. Apparently this effect accounts for the
- >added toxicity of such compounds.
-
- Yes, the excessive lopsidedness of such substances would make them more toxic.
- I should point out, though, that in most cases, the toxicity of the alcohol
- itself isn't the problem, but the toxicity of the metabolic byproduct as the
- body attempts to rid itself of the alcohol.
-
- You can work out the oxidation reactions for the chlorinated alcohols yourself.
- Some of the products of their oxidation are extremely vile looking, and are
- definitely not things which I would want in my body.
-
- The original question, however, was one of psychoactive effects and not one
- of toxicity.
- --scott
-