Check Perrin, Perrin and Armarego's "Purification of
Laboratory Chemicals". They have recommendations, which I
have long since forgotten (because I have long since given
up the foolhardy excercise of using acetone with highly
water-sensitive reagents.) Just a guess, but I might
suggest thinking about drying it over activated 3A molecular
seives or passing it down a column of activated neutral
alumina.
Eric Lucas
jason hathaway wrote:
> Hello,
>
> How would one make acetone anhydrous?
> Simple distilliation?
> Is an azeotrope formed (hi or low BP)?
> Any dehydrating agents?
>
> Thanks,
>
> Jason
>
> ______________________________________________________
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How dry do you need it and what are you going to use it for? I distill
acetone off of potassium carbonate and that gets it good enough for the
reactions I do, however I'm not using anything that's terribly water
sensitive, I just need to get the acetone dry enough that the slurry of my
reaction doesn't clump up.
If you're looking for azeotropes, find a CRC handbook. There's a table
with a lot of common solvent azeotropes somewhere in there.
Good luck.
--------------------------------**--------------------------------
| Jeffrey J. Bodwin I got lots of good ideas, I just |
| bodw...@umich.edu ain't in charge. - Gallagher |
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