We seem to be going around in circles, however -- if you heat something hotter than its boiling point, but pressurize it so it doesn't boil. Won't it boil when you reduce the pressure? And doesn't that have to happen, when you open the autoclave?
I remember moving this thread from Physical chemistry, where you initially posted it, to Biochemistry where it is now. This was because I thought you could use some tips, from some people with experience.
However one more question: if the liquids should not boil, than why is boil over such a big problem? You are not supposed to fill the bottles completely, because of boil over, but why? If it should not happen?
The reason why is because its a good idea, at all times, to be generous with safety and handling procedures to avoid making a mess. Consider, if the pressure on a bottle is just slightly high, if it hasn't cooled off just slightly not enough, if it is just slightly overfilled, if a surface nucleation site not present in 99 other bottles is present -- hot media boils over, onto the user, into the autoclave, making a mess.
You seem to have been going though this entire thread, under the theory that the phase diagram for water applies precisely to a media solution (it doesn't, of course, given coligative properties), and that the temperature and pressure gauges are accurate and precise to 0.1 units, and you should be able to handle the entire autoclave contents without concern at the very instant your instruments read at the correct point. Basically to save time? It seems like this is an interesting thought problem, or a creative argument, but rapidly becoming an impractical discussion, as we continue to try to "logic" away real world concerns. Are you seeing where I'm coming from?