Reheating a bowl of chilli con carnage (I.e one my old man made, because he doesn't use fly agaric and peppery boletus in it OR
the correct extra spices when he does one. Its edible enough and not BAD, its just, not excellent as it should be with a bit of dried cured Amanita muscaria mushrooms.
Listening to music (Otep-Atom to Adam
https://youtu.be/vbOSSiBEZD4 )
Smoking a fag. Wishing I had bud, tried random likely looking types but the fucker wouldn't help, hadn't got a phone. Hadn't got mine on me either. Haven't had anything but synthetics in a couple of years

don't know anybody anymore, since my old phone got jacked and I lost all my contacts.
Just plugged 100-120mg or so of oxy IR and a few mg of pramipexole (a dopamine agonist)
Got to ring my lawyer to rearrange a bail date.
Hunting around for a plug, to wire to my better water pump. I have another but its tiny and crappy, and I can't find it anyway. Got an experiment to perform regarding acetaldehyde synthesis. Have to do a distillation through a condenser recirculating salted ice-water, and collect product in a flask situated within a salt/diethylene glycol/a little water to ensure good contact with the receiver flask/ice bath since the boiling point of acetaldehyde is only 20.2 degrees 'C. So going to collect it in a cryo bath at -30something (I forget exactly how cold that particular mixture gets, but with some methylated spirits added to the antfreeze poured over the salted ice, it gets just a few degrees short of the temperature requited to render gaseous ammonia liquid.
Also got to purify some willy pete, by distillation followed by a bath in hot chromic acid (potassium dichromate/98% sulfuric mixture) and melting the W P under the surface of the chromic acid bath to clean the inside from oxides; all done under inert gas. Its a fairly extreme length to go to get it clean but this is not for making meth etc. but rather, symthesis of a little-studied allotrope of the element where impurities could conceivably have all manner of effects upon things like crystal substructure at the molecular level, success v failure and the quality of the crystals. The method involves recrystallizing either red or white phosphorus after heating it under molten lead for between 18 hours and two days. Got an electrically controlled moten metal-based heating bath. Going to build myself some custom sealed retorts from copper pipe and fittings; then before use, several spray-burn cyc;les of potassium sillicate solution to give it a glass coating, doesn't need to be thermal shock resistant, its just to avoid contact with the searing hot phosphorus with the copper and formation of phosphine gas, PH3, the phosphorus analogue of NH3m annonia but which is extremely poisonous.
Or I intended to. Will have to do it tomorrow, since my morning dose of nitrazepam left me nodding out HARD combined with 300mg morphine IM and 200 of oxy plugged. I'm still nodding in and out, so no way am I going to start roasting elemental phosphorus when I can hardly see straight or type correctly

(not sure which so am going to try both as two separate experiments in parallel, possibly three, using Schlenk;s scarlet allotrope and see what happens)