Just took 10 H.B. Woodrose Seeds

I just don't what some kid to read this and try to distill gasoline and blow himself up.
Or start snorting rat poison or something.
You know how stupid Kids are nowadays.
Some people will do just about anything to get high.

I think that it is legal to distill wine, but, it is Illegal to distill products from one form to another.
Thats why solvents and fuels you buy are denaturated so that they cannot be consumed in the case of ethanol.
Ethanol is usually denaturated with methanol.
The additives in fuels are probably present so they burn more efficiently and so they cannot be used for illicit manufacture.

Another method of distillation that might work would be to take a large relatively flat aluminum baking sheet and put the impure liquid in the sheet. Then take a smaller aluminum baking sheet and anchor it in the center somehow and put plastic wrap over the top concaved inward so when the liquid evaporates under sunlight or some other uv/vis radiation source it condenses on the wrap covering and drips into the smaller baking sheet. An organic solvent might dissolve the plastic wrap though. This might work with water though. I don't know I have never tried it.

Haha you're pretty fucked up or something... did you just drink petroleum? Christ.

No.
Is all fun and Games. No?
Just disscussion.

Down South in the forests where in the first year "virgin gum" bleeds from the rabbits ear.
And the second year the "yellow dip" dribbles from the buck box.
The "Crude Turpentine" is then distilled in the presence of water to separate the volatile hydrocarbons "oil of turpentine" from the non-volatiles "rosin"
Ahhh the "Spirits" from the pine forests.

Apparatus: A 25- and 50-mL round bottom flask, ice-water bath, apparatus for heating under reflux, magnetic stirring, simple distillation, vacume filtration, and flameless heating.

Setting up: Place about 4-g of ground nutmeg in the 50-mL round bottom flask containing a stirbar and add 10-mL of diethyl ether. If only seeds of nutmeg are available, grind the seeds in a mortar and pestle or a blender. Attach water-cooled condeser to the flask, and set up the apparatus for heating under reflux.

Extraction and Isolation: Heat the mixture under refux for approximately 1/2 hr. Allow the contents of the flask to cool to room temperature. Filter the mixture through fluted filter paper into 25-mL round bottom flask, rinsing any residue remaining in the 50-mL flask onto the filter paper with an additional 2-4-mL of diethyl ether.
Equip the flask containing the filtrate for simple distillation, and remove the diethyl ether by distillation. Dissolve the resulting yellow oil in 3-4-mL of acetone while warming the mixture (no flames). Immediately pour the hot solution into a 25-mL Erlenmeyer flask. Allow the solution to stand at room temperature for about 1/2 hr. If crystallization has not occured during this time gently scratch the flask with a glass stirring rod at the air/liquid interface. Complete crystallization by cooling the flask in an ice water bath for an additional 15 min. Collect the trimyristin on a Buchner of Hirsch funnel by vacuum filtration. Transfer it to a watch glass or weighing paper and air dry.

123

1. Ergotamine Group:
ergotamine C33H35O5N5
ergotaminine

ergosine C30H37O5N5
ergosinine

2. Ergotoxine Group:
ergocristine C35H39O5N5
ergocristinine

ergokryptine C32H41O5N5
ergokryptinine

ergocornine C31H39O5N5
ergocorninine

3. Ergobasine Group:
ergobasine C19H23O2N3
ergobasinine

Each pair above are stereoisomers due to rearrangements between lysergic and isolysergic acids. The natural levorotataory ergot alkaloids are derived from lysergic acid, such as, ergotamine. the dextrorataory members such as ergotaminine are derived from isolysergic acid. The natural levorotatory alkaloids have powerful pharmacological action, whereas the corresponding dextrorotatory compounds posses only a fraction of the activity.