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.
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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.
..this is what happens when you do acid to many times boys and girls...
rofl ya that's what I was thinking... ;)
Hymm?
Well this is a web page for drug users?
Kava Kava root has been used by Native Americans to relieve nervous anxiety, tension, and restlessness. Studies have shown that heavy chronic use of commercially produced kava root extract may be linked to liver damage such as cirrosis, ect.
San Pedro cacus has been said to contain mescaline, which is available in the south western united states and mexico. It would howerver require much higher does of cacus when compaired to peyote to induce hallucinogenic effects. San Pedro cacus may also contain other noxious and poisonous alkaloids so use as a peyote substitute is probably discouraged.
The folowing species of mushrooms have been found to contain psilocybin or psilocin, d (dry), f (fresh).
Species, psilocybin (%), psilocin (%)
pluteus atricapillus (d) 0.004, 0
pluteus salicinus (d) 0.005, 0
panaeolus olivaceus (f) 0.21, 0
panaeolus subbalteatus (d) 0.30, 0.05
panaeolina foenisecii (d) 0.03, 0
psathyrella candolleana (d) 0.004, 0.005
conocybe cyanopus (f) 0.45, 0.07
conocybe kuehneriana (d) 0, 0.004
psilocybe semilanceata (f) 0.80, 0.003
(f) 0.19, 0.004
(d) 0.87, 0
(f) 0.82, 0.025
(d) 0.20, 0
agrocybe (d) 0.003, 0
"Contanimation of cereal grain with ergot sclerotia formed by claviceps purpurea and related fungal species is a widely recognized phenomenon. The sclerotia contain a variety of potentially toxic ergot alkaloids some of which, such as ergonovine (ergometrine), are also used as drugs. Wheat, rye, and related Gramineaceous cereal seeds and seed stock also become contaminated by ergot alkaloids from the widely distributed wild-typ higher plants of the family Convolvulaceae. The most importand member of this family is the morning glory weed plant (ipomoea). In a previous paper we reported that the heavenly blue variety of this plant contains substantial amounts of ergot alkaloids.
Chlorogenic acid, a chromosome-damaging or clastogenic compound, was also found to be present in a series of morning glory varieties.
Although harvesting, cleaning, and milling of grain generally removes most of the ergot from contaminated crops, this is not always the case. Commercial wheat and rye flours are reported to contain smallamounts of ergot alkaloids. Lorenz (1979) reports that the consumption of ergot-contaminated grain may result in serious illness or even death."
"Heavenly Blue morning glory seeds contain about 20% high-quality protein, about 16% fat, and 55% carbohydrate and inhibited the activity of trypsin to the extent of about 11mg/g of seed flour. The total ergot content of of 52mg/100g of the seeds was reduced by 8-21% when the seed flour was mixed with a commercial wheat flour preperation in a ratio of 1:9 and baked as a muffin in a autoclave at 121 degree C for 18-min."
"These findings show that varying degrees of thermal destruction of ergot alkaloids and chlorogenic acid occur in a typical flour mix at ordinary baking temperatures."
So yea It looks like Ergot alkaloids are present in Heavenly Blue Morning Glory Seeds from Holland and Germany along with Chlorogenic acid which can decompose upon heat and light.
Solvent reports have said that Colman camp fuel was a poor petroleum ether solvent when distilled. Ozark trail camp fuel was a good petromeum ether solvent when distilled and is available at wal-mart. Grain alcohol from the liquor store is ethanol diluted with water 80 proof = 40%alcohol by volume.
distillation apparatus can be made from copper tubing available at home-depot. Directions for assembly of a distillation apparatus is available at www.moonshine-still.com
Wal-Mart is excellent source for all you crack-lab needs, with flameless portable burners, kitchen utensils, sovents.
Ahhh theres nothing like a good can of mooshine in morning along with the smell of burning coal and refined petrols.
Trichocereus pachanio "San Pedro contains appreciable mescaline (Crosby, D.M. McLaughlin, J.L. 36, 417 (1976)."
Pummangura, S. McLaughlin, J.L., Schifferdecker, R.C. "Cactus Alkaloids. LI. Lack of Mescaline Translocation in Grafted Trichocereus", 1981.
Experimental:
Plant Material- Small plants of Trichocereus pachanoi (control) along with others were obtained commercially and maintained under greenhouse conditions. The Cactus was sliced into small peices, frozen, and freeze-dried. The Sample were pulverized in a Wiley Mill.
Exactly 5.00g of sample was extracted with basic chloroform and acid-base partitioning. The extract was dissolved in 0.8mL of methanol. The Methanol-Alkaloid-extracts were analyzed using thin-layer and gas-liquid chromatography mescaline was detected by gas-liquid chromatography in the trichocereus pachanoi sample which agreed with the tlc analysis.
"Two papers with Dr. Carlos Gutierrez-Noriega reported the effects of oral administration of this alkaloid in doses varying from 5 to 11.5 g per kilo in 43 subjects, of whom developed a brief psycotic state. The method of preparation of the alkaloid, some of its physical and chemical properties, the psychological changes, as well as the dosage of the alkaloid employed, suggested the presence of mescaline."
"The only other reference to opuntia cylindrica we have been able to find is in a review artical by Buscaino"
"We have been able to identify the alkaloid present as mescaline, present in a concentration of 0.9% of the whole dried plant. There is no more than a slight trace of additional alkaloids."
-Received March 21, 1960
"Cactus Alkaloids, LXI. Identification of Mescaline and Related Compounds in Eight Additional Species Using TLC and MS/MS"
Ma, W.W. Jiang, X.Y., Cooks, R.G. McLaughlin, Gibson, A.C. Zeyemaker, F. and Ostolaza, C.N.
Apartado 5545, Lima 100, Peru
"The well-known catus alkaloid mescaline (3,4,5-trimethoxy-beta-phenethyamine) is present in lophophora and some species of trichocereus in sufficient concentrations to impart hallucinogenic activity upon ingestion by humans. It is less well known that additional cactus species, representing all three catus sub-families, can also contain this hallucinogen although in lesser concentrations. "
"The detection of small traces of mescaline were reported in eight additional species: opuntia acanthocarpa, opuntia basilaria, opuntia echinocarpa, polaski chende, pterocereus gaumeri, stenocereus beneckei, stenocereus stellatus, and stenocereus treleasei"
In 1986...
Source 1: Cactus Ranchito, Tarzana, California.
Source 2: purchased from Abbey Garden, 4620 Carpinteria, California 93013.
Source 5: cuttings from plants grown at the Huntington Botanical Garden, 1151 Oxford road, Marino, California 81108.
"This was a report of the detection of mescaline in polaskia, pterocereus, and stenocereus."
"Quantitative tlc estimated the maximum concentration in the richest of the reported species (stenocereus stellatus) to be at the level of 0.01% of the dry weight, an isuficient amount to cause hallucinations upon ingestion."
"'Neoraimondia macrostibas' is an ingredient, with 'Trichocereus pachanoi' and several noncactaceous plant species of the Peruvian hallucinogenic drink 'cimora' ; the absence of mescaline in Neoraimondia arequipensis var. roseiflora, formerly treated as a variety of N. macrostibas, leaves unexplained this folkloric use."
Brief Report Jul-Aug 1986.
"Endless curse, blood runs cold
Evil stare, will turn your flesh to stone."
So it is a decent guess to predict that LSD production may stem from rural America wheat and rye fields and through the agricultural industry. If you visit a Wheat field you might be able to find it. It is highly toxic I think.
"Abstract- A memeber of the family Orchidacea, Oncidium cebolleta, is used by the Tarahumara Indians of northern Mexico as a temporary replacement for peyote. We have found it to contain the known compounds: 2,7-dihydroxy-3,4,6-trimethoxyphenanthrene; 2,7-dihydroxy-3,4,6-trimethoxy-9,10-dihydrophenanthrene; 2,3-dihydroxy-4,7,8-trimethoxyphenanthrene; and the new compounds: 2,7-dihydroxy-3,4-dimethoxyphenanthrene; and 2,7-dihydroxy-4,8-dimethoxyphenanthrene."
"The Tarahumara Indians of northern Mexico use a number of hallucinogenic plants in religious ceremonies and were one of the first peoples to gain publicity for their used of Lophophora williamsii (peyote). Along with other plants, one important tempory replacement for peyote among the Tarahumara is Oncidium cebolleta. The whole green leaf is said to be consumed after it is crushed in water. This member of the so called "rat-tail" of Oncidium orchids was one of the first introduced from the Carribean Islands into Europe for culture. It was reported that 'the natives use it externally...crushed with salt...wherein it has agreat reputation [in treatment] of serious contusions, bone fractures, and other diseases'"