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time to update the FAQ already! Much thanks, folks. And of
course, just note that you want ---> ANONYMITY <---, and I will
erase all names, addresses, etc. Just make sure that the note is
very visible! I will use no identifying information anyway,
unless the source is published, or the author states that she/he
Well, anyway, the following topics are updated: we now have
an alkaline estimate for P. Arundinacae, we have more information
on bufotenine, we have a possible lead on why phalaris kills
sheep and not man, and we have a new factor in maximizing
alkaloid growth! Growing phalaris is now a separate section. Plus
LSD and MAOIs. No small update in so short a time! Plus, there
are a bunch of small tidbit thrown in, corrections made etc.
XXXXXXXXX INITIAL NOTES XXXXXXXXXXX
This author assumes absolutely no responsibility for
anything you do, as a result of reading this material, or for any
other reason. I make no claims as to accuracy. Always assume your
own responsibility for research and for your actions. Read all
the warnings. Read the articles. Decide what you may be willing
and unwilling to put in your head.
XXXXXXXXX ABBREVIATIONS/NOMENCLATURE/MISC XXXXXXXXXX
The following alkaloids are discussed and abbreviated as
indicated: N,N-dimethyltryptamine (DMT), 5-Hydroxy-N,NDimethyltryptamine
(5-Me-DMT) and 5-Hydroxy-N,NDimethyltryptamine
(5-OH-DMT or bufotenine).
file:///C|/Documents%20and%20Settings/All%20Users/...0Culture/Ayahuasca%20and%20DMT/DMT%20FAQ%202.0.txt (1 of 13)4/14/2004 9:11:34 PM
Phalaris aquatica is also called phalaris tuberosa. I use p.
tuberosa in this text.
XXXXXXXXXX THE DRUGS IN QUESTION XXXXXXXXXX
The main drug of interest here is DMT. DMT causes intense
visual hallucinations and other psychedelic phenomena. It has
been mostly encountered in the technologically developed world as
a pink (cool) crystalline powder, which was smoked or injected.
This caused nearly instant, brief, and intense trips. Peaks occur
immediately and last around 10 minutes, with another 30 or so
minutes of mild effects.
5-Me-DMT is a close relative of DMT. 5-Me-DMT is reported to
be about 4 times as potent as DMT and is often regarded as
preferable to DMT. 5-Me-DMT has most of the psychedelic qualities
as DMT but does not cause visual hallucinations. It follows the
same time course.
Bufotenine (5-OH-DMT) is another DMT relative. This compound
is vaguely referred to as "noxious" by Jonathan Ott. Apparently
10mg of pure 5-OH-DMT injected is enough to cause "dramatic
circulatory crises." There appears to be debate over the
psychedelic qualities of bufotenine. However, McLeod & Sitaram,
Shulgin, and Fabins & Hawkings all report the presence of
psychotomimetic effects. Bufotenine causes anxiety, cir Dmt Plant In Colorado FOR FOR ECSTASY
extractions can be made acidic (pH 9.5) with 1-N hydrochloric acid, filtered and
washed in a separatory funnel or improvised siphon-jug apparatus with diethyl
ether, neutralized with ammonium hydroxide and evaporated to dryness.
However, most of these solvents are difficult for the non-professional to obtain.
Perhaps it is just as well since many of these solvents are either toxic or
explosive if handled improperly. Also, we do not always know precisely what we
are trying to extract. Some of the active principles may be non-alkaloidal. Too
much purification might remove some of the active substances. The approach
given here employs materials which may be purchased inexpensively at any
supermarket and are safe to work with. This procedure extracts all of the alcohol
and water-soluable alkaloids and non-alkaloidal materials and permits only the
fibrous pulp to be discarded.
Pulverize the dried cactus (tufts and spines need not be removed). Prepare a
mixture of two parts isopropyl rubbing alcohol and one part clear, non-sudsing,
unscented and untinted ammonia. Make the pulverized material soggy with this
mixture and allow it to stand covered overnight. Do not use aluminum or iron
wares during any of these steps. After soaking, cover the mash with isopropyl
alcohol and boil in a heat bath for six hours. Strain the liquids through muslin and
press as much liquid as possible from the pulp. With fresh alcohol repeat the
boiling and straining three more times. Combine the strained liquids. Evaporate
this in a heat bath until only a tar remains. (When evaporating a solvent use and
electric range or hot plate rather than a gas stove. Have adequate ventilation and
avoid breathing the fumes.) The tar can be further dried by spreading it thinly on
a baking tray and placing it in an oven set at the lowest possible heat. Remove
the tray once every fifteen minutes to examine the material. When it appears to
be almost dry place it back in the oven, shut the heat off, and let it stay there until
the oven cools.
DICTIONARY OF CACTUS ALKALOIDS
• Anhalidine: Tetrahydroisoquinoline alkaloid (2-methyl-6,7-dimeethoxy-8-
hydroxy-1,2,3,4,-tetrahydroisoquinoline) Found in Lophophora and
• B-O-methylsynephrine: Phenolic B-phenethylamine found in citrus trees
and some cacti. No data on pharmacology, but similar compound B-Omethylepin-
ephrine produces considerable CNS stimulation.
• 3-dimethyltrichocereine: B-phenethylamine alkaloid (N,N-dimethyl-3-
hydroxy-4,5-dimethoxy-B-phenethylamine). Found in Pelecyphora and
some Trichocereus species.
• Dolichotheline: Imidazole alkaloid properly known as N-isovalerylhistamine
or 4(5)-2-N-isovalerylaminoethylimidazole. Found only in Dolichothele
and Gymnocactus species. Pharmacological action still unknown.
• Homoveratrilamine: a dimethoxy form of the mescaline molecule (3,4-
dimethoxy-B-phenethylamine). It has no activity by itself, but may alter the
mescaline experience s
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