476 lines
20 KiB
Plaintext
476 lines
20 KiB
Plaintext
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Okay 2C-B is 4-bromo-2,5-dimethoxyphenethylamine. Its the phenethylamine
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analogue of DOB. The 2C is because its had a 2-carbon chain sticking off
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of the phenyl ring (which is why its a phenethylamine instead of an
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amphetamine), and I *assume* the B is because of the Br atom in the 4
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position.
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+--------- the second (beta - carbon)
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v
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CH3O /\\ / \ NH2
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\ / \\ / \ /
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/ \ // \ |
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Br \// OCH3 +------------ the first (alpha - carbon)
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Doses are 12-24mg, Duration is 4-8 hours. Doses of 100mg have been taken
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safely. 2C-B seems to be an extraordinarily colorful hallucingen similar
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to LSD -- apparently somewhat analytical and dissasociative in higher doses
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or in those sensitive to those effects.
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Quote from Ecstasy: The MDMA Story...
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[begins with a quotation from Alexander Shulgin]:
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2C-B... is a tool... which ties the mental processes directly
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and constructively into the physical soma.
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The analgesic effects experienced with many, if not most,
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psychedelic drugs, are not present with 2C-B. On the
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contrary, there is increased body awareness of every kind,
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including skin sensitivity, heightened responsiveness to
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smells, tastes, and sexual stimulation.
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One experiences increased consciousness of physical
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health and energy, or, on the other hand, sharpened
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awareness of any body imbalance or discomfort.
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2C-B allows for rich visual imagery and intesnse eyes-
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closed fantasy without the cluttering up of the mental field
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with too much elaboration... It is a superb tool for learning
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and growth.
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[...] At high doses (above 30 mgs.), 2C-B is intensely hallucinogenic,
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and, like any major psychedelic, can be frightening for certain people.
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In small doses, it becomes a mild sensory enhancer but does not have the
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strongly empathogenic qualities that MDMA has.
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Perhaps the best use that has been found for 2C-B is as a synergist
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with MDMA. When taken together, the MDMA pushes the non-specific 2C-B
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reaction in a more warm and emphathetic direction. Because 2C-B is a
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psychedelic drug, and therefore not fully predictable, its action can take
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the user in many different directions. But if the set and setting are right,
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2C-B can enhance the desire for sexual orgasm during an MDMA experience.
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The synergy of the two substances can on occasion be a true aphrodisiac.
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Shulgin writes in PiHKAL:
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"The most succesfful reports have followed a program in which the two drugs
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are not used at the same time, nor even too closely spaced. It appears that
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the optimum time for the 2C-B is at, or just before, the final baseline
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recovery of the MDMA."
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DOB: 2,5-Dimethoxy-4-Bromoamphetamine. The only chemical difference is
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the addition of an extra carbon to the chain. This turns the
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phenethylamine into an alpha-methyl-phenethylamine (because the
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addition of a carbon means attatching a methyl group to the
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alpha carbon of the phenethylamine) also called a phenylisopropylamine
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or simply an amphetamine.
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CH3O /\\ / \ NH2
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\ / \\ / \ /
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/ \ // \
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Br \// OCH3
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DOB has a potency of 1.0-3.0 mg and duration of 18-30 hours. Its very
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similar to LSD. It seems to be more colorful than LSD and less dissociative
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than 2C-B based on the reports I've read. The index of safety is probably
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something like over 1,000 times the effective dose.
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2C-D (LE-25): 2,5-Dimethoxy-4-Methylphenethylamine. This is the 2 carbon
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homologue of DOM (2C-B is to DOB as 2C-D is to DOM). The difference
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between 2C-D and 2C-B is simply the replacement of the Br atom with
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a methyl group.
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CH3O /\\ / \ NH2
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\ / \\ / \ /
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/ \ // \
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H3C \// OCH3
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2C-D has a potency of 20-60mg and a duration of 4-6 hours. Seems to also
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be very colorful. Shulgin notes: "Wow! This particular compound is what
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I call a pharmacological tofu. It doesn't seem to do much by itself, always
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teasing, until you get to heroic levels. But a goodly number of experimental
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therapists have said that it is excellent in extending the action of some
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other materials. It seems to boost the waning action of another drug, without
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adding its own color to the experience." At 150mg+ it appears it might be
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a full blown 2C-B-like psychedelic, however. No info on the toxic dose.
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DOM (STP): 2,5-Dimethoxy-4-Methylamphetamine. Again, simply the addition
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of an extra carbon to the chain to turn the phenethylamine 2C-D into
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the ampehtamine DOM. And the replacement of the Br atom in DOB with
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a methyl group would give you DOM also.
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CH3O /\\ / \ NH2
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\ / \\ / \ /
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/ \ // \
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H3C \// OCH3
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DOM has a potency of about 3-10mg and a duration of 14-20 hours. This was
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first synthesized by Shulgin, and is what he calls his "Problem Child" (in
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reference to Albert Hofmann's name for LSD). It gained a considerable
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amount of use in the 60's and people taking 30mg+ (a whopping dose) had
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some very dissasociative, bad trips. It was known as STP, which stands for
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the motor oil additive actually, but was also known as "Serenity,
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Tranquility and Peace". From the descriptions it seems LSD-like, with
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possibly even more of a head-trip. 5-10mg seems *much* more appropriate
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from the descriptions with very good effects. Only at higher (20-30mg)
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doses does it appear to get really nasty.
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And for chemical comparison, MDA and MDMA: 3,4-methylenedioxyamphetamine and
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3,4-methylenedioxymethamphetamine respectively... They're somewhat similar
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to DOM and DOB -- all the ring substituents need to be knocked off and
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replaced with the 3,4-methylenedioxy ring. Then for MDMA you've got the
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addition of a methyl group to the nitrogen amine.
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MDA:
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O /\\ / \ NH2
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/ \ / \\ / \ /
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/ || | |
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H2C || | |
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\ || | CH3
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\ / \ //
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O \//
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MDMA:
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O /\\ / \ NHCH3
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/ \ / \\ / \ /
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/ || | |
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H2C || | |
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\ || | CH3
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\ / \ //
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O \//
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Also we might as well throw in amphetamine if you all haven't figured out
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what that should look like yet (replace the NH2 with NHCH3 to get
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methamphetamine -- identical substitution as between MDA and MDMA).
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Also, if you knock off the CH2 from amphetamine, you'll get phenethylamine
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which is the prototype chemical for all the drugs I've listed so far, although
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itself its inactive.
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amphetamine:
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/\\ / \ NH2
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/ \\ / \ /
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\ //
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\//
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And just for kicks here we have good old LSD which looks nothing like all
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these other chemicals:
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/ C2H5
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H. CON
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'. / \ C2H5
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/ \
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/ \
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/\\ /\ / \
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/ \\ / \ / CH3
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\ // \ /
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\// \/
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HN-------
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Hope you enjoyed that. Chem dweebs please check to make sure I got
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everything correct. I didn't have time to go over this with a fine-toothed
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comb.
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=============================================================================
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From: cutrell@nic.cerf.net (Doug Cutrell)
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Date: 8 Jul 92 23:31:16 GMT
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Newsgroups: alt.drugs
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Subject: Re: LSD.
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Lamont Granquist writes:
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>DOB has a potency of 1.0-3.0 mg and duration of 18-30 hours. Its very
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>similar to LSD. It seems to be more colorful than LSD and less dissociative
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>than 2C-B based on the reports I've read. The index of safety is probably
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>something like over 1,000 times the effective dose.
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This figure is probably based on animal experiments described
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by Shulgin in Pihkal. However, he goes on to say that the
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index of safety is probably much lower than this. He says
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there are numerous reports of overdoses causing vascular
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arterial spasm, and gives one verified account of a couple who
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thought they had MDA and took quantities appropriate for that
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compound... i.e. around 100 mg. The woman died, the man lived
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after convulsions and a week in a coma. Since the standard dose
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is 1-3 mg., the lethal dose is more like 30 times the effective
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dose.
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Doug Cutrell
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cutrell@cerf.net
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=============================================================================
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Well, in a thread recently, there was some talk aabout bromo
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mescaline, and mention was made of the entry in the Student Handbook of
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our esteemed institution that deals with the drug in question. Well, it is
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Reed folklore that tells us that bromo mescaline was first synthesized here
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at Reed (BTW, it is not folklore that Dr. Demento graduated from Reed),
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but the drug is real, to which several friends can attest. Since I have the
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ol' Student Handbook right in front of me, I'll tell y'all what it sez.
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----------------------------------------------------------------------------
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From _The Reed College Student Handbook_, in the "Drug Article That Ate Reed
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College", by Marty Smith:
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Bromo-mescaline. The most terrifying hallucinogen known to man. The effects
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last 3-5 hours, the visuals are awe-inspiring and the head trip is light,
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usually. The catch is, first, for it to act like bromo, you have to snort
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it. This is really intense, because in about two to five minutes, you're
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tripping you ass off, the world is melting. The incredible speed with which
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this happens is one of the things those who like it like about it. However,
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when it gets up your nose it hurts. This is probably an understatement. It's
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really amazingly painful. You'll be suprised that you would actually do this
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to yourself. It has been described as having red hot knives shoved up your
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nose, or being kicked in the face by a psychedelic horse. You may briefly
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entertain notions of dying. This all dies down after about twenty minutes,
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though, and you're lucky there will be no nausea at all afterward. (It helps
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to have eaten a starchy meal about an hour and a half earlier.) Otherwise,
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you might have about 20 minutes of mild nausea. The visuals are real good.
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To have visuals this intense on acid you'd have to be on so much that you
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couldn't talk. On bromo you could discuss them reasonably coherently.
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A word about dosage. One hit is one fourtieth of a gram. This is a
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fact. Do not say something stupid like, "Oh, let's do a lot," and hoot up a
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couple of lines the size of your thumb. I have some friends who did this,
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and they ended up lying under some bushes, at night, in the rain, unable
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even to yell for help, and now they will not do drugs for the next five
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million jillion years.
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---------------------------------------------------------------------------
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That's the straight dope (none of the many puns intended).
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late,
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miguel
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=============================================================================
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pierre@media.mit.edu (Pierre St. Hilaire) writes:
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> Sure. And table salt releases sodium and chlorine in your
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>body, so you will both catch fire and suffocate if you take it.
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>
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> Adding halogen atoms to psychedelic amines can significantly
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>modify their potency, duration, and effects. Read Alexander Shulgin's
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>PIKHAL for an extensive discussions on halogenated substituted
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>phenylethylamines.
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yes, i believe that "bromomescaline" 2-CB aka CBr... 2,5-dimethoxy-4-
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bromophenethylamine. the reason why it probably burns going up your nose
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is that it may lack any kind of anaesthetic action (unlike MDA, MDMA, and
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particularly cocaine), while still being in the form (probably) of a
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hydrochloric salt (where the HCl comes from).
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culled from the MDMA FAQ:
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}
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} CBr is 2,5-Dimethoxy-4-Bromophenethylamine. The
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} "sometimes frightening" part probably comes from taking more than the
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} full dose, and the literature suggests that with larger dosages come
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} disproportionately larger responses, unlike some other psychedelics
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} we all know and love. I've had very enlightening experiences with CBr,
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} and they grew better in quantum leap fashion.
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}
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} + wonderful and gently insightful (semi-wilderness, daytime, friends).
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} + profoundly sexual with glimpses of bird-animal forms (indoors, nightime,
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} lover) minor telepathic imagery.
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} + sexual and shamanic, native american imagery (indoors, day-night, alone).
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} + profound native american imagery (indoors, night, after cannabis, friend)
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} actually slept a bit (too much cannabis) and awoke to the most wonderful
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} visuals (friend in other room - ditto).
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} + full-blown spirit animals all night long (desert, night, friend, good THC
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} 1/2 way thru trip) - mountain lion (very playful) and eagle most prominent
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} two deer (incredibly loving), a wolf (very brief), fantastic living plant
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} spirits, entities in mountain, mucho native american imagery, et. al.
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} very telepathic with friend. brief teleportation/desert-zoom experience.
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} understood the ancients' fascination with constellations. imparted with
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} sudden knowledge in extreme detail - confirmed later by ex-lover, scared
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} ex-lover shitless.
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}
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} My last experience with CBr changed my life in many profound ways (for the
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} better). With THC and a little concentration I can get back to some of those
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} places. With no THC and a lot of concentration I can get back to some of
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} those places. Remember.
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}
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} I believe CBr is recognized as an enthogen and an entactogen, and
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} unfortunately it's now Schedule 1. :-( Put this one on the top of
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} the list of drugs to be legalized.
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=============================================================================
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Date: Sun, 28 Feb 1993 00:22:14 -0800
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From: Alexander T. Shulgin
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To: lamontg@milton.u.washington.edu
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Subject: bromo
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} Hi:
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}
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} There has been quite a flow of stuff on the subject of BROMO on
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} alt.drugs entry. Maybe you can post some parts of the following
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} that might answer some of the comments, questions, or errors
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} being put out there on the topic.
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}
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} (1) Bromomescaline is without doubt 2C-B. The dosage, the
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} duration, the nature of the experience, all seem consistent with
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} this assignment. Also, as you have indicated, the replacement of
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} a methoxy group (of mescaline) with a bromo atom gives the
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} isomeric structure (a little rearrangement needed) of 2C-B.
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}
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} (2) It releases bromic acid. Of course not. Bromic acid
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} (HBrO3) is an unstable chimera which is substantially unknown.
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} Probably what is meant is that it releases hydrobromic acid
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} (HBr) but then there is no experimental evidence that HBr is
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} released either. I suspect that the bromine atom stays on the
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} drug molecule all the way through the kidney, and that there
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} is no release of this element at any time in the body.
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}
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} (3) It is illegal, or a scheduled drug. No so. 2C-B was added
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} to the German law in January of this year, but in the US it is
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} still an unnamed drug in Federal law.
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}
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} (4) It burns on snorting (insufflation). It sure does, but this
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} is most likely due to the fact that it is extremely insoluble in
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} water, and probably sits on the mucous membranes for quite a
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} while until it dissolves and is absorbed. And until this happens
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} it irritates and blisters the skin at the sites where the solid
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} particles of the drug happen to settle. Once absorbed, the
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} pain disappears, and the effects start. A challenge to this
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} would be to snort the acetate or the hydrobromide salt, both of
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} which are quite a bit more soluble in water. These should have
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} the same psychological effect, and they should act even more
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} quickly (no slow dissolving) and act with little or no pain.
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}
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} I would love to know who in the wide wide world of information
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} input discovered the term bromic!! It cannot believe it has any
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} merit.
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}
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} Can you drift some of this on to the world of alt.drugs and
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} satisfy this search for information?
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}
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} Thanks.
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}
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} Sasha
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=============================================================================
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From: Mark_Farone@sfa.ufl.edu (Mark Farone)
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Newsgroups: alt.psychoactives
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Subject: Re: 2CB
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Date: 18 Apr 1994 12:28:10 GMT
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Message-ID: <Mark_Farone-180494082742@128.227.37.18>
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In article <766538637-0-4072@chop.isca.uiowa.edu>, David Roknich
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<Hologram@chop.isca.uiowa.edu> wrote:
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> dg596@cleveland.Freenet.Edu (Russell Faraday)writes:
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> Another new sensation gripping our little pocket of cultural
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> coolness is something called 2CB. As a discussion starter, I'd
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> ......
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> 2CB is a designer drug that was not illegal until a few morons
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> blathered publicly about its existance in the early 80s
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With respect to US laws, 2cb (aka Nexus, Zenith) wasn't scheduled until
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late 1993.
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Its actual chemical name is 4-Bromo-2,5-Dimethoxyphenethylamine.
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The Feds were alerted when a rather rich fella in Tampa, FL took some to
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relieve impotence, as it was being promoted. When started tripping he
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called the DEA and the next thing you know...
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See _Federal Register_, Vol. 58, No. 212, Thurs. Nov 4,1993 page 58819-20.
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--
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|
__________________________________________________________________________
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|
Mark Farone "A pile of rocks ceases to be a rock pile when
|
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|
University of Florida somebody comtemplates it with the idea
|
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|
Mark_Farone@sfa.ufl.edu of a cathedral in mind." -Saint Exupery
|
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|
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|
=============================================================================
|
||
|
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|
From: bgg@connect.com.au (Ben Golding)
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|
Newsgroups: alt.drugs
|
||
|
Subject: 2CB report from Sydney Morning Herald (18 May 94)
|
||
|
Date: 20 May 1994 11:34:39 +1000
|
||
|
Message-ID: <2rh43f$81k@warrane.connect.com.au>
|
||
|
|
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|
A wonderfully fact-free article from the SMH.
|
||
|
|
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|
Operation Noah is an annual campaign where people are encouraged to
|
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|
call the police to dob in a drug users and suppliers. Over the years
|
||
|
it has been running it has been steadily galvanising public opinion
|
||
|
against the operation and pushing discussion of drug policy to the
|
||
|
fore. As you can imagine, most of the busts are people with a plant
|
||
|
in their backyard with neighbours who don't like them, you know,
|
||
|
exactly the sort of people that pose the greatest threat to society.
|
||
|
|
||
|
Ben.
|
||
|
--
|
||
|
Noah Hunts New Drug, Emma Tom, Sydney Morning Herald, Wed.18th, 1994
|
||
|
|
||
|
A dangerous new designer drug similar to ecstasy is among the
|
||
|
amphetamines to be targeted today in operation Noah, the annual national
|
||
|
drugs phone-in.
|
||
|
Detective Sergeant Mal Brammer, from the NSW Drug Enforcement
|
||
|
Agency, said the new drug, known as nexus or 2CD (sic), had originated
|
||
|
at dance parties in the United States.
|
||
|
He said nexus differed from ecstasy in that it was stronger,
|
||
|
lasted longer and caused hallucinations. Part of its attraction was that
|
||
|
it "temporarily alleviated impotency and frigidity".
|
||
|
"We are concerned that nexus is being mixed with or sold as
|
||
|
ecstasy," he said.
|
||
|
|
||
|
=============================================================================
|
||
|
|
||
|
From: bgg@connect.com.au (Ben Golding)
|
||
|
Newsgroups: alt.drugs
|
||
|
Subject: Re: 2CB report from Sydney Morning Herald (18 May 94)
|
||
|
Date: 21 May 1994 12:56:56 +1000
|
||
|
Message-ID: <2rjt9o$ip6@warrane.connect.com.au>
|
||
|
|
||
|
[quoted text deleted -cak]
|
||
|
|
||
|
Further to this article, Here's a response to the letters page:
|
||
|
|
||
|
Re: "Noah hunts new drug", Emma Tom, April 18th 1994, p.10
|
||
|
|
||
|
Before we panic about a new designer amphetamine, which Nexus is not, I
|
||
|
feel some clarification is in order. I am a medicinal chemist in
|
||
|
regular contact with Dr. Alexander Shulgin, who has devoted his life to
|
||
|
producing new drugs for use in therapy, and names 2C-B (not 2CD) as his
|
||
|
greatest discovery. Not originating at dance parties, it has been
|
||
|
known to the scientific community for years. Concerning legality: the
|
||
|
NSW poisons list prohibits chemicals of its class with hallucinogenic
|
||
|
properties. 2C-B is unlisted, and its hallucinogenic properties
|
||
|
debatable . It does not cause true hallucinations but visual
|
||
|
distortions at high do ses, and is subjectively different from other
|
||
|
drugs such as ecstasy. It is not a stimulant, and lacks side-effects
|
||
|
such as overheating and post-use fatigue. Unlike LSD it leaves the
|
||
|
user mentally clear and lucid, and so is unlikely to cause a panic
|
||
|
reaction. As for dangerous, 2C-B is essentially non-addictive, rel
|
||
|
atively short acting, has no known serious side-effects, and no
|
||
|
recorded overdose cases. Legal or illegal, like it or not, it will
|
||
|
probably be increasingly popular.
|
||
|
|
||
|
|
||
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|