3,4-methylenedioxyamphetamine

From Academic Kids

MDA
Chemical name3,4-Methylenedioxyamphetamine or
1-(benzo[d][1,3]dioxol-5-yl)propan-2-amine
Chemical formulaC10H13NO2
Molecular mass179.22 g/mol
Melting point187 - 188 C (hydrochloride)
CAS numbers4764-17-4, 51497-09-7, 61614-60-6, 65620-66-8
SMILESNC(C)CC1=CC=C(OCO2)C2=C1
Chemical structure of MDA


3,4-methylenedioxyamphetamine, or MDA, is a psychedelic hallucinogenic drug and Empathogen/Entactogen of the phenethylamine family. It was first synthesized by G. Mannish and W. Jacobson in 1910. There are about 20 different synthetic routes described in the literature for its preparation.

Contents

Medical use

MDA was first used in animal tests in 1939, and human trials began in 1941 in the exploration of possible therapies for Parkinson's disease. From 1949 to 1957, more than 500 human subjects were given MDA in an investigation of its potential use as an antidepressant and/or anorectic by Smith, Klein, and French. The United States Army also experimented with the drug, code named EA-1298, while working to develop a truth drug or incapacitating agent. One human subject died in January 1953 after being intravenously injected with 500mg of the drug. MDA was patented as a cough suppressant by H. D. Brown in 1958, as an ataractic by Smith, Klein, and French in 1960, and as an anorectic under the trade name “Amphedoxamine” in 1961. Several researchers, including Claudio Naranjo, have explored MDA in the field of psychotherapy.

Recreational use

MDA began to appear on the recreational drug scene around 1963 to 1964. It was then inexpensive and readily available as a research chemical from several scientific supply houses. Although now illegal, MDA continues to be bought, sold, and used for recreational purposes, often in the form of tablets purporting to contain MDMA (Ecstacy).

Effects

A recreational dose of MDA is commonly between 80 and 160mg. The “R” optical isomer is more potent than the “S” optical isomer. Although there is some debate, the duration of the drug is now generally believed to be roughly 4 to 6 hours. The effects of the drug are quite similar to those of MDMA (Ecstacy), including Empathogen/Entactogenic effects. Because of these effects, MDA was called the “hug drug” and was alleged to stand for “Mellow Drug of America” in the 1960s. Some users feel that MDA has more psychedelic or hallucinogenic qualities than MDMA.

The toxicity of MDA is not fully known. The LD50 in mice has been reported as 92mg/kg by intraperitoneal injection.

Legality

In 1970, the Controlled Substances Act was enacted in the United States, placing MDA into Schedule I. It is similarly controlled in other nations. Internationally, MDA is a Schedule I drug under the Convention on Psychotropic Substances[1] (http://www.incb.org/pdf/e/list/green.pdf).

See also

External links

References

  • Lee, M.A. and Shlain, B., Acid Dreams: The CIA, LSD, and the Sixties Rebellion. Grove, 1985.
  • Stafford, P. Psychedelics Encyclopedia. Ronin, 1992.

Categorization

Template:Entactogens Template:Hallucinogenic phenethylaminesde:3,4-Methylendioxyamphetamin nl:MDA pl:MDA (farmakologia)

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