3-4-Methylenedioxy-N-ethylamphetamine (MDEA; also called MDE and colloquially, Eve) is an empathogenic psychoactive drug. MDEA is a substituted amphetamine and a substituted methylenedioxyphenethylamine. 3-4-Methylenedioxy-N-ethylamphetamine acts as a serotonin, norepinephrine, and dopamine releasing agent and reuptake inhibitor. It is a Pharmaceutical Chemicals controlled-substances products
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3,4-Methylenedioxy-N-ethylamphetamine (also known as MDEA, MDE, and colloquially as Eve) is a lesser-known entactogen substance of the amphetamine class. MDEA is chemically similar to MDMA and MDA. It produces its effects by increasing levels of serotonin, norepinephrine, and dopamine in the brain.
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3,4-Methylenedioxy-N-ethylamphetamine Online. The first recorded human use of MDEA was in 1976 by Alexander Shulgin, who noted its similarity to MDMA in both effects and potency, though faster to act and shorter in duration. The synthesis and pharmacological evaluation of MDEA and a series of related compounds were published in 1980. MDEA is included in Shulgin’s 1991 book “PiHKAL” (“Phenethylamines I Have Known and Loved”).
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3,4-Methylenedioxy-N-ethylamphetamine Online. In the United States, MDEA was introduced recreationally in 1985 as a legal substitute to the newly banned MDMA before it was made a Schedule I substance two years later. Since then, MDEA has rarely been sold on its own and has largely been used as an occasional additive or substitute ingredient in pills of “Ecstasy”.
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Very little data exists about the pharmacological properties, metabolism, and toxicity of 3,4-Methylenedioxy-N-ethylamphetamine (MDEA). As a result it is highly advised to approach this potentially habit-forming entactogenic substance with the proper amount of precaution and harm reduction practices if choosing to use it.
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MDEA, also known as 3,4-Methylenedioxy-N-ethylamphetamine, is a synthetic molecule of the substituted amphetamine chemical class. Molecules of the amphetamine class contain a phenethylamine core featuring a phenyl ring bound to an amino (NH2) group through an ethyl chain with an additional methyl substitution at Rα. Additionally, MDEA contains an ethyl substitution on RN, which is a single carbon extension of the methyl group present in MDMA. MDEA also contains substitutions at R3 and R4 of the phenyl ring with oxygen groups that are incorporated into a methylenedioxy ring through a methylene bridge. MDEA shares this methylenedioxy ring with other entactogens like MDMA, MDA and MDAI.
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MDEA; MDE; Eve; МДЭА; МДЭ; Ева; Vorabend; Víspera; Methylendioxyethylamphetamin; N-Ethyl MDA; Methylenedioxyethylamphetamine; Метилендиоксиэтиламфетамин; Metilendioxietilanfetamina; N-etilo MDA; N-этил МДА; CAS 82801-81-8; Metilendioxietanfetamina; Метилендиоксиэтамфетамин; Methylendioxyethamphetamin; 3,4-Methylendioxyethamphetamin; 3,4-метилендиоксиэтамфетамин; 3,4-metilendioxietanfetamina
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