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Al 2 Me 6 + 3 H 2 O → Al 2 O 3 + 6 CH 4. Under controlled conditions, the reaction can be stopped to give methylaluminoxane: AlMe 3 + H 2 O → 1/n [AlMeO] n + 2 CH 4. Alcoholysis and aminolysis reactions proceed comparably. For example, dimethylamine gives the dialuminium diamide dimer: [7] 2 AlMe 3 + 2 HNMe 2 → [AlMe 2 NMe 2] 2 + 2 CH 4
Sveriges riksdag added TMA-2 to schedule I ("substances, plant materials and fungi which normally do not have medical use") as narcotics in Sweden as of Dec 30, 1999, published by Medical Products Agency in their regulation LVFS 2004:3 listed as 2,4,5-trimetoxiamfetamin (TMA-2).
Tetramethylammonium (TMA) is the simplest quaternary ammonium cation. It has the chemical formula [Me 4 N] + and consists of four methyl groups (−CH 3, denoted Me) attached to a central nitrogen atom. The cation is isoelectronic with neopentane (Me 4 C). It is positively-charged and can only be isolated in association with a counter-ion.
Shulgin explains in his book that DMMDA has 6 isomers similar to TMA. [1] DMMDA-2 is the only other isomer that has been synthesized as of yet. DMMDA-3 could be made from exalatacin (1-allyl-2,6-dimethoxy-3,4-methylenedioxybenzene). Exalatacin can be found in the essential oil of both Crowea exalata and Crowea angustifolia var. angustifolia. [2]
The mechanism that produces the hallucinogenic and entheogenic effects of 2C-TFM is most likely to result from action as a 5-HT 2A serotonin receptor agonist in the brain, a mechanism of action shared by all of the hallucinogenic tryptamines and phenethylamines. 2C-TFM displaced radiolabelled ketanserin from 5-HT 2A/C receptors with a K i of 74.5 nM, as compared to a K i of 80.9 nM for the ...
TMA-2 may be: TMA-2 mine; Soyuz TMA-2, a Russian space exploration mission; 2,4,5-trimethoxyamphetamine, a hallucinogenic drug;
An assortment of several designer drugs. Designer drugs are structural or functional analogues of controlled substances that are designed to mimic the pharmacological effects of the parent drug while avoiding detection or classification as illegal.
The activity of ψ-DOM (and ψ-2C-T-4) demonstrates that the two methoxy groups on the psychedelic phenethylamines are not strictly limited to the 2,5-positions on the phenyl ring. Indeed, any of the 2Cx or DOx series of drugs could alternatively be made as the 2,6-isomer and would still be expected to show similar activity, although slightly ...