2C-T (hydrochloride) (Synonyms: 2,5-Dimethoxy-4-methylthiophenethylamine) |
| Katalog-Nr.GC42145 |
A series of 2,5-dimethoxy phenethylamines, collectively referred to as 2Cs, have psychoactive effects.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 61638-10-6
Sample solution is provided at 25 µL, 10mM.
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A series of 2,5-dimethoxy phenethylamines, collectively referred to as 2Cs, have psychoactive effects.[1][2] The most effective 2C compounds are substituted at the 4 position of the aromatic ring. Many are scheduled as illegal substances. [3][4] 2C-T (hydrochloride) is described formally as 2,5-dimethoxy-4-methylthiophenylethylamine hydrochloride. It has structural and pharmacokinetic properties similar to the drugs mescaline (hydrochloride) and 2C-T-2 (hydrochloride) . [5] This product is intended for forensic and research purposes.
Reference:
[1]. Bruno, R., Matthews, A.J., Dunn, M., et al. Emerging psychoactive substance use among regular ecstasy users in Australia. Drug Alcohol Depend. 124(1-2), 19-25 (2012).
[2]. Moya, P.R., Berg, K.A., Gutiérrez-Hernandez, M.A., et al. Functional selectivity of hallucinogenic phenethylamine and phenylisopropylamine derivatives at human 5-hydroxytryptamine (5-HT)2A and 5-HT2C receptors. Journal of Pharmacology and Experimental Therapeutics 321, 1054-1061 (2007).
[3]. Meyer, M.R., and Maurer, H.H. Metabolism of designer drugs of abuse: An updated review. Curr. Drug Metab. 11(5), 468-482 (2010).
[4]. Nagai, F., Nonaka, R., and Satoh Hisashi Kamimura, K. The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. Eur. J. Pharmacol. 559(2-3), 132-137 (2007).
[5]. Nichols, D.E., and Shulgin, A.T. Sulfur analogs of psychotomimetic amines. Journal of Pharmaceutical Sciences 65(10), 1554-1556 (1976).
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