Derivatives of N,N-diethyltryptamine (DET) are hallucinogenic compounds with activity at the serotonin (5-hydroxytryptamine) receptors.[1] 4-acetoxy DET is a DET derivative that is expected to be hydrolyzed in the blood to 4-hydroxy DET, a designer drug of abuse.[2] The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.
Reference:
[1]. Blair, J.B., Kurrasch-Orbaugh, D., Marona-Lewicka, D., et al. Effect of ring fluorination on the pharmacology of hallucinogenic tryptamines. J. Med. Chem. 43(24), 4701-4710 (2000).
[2]. Uchiyama, N., Kawamura, M., Kikura-Hanajiri, R., et al. URB-754: A new class of designer drug and 12 synthetic cannabinoids detected in illegal products. Forensic Science International 227(1-3), 21-32 (2013).