- DME
- 3,4-Dimethoxy-β-hydroxyphenethylamine
- 2-Amino-1-(3,4-dimethoxyphenyl)ethan-1-ol
- 2-Amino-1-(3,4-dimethoxyphenyl)ethanol
Butterick, JR; Unrau, AM. Studies on theoretical psychotogens. Synthesis of O-methylated analogs of catecholamine neurotransmitters and metabolic precursors. Can. J. Chem., 1 Jan 1974, 52 (16), 2873–2879. 305 kB. https://doi.org/10.1139/v74-418 #4 MS,NMR,IR,TLC
Butterick, JR. Synthesis of O-transmethylated catecholamines and psychodysleptic β-phenylisopropylamines. Ph. D. Thesis, Simon Faser University, Burnaby, BC, Canada, 11 Mar 1975. 6.1 MB. #4 External examiner: A. T. Shulgin! NMR,IR,UV,TLC
Shulgin, AT; Sargent, T; Naranjo, C. Structure-activity relationships of one-ring psychotomimetics. Nature, 1 Jan 1969, 221, 537–541. 537 kB. https://doi.org/10.1038/221537a0 #XLV
Shulgin, AT. Basic Pharmacology and Effects. In Hallucinogens. A Forensic Drug Handbook; Laing, R; Siegel, JA, Eds., Academic Press, London, 24 Apr 2003; pp 67–137. 6.3 MB.
Anon. New ways with hallucinogens. Lancet, 8 Mar 1969, 293 (7593), 510. 181 kB. https://doi.org/10.1016/S0140-6736(69)91603-1 #3,4-dimethoxyphenylethanolamine
Vogel, WH; Evans, BD. Structure-activity-relationships of certain hallucinogenic substances based on brain levels. Life Sci., 15 May 1977, 20 (10), 1629–1635. 419 kB. https://doi.org/10.1016/0024-3205(77)90335-6 #3,4-Dimethoxy-PEOH