Exploring Fentanyl. To explore a different substance…

Name:
Fentanyl
IUPAC name:
N-Phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide
ID: 10715 · Formula: C22H28N2O · Molecular weight: 336.471
Tags: Fentanyl
InChI: InChI=1S/C22H28N2O/c1-2-22(25)24(20-11-7-4-8-12-20)21-14-17-23(18-15-21)16-13-19-9-5-3-6-10-19/h3-12,21H,2,13-18H2,1H3
InChI Key: PJMPHNIQZUBGLI-UHFFFAOYSA-NThis stereoisomerAny stereoisomer

Breindahl, T; Kimergård, A; Findal Andreasen, M; Pedersen, DS. Identification of a new psychoactive substance in seized material: the synthetic opioid N-phenyl-N-[1-(2-phenethyl)piperidin-4-yl]prop-2-enamide (Acrylfentanyl). Drug Test. Analysis, 1 Jan 2016, 9 (3), 415-422. 516 kB. https://doi.org/10.1002/dta.2046

Rojkiewicz, M; Majchrzak, M; Celiński, R; Kuś, P; Sajewicz, M. Identification and physicochemical characterization of 4-fluorobutyrfentanyl (1-((4-fluorophenyl)(1-phenethylpiperidin-4-yl)amino)butan-1-one, 4-FBF) in seized materials and post-mortem biological samples. Drug Test. Analysis, 1 Jan 2016, 9 (3), 405-414. 614 kB. https://doi.org/10.1002/dta.2135

Ziporyn, T. A growing industry and menace: makeshift laboratory’s designer drugs. JAMA, 12 Dec 1986, 256 (22), 3061–3063. 486 kB. https://doi.org/10.1001/jama.1986.03380220011003

Ohta, H; Suzuki, S; Ogasawara, K. Studies on Fentanyl and Related Compounds IV. Chromatographic and Spectrometric Discrimination of Fentanyl and its Derivatives. J. Anal. Toxicol., 1 Jul 1999, 23 (4), 280-285. 354 kB. https://doi.org/10.1093/jat/23.4.280 #2

Suzuki, S. Studies on fentanyl and related compounds: II. Spectrometric discrimination of five monomethylated fentanyl isomers by gas chromatography/Fourier transform-infrared spectrometry. Forensic Sci. Int., 1 Sep 1989, 43 (1), 15–19. 289 kB. https://doi.org/10.1016/0379-0738(89)90117-5 #a

Spahn, V; Vecchio, GD; Labuz, D; Rodriguez-Gaztelumendi, A; Massaly, N; Temp, J; Durmaz, V; Sabri, P; Reidelbach, M; Machelska, H; Weber, M; Stein, C. A nontoxic pain killer designed by modeling of pathological receptor conformations. Science, 3 Mar 2017, 355 (6328), 966–969. 2.8 MB. https://doi.org/10.1126/science.aai8636 The erratum and revised supplementary material are appended

Vuckovic, S; Prostran, M; Ivanovic, M; Dosen-Micovic, L; Todorovic, Z; Nesic, Z; Stojanovic, R; Divac, N; Mikovic, Z. Fentanyl analogs: Structure-activity-relationship study. Curr. Med. Chem., 1 Jul 2009, 16 (19), 2468–2474. 211 kB. https://doi.org/10.2174/092986709788682074 #1

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27 May 2018 · Creative Commons BY-NC-SA ·