Exploring Dimethylcathinone. To explore a different substance…

Names:
DMAP
DMC
Dimethylcathinone
Dimethylpropion
Metamfepramone
IUPAC name:
2-(Dimethylamino)-1-phenylpropan-1-one
2110 · C11H15NO · 177.243
InChI=1S/C11H15NO/c1-9(12(2)3)11(13)10-7-5-4-6-8-10/h4-9H,1-3H3
KBHMHROOFHVLBA-UHFFFAOYSA-N This stereoisomer Any stereoisomer

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Iversen, LL. Consideration of the cathinones, Advisory Council on the Misuse of Drugs, 31 Mar 2010. 286 kB.

Tsujikawa, K; Mikuma, T; Kuwayama, K; Miyaguchi, H; Kanamori, T; Iwata, YT; Inoue, H. Degradation pathways of 4-methylmethcathinone in alkaline solution and stability of methcathinone analogs in various pH solutions. Forensic Sci. Int., 10 Jul 2012, 220 (1–3), 103–110. 671 kB. https://doi.org/10.1016/j.forsciint.2012.02.005

Toole, KE; Fu, S; Shimmon, RG; Kraymen, M; Taflaga, S. Color tests for the preliminary identification of methcathinone and analogues of methcathinone. Microgram J., 2012, 9 (1), 27–32. 496 kB.

Dal Cason, TA. Synthesis and identification of N,N-dimethylcathinone hydrochloride. Microgram J., 1 Jan 2007, 5 (1–4), 3–12. 93 kB.

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EMCDDA. New drugs in Europe, 2011, European Monitoring Centre for Drugs and Drug Addiction, 1 Apr 2012. 401 kB.

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Adamowicz, P; Zuba, D. Discrimination among designer drug isomers by chromatographic and spectrometric methods. In Chromatographic Techniques in the Forensic Analysis of Designer Drugs; Kowalska, T; Sajewicz, M; Sherma, J, Eds., CRC Press, Taylor & Francis Group, 1 Jan 2018; pp 211–232. 1.1 MB.

Takahashi, M; Nagashima, M; Suzuki, J; Seto, T; Yasuda, I; Yoshida, T. Creation and application of psychoactive designer drugs data library using liquid chromatography with photodiode array spectrophotometry detector and gas chromatography–mass spectrometry. Talanta, 15 Feb 2009, 77 (4), 1245–1272. 1.2 MB. https://doi.org/10.1016/j.talanta.2008.07.062 #Dimethylcathinone

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MMAI
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5-APDB
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6-MAT
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IBF5AP
MHAT
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3-HO-CPDMA
2-Methylmethcathinone
3-MMC
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10831
10743
10735
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19 September 2018 · Creative Commons BY-NC-SA ·