MDPHP – Wikipedia

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Chemical compound

MDPHP (3′,4′-Methylenedioxy-α-pyrrolidinohexiophenone) is a stimulant of the cathinone class originally developed in the 1960s,[1] which has been reported as a novel designer drug. In the UK its slang name is monkey dust.[2] It is closely related to the potent stimulant MDPV though with slightly milder effects, and has been used as an alternative in some countries following the banning of MDPV.[3][4][5][6]

Legal Status[edit]

MDPHP is specifically listed as a controlled substance in Japan [7] and Hungary,[8] and is controlled under analogue provisions in a number of other jurisdictions.

See also[edit]

References[edit]

  1. ^ DE 1545591, Koeppe H, Zeile K, Ludwig G, “Patent DE – Verfahren zur Herstellung von α-Aminoketonen mit heterocyclischer Aminogruppe”, issued 28 May 1965 
  2. ^ “Monkey Dust drug use ‘an epidemic’, emergency workers warn”. BBC. 10 August 2018. Retrieved 16 August 2018.
  3. ^ Zaitsu K, Katagi M, Tsuchihashi H, Ishii A (2013). “Recently abused synthetic cathinones, α-pyrrolidinophenone derivatives: A review of their pharmacology, acute toxicity, and metabolism”. Forensic Toxicology. 32: 1–8. doi:10.1007/s11419-013-0218-1. S2CID 25604845.
  4. ^ Kaizaki-Mitsumoto A, Noguchi N, Yamaguchi S, Odanaka Y, Matsubayashi S, Kumamoto H, et al. (January 2016). “Three 25-NBOMe-type drugs, three other phenethylamine-type drugs (25I-NBMD, RH34, and escaline), eight cathinone derivatives, and a phencyclidine analog MMXE, newly identified in ingredients of drug products before they were sold on the drug market”. Forensic Toxicology. 34 (1): 108–14. doi:10.1007/s11419-015-0293-6. S2CID 45890497.
  5. ^ Beck O, Bäckberg M, Signell P, Helander A (April 2018). “Intoxications in the STRIDA project involving a panorama of psychostimulant pyrovalerone derivatives, MDPV copycats”. Clinical Toxicology. Philadelphia, Pa. 56 (4): 256–263. doi:10.1080/15563650.2017.1370097. PMID 28895757. S2CID 3401681.
  6. ^ Fowble KL, Shepard JR, Musah RA (March 2018). “Identification and classification of cathinone unknowns by statistical analysis processing of direct analysis in real time-high resolution mass spectrometry-derived “neutral loss” spectra”. Talanta. 179: 546–553. doi:10.1016/j.talanta.2017.11.020. PMID 29310273.
  7. ^ “指定薬物名称・構造式一覧（平成27年9月16日現在）” (PDF) (in Japanese). 厚生労働省. 16 September 2015. Retrieved 8 October 2015.
  8. ^ “A Daath.hu kiegészítése a BSZKI “designer jogi listáján” nem szereplő, de a C-lista 1.-4. szerkezeti leírásainak megfelelő, illetve a C-lista 5. felsorolásában szereplő néhány anyagról” [The addition to Daath.hu is not included in the “designer legal list” of the BSZKI, but C-list 1.-4. and some of the substances in list 5 of list C.] (PDF) (in Hungarian).


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