| 词条 | 3,4-Methylenedioxy-N-hydroxy-N-methylamphetamine |
| 释义 |
| IUPAC_name = 1-(1,3-Benzodioxol-5-yl)-N-hydroxy-N-methylpropan-2-amine | image = FLEA.svg | width = 200px | tradename = | pregnancy_category = | legal_UK = Class A | legal_DE = Anlage I | routes_of_administration = | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number = 214414-88-7 | ATC_prefix = | ATC_suffix = | PubChem = | DrugBank = | ChemSpiderID = 21106310 | chemical_formula = | C=11 | H=15 | N=1 | O=3 | molecular_weight = 209.24 g/mol | smiles = C1=C2C(=CC=C1CC(C)N(C)O)OCO2 }}3,4-Methylenedioxy-N-hydroxy-N-methylamphetamine (MDHMA; FLEA) is an entactogen, psychedelic, and stimulant of the phenethylamine and amphetamine chemical classes. It is the N-hydroxy homologue of MDMA ("Ecstasy"), and the N-methyl homologue of MDOH. MDHMA was first synthesized and assayed by Alexander Shulgin.[1] In his book PiHKAL (Phenethylamines i Have Known And Loved), Shulgin listed the dosage range as 100–160 mg, and the duration as approximately 4–8 hours.[2] He describes MDHMA as causing entactogenic and open MDMA-like effects, easing communication, and increasing appreciation of the senses.[3] LegalityUnited KingdomThis substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[4] References1. ^{{CitePiHKAL}} 2. ^{{CitePiHKAL}} 3. ^{{CitePiHKAL}} 4. ^{{cite web | title = UK Misuse of Drugs act 2001 Amendment summary | url = http://isomerdesign.com/Cdsa/scheduleUK.php?schedule=1&ion=30&structure=C | accessdate = 12 March 2014 | publisher = Isomer Design}} External links
7 : Substituted amphetamines|Designer drugs|Benzodioxoles|Serotonin-norepinephrine-dopamine releasing agents|Methamphetamines|Entactogens and empathogens|Hydroxylamines |
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