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74341-83-6

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74341-83-6 Structure

74341-83-6 Structure
IdentificationBack Directory
[Name]

N-Hydroxy-MDA Hydrochloride
[CAS]

74341-83-6
[Synonyms]

N-Hydroxy-MDA Hydrochloride
N-hydroxy MDA (hydrochloride) (exempt preparation)
[Molecular Formula]

C10H14ClNO3
[MDL Number]

MFCD00171386
[MOL File]

74341-83-6.mol
[Molecular Weight]

231.676
Chemical PropertiesBack Directory
[solubility ]

DMF: 10 mg/ml
DMSO: 10 mg/ml
Ethanol: 15 mg/mlPBS (pH 7.2): 5 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H330-H310-H300
[Precautionary statements ]

P264-P270-P301+P310-P321-P330-P405-P501-P260-P271-P284-P304+P340-P310-P320-P403+P233-P405-P501-P262-P264-P270-P280-P302+P350-P310-P322-P361-P363-P405-P501
Hazard InformationBack Directory
[Description]

3,4-Methylenedioxyamphetamine (MDA) is psychedelic and entactogenic drug that is scheduled as a controlled substance in the United States. N-hydroxy-MDA is an analog of MDA (, hydrochloride form) which inhibits reuptake of noradrenaline (IC50 = 87.8 μM) more effectively than serotonin (IC50 = 215 μM). Like MDA, N-hydroxy-MDA is regulated in the United States. This product is intended for forensic and research applications.
[Uses]

N-Hydroxy-MDA is an 3,4-methylenedioxymethamphetamine (M303985) analogue and was studied as a inhibitor of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines.
[References]

[1] T MONTGOMERY. Comparative potencies of 3,4-methylenedioxymethamphetamine (MDMA) analogues as inhibitors of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines[J]. British Journal of Pharmacology, 2009, 152 7: 1121-1130. DOI: 10.1038/sj.bjp.0707473
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86029-48-3 74341-83-6 2747917-68-4 6292-91-7 42542-07-4