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1286588-92-8

1286588-92-8 Structure

1286588-92-8 Structure
IdentificationBack Directory
[Name]

3,4-MDEA-d5 (hydrochloride)
[CAS]

1286588-92-8
[Synonyms]

MDE-d5 Hydrochloride
3,4-MDEA-d5 (hydrochloride)
(±)-MDEA-d5 hydrochloride (Ethyl d5)
3,4-MDEA-d5 (hydrochloride) (exempt preparation)
1-(1,3-benzodioxol-5-yl)-N-(1,1,2,2,2-pentadeuterioethyl)propan-2-amine:hydrochloride
[Molecular Formula]

C12H13ClD5NO2
[MDL Number]

MFCD30718258
[MOL File]

1286588-92-8.mol
[Molecular Weight]

248.761
Chemical PropertiesBack Directory
[solubility ]

DMF: 5 mg/ml
DMSO: 10 mg/ml
Ethanol: 0.3 mg/mlPBS (pH 7.2): 5 mg/ml
Safety DataBack Directory
[Symbol(GHS) ]

Flame (GHS02)Skull and Crossbones (GHS06)Health Hazard (GHS08)
GHS02,GHS06,GHS08
[Signal word ]

Danger
[Hazard statements ]

H225-H301+H311+H331-H370
[Precautionary statements ]

P210-P240-P241-P242-P243-P260-P264-P270-P271-P280-P301+P310-P321-P330-P303+P361+P353-P304+P340-P307+P311-P312-P361+P364-P370+P378-P403+P233-P403+P235-P405-P501
Hazard InformationBack Directory
[Description]

3,4-MDEA-d5 (hydrochloride) (exempt preparation) (Item No. 22876) is intended for use as an internal standard for the quantification of 3,4-MDEA (Item Nos. 14085 | ISO60196) by GC- or LC-MS. 3,4-MDEA is categorized as an amphetamine. It has similar psychotropic action to MDMA and shares the common name of "ecstasy". Postmortem findings in human deaths associated with 3,4-MDEA as well as 3,4-MDMA indicate striking brain and myocardial damage as well as liver necrosis. 3,4-MDEA is regulated as a Schedule I compound in the United States. 3,4-MDEA-d5 (hydrochloride) (exempt preparation) (Item No. 22876) is provided as a DEA exempt preparation. This product is intended for research and forensic applications.
[Uses]

1-(1,3-Benzodioxol-5-yl)-N-(1,1,2,2,2-pentadeuterioethyl)propan-2-amine Hydrochloride is used as an internal standard for the quantification of 3,4-MDEA, which has similar psychotropic action to methylenedioxyamphetamine (MDMA) and produces significant retention deficits in learning tasks in rats.
[References]

[1] ROLAND W. FREUDENMANN  Manfred S. The Neuropsychopharmacology and Toxicology of 3,4-methylenedioxy-N-ethyl-amphetamine (MDEA)[J]. CNS drug reviews, 2006, 10 2: 89-116. DOI: 10.1111/j.1527-3458.2004.tb00007.x
[2] C M MILROY  A R F  J C Clark. Pathology of deaths associated with “ecstasy” and “eve” misuse.[J]. Journal of Clinical Pathology, 1996, 49 2: 149-153. DOI: 10.1136/jcp.49.2.149
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