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22004-32-6

22004-32-6 Structure

22004-32-6 Structure
IdentificationBack Directory
[Name]

2,5-DIMETHOXY-4-ETHYLAMPHETAMIN
[CAS]

22004-32-6
[Synonyms]

DOET
Dea no. 7399
DOET (exempt preparation)
2,5-DIMETHOXY-4-ETHYLAMPHETAMIN
2,5-dimethoxy-4-ethylamphetamine
4-Ethyl-2,5-diMethoxyaMphetaMine
2,5-DIMETHOXY-4-ETHYLAMPHETAMIN, >99% (HPLC)
1-(4-Ethyl-2,5-dimethoxyphenyl)-2-propanamine
4-Ethyl-2,5-diMethoxy-α- MethylphenethylaMine
1-(4-ethyl-2,5-dimethoxyphenyl)propan-2-amine
2,5-Dimethoxy-4-ethyl-α-methylbenzeneethanamine
4-Ethyl-2,5-dimethoxy-α-methylbenzeneethanamine
1-Methyl-2-(4-ethyl-2,5-dimethoxyphenyl)ethanamine
Benzeneethanamine, 4-ethyl-2,5-dimethoxy-α-methyl-
(±)-1-(2,5-DiMethoxy-4-ethylphenyl)-2-aMinopropane
Benzeneethanamine, 4-ethyl-2,5-dimethoxy-alpha-methyl-
[Molecular Formula]

C13H21NO2
[MDL Number]

MFCD09752943
[MOL File]

22004-32-6.mol
[Molecular Weight]

223.31
Chemical PropertiesBack Directory
[Boiling point ]

322.7±37.0 °C(Predicted)
[density ]

0.998±0.06 g/cm3(Predicted)
[solubility ]

DMF: 0.5 mg/ml
Ethanol: 0.3 mg/ml
[pka]

9.77±0.10(Predicted)
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
[DEA Controlled Substances]

CSCN: 7399
CSA SCH: Schedule I
NARC: No
Hazard InformationBack Directory
[Uses]

DOET is a potent, long-acting psychoactive drug of the phenethylamine and amphetamine chemical classes that, similar to other substituted amphetamines, likely acts as a serotonin 5-HT2 receptor partia l agonist. This compound is intended only for research and forensic applications.
[Definition]

ChEBI: 2,5-Dimethoxy-4-ethylamphetamine is a member of amphetamines.
[References]

[1] ANDREAS H. EWALD  Hans H M. 2,5-Dimethoxyamphetamine-derived designer drugs: Studies on the identification of cytochrome P450 (CYP) isoenzymes involved in formation of their main metabolites and on their capability to inhibit CYP2D6[J]. Toxicology letters, 2008, 183 1: Pages 52-57. DOI: 10.1016/j.toxlet.2008.09.014
[2] S H SNYDER L A F H Weingartner. DOET (2,5-dimethoxy-4-ethylamphetamine), a new psychotropic drug. Effects of varying doses in man.[J]. Archives of general psychiatry, 1971, 24 1: 50-55. DOI: 10.1001/archpsyc.1971.01750070052006
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