Ethylone
Chemical compound
From Wikipedia, the free encyclopedia
Ethylone, also known as 3,4-methylenedioxy-N-ethylcathinone (MDEC, βk-MDEA), is a recreational designer drug of the phenethylamine, amphetamine, and cathinone chemical classes.[1] It is the β-keto analogue of MDEA ("Eve"). Ethylone has only a short history of human use and is reported to be less potent than its relative methylone.[citation needed] In the United States, it began to be found in cathinone products in late 2011.[4]
category
- N (US)
| Clinical data | |
|---|---|
| Other names | 3,4-Methylenedioxy-N-ethylcathinone; MDEC; βk-MDEA |
| Pregnancy category |
|
| Routes of administration | Oral[1] |
| Drug class | Serotonin–norepinephrine–dopamine releasing agent; Entactogen |
| ATC code |
|
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Duration of action | 2–4 hours[1] |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| KEGG | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C12H15NO3 |
| Molar mass | 221.256 g·mol−1 |
| 3D model (JSmol) | |
| Chirality | Racemic mixture |
| |
| |
| | |
Very little data exists about the pharmacological properties, metabolism, and toxicity of ethylone, and although several ethylone-related deaths have been reported, the cause of death was not due to ingestion of ethylone.[4]
Interactions
Pharmacology
Pharmacokinetics
Analysis of human and rat urine for the metabolites of bk-amphetamines suggested that ethylone was degraded in the following metabolic steps:[5]
- N-deethylation to the primary amine.
- Reduction of the keto moiety to the respective alcohol.
Society and culture
Legal status
As of October 2015 Ethylone is a controlled substance in China.[6]