![]() | |
Clinical data | |
---|---|
Routes of administration | Oral |
ATC code |
|
Legal status | |
Legal status |
|
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
CompTox Dashboard ( EPA) | |
Chemical and physical data | |
Formula | C12H17NO2 |
Molar mass | 207.273 g·mol−1 |
3D model ( JSmol) | |
| |
| |
(verify) |
3,4-Ethylenedioxy-N-methylamphetamine (EDMA) is an entactogen drug of the methamphetamine class. [1] [2] It is an analogue of MDMA where the methylenedioxy ring has been replaced by an ethylenedioxy ring. [1] [2] EDMA was first synthesized by Alexander Shulgin. [1] In his book PiHKAL, the dosage is listed as 150–250 mg, and the duration listed as 3–5 hours. [1] According to Shulgin, EDMA produces a bare threshold consisting of paresthesia, nystagmus, and hypnogogic imagery, with few to no other effects. [1] Scientific research has demonstrated that EDMA acts as a non- neurotoxic serotonin releasing agent with moderately diminished potency relative to MDMA, and with negligible effects on dopamine release. [2]
![]() | |
Clinical data | |
---|---|
Routes of administration | Oral |
ATC code |
|
Legal status | |
Legal status |
|
Identifiers | |
| |
CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
CompTox Dashboard ( EPA) | |
Chemical and physical data | |
Formula | C12H17NO2 |
Molar mass | 207.273 g·mol−1 |
3D model ( JSmol) | |
| |
| |
(verify) |
3,4-Ethylenedioxy-N-methylamphetamine (EDMA) is an entactogen drug of the methamphetamine class. [1] [2] It is an analogue of MDMA where the methylenedioxy ring has been replaced by an ethylenedioxy ring. [1] [2] EDMA was first synthesized by Alexander Shulgin. [1] In his book PiHKAL, the dosage is listed as 150–250 mg, and the duration listed as 3–5 hours. [1] According to Shulgin, EDMA produces a bare threshold consisting of paresthesia, nystagmus, and hypnogogic imagery, with few to no other effects. [1] Scientific research has demonstrated that EDMA acts as a non- neurotoxic serotonin releasing agent with moderately diminished potency relative to MDMA, and with negligible effects on dopamine release. [2]