| | |
| Clinical data | |
|---|---|
| Other names | 2-Methoxy-4-methyl-5-methylsulfinylamphetamine |
| Routes of administration | Oral [1] |
| Drug class | Serotonergic psychedelic; Hallucinogen |
| ATC code |
|
| Pharmacokinetic data | |
| Duration of action | 10–16 hours [1] |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider |
|
| UNII | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C12H19NO2S |
| Molar mass | 241.35 g·mol−1 |
| 3D model (JSmol) | |
| |
| |
| (verify) | |
TOMSO, or 5-TOMSO, also known as 2-methoxy-4-methyl-5-methylsulfinylamphetamine, is a psychedelic drug of the phenethylamine and amphetamine families related to the DOx series. [1] [2] It is the analogue of DOM in which the methoxy group at the 5 position has been replaced with a sulfur-containing methyl sulfinyl group. [1] [2] In his book PiHKAL (Phenethylamines I Have Known and Loved), Alexander Shulgin lists TOMSO's dose as >150 mg orally alone or 100 to 150 mg orally in combination with alcohol and its duration as 10 to 16 hours. [1] TOMSO was reported to produce no or only threshold effects by itself at the assessed doses, but when alcohol was concomitantly ingested, clear hallucinogenic effects occurred. [1] These effects included facial distortion and remarkable time dilation, among others. [1] When combined with alcohol, "plus-two" and "plus-three" experiences occurred on the Shulgin Rating Scale. [1] TOMSO was first described in the scientific literature by Alexander Shulgin and Peyton Jacob III in 1983. [2] Subsequently, it was described in greater detail by Shulgin in PiHKAL in 1991. [1]
| Phenethylamines |
| ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Amphetamines |
| ||||||||||||||||
| Phentermines |
| ||||||||||||||||
| Cathinones |
| ||||||||||||||||
| Phenylisobutylamines (and further-extended) | |||||||||||||||||
| Catecholamines (and close relatives) |
| ||||||||||||||||
| Cyclized phenethylamines |
| ||||||||||||||||
| Related compounds |
| ||||||||||||||||
| | This hallucinogen-related article is a stub. You can help Wikipedia by expanding it. |