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IDNNA
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This article relies largely or entirely on a single source. (October 2019) |
| Clinical data | |
|---|---|
| Other names | 4-Iodo-2,5-dimethoxy-N,N-dimethylamphetamine; 2,5-Dimethoxy-4-iodo-N,N-dimethylamphetamine; N,N-Dimethyl-DOI |
| Routes of administration | Oral[1] |
| ATC code |
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| Pharmacokinetic data | |
| Duration of action | Unknown[1] |
| Identifiers | |
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| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C13H20INO2 |
| Molar mass | 349.212 g·mol−1 |
| 3D model (JSmol) | |
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| (verify) | |
IDNNA, also known as 4-iodo-2,5-dimethoxy-N,N-dimethylamphetamine or as N,N-dimethyl-DOI, is a lesser-known psychoactive drug and a substituted amphetamine.[1] It is also the N,N-dimethyl analogue of DOI.[1]
Use and effects
[edit]In his book PiHKAL (Phenethylamines I Have Known and Loved), the minimum dose is listed as 2.6 mg and the duration as unknown.[1] IDNNA produces few to no effects.[1]
Society and culture
[edit]Legal status
[edit]Canada
[edit]IDNNA is a controlled substance in Canada under phenethylamine blanket-ban language.[2]
United Kingdom
[edit]This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[3]
See also
[edit]- DOx (psychedelics)
- N-Methyl-DOI
- Methyl-DOB (N-methyl-DOB)
- N-Methyl-2C-I
- N-Methyl-2C-B
- Beatrice (N-methyl-DOM)
- N-Methyl-DOET
References
[edit]- ^ a b c d e f IDNNA Entry in PiHKAL
- ^ "Controlled Drugs and Substances Act". Department of Justice Canada. Retrieved 19 January 2026.
- ^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Archived from the original on 22 October 2017. Retrieved 12 March 2014.
