:IDNNA
{{one source|date=October 2019}}
{{chembox
| verifiedrevid = 415659854
| ImageFile1 = IDNNA.png
| ImageSize1 = 200px
| ImageFile2 =
| ImageSize2 = 200px
| PIN = 1-(4-Iodo-2,5-dimethoxyphenyl)-N,N-dimethylpropan-2-amine
| OtherNames = 2,5-Dimethoxy-4-iodo-N,N-dimethylamphetamine
2,5-Dimethoxy-4-iodo-1-ethyl-(α-methyl)amine
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 119009
| InChI = 1/C13H20INO2/c1-9(15(2)3)6-10-7-13(17-5)11(14)8-12(10)16-4/h7-9H,6H2,1-5H3
| InChIKey = XBCUSBRGRALQID-UHFFFAOYAY
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 11043
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C13H20INO2/c1-9(15(2)3)6-10-7-13(17-5)11(14)8-12(10)16-4/h7-9H,6H2,1-5H3
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = XBCUSBRGRALQID-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 85563-10-6
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = M6Q9NK9RFD
| PubChem = 135056
| SMILES = Ic1cc(OC)c(cc1OC)CC(N(C)C)C
}}
|Section2={{Chembox Properties
| Formula = C13H20NO2I
| MolarMass = 349.211 g/mol
| Appearance =
| Density =
| MeltingPt =
| BoilingPt =
| Solubility = }}
|Section3={{Chembox Hazards
| MainHazards =
| FlashPt =
| AutoignitionPt = }}
}}
IDNNA (2,5-dimethoxy-4-iodo-N,N-dimethylamphetamine) is a lesser-known psychedelic drug and a substituted amphetamine. It is also the N,N-dimethyl analog of DOI. IDNNA was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 2.6 mg, and the duration unknown.[http://www.erowid.org/library/books_online/pihkal/pihkal090.shtml IDNNA Entry in PiHKAL] IDNNA produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of IDNNA.
Legality
=United Kingdom=
This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.{{cite web | title = UK Misuse of Drugs act 2001 Amendment summary | url = http://isomerdesign.com/Cdsa/scheduleUK.php?schedule=1&ion=30&structure=C | access-date = 12 March 2014 | publisher = Isomer Design | archive-date = 22 October 2017 | archive-url = https://web.archive.org/web/20171022085110/http://isomerdesign.com/Cdsa/scheduleUK.php?schedule=1&ion=30&structure=C | url-status = dead }}
See also
References
{{Reflist}}
{{Phenethylamines}}
Category:Dimethylamino compounds
Category:Iodobenzene derivatives
{{Psychoactive-stub}}