IRIS (psychedelic)

IRIS (2-methoxy-5-ethoxy-4-methylamphetamine) is a lesser-known psychedelic drug and a substituted amphetamine. It is also the 5-ethoxy analog of DOM. IRIS was first synthesized by Alexander Shulgin. In his book PiHKAL, the minimum dosage is listed as 9 mg, and the duration unknown.[1] IRIS produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of IRIS.

IRIS
Names
Preferred IUPAC name
1-(5-Ethoxy-2-methoxy-4-methylphenyl)propan-2-amine
Other names
2-Methoxy-5-ethoxy-4-methylamphetamine
2-Methoxy-5-ethoxy-4-methyl-1-ethyl-(alpha-methyl)amine
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
InChI
  • InChI=1S/C13H21NO2/c1-5-16-12-8-11(7-10(3)14)13(15-4)6-9(12)2/h6,8,10H,5,7,14H2,1-4H3 Y
    Key: IPJRCKIREPMKNE-UHFFFAOYSA-N Y
  • InChI=1/C13H21NO2/c1-5-16-12-8-11(7-10(3)14)13(15-4)6-9(12)2/h6,8,10H,5,7,14H2,1-4H3
    Key: IPJRCKIREPMKNE-UHFFFAOYAV
SMILES
  • COc1cc(C)c(cc1CC(C)N)OCC
Properties
Chemical formula
 C13H21NO2
Molar mass 223.316 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

See also

References
  1. IRIS entry in PiHKAL


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