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	952016-59-0 Y
3D model (JSmol)	Interactive image
ChemSpider	21106327 Y
PubChem CID	44719575
UNII	V3WW7XL92Q
CompTox Dashboard (EPA)	DTXSID20660367
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

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.

See also[edit]

• Beatrice (psychedelic)
• Phenethylamine
• Psychedelics, dissociatives and deliriants

References[edit]