EEM (psychedelic)

EEM

Names
Preferred IUPAC name 1-(2,4-Diethoxy-5-methoxyphenyl)propan-2-amine
Identifiers
CAS Number	23693-33-6 Y
3D model (JSmol)	Interactive image
ChemSpider	21106297 Y
PubChem CID	44719558
UNII	EYL9ME7KPM Y
CompTox Dashboard (EPA)	DTXSID20660362
InChI InChI=1S/C14H23NO3/c1-5-17-12-9-14(18-6-2)13(16-4)8-11(12)7-10(3)15/h8-10H,5-7,15H2,1-4H3 Y Key: SAFDWWQYGOOGMX-UHFFFAOYSA-N Y InChI=1/C14H23NO3/c1-5-17-12-9-14(18-6-2)13(16-4)8-11(12)7-10(3)15/h8-10H,5-7,15H2,1-4H3 Key: SAFDWWQYGOOGMX-UHFFFAOYAW
SMILES CCOc1cc(OCC)c(cc1OC)CC(C)N
Properties
Chemical formula	C14H23NO3
Molar mass	253.342 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

EEM (2,4-diethoxy-5-methoxyamphetamine) is a lesser-known substituted amphetamine. It is a diethoxy-methoxy analog of trimethoxyamphetamine (TMA-2). EEM was first synthesized by Alexander Shulgin. In his book PiHKAL, both the dosage and duration are unknown. EEM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EEM.

See also

• Phenethylamine
• Psychedelics, dissociatives and deliriants