EEM (psychedelic)

EEM
Names
	Preferred IUPAC name 1-(2,4-Diethoxy-5-methoxyphenyl)propan-2-amine
Identifiers
CAS Number	23693-33-6 ;
3D model (JSmol)	Interactive image;
ChemSpider	21106297 ;
PubChem CID	44719558;
UNII	EYL9ME7KPM ;
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 Key: SAFDWWQYGOOGMX-UHFFFAOYSA-N ; 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). verify (what is ?) 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.^[1] EEM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EEM.

References

^ EEM Entry in PiHKAL

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[1] EEM Entry in PiHKAL

[1]

See also

References