EMM (drug)

EMM

Clinical data
Other names	2-Ethoxy-4,5-dimethoxyamphetamine
Routes of administration	Oral[1]
ATC code	None
Pharmacokinetic data
Duration of action	Unknown[1]
Identifiers
IUPAC name 1-(2,4,5-trimethoxyphenyl)propan-2-amine
CAS Number	23693-30-3^Y
PubChem CID	44719565
ChemSpider	21106299^Y
UNII	8S8UH2M5JV
CompTox Dashboard (EPA)	DTXSID40660364
Chemical and physical data
Formula	C13H21NO3
Molar mass	239.315 g·mol^−1
3D model (JSmol)	Interactive image
SMILES C1(=CC(=C(C=C1CC(C)N)OC)OC)OCC
InChI InChI=1S/C13H21NO3/c1-5-17-11-8-13(16-4)12(15-3)7-10(11)6-9(2)14/h7-9H,5-6,14H2,1-4H3^Y Key:SKRNTJDDBVAEGB-UHFFFAOYSA-N^Y
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EMM, also known as 2-ethoxy-4,5-dimethoxyamphetamine, is a substituted amphetamine.^[1] It is a dimethoxy-ethoxy analogue of trimethoxyamphetamine (TMA-2).^[1] EMM was first synthesized by Alexander Shulgin.^[1] In his book PiHKAL, both the dose and duration are unknown.^[1] EMM produces few to no effects.^[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of EMM.^[1]

See also

• DOx (psychedelics)
• TWEETIO (psychedelics)

References

1. Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. EMM Entry in PiHKAL