EEM (drug)

EEM
Clinical data
Other names2,4-Diethoxy-5-methoxyamphetamine
Routes of
administration		Oral[1]
ATC code
  • None
Pharmacokinetic data
Duration of actionUnknown[1]
Identifiers
  • 1-(2,4-diethoxy-5-methoxyphenyl)propan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC14H23NO3
Molar mass253.342 g·mol−1
3D model (JSmol)
  • CCOc1cc(OCC)c(cc1OC)CC(C)N
  • 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
  (verify)

EEM, also known as 2,4-diethoxy-5-methoxyamphetamine, is a substituted amphetamine.[1] It is a diethoxy-methoxy analogue of trimethoxyamphetamine (TMA-2).[1] EEM was first synthesized by Alexander Shulgin.[1] In his book PiHKAL, both the dose and duration are unknown.[1] EEM produces few to no effects.[1] Very little data exists about the pharmacological properties, metabolism, and toxicity of EEM.[1]

See also

References

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