EMM (psychedelic)

EMM
Names
Preferred IUPAC name
1-(2,4,5-Trimethoxyphenyl)propan-2-amine
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • 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 checkY
    Key: SKRNTJDDBVAEGB-UHFFFAOYSA-N checkY
  • InChI=1/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
    Key: SKRNTJDDBVAEGB-UHFFFAOYAE
  • C1(=CC(=C(C=C1CC(C)N)OC)OC)OCC
  • COc1cc(OCC)c(cc1OC)CC(C)N
Properties
C13H21NO3
Molar mass 239.315 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

EMM (2-ethoxy-4,5-dimethoxyamphetamine) is a lesser-known substituted amphetamine. It is a dimethoxy-ethoxy analog of trimethoxyamphetamine (TMA-2). EMM was first synthesized by Alexander Shulgin. In his book PiHKAL, both the dosage and duration are unknown.[1] EMM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EMM.

See also

References

  1. ^ EMM Entry in PiHKAL


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