Chemistry:EMM (psychedelic)

EMM

Names
Preferred IUPAC name 1-(2,4,5-Trimethoxyphenyl)propan-2-amine
Identifiers
CAS Number	23693-30-3 Y
3D model (JSmol)	Interactive image Interactive image
ChemSpider	21106299 Y
PubChem CID	44719565
UNII	8S8UH2M5JV Y
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 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
SMILES C1(=CC(=C(C=C1CC(C)N)OC)OC)OCC COc1cc(OCC)c(cc1OC)CC(C)N
Properties
Chemical formula	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).
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Infobox references

Tracking categories (test):

• SizeSet

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. EMM produces few to no effects. Very little data exists about the pharmacological properties, metabolism, and toxicity of EMM.

See also

• Phenethylamine
• Psychedelics, dissociatives and deliriants