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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
CompTox Dashboard ( EPA)	DTXSID40660364
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). Y  verify ( what is YN ?) 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

• Phenethylamine
• Psychedelics, dissociatives and deliriants

References

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