MPM (psychedelic)

Last updated
MPM
MPM.png
Names
Preferred IUPAC name
1-(2,5-Dimethoxy-4-propoxyphenyl)propan-2-amine
Other names
2,5-Dimethoxy-4-propoxyamphetamine; 2,5-Dimethoxy-α-methyl-4-propoxybenzeneethanamine
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
UNII
  • InChI=1S/C14H23NO3/c1-5-6-18-14-8-11(7-10(2)15)12(16-3)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3 Yes check.svgY
    Key: FTJOFRCENIVFLC-UHFFFAOYSA-N Yes check.svgY
  • InChI=1/C14H23NO3/c1-5-6-18-14-8-11(7-10(2)15)12(16-3)9-13(14)17-4/h8-10H,5-7,15H2,1-4H3
    Key: FTJOFRCENIVFLC-UHFFFAOYAE
  • COc1cc(OC)c(cc1OCCC)CC(C)N
Properties
C14H23NO3
Molar mass 253.342 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Yes check.svgY  verify  (what is  Yes check.svgYX mark.svgN ?)

MPM (2,5-dimethoxy-4-propoxyamphetamine) is a lesser-known psychedelic drug and a substituted amphetamine.

MPM was first synthesized by Alexander Shulgin. In his book PiHKAL , dosage is given as "30 mg or more" and duration "probably short". [1] MPM is of low potency and produced only slight effects at the highest dose reported in PiHKAL of 30 mg, although its effects at higher doses than this have not been reported.

Very little data exists about the pharmacological properties, metabolism, and toxicity of MPM.

See also

Related Research Articles

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2,5-Dimethoxy-4-ethoxyamphetamine Psychedelic drug

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Animal studies that have compared DOF to the highly potent DOI and DOB imply that the human activity will be some four to six times less than these two heavier halide analogues.

References