Methylenedioxydimethylamphetamine

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Methylenedioxydimethylamphetamine
Names
IUPAC name
(2-Benzo[1,3]dioxol-5-yl-1-methyl-ethyl)-dimethylamine
Other names
3,4-Methylenedioxy-N,N-dimethylamphetamine
3,4-Methylenedioxy-(alpha,N,N-trimethyl)-1-ethane
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C12H17NO2/c1-9(13(2)3)6-10-4-5-11-12(7-10)15-8-14-11/h4-5,7,9H,6,8H2,1-3H3 ☒N
    Key: JEJGUIDNYBAPGN-UHFFFAOYSA-N ☒N
  • InChI=1/C12H17NO2/c1-9(13(2)3)6-10-4-5-11-12(7-10)15-8-14-11/h4-5,7,9H,6,8H2,1-3H3
    Key: JEJGUIDNYBAPGN-UHFFFAOYAU
  • CC(Cc1ccc2c(c1)OCO2)N(C)C
Properties
C12H17NO2
Molar mass 207.27 g/mol
Melting point 172 to 173 °C (342 to 343 °F; 445 to 446 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

3,4-Methylenedioxy-N,N-dimethylamphetamine (MDDM) is a lesser-known psychedelic drug. It is also the N,N-dimethyl analog of 3,4-methylenedioxyamphetamine (MDA). MDDM was first synthesized by Alexander Shulgin. In his book PiHKAL (Phenethylamines i Have Known And Loved), the dosage is unspecified and the duration unknown. MDDM produces only mild effects that are not well characterized in PiHKAL. Very little data exists about the pharmacological properties, metabolism, and toxicity of MDDM. This compound is however occasionally encountered as an impurity in 3,4-methylenedioxy-N-methylamphetamine (MDMA) which has been synthesized by methylation of MDA using methylating reagents such as methyl iodide. An excess of reagent or a reaction temperature that is too high results in some double methylation of the amine nitrogen, yielding MDDM as well as MDMA. The presence of MDDM as an impurity can thus reveal which synthetic route was used to manufacture seized samples of MDMA.

Legality

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[1]

See also

References

  1. ^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.

External links

Template:PiHKAL