Methylenedioxyhydroxyethylamphetamine

MDHOET
Clinical data
Other names3,4-Methylenedioxy-N-hydroxyethylamphetamine; MDOHET; MDHET; MDHEA; N-Hydroxyethyl-MDA
Routes of
administration		Oral[1]
ATC code
  • None
Pharmacokinetic data
Duration of actionUnknown[1]
Identifiers
  • 2-{[(2H-1,3-benzodioxol-5-yl)propan-2-yl]amino}ethan-1-ol
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC12H17NO3
Molar mass223.272 g·mol−1
3D model (JSmol)
  • C1=C2C(=CC=C1CC(C)NCCO)OCO2
  • InChI=1S/C12H17NO3/c1-9(13-4-5-14)6-10-2-3-11-12(7-10)16-8-15-11/h2-3,7,9,13-14H,4-6,8H2,1H3 N
  • Key:SCUUYKMQDUDNBP-UHFFFAOYSA-N N
 NY (what is this?)  (verify)

MDHOET, also known as 3,4-methylenedioxy-N-hydroxyethylamphetamine or as N-hydroxyethyl-MDA, is a lesser-known drug and a substituted amphetamine.[1] It is also the N-hydroxyethyl analogue of MDA.[1]

Use and effects

In his book PiHKAL (Phenethylamines I Have Known and Loved), Alexander Shulgin lists MDHOET's dose as greater than 50 mg orally and its duration as unknown.[1] MDHOET produced few to no effects.[1]

Chemistry

Synthesis

The chemical synthesis of MDHOET has been described.[1]

Society and culture

United Kingdom

This substance is a Class A drug in the Drugs controlled by the UK Misuse of Drugs Act.[2]

See also

References

  1. ^ a b c d e f g Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
  2. ^ "UK Misuse of Drugs act 2001 Amendment summary". Isomer Design. Retrieved 12 March 2014.
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