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3,4-Methylenedioxy-N-isopropylamphetamine

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MDIP
BERJAYA
Clinical data
Other names3,4-Methylenedioxy-N-isopropylamphetamine; MDIP; MDIPA; N-Isopropyl-MDA
Routes of
administration		Oral[1]
ATC code
  • None
Pharmacokinetic data
Duration of actionUnknown[1]
Identifiers
  • 1-(2H-1,3-benzodioxol-5-yl)-N-(propan-2-yl)propan-2-amine
CAS Number
PubChem CID
ChemSpider
UNII
CompTox Dashboard (EPA)
Chemical and physical data
FormulaC13H19NO2
Molar mass221.300 g·mol−1
3D model (JSmol)
  • C1=C2C(=CC=C1CC(C)NC(C)C)OCO2
  • InChI=1S/C13H19NO2/c1-9(2)14-10(3)6-11-4-5-12-13(7-11)16-8-15-12/h4-5,7,9-10,14H,6,8H2,1-3H3
  • Key:XKEVWMVUIDDRMC-UHFFFAOYSA-N
  (verify)

MDIP, also known as 3,4-methylenedioxy-N-isopropylamphetamine or as N-isopropyl-MDA, is a psychoactive drug of the phenethylamine and amphetamine families.[1][2] It is the N-isopropyl analogue of 3,4-methylenedioxyamphetamine (MDA).[1][2]

Use and effects

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In his book PiHKAL (Phenethylamines I Have Known and Loved), Alexander Shulgin lists MDIP's dose as greater than 250 mg orally and its duration as unknown.[1][2] MDIP produces a brief mild threshold and no other effects.[1]

Chemistry

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Synthesis

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

See also

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References

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  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. MDIP entry
  2. ^ a b c Shulgin AT (2003). "Basic Pharmacology and Effects". In Laing RR (ed.). Hallucinogens: A Forensic Drug Handbook. Forensic Drug Handbook Series. Elsevier Science. pp. 67–137. ISBN 978-0-12-433951-4. Archived from the original on 13 July 2025.
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