Anodyne

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DOIP
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
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Conformer structure via JSmol
Physical properties
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237.34 g/mol [1]
3 [1]
Structural Identifiers
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C14H23NO2 [1]
1-(2,5-dimethoxy-4-propan-2-ylphenyl)propan-2-amine [1]
CC(C)C1=C(C=C(C(=C1)OC)CC(C)N)OC [1]
InChI=1S/C14H23NO2/c1-9(2)12-8-13(16-4)11(6-10(3)15)7-14(12)17-5/h7-10H,6,15H2,1-5H3 [1]
InChIKeySPKSLAUXKHSASF-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-isopropylamphetamine

2,5-Dimethoxy-4-isopropylamphetamine (also known as Doipr, 4-Isopropyl-2,5-dimethoxyamphetamine, Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-(1-methylethyl)-, Doip or Q20706958) is a psychedelic substance of the 2,5-dimethoxyamphetamine class.

Chemistry

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2,5-Dimethoxy-4-isopropylamphetamine is a racemic mixture of the

Stereoisomers
(S)-2,5-Dimethoxy-4-isopropylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(R)-2,5-Dimethoxy-4-isopropylamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • 4-Substituted 2,5-dimethoxyamphetamines (DOx)
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 44265275, 2,5-Dimethoxy-4-isopropylamphetamine. Accessed July 14, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/44265275

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-isopropylamphetamine. UNII: PF0P8RBU0X. Global Substance Registration System. Accessed July 14, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/PF0P8RBU0X