DOIP | |
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Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C14H23NO2[1] |
Molecular mass | 237.34 g/mol[1] |
Predicted LogP | 3[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-(2,5-dimethoxy-4-propan-2-ylphenyl)propan-2-amine[1] |
SMILES | CC(C)C1=C(C=C(C(=C1)OC)CC(C)N)OC[1] |
InChI | 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] |
InChIKey | SPKSLAUXKHSASF-UHFFFAOYSA-N[1] |
Dosing |
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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)- or Doip) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.
Chemistry
Stereochemistry
(RS)-2,5-Dimethoxy-4-isopropylamphetamine is a racemic mixture of the optical stereoisomers
Legal status
- Canada: 2,5-Dimethoxy-4-isopropylamphetamine is a Schedule I.
- Germany: 2,5-Dimethoxy-4-isopropylamphetamine is a Neuer-Psychoaktiver-Stoff under the "Neue-psychoaktive-Stoffe-Gesetz (NpSG)".
- United Kingdom: 2,5-Dimethoxy-4-isopropylamphetamine is a Class A.
See also
External links
- 2,5-Dimethoxy-4-isopropylamphetamine (Wikipedia)
- 2,5-Dimethoxy-4-isopropylamphetamine (Wikidata)
- 2,5-Dimethoxy-4-isopropylamphetamine (PubChem)
- 2,5-Dimethoxy-4-isopropylamphetamine (ChEMBL)
- 2,5-Dimethoxy-4-isopropylamphetamine (Common Chemistry)
- 2,5-Dimethoxy-4-isopropylamphetamine (UNII)
- 2,5-Dimethoxy-4-isopropylamphetamine (EPA DSSTox)
References
National Center for Biotechnology Information. PubChem Compound Summary for CID 44265275, 2,5-Dimethoxy-4-isopropylamphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/44265275.
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-isopropylamphetamine. UNII: PF0P8RBU0X. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/PF0P8RBU0X