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6-(2-Aminopropyl)benzofuran

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6-APB
6-(2-Aminopropyl)benzofuran
Salts
[]
6-(2-Aminopropyl)benzofuran hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Physical properties
[]
175.23 g/mol [1]
2.1 [1]
Structural Identifiers
[]
C11H13NO [1]
1-(1-benzofuran-6-yl)propan-2-amine [1]
CC(CC1=CC2=C(C=C1)C=CO2)N [1]
InChI=1S/C11H13NO/c1-8(12)6-9-2-3-10-4-5-13-11(10)7-9/h2-5,7-8H,6,12H2,1H3 [1]
InChIKeyFQDAMYLMQQKPRX-UHFFFAOYSA-N [1]

6-(2-Aminopropyl)benzofuran (also known as 6-(2-Aminopropyl)benzofuran, 6-APB, Benzofury, J3.334.441d, RefChem:103992, 1-(benzofuran-6-yl)propan-2-amine, LLA83485 or 6-Benzofuranethanamine, α-methyl-) is a substance of the amphetamine class.

Chemistry

Salts []

6-(2-Aminopropyl)benzofuran is typically found in the form of its hydrochloride salt.

 []

6-(2-Aminopropyl)benzofuran is a racemic mixture of the .

(R)-6-(2-Aminopropyl)benzofuranGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-6-(2-Aminopropyl)benzofuranGenerated by the Chemistry Development Kit (http://github.com/cdk)
Stereoisomer enumberation with rdkit

Subjective effects []

Mere / 6-(2-Aminopropyl)benzofuran []
magnus / 6-(2-Aminopropyl)benzofuran []
Routes:
  • Oral
Forms:
  • Succinate
Effects:Notes:
  • the first half of the experience is more mdma like, after a few hours the experience becomes more psychedelic

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 9794343, 6-(2-Aminopropyl)benzofuran. Accessed September 1, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/9794343

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 6-(2-Aminopropyl)benzofuran. UNII: 285VE60914. Global Substance Registration System. Accessed September 1, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/285VE60914