Anodyne

DOBU
2,5-Dimethoxy-4-butylamphetamine
Salts
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2,5-Dimethoxy-4-butylamphetamine hydrochloride
2,5-Dimethoxy-4-butylamphetamine hydrochloride
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC15H25NO2[1]
Molecular mass251.36 g/mol[1]
Predicted LogP3.9[1]
Chiralityracemic[2]
Identifiers
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IUPAC name1-(4-butyl-2,5-dimethoxyphenyl)propan-2-amine[1]
SMILESCCCCC1=CC(=C(C=C1OC)CC(C)N)OC[1]
InChIInChI=1S/C15H25NO2/c1-5-6-7-12-9-15(18-4)13(8-11(2)16)10-14(12)17-3/h9-11H,5-8,16H2,1-4H3[1]
InChIKeyNGVDYAULSQKEGW-UHFFFAOYSA-N[1]
Dosing

2,5-Dimethoxy-4-butylamphetamine

2,5-Dimethoxy-4-butylamphetamine (also known as Benzeneethanamine, 4-butyl-2,5-dimethoxy-α-methyl-, 4-Butyl-2,5-dimethoxy-α-methylbenzeneethanamine, -1-(2,5-Dimethoxy-4-n-butylphenyl)-2-aminopropane, α-Methyl-4-butyl-2,5-dimethoxyphenethylamine, 1-(4-Butyl-2,5-dimethoxyphenyl)propan-2-amine, -1-(2,5-Dimethoxy-4-N-butylphenyl)-2-aminopropane, NCA77989, Pdsp1_001368, Pdsp2_001352 or 2-(4-Butyl-2,5-dimethoxy-phenyl)-1-methyl-ethylamine) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

2,5-Dimethoxy-4-butylamphetamine is typically found in the form of its hydrochloride salt.

Stereochemistry

(RS)-2,5-Dimethoxy-4-butylamphetamine is a racemic mixture of the optical stereoisomers

See also

References

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 10060720, 2,5-Dimethoxy-4-butylamphetamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/10060720.

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-butylamphetamine. UNII: 6ARH6DPN4N. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/6ARH6DPN4N