Anodyne

2C-G
2,5-Dimethoxy-3,4-dimethylphenethylamine
Salts
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2,5-Dimethoxy-3,4-dimethylphenethylamine hydrochloride
2,5-Dimethoxy-3,4-dimethylphenethylamine hydrochloride
Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formulaC12H19NO2[1]
Molecular mass209.28 g/mol[1]
Predicted LogP1.9[1]
Chiralityachiral[2]
Identifiers
[]
IUPAC name2-(2,5-dimethoxy-3,4-dimethylphenyl)ethanamine[1]
SMILESCC1=C(C=C(C(=C1C)OC)CCN)OC[1]
InChIInChI=1S/C12H19NO2/c1-8-9(2)12(15-4)10(5-6-13)7-11(8)14-3/h7H,5-6,13H2,1-4H3[1]
InChIKeyNFOHGLKGLZIHJQ-UHFFFAOYSA-N[1]
Dosing

2,5-Dimethoxy-3,4-dimethylphenethylamine

2,5-Dimethoxy-3,4-dimethylphenethylamine (also known as 2,5-Dimethoxy-3,4-dimethylbenzeneethanamine, 3,4-Dimethyl-2,5-dimethoxyphenethylamine or Benzeneethanamine, 2,5-dimethoxy-3,4-dimethyl-) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

2,5-Dimethoxy-3,4-dimethylphenethylamine is typically found in the form of its hydrochloride salt.

Stereochemistry

2,5-Dimethoxy-3,4-dimethylphenethylamine is a achiral mixture

See also

References

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 22238091, 2,5-Dimethoxy-3,4-dimethylphenethylamine. Accessed June 17, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/22238091.

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-3,4-dimethylphenethylamine. UNII: DTG7FMO01J. Global Substance Registration System. Accessed June 17, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/DTG7FMO01J