AnodyneWiki

Disable conformers
Collapse all
Light theme

2,5-Dimethoxyphenethylamine

Read
2C-H
2,5-Dimethoxyphenethylamine
Salts
[]
2,5-Dimethoxyphenethylamine hemisulfate
Generated by the Chemistry Development Kit (http://github.com/cdk)
2,5-Dimethoxyphenethylamine hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Rotamer
[]
Conformer structure via 3Dmol.js
Enable javascript to view conformer structure via 3Dmol.js
Physical properties
[]
181.23 g/mol [1]
1.3 [1]
Structural Identifiers
[]
C10H15NO2 [1]
2-(2,5-dimethoxyphenyl)ethanamine [1]
COC1=CC(=C(C=C1)OC)CCN [1]
InChI=1S/C10H15NO2/c1-12-9-3-4-10(13-2)8(7-9)5-6-11/h3-4,7H,5-6,11H2,1-2H3 [1]
InChIKeyWNCUVUUEJZEATP-UHFFFAOYSA-N [1]

2,5-Dimethoxyphenethylamine (also known as NSC 168525, Dtxcid40112055, 625-021-8, 2-(2,5-Dimethoxyphenyl)ethanamine, 2-(2,5-Dimethoxy-phenyl)-ethylamine, 2-(2,5-Dimethoxyphenyl)Ethan-1-Amine, 2C-H, 2,5-Dimethoxyphenethylamine-d6, 2-(2,5-Dimethoxyphenyl)Ethylamine or Chembl287047) is a substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

Salts []

2,5-Dimethoxyphenethylamine is typically found in the form of its hemisulfate and hydrochloride salts.

 []

2,5-Dimethoxyphenethylamine is a achiral mixture.

There are currently 6 reagent-interactions on

ReagentColor change
Marquis
Mecke
Mandelin
Froehde
Simon's
Scott

Experience reports

Erowid

There are currently 1 experience reports involving 2,5-dimethoxyphenethylamine on : []

See also []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 76632, 2,5-Dimethoxyphenethylamine. Accessed June 7, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/76632

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxyphenethylamine. UNII: 9A8XF4GA0X. Global Substance Registration System. Accessed June 7, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/9A8XF4GA0X