Anodyne

Disable conformers
Expand all
Toggle theme
DOC
Generated by the Chemistry Development Kit (http://github.com/cdk)
Salts
[]
Hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
[]
Enable javascript to view conformer structure via 3Dmol.js
Physical properties
[]
229.70 g/mol [1]
2.5 [1]
Structural Identifiers
[]
C11H16ClNO2 [1]
1-(4-chloro-2,5-dimethoxyphenyl)propan-2-amine [1]
CC(CC1=CC(=C(C=C1OC)Cl)OC)N [1]
InChI=1S/C11H16ClNO2/c1-7(13)4-8-5-11(15-3)9(12)6-10(8)14-2/h5-7H,4,13H2,1-3H3 [1]
InChIKeyACRITBNCBMTINK-UHFFFAOYSA-N [1]

2,5-Dimethoxy-4-chloroamphetamine

2,5-Dimethoxy-4-chloroamphetamine (also known as 4-Chloro-2,5-dimethoxyamphetamine, 4-Cl-2,5-dma, J275.082A, 1-(4-Chloro-2,5-dimethoxyphenyl)-2-aminopropaneHCL, Benzeneethanamine, 4-chloro-2,5-dimethoxy-α-methyl-, C22719 or Q4029756) is a psychedelic substance of the 2,5-dimethoxyamphetamine class.

Chemistry

Salts []

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

 []

2,5-Dimethoxy-4-chloroamphetamine is a racemic mixture of the

Stereoisomers
(R)-2,5-Dimethoxy-4-chloroamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)
(S)-2,5-Dimethoxy-4-chloroamphetamineGenerated by the Chemistry Development Kit (http://github.com/cdk)

See also []

  • 4-Substituted 2,5-dimethoxyamphetamines (DOx)
  • Anodyne

    • External links []

    References []

    1. National Center for Biotechnology Information. PubChem Compound Summary for CID 542036, 2,5-Dimethoxy-4-chloroamphetamine. Accessed July 13, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/542036

    2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. 2,5-Dimethoxy-4-chloroamphetamine. UNII: 8Y1C6K0PCA. Global Substance Registration System. Accessed July 13, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/8Y1C6K0PCA