DOAM

Salts []
2,5-Dimethoxy-4-amylamphetamine hydrochloride

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C16H27NO2[1]
Molecular mass	265.39 g/mol[1]
Predicted LogP	4.4[1]
Chirality	racemic[2]

Identifiers []
IUPAC name	1-(2,5-dimethoxy-4-pentylphenyl)propan-2-amine[1]
SMILES	CCCCCC1=CC(=C(C=C1OC)CC(C)N)OC[1]
InChI	InChI=1S/C16H27NO2/c1-5-6-7-8-13-10-16(19-4)14(9-12(2)17)11-15(13)18-3/h10-12H,5-9,17H2,1-4H3[1]
InChIKey	VLJORLCVOAUUKM-UHFFFAOYSA-N[1]

Dosing

2,5-Dimethoxy-4-amylamphetamine

2,5-Dimethoxy-4-amylamphetamine (also known as 2,5-Dimethoxy-4-pentylamphetamine, α-Methyl-4-amyl-2,5-dimethoxyphenethylamine, 1-(2,5-Dimethoxy-4-pentylphenyl)propan-2-amine, US20240166618, Compound 23, US20240166618, Compound 29, CS-0083652, 2,5-Dimethoxy-I+/--methyl-4-pentylbenzeneethanamine or Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-pentyl-) is a substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

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

Stereochemistry

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

See also

• 2,5-Dimethoxyphenethylamine
• Substituted 2,5-dimethoxyphenethylamines
• Anodyne

External links

• 2,5-Dimethoxy-4-amylamphetamine (Wikipedia)
• 2,5-Dimethoxy-4-amylamphetamine (Wikidata)
• 2,5-Dimethoxy-4-amylamphetamine (PubChem)
• 2,5-Dimethoxy-4-amylamphetamine (ChEMBL)
• 2,5-Dimethoxy-4-amylamphetamine (Common Chemistry)
• 2,5-Dimethoxy-4-amylamphetamine (UNII)
• 2,5-Dimethoxy-4-amylamphetamine (EPA DSSTox)

References