DON

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

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C11H16N2O4[1]
Molecular mass	240.26 g/mol[1]
Predicted LogP	1.7[1]
Chirality	racemic[2]

Identifiers []
IUPAC name	1-(2,5-dimethoxy-4-nitrophenyl)propan-2-amine[1]
SMILES	CC(CC1=CC(=C(C=C1OC)[N+](=O)[O-])OC)N[1]
InChI	InChI=1S/C11H16N2O4/c1-7(12)4-8-5-11(17-3)9(13(14)15)6-10(8)16-2/h5-7H,4,12H2,1-3H3[1]
InChIKey	JQJRESSXOVAECC-UHFFFAOYSA-N[1]

Dosing

2,5-Dimethoxy-4-nitroamphetamine

2,5-Dimethoxy-4-nitroamphetamine (also known as 1-(2,5-Dimethoxy-4-nitrophenyl)-2-aminopropane, Don, J275.080E, L000870, 2-(2,5-Dimethoxy-4-nitro-phenyl)-1-methyl-ethylamine, Benzeneethanamine, 2,5-dimethoxy-α-methyl-4-nitro-, (-)2-(2,5-Dimethoxy-4-nitro-phenyl)-1-methyl-ethylamine, 2-(2,5-Dimethoxy-4-nitro-phenyl)-1-methyl-ethylamine(DON), -1-(2,5-Dimethoxy-4-nitrophenyl)-2-aminopropane or -1-(4-Nitro-2,5-dimethoxyphenyl)-2-aminopropane) is a psychedelic substance of the 2,5-dimethoxyphenethylamine class.

Chemistry

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

Stereochemistry

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

See also

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

External links

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

References