Beatrice, N-methyl-DOM, MDO-D, MDOM

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	223.31 g/mol ^[1]
Predicted LogP	2.8 ^[1]

Structural Identifiers []
Molecular formula	C₁₃H₂₁NO₂ ^[1]
IUPAC name	1-(2,5-dimethoxy-4-methylphenyl)-N-methylpropan-2-amine ^[1]
SMILES	CC1=CC(=C(C=C1OC)CC(C)NC)OC ^[1]
InChI	InChI=1S/C13H21NO2/c1-9-6-13(16-5)11(7-10(2)14-3)8-12(9)15-4/h6,8,10,14H,7H2,1-5H3 ^[1]
InChIKey	IWYGVDBZCSCJGT-UHFFFAOYSA-N ^[1]

2,5-Dimethoxy-4-methylmethamphetamine

2,5-Dimethoxy-4-methylmethamphetamine (also known as Beatrice, 2,5-Dimethoxy-N,α,4-trimethylbenzeneethanamine, Phenethylamine, 2,5-dimethoxy-α,N,4-trimethyl-, 2,5-Dimethoxy-α,N,4-trimethylphenethylamine, N-methyl-2,5-dimethoxy-4-methylamphetamine, Q4877113, 2,5-Dimethoxy-n,α,4-trimethylbenzeneethanamine, Benzeneethanamine, 2,5-dimethoxy-N,α,4-trimethyl- or Benzeneethanamine, 2,5-dimethoxy-n,α,4-trimethyl-) is a stimulant substance of the 2,5-dimethoxyamphetamine class.

Chemistry

Stereochemistry []

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

Stereoisomers
(S)-2,5-Dimethoxy-4-methylmethamphetamine (R)-2,5-Dimethoxy-4-methylmethamphetamine

Subjective effects []

Physical effects
Abnormal heartbeat Appetite suppression Dehydration Dry mouth Increased blood pressure Increased heart rate Increased libido Restless legs Shakiness Stamina enhancement Stimulation Teeth grinding Vasoconstriction

Cognitive effects
Analysis enhancement Cognitive euphoria Compulsive redosing Disinhibition Ego inflation Focus enhancement Increased music appreciation Mania Motivation enhancement Suggestibility suppression Thought acceleration Wakefulness

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 212480, 2,5-Dimethoxy-4-methylmethamphetamine. Accessed August 3, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/212480

Anodyne