Bromantane

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	306.24 g/mol ^[1]
Predicted LogP	5 ^[1]

Structural Identifiers []
Molecular formula	C₁₆H₂₀BrN ^[1]
IUPAC name	N-(4-bromophenyl)adamantan-2-amine ^[1]
SMILES	C1C2CC3CC1CC(C2)C3NC4=CC=C(C=C4)Br ^[1]
InChI	InChI=1S/C16H20BrN/c17-14-1-3-15(4-2-14)18-16-12-6-10-5-11(8-12)9-13(16)7-10/h1-4,10-13,16,18H,5-9H2 ^[1]
InChIKey	LWJALJDRFBXHKX-UHFFFAOYSA-N ^[1]

Bromantane

Bromantane (also known as Bromantan, bromontan, 2-bromophenyl-1-amino adamantane, N-(4-Bromophenyl)tricyclo(3.3.1.13,7)decan-2-amine, Tricyclo(3.3.1.13,7)decan-2-amine, N-(4-bromophenyl)-, Tricyclo[3.3.1.13,7]decan-2-amine, N-(4-bromophenyl)-, Ladasten, N-(2-adamantyl)-n-(4-bromophenyl)amine, Tricyclo[3.3.1.13,7]decan-2-amine,N-(4-bromophenyl)- or 2-(4-Bromophenyl)aminoadamantane) is a stimulant substance of the aniline class.

Chemistry

Stereochemistry []

Bromantane is a racemic mixture of the enantiomers

Stereoisomers
(1r,3R)-5r)-7S)-9Tet_CCW)-Bromantane (1r,3S)-5r)-7R)-9Tet_CW)-Bromantane

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 4660557, Bromantane. Accessed July 25, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/4660557

Anodyne