Bromadoline

U-47931E

Salts []
Bromadoline maleate

Molecular structure via molpic based on CDK

Physical properties []
Molecular mass	325.24 g/mol ^[1]
Predicted LogP	3.3 ^[1]

Structural Identifiers []
Molecular formula	C₁₅H₂₁BrN₂O ^[1]
IUPAC name	4-bromo-N-[(1S,2S)-2-(dimethylamino)cyclohexyl]benzamide ^[1]
SMILES	CN(C)[C@H]1CCCC[C@@H]1NC(=O)C2=CC=C(C=C2)Br ^[1]
InChI	InChI=1S/C15H21BrN2O/c1-18(2)14-6-4-3-5-13(14)17-15(19)11-7-9-12(16)10-8-11/h7-10,13-14H,3-6H2,1-2H3,(H,17,19)/t13-,14-/m0/s1 ^[1]
InChIKey	UFDJFJYMMIZKLG-KBPBESRZSA-N ^[1]

Bromadoline (also known as Bromadoline, Bromadolina, Bromadolinum, trans-p-Bromo-N-(2-(dimethylamino)cyclohexyl)benzamide, Dtxsid40217897, 4-Bromo-N-(trans-2-(dimethylamino)cyclohexyl)benzamide, Benzamide, 4-bromo-N-(2-(dimethylamino)cyclohexyl)-, trans-, 4-bromo-N-(2-(dimethylamino)cyclohexyl)benzamide, Bromadolium or Dtxcid901774251) is a opioid substance of the benzylamine class.

Chemistry

Salts []

Bromadoline is typically found in the form of its maleate salt.

Stereochemistry []

Bromadoline is a achiral mixture of the optical stereoisomers.

Subjective effects []

class / Opioid

Physical effects
Constipation Cough suppression Difficulty urinating Itchiness Nausea Pain relief Pupil constriction Respiratory depression Sedation Stomach cramp

Cognitive effects
Anxiety suppression Cognitive euphoria Compulsive redosing Increased music appreciation Thought deceleration

Visual effects
Double vision

External links []

References []

National Center for Biotechnology Information. PubChem Compound Summary for CID 54753, Bromadoline. Accessed April 19, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/54753
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Bromadoline. UNII: R8DWN01P1M. Global Substance Registration System. Accessed April 19, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/R8DWN01P1M

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