Fenfluramine

Salts []
Fenfluramine hydrochloride

Molecular structure via molpic
Conformer structure via 3Dmol.js
Molecular formula	C12H16F3N[1]
Molecular mass	231.26 g/mol[1]
Predicted LogP	3.4[1]
Melting point	160-170[1]
Boiling point	108-112[1]
Decomposition	When heated to decomp it emits very toxic fumes of fluoride ion and oxides of nitrogen.[1]
Chirality	racemic[2]

Identifiers []
IUPAC name	N-ethyl-1-[3-(trifluoromethyl)phenyl]propan-2-amine[1]
SMILES	CCNC(C)CC1=CC(=CC=C1)C(F)(F)F[1]
InChI	InChI=1S/C12H16F3N/c1-3-16-9(2)7-10-5-4-6-11(8-10)12(13,14)15/h4-6,8-9,16H,3,7H2,1-2H3[1]
InChIKey	DBGIVFWFUFKIQN-UHFFFAOYSA-N[1]

Dosing
Elimination half-life	13–30 hours

Fenfluramine

(Redirected from (+)-Fenfluramine)

Fenfluramine (also known as Obedrex, Rotondin, Pesos, Ponderax PA, DL-Fenfluramine, Fenfluramina, Acino, Fenfluraminum, (+-)-Fenfluramine or Fenfluramin) is a substance of the amphetamine class.

Chemistry

Fenfluramine is typically found in the form of its hydrochloride salt.

Stereochemistry

(RS)-Fenfluramine is a racemic mixture of the optical stereoisomers:

Stereoisomers []
(+)-Fenfluramine (-)-Fenfluramine

Legal status

• Brazil: Fenfluramine is a F4 substance.
• United States: Fenfluramine is a prescription only substance.
• European Union: Fenfluramine is a prescription only substance.

See also

• Amphetamine
• Substituted amphetamines
• Anodyne

External links

• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (Wikipedia)
• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (Wikidata)
• Fenfluramine / (+)-Fenfluramine (DrugBank)
• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (PubChem)
• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (ChEMBL)
• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (ChEBI)
• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (Common Chemistry)
• Fenfluramine / (+)-Fenfluramine (HMDB)
• Fenfluramine / (+)-Fenfluramine (KEGG)
• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (UNII)
• Fenfluramine / (+)-Fenfluramine / (-)-Fenfluramine (EPA DSSTox)