Cathinone

Salts []
Cathinone hydrochloride

Molecular structure via molpic

Conformer structure via 3Dmol.js
Molecular formula	C₉H₁₁NO
Molecular mass	149.19 g/mol
Appearance	Pale yellow leaf from petroleum ether
Predicted LogP	1.1
Melting point	46.5 °C
Boiling point	93 °C
Decomposition	Hazardous decomposition products formed under fire conditions. - Carbon oxides, nitrogen oxides (NOx), Hydrogen chloride gas. /S(-)-Cathinone hydrochloride/
Solubility	Very soluble in ether, ethanol
Chirality	racemic

Identifiers []
IUPAC name	2-amino-1-phenylpropan-1-one
SMILES	CC(C(=O)C1=CC=CC=C1)N
InChI	InChI=1S/C9H11NO/c1-7(10)9(11)8-5-3-2-4-6-8/h2-7H,10H2,1H3
InChIKey	PUAQLLVFLMYYJJ-UHFFFAOYSA-N

Dosing
Elimination half-life	0.7–2.3 h

Cathinone

Cathinone (also known as (+-)-cathinone, 2-Aminopropiophenone, 2-Amino-1-phenyl-1-propanone, (+/-)-Cathinone, dl-Cathinone, 1-Propanone, 2-amino-1-phenyl-, 2-Amino-2-methylacetophenone, Abyssiniantea, Bathtabspeed or Looderstar) is a stimulant substance of the cathinone class.

Chemistry

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

Stereochemistry

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

Stereoisomers []
(+)-Cathinone	(-)-Cathinone

Legal status

Australia: Cathinone is a S9 substance.
Brazil: Cathinone is a F2 substance.
Canada: Cathinone is a Schedule III substance.
Germany: Cathinone is a Anlage I substance.
United Kingdom: Cathinone is a Class c substance.
United States: Cathinone is a Schedule I substance.
United Nations: Cathinone is a Schedule I drug under the "Convention on Psychotropic Substances 1971".

Anodyne

Cathinone

Chemistry

Stereochemistry

Legal status

See also

External links