Propylamphetamine

Propylamphetamine
	File:Propylamphetamine.png
Pharmacokinetic data
Metabolism	hepatic
Excretion	renal
Identifiers
	IUPAC name N-propyl-1-phenyl-propan-2-amine;
CAS Number	51799-32-7;
PubChem CID	103544;
E number	{{#property:P628}}
ECHA InfoCard	{{#property:P2566}}Lua error in Module:EditAtWikidata at line 36: attempt to index field 'wikibase' (a nil value).
Chemical and physical data
Formula	C12H19N
Molar mass	177.286 g/mol

N-propylamphetamine is a stimulant drug derived from amphetamine which was invented in the 1970s.

Propylamphetamine was used mainly for research into the metabolism of amphetamines,^[1] and as a reference compound to compare to other amphetamines,^[2] but animal research has shown it to be an active stimulant slightly less potent than amphetamine.^[3]

References

↑ Nazarali AJ, Baker GB, Coutts RT, Pasutto FM. Amphetamine in rat brain after intraperitoneal injection of N-alkylated analogues. Progress in Neuropsychopharmacology and Biological Psychiatry. 1983;7(4-6):813-6.
↑ Valtier S, Cody JT. Evaluation of internal standards for the analysis of amphetamine and methamphetamine. Journal of Analytical Toxicology. 1995 Oct;19(6):375-80.
↑ Woolverton WL, Shybut G, Johanson CE. Structure-activity relationships among some d-N-alkylated amphetamines. Pharmacology Biochemistry and Behavior. 1980 Dec;13(6):869-76.

Template:Stimulants Template:Amphetamines

[1] Nazarali AJ, Baker GB, Coutts RT, Pasutto FM. Amphetamine in rat brain after intraperitoneal injection of N-alkylated analogues. Progress in Neuropsychopharmacology and Biological Psychiatry. 1983;7(4-6):813-6.

[2] Valtier S, Cody JT. Evaluation of internal standards for the analysis of amphetamine and methamphetamine. Journal of Analytical Toxicology. 1995 Oct;19(6):375-80.

[3] Woolverton WL, Shybut G, Johanson CE. Structure-activity relationships among some d-N-alkylated amphetamines. Pharmacology Biochemistry and Behavior. 1980 Dec;13(6):869-76.

[1]

[2]

[3]

Propylamphetamine

References

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