Propylamphetamine

Chemical compound
  • none
Legal statusLegal status
  • UK: Not controlled
Pharmacokinetic dataMetabolismHepaticExcretionRenalIdentifiers
  • N-(1-methyl-2-phenylethyl)propan-1-amine
CAS Number
  • 51799-32-7 ☒N
PubChem CID
  • 103544
ChemSpider
  • 11655332 checkY
UNII
  • E52ZLB6J7C
CompTox Dashboard (EPA)
  • DTXSID30966120 Edit this at Wikidata
ECHA InfoCard100.215.934 Edit this at WikidataChemical and physical dataFormulaC12H19NMolar mass177.291 g·mol−13D model (JSmol)
  • Interactive image
  • NC(C)Cc1ccccc1CCC
InChI
  • InChI=1S/C12H19N/c1-3-6-11-7-4-5-8-12(11)9-10(2)13/h4-5,7-8,10H,3,6,9,13H2,1-2H3 checkY
  • Key:VMVXCJCVBKWYTF-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Propylamphetamine is a psychoactive drug and research chemical of the phenethylamine and amphetamine chemical classes which acts as a stimulant. It was first developed in the 1970s, mainly for research into the metabolism of,[1] and as a comparison tool to, other amphetamines.[2] A study in rats found propylamphetamine to be 1/4 as potent as amphetamine.[3]

See also

References

  1. ^ Nazarali AJ, Baker GB, Coutts RT, Pasutto FM (1983). "Amphetamine in rat brain after intraperitoneal injection of N-alkylated analogues". Progress in Neuro-Psychopharmacology & Biological Psychiatry. 7 (4–6): 813–6. doi:10.1016/0278-5846(83)90073-8. PMID 6686713. S2CID 35531794.
  2. ^ Valtier S, Cody JT (October 1995). "Evaluation of internal standards for the analysis of amphetamine and methamphetamine". Journal of Analytical Toxicology. 19 (6): 375–80. doi:10.1093/jat/19.6.375. PMID 8926730.
  3. ^ Woolverton WL, Shybut G, Johanson CE (December 1980). "Structure-activity relationships among some d-N-alkylated amphetamines". Pharmacology, Biochemistry, and Behavior. 13 (6): 869–76. CiteSeerX 10.1.1.687.9187. doi:10.1016/0091-3057(80)90221-x. PMID 7208552. S2CID 25123820.
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AdamantanesAdenosine antagonistsAlkylaminesAmpakinesArylcyclohexylaminesBenzazepinesCathinonesCholinergicsConvulsantsEugeroicsOxazolinesPhenethylamines
PhenylmorpholinesPiperazinesPiperidinesPyrrolidinesRacetamsTropanesTryptaminesOthers
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DRAsTooltip Dopamine releasing agents
NRAsTooltip Norepinephrine releasing agents
SRAsTooltip Serotonin releasing agents
Others
See also: Receptor/signaling modulators • Monoamine reuptake inhibitors • Adrenergics • Dopaminergics • Serotonergics • Monoamine metabolism modulators • Monoamine neurotoxins
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Phenethylamines


Stimulants: Phenylethanolamine

Amphetamines
Phentermines
Cathinones
Phenylisobutylamines
Phenylalkylpyrrolidines
Catecholamines
(and close relatives)
Miscellaneous
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