Prolintane

Source: Wikipedia, the free encyclopedia.
Prolintane
Clinical data
Routes of
administration
oral, intranasal, rectal
ATC code
Legal status
Legal status
Identifiers
  • 1-(1-phenylpentan-2-yl)pyrrolidine
JSmol)
Melting point133 °C (271 °F)
Boiling point153 °C (307 °F)
  • CCCC(N1CCCC1)CC2=CC=CC=C2
  • InChI=1S/C15H23N/c1-2-8-15(16-11-6-7-12-16)13-14-9-4-3-5-10-14/h3-5,9-10,15H,2,6-8,11-13H2,1H3 checkY
  • Key:OJCPSBCUMRIPFL-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Prolintane (Catovit, Katovit, Promotil, Villescon) is a

MDPV, and propylhexedrine and it has a similar mechanism of action.[4] Many cases of prolintane abuse have been reported.[5]

Under the trade-name "Katovit", prolintane was commercialized by the Spanish pharmaceutical company, FHER. Katovit was sold until 2001, and was most often used by students and workers as a stimulant to provide energy, promote alertness and concentration.[medical citation needed]

See also

References

  1. ^ Anvisa (2023-03-31). "RDC Nº 784 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial" [Collegiate Board Resolution No. 784 - Lists of Narcotic, Psychotropic, Precursor, and Other Substances under Special Control] (in Brazilian Portuguese). Diário Oficial da União (published 2023-04-04). Archived from the original on 2023-08-03. Retrieved 2023-08-16.
  2. PMID 4392006
    .
  3. ^ GB Patent 807835
  4. PMID 7437258
    .
  5. .