Pindolol

CAS Number 13523-86-9
Molecular Formula C14H20N2O2
Molecular Weight 248.327 g/mol
InChI Key JZQKKSLKJUAGIC-UHFFFAOYSA-N
LogP 1.75
Synonyms
  • Pindolol
  • 1-[(1H-Indol-4-yl)oxy]-3-[(propan-2-yl)amino]propan-2-ol
  • 2-Propanol, 1-(1H-indol-4-yloxy)-3-[(1-methylethyl)amino]-
  • 13523-86-9
  • 5-21-03-00017
  • 2-Propanol, 1-(1H-indol-4-yloxy)-3-[(1-methylethyl)amino]-
  • (.+-.)-4-[2-Hydroxy-3-(isopropylamino)propoxy]indole
  • (.+-.)-LB 46
  • (.+-.)-Pindolol
  • (RS)-Pindolol
  • 1-[(1-Methylethyl)amino]-3-(4-indolyloxy)-2-propanol
  • 2-Propanol, 1-(indol-4-yloxy)-3-(isopropylamino)-
  • 4-(2-Hydroxy-3-isopropylaminopropoxy)indole
  • 4-(3-Isopropylamino-2-hydroxypropoxy)indole
  • Apo-pindol
  • Betapindol
  • Blocklin L
  • Calvisken
  • Carvisken
  • Decreten
  • DL-4-[2-Hydroxy-3-(isopropylamino)propoxy]indole
  • DL-Pindolol
  • Durapindol
  • Glauco-Visken
  • N-[2-Hydroxy-3-(1H-indol-4-yloxy)propyl]-N-isopropylamine
  • Pectobloc
  • Pinbetol
  • Prinodolol
  • Pynastin
  • BRN 1536506
  • EINECS 236-867-9
  • EINECS 244-623-8
  • Glauco-Viskin
  • 4-(2-Hydroxy-3-isopropylaminopropoxy)-indole
  • 1-(Indol-4-yloxy)-3-(isopropylamino)-2-propanol
  • 1-(1H-Indol-4-yloxy)-3-((1-methylethyl)amino)-2-propanol
  • 4-(3-(Isopropylamino)-2-hydroxypropoxy)indole
  • 1-((1-Methylethyl)amino)-3-(4-indolyloxy)-2-propanol
  • (+-)-Pindolol
  • 2-Propanol, 1-(4-indolyloxy)-3-(isopropylamino)-
  • Pindololum
  • UNII-BJ4HF6IU1D
  • 1-(1H-indol-4-yloxy)-3-(isopropylamino)propan-2-ol
  • 1-(1H-indol-4-yloxy)-3-(propan-2-ylamino)-propan-2-ol
  • 1-(1H-indol-4-yloxy)-3-[(1-methylethyl)amino]propan-2-ol
  • 4-(2-hydroxy-3-isopropylaminopropoxy)-indole

Applications:


HPLC Separation of Pyrilamine, Trimipramine, Pindolol Using Hydrogen Bonding Mode
  Application Notes: Many drugs contain small hydrophobic and hydrophilic compounds. There are several ways to retain and analyze these compounds including, reversed-phase chromatography, cation-exchange chromatography, and HILIC. Our method includes separation based on hydrogen-bonding interactions between the analytes and the stationary phase. Hydrogen bonding offers unique selectivity of separation with good peak shape and retention control. Our method is fully compatible with ELSD, LC/MS and preparative chromatography. This approach can also be applied to the analysis of other drug molecules. Application Columns: SHARC 1, 3.2x100 mm, 5 um, 100A. To learn more about SHARC 1 columns click here. To order this column click here. To see more chromatographic separations check our web site. Application Compounds: Pyrilamine, trimipramine, and pindolol Detection Technique: UV, LC/MS

Application Analytes:

Pindolol
Pyrilamine