Pindolol

Pindolol structural formula

CAS Number13523-86-9
Molecular FormulaC14H20N2O2
Molecular Weight248.327
InChI KeyJZQKKSLKJUAGIC-UHFFFAOYSA-N
LogP1.75
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:

Uv-Vis Spectrum of Pindolol

February 17, 2026

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If you are looking for optimized HPLC method to analyze Pindolol check our HPLC Applications library

For optimal results in HPLC analysis, it is recommended to measure absorbance at a wavelength that matches the absorption maximum of the compound(s) being analyzed. The UV spectrum shown can assist in selecting an appropriate wavelength for your analysis. Please note that certain mobile phases and buffers may block wavelengths below 230 nm, rendering absorbance measurement at these wavelengths ineffective. If detection below 230 nm is required, it is recommended to use acetonitrile and water as low UV-transparent mobile phases, with phosphoric acid and its salts, sulfuric acid, and TFA as buffers.
For some compounds, the UV-Vis Spectrum is affected by the pH of the mobile phase. The spectra presented here are measured with an acidic mobile phase that has a pH of 3 or lower.

Application Analytes:
Pindolol
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Method for Analysis of Pindolol on Primesep 200

May 3, 2016

Chr_1060

Application Column

Primesep 200

Column Diameter: 3.2 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A
Column options: dual ended

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Application Analytes:
Pindolol
Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.

HPLC Separation of Pyrilamine, Trimipramine, Pindolol Using Hydrogen Bonding Mode

June 15, 2012

 

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, 3.2×100 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

Condition
Column Sharc 1, 3.2×100 mm, 5 µm, 100A
Mobile Phase MeCN/MeOH
Buffer AmFm, Formic acid
Flow Rate 0.5 ml/min
Detection UV, 270 nm

 

Description
Class of Compounds
 Drug, Acid, Hydrophilic, Ionizable, Vitamin, Supplements
Analyzing Compounds Pyrilamine, Trimipramine, Pindolol

 

Application Column

SHARC 1

The SHARC™ family of innovative columns represents the first commercially available columns primarily utilizing separation based on hydrogen bonding. SHARC stands for Specific Hydrogen-bond Adsorption Resolution Column. Hydrogen bonding involves an interaction or attraction between a bound hydrogen atom and molecules containing electronegative atoms, such as oxygen, nitrogen, and fluorine.

Select options
Application Analytes:
Pindolol
Pyrilamine
Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.