5-Aminoindole

5-Aminoindole structural formula

CAS Number5192-03-0
Molecular FormulaC8H8N2
Molecular Weight132.167
InChI KeyZCBIFHNDZBSCEP-UHFFFAOYSA-N
LogP0.7
Synonyms
  • 5-Aminoindole
  • 1H-Indol-5-amine
  • 5192-03-0
  • EINECS 225-977-2
  • Indole, 5-amino-
  • NSC 61452
  • UNII-Q732PG0Y16
  • indol-5-ylamine
  • 1H-indol-5-amine

Applications:

HPLC Method for Analysis of 5-Aminoindol on Primesep 100 Column

July 30, 2024

High Performance Liquid Chromatography (HPLC) Method for Analysis of 5-Aminoindole on Primesep 100 by SIELC Technologies

Separation type: Liquid Chromatography Mixed-mode SIELC Technologies

HPLC Method for Analysis of 5-Aminoindol on Primesep 100 Column


 High Performance Liquid Chromatography (HPLC) Method for Analysis of 5-Aminoindole

5-Aminoindole is an organic compound with the chemical formula C8H8N2. It is a derivative of indole and features an amino group at the 5-position.

Applications:
Pharmaceuticals: It can serve as a building block in the synthesis of various pharmaceutical compounds.
Research: Used in studies related to indole derivatives, which are important in medicinal chemistry.
5-Aminoindole be retained and analyzed using a Primesep 100 mixed-mode stationary phase column. The analysis employs an isocratic method with a simple mobile phase comprising water, acetonitrile (MeCN), and sulfuric acid as a buffer. This method allows for detection using UV 200 nm

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseMeCN – 55%
BufferH2SO4 -0.05%
Flow Rate1.0 ml/min
DetectionUV 200 nm
Samples1.0 mg/ml MeCN/H2O – 50/50%
Injection volume1 µl
LOD*30 ppb (200 nm)
* LOD was determined for this combination of instrument, method, and analyte, and it can vary from one laboratory to another even when the same general type of analysis is being performed.

Class of Compounds
Pyridines
Analyzing Compounds5-Aminoindole

Application Column

Primesep 100

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
5-Aminoindole

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.

Separation of Model Compounds in Reversed-Phase and Mixed-Mode

April 25, 2019

Separation type: Liquid Chromatography Mixed-mode








 
Many compounds are difficult, if not impossible, to separate on reverse-phase columns in HPLC. Other compounds cannot be separated on ion-exchange columns. That’s where the mixed-mode columns come in. By using a stationary phase with both hydrophobic and ion-exchange properties, allows the chromatographer to have additional controls over separation conditions. Here, we demonstrate the separation of compounds that can’t be achieved on a C18 column. By using both an organic gradient and buffer gradient of ammonium formate (AmFm), we can separate structurally similar compounds that can’t be separated on a reverse-phase column alone.




 

Condition

Column Primesep 100, 3,2×50 mm, 2,7 µm, 100A
Mobile Phase Gradient  MeCN – 10-60%, 5 min
Buffer Gradient AmFm pH 3.5- 30 – 70 mM, 5 min
Flow Rate 1.2 ml/min
Detection UV, 270 nm

 

Description

Class of Compounds
Drug,  Basic, Hydrophilic, Hydrophobic, Ionizable.
Analyzing Compounds Adenosine, 3,4-Difluroaniline, 4-Amino-2-chloropyridine, 5-Aminoindole, 4-Amino-3-chloropyridine, 2-Amino 5-methylthiadiazole, 4-Ethylaniline

 

Application Column

Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
2-Amino-5-Methylthiadiazole
2-Amino-5-methyl-thiazole
3,4-Difluoroaniline
4-Amino-2-Chloropyridine
4-Amino-3-Chloropyridine
4-Ethylaniline
5-Aminoindole
Adenosine
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.