3-Aminopyrazole-4-carboxylic acid

3-Aminopyrazole-4-carboxylic acid structural formula

CAS Number41680-34-6
Molecular FormulaC4H5N3O2
Molecular Weight127.103
InChI KeyKMRVTZLKQPFHFS-UHFFFAOYSA-N
LogP-0.311
Synonyms
  • 3-Aminopyrazole-4-carboxylic acid
  • 5-Amino-1H-pyrazole-4-carboxylic acid
  • 1H-Pyrazole-4-carboxylic acid, 5-amino-
  • 41680-34-6
  • 3-Amino-4-carboxypyrazole
  • EINECS 255-493-7
  • NSC 89246
  • Pyrazole-4-carboxylic acid, 3-amino-

Applications:

HPLC Separation of Pyrazinecarboxamide and Related Compounds

June 25, 2020


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Pyrazinamide is a medication used in the treatment of infectious disease tuberculosis and is on the World Health Organization’s (WHO) list of essential medicines. It can be retained and separated from other pyrazine compounds, which are structurally similar and can be difficult to separate in reverse-phase HPLC, by using Primesep A mixed-mode column. Primesep A’s stationary phase is embedded with strong acidic ion-pairing groups. The analytical method is isocratic and uses the mobile phase of acetonitrile (ACN) and water with sulfuric acid (H2SO4) as buffer and UV detection at 275nm.

Condition

Column Primesep A, 4.6×100 mm, 5 µm, 100A
Mobile Phase MeCN/H2O – 5/95%
Buffer H2SO4
Flow Rate 1.0 ml/min
Detection UV 275 nm

Description

Class of Compounds Hydrophilic,  Heterocyclic, Aromatic
Analyzing Compounds Pyrazine,  Aminopyrazine, Pyrazinamide, 3-Aminopyrazole-4-carboxylic acid

 

Application Column

Primesep A

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.

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Application Analytes:
2-Aminopyrazine
3-Aminopyrazole-4-carboxylic acid
Pyrazinamide
Pyrazine
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 3-Aminopyrazole-4-carboxylic acid on Newcrom R1 HPLC column

May 16, 2018
Separation of 3-Aminopyrazole-4-carboxylic acid on Newcrom R1 HPLC column

3-Aminopyrazole-4-carboxylic acid can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

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Application Analytes:
3-Aminopyrazole-4-carboxylic acid
The result was obtained by a proprietary SIELC algorithm. It may deviate from the actual experimental data. The experimental data are available upon request. Contact us by e-mail: support@sielc.com or by phone: 847-229-2629.