3-Hydroxyanthranilic acid

CAS Number548-93-6
Molecular Formula C7H7NO3
Molecular Weight153.14
InChI KeyWJXSWCUQABXPFS-UHFFFAOYSA-N
LogP2.9
Synonyms
  • 2-Amino-3-hydroxybenzoic acid
  • 3-Hydroxyanthranilic acid
  • 548-93-6
  • 3-Oxyanthranilic acid
  • 3-hydroxyanthranilate
  • 2-AMINO-3-HYDROXY-BENZOIC ACID
  • Anthranilic acid, 3-hydroxy-
  • Benzoic acid, 2-amino-3-hydroxy-
  • 3-Ohaa
  • 3-Hydroxy-anthranilsaeure
  • 3-Hydroxy-anthranilsaeure [German]
  • 3-Hydroxy anthranilic acid
  • MFCD00007700
  • 1UQB1BT4OT
  • CHEBI:15793
  • NSC-522891
  • 3-oh-anthranilic acid
  • CCRIS 4427
  • 3-hydroxy-anthranilate
  • HSDB 4040
  • EINECS 208-962-5
  • UNII-1UQB1BT4OT
  • NSC 522891
  • BRN 0973356
  • AI3-52837
  • 3-Oxyanthranilate
  • 3-hydroxanthranilate
  • 1u1w
  • 3-hydroxyantranilic acid
  • WLN: ZR BQ FVQ
  • 3-Hydroxy-2-aminobenzoate
  • 3-hydroxy-Anthranilic acid
  • bmse000321
  • 2-amino-3-hydroxy-Benzoate

Applications:

UV-Vis Spectrum of 3-Hydroxyanthranilic Acid

July 12, 2024

Access the UV-Vis Spectrum SIELC Library

UV-Vis Spectrum of 3-Hydroxyanthranilic Acid. Absorption Maxima: 212 nm, 310 nm, 342 nm.

If you are looking for optimized HPLC method to analyze 3-Hydroxyanthranilic acid 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.

Application Analytes:
3-Hydroxyanthranilic acid
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 Separation of a Mixture of Tryptophan and its Catabolites on Primesep 100 Column

October 3, 2023

High Performance Liquid Chromatography (HPLC) Method for Analysis of Mixture of Tryptophan and its Catabolites on Primesep 100 by SIELC Technologies

Separation type: Liquid Chromatography Mixed-mode

HPLC Method for Analysis of Mixture of Tryptophan and its Catabolites on Primesep 100 Column by SIELC Technologies

Tryptophan and its catabolites participate in several biological pathways, having roles in protein synthesis, serving as precursors to bioactive molecules, and influencing several physiological processes. Here’s an overview considering a mixture of tryptophan and its catabolites:

Tryptophan:

  • Essential Amino Acid: Tryptophan is a precursor to several important compounds, including serotonin and melatonin.
  • In Protein Synthesis: Incorporated into proteins during protein synthesis.

Catabolites:

1. Serotonin:

  • Neurotransmitter: Regulates mood, appetite, and sleep, among other functions.
  • Derivative: Melatonin, which regulates the sleep-wake cycle.

2. Kynurenine Pathway (Major catabolic pathway of tryptophan):

  • Kynurenine: An intermediate and precursor to several bioactive compounds.
  • Kynurenic Acid: An NMDA receptor antagonist, believed to have neuroprotective effects.
  • Xanthurenic Acid: Its physiological roles are still being explored, but it’s often studied for its relation to diabetes and neurological conditions.
  • 3-Hydroxykynurenine: Can generate reactive oxygen species, potentially contributing to cellular stress.
  • Quinolinic Acid: A neuroactive metabolite that can act as an NMDA receptor agonist.

3. Indoleamine 2,3-dioxygenase (IDO) Pathway:

  • Tryptophan can be degraded into several catabolites via the IDO pathway, influencing immune response and cell proliferation.

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Tryptophan and its Catabolites can be retained, separated and analyzed on a Primesep 100 mixed-mode stationary phase column using an gradient analytical method with a simple mobile phase of water, Acetonitrile (MeCN), and a sulfuric acid as a buffer. This analysis method can be detected using UV at 220 nm.

High Performance Liquid Chromatography (HPLC) Method for Analyses of Mixture of Tryptophan and its Catabolites

Condition

ColumnPrimesep 100, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile PhaseGradient MeCN 5-50% in 10 min, with 2 min hold afterwards
BufferGradient H2SO4 from 0.1-0.2% in 10 min, with 2 min hold afterwards
Flow Rate1.0 ml/min
DetectionUV 220 nm

Description

Class of CompoundsEssential Amino Acid Tryptophan and its Catabolites
Analyzing CompoundsTryptophan, Picolinic Acid, Kynurenine, 3-Hydroxykynurenine, 3-Hydroxyanthranilic acid

Application Column

Primesep 100

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

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Application Analytes:
3-Hydroxyanthranilic acid
3-Hydroxykynurenine
Kynurenine
Picolinic Acid
Tryptophan

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.