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Atomfair 5,6-Dihydroxyindoline C8H9NO2

Description 5,6-Dihydroxyindoline (CAS No. 29539-03-5) is a high-purity biochemical intermediate with the molecular formula C8H9NO2and IUPAC name 2,3-dihydro-1H-indole-5,6-diol . This compound is a critical precursor in the synthesis of melanin-related polymers and neuromelanin, making it invaluable for biochemical and pharmacological research. Its dihydroxy-substituted indoline structure enables versatile reactivity in oxidative coupling and polymerization studies. Provided as an off-white to light brown crystalline powder, our product is rigorously tested for purity (??98% by HPLC) and stability, ensuring reproducibility in sensitive applications. Suitable for use as a reference standard or synthetic building block, it is packaged under inert gas to prevent oxidation.…

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Description

Description

5,6-Dihydroxyindoline (CAS No. 29539-03-5) is a high-purity biochemical intermediate with the molecular formula C8H9NO2 and IUPAC name 2,3-dihydro-1H-indole-5,6-diol. This compound is a critical precursor in the synthesis of melanin-related polymers and neuromelanin, making it invaluable for biochemical and pharmacological research. Its dihydroxy-substituted indoline structure enables versatile reactivity in oxidative coupling and polymerization studies. Provided as an off-white to light brown crystalline powder, our product is rigorously tested for purity (??98% by HPLC) and stability, ensuring reproducibility in sensitive applications. Suitable for use as a reference standard or synthetic building block, it is packaged under inert gas to prevent oxidation. Store at 2-8??C in a tightly sealed container.

  • CAS No: 29539-03-5
  • Molecular Formula: C8H9NO2
  • Molecular Weight: 151.16
  • Exact Mass: 151.063328530
  • Monoisotopic Mass: 151.063328530
  • IUPAC Name: 2,3-dihydro-1H-indole-5,6-diol
  • SMILES: C1CNC2=CC(=C(C=C21)O)O
  • Synonyms: 29539-03-5, Indoline-5,6-diol, 5,6-Indolinediol, 5,6-Dihydroxyindoline, Leukoaminochrome

Application

5,6-Dihydroxyindoline serves as a key monomer in the synthesis of eumelanin-inspired polymers for conductive biomaterials and UV-absorbing coatings. Researchers utilize it to model neuromelanin formation in Parkinson’s disease studies due to its structural similarity to dopamine oxidation products. The compound also finds application in developing hair dye intermediates and as a radical scavenger in antioxidant assays.

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