4-Hydroxyindole丨CAS 2380-94-1

4-Hydroxyindole丨CAS 2380-94-1
Product Introduction:
Catalog No.: SS129430
CAS No.: 2380-94-1
Assay(HPLC): 98.5% min
Product Name: 4-Hydroxyindole
Molecular Formula: C8H7NO
Molecular Weight: 133.15
Synonym(s): 4-Indolol
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Technical Parameters
Description

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Specifications of 4-Hydroxyindole丨CAS 2380-94-1

 

Appearance

Light grey, greenish-grey or greenish-brown powder

Assay (HPLC)

98.5% min

Melting point

95–100 °C

Loss on drying

0.5% max

Sum of impurities (GC)

1.0% max

 

 

 

Applications

1. Pharmaceutical and Medicinal Chemistry

Intermediate in drug synthesis:
Serves as a building block in the synthesis of bioactive compounds, especially those with serotonin-related activity.

Lead structure for CNS drugs:
The indole ring is a privileged scaffold in neuropharmacology; 4-hydroxyindole is used to explore analogs for antidepressant, anxiolytic, or antipsychotic agents.

2. Neurochemical Research

Metabolite mimic:
Structurally similar to serotonin and melatonin analogs, making it valuable in the study of neurotransmitter pathways.

Useful for developing radiolabeled tracers or fluorescent probes for indole-containing biomolecules.

3. Chemical and Biochemical Research

Synthetic precursor:
Used in organic synthesis for the preparation of indole-based ligands, catalysts, and functional materials.

4-Hydroxyindole丨CAS 2380-94-1 plays a role in the development of bioinspired materials or heterocyclic libraries for screening.

4. Pigment and Dye Chemistry

Can be used as a starting material for the development of functional dyes and colorants, particularly those mimicking natural indole-derived pigments.


 

Benefits

✅ 1. Versatile Synthetic Intermediate

The hydroxyl group at the 4-position provides a handle for functionalization through etherification, acylation, or oxidation, enabling the construction of a wide range of derivatives.

✅ 2. Biocompatible Scaffold

As a derivative of indole, which is naturally found in tryptophan, serotonin, and melatonin, 4-hydroxyindole offers biocompatibility and pharmacological relevance.

✅ 3. Electron-Rich Aromatic System

The molecule's electron-donating hydroxyl group enhances reactivity, making it useful in electrophilic aromatic substitution reactions and coupling chemistry.

✅ 4. Research Tool for Neuroscience and Biochemistry

Enables the study of indole metabolism, receptor binding, and enzyme activity in brain and endocrine systems.


 

Summary

4-Hydroxyindole丨CAS 2380-94-1 is a valuable compound in chemical synthesis, pharmaceutical R&D, and neurochemical research, owing to its structural similarity to bioactive indoles and its functional versatility. Its applications range from drug discovery and metabolite studies to the design of pigments and dyes, making it an important tool in both academic and industrial laboratories.

 

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