5-Hydroxyindole

99.0%

  • Product Code: 120327
  Alias:    5-Hydroxyindole
  CAS:    1953-54-4
Molecular Weight: 133.15 g./mol Molecular Formula: C₈H₇NO
EC Number: 217-782-6 MDL Number: MFCD00005677
Melting Point: 106-108 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: 5-Hydroxyindole is primarily utilized in biochemical research as a precursor or intermediate in the synthesis of more complex compounds, particularly those related to neurotransmitters. It plays a significant role in studies involving serotonin pathways, as it is structurally similar to serotonin, a key neurotransmitter in the human body. Researchers use it to investigate the effects of serotonin on mood, appetite, and sleep, as well as its role in neurological disorders. Additionally, 5-Hydroxyindole is employed in the development of pharmaceuticals targeting conditions like depression, anxiety, and migraines. Its applications also extend to organic synthesis, where it serves as a building block for creating indole derivatives with potential biological activity.
Product Specification:
Test Specification
Melting Point 107-110
Purity (%) 98.5-100
Appearance Light Beige To Dark Brown Powder Or Solid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿1,920.00
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5.000 10-20 days ฿7,320.00
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5-Hydroxyindole
5-Hydroxyindole is primarily utilized in biochemical research as a precursor or intermediate in the synthesis of more complex compounds, particularly those related to neurotransmitters. It plays a significant role in studies involving serotonin pathways, as it is structurally similar to serotonin, a key neurotransmitter in the human body. Researchers use it to investigate the effects of serotonin on mood, appetite, and sleep, as well as its role in neurological disorders. Additionally, 5-Hydroxyindole is employed in the development of pharmaceuticals targeting conditions like depression, anxiety, and migraines. Its applications also extend to organic synthesis, where it serves as a building block for creating indole derivatives with potential biological activity.
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