5-Hydroxyindole
99.0%
- Product Code: 120327
Alias:
5-Hydroxyindole
CAS:
1953-54-4
Molecular Weight: | 133.15 g./mol | Molecular Formula: | C₈H₇NO |
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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 |
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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 |
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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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