4-Aminobutyric Acid Hydroiodide
≥98%
- Product Code: 93788
CAS:
2096495-60-0
| Molecular Weight: | 231.03 g./mol | Molecular Formula: | C₄H₉NO₂HI |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
Used primarily in biochemical research, this compound serves as a precursor in the synthesis of gamma-aminobutyric acid (GABA), a crucial neurotransmitter in the central nervous system. It plays a significant role in studies focused on understanding GABAergic signaling and its impact on neurological disorders such as epilepsy, anxiety, and insomnia. Additionally, it is utilized in the development of pharmaceuticals aimed at modulating GABA receptors to treat these conditions. In organic chemistry, it acts as a building block for creating more complex molecules, particularly in the synthesis of heterocyclic compounds. Its iodide component also makes it valuable in certain iodination reactions, where it serves as a source of iodine.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Dark-Brown Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,180.00 |
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| 1.000 | 10-20 days | ฿6,680.00 |
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| 5.000 | 10-20 days | ฿24,600.00 |
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4-Aminobutyric Acid Hydroiodide
Used primarily in biochemical research, this compound serves as a precursor in the synthesis of gamma-aminobutyric acid (GABA), a crucial neurotransmitter in the central nervous system. It plays a significant role in studies focused on understanding GABAergic signaling and its impact on neurological disorders such as epilepsy, anxiety, and insomnia. Additionally, it is utilized in the development of pharmaceuticals aimed at modulating GABA receptors to treat these conditions. In organic chemistry, it acts as a building block for creating more complex molecules, particularly in the synthesis of heterocyclic compounds. Its iodide component also makes it valuable in certain iodination reactions, where it serves as a source of iodine.
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