L-2-Amino-3-guanidinopropionic acid hydrochloride
98%
- Product Code: 105219
Alias:
L-3-guanidinoalanine hydrochloride
CAS:
1482-99-1
| Molecular Weight: | 182.61 g./mol | Molecular Formula: | C₄H₁₀N₄O₂HCl |
|---|---|---|---|
| EC Number: | 216-044-0 | MDL Number: | MFCD00036989 |
| Melting Point: | ~220 °C (dec.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
L-2-Amino-3-guanidinopropionic acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of more complex organic compounds, particularly those with potential therapeutic applications. The compound is often utilized in studies related to amino acid metabolism and protein synthesis due to its structural similarity to naturally occurring amino acids. Additionally, it finds application in the development of peptide-based drugs, where it can be incorporated into peptide chains to modify their biological activity or stability. Its guanidinium group also makes it useful in research involving enzyme inhibition and receptor binding studies, as it can interact with various biological targets.
Product Specification:
| Test | Specification |
|---|---|
| Purity (Tlc) | 98-100 |
| Specific Rotation | 16-18 |
| A20D50MGMLWATER | |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
| Solubility In Water | Colorless And Transparent Solution |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,680.00 |
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| 0.500 | 10-20 days | ฿9,390.00 |
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| 1.000 | 10-20 days | ฿16,020.00 |
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L-2-Amino-3-guanidinopropionic acid hydrochloride
L-2-Amino-3-guanidinopropionic acid hydrochloride is primarily used in biochemical research and pharmaceutical development. It serves as a precursor or intermediate in the synthesis of more complex organic compounds, particularly those with potential therapeutic applications. The compound is often utilized in studies related to amino acid metabolism and protein synthesis due to its structural similarity to naturally occurring amino acids. Additionally, it finds application in the development of peptide-based drugs, where it can be incorporated into peptide chains to modify their biological activity or stability. Its guanidinium group also makes it useful in research involving enzyme inhibition and receptor binding studies, as it can interact with various biological targets.
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