(2R,3R)-2-Amino-3-hydroxybutyric acid
97%
- Product Code: 67146
Alias:
D-Allotreonine
CAS:
24830-94-2
| Molecular Weight: | 119.12 g./mol | Molecular Formula: | CH₃CHOHCHNH₂CO₂H |
|---|---|---|---|
| EC Number: | 246-488-0 | MDL Number: | MFCD00004526 |
| Melting Point: | 276 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of biochemistry and pharmaceutical research. It serves as a chiral building block in the synthesis of various biologically active molecules, particularly in the development of antibiotics and other therapeutic agents. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial for drug efficacy and safety. Additionally, it is used in studies related to amino acid metabolism and enzyme mechanisms, providing insights into biochemical pathways. Its role in peptide synthesis also highlights its importance in producing specific peptide sequences for research and therapeutic purposes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Solid |
| PURITY | 96.5 |
| SOLUBILITY IN HOT WATER | ALMOST TRANSPARENCY |
| SPECIFIC ROTATION A20DC5WATER | -11 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿380.00 |
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| 1.000 | 10-20 days | ฿500.00 |
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| 5.000 | 10-20 days | ฿2,460.00 |
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(2R,3R)-2-Amino-3-hydroxybutyric acid
This compound is primarily utilized in the field of biochemistry and pharmaceutical research. It serves as a chiral building block in the synthesis of various biologically active molecules, particularly in the development of antibiotics and other therapeutic agents. Its stereochemistry makes it valuable for creating enantiomerically pure compounds, which are crucial for drug efficacy and safety. Additionally, it is used in studies related to amino acid metabolism and enzyme mechanisms, providing insights into biochemical pathways. Its role in peptide synthesis also highlights its importance in producing specific peptide sequences for research and therapeutic purposes.
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