D-allo-Isoleucine
98%
- Product Code: 67145
Alias:
D-Alloisoleucine; (2R,3S)-2-amino-3-methylvaleric acid
CAS:
1509-35-9
| Molecular Weight: | 131.17 g./mol | Molecular Formula: | C₆H₁₃NO₂ |
|---|---|---|---|
| EC Number: | 216-143-9 | MDL Number: | MFCD00066445 |
| Melting Point: | 291 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
D-allo-Isoleucine is primarily used in the field of biochemistry and pharmaceutical research. It serves as a valuable chiral building block in the synthesis of peptides and proteins, aiding in the study of their structure and function. This compound is also utilized in the development of nutritional supplements, particularly those aimed at enhancing muscle recovery and growth, due to its role in protein synthesis. Additionally, D-allo-Isoleucine is employed in metabolic studies to understand the pathways and mechanisms of amino acid metabolism in various organisms. Its unique stereochemistry makes it a useful tool in enantioselective synthesis, contributing to the production of optically active compounds in medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 97.5-100 |
| HCL | -39.0--35.0 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $39.18 |
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| 5.000 | 10-20 days | $152.69 |
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| 25.000 | 10-20 days | $688.10 |
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D-allo-Isoleucine
D-allo-Isoleucine is primarily used in the field of biochemistry and pharmaceutical research. It serves as a valuable chiral building block in the synthesis of peptides and proteins, aiding in the study of their structure and function. This compound is also utilized in the development of nutritional supplements, particularly those aimed at enhancing muscle recovery and growth, due to its role in protein synthesis. Additionally, D-allo-Isoleucine is employed in metabolic studies to understand the pathways and mechanisms of amino acid metabolism in various organisms. Its unique stereochemistry makes it a useful tool in enantioselective synthesis, contributing to the production of optically active compounds in medicinal chemistry.
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