(S)-2,2'-((5-(((Benzyloxy)carbonyl)amino)-1-carboxypentyl)azanediyl)diacetic acid
97%
- Product Code: 57125
CAS:
113231-04-2
| Molecular Weight: | 396.39 g./mol | Molecular Formula: | C₁₈H₂₄N₂O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27977806 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in peptide synthesis and biochemical research. It serves as a key intermediate in the production of complex peptides and proteins, enabling the introduction of specific functional groups or modifications. Its structure is particularly useful in creating peptide bonds and facilitating the assembly of amino acid sequences. Additionally, it is employed in the development of peptide-based drugs and therapeutic agents, where precise molecular design is critical. Its role in protecting amino groups during synthesis ensures the integrity and specificity of the final peptide product. This compound is also valuable in studies involving enzyme kinetics and protein interactions, contributing to advancements in biochemistry and medicinal chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White to yellow solid |
| Purity | 96.5-100 |
| Infrared Spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 G | 10-20 days | ฿22,090.00 |
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| 0.250 G | 10-20 days | ฿33,110.00 |
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(S)-2,2'-((5-(((Benzyloxy)carbonyl)amino)-1-carboxypentyl)azanediyl)diacetic acid
This chemical is primarily utilized in peptide synthesis and biochemical research. It serves as a key intermediate in the production of complex peptides and proteins, enabling the introduction of specific functional groups or modifications. Its structure is particularly useful in creating peptide bonds and facilitating the assembly of amino acid sequences. Additionally, it is employed in the development of peptide-based drugs and therapeutic agents, where precise molecular design is critical. Its role in protecting amino groups during synthesis ensures the integrity and specificity of the final peptide product. This compound is also valuable in studies involving enzyme kinetics and protein interactions, contributing to advancements in biochemistry and medicinal chemistry.
| Mechanism | - |
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| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
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