(S)-4-Amino-2-(tert-butoxycarbonylamino)butyric acid
98.0%
- Product Code: 96150
Alias:
(S)-Nα-Boc-2,4-diaminobutyric acid
(S)-4-amino-2-(Boc-amino)butanoic acid
CAS:
25691-37-6
| Molecular Weight: | 218.25 g./mol | Molecular Formula: | C₉H₁₈N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00236841 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the synthesis of peptides and peptidomimetics, where it serves as a building block for creating specific amino acid sequences. It is particularly valuable in the development of biologically active peptides due to its ability to introduce a protected amino group, which can be selectively deprotected during synthesis. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, making it a preferred choice in solid-phase peptide synthesis (SPPS). Additionally, it is employed in the preparation of modified peptides for research in drug discovery, enabling the study of structure-activity relationships and the design of therapeutic agents. Its application extends to the production of custom peptides for biochemical assays and the development of peptide-based pharmaceuticals.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Powder or Solid or Chunks |
| PURITY | 97.5-100 |
| PROTON NMR SPECTRUM | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
| Specific rotation a20DC2 AcOH | -9 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿720.00 |
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| 5.000 | 10-20 days | ฿2,680.00 |
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| 25.000 | 10-20 days | ฿10,010.00 |
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(S)-4-Amino-2-(tert-butoxycarbonylamino)butyric acid
This chemical is primarily utilized in the synthesis of peptides and peptidomimetics, where it serves as a building block for creating specific amino acid sequences. It is particularly valuable in the development of biologically active peptides due to its ability to introduce a protected amino group, which can be selectively deprotected during synthesis. The tert-butoxycarbonyl (Boc) group provides stability under various reaction conditions, making it a preferred choice in solid-phase peptide synthesis (SPPS). Additionally, it is employed in the preparation of modified peptides for research in drug discovery, enabling the study of structure-activity relationships and the design of therapeutic agents. Its application extends to the production of custom peptides for biochemical assays and the development of peptide-based pharmaceuticals.
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