N-Cbz-D-alanine
96%
- Product Code: 105652
Alias:
N-CBZ-D-alanine ; N-benzyloxycarbonyl-D-alanine
CAS:
26607-51-2
| Molecular Weight: | 223.23 g./mol | Molecular Formula: | C₁₁H₁₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00063126 | |
| Melting Point: | 83-84°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
N-Cbz-D-alanine is widely used in peptide synthesis as a protecting group for the amine functionality of D-alanine. The carbobenzyloxy (Cbz) group shields the amine during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids in the final peptide. This compound is particularly valuable in the production of complex peptides and pharmaceuticals, where precise control over the assembly of amino acids is critical. Additionally, it is employed in the development of chiral molecules and intermediates for organic synthesis, contributing to the creation of enantiomerically pure compounds used in drug development and research. Its stability and ease of removal under mild conditions make it a preferred choice in synthetic organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Specific Rotation [A]20/D (C=1, ACOH) | 9-15 |
| Appearance | White To Light Yellow Powder |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $12.04 |
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| 5.000 | 10-20 days | $17.03 |
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| 25.000 | 10-20 days | $34.88 |
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| 100.000 | 10-20 days | $100.50 |
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| 500.000 | 10-20 days | $471.77 |
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N-Cbz-D-alanine
N-Cbz-D-alanine is widely used in peptide synthesis as a protecting group for the amine functionality of D-alanine. The carbobenzyloxy (Cbz) group shields the amine during the synthesis process, preventing unwanted reactions and ensuring the correct sequence of amino acids in the final peptide. This compound is particularly valuable in the production of complex peptides and pharmaceuticals, where precise control over the assembly of amino acids is critical. Additionally, it is employed in the development of chiral molecules and intermediates for organic synthesis, contributing to the creation of enantiomerically pure compounds used in drug development and research. Its stability and ease of removal under mild conditions make it a preferred choice in synthetic organic chemistry.
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