Boc-β-Glu(OBzl)-OH
98%
- Product Code: 104758
Alias:
N-tert-butoxycarbonyl-L-beta-glutamic acid 5-benzyl ester
CAS:
254101-10-5
| Molecular Weight: | 337.37 g./mol | Molecular Formula: | C₁₇H₂₃NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01862861 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in peptide synthesis as a protecting group for glutamic acid. It helps in preventing unwanted reactions at the glutamic acid site during the formation of peptide bonds. The Boc group protects the amino group, while the OBzl group protects the carboxyl group, allowing selective deprotection and coupling in multi-step peptide synthesis. This compound is particularly useful in the synthesis of complex peptides and proteins, where precise control over the addition of amino acids is required. It is also employed in the development of pharmaceuticals, especially in the production of peptide-based drugs, where maintaining the integrity of specific amino acids is crucial for the drug's activity and stability.
Product Specification:
| Test | Specification |
|---|---|
| Carbon By Elemental Analysis | 59-60.9 |
| Purity (HPLC) | 97.5-100 |
| Infrared Spectrometry | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
| Appearance | White To Light Yellow Powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿1,773.00 |
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| 1.000 | 10-20 days | ฿5,706.00 |
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| 5.000 | 10-20 days | ฿18,690.00 |
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Boc-β-Glu(OBzl)-OH
Used primarily in peptide synthesis as a protecting group for glutamic acid. It helps in preventing unwanted reactions at the glutamic acid site during the formation of peptide bonds. The Boc group protects the amino group, while the OBzl group protects the carboxyl group, allowing selective deprotection and coupling in multi-step peptide synthesis. This compound is particularly useful in the synthesis of complex peptides and proteins, where precise control over the addition of amino acids is required. It is also employed in the development of pharmaceuticals, especially in the production of peptide-based drugs, where maintaining the integrity of specific amino acids is crucial for the drug's activity and stability.
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