Boc-Lys(Boc)-OH
97%
- Product Code: 60763
Alias:
(S)-2,6-di-tert-butoxycarbonylaminocaproic acid; (S)-2,6-di-tert-butoxycarbonylaminocaproic acid
CAS:
2483-46-7
| Molecular Weight: | 346.4 g./mol | Molecular Formula: | C₁₆H₃₀N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00038515 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is widely used in peptide synthesis as a protecting group for amino acids. It helps in preventing unwanted reactions at the amino group during the synthesis process, ensuring the correct sequence of amino acids in the final peptide. It is particularly useful in solid-phase peptide synthesis (SPPS) due to its stability under various reaction conditions. Additionally, it is employed in the preparation of complex peptides and proteins for pharmaceutical research, enabling the development of therapeutic agents and biochemical studies. Its compatibility with other protecting groups makes it a versatile tool in organic chemistry and biochemistry laboratories.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | COLORLESS TO WHITE CRYSTALS AND/OR CHUNKS |
| INFRARED SPECTRUM | Conforms to Structure |
| PURITY | 96.5 |
| SPECIFIC ROTATION A20DC1MEOH | -4 -2 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿330.00 |
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| 5.000 | 10-20 days | ฿440.00 |
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| 25.000 | 10-20 days | ฿2,510.00 |
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Boc-Lys(Boc)-OH
This chemical is widely used in peptide synthesis as a protecting group for amino acids. It helps in preventing unwanted reactions at the amino group during the synthesis process, ensuring the correct sequence of amino acids in the final peptide. It is particularly useful in solid-phase peptide synthesis (SPPS) due to its stability under various reaction conditions. Additionally, it is employed in the preparation of complex peptides and proteins for pharmaceutical research, enabling the development of therapeutic agents and biochemical studies. Its compatibility with other protecting groups makes it a versatile tool in organic chemistry and biochemistry laboratories.
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