Boc-L-Lys(Z)-OH
98%
- Product Code: 105417
Alias:
Nα-(tert-butoxycarbonyl)-Nε-benzyloxycarbonyl-L-lysine
CAS:
2389-45-9
Molecular Weight: | 380.44 g./mol | Molecular Formula: | C₁₉H₂₈N₂O₆ |
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EC Number: | 219-221-0 | MDL Number: | MFCD00065584 |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
- Used in peptide synthesis as a protecting group for amino acids, ensuring selective reactions during the formation of peptide bonds.
- Helps in the preparation of complex peptides and proteins by safeguarding the lysine side chain during chemical processes.
- Commonly applied in pharmaceutical research for developing peptide-based drugs and bioactive compounds.
- Facilitates the synthesis of modified peptides with specific functional properties for biochemical studies.
- Enhances the stability and solubility of intermediates in organic synthesis, making it easier to handle and purify compounds.
- Plays a role in the production of custom peptides for diagnostic tools and therapeutic agents.
Product Specification:
Test | Specification |
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Carbon | 58.5-61.5 |
Melting Point | 75-79 |
Nitrogen | 7.1-7.7 |
Purity (HPLC) | 98-100 |
Purity (Neutralization Titration) | 98-100 |
Appearance | White To Light Yellow Powder |
Solubility | Colorless Clear (50Mg/Ml, Methanol) |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $13.37 |
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5.000 | 10-20 days | $18.88 |
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25.000 | 10-20 days | $73.93 |
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100.000 | 10-20 days | $231.24 |
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Boc-L-Lys(Z)-OH
- Used in peptide synthesis as a protecting group for amino acids, ensuring selective reactions during the formation of peptide bonds.
- Helps in the preparation of complex peptides and proteins by safeguarding the lysine side chain during chemical processes.
- Commonly applied in pharmaceutical research for developing peptide-based drugs and bioactive compounds.
- Facilitates the synthesis of modified peptides with specific functional properties for biochemical studies.
- Enhances the stability and solubility of intermediates in organic synthesis, making it easier to handle and purify compounds.
- Plays a role in the production of custom peptides for diagnostic tools and therapeutic agents.
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