(R)-N-Fmoc-Α-(4-Pentynyl)Alanine
98%
- Product Code: 231575
CAS:
1198791-56-8
Molecular Weight: | 391.46 g./mol | Molecular Formula: | C₂₄H₂₅NO₄ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature |
Product Description:
Widely used in peptide synthesis, this compound serves as a chiral building block for introducing alkyne functionality into peptide chains. The presence of the terminal alkyne allows for site-specific modification via click chemistry, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC). This is valuable in bioconjugation, enabling attachment of fluorophores, biotin, or other functional tags for detection, imaging, or immobilization. The Fmoc group ensures compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly under mild basic conditions. Its stereochemistry helps maintain desired peptide conformation, making it useful in the development of structured peptides, probes, and peptide-based therapeutics.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿16,840.00 |
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0.250 | 10-20 days | ฿28,140.00 |
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1.000 | 10-20 days | ฿76,750.00 |
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(R)-N-Fmoc-Α-(4-Pentynyl)Alanine
Widely used in peptide synthesis, this compound serves as a chiral building block for introducing alkyne functionality into peptide chains. The presence of the terminal alkyne allows for site-specific modification via click chemistry, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC). This is valuable in bioconjugation, enabling attachment of fluorophores, biotin, or other functional tags for detection, imaging, or immobilization. The Fmoc group ensures compatibility with standard solid-phase peptide synthesis (SPPS), allowing stepwise assembly under mild basic conditions. Its stereochemistry helps maintain desired peptide conformation, making it useful in the development of structured peptides, probes, and peptide-based therapeutics.
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