6-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoic acid
95%
- Product Code: 191381
CAS:
1313183-12-8
| Molecular Weight: | 368.43 g./mol | Molecular Formula: | C₂₁H₂₄N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16036312 | |
| Melting Point: | Boiling Point: | 609.9±55.0 °C(Predicted) | |
| Density: | 1.245±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry, light-proof |
Product Description:
Used primarily in solid-phase peptide synthesis as a protected amino acid building block. The Fmoc group provides temporary protection for the alpha-amino group, allowing selective deprotection under mild basic conditions while the peptide chain is assembled on a resin. The side-chain amino group is left unprotected or can be selectively protected depending on the synthesis strategy, enabling the incorporation of lysine derivatives into target peptides. Its structure supports the synthesis of complex peptides and proteins in research settings, especially in pharmaceutical development and biochemical studies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 G | 10-20 days | ฿2,770.00 |
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| 25.000 G | 10-20 days | ฿9,690.00 |
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| 100.000 G | 10-20 days | ฿31,960.00 |
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6-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoic acid
Used primarily in solid-phase peptide synthesis as a protected amino acid building block. The Fmoc group provides temporary protection for the alpha-amino group, allowing selective deprotection under mild basic conditions while the peptide chain is assembled on a resin. The side-chain amino group is left unprotected or can be selectively protected depending on the synthesis strategy, enabling the incorporation of lysine derivatives into target peptides. Its structure supports the synthesis of complex peptides and proteins in research settings, especially in pharmaceutical development and biochemical studies.
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