2-[2-(Fmoc-amino)ethoxy]ethylamine hydrochloride
≥97% (HPLC)
- Product Code: 104470
CAS:
221352-88-1
| Molecular Weight: | 362.85 g./mol | Molecular Formula: | C₁₉H₂₃ClN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01321025 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily used in peptide synthesis as a protecting group for amines. The Fmoc (fluorenylmethyloxycarbonyl) group ensures selective deprotection during the synthesis process, allowing for precise control over peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis, where it helps in building complex peptides with high efficiency. The hydrochloride form enhances its stability and solubility, making it easier to handle in laboratory settings. Additionally, it finds applications in the development of pharmaceuticals and biochemical research, where protecting amine groups is crucial for synthesizing specific molecular structures. Its utility in creating custom peptides makes it a key reagent in drug discovery and protein engineering studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,590.00 |
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| 1.000 | 10-20 days | ฿12,960.00 |
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2-[2-(Fmoc-amino)ethoxy]ethylamine hydrochloride
This compound is primarily used in peptide synthesis as a protecting group for amines. The Fmoc (fluorenylmethyloxycarbonyl) group ensures selective deprotection during the synthesis process, allowing for precise control over peptide chain assembly. It is particularly valuable in solid-phase peptide synthesis, where it helps in building complex peptides with high efficiency. The hydrochloride form enhances its stability and solubility, making it easier to handle in laboratory settings. Additionally, it finds applications in the development of pharmaceuticals and biochemical research, where protecting amine groups is crucial for synthesizing specific molecular structures. Its utility in creating custom peptides makes it a key reagent in drug discovery and protein engineering studies.
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