Fmoc-3-(4-aminophenyl)-propionic Acid
≥95%
- Product Code: 117426
CAS:
882847-07-6
| Molecular Weight: | 387.44 g./mol | Molecular Formula: | C₂₄H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656461 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
Fmoc-3-(4-aminophenyl)-propionic acid is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for introducing aromatic amine functionalities into peptide chains. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amine, allowing selective deprotection during synthesis. This compound is especially valuable in the development of peptide-based drugs, biomaterials, and research tools, where precise incorporation of aromatic amines is required. Its applications extend to the creation of peptide conjugates, probes, and modified peptides for studying protein interactions, drug delivery systems, and biochemical assays. The compound’s stability and compatibility with standard peptide synthesis protocols make it a versatile reagent in both academic and industrial settings.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | Ft60,119.52 |
+
-
|
Fmoc-3-(4-aminophenyl)-propionic Acid
Fmoc-3-(4-aminophenyl)-propionic acid is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key building block for introducing aromatic amine functionalities into peptide chains. The Fmoc (fluorenylmethyloxycarbonyl) group acts as a protective group for the amine, allowing selective deprotection during synthesis. This compound is especially valuable in the development of peptide-based drugs, biomaterials, and research tools, where precise incorporation of aromatic amines is required. Its applications extend to the creation of peptide conjugates, probes, and modified peptides for studying protein interactions, drug delivery systems, and biochemical assays. The compound’s stability and compatibility with standard peptide synthesis protocols make it a versatile reagent in both academic and industrial settings.
| Mechanism | - |
| Appearance | - |
| Longevity | - |
| Strength | - |
| Storage | - |
| Shelf Life | - |
| Allergen(s) | - |
| Dosage (Range) | - |
| Recommended Dosage | - |
| Dosage (Per Day) | - |
| Recommended Dosage (Per Day) | - |
| Mix Method | - |
| Heat Resistance | - |
| Stable in pH range | - |
| Solubility | - |
| Product Types | - |
| INCI | - |
Cart
No products
Subtotal:
Ft0.00
Ft0.00
Total :