2,5-Dioxopyrrolidin-1-yl 1-(9H-fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31,34,37,40-tridecaoxa-4-azatritetracontan-43-oate
≥98%
- Product Code: 61651
CAS:
2227246-92-4
Molecular Weight: | 937.03 g./mol | Molecular Formula: | C₄₆H₆₈N₂O₁₈ |
---|---|---|---|
EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key reagent for the introduction of the fluorenylmethyloxycarbonyl (Fmoc) protecting group, which is essential for protecting amino groups during the peptide chain assembly. The Fmoc group is highly favored due to its stability under various reaction conditions and its ease of removal under mild basic conditions, making it ideal for synthesizing complex peptides.
Additionally, the polyethyleneglycol (PEG) linker in the molecule enhances solubility in organic solvents, facilitating efficient coupling reactions. This feature is particularly beneficial in the synthesis of long or hydrophobic peptides, where solubility issues often arise. The compound’s design ensures high reactivity and selectivity, enabling precise control over peptide elongation and minimizing side reactions. Its application extends to the production of peptides for pharmaceutical research, drug development, and biochemical studies, where high-purity peptides are critical.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
1.000 | 10-20 days | $2,127.33 |
+
-
|
2,5-Dioxopyrrolidin-1-yl 1-(9H-fluoren-9-yl)-3-oxo-2,7,10,13,16,19,22,25,28,31,34,37,40-tridecaoxa-4-azatritetracontan-43-oate
This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a key reagent for the introduction of the fluorenylmethyloxycarbonyl (Fmoc) protecting group, which is essential for protecting amino groups during the peptide chain assembly. The Fmoc group is highly favored due to its stability under various reaction conditions and its ease of removal under mild basic conditions, making it ideal for synthesizing complex peptides.
Additionally, the polyethyleneglycol (PEG) linker in the molecule enhances solubility in organic solvents, facilitating efficient coupling reactions. This feature is particularly beneficial in the synthesis of long or hydrophobic peptides, where solubility issues often arise. The compound’s design ensures high reactivity and selectivity, enabling precise control over peptide elongation and minimizing side reactions. Its application extends to the production of peptides for pharmaceutical research, drug development, and biochemical studies, where high-purity peptides are critical.
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 | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
$0.00
$0.00
Total :