Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 2095488-98-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Fmoc-L-Ala(BCP)-OH features a benzylcyclopropyl (BCP) side chain that enhances conformational rigidity and metabolic stability in peptide synthesis. This derivative integrates seamlessly into solid-phase workflows, offering improved solubility and reduced aggregation during chain elongation. The Fmoc group enables efficient deprotection under mild basic conditions.
Fmoc-L-Ala(BCP)-OH serves as a versatile building block for solid-phase peptide synthesis, enabling the incorporation of a bioorthogonal click handle via its benzylcyclopropyl (BCP) side chain. The Fmoc group provides efficient protection for the amine, while the BCP moiety facilitates reliable copper-free ligation under physiological conditions. This derivative offers excellent bench stability, straightforward purification, and compatibility with standard coupling protocols, making it ideal for site-specific conjugation in peptide-drug conjugates and functionalized biomolecules.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319
|
|
|
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: