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 1948-48-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
β-Glutamic acid features a γ-carboxyl group positioned two atoms away from the α-amino nitrogen, enabling unique coordination in metal-binding systems and facilitating incorporation into bioactive peptides. This structural arrangement supports applications in chelation chemistry and peptide synthesis where side-chain functionality is critical.
β-Glutamic acid serves as a key building block for the synthesis of γ-amino acids, peptidomimetics, and bioactive heterocycles. Its bifunctional nature—carboxylic acid and amine groups separated by two methylene units—enables straightforward incorporation into peptide backbones and facilitates ring formation under standard conditions. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: