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 158257-40-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral diol motif with defined (3S,4S) stereochemistry, enabling precise incorporation into peptide synthesis workflows. The C-terminal hydroxyl and methyl-substituted heptanoic acid chain offer tailored reactivity for conjugation strategies. Bench-stable and moisture-tolerant, it facilitates efficient coupling under standard conditions.
(3S,4S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-hydroxy-6-methylheptanoic acid serves as a stereochemically defined amino acid building block for peptide synthesis, enabling efficient incorporation of hydroxylated side chains. The fluorenylmethoxycarbonyl (Fmoc) group provides orthogonal protection and facilitates straightforward purification by chromatography. Its bench-stable nature and compatibility with standard coupling protocols make it suitable for both manual and automated synthesis workflows.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: