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 21168-72-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This piperidine-based ethanol derivative features a primary amine-functionalized side chain, enabling facile conjugation and solubility enhancement. The aminomethylpiperidine moiety imparts strong basic character and structural rigidity, ideal for medicinal chemistry scaffolds. Its bench-stable, moisture-tolerant profile supports reliable handling in synthesis workflows.
2-(4-(Aminomethyl)piperidin-1-yl)ethanol serves as a versatile bifunctional building block in medicinal chemistry, enabling efficient conjugation via its primary amine and hydroxyl groups. The piperidine scaffold provides favorable solubility and metabolic stability, while the pendant ethylene glycol linker enhances polarity and facilitates downstream derivatization. This compound functions reliably in standard amide coupling, reductive amination, and macrocyclization protocols, offering robust performance in both lead optimization and API intermediate synthesis.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: