Cuprate(1-), (glycyl-L-histidyl-κN1-L-lysinato)[glycyl-κN-L-histidyl-κN,κN3-L-lysinato(2-)]-, hydrogen, acetate (1:1:2)(CAS: 130120-57-9)

Cuprate(1-), (glycyl-L-histidyl-κN1-L-lysinato)[glycyl-κN-L-histidyl-κN,κN3-L-lysinato(2-)]-, hydrogen, acetate (1:1:2) is a complex organometallic compound with a high molecular weight. It crystallizes in the monoclinic system. The compound has a relatively high solubility in water and organic solvents. It exhibits good reactivity with Lewis acids. This compound is known for its stability under normal conditions but is susceptible to hydrolysis in the presence of moisture.

Cuprate(1-), (glycyl-L-histidyl-κN1-L-lysinato)[glycyl-κN-L-histidyl-κN,κN3-L-lysinato(2-)]-, hydrogen, acetate (1:1:2) can be synthesized through multi-step reactions involving metalation of the ligands followed by the addition of hydrogen acetate. The process requires precise control of reaction conditions, including temperature and the use of appropriate catalysts to achieve high selectivity and yield.

Cuprate(1-), (glycyl-L-histidyl-κN1-L-lysinato)[glycyl-κN-L-histidyl-κN,κN3-L-lysinato(2-)]-, hydrogen, acetate (1:1:2) is primarily used in the pharmaceutical industry for the synthesis of complex organometallic compounds. It is also utilized in the development of novel sensor technologies and semiconductor materials due to its unique electronic properties.

When handling Cuprate(1-), (glycyl-L-histidyl-κN1-L-lysinato)[glycyl-κN-L-histidyl-κN,κN3-L-lysinato(2-)]-, hydrogen, acetate (1:1:2), it is crucial to use appropriate personal protective equipment (PPE) such as gloves, goggles, and a lab coat. Work should be conducted in a well-ventilated area or a fume hood to avoid inhalation. In case of a spill, it is recommended to absorb with an appropriate material and dispose of the waste according to local regulations. Always refer to the Safety Data Sheet (SDS) for detailed handling instructions.