
CAS 222159-87-7
:N-(5-Aminopentyl)maleimide trifluoroacetate salt
Description:
N-(5-Aminopentyl)maleimide trifluoroacetate salt is a chemical compound characterized by its maleimide functional group, which is known for its reactivity towards thiols, making it useful in bioconjugation and polymer chemistry. The presence of the trifluoroacetate salt form enhances its solubility in polar solvents, facilitating its application in various chemical reactions. The compound features a five-carbon alkyl chain (pentyl) attached to the amino group, which can influence its biological activity and interaction with other molecules. This compound is typically utilized in the synthesis of conjugates for drug delivery systems, as well as in the development of biomaterials due to its ability to form stable linkages with biomolecules. Its unique structure allows for selective reactions, making it a valuable tool in chemical biology and materials science. Safety and handling precautions should be observed, as with any chemical substance, to mitigate potential hazards associated with its use.
- N-(5-Aminopentyl)maleimide trifluoroacetate salt
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Found 4 products.
N-(5-AMINOPENTYL)MALEIMIDE TRIFLUOROACETATE SALT
CAS:Formula:C11H15F3N2O4Purity:95%Color and Shape:SolidMolecular weight:296.24301-(5-Aminopentyl)-1H-Pyrrole-2,5-Dione 2,2,2-Trifluoroacetate
CAS:1-(5-Aminopentyl)-1H-Pyrrole-2,5-Dione 2,2,2-TrifluoroacetatePurity:99%Molecular weight:296.24g/molN-(5-Aminopentyl)maleimide Trifluoroacetic Acid Salt
CAS:Controlled ProductApplications N-(5-Aminopentyl)maleimide Trifluoroacetic Acid Salt is used in the preparation of site directed maleimide bifunctional chelators for technetium and rhenium.
References Banerjee, S. et al.: Dalton Trans., 24, 3886 (2005);Formula:C9H14N2O2·C2HF3O2Color and Shape:NeatMolecular weight:296.243



