CAS 499-86-5
:Ac-Lys(Ac)-OH
Description:
The chemical substance known as Ac-Lys(Ac)-OH, with the CAS number 499-86-5, is a derivative of lysine, an essential amino acid. This compound features an acetyl group attached to the amino group of lysine, which enhances its solubility and stability. Ac-Lys(Ac)-OH is characterized by its ability to participate in peptide bond formation, making it relevant in biochemical research and peptide synthesis. The acetylation of lysine can influence protein function and interactions, as it is a common post-translational modification. This compound is typically used in studies related to protein chemistry, enzymatic activity, and the development of peptide-based therapeutics. Its molecular structure includes both an amino group and a carboxylic acid group, which are characteristic of amino acids, along with the acetyl modifications that alter its reactivity and properties. Overall, Ac-Lys(Ac)-OH serves as a valuable tool in the fields of biochemistry and molecular biology.
Formula:C10H18N2O4
Synonyms:- Ac-Lys(Ac)-OH・DCHA
- Ac-Lys (Ac)-Oh
- alpha,epsilon-Diacetyl-L-lysine
- N-ALPHA,N-EPSILON-DI-ACETYL-L-LYSINE
- AC-LYSINE (AC)-OH
- L-Lysine, N2,N6-diacetyl-
- N-ALPHA,EPSILON-BIS-ACETYL-L-LYSINE
- Diacetyl-L-lysine
- Na,e-Bis-acetyl-L-lysine≥ 99% (TLC)
- Ac-L-Lys(Ac)-OH
- N2,N6-Diacetyl-L-lysine
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Found 5 products.
Ac-Lys(Ac)-OH
CAS:<p>Bachem ID: 4025494.</p>Formula:C10H18N2O4Purity:> 99%Color and Shape:White PowderMolecular weight:230.26Ac-lys(ac)-OH
CAS:Controlled Product<p>Applications Ac-lys(ac)-oh was used in the reaction of HOCl with amino acids and peptides with ESR evidence for rapid rearrangement and fragmentation reactions of nitrogen-centered radicals.<br>References Hawkins, C., et al.: J. Chem. Soc. Perkin Trans. 2, 9, 1937 (1998);<br></p>Formula:C10H18N2O4Color and Shape:NeatMolecular weight:237.768Na,e-Bis-acetyl-L-lysine
CAS:Formula:C10H18N2O4Purity:95.0%Color and Shape:SolidMolecular weight:230.264





