Nε-Palmitoyl-L-glutamic Acid γ-Succinimidyl-α-tert-butyl Ester

• CAT Number: R050652
• CAS Number: 204521-63-1
• Molecular Formula: C29H50N2O7
• Molecular Weight: 538.726
• Purity: ≥95%
• Synonyms: Nε-Palmitoyl-Glu-γ-succinimidyl-α-tert-butyl Ester; (2S)-5-[(2,5-Dioxo-1-pyrrolidinyl)?oxy]-5-oxo-2-[(1-oxohexadecyl)amino]pentanoic Acid 1,1-Dimethylethyl Ester; Nε-Hexadecanoyl-L-glutamic Acid α-t-Butyl-γ-2,5-dioxopyrrolidin-1-yl-diester
• Storage: -20°C
• IUPAC Name: 1-O-tert-butyl 5-O-(2,5-dioxopyrrolidin-1-yl) (2S)-2-(hexadecanoylamino)pentanedioate
• InChI: InChI=1S/C29H50N2O7/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-24(32)30-23(28(36)37-29(2,3)4)19-22-27(35)38-31-25(33)20-21-26(31)34/h23H,5-22H2,1-4H3,(H,30,32)/t23-/m0/s1
• InChIKey: MKJFKKLCCRQPHN-QHCPKHFHSA-N
• SMILES: CCCCCCCCCCCCCCCC(=O)NC(CCC(=O)ON1C(=O)CCC1=O)C(=O)OC(C)(C)C

Nε-Palmitoyl-L-glutamic acid γ-succinimidyl-α-tert-butyl ester is a specialized compound used in peptide synthesis and bioconjugation chemistry. It consists of a glutamic acid residue modified with a palmitoyl group, a succinimidyl ester, and a tert-butyl ester. This compound is employed in the conjugation of peptides and proteins to lipids or surfaces for applications in drug delivery and biomaterials research. Research on this compound focuses on optimizing bioconjugation methods and developing novel biomaterials with tailored properties.