Description

• General description: High purity Fmoc-protected amino acid for research and process production of peptides, with very low levels of dipeptide, free-amino acids and acetic acid impurities. Standard building block for introduction of isoleucine amino-acid residues by Fmoc SPPS Associated Protocols and Technical ArticlesFmoc-amino acids for Peptide Production Cleavage and Deprotection Protocols for Fmoc SPPS
• Application: Total synthesis of teixobactin: This article describes the challenges and strategies in synthesizing teixobactin, a promising new antibiotic, highlighting the role of Fmoc-Ile-OH in the synthesis process (Jin et al., 2016). Synthesis and structure–activity relationship studies of teixobactin analogues: Discusses the synthesis of teixobactin analogues using Fmoc-Ile-OH, providing insights into developing more effective antibiotics (Wu et al., 2017).
• Linkage: Replaces: 04-12-1024
• Analysis Note: Color (visual): white to off whiteAppearance of substance (visual): powderColor index (0,5 M in DMF): ≤ 150 HazenIdentity (IR): passes testEnantiomeric purity: ≥ 99.7 % (a/a)Purity (HPLC): ≥ 99.0 % (a/a)Fmoc-ß-Ala-OH (HPLC): ≤ 0.1 % (a/a)Fmoc-ß-Ala-Ile-OH (HPLC): ≤ 0.1 % (a/a)Fmoc-Ile-Ile-OH (HPLC): ≤ 0.1 % (a/a)Fmoc-Leu-OH (GC): ≤ 0.1 % (a/a)Assay free amino acid (GC): ≤ 0.2 %Purity (TLC(011A)): ≥ 98 %Purity (TLC(0811)): ≥ 98 %Solubility (25 mmole in 50 ml DMF): clearly solubleAssay (acidimetric): ≥ 98.0 %Water (K. F.): ≤ 2.0 %Ethyl acetate (HS-GC): ≤ 0.5 %Acetate (IC): ≤ 0.02 %To see the solvent systems used for TLC of Novabiochem® products please click here.
• Legal Information: Novabiochem is a registered trademark of Merck KGaA, Darmstadt, Germany