Description

• Application: Computer modeling of adsorption on an activated charcoal surface.: This study uses computational modeling to simulate adsorption processes, where Dimethyl sulfoxide-d₆ is likely used as a model solvent to analyze interactions at the molecular level (Wurster et al., 1994). Solvent effects on the conformation of cyclo(-D-Trp-D-Asp-Pro-D-Val-Leu-). An NMR spectroscopy and molecular modeling study.: Investigates how solvents like Dimethyl sulfoxide-d₆ influence peptide conformations, enhancing our understanding of peptide behavior in different chemical environments (Gonnella et al., 1994). Role of the NH2-terminal domain of angiotensin II (ANG II) and [Sar1]angiotensin II on conformation and activity. NMR evidence for aromatic ring clustering and peptide backbone folding compared with [des-1,2,3]angiotensin II.: Discusses the structural and functional aspects of angiotensin II with Dimethyl sulfoxide-d₆ as a solvent to facilitate NMR analysis, providing insights into peptide structure-activity relationships (Matsoukas et al., 1994). Cyclic lactam analogues of Ac-[Nle4]alpha-MSH4-11-NH2.: Focuses on cyclic lactam analogues using Dimethyl sulfoxide-d₆ in NMR studies to investigate molecular conformations, contributing to peptide chemistry research (Sugg et al., 1988). NMR study of a lymphocyte differentiating thymic factor. An investigation of the Zn(II)-nonapeptide complexes (thymulin).: Utilizes Dimethyl sulfoxide-d₆ in detailed NMR studies to explore the interactions of metal-peptide complexes, which are crucial for understanding the bioactive conformation and function of peptides in analytical biochemistry (Cung et al., 1988).
• Analysis Note: Deuteration degree: ≥ 99.80 %Water (K. Fischer, H₂O + D₂O): ≤ 0.030 %Performance test (NMR-spectrum): passes testWater (NMR, H₂O): ≤ 0.020 %
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• Legal Information: MAGNISOLV is a trademark of Merck KGaA, Darmstadt, Germany