1.03424
Dimethyl sulfoxide-d6
deuteration degree min. 99.8% for NMR spectroscopy MagniSolv™
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vapor pressure
0.42 mmHg ( 20 °C)
Quality Level
form
liquid
autoignition temp.
573 °F
potency
14500 mg/kg LD50, oral (Rat)
40000 mg/kg LD50, skin (Rat)
expl. lim.
42 %
technique(s)
NMR: suitable
impurities
≤0.020% Water (H<SUB>2</SUB>O) (NMR)
≤0.030% Water (H<SUB>2</SUB>O + D<SUB>2</SUB>O) (Karl Fischer)
refractive index
n20/D 1.476 (lit.)
bp
189 °C (lit.)
mp
20.2 °C
transition temp
flash point 88 °C
density
1.190 g/mL at 25 °C (lit.)
mass shift
M+6
storage temp.
no temp limit
SMILES string
[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]
InChI
1S/C2H6OS/c1-4(2)3/h1-2H3/i1D3,2D3
InChI key
IAZDPXIOMUYVGZ-WFGJKAKNSA-N
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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
Water (K. Fischer, H₂O + D₂O): ≤ 0.030 %
Performance test (NMR-spectrum): passes test
Water (NMR, H₂O): ≤ 0.020 %
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Legal Information
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point(F)
190.4 °F
Flash Point(C)
88 °C
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