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About This Item
Linear Formula:
(CD3)2SO
CAS Number:
Molecular Weight:
84.17
UNSPSC Code:
12191502
NACRES:
NA.21
PubChem Substance ID:
EC Number:
218-617-0
Beilstein/REAXYS Number:
1237248
MDL number:
Product Name
Dimethyl sulfoxide-d6, 99.5 atom % D
InChI key
IAZDPXIOMUYVGZ-WFGJKAKNSA-N
InChI
1S/C2H6OS/c1-4(2)3/h1-2H3/i1D3,2D3
SMILES string
[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]
vapor pressure
0.42 mmHg ( 20 °C)
isotopic purity
99.5 atom % D
assay
99% (CP)
form
liquid
autoignition temp.
573 °F
expl. lim.
42 %
technique(s)
NMR: suitable
impurities
≤0.0250% water
water
refractive index
n20/D 1.476 (lit.)
bp
189 °C (lit.)
mp
20.2 °C (lit.)
density
1.190 g/mL at 25 °C (lit.)
mass shift
M+6
Quality Level
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Application
DMSO-d6 along with glycerol or glycerol-d8 forms highly viscous binary solvents with high dissolution power for complex biological active compounds.
Dimethyl sulfoxide-d6 (DMSO-d6) has been employed as solvent for the dissolution of 1-allyloxy-2-hydroxy-propyl-starch (AHP-starch) to record its high resolution 1H NMR (Proton Nuclear Magnetic Resonance) spectrum.
General description
Dimethyl sulfoxide-d6 (DMSO-d6) is a deuterated solvent. On photoirradiation in the range of 193 and 222nm, it undergoes decomposition to afford CD3 radicals. Quantum yields of CD3 have been evaluated by infrared diode laser absorption spectroscopy. 100% DMSO-d6 has been used as solvent in the long-range COSY (Correlation Spectroscopy) experiment.
Other Notes
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Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
190.4 °F
flash_point_c
88 °C
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Optimization of the synthesis of 1-allyloxy-2-hydroxy-propyl-starch through statistical experimental design.
Huijbrechts AML, et al.
Carbohydrate Polymers, 77(5), 25-31 (2009)
Highly Viscous Binary Solvents: DMSO-d6/Glycerol and DMSO-d6/Glycerol-d8 for Polar and Apolar Mixture Analysis by NMR.
Lameiras P and Nuzillard J-M.
Analytical Chemistry, 88(8), 4508-4515 (2016)
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Applied and environmental microbiology, 57(2), 434-439 (1991-02-01)
Two isoflavonoids isolated from clover roots grown under phosphate stress were characterized as formononetin (7-hydroxy,4'-methoxy isoflavone) and biochanin A (5,7-dihydroxy,4'-methoxy isoflavone). At 5 ppm, these compounds stimulated hyphal growth in vitro and root colonization of an undescribed vesicular-arbuscular mycorrhiza, a
Using high-performance quantitative NMR (HP-qNMR?) for certifying traceable and highly accurate purity values of organic reference materials with uncertainties< 0.1%.
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Accreditation and Quality Assurance, 18(2), 91-98 (2013)
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