175943

Sigma-Aldrich

Dimethyl sulfoxide-d6

99.5 atom % D

Synonym(s):
Hexadeuterodimethyl sulfoxide, (Methyl sulfoxide)-d6, DMSO-d6
Linear Formula:
(CD3)2SO
CAS Number:
Molecular Weight:
84.17
Beilstein/REAXYS Number:
1237248
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.21

Quality Level

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 %

application(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

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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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.

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.

Packaging

10 g in ampule
50, 100, 250 g in glass bottle

RIDADR

NONH for all modes of transport

WGK Germany

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

Certificate of Origin

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)
Akira Minami et al.
Scientific reports, 11(1), 3302-3302 (2021-02-10)
Reduction of elastin in the skin causes various skin diseases as well as wrinkles and sagging with aging. Sialidase is a hydrolase that cleaves a sialic acid residue from sialoglycoconjugate. Cleavage of sialic acid from microfibrils by the sialidase isozyme...
M G Nair et al.
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%.
Weber M, et al.
Accreditation and Quality Assurance, 18(2), 91-98 (2013)
Related Content
NMR spectroscopy is an analytic technique to determine molecular structure, chemical composition and purity. NMR detects the energy absorbed due to nuclear spin states in the presence of a strong magnetic field.
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