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Merck

453323

Dimethyl sulfoxide-d6

"100%", 99.96 atom % D

Synonym(s):

(Methyl sulfoxide)-d6, DMSO-d6, Hexadeuterodimethyl sulfoxide

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About This Item

Linear Formula:
(CD3)2SO
CAS Number:
2206-27-1
Molecular Weight:
84.17
EC Number:
218-617-0
UNSPSC Code:
12191502
PubChem Substance ID:
24868790
Beilstein/REAXYS Number:
1237248
MDL number:
MFCD00002090

Product Name

Dimethyl sulfoxide-d6, "100%", 99.96 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

99.96 atom % D

assay

≥99.0%

form

liquid

autoignition temp.

573 °F

expl. lim.

42 %

packaging

pk of 10 × 0.25 mL

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

100

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Application

Dimethyl sulfoxide-d6 may be used as an NMR solvent for 1H and 13C NMR experiments.

General description

Dimethyl sulfoxide-d6 (DMSO-d6) is a deuterated NMR solvent. It undergoes photodissociation to generate CD3 radical photoproducts, which have been analyzed by infrared diode laserabsorption spectroscopy. Dissociation dynamics of DMSO-d6 at 193nm was examined using photo fragment translational spectroscopy method.

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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Certificates of Analysis (COA)

Lot/Batch Number
MKBJ8908V
MKBD1592
03213DE
02423CD
19414PN

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Solution forms of an antitumor cyclic hexapeptide, RA-VII in dimethyl sulfoxide-d6 from nuclear magnetic resonance studies.
Itokawa H, et al.
Chemical & Pharmaceutical Bulletin, 40(4), 1050-1052 (1992)
Unraveling the dissociation of dimethyl sulfoxide following absorption at 193 nm.
Blank DA, et al.
J. Chem. Phys. , 106(2), 539-550 (1997)
Diode laser measurements of CD3 quantum yields and internal energy for the dissociation of dimethyl sulfoxide-d6.
Rudolph RN, et al.
J. Chem. Phys. , 106(4), 1346-1352 (1997)
Papawee Suabjakyong et al.
PloS one, 10(3), e0122733-e0122733 (2015-03-27)
The basidiomycetous mushroom Phellinus igniarius (L.) Quel. has been used as traditional medicine in various Asian countries for many years. Although many reports exist on its anti-oxidative and anti-inflammatory activities and therapeutic effects against various diseases, our current knowledge of
Barbara Parrino et al.
European journal of medicinal chemistry, 94, 367-377 (2015-03-18)
Three new ring systems, pyrido[2',3':3,4]pyrrolo[1,2-a]quinoxalines, pyrido[3',2':3,4]pyrrolo[1,2-a]quinoxalines and pyrido[2',3':5,6]pyrazino[2,1-a]isoindoles, were synthesized through an aza-substitution on the already active isoindolo-quinoxaline system and in particular in the position 7 or 4 of the isoindole moiety and in position 5 of the quinoxaline portion.
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