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716731

Dimethyl sulfoxide-d6

"Special HOH", ≥99.9 atom % D

Synonym(s):

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

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10 X 0.75 ML

$75.20

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$91.60

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$316.00

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Estimated to ship onDecember 15, 2025fromMILWAUKEE

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About This Item

Linear Formula:
(CD3)2SO
CAS Number:
2206-27-1
Molecular Weight:
84.17
Beilstein/REAXYS Number:
1237248
EC Number:
218-617-0
MDL number:
MFCD00002090
UNSPSC Code:
12142201
PubChem Substance ID:
329763425
NACRES:
NA.21

Key Documents

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vapor pressure

0.42 mmHg ( 20 °C)

isotopic purity

≥99.9 atom % D

assay

≥99% (CP)

form

liquid

autoignition temp.

573 °F

expl. lim.

42 %

technique(s)

NMR: suitable

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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This Item
296147417939900749
Dimethyl sulfoxide-d6 "Special HOH", ≥99.9 atom % D

Sigma-Aldrich

716731

Dimethyl sulfoxide-d6

Dimethyl sulfoxide-d6 99.9 atom % D, contains 0.03 % (v/v) TMS

Sigma-Aldrich

296147

Dimethyl sulfoxide-d6

Dimethyl sulfoxide-d6 "100%", 99.96 atom % D, contains 0.03 % (v/v) TMS

Sigma-Aldrich

417939

Dimethyl sulfoxide-d6

Dimethyl sulfoxide-d6 "Special HOH", ≥99 atom % D, contains 0.05 % (v/v) TMS

900749

Dimethyl sulfoxide-d6

mass shift

M+6

mass shift

M+6

mass shift

M+6

mass shift

M+6

isotopic purity

≥99.9 atom % D

isotopic purity

99.9 atom % D

isotopic purity

99.96 atom % D

isotopic purity

≥99 atom % D

technique(s)

NMR: suitable

technique(s)

NMR: suitable

technique(s)

NMR: suitable

technique(s)

NMR: suitable

assay

≥99% (CP)

assay

99% (CP)

assay

≥99% (CP)

assay

≥99% (CP)

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

-

form

liquid

form

liquid

form

liquid

form

liquid

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.[1] Dissociation dynamics of DMSO-d6 at 193nm was examined using photo fragment translational spectroscopy method.[2]

Application

Dimethyl sulfoxide-d6 may be used as an NMR solvent for 1H and 13C NMR experiments.[3]

Other Notes

Check out ChemisTwin®, our brand new online portal for identity confirmation and quantification of NMR spectra. Learn more or reach out to us for a free trial.

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

190.4 °F

flash_point_c

88 °C

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Certificates of Analysis (COA)

Lot/Batch Number
MBBD8549
MBBD6764
MBBD7099
MBBD4452
MBBD1706

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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)
Priya P Netalkar et al.
European journal of medicinal chemistry, 79, 47-56 (2014-04-12)
Air and moisture stable coordination compounds of late first row transition metals, viz. Co(II), Ni(II), Cu(II) and Zn(II), with a newly designed ligand, 2-(2-benzo[d]thiazol-2-yl)hydrazono)propan-1-ol (LH), were prepared and successfully characterized using various spectro-analytical techniques. The molecular structures of the ligand
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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