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Key Documents

V800164

Sigma-Aldrich

Dimethyl sulfoxide

AR, ≥99.5%

Synonym(s):

DMSO

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About This Item

Linear Formula:
(CH3)2SO
CAS Number:
Molecular Weight:
78.13
Beilstein/REAXYS Number:
506008
EC Number:
MDL number:
UNSPSC Code:
12191502
PubChem Substance ID:
grade:
AR
assay:
≥99.5%
bp:
189 °C (lit.)
vapor pressure:
0.42 mmHg ( 20 °C)
Pricing and availability is not currently available.

grade

AR

vapor density

2.7 (vs air)

vapor pressure

0.42 mmHg ( 20 °C)

product line

Vetec

assay

≥99.5%

form

liquid

autoignition temp.

573 °F

expl. lim.

42 %, 63 °F

dilution

(for analytical testing)

refractive index

n20/D 1.479 (lit.)

bp

189 °C (lit.)

mp

16-19 °C (lit.)

density

1.10 g/mL (lit.)

SMILES string

CS(C)=O

InChI

1S/C2H6OS/c1-4(2)3/h1-2H3

InChI key

IAZDPXIOMUYVGZ-UHFFFAOYSA-N

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General description

Dimethyl sulfoxide (DMSO) is a high-boiling polar aprotic solvent and mild oxidant used in organic synthesis. DMSO can also act as a one-carbon synthon in organic chemistry.[1] It is a source of -Me, -SMe, -SO2Me functional groups. It is also used as a versatile reagent in Pfitzner-Moffatt oxidation, Swern oxidation, and Corey-Chaykovsky reaction.[2]

Caution

Supercools easily and remelts slowly at room temperature. Solidified product can be re-liquified by warming to room temperature without detriment to the product.

Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

10 - Combustible liquids

wgk_germany

WGK 1

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup


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Dimethyl sulfoxide as a synthon in organic chemistry
Jones-Mensah E, et al.
Synthesis, 48, 1421-1436 (2016)
The applications of dimethyl sulfoxide as reagent in organic synthesis
Wu X-F and Natte K
advanced synthesis and catalysis, 358, 336-352 (2016)
A Oguro-Ando et al.
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Medulloblastoma is the most common malignant pediatric brain tumor, with metastases present at diagnosis conferring a poor prognosis. Mechanisms of dissemination are poorly understood and metastatic lesions are genetically divergent from the matched primary tumor. Effective and less toxic therapies

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