441392
Dimethyl sulfoxide-d6
99.9 atom % D
Synonym(s):
(Methyl sulfoxide)-d6, DMSO-d6, Hexadeuterodimethyl sulfoxide
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
(CD3)2SO
CAS Number:
Molecular Weight:
84.17
EC Number:
218-617-0
UNSPSC Code:
12191502
PubChem Substance ID:
Beilstein/REAXYS Number:
1237248
MDL number:
Isotopic purity:
99.9 atom % D
Assay:
99% (CP)
Mass shift:
M+6
Form:
liquid
vapor pressure
0.42 mmHg ( 20 °C)
Quality Level
isotopic purity
99.9 atom % D
assay
99% (CP)
form
liquid
autoignition temp.
573 °F
expl. lim.
42 %
packaging
pk of 10 × 0.75 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
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
Still not finding the right product?
Explore all of our products under Dimethyl sulfoxide-d6
Storage Class
10 - Combustible liquids
wgk
WGK 1
flash_point_f
190.4 °F
flash_point_c
88 °C
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
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.
Pedro Aqueveque et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 70(3-4), 97-102 (2015-05-29)
Liquid fermentations of the fungus Stereum rameale (N° 2511) yielded extracts with antibacterial activity. The antibacterial activity reached its peak after 216 h of stirring. Bioassay-guided fractionation methods were employed for the isolation of the bioactive metabolites. Three known compounds
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 441392-0.75ML | 04061837614910 |