437697
二甲基亚砜-d 6
99.5 atom % D, contains 0.1 % (v/v) TMS
别名:
DMSO-d6, 二甲基亚砜-d6, 氘代二甲亚砜
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关于此项目
线性分子式:
(CD3)2SO
化学文摘社编号:
分子量:
84.17
EC Number:
218-617-0
UNSPSC Code:
12142201
PubChem Substance ID:
Beilstein/REAXYS Number:
1237248
MDL number:
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
99.5 atom % D
assay
≥99.00%
form
liquid
autoignition temp.
573 °F
contains
0.1 % (v/v) TMS
expl. lim.
42 %
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
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General description
Dimethyl sulfoxide-d6 (DMSO-d6) is a deuterated NMR solvent containing 0.1%(v/v) TMS (tetramethylsilane). 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.
Application
Dimethyl sulfoxide-d6 may be used as an NMR solvent for 1H and 13C NMR experiments.
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
190.4 °F
flash_point_c
88 °C
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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
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
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