569585
二甲基亚砜-d 6
99.9 atom % D, anhydrous
别名:
DMSO-d6, 二甲基亚砜-d6, 氘代二甲亚砜
等级
anhydrous
蒸汽压
0.42 mmHg ( 20 °C)
同位素纯度
99.9 atom % D
方案
≥99.00%
自燃温度
573 °F
expl. lim.
42 %
杂质
<50 ppm water
折射率
n20/D 1.476 (lit.)
沸点
189 °C (lit.)
mp
20.2 °C (lit.)
密度
1.190 g/mL at 25 °C (lit.)
质量偏移
M+6
SMILES字符串
[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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一般描述
Dimethyl sulfoxide-d6 (DMSO-d6) is a deuterated NMR solvent. It is an anhydrous solvent, which minimizes any interference from water peaks. It is useful in performing critical air- and moisture-sensitive NMR analysis. 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.
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
190.4 °F
闪点(°C)
88 °C
法规信息
新产品
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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)
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
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)
Luís Novo et al.
Molecular pharmaceutics, 12(1), 150-161 (2014-11-11)
The applicability of small interfering RNA (siRNA) in future therapies depends on the availability of safe and efficient carrier systems. Ideally, siRNA delivery requires a system that is stable in the circulation but upon specific uptake into target cells can
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