推荐产品
蒸汽压
0.42 mmHg ( 20 °C)
质量水平
同位素纯度
≥99.9 atom % D
方案
≥99% (CP)
表单
liquid
自燃温度
573 °F
expl. lim.
42 %
技术
NMR: suitable
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
正在寻找类似产品? 访问 产品对比指南
一般描述
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. Dissociation dynamics of DMSO-d6 at 193nm was examined using photo fragment translational spectroscopy method.
应用
Dimethyl sulfoxide-d6 may be used as an NMR solvent for 1H and 13C NMR experiments.
推荐产品
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.
储存分类代码
10 - Combustible liquids
WGK
WGK 1
闪点(°F)
190.4 °F
闪点(°C)
88 °C
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.
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系技术服务部门