推薦產品
蒸汽壓力
0.42 mmHg ( 20 °C)
品質等級
同位素純度
99.96 atom % D
化驗
≥99.00%
形狀
liquid
自燃溫度
573 °F
expl. lim.
42 %
包裝
pk of 10 × 1 mL
技術
NMR: suitable
雜質
≤0.0250% water
water
折射率
n20/D 1.476 (lit.)
bp
189 °C (lit.)
mp
20.2 °C (lit.)
密度
1.190 g/mL at 25 °C (lit.)
質量偏移
M+6
SMILES 字串
[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]
InChI
1S/C2H6OS/c1-4(2)3/h1-2H3/i1D3,2D3
InChI 密鑰
IAZDPXIOMUYVGZ-WFGJKAKNSA-N
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一般說明
Dimethyl sulfoxide-d6 (DMSO-d6) is a deuterated NMR solvent useful in NMR-based research and analyses. It undergoes photodissociation to generate CD3 radical photoproducts, which have been analyzed by infrared diode laser-absorption spectroscopy. Dissociation dynamics of DMSO-d6 at 193nm was examined using photo fragment translational spectroscopy method.
應用
Dimethyl sulfoxide-d6 may be used as an NMR solvent for 1H and 13C NMR experiments.
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儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 1
閃點（°F）
190.4 °F
閃點（°C）
88 °C
分析證明 (COA)
輸入產品批次/批號來搜索 分析證明 (COA)。在產品’s標籤上找到批次和批號，寫有 ‘Lot’或‘Batch’.。
Unraveling the dissociation of dimethyl sulfoxide following absorption at 193 nm.
Blank DA, et al.
J. Chem. Phys. , 106(2), 539-550 (1997)
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)
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
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.
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