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蒸汽壓力
0.42 mmHg ( 20 °C)
同位素純度
99.9 atom % D
化驗
≥99% (CP)
形狀
liquid
自燃溫度
573 °F
包含
1 % (v/v) TMS
expl. lim.
42 %
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
尋找類似的產品？ 前往 產品比較指南
一般說明
二甲基亚砜-d 6 (DMSO-d 6 ) 是氘代溶剂 ，含有 1% (v/v) TMS（四甲基硅烷，作为稳定剂加入）。在 193 和 222 nm 的光辐射下，它发生分解，生成 CD 3 自由基。用红外二极管激光吸收光谱法计算了 CD 3 的量子产率。100%DMSO-d 6 已被用作长程 COSY（相关光谱）实验的溶剂。
應用
DMSO-d6与甘油或甘油-d8一起可形成高粘度的二元溶剂，对复杂的生物活性化合物具有高溶解能力。
推薦產品
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 2
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’.。
Highly Viscous Binary Solvents: DMSO-d6/Glycerol and DMSO-d6/Glycerol-d8 for Polar and Apolar Mixture Analysis by NMR.
Lameiras P and Nuzillard J-M.
AZo Journal of Materials Online, 88(8), 4508-4515 (2016)
M G Nair et al.
Applied and environmental microbiology, 57(2), 434-439 (1991-02-01)
Two isoflavonoids isolated from clover roots grown under phosphate stress were characterized as formononetin (7-hydroxy,4'-methoxy isoflavone) and biochanin A (5,7-dihydroxy,4'-methoxy isoflavone). At 5 ppm, these compounds stimulated hyphal growth in vitro and root colonization of an undescribed vesicular-arbuscular mycorrhiza, a
Using high-performance quantitative NMR (HP-qNMR?) for certifying traceable and highly accurate purity values of organic reference materials with uncertainties< 0.1%.
Weber M, et al.
Accreditation and Quality Assurance, 18(2), 91-98 (2013)
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)
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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