417939
Dimethyl sulfoxide-d6
"100%", 99.96 atom % D, contains 0.03 % (v/v) TMS
동의어(들):
(Methyl sulfoxide)-d6, DMSO-d6, Hexadeuterodimethyl sulfoxide
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10 X 0.75 ML
₩278,922
25 ML
₩753,536
About This Item
Linear Formula:
(CD3)2SO
CAS Number:
Molecular Weight:
84.17
Beilstein:
1237248
EC Number:
MDL number:
UNSPSC 코드:
12191502
PubChem Substance ID:
NACRES:
NA.21
추천 제품
vapor pressure
0.42 mmHg ( 20 °C)
Quality Level
동위원소 순도
99.96 atom % D
분석
≥99% (CP)
양식
liquid
autoignition temp.
573 °F
포함
0.03 % (v/v) TMS
expl. lim.
42 %
기술
NMR: suitable
불순물
≤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.)
질량 이동
M+6
SMILES string
[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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일반 설명
Dimethyl sulfoxide-d6 (DMSO-d6) is a deuterated NMR solvent containing 0.03% (v/v) TMS (tetramethylsilane). It is 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.[1] Dissociation dynamics of DMSO-d6 at 193nm was examined using photo fragment translational spectroscopy method.[2]
애플리케이션
Dimethyl sulfoxide-d6 (DMSO-d6) may be used as an NMR solvent for 1H and 13C NMR experiments.[3]
추천 제품
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Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point (°F)
190.4 °F
Flash Point (°C)
88 °C
개인 보호 장비
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)
Luís Novo et al.
Molecular pharmaceutics, 12(1), 150-161 (2014-11-11)
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Papawee Suabjakyong et al.
PloS one, 10(3), e0122733-e0122733 (2015-03-27)
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