추천 제품
Grade
anhydrous
Quality Level
vapor pressure
0.42 mmHg ( 20 °C)
동위원소 순도
99.9 atom % D
분석
≥99.00%
형태
liquid
autoignition temp.
573 °F
expl. lim.
42 %
기술
NMR: suitable
불순물
<50 ppm 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. 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.
애플리케이션
Dimethyl sulfoxide-d6 may be used as an NMR solvent for 1H and 13C NMR experiments.
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
Carbohydrate polymers, 250, 116929-116929 (2020-10-15)
Xylan extracted from corn cobs was used to produce mesalamine-loaded xylan microparticles (XMP5-ASA) by cross-linking polymerization using a non-hazardous cross-linking agent. The microparticles were characterized by thermal analysis (DSC/TG), X-ray diffraction (XRD), Infrared spectroscopy (FTIR-ATR) and scanning electron microscopy (SEM).
Unraveling the dissociation of dimethyl sulfoxide following absorption at 193 nm.
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.
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.
J. Chem. Phys. , 106(4), 1346-1352 (1997)
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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