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151874

Sigma-Aldrich

Sulfoxyde de diméthyle-d6, Diméthylsulfoxyde-d6

99.9 atom % D

Synonyme(s) :

(Sulfoxyde de méthyle)-d6, (Méthylsulfoxyde)-d6, DMSO-d6, Hexadeutérodiméthyl sulfoxyde, Hexadeutérodiméthylsulfoxyde

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About This Item

Formule linéaire :
(CD3)2SO
Numéro CAS:
Poids moléculaire :
84.17
Numéro Beilstein :
1237248
Numéro CE :
Numéro MDL:
Code UNSPSC :
12191502
ID de substance PubChem :
Nomenclature NACRES :
NA.11

Pression de vapeur

0.42 mmHg ( 20 °C)

Niveau de qualité

Pureté isotopique

99.9 atom % D

Pureté

99% (CP)

Forme

liquid

Température d'inflammation spontanée

573 °F

Limite d'explosivité

42 %

Technique(s)

NMR: suitable

Impuretés

≤0.0250% water
water

Indice de réfraction

n20/D 1.476 (lit.)

Point d'ébullition

189 °C (lit.)

Pf

20.2 °C (lit.)

Densité

1.190 g/mL at 25 °C (lit.)

Changement de masse

M+6

Chaîne SMILES 

[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]

InChI

1S/C2H6OS/c1-4(2)3/h1-2H3/i1D3,2D3

Clé InChI

IAZDPXIOMUYVGZ-WFGJKAKNSA-N

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Application


  • Investigation of the Spatial Structure of Flufenamic Acid in Supercritical Carbon Dioxide Media via 2D NOESY.: This research explores the molecular interactions of flufenamic acid in supercritical CO2, highlighting analytical techniques using Dimethyl sulfoxide-d₆ as a solvent to enhance spectral readings (Khodov et al., 2023).

  • Taguchi Approach for Optimization of a Green Quantitative 1H-NMR Practice for Characterization of Levetiracetam and Brivaracetam in Pharmaceuticals.: Utilizes Dimethyl sulfoxide-d₆ in NMR spectroscopy to refine analytical methods for characterizing pharmaceuticals, aiming for environmental sustainability (Mansour et al., 2022).

  • Counterintuitive torsional barriers controlled by hydrogen bonding.: Investigates molecular torsion influenced by hydrogen bonding, with Dimethyl sulfoxide-d₆ employed to study solvent effects, contributing to our understanding of molecular dynamics in analytical chemistry (Barbero et al., 2020).

  • Elucidating Interactions between DMSO and Chelate-Based Ionic Liquids.: Examines the interaction dynamics between Dimethyl sulfoxide-d₆ and ionic liquids, offering insights into solvent-solute interactions critical in analytical methodologies (Chen et al., 2015).

  • Conformation of an octapeptide fragment (2-9) of kaliocin-1 in DMSO-d6 by 1H NMR and restrained molecular dynamics.: This study uses Dimethyl sulfoxide-d₆ in NMR to elucidate the conformational properties of a peptide, aiding in the understanding of peptide structure under analytical conditions (Sunilkumar et al., 2007).

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À utiliser avec

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

190.4 °F

Point d'éclair (°C)

88 °C


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Mika Henrikki Sipponen et al.
Nature communications, 9(1), 2300-2300 (2018-06-14)
Dehydration reactions proceed readily in water-filled biological cells. Development of biocatalysts that mimic such compartmentalized reactions has been cumbersome due to the lack of low-cost nanomaterials and associated technologies. Here we show that cationic lignin nanospheres function as activating anchors
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.
Pedro Aqueveque et al.
Zeitschrift fur Naturforschung. C, Journal of biosciences, 70(3-4), 97-102 (2015-05-29)
Liquid fermentations of the fungus Stereum rameale (N° 2511) yielded extracts with antibacterial activity. The antibacterial activity reached its peak after 216 h of stirring. Bioassay-guided fractionation methods were employed for the isolation of the bioactive metabolites. Three known compounds
Nik Khairunissa Nik Abdullah Zawawi et al.
Bioorganic & medicinal chemistry, 23(13), 3119-3125 (2015-05-24)
A library of novel 2,5-disubtituted-1,3,4-oxadiazoles with benzimidazole backbone (3a-3r) was synthesized and evaluated for their potential as β-glucuronidase inhibitors. Several compounds such as 3a-3d, 3e-3j, 3l-3o, 3q and 3r showed excellent inhibitory potentials much better than the standard (IC50=48.4±1.25μM: d-saccharic

Articles

Use this reference table to find the coupling values and chemical shifts of our NMR (deuterated) solvents. Melting and boiling points, molecular weight, density, and CAS number are also listed.

Contenu apparenté

NMR spectroscopy elucidates molecular structure and purity via nuclear spin states in a strong magnetic field.

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