Skip to Content
Merck

441392

Dimethyl sulfoxide-d6

99.9 atom % D

Synonym(s):

(Methyl sulfoxide)-d6, DMSO-d6, Hexadeuterodimethyl sulfoxide

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(1)

About This Item

Linear Formula:
(CD3)2SO
CAS Number:
2206-27-1
Molecular Weight:
84.17
EC Number:
218-617-0
UNSPSC Code:
12191502
PubChem Substance ID:
24867659
Beilstein/REAXYS Number:
1237248
MDL number:
MFCD00002090

Product Name

Dimethyl sulfoxide-d6, 99.9 atom % D

InChI key

IAZDPXIOMUYVGZ-WFGJKAKNSA-N

InChI

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

SMILES string

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

vapor pressure

0.42 mmHg ( 20 °C)

isotopic purity

99.9 atom % D

assay

99% (CP)

form

liquid

autoignition temp.

573 °F

expl. lim.

42 %

packaging

pk of 10 × 0.75 mL

technique(s)

NMR: suitable

impurities

≤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.)

mass shift

M+6

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Storage Class

10 - Combustible liquids

wgk

WGK 1

flash_point_f

190.4 °F

flash_point_c

88 °C

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKBJ4100V
STBC8888V
STBC6337V
MKBH8447V
MKBJ2066V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Gianni Colotti et al.
Amino acids, 52(2), 247-259 (2019-05-01)
Leishmania protozoans are the causative agent of leishmaniasis, a neglected tropical disease consisting of three major clinical forms: visceral leishmaniasis (VL), cutaneous leishmaniasis, and mucocutaneous leishmaniasis. VL is caused by Leishmania donovani in East Africa and the Indian subcontinent and
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
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.
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
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
View All Related Papers

Related Content

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service