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Merck

94563

Supelco

Dimethylsulfoxid

analytical standard

Synonym(e):

DMSO, Methylsulfoxid

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About This Item

Lineare Formel:
(CH3)2SO
CAS-Nummer:
Molekulargewicht:
78.13
Beilstein:
506008
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12191502
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

Dampfdichte

2.7 (vs air)

Dampfdruck

0.42 mmHg ( 20 °C)

Assay

≥99.95% (GC)

Selbstzündungstemp.

573 °F

Haltbarkeit

limited shelf life, expiry date on the label

Expl.-Gr.

42 %, 63 °F

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Brechungsindex

n20/D 1.479 (lit.)
n20/D 1.479

bp

189 °C (lit.)

mp (Schmelzpunkt)

16-19 °C (lit.)

Löslichkeit

H2O: miscible (completely)

Dichte

1.10 g/mL (lit.)

Anwendung(en)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

Format

neat

SMILES String

CS(C)=O

InChI

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

InChIKey

IAZDPXIOMUYVGZ-UHFFFAOYSA-N

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Allgemeine Beschreibung

Dimethyl Sulfoxide (DMSO) contains both highly polar and apolar groups, which impart it an amphipathic character. It can dissolve in both aqueous and organic solvents. It is a commonly used solvent in hydrophobic pharmaceutical agents, exhibiting effective hydroxyl radical scavenging ability.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food. Find all available reference materials for compounds listed in 10/2011 here

Anwendung

DMSO may be used as an analytical standard for the determination of the analyte in environmental samples by gas chromatography (GC) technique.
Dimethyl sulfoxide may be used as a molecular probe in the detection and analysis of hydroxyl radicals generated in advanced oxidation processes using high performance liquid chromatography(HPLC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Vorsicht

Unterkühlt leicht und schmilzt langsam bei Raumtemperatur. Das verfestigte Produkt kann durch Erwärmen auf Raumtemperatur wieder verflüssigt werden, ohne dabei geschädigt zu werden.

Sonstige Hinweise

For information on dimethyl sulfoxide miscibility, please visit the following link:
Dimethyl Sulfoxide Miscibility/Immiscibility Table

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 1

Flammpunkt (°F)

188.6 °F - closed cup

Flammpunkt (°C)

87 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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Analysenzertifikate (COA)

Lot/Batch Number

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Kunden haben sich ebenfalls angesehen

Determination of hydroxyl radicals in advanced oxidation processes with dimethyl sulfoxide trapping and liquid chromatography
Tai C, et al.
Analytica Chimica Acta, 527(1), 73-80 (2004)
Determination of hydroxyl radicals in advanced oxidation processes with dimethyl sulfoxide trapping and liquid chromatography
Tai C, et al.
Analytica Chimica Acta, 527, 73-80 (2004)
Nuno C Santos et al.
Biochemical pharmacology, 65(7), 1035-1041 (2003-03-29)
DMSO is an amphipathic molecule with a highly polar domain and two apolar methyl groups, making it soluble in both aqueous and organic media. It is one of the most common solvents for the in vivo administration of several water-insoluble
Mulmudi Hemant Kumar et al.
Advanced materials (Deerfield Beach, Fla.), 26(41), 7122-7127 (2014-09-13)
Lead free perovskite solar cells based on a CsSnI3 light absorber with a spectral response from 950 nm is demonstrated. The high photocurrents noted in the system are a consequence of SnF2 addition which reduces defect concentrations and hence the
Björn Zörner et al.
Brain : a journal of neurology, 137(Pt 6), 1716-1732 (2014-04-17)
Anatomical plasticity such as fibre growth and the formation of new connections in the cortex and spinal cord is one known mechanism mediating functional recovery after damage to the central nervous system. Little is known about anatomical plasticity in the

Protokolle

GC Analysis of Class 3 Residual Solvents on SUPELCOWAX® 10

Verwandter Inhalt

Butyl methyl ether; Acetic acid; 2-Butanone; Ethyl acetate; Tetrahydrofuran; 1-Butanol; Isopropyl acetate; Heptane; Propyl acetate; 3-Methylbutanol; 4-Methyl-2-pentanone; Isobutyl acetate; Butyl acetate; Dimethyl sulfoxide; Anisole; Cumene

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