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328502

Sigma-Aldrich

Dimethyl diselenide

96%

Synonym(s):

Methyl diselenide

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About This Item

Linear Formula:
(CH3)2Se2
CAS Number:
Molecular Weight:
187.99
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

form

liquid

refractive index

n20/D 1.6388 (lit.)

bp

155-157 °C (lit.)

density

1.987 g/mL at 25 °C (lit.)

SMILES string

C[Se][Se]C

InChI

1S/C2H6Se2/c1-3-4-2/h1-2H3

InChI key

VLXBWPOEOIIREY-UHFFFAOYSA-N

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General description

Dimethyl diselenide is a volatile selenium species and its determination in biological samples by HPLC-inductively coupled argon plasma mass spectrometry was reported. Selenium alkylation with dimethyl diselenide was reported by solid-phase microextraction gas chromatography-mass spectrometry.

Application

Dimethyl diselenide is the most powerful reagent used to identify distonic radical cations.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Flam. Liq. 3 - STOT RE 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

140.0 °F - closed cup

Flash Point(C)

60 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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K K Thoen et al.
Journal of the American Society for Mass Spectrometry, 7(12), 1245-1250 (1996-12-01)
Dimethyl diselenide is demonstrated to be among the most powerful reagents used to identify distonic radical cations. Most such ions readily abstract CH3Se from dimethyl diselenide. The reaction is faster and more exclusive than CH3S(·) abstraction from dimethyl disulfide, a
William J Hunter et al.
Journal of chromatography. A, 1038(1-2), 295-297 (2004-07-06)
A simple method for the determination of volatile selenium compounds employing a gas chromatograph equipped with a photoionization detector is described. The method involves the direct injection of dimethylselenide (DMS) or dimethyldiselenide (DMDS) into the gas chromatograph; no derivatization of
Kathrin Schilling et al.
Journal of environmental quality, 40(3), 1021-1027 (2011-05-07)
If volatile organoselenides are to be analyzed for their stable Se isotope composition to elucidate sources and formation processes, organoselenides need to be trapped quantitatively to avoid artificial Se isotope fractionation. We developed an efficient trap of organoselenides to be
Elimination of selenium compounds by mice through formation of different volatile selenides.
S Jiang et al.
Experientia, 39(3), 293-294 (1983-03-15)
Yiqiang Zhang et al.
Journal of environmental quality, 31(4), 1124-1128 (2002-08-15)
Volatilization of dimethyldiselenide (DMDSe) is one of the most important processes for removing selenium (Se) from Se-contaminated environments. However, the fate of DMDSe in soil is not known. In this study, we monitored the changes of DMDSe in the head

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