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Sigma-Aldrich

Dibenzyl diselenide

95%

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About This Item

Linear Formula:
(C6H5CH2)2Se2
CAS Number:
1482-82-2
Molecular Weight:
340.18
MDL number:
MFCD00004767
UNSPSC Code:
12352100
PubChem Substance ID:
24857671

assay

95%

mp

91-93 °C (lit.)

SMILES string

C([Se][Se]Cc1ccccc1)c2ccccc2

signalword

Danger

Hazard Classifications

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

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
06910AI
05714KR
05714EC
16530MN

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T Shimada et al.
Cancer research, 57(21), 4757-4764 (1997-11-14)
The effects of synthetic chemopreventive organoselenium compounds 1,2-, 1,3-, and 1,4-phenylenebis(methylene)selenocyanate (o-, m-, and p-XSC, respectively), benzyl selenocyanate (BSC), and dibenzyl diselenide (DDS) and inorganic sodium selenite on the oxidation of xenobiotics and procarcinogens by human cytochrome P450 (P450 or
K el-Bayoumy et al.
Chemical research in toxicology, 4(5), 560-565 (1991-09-01)
Benzyl selenocyanate (BSC), a synthetic organoselenium compound, has been shown to inhibit chemically induced tumors in several animal model systems. However, it is not known whether BSC or one of its metabolites is responsible for the chemopreventive effect. An initial
B S Reddy et al.
Anticancer research, 16(3A), 1123-1127 (1996-05-01)
Our previous studies have demonstrated that dietary benzylselenocyanate (BSC) and 1,4-phenylenebis (methylene) selenocyanate (p-XSC); organoselenium compounds, act as potential chemopreventive agents in colon carcinogenesis in F344 rats. As a part of a program aimed to develop less toxic and more
Yapei Wang et al.
Langmuir : the ACS journal of surfaces and colloids, 22(13), 5552-5555 (2006-06-14)
We report on the use of block copolymer micelles of polystyrene-b-poly(acrylic acid) (PS-b-PAA) as matrixes for incorporating dibenzyl diselenide. We found that the water-insoluble diselenide, after being incorporated into the micelles, demonstrates glutathione peroxidase (GPx) activity in water. Surprisingly, the

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