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33820

Sigma-Aldrich

Dibenzyl sulfide

≥95.0% (HPLC)

Synonym(s):

Benzyl sulfide

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100 G
$111.00

About This Item

Linear Formula:
(C6H5CH2)2S
CAS Number:
538-74-9
Molecular Weight:
214.33
Beilstein/REAXYS Number:
1911157
EC Number:
208-703-6
MDL number:
MFCD00004784
UNSPSC Code:
12352100
PubChem Substance ID:
57648912
NACRES:
NA.22

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assay

≥95.0% (HPLC)

form

solid

mp

44-47 °C (lit.)

functional group

phenyl
thioether

SMILES string

C(SCc1ccccc1)c2ccccc2

InChI

1S/C14H14S/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2

InChI key

LUFPJJNWMYZRQE-UHFFFAOYSA-N

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General description

Sulfur K-edge XANES spectra of dibenzyl sulfide has been measured.[1] Adsorption modes of dibenzyl disulphide on bare and iron-coated silver in 0.5M HCl was studied by surface-enhanced Raman scattering (SERS) spectroscopy.[2] Dibenzyl sulfide undergoes oxidation to dibenzyl sulfoxide by SiO2-HNO3/KBr.[3]

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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H Rösner et al.
Biochimica et biophysica acta, 1540(2), 166-177 (2001-08-22)
Dibenzyl trisulphide (DTS), a main lipophilic compound in Petiveria alliacea L. (Phytolaccaceae), was identified as one of the active immunomodulatory compounds in extracts of the plant. To learn more about its biological activities and molecular mechanisms, we conducted one-dimensional NMR
A SERS Study on Adsorption of Dibenzyl Disulfide, Sulfide, and Sulfoxide on an Iron-Deposited Silver Electrode in a Hydrochloric Acid Solution.
Ohno N, et al.
Journal of the Electrochemical Society, 140(9), 2512-2519 (1993)
Francesco Naso et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(48), 13417-13426 (2009-11-13)
An experimental investigation of the enantioselective oxidation of aryl benzyl sulfides by tert-butyl hydroperoxide in the presence of a titanium/hydrobenzoin catalyst has shown that these sulfides are ideal substrates for this catalytic system, with negligible interference by the substituents on
Jonathan D Van Hamme et al.
Applied and environmental microbiology, 69(2), 1320-1324 (2003-02-07)
Microbial metabolism of organosulfur compounds is of interest in the petroleum industry for in-field viscosity reduction and desulfurization. Here, dibenzyl sulfide (DBS) metabolism in white rot fungi was studied. Trametes trogii UAMH 8156, Trametes hirsuta UAMH 8165, Phanerochaete chrysosporium ATCC
B Lei et al.
Journal of bacteriology, 178(19), 5699-5705 (1996-10-01)
The oxidation of dibenzothiophene to dibenzothiophene sulfone has been linked to the enzyme encoded by the sox/dszC gene from Rhodococcus sp. strain IGTS8 (S. A. Denome, C. Oldfield, L. J. Nash, and K. D. Young, J. Bacteriol. 176:6707-6717, 1994; C.
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