33820
Dibenzyl sulfide
≥95.0% (HPLC)
Synonym(s):
Benzyl sulfide
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About This Item
Linear Formula:
(C6H5CH2)2S
CAS Number:
Molecular Weight:
214.33
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-703-6
Beilstein/REAXYS Number:
1911157
MDL number:
Assay:
≥95.0% (HPLC)
Form:
solid
InChI key
LUFPJJNWMYZRQE-UHFFFAOYSA-N
InChI
1S/C14H14S/c1-3-7-13(8-4-1)11-15-12-14-9-5-2-6-10-14/h1-10H,11-12H2
SMILES string
C(SCc1ccccc1)c2ccccc2
assay
≥95.0% (HPLC)
form
solid
mp
44-47 °C (lit.)
functional group
phenyl, thioether
Quality Level
Related Categories
General description
Sulfur K-edge XANES spectra of dibenzyl sulfide has been measured. Adsorption modes of dibenzyl disulphide on bare and iron-coated silver in 0.5M HCl was studied by surface-enhanced Raman scattering (SERS) spectroscopy. Dibenzyl sulfide undergoes oxidation to dibenzyl sulfoxide by SiO2-HNO3/KBr.
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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)
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
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
N Itoh et al.
FEBS letters, 412(2), 281-284 (1997-07-28)
The degradation of thiodiglycol (I) and benzyl sulfide (II) was attempted using Coriolus versicolor and Tyromyces palustris to investigate the potential ability of basidiomycetes to degrade Yperite (bis(2-chloroethyl) sulfide), a mass-produced and stored chemical warfare agent. I was very rapidly
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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