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33820

Dibenzyl sulfide

≥95.0% (HPLC)

Synonym(s):

Benzyl sulfide

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100 G

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$119.00

Estimated to ship onDecember 15, 2025Details

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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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Quality Level

100

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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Show Differences

1 of 4

This Item
3435281392933630
Dibenzyl sulfide ≥95.0% (HPLC)

Sigma-Aldrich

33820

Dibenzyl sulfide

Benzyl sulfone 99%

Sigma-Aldrich

343528

Benzyl sulfone

Benzyl thiocyanate ≥95.0% (GC)

Sigma-Aldrich

13929

Benzyl thiocyanate

Dibenzyl ether purum, ≥98.0% (GC)

Sigma-Aldrich

33630

Dibenzyl ether

assay

≥95.0% (HPLC)

assay

99%

assay

≥95.0% (GC)

assay

≥98.0% (GC)

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

form

solid

form

solid

form

solid

form

liquid

mp

44-47 °C (lit.)

mp

-

mp

39-41 °C (lit.)

mp

1.5-3.5 °C (lit.)

functional group

phenyl

functional group

phenyl, sulfone

functional group

phenyl, thiocyanate, thioether

functional group

ether, phenyl

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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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
I L Genz et al.
Zentralblatt fur Bakteriologie, Parasitenkunde, Infektionskrankheiten und Hygiene. Zweite naturwissenschaftliche Abteilung: Mikrobiologie der Landwirtschaft der Technologie und des Umweltschutzes, 135(4), 308-312 (1980-01-01)
A diffusion cell type which is suitable for investigation of water-insoluble compounds is shown. The chamber consists of two compartments, the so-called bottom-chamber, which contains the solid substance under investigation, and the main chamber, which is above it. In this
Chemo and homoselective catalytic oxidation of sulfides to sulfoxides with supported nitric acid on silica gel and poly vinyl pyrrolidone (PVP) catalyzed by KBr and/or NaBr.
Zolfigol MA, et al.
Catalysis Communications, 9(8), 1739-1744 (2008)
Robert Beck et al.
Dalton transactions (Cambridge, England : 2003), (37)(37), 4981-4983 (2008-09-20)
C-H activation through the coordination of a benzyl sulfide anchoring group with a C-S bond cleavage at a Co(v) center constitutes a regiospecific access to four- and five-membered metallacycles under mild conditions.
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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