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479411

Sigma-Aldrich

4,6-Dimethyldibenzothiophene

97%

Synonym(s):

4,6-DMDBT

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About This Item

Empirical Formula (Hill Notation):
C14H12S
CAS Number:
1207-12-1
Molecular Weight:
212.31
EC Number:
214-894-7
MDL number:
MFCD00216264
UNSPSC Code:
12352100
PubChem Substance ID:
24871616
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

153-157 °C (lit.)

SMILES string

Cc1cccc2c3cccc(C)c3sc12

InChI

1S/C14H12S/c1-9-5-3-7-11-12-8-4-6-10(2)14(12)15-13(9)11/h3-8H,1-2H3

InChI key

MYAQZIAVOLKEGW-UHFFFAOYSA-N

General description

4,6-Dimethyldibenzothiophene (4,6-DMDBT), a high refractory sulfur compound, is commonly found in diesel fuel. Its synthesis has been reported. The hydrodesulfurization of 4,6-DMDBT using bulk nickel alloy, bulk tungsten phosphide (WP), NiMo sulfide supported on active carbons and molecularly imprinted polymers have been reported. The dielectric behavior of 4,6-DMDBT under different microwave frequencies and temperature has been investigated.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBH6801
SHBD7685V
SHBC7015V
SHBC3632V
SHBC6994V

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Meiqin Zheng et al.
Journal of hazardous materials, 362, 424-435 (2018-09-28)
In this work, the adsorption desulfurization performance and adsorption diffusion study of B2O3 modified Ag-CeOx/TiO2-SiO2 adsorbent were investigated. The adsorption desulfurization performance was studied by batch and fixed bed tests. The homogeneous surface diffusion model (HSDM) was employed to investigate
Hussein N Nassar et al.
Environmental science and pollution research international, 28(7), 8102-8116 (2020-10-14)
One of the main precursors of air pollution and acid rains is the presence of the recalcitrant thiophenic compounds, for example dibenzothiophene (DBT) and its derivatives in transportation fuels. In an attempt to achieve the worldwide regulations of ultra-low sulfur
Hydrodesulfurization kinetics and mechanism of 4,6-dimethyldibenzothiophene over NiMo catalyst supported on carbon.
Sakanishi K, et al.
J. Mol. Catal. A: Chem., 155(1), 101-109 (2000)
Development of a novel molecularly imprinted polymer for the retention of 4,6-dimethyldibenzothiophene.
Tom LA, et al.
Microchimica Acta, 176(3-4), 375-380 (2012)
Hydrodesulfurization of dibenzothiophene, 4,6-dimethyldibenzothiophene, and their hydrogenated intermediates over bulk tungsten phosphide.
Yang L, et al.
J. Catal., 330, 330-343 (2015)
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