479411
4,6-Dimethyldibenzothiophene
97%
Synonym(s):
4,6-DMDBT
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About This Item
Empirical Formula (Hill Notation):
C14H12S
CAS Number:
Molecular Weight:
212.31
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
214-894-7
MDL number:
Product Name
4,6-Dimethyldibenzothiophene, 97%
InChI key
MYAQZIAVOLKEGW-UHFFFAOYSA-N
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
SMILES string
Cc1cccc2c3cccc(C)c3sc12
assay
97%
mp
153-157 °C (lit.)
Quality Level
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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
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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
An efficient synthesis of pure 4,6-dimethyldibenzothiophene.
Meille V, et al.
Tetrahedron, 52(11), 3953-3960 (1996)
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
Gan Ye et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(14), 1903-1908 (2017-04-25)
Oxidative desulfurization is considered to be one of the most promising methods for producing ultra-low-sulfur fuels because it can effectively remove refractory sulfur-containing aromatic compounds under mild conditions. In this work, the oxidative desulfurization performance over UiO-66(Zr) is greatly enhanced
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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