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
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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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Hydrotreating activity of bulk NiB alloy in model reaction of hydrodesulfurization 4,6-dimethyldibenzothiophene.
Lewandowski M.
Applied Catalysis. B, Environmental, 160, 10-21 (2014)
Peiwen Wu et al.
Journal of hazardous materials, 391, 122183-122183 (2020-02-10)
Metal-free catalysts have been proved to be a low-cost and environmentally friendly species in aerobic oxidative desulfurization (ODS). In this work, exfoliated metal-free boron carbide with few-layered structure, small size, and abundant defects, was first employed in an aerobic ODS
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)
Dielectric properties of quinoline, 4,6-dimethyldibenzothiophene and hexadecane as model compounds in the upgrading of LCO.
Donaldson AA, et al.
Fuel Processing Technology, 92(9), 1733-1737 (2011)
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