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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

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
Hydrotreating activity of bulk NiB alloy in model reaction of hydrodesulfurization 4,6-dimethyldibenzothiophene.
Lewandowski M.
Applied Catalysis. B, Environmental, 160, 10-21 (2014)
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)
An efficient synthesis of pure 4,6-dimethyldibenzothiophene.
Meille V, et al.
Tetrahedron, 52(11), 3953-3960 (1996)
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)
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