Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

479411

Sigma-Aldrich

4,6-Dimethyldibenzothiophene

97%

Synonym(s):

4,6-DMDBT

Sign Into View Organizational & Contract Pricing
All Photos(3)

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SHBH6801
SHBD7685V
SHBC7015V
SHBC3632V
SHBC6994V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
Yanqi Xu et al.
Dalton transactions (Cambridge, England : 2003), 45(48), 19511-19518 (2016-11-30)
Deep desulfurization is a challenging task and global efforts are focused on the development of new approaches for the reduction of sulfur-containing compounds in fuel oils. In this work, we have proposed a new design strategy for the development of
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
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)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service