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D32202

Sigma-Aldrich

Dibenzothiophene

98%

Synonym(s):

DBT, Diphenylene sulfide

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About This Item

Empirical Formula (Hill Notation):
C12H8S
CAS Number:
132-65-0
Molecular Weight:
184.26
Beilstein/REAXYS Number:
121101
EC Number:
205-072-9
MDL number:
MFCD00004969
UNSPSC Code:
12352100
PubChem Substance ID:
24893734
NACRES:
NA.22

Quality Level

200

assay

98%

form

powder or crystals

bp

332-333 °C (lit.)

mp

97-100 °C (lit.)

SMILES string

c1ccc2c(c1)sc3ccccc23

InChI

1S/C12H8S/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H

InChI key

IYYZUPMFVPLQIF-UHFFFAOYSA-N

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Application

Dibenzothiophene (DBT) can be used as:
  • A starting material for the synthesis of corresponding sulfoxide and sulfone by oxidative desulfurization using various catalysts.
  • A template for the synthesis of surface molecular imprinted polymer (SMIP). SMIP is applicable for the removal of dibenzothiophene during desulfurization of the gasoline
  • A precursor for the synthesis of DBT based π-conjugating polymers.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

338.0 °F

flash_point_c

170 °C

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCG4704
BCCC9424
BCCC5301
BCCB1195
BCCB1193

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Synthesis of novel π-conjugating polymers based on dibenzothiophene
Nemoto N, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 41(10), 1521-1526 (2003)
Hydrodesulfurization of dibenzothiophene over siliceous MCM-41-supported nickel phosphide catalysts
Wang, A, et al.
J. Catal., 229(2), 314-321 (2005)
Hydrodesulfurization of dibenzothiophene and 4, 6-dimethyldibenzothiophene over sulfided NiMo/γ-Al2O3, CoMo/γ-Al2O3, and Mo/γ-Al2O3 catalysts
Egorova, Marina and Prins, Roel
J. Catal., 225(2), 417-427 (2004)
Synthesis and characterization of a surface molecular imprinted polymer as a new adsorbent for the removal of dibenzothiophene
Yang W, et al.
Journal of Chemical and Engineering Data, 57(6), 1713-1720 (2012)
Olga Senko et al.
Molecules (Basel, Switzerland), 24(9) (2019-05-08)
Sulfur recovery from organic molecules such as toxic sulfones is an actual problem, and its solution through the use of environmentally friendly and nature-like processes looks attractive for research and application. For the first time, the possible bioconversion of organic
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Protocols

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GC Analysis of Polynuclear Aromatic Hydrocarbons (PAHs) in Salmon on SPB®-608 (20 m x 0.18 mm I.D., 0.18 µm) after QuEChERS Cleanup using Supel™ QuE Z-Sep, Fast GC Analysis

GC Analysis of Polynuclear Aromatic Hydrocarbons (PAHs) in Salmon on SPB®-608 (20 m x 0.18 mm I.D., 0.18 µm) after QuEChERS Cleanup using Supel™ QuE Z-Sep, Fast GC Analysis

GC Analysis of Polynuclear Aromatic Hydrocarbons (PAHs) in Salmon on SPB®-608 (20 m x 0.18 mm I.D., 0.18 µm) after QuEChERS Cleanup using Supel™ QuE Z-Sep, Fast GC Analysis

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