45776
Dibenzothiophene
analytical standard
Synonym(s):
DBT, Diphenylene sulfide
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About This Item
Empirical Formula (Hill Notation):
C12H8S
CAS Number:
Molecular Weight:
184.26
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
205-072-9
Beilstein/REAXYS Number:
121101
MDL number:
grade
analytical standard
Quality Level
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
332-333 °C (lit.)
mp
97-100 °C (lit.)
application(s)
environmental
format
neat
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
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1
Storage Class
11 - Combustible Solids
wgk
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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Mykola Seredych et al.
ChemSusChem, 4(1), 139-147 (2011-01-13)
Adsorption of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (DMDBT) from simulated diesel fuel was investigated with polymer-derived carbon matrices. Sulfur was incorporated to the carbon surface via a high-temperature hydrogen sulfide reduction of oxygen-containing groups. The resultant carbons were characterized by nitrogen
A Stephen K Hashmi et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(21), 6576-6580 (2012-04-21)
With the IPr ligand (IPr=1,3-bis-(2,6-diisopropylphenyl)imidazol-2-ylidene) on gold(I) excellent yields in the benzanellation of 2-substituted thiophenes, benzothiophenes, pyrroles, benzofurans, and indoles were achieved. The 1-siloxybut-3-ynyl side chains, incorporated in the anellation, are easily accessible by the addition of a propargyl metal
Santhosh Reddy Patpi et al.
Journal of medicinal chemistry, 55(8), 3911-3922 (2012-03-28)
A molecular hybridization approach is an emerging structural modification tool to design new molecules with improved pharmacophoric properties. In this study, 1,2,3-triazole-based Mycobacterium tuberculosis inhibitors and synthetic and natural product-based tricyclic (carbazole, dibenzo[b,d]furan, and dibenzo[b,d]thiophene) antimycobacterial agents were integrated in