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45776

Dibenzothiophene

analytical standard

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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756946
EC Number:
205-072-9
Beilstein/REAXYS Number:
121101
MDL number:
MFCD00004969
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grade

analytical standard

Quality Level

100

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

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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.

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

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
BCCH0631
BCBV0147

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Meijun Li et al.
Journal of chromatography. A, 1233, 126-136 (2012-03-03)
Polycyclic aromatic sulfur heterocyclics (PASHs) consist mainly of thiophene class compounds, and are the most important organosulfur compounds in crude oils and sediment extracts. Dibenzothiophene (DBT) and its methylated homologues were identified on mass chromatograms by comparison with retention indices
Christian Zeigler et al.
Analytical chemistry, 84(5), 2245-2252 (2012-02-22)
Polycyclic aromatic sulfur heterocycles (PASH) are sulfur analogues of polycyclic aromatic hydrocarbons (PAH). Alkylated PAH attract much attention as carcinogens, mutagens, and as diagnostics for environmental forensics. PASH, in contrast, are mostly ignored in the same studies due to the
Shilpi Aggarwal et al.
FEMS microbiology letters, 315(2), 115-121 (2010-12-25)
Rhodococcus erythropolis has been studied widely for potential applications in biodesulfurization. Previous works have been largely experimental with an emphasis on the characterization and genetic engineering of desulfurizing strains for improved biocatalysis. A systems modeling approach that can complement these
Ellen M Cooper et al.
Environmental toxicology and chemistry, 29(11), 2409-2416 (2010-09-24)
Biodegradation of pollutants often results in incomplete mineralization and formation of degradation products with unknown chemical and toxicological characteristics. Ultraviolet (UV) irradiation, a common technology used in water and wastewater treatment, may help reduce aqueous concentrations of degradation products produced
Adeniyi S Ogunlaja et al.
Dalton transactions (Cambridge, England : 2003), 41(45), 13908-13918 (2012-10-02)
The reaction between [V(IV)OSO(4)] and the tetradentate N(2)O(2)-donor Schiff base ligand, N,N-bis(o-hydroxybenzaldehyde)phenylenediamine (sal-HBPD), obtained by the condensation of salicylaldehyde and o-phenylenediamine in a molar ratio of 2 : 1 respectively, resulted in the formation of [V(IV)O(sal-HBPD)]. The molecular structure of
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Global Trade Item Number

SKUGTIN
45776-250MG04061832342399

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