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Merck

45776

Dibenzothiophene

analytical standard

Sinónimos:

DBT, Diphenylene sulfide

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Fórmula empírica (notación de Hill):
C12H8S
Número CAS:
132-65-0
Peso molecular:
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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Nombre del producto

Dibenzothiophene, analytical standard

InChI key

IYYZUPMFVPLQIF-UHFFFAOYSA-N

InChI

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

SMILES string

c1ccc2c(c1)sc3ccccc23

grade

analytical standard

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

Quality Level

100

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Categorías relacionadas

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

Clase de almacenamiento

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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Certificados de análisis (COA)

Lot/Batch Number
BCCH0631
BCBV0147

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Visite la Librería de documentos

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
Shilpi Aggarwal et al.
Molecular bioSystems, 8(10), 2724-2732 (2012-07-27)
Rhodococcus erythropolis has been widely studied for desulfurization. However, activity levels required for commercial application have not been achieved. A major limitation of the current work in biodesulfurization is inadequate information regarding sulfur metabolism generally, and in particular the metabolism
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