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Merck
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Key Documents

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45776

Supelco

Dibenzothiophene

analytical standard

Sinónimos:

DBT, Diphenylene sulfide

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About This Item

Fórmula empírica (notación de Hill):
C12H8S
Número de CAS:
132-65-0
Peso molecular:
184.26
Beilstein/REAXYS Number:
121101
EC Number:
205-072-9
MDL number:
MFCD00004969
UNSPSC Code:
41116107
PubChem Substance ID:
329756946
NACRES:
NA.24

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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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.

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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_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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Certificados de análisis (COA)

Lot/Batch Number
BCCH0631
BCBV0147
SZBC340XV
SZB9315XV
SZE9315X

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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
Palladium-catalyzed double C-H activation directed by sulfoxides in the synthesis of dibenzothiophenes.
Rajarshi Samanta et al.
Angewandte Chemie (International ed. in English), 50(22), 5217-5220 (2011-04-21)
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
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
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