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Merck
CN

347833

Sigma-Aldrich

二苯并噻吩

≥99%

别名:

DBT, 二苯噻吩

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About This Item

经验公式(希尔记法):
C12H8S
CAS号:
分子量:
184.26
Beilstein:
121101
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

≥99%

表单

crystalline (powder)

颜色

white

沸点

332-333 °C (lit.)

mp

97-100 °C (lit.)

SMILES字符串

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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一般描述

二苯并噻吩是多环芳烃((PAH)的重要代表。在高压流动微反装置上研究了预硫化钼铝催化剂上二苯并噻吩加氢脱硫的动力学。已经报道了高温菌 枯草芽孢杆菌 WU-S2B 对二苯并噻吩的生物脱硫。

应用

以二苯并噻吩作为重质硫化物,研究了重质硫化物对流化催化裂化 (FCC) 汽油馏分中硫含量的影响。

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

预防措施声明

危险分类

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

338.0 °F

闪点(°C)

170 °C

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The effect of heavy aromatic sulfur compounds on sulfur in cracked naphtha.
Valla JA, et al.
Catalysis Today, 127(1), 92-98 (2007)
K Kirimura et al.
Journal of bioscience and bioengineering, 91(3), 262-266 (2005-10-20)
Heterocyclic organosulfur compounds such as dibenzothiophene (DBT) in petroleum cannot be completely removed by hydrodesulfurization using chemical catalysts. A moderately thermophilic bacterium Bacillus subtilis WU-S2B, which could desulfurize DBT at 50 degrees C through the selective cleavage of carbon-sulfur (CS)
Selectivity of molybdenum catalyst in hydrodesulfurization, hydrodenitrogenation, and hydrodeoxygenation: Effect of additives on dibenzothiophene hydrodesulfurization.
Nagai M and Toshiaki Kabe.
J. Catal., 81(2), 440-449 (1983)
Kristina Lång et al.
European radiology, 26(1), 184-190 (2015-05-02)
To assess the performance of one-view digital breast tomosynthesis (DBT) in breast cancer screening. The Malmö Breast Tomosynthesis Screening Trial is a prospective population-based one-arm study with a planned inclusion of 15000 participants; a random sample of women aged 40-74
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

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