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Merck
CN

141062

Sigma-Aldrich

蒽

ReagentPlus®, 99%

别名:

蒽, 蒽醌

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关于此项目

经验公式（希尔记法）:
C14H10
CAS Number:
120-12-7
分子量:
178.23
颜色索引号:
10790
Beilstein:
1905429
EC 号:
204-371-1
MDL编号:
MFCD00001240
UNSPSC代码:
12352100
eCl@ss:
39011608
PubChem化学物质编号:
57647135
NACRES:
NA.22

主要文件

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蒸汽密度

6.15 (vs air)

质量水平

200

蒸汽压

1 mmHg ( 145 °C)

产品线

ReagentPlus®

方案

99%

表单

powder or flakes

自燃温度

1004 °F

颜色

blue-violet fluorescence

沸点

340 °C (lit.)

mp

210-215 °C (lit.)

溶解性

toluene: soluble 20 mg/mL, clear, colorless to faintly yellow
alcohols: soluble
benzene: soluble
chloroform: soluble
hydronaphthalenes: soluble
supercritical carbon dioxide: soluble

SMILES字符串

c1ccc2cc3ccccc3cc2c1

InChI

1S/C14H10/c1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1/h1-10H

InChI key

MWPLVEDNUUSJAV-UHFFFAOYSA-N

基因信息

human ... CYP1A2(1544)

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相关类别

一般描述

蒽衍生物可用于制备稳定的蓝光发射有机电致发光器件 。 分枝杆菌 sp 将其氧化为蒽 顺式 -1,2-二氢二醇。菌株 PYR-12 。它通过与[5,6]-富勒烯C60的[4 + 2]-环加成反应形成双加合物。

应用

蒽已被证明可溶于各种环己酮、乙酸乙酯和甲醇的二元和三元混合物中。
蒽用于研究蒽在超临界CO2中的光二聚反应。

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation markEnvironment
GHS07,GHS09

警示用语：

Warning

危险声明

H319,H410

危险分类

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 2

闪点(°F)

249.8 °F - closed cup

闪点(°C)

121.0 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000460031
0000460031
MKCX9617
0000431141
0000431140

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Christopher E. Bunker et al.
The Journal of organic chemistry, 62(21), 7324-7329 (2001-10-24)
The photodimerization reaction of anthracene in supercritical CO(2) was studied systematically at different CO(2) densities. Unlike in normal liquid solvents, the reaction in supercritical CO(2) is significant even at anthracene concentrations as low as a few micromolar. At comparable anthracene
The bis-adducts of the [5, 6]-fullerene C60 and anthracene.
Duarte-Ruiz A, et al.
Tetrahedron, 57(17), 3709-3714 (2001)
Anthracene derivatives for stable blue-emitting organic electroluminescence devices.
Jianmin S and Tang CW.
Applied Physics Letters, 80(17), 3201-3203 (2002)
J D Moody et al.
Applied and environmental microbiology, 67(4), 1476-1483 (2001-04-03)
Cultures of Mycobacterium sp. strain PYR-1 were dosed with anthracene or phenanthrene and after 14 days of incubation had degraded 92 and 90% of the added anthracene and phenanthrene, respectively. The metabolites were extracted and identified by UV-visible light absorption
Jiang-Fei Xu et al.
Organic letters, 15(24), 6148-6151 (2013-11-19)
Dynamic covalent bonds supplied by reversible anthracene dimerization were combined with pillar[5]arene/imidazole host-guest interactions to construct double-dynamic polymers. Heating such polymers (in solution or as a gel) led to depolymerization by dissociation of either the host-guest complexes alone or the
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