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Merck
CN

694959

蒽

sublimed grade, ≥99%

别名:

蒽, 蒽醌

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关于此项目

经验公式（希尔记法）:
C14H10
化学文摘社编号:
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:
329761702
NACRES:
NA.22

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等级

sublimed grade

质量水平

100

蒸汽密度

6.15 (vs air)

蒸汽压

1 mmHg ( 145 °C)

方案

≥99%

表单

crystalline

自燃温度

1004 °F

缺失

0.5 wt. % loss on heating, 155°C (typical, TGA)

沸点

340 °C (lit.)

mp

210-215 °C (lit.)

溶解性

alcohols: soluble
benzene: soluble
chloroform: soluble
hydronaphthalenes: soluble
supercritical carbon dioxide: soluble

轨道能量

HOMO 5.7 eV 
LUMO 1.7 eV 

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

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相关类别

一般描述

可按要求提供 TGA/DSC 指定批次追溯

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。

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

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0000343454
0000343454
0000266482
0000266482
0000015863

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Kohei Yazaki et al.
Chemical communications (Cambridge, England), 49(16), 1630-1632 (2013-01-23)
A bowl-shaped organic host was prepared by linking two anthracene-embedded bispyridine ligands with two methylene spacers. The water-soluble host has a hemispherical hydrophobic cavity (∼1 nm in diameter) with two cationic methylenebispyridinyl (Lewis acidic) moieties and shows the selective recognition
Ling-Bao Xing et al.
Langmuir : the ACS journal of surfaces and colloids, 29(9), 2843-2848 (2013-02-12)
A new type of anthracene organogelator based on uracil was obtained using organic aromatic solvents, cyclohexane, DMSO, ethanol, and ethyl acetate. It was further characterized by field-emission scanning electron microscopy and transmission electron microscopy. Specifically, the resulting organogels were demonstrated
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
Yongshu Xie et al.
Chemical communications (Cambridge, England), 48(94), 11513-11515 (2012-10-24)
2,2'-Dipyridylamine and anthracene units were linked to afford highly emissive compounds whose Cu(2+) ensembles were developed as effective fluorescence turn-on CN(-) probes.
Payam Payamyar et al.
Chimia, 67(4), 283-285 (2013-08-24)
We describe the challenges involved with extending the limited lateral size of two-dimensional polymers (2DPs). An amphiphilic monomer with three-fold symmetry is chosen to form an ideally tessellated monolayer at the air/water interface. Anthracene [4+4] photo-dimerization is chosen as the
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