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Merck
CN

694959

Anthracene

sublimed grade, ≥99%

Synonym(s):

Anthraxcene, Paranaphthalene

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About This Item

Empirical Formula (Hill Notation):
C14H10
CAS Number:
120-12-7
Molecular Weight:
178.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329761702
eCl@ss:
39011608
EC Number:
204-371-1
MDL number:
MFCD00001240
Colour Index Number:
10790
Beilstein/REAXYS Number:
1905429
Assay:
≥99%
Form:
crystalline

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InChI

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

SMILES string

c1ccc2cc3ccccc3cc2c1

InChI key

MWPLVEDNUUSJAV-UHFFFAOYSA-N

grade

sublimed grade

vapor density

6.15 (vs air)

vapor pressure

1 mmHg ( 145 °C)

assay

≥99%

form

crystalline

autoignition temp.

1004 °F

loss

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

bp

340 °C (lit.)

Quality Level

100

mp

210-215 °C (lit.)

solubility

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

orbital energy

HOMO 5.7 eV , LUMO 1.7 eV 

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General description

TGA/DSC Lot specific traces available upon request

Application

Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol .

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

249.8 °F - closed cup

flash_point_c

121.0 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - PBT

pictograms

Environment
GHS09

signalword

Danger

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
0000343454
0000343454
0000266482
0000266482
0000015863

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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
Hyunjung Lee et al.
Inorganic chemistry, 51(20), 10904-10915 (2012-09-26)
The tendency of a Hg(II) ion to strongly quench fluorescence of potential fluorescent sensors is explored. Fluorescence measurements show the expected order of the chelation-enhanced fluorescence (CHEF) effect of Zn(II) > Cd(II) > Hg(II) ~ Cu(II), which is interpreted as
Alina P Sergeeva et al.
Journal of the American Chemical Society, 134(43), 18065-18073 (2012-10-04)
Clusters of boron atoms exhibit intriguing size-dependent structures and chemical bonding that are different from bulk boron and may lead to new boron-based nanostructures. We report a combined photoelectron spectroscopic and ab initio study of the 22- and 23-atom boron
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
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
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