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141062

Sigma-Aldrich

Anthracene

ReagentPlus®, 99%

Sinónimos:

Anthraxcene, Paranaphthalene

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About This Item

Fórmula empírica (notación de Hill):
C14H10
Número de CAS:
120-12-7
Peso molecular:
178.23
Colour Index Number:
10790
Beilstein/REAXYS Number:
1905429
EC Number:
204-371-1
MDL number:
MFCD00001240
UNSPSC Code:
12352100
eCl@ss:
39011608
PubChem Substance ID:
57647135
NACRES:
NA.22

vapor density

6.15 (vs air)

Quality Level

200

vapor pressure

1 mmHg ( 145 °C)

product line

ReagentPlus®

assay

99%

form

powder or flakes

autoignition temp.

1004 °F

color

blue-violet fluorescence

bp

340 °C (lit.)

mp

210-215 °C (lit.)

solubility

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

SMILES string

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

Gene Information

human ... CYP1A2(1544)

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General description

Anthracene derivatives are useful in preparing stable blue-emitting organic electroluminescence devices. It is oxidized to anthracene cis-1,2-dihydrodiol by Mycobacterium sp. strain PYR-12. It forms bis-adducts by [4+2]-cycloaddition reaction with [5,6]-fullerene C60.

Application

Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol .
Anthracene was used to study the photodimerization reaction of anthracene in supercritical CO2.

Legal Information

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

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H319,H410

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

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

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Certificados de análisis (COA)

Lot/Batch Number
MKCW9141
0000239624
MKCS8831
MKCR0570
MKCS0894

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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
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)
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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