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A89200

Anthracene

Name: Anthracene
Brand: ALDRICH

reagent grade, 97%

Sinónimos:

Anthraxcene, Paranaphthalene

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Fórmula empírica (notación de Hill):

C₁₄H₁₀

Número CAS:

120-12-7

Peso molecular:

178.23

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891381

eCl@ss:

39011608

EC Number:

204-371-1

MDL number:

MFCD00001240

Colour Index Number:

10790

Beilstein/REAXYS Number:

1905429

Assay:

97%

Form:

flakes, powder or solid

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Propiedades

grade

reagent grade

Quality Level

200

vapor density

6.15 (vs air)

vapor pressure

1 mmHg ( 145 °C)

assay

97%

form

flakes, powder or solid

autoignition temp.

1004 °F

bp

340 °C (lit.)

mp

210-215 °C (lit.)

solubility

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)

Descripción

General description

Anthracene, a polycyclic aromatic hydrocarbon, is an important moiety in supramolecular chemistry due to its size and shape and photophysical properties. Its closed-shelled Huckel aromatic structure, fluorescence property, well-resolved absorption and emission bands, high fluorescence quantum yield and nanosecond lifetime makes it an ideal organic fluorophore.

Application

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

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Clase de almacenamiento

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

pictograms

GHS09

signalword

Danger

hcodes

H410,EUH440

pcodes

P201 - P202 - P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - PBT

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Molecular architectures of multi-anthracene assemblies.

Yoshizawa M & Klosterman JK.

Chemical Society Reviews, 43(6), 1885-1898 (2014)

Approaching two-dimensional polymers with macroscopic sizes.

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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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

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