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694959

Sigma-Aldrich

Anthracene

sublimed grade, ≥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:
329761702
NACRES:
NA.22

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.)

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 

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

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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 .

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Quinine sulfate meets USP testing specifications, monograph mol wt. 782.94 ((C20H24N2O2)2 . H2SO4 . 2H2O)

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Naphthalene 99%

Sigma-Aldrich

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Naphthalene

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
Dabin Shi et al.
Dalton transactions (Cambridge, England : 2003), 42(2), 484-491 (2012-10-20)
A novel three-dimensional (3D) porous metal-organic framework, {[Cd(L)(H(2)O)]·3H(2)O}(∞) (1) (L-H(2) = 4,4'-(9,10-anthracenediyl)dibenzoic acid), was synthesized. 1 has a 3D framework formed by L connectors and the infinite {Cd(O(2)CR)(2)}(∞) secondary building units (SBUs). Compound 1 was characterized by IR spectroscopy, thermogravimetry
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
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