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694959

Sigma-Aldrich

Anthracene

sublimed grade, ≥99%

Sinonimo/i:

Anthraxcene, Paranaphthalene

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About This Item

Formula empirica (notazione di Hill):
C14H10
Numero CAS:
120-12-7
Peso molecolare:
178.23
Colour Index:
10790
Beilstein:
1905429
Numero CE:
204-371-1
Numero MDL:
MFCD00001240
Codice UNSPSC:
12352100
eCl@ss:
39011608
ID PubChem:
329761702
NACRES:
NA.22

Grado

sublimed grade

Densità del vapore

6.15 (vs air)

Tensione di vapore

1 mmHg ( 145 °C)

Saggio

≥99%

Forma fisica

crystalline

Temp. autoaccensione

1004 °F

Perdita

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

P. eboll.

340 °C (lit.)

Punto di fusione

210-215 °C (lit.)

Solubilità

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

Energia dell’orbitale

HOMO 5.7 eV 
LUMO 1.7 eV 

Stringa SMILE

c1ccc2cc3ccccc3cc2c1

InChI

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

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Descrizione generale

TGA/DSC Lot specific traces available upon request

Applicazioni

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

Pittogrammi

Exclamation markEnvironment
GHS07,GHS09

Avvertenze

Warning

Indicazioni di pericolo

H319,H410

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

249.8 °F - closed cup

Punto d’infiammabilità (°C)

121.0 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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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
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
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
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
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.
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