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694959

Sigma-Aldrich

Anthracene

sublimed grade, ≥99%

Synonyme(s) :

Anthraxcene, Paranaphthalene

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About This Item

Formule empirique (notation de Hill):
C14H10
Numéro CAS:
120-12-7
Poids moléculaire :
178.23
Numéro C.I. (Colour Index):
10790
Numéro Beilstein :
1905429
Numéro CE :
204-371-1
Numéro MDL:
MFCD00001240
Code UNSPSC :
12352100
eCl@ss :
39011608
ID de substance PubChem :
329761702
Nomenclature NACRES :
NA.22

Qualité

sublimed grade

Densité de vapeur

6.15 (vs air)

Pression de vapeur

1 mmHg ( 145 °C)

Pureté

≥99%

Forme

crystalline

Température d'inflammation spontanée

1004 °F

Perte

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

Point d'ébullition

340 °C (lit.)

Pf

210-215 °C (lit.)

Solubilité

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

Énergie orbitale

HOMO 5.7 eV 
LUMO 1.7 eV 

Chaîne SMILES 

c1ccc2cc3ccccc3cc2c1

InChI

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

Clé InChI

MWPLVEDNUUSJAV-UHFFFAOYSA-N

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Description générale

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 .

Pictogrammes

Exclamation markEnvironment
GHS07,GHS09

Mention d'avertissement

Warning

Mentions de danger

H319,H410

Classification des risques

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

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

249.8 °F - closed cup

Point d'éclair (°C)

121.0 °C - closed cup

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Naphthalene 99%

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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
Gang Liu et al.
Journal of the American Chemical Society, 135(12), 4805-4814 (2013-03-05)
We have been developing the methodology to discriminate the handedness and diameter of single-walled carbon nanotubes (SWNTs) through molecular recognition using chiral diporphyrin nanotweezers. Although relatively small diameters of SWNTs (<1.0 nm) were recognized well, nanotweezers were not able to
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
Kohei Yazaki et al.
Chemical communications (Cambridge, England), 49(16), 1630-1632 (2013-01-23)
A bowl-shaped organic host was prepared by linking two anthracene-embedded bispyridine ligands with two methylene spacers. The water-soluble host has a hemispherical hydrophobic cavity (∼1 nm in diameter) with two cationic methylenebispyridinyl (Lewis acidic) moieties and shows the selective recognition
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