31581

Supelco

Anthracene

analytical standard

Sinônimo(s):
Anthraxcene, Paranaphthalene
Empirical Formula (Hill Notation):
C14H10
Número CAS:
Peso molecular:
178.23
Número do índice de cores:
10790
Beilstein/REAXYS Number:
1905429
Número EC:
Número MDL:
eCl@ss:
39011608
ID de substância PubChem:
NACRES:
NA.24

Nível de qualidade

100

grau

analytical standard

densidade de vapor

6.15 (vs air)

pressão de vapor

1 mmHg ( 145 °C)

forma

neat

temperatura de autoignição

1004 °F

prazo de validade

limited shelf life, expiry date on the label

aplicação(ões)

HPLC: suitable
gas chromatography (GC): suitable

pb

340 °C (lit.)

pf

210-215 °C (lit.)

solubilidade

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

Setor em destaque

Environmental

formato

neat

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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Descrição geral

Anthracene is a low-molecular weight polycyclic aromatic hydrocarbon (PAH). It acts as starting material for the production of anthraquinone.

Aplicação

Anthracene has been used as reference standard in identifying and quantifying PAHs in edible oils using GC–MS method.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol .

Pictogramas

Environment

Palavra indicadora

Warning

Frases de perigo

Declarações de precaução

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

RIDADR

UN 3077 9 / PGIII

Ponto de fulgor (ºF)

249.8 °F - closed cup

Ponto de fulgor (ºC)

121.0 °C - closed cup

Polycyclic aromatic hydrocarbons (PAHs) in edible oils by gas chromatography coupled with mass spectroscopy.
Hossain, M. Amzad, and S. M. Salehuddin.
Arabian Journal of Chemistry, 5.3, 391-396 (2012)
Oxidation of Anthracene and Benzo[a]pyrene by Laccases from Trametes versicolor.
Collins PJ
Applied and Environmental Microbiology, 62(12), 4563-4567 (1996)
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...
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...
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.
Protocolos
US EPA Method 610 describes the analysis of polynuclear aromatic hydrocarbons (commonly referred to as PAHs or PNAs) by both HPLC and GC.
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