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Supelco

Anthracen

analytical standard

Synonym(e):

Anthrazen, Paranaphthalin

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About This Item

Empirische Formel (Hill-System):
C14H10
CAS-Nummer:
120-12-7
Molekulargewicht:
178.23
Farbindexnummer:
10790
Beilstein:
1905429
EG-Nummer:
204-371-1
MDL-Nummer:
MFCD00001240
UNSPSC-Code:
41116107
eCl@ss:
39011608
PubChem Substanz-ID:
329753832
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Dampfdichte

6.15 (vs air)

Dampfdruck

1 mmHg ( 145 °C)

Selbstzündungstemp.

1004 °F

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

340 °C (lit.)

mp (Schmelzpunkt)

210-215 °C (lit.)

Löslichkeit

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

Anwendung(en)

environmental

Format

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

InChIKey

MWPLVEDNUUSJAV-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Anwendung

Anthracen ist in einer Vielzahl von binären und ternären Mischungen aus Cyclohexanon, Ethylacetat und Methanol löslich.
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.

Empfohlene Produkte

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Piktogramme

Exclamation markEnvironment
GHS07,GHS09

Signalwort

Warning

H-Sätze

H319,H410

Gefahreneinstufungen

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

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 2

Flammpunkt (°F)

249.8 °F - closed cup

Flammpunkt (°C)

121.0 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

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Analysenzertifikate (COA)

Lot/Batch Number
BCCH3998
BCCB5640
BCBW1144
SZBD155XV
SZBB235XV

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Die Dokumentenbibliothek aufrufen

Oxidation of Anthracene and Benzo[a]pyrene by Laccases from Trametes versicolor.
Collins PJ
Applied and Environmental Microbiology, 62(12), 4563-4567 (1996)
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)
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
Mohammed S Almeataq et al.
Chemical communications (Cambridge, England), 49(22), 2252-2254 (2013-02-12)
The preparation of anthracene-based low band gap conjugated polymers comprising 2,6-linked anthracene and dithienyl-benzo[c][1,2,5]thiadiazole or dibithiophenyl-benzo[c][1,2,5]thiadiazole alternate repeat units is presented. The photophysical, electrochemical and photovoltaic properties of the polymers in bulk heterojunction solar cells using PC(71)BM as an acceptor
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