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Merck

31581

Anthracene

analytical standard

Synonyme(s) :

Anthraxcene, Paranaphthalene

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A propos de cet article

Formule empirique (notation de Hill) :
C14H10
Numéro CAS:
120-12-7
Poids moléculaire :
178.23
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329753832
eCl@ss:
39011608
EC Number:
204-371-1
MDL number:
MFCD00001240
Colour Index Number:
10790
Beilstein/REAXYS Number:
1905429

Principaux documents

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Nom du produit

Anthracene, analytical standard

InChI key

MWPLVEDNUUSJAV-UHFFFAOYSA-N

InChI

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

SMILES string

c1ccc2cc3ccccc3cc2c1

grade

analytical standard

vapor density

6.15 (vs air)

vapor pressure

1 mmHg ( 145 °C)

autoignition temp.

1004 °F

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

340 °C (lit.)

mp

210-215 °C (lit.)

solubility

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

application(s)

environmental

format

neat

Quality Level

100

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Catégories apparentées

Application

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

General description

Anthracene is a low-molecular weight polycyclic aromatic hydrocarbon (PAH). It acts as starting material for the production of anthraquinone.
This compound is listed in the SVHC (Substances of very high concern) candidate list of ECHA (European Chemicals Agency)

Other Notes

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.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H319,H410

Hazard Classifications

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

Classe de stockage

11 - Combustible Solids

wgk

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

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Certificats d'analyse (COA)

Lot/Batch Number
BCCN6456
BCCH3998
BCCB5640
BCBW1144

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Consulter la Bibliothèque de documents

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
Qiuli Zhao et al.
Chemical communications (Cambridge, England), 48(95), 11671-11673 (2012-10-26)
Perylene bisimide derivatives substituted with one and two tetraphenylethene moieties at 1 and 1,7-postions show distinct optical properties. The former displays characteristic emission features of perylene bisimides in solution and red emission in the aggregate state, while the latter is
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