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Anthracene

analytical standard

Synonym(s):

Anthraxcene, Paranaphthalene

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250 MG
€102.00

€102.00


Estimated to ship on16 April 2025


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250 MG
€102.00

About This Item

Empirical Formula (Hill Notation):
C14H10
CAS Number:
Molecular Weight:
178.23
Colour Index Number:
10790
Beilstein:
1905429
EC Number:
MDL number:
UNSPSC Code:
41116107
eCl@ss:
39011608
PubChem Substance ID:
NACRES:
NA.24

€102.00


Estimated to ship on16 April 2025


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grade

analytical standard

Quality Level

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

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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General description

Anthracene is a low-molecular weight polycyclic aromatic hydrocarbon (PAH). It acts as starting material for the production of anthraquinone.[1]

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.[2]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Recommended products

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

249.8 °F - closed cup

Flash Point(C)

121.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

EU REACH SVHC Candidate List

CAS No.

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Certificates of Analysis (COA)

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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)
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
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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