Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

48567

Supelco

Anthracene

analytical standard

Synonym(s):

Anthraxcene, Paranaphthalene

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Empirical Formula (Hill Notation):
C14H10
CAS Number:
120-12-7
Molecular Weight:
178.23
Colour Index Number:
10790
Beilstein/REAXYS Number:
1905429
EC Number:
204-371-1
MDL number:
MFCD00001240
UNSPSC Code:
12000000
PubChem Substance ID:
24872114
Pricing and availability is not currently available.

grade

analytical standard

vapor density

6.15 (vs air)

vapor pressure

1 mmHg ( 145 °C)

CofA

current certificate can be downloaded

autoignition temp.

1004 °F

packaging

ampule of 5000 mg

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

storage temp.

2-30°C

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

Gene Information

human ... CYP1A2(1544)

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Anthracene is a polycyclic aromatic hydrocarbon often formed by incomplete combustion of organic materials.[1]

Application

Anthracene has been shown to be soluble in a variety of binary and ternary mixtures of cyclohexanone, ethyl acetate, and methanol .
Anthracene may be used as an analytical reference standard for the determination of the analyte in aqueous solution by synchronous fluorimetry.[2]
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H319,H410

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk_germany

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LC27038V
LC20963V
LC10254V
LC02331V
LB96498V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 5

1 of 5

Acenaphthene analytical standard

Supelco

48500-U

Acenaphthene

Fluoranthene analytical standard

Supelco

48535

Fluoranthene

Anthanthrene BCR®, certified reference material

BCR091

Anthanthrene

Benzo[ghi]perylene analytical standard

Supelco

48491

Benzo[ghi]perylene

Benz[a]anthracene analytical standard

Supelco

48563

Benz[a]anthracene

Determination of polycyclic aromatic hydrocarbons in water samples using high-performance liquid chromatography with amperometric detection.
Nirmaier HP, et al.
Journal of Chromatography A, 730(1-2), 169-175 (1996)
Simultaneous determination of dissolved anthracene and pyrene in aqueous solution by synchronous fluorimetry.
Cai ZQ, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 69(1), 130-133 (2008)
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
View All Related Papers

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service