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Key Documents

Safety Information

694959

Sigma-Aldrich

Anthracene

sublimed grade, ≥99%

Synonym(s):

Anthraxcene, Paranaphthalene

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¥5,314.03

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:
12352100
eCl@ss:
39011608
PubChem Substance ID:
NACRES:
NA.22

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grade

sublimed grade

Quality Level

vapor density

6.15 (vs air)

vapor pressure

1 mmHg ( 145 °C)

Assay

≥99%

form

crystalline

autoignition temp.

1004 °F

loss

0.5 wt. % loss on heating, 155°C (typical, TGA)

bp

340 °C (lit.)

mp

210-215 °C (lit.)

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This Item
MABE326MABE222ABE498
antibody form

affinity isolated antibody

antibody form

purified antibody

antibody form

purified immunoglobulin

antibody form

affinity isolated antibody

biological source

rabbit

biological source

mouse

biological source

rabbit

biological source

rabbit

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

UniProt accession no.

Q9BY66

UniProt accession no.

Q9BY66

UniProt accession no.

O75164

UniProt accession no.

Q6ZMT4

species reactivity

mouse, human

species reactivity

human

species reactivity

human

species reactivity

human

General description

TGA/DSC Lot specific traces available upon request

Application

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

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 Information

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Payam Payamyar et al.
Chimia, 67(4), 283-285 (2013-08-24)
We describe the challenges involved with extending the limited lateral size of two-dimensional polymers (2DPs). An amphiphilic monomer with three-fold symmetry is chosen to form an ideally tessellated monolayer at the air/water interface. Anthracene [4+4] photo-dimerization is chosen as the
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
Ling-Bao Xing et al.
Langmuir : the ACS journal of surfaces and colloids, 29(9), 2843-2848 (2013-02-12)
A new type of anthracene organogelator based on uracil was obtained using organic aromatic solvents, cyclohexane, DMSO, ethanol, and ethyl acetate. It was further characterized by field-emission scanning electron microscopy and transmission electron microscopy. Specifically, the resulting organogels were demonstrated
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.
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

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