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N10970

Anthraquinone

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C14H8O2
CAS Number:
84-65-1
Molecular Weight:
208.21
Beilstein/REAXYS Number:
390030
EC Number:
201-549-0
MDL number:
MFCD00001188
UNSPSC Code:
41116107
PubChem Substance ID:
329818484

grade

analytical standard

vapor density

7.16 (vs air)

vapor pressure

1 mmHg ( 190 °C)

packaging

ampule of 1 g

manufacturer/tradename

Chem Service, Inc. PS-926

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

379-381 °C (lit.)

mp

284-286 °C (lit.)

format

neat

SMILES string

O=C1c2ccccc2C(=O)c3ccccc13

InChI

1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H

InChI key

RZVHIXYEVGDQDX-UHFFFAOYSA-N

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Application

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

pictograms

Health hazardExclamation mark
GHS08,GHS07

signalword

Danger

hcodes

H317,H350

Hazard Classifications

Carc. 1B - Skin Sens. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 1

flash_point_f

482.0 °F - closed cup

flash_point_c

250 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number

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Leila Qasemian et al.
Chemosphere, 84(10), 1321-1328 (2011-06-15)
Mediterranean coastal ecosystems are known to be highly subject to natural and anthropic environmental stress. In this study, we examine the effects of anthracene as a common pollutant on the total microbial communities from a Pinus halepensis litter of a
A A Stepanov et al.
The Journal of organic chemistry, 76(21), 8737-8748 (2011-09-14)
The nature of products in the diazotization of 1-amino-2-acetylenyl-9,10-anthraquinones strongly depends on the nature of substituents at both the alkyne and at the anthraquinone core. Donor substitution (NHAr, OH) at the fourth position stabilizes the diazonium salt at C1, decelerating
Witold Nowik et al.
Journal of chromatography. A, 1218(23), 3636-3647 (2011-05-03)
A series of reversed phases bonded with several functional groups was investigated for separation of anthraquinone derivatives, following the previous work, dedicated to the selectivity of octadecyl silica bonded phases. Considering wide diversity of substitutions in hydrophobic anthraquinone skeleton, interactions
Gui'e Xie et al.
British journal of pharmacology, 159(3), 689-697 (2010-02-05)
The aims of this study were to investigate the anti-cancer activity of SZ-685C, an anthracycline analogue isolated from marine-derived mangrove endophytic fungi, and to explore the molecular mechanisms underlying such activity. The effect of SZ-685C on the viability of cancer
Rakesh Kumar et al.
Molecular diversity, 15(3), 687-695 (2010-11-30)
H(2)O(2) mediated oxidation of alcohols in ionic liquid is revisited, wherein, ionic liquids under the influence of microwave irradiation have been found to facilitate activation of H(2)O(2) without any metal catalyst in aqueous condition. The method utilizes a neutral ionic
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