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N10970

Anthraquinone

analytical standard

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About This Item

Formula empirica (notazione di Hill):
C14H8O2
Numero CAS:
84-65-1
Peso molecolare:
208.21
Beilstein:
390030
Numero CE:
201-549-0
Numero MDL:
MFCD00001188
Codice UNSPSC:
41116107
ID PubChem:
329818484

Grado

analytical standard

Densità del vapore

7.16 (vs air)

Tensione di vapore

1 mmHg ( 190 °C)

Confezionamento

ampule of 1 g

Produttore/marchio commerciale

Chem Service, Inc. PS-926

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. ebollizione

379-381 °C (lit.)

Punto di fusione

284-286 °C (lit.)

Formato

neat

Stringa SMILE

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
RZVHIXYEVGDQDX-UHFFFAOYSA-N

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Applicazioni

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

Pittogrammi

Health hazardExclamation mark
GHS08,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H317,H350

Classi di pericolo

Carc. 1B - Skin Sens. 1

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

482.0 °F - closed cup

Punto d’infiammabilità (°C)

250 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number

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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
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
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
Sana Zafar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 114, 164-169 (2013-06-19)
Nonlinear optical properties of 1,4-Diamino-9,10-Anthraquinone dye in solution at different concentrations are investigated by utilizing single beam Z-scan technique using a low power continuous wave laser (λ=532 nm). The anthraquinone dye is found to exhibit self-defocusing and reverse saturable absorption
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