31466
蒽醌
PESTANAL®, analytical standard
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关于此项目
经验公式（希尔记法）:
C14H8O2
化学文摘社编号:
分子量:
208.21
EC Number:
201-549-0
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
390030
MDL number:
InChI key
RZVHIXYEVGDQDX-UHFFFAOYSA-N
InChI
1S/C14H8O2/c15-13-9-5-1-2-6-10(9)14(16)12-8-4-3-7-11(12)13/h1-8H
SMILES string
O=C1c2ccccc2C(=O)c3ccccc13
grade
analytical standard
vapor density
7.16 (vs air)
vapor pressure
1 mmHg ( 190 °C)
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
379-381 °C (lit.)
mp
284-286 °C (lit.)
application(s)
agriculture
environmental
format
neat
Quality Level
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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.
Other Notes
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Carc. 1B - Skin Sens. 1
存储类别
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
wgk
WGK 1
flash_point_f
482.0 °F - closed cup
flash_point_c
250 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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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
Ying-Jung Chen et al.
Chemistry, an Asian journal, 10(4), 1025-1034 (2015-01-27)
Fluorescent chemosensors 1 and 2, with 1,2,4-oxadiazoles as the binding ligands and anthracene as the fluorophore, were synthesized through sequential 1,3-dipolar cycloaddition reactions of 25,27-dioxyacetonitrilecalix[4]arenes 8 and 11. The fluorescence of 1 was severely quenched by both Fe(3+) and Cu(2+)
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