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Merck
CN

31466

Supelco

蒽醌

PESTANAL®, analytical standard

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About This Item

经验公式(希尔记法):
C14H8O2
CAS号:
分子量:
208.21
Beilstein:
390030
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:

等级

analytical standard

质量水平

蒸汽密度

7.16 (vs air)

蒸汽压

1 mmHg ( 190 °C)

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

沸点

379-381 °C (lit.)

mp

284-286 °C (lit.)

应用

agriculture
environmental

包装形式

neat

SMILES字符串

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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应用

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

推荐产品

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.

法律信息

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Health hazardExclamation mark

警示用语:

Danger

危险声明

危险分类

Carc. 1B - Skin Sens. 1

储存分类代码

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 1

闪点(°F)

482.0 °F - closed cup

闪点(°C)

250 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(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
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
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
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
Myriam Bonose-Crosnier de Bellaistre et al.
Journal of chromatography. A, 1218(6), 778-786 (2011-01-14)
Chromatographic study of natural products helps to determine their molecular composition and to identify their sources (biological, geographical, etc.). However, identifying anthraquinoids is still a challenge because this chemical family is composed of more than half a thousand molecules. In

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