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N10970

Anthraquinone

analytical standard

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About This Item

Fórmula empírica (Notação de Hill):
C14H8O2
Número CAS:
84-65-1
Peso molecular:
208.21
Beilstein:
390030
Número CE:
201-549-0
Número MDL:
MFCD00001188
Código UNSPSC:
41116107
ID de substância PubChem:
329818484

grau

analytical standard

densidade de vapor

7.16 (vs air)

pressão de vapor

1 mmHg ( 190 °C)

embalagem

ampule of 1 g

fabricante/nome comercial

Chem Service, Inc. PS-926

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

p.e.

379-381 °C (lit.)

pf

284-286 °C (lit.)

Formato

neat

cadeia de caracteres SMILES

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

chave InChI

RZVHIXYEVGDQDX-UHFFFAOYSA-N

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Aplicação

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

Pictogramas

Health hazardExclamation mark
GHS08,GHS07

Palavra indicadora

Danger

Frases de perigo

H317,H350

Classificações de perigo

Carc. 1B - Skin Sens. 1

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

482.0 °F - closed cup

Ponto de fulgor (°C)

250 °C - closed cup

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Lot/Batch Number

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C Ma et al.
Journal of applied microbiology, 112(5), 883-891 (2012-03-06)
To isolate an alkaliphilic bacterium and to investigate its ability of extracellular reduction. An alkaliphilic and halotolerant humus-reducing anaerobe, Bacillus pseudofirmus MC02, was successfully isolated from a pH 10·0 microbial fuel cell. To examine its ability of extracellular reduction, AQDS
Seyed Hadi Ebrahimia et al.
Archives of animal nutrition, 65(4), 267-277 (2011-09-06)
The objective of the present study was to investigate the hypothesis that 9,10-anthraquinone (AQ) in combination with fumaric acid (FMA) may provide complementary effects to inhibit methanogens and enhance rumen's capacity for better utilisation of FMA towards propionate production. Three
Hai-Yu Hu et al.
Organic letters, 10(21), 5035-5038 (2008-10-11)
The first selective catalytic hydrogenation induced by the artificial helix based on oligo(phenanthroline dicarboxamide)s containing a 9,10-anthraquinone subunit is described. Due to the steric hindrance within the helically folded oligomers, the selective reductions of the anthraquinone units were completely different
B Hemmateenejad et al.
Talanta, 77(1), 351-359 (2008-09-23)
The retention behavior of 28 synthesized 9,10-anthraquinone derivatives in a reversed-phase (RP) high performance liquid chromatography (HPLC) system has been studied on a C18-RP column using acetonitrile-water mixtures as mobile phase. The influences of the composition of mobile phase and
Guillaume Fayet et al.
Journal of molecular graphics & modelling, 28(6), 465-471 (2009-12-29)
This work presents a quantitative structure-property relationship (QSPR)-based approach allowing an accurate prediction of the excited-state properties of organic dyes (anthraquinones and azobenzenes) from ground-state molecular descriptors, obtained within the (conceptual) density functional theory (DFT) framework. The ab initio computation
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